Polymorphic form of reduced beta-nicotinamide mononucleotide calcium salt and preparation method and application thereof

Abstract

The invention relates to a compound NMNH calcium salt, in particular to a polymorphic substance of a reduced beta-nicotinamide mononucleotide calcium salt, a preparation method of the polymorphic substance, application of the polymorphic substance as a pharmaceutical ingredient, a health care product ingredient, a cosmetic ingredient or a food additive, and preparations containing the salts. Belongs to the fields of medicines, health-care products, cosmetics and food additives. Specifically, the invention describes an NMNH calcium salt polymorphic substance, the crystal shows long-term continuous stability, the stability performance and moisture absorption resistance of the crystal are obviously superior to those of NMNH disodium salt, and the crystal is more beneficial to long-term storage, popularization and marketing. The preparation process of the NMNH calcium salt crystal is simple, easy to control and suitable for large-scale production.

Description

Technical Field

[0001] The present invention relates to the field of chemical raw materials for medicines, health products, cosmetics and food additives, and in particular to a polymorph of reduced β-nicotinamide mononucleotide calcium salt and a preparation method and use thereof. Background Art

[0002] As one of the most popular molecules in the field of anti-aging, nicotinamide adenine dinucleotide (NAD + ) has become the core of anti-aging substances in all generations. + It is an important coenzyme required for more than 500 enzymatic reactions and is well known for its role in oxidation and reduction (Ansari and Raghava, 2010; Rajman et al., 2018; Stein and Imai, 2012). More and more studies indicate that increasing NAD + Equivalent amounts can significantly improve multiple organ functions, including liver function, kidney function, cardiac function, and skeletal muscle function (Canto et al., 2012; Mills et al., 2016; Rajman et al., 2018). + It can be synthesized using tryptophan in the de novo biosynthesis pathway, nicotinic acid (NA) in the preiss-handler pathway, and nicotinamide (NAM), nicotinamide riboside (NR), and nicotinamide mononucleotide (NMN) in the salvage pathway (Canto et al., 2015; Chiarugi et al., 2012; Johnson and Imai, 2018). In particular, as NAD + The key intermediates, NAM, NR, and NMN, have been extensively studied for their potential therapeutic effects in many mouse disease models (Mills et al., 2016), among which NMN is currently considered the most suitable NAD + Precursor, and currently NMN is hot-selling in the global market and is highly favored by consumers.

[0003] NMNH (molecular structure as shown in formula (A)) is called "reduced nicotinamide mononucleotide" or "reduced β-nicotinamide mononucleotide" in Chinese. It is the reduced form of NMN and is a supplement to NAD. + A new precursor of NAD with better NMN properties + The promoting effect and other biological functions such as increasing cellular antioxidant capacity, reducing fat accumulation, reducing inflammatory response and inhibiting tumor cell growth are health-promoting agents with significant commercial potential (WO2021098725A1).

[0004]

[0005] NMNH is the reduced form of NMN, which is sensitive to air, easily oxidized, and unstable, making it unfavorable for long-term storage and market promotion. WO2023160405 (A1) reports NMNH disodium salt compounds and their crystal forms and amorphous forms. When left open in a stability test chamber at 25°C and 65% RH, the amorphous powder of NMNH disodium salt turned into oil after one day and the purity dropped from 99.30% to 99.02%. The purity of NMNH disodium salt crystal form A solid dropped from 99.33% to 99.01% after 5 days. Such stability cannot meet the shelf life of the product and is not conducive to the market promotion of the product.

[0006] Therefore, there is still an urgent need in this field to develop new salt forms of NMNH compounds with better stability, better suitability for long-term storage and market promotion. Summary of the invention

[0007] The present invention aims to provide a new salt form of NMNH compounds with better stability and better convenience for long-term storage and market promotion, and specifically relates to a polymorph of reduced β-nicotinamide mononucleotide calcium salt, a preparation method and uses thereof.

[0008] In the first aspect of the present invention, a calcium salt crystal of reduced β-nicotinamide mononucleotide represented by formula (I) is provided.

[0009]

[0010] The crystal is a crystalline form selected from the group consisting of crystalline form A, crystalline form B, crystalline form C, crystalline form D, or crystalline form E.

[0011] In another preferred embodiment, the XRPD spectrum of the crystalline form A includes 3 or more (such as 4, 5, 6, 7 or 8) 2θ values ​​selected from the following group: 6.9°±0.2°, 9.5°±0.2°, 12.6°±0.2°, 15.6°±0.2°, 17.9°±0.2°, 21.0°±0.2°, 21.8°±0.2°, 25.4°±0.2°;

[0012] The XRPD spectrum of the crystalline form B comprises 3 or more (e.g., 4, 5, 6, 7 or 8) 2θ values ​​selected from the group consisting of 6.5°±0.2°, 8.1°±0.2°, 11.9°±0.2°, 13.1°±0.2°, 17.6°±0.2°, 21.4°±0.2°, 23.7°±0.2°, and 26.9°±0.2°;

[0013] The XRPD spectrum of the crystalline form C includes 3 or more (such as 4, 5, 6, 7 or 8) 2θ values ​​selected from the following group: 6.2°±0.2°, 9.7°±0.2°, 12.4°±0.2°, 16.1°±0.2°, 17.1°±0.2°, 18.7°±0.2°, 20.8°±0.2°, and 26.6°±0.2°.

[0014] In another preferred embodiment, the crystal of the reduced β-nicotinamide mononucleotide calcium salt is a hydrate, a solvate or an organic solvent-hydrate.

[0015] In another preferred embodiment, the organic solvent-hydrate of the reduced β-nicotinamide mononucleotide calcium salt is ethanol-hydrate or acetone-hydrate.

[0016] In another preferred embodiment, the structural formula of the reduced β-nicotinamide mononucleotide calcium salt is as shown in Formula II:

[0017]

[0018] In the formula, S represents an organic solvent, and H2O is water; when x=0, n>0, it is a hydrate; when x>0, n=0, it is an organic solvate; when x>0, n>0, it is an organic solvent-hydrate.

[0019] In another preferred embodiment, x and / or n are independently an integer or a non-integer.

[0020] In another preferred embodiment, the crystalline form A further has one or more characteristics selected from the following group:

[0021] 1) the XRPD spectrum of the crystalline form A comprises 6 or more 2θ values ​​selected from the group consisting of 6.9°±0.2°, 9.5°±0.2°, 12.6°±0.2°, 13.9°±0.2°, 14.4°±0.2°, 15.6°±0.2°, 16.7°±0.2°, 17.2°±0.2°, 17.9°±0.2°, 18.8°±0.2°, 21.0°±0.2°, 21.8°±0.2°, 23.1°±0.2°, 25.4°±0.2°, 26.5°±0.2°, 27.3°±0.2°, 28.1°±0.2°, 31.5°±0.2°, 32.8°±0.2°, and 35.6°±0.2°;

[0022] 2) The XRPD pattern of the crystalline form A is substantially as follows Figure 1 represented;

[0023] 3) The crystal form A is a hydrate with a water content of 4%wt-13%wt; preferably, the crystal form A is a 1-3 hydrate.

[0024] In another preferred embodiment, the crystalline form A is a hydrate with a water content of 5%wt-12%wt.

[0025] In another preferred embodiment, the crystalline form A is a hydrate with a water content of 6%wt-11%wt.

[0026] In another preferred embodiment, the crystalline form B further has one or more characteristics selected from the following group:

[0027] 1) The XRPD pattern of the crystalline form B comprises 6 or more 2θ values ​​selected from the group consisting of 6.5°±0.2°, 8.1°±0.2°, 11.9°±0.2°, 13.1°±0.2°, 13.5°±0.2°, 14.5°±0.2°, 17.6°±0.2°, 18.0°±0.2°, 18.9°±0.2°, 19.4°±0.2°, 19.7°±0.2°, 20.3°±0.2°, 21.4°±0.2°, 23.7°±0.2°, 24.3°±0.2°, 25.1°±0.2°, 26. 6.4°±0.2°, 26.9°±0.2°, 27.5°±0.2°, 28.7°±0.2°, 29.3°±0.2°, 30.5°±0.2°, 30.9°±0.2°, 31.6°±0.2°, 32.4°±0.2°, 32.9°±0.2°, 34.2°±0.2°, 35.0°±0.2°, 35.4°±0.2°, 36.7°±0.2°, 37.5°±0.2°, 37.9°±0.2°, 38.2°±0.2°, 38.9°±0.2°, 40.2°±0.2°;

[0028] 2) The XRPD pattern of the crystalline form B is substantially as follows Figure 2 represented;

[0029] 3) The crystal form B is a hydrate with a water content of 4%-20%wt; preferably, the crystal form B is a 1-5 hydrate.

[0030] In another preferred embodiment, the crystalline form B is a hydrate with a water content of 5%wt-19%wt.

[0031] In another preferred embodiment, the crystalline form B is a hydrate with a water content of 6% wt-18% wt.

[0032] In another preferred embodiment, the crystalline form C further has one or more characteristics selected from the following group:

[0033] 1) The XRPD spectrum of the crystalline form C comprises 6 or more 2θ values ​​selected from the group consisting of 6.2°±0.2°, 6.8°±0.2°, 9.7°±0.2°, 11.8°±0.2°, 12.4°±0.2°, 14.2°±0.2°, 15.5°±0.2°, 16.1°±0.2°, 17.1°±0.2°, 17.9°±0.2°, 18.7°±0.2°, 20.1°±0.2°, 20.8°±0.2°, 21.5°±0.2°, 22.9°±0.2°, 23.5°±0.2°, 24.1°±0.2°, 24.5°±0.2° .2°, 25.0°±0.2°, 25.8°±0.2°, 26.6°±0.2°, 27.3°±0.2°, 27.7°±0.2°, 28.3°±0.2°, 28.5°±0.2°, 29.7°±0.2°, 30.3°±0.2°, 30.8°±0.2°, 31.4°±0.2°, 32.8°±0.2°, 33.4°±0.2°, 34.4°±0.2°, 35.3°±0.2°, 36.0°±0.2°, 37.1°±0.2°, 38.0°±0.2°, 39.0°±0.2°, 39.8°±0.2°;

[0034] 2) The XRPD pattern of the crystalline form C is substantially as follows Figure 3 represented;

[0035] 3) The crystal form C is a hydrate with a water content of 4%wt-13%wt; preferably, the crystal form C is a 1-3 hydrate.

[0036] In another preferred embodiment, the crystalline form C is a hydrate with a water content of 5%wt-12%wt.

[0037] In another preferred embodiment, the crystalline form C is a hydrate with a water content of 6% wt-11% wt.

[0038] In another preferred embodiment, the crystalline form D has one or more characteristics selected from the following group:

[0039] 1) the XRPD spectrum of the crystalline form D comprises 3 or more 2θ values ​​selected from the group consisting of 7.0°±0.2°, 8.0°±0.2°, 12.0°±0.2°, 17.8°±0.2°, 20.2°±0.2°, and 26.9°±0.2°;

[0040] 2) the XRPD spectrum of the crystalline form D further comprises one or more 2θ values ​​selected from the following group: 13.5°±0.2°, 14.2°±0.2°, 24.0°±0.2°;

[0041] 3) the XRPD spectrum of the crystalline form D comprises 6 or more 2θ values ​​selected from the group consisting of 7.0°±0.2°, 8.0°±0.2°, 12.0°±0.2°, 13.5°±0.2°, 14.2°±0.2°, 15.7°±0.2°, 17.8°±0.2°, 19.2°±0.2°, 20.2°±0.2°, 23.5°±0.2°, 24.0°±0.2°, 24.5°±0.2°, 26.1°±0.2°, 26.9°±0.2°, 28.7°±0.2°, 30.5°±0.2°, and 33.8°±0.2°;

[0042] 4) The XRPD pattern of the crystal form D is substantially as follows Figure 4 represented;

[0043] 5) The crystal form D 1 The H NMR spectrum is basically Figure 7 represented;

[0044] 6) The crystal form D is an ethanol-hydrate, containing about 0.2-0.5 ethanol and a water content of 16%wt-23%wt; preferably, the crystal form D is a 3-6 hydrate.

[0045] In another preferred embodiment, the crystal form D is ethanol-hydrate with a water content of 18% wt-21% wt.

[0046] In another preferred embodiment, the crystalline form E has one or more characteristics selected from the following group:

[0047] 1) the XRPD spectrum of the crystalline form E comprises 3 or more 2θ values ​​selected from the following group: 6.9°±0.2°, 8.0°±0.2°, 11.9°±0.2°, 17.8°±0.2°, 20.2°±0.2°, 26.9°±0.2°;

[0048] 2) the XRPD spectrum of the crystalline form E further comprises one or more 2θ values ​​selected from the following group: 13.5°±0.2°, 14.2°±0.2°, 24.0°±0.2°;

[0049] 3) the XRPD spectrum of the crystalline form E comprises 6 or more 2θ values ​​selected from the group consisting of 6.9°±0.2°, 8.0°±0.2°, 11.9°±0.2°, 13.5°±0.2°, 14.2°±0.2°, 15.7°±0.2°, 17.8°±0.2°, 18.8°±0.2°, 19.2°±0.2°, 20.2°±0.2°, 24.1°±0.2°, 26.0°±0.2°, 26.9°±0.2°, 28.7°±0.2°, 30.7°±0.2°, and 33.9°±0.2°;

[0050] 4) The XRPD pattern of the crystalline form E is substantially as follows Figure 5 represented;

[0051] 5) The crystal form E 1 The H NMR spectrum is basically Figure 8 represented;

[0052] 6) The crystal form E is an acetone monohydrate, containing about 0.2-0.5 acetone and a water content of 16%wt-23%wt; preferably, the crystal form E is a 3-6 hydrate.

[0053] In another preferred embodiment, the crystalline form E is acetone-hydrate with a water content of 18% wt-21% wt.

[0054] In a second aspect of the present invention, there is provided a method for preparing the crystal according to the first aspect, the method comprising the following steps:

[0055] (I) Preparation of Form A:

[0056] I-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent;

[0057] I-2) adding a second solvent dropwise to the reduced β-nicotinamide mononucleotide calcium salt solution described in step I-1) at 40-50° C., filtering the crystals and drying at 40-50° C. to obtain a crystalline form A of the reduced β-nicotinamide mononucleotide calcium salt, wherein the first solvent is selected from water; the second solvent is selected from water, methanol, ethanol, n-propanol, isopropanol, acetone, acetonitrile, tetrahydrofuran, or a mixed solvent thereof;

[0058] (II) Preparation of Form B:

[0059] II-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent;

[0060] II-2) adding a second solvent dropwise to the reduced β-nicotinamide mononucleotide calcium salt solution described in step II-1) at 20-30° C., filtering the crystals and drying at 20-30° C. to obtain reduced β-nicotinamide mononucleotide calcium salt crystalline form B, wherein the first solvent is selected from water; the second solvent is selected from water, methanol, or a mixed solvent thereof;

[0061] (III) Preparation of Form C:

[0062] III-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent;

[0063] III-2) adding a second solvent to the reduced β-nicotinamide mononucleotide calcium salt solution of step III) at 20-30° C., filtering the crystals, and then drying at 40-50° C. to obtain reduced β-nicotinamide mononucleotide calcium salt crystalline form C, wherein the first solvent is selected from water; the second solvent is selected from water, methanol, or a mixed solvent thereof;

[0064] (IV) Preparation of Form D:

[0065] IV-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent;

[0066] IV-2) adding a second solvent to the reduced β-nicotinamide mononucleotide calcium salt solution of step IV-1) at 20-30° C., filtering the crystals, and then drying at 30-40° C. to obtain a crystalline form D of the reduced β-nicotinamide mononucleotide calcium salt, wherein the first solvent is selected from water; and the second solvent is selected from water, ethanol, or a mixed solvent thereof;

[0067] (V) Preparation of Form E:

[0068] V-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent;

[0069] V-2) adding a second solvent dropwise to the reduced β-nicotinamide mononucleotide calcium salt solution described in step V-1) at 20-30° C., filtering the solution by crystallization, and then drying at 30-40° C. to obtain the reduced β-nicotinamide mononucleotide calcium salt crystalline form E, wherein the first solvent is selected from water; and the second solvent is selected from water, acetone, or a mixed solvent thereof.

[0070] In another preferred embodiment, the solution containing reduced β-nicotinamide mononucleotide calcium salt is provided by the following method: adding reduced β-nicotinamide mononucleotide calcium salt to a first solvent to obtain a solution containing reduced β-nicotinamide mononucleotide calcium salt, or generating a reduced β-nicotinamide mononucleotide calcium salt solution in situ in the reaction solution.

[0071] In another preferred embodiment, the method for preparing the crystal form comprises the steps of:

[0072] 1) providing a solution comprising reduced β-nicotinamide mononucleotide calcium salt in a first solvent;

[0073] 2) Under stirring conditions, a second solvent is added dropwise to the reduced β-nicotinamide mononucleotide calcium salt solution described in step 1) to obtain reduced β-nicotinamide mononucleotide calcium salt crystals by crystallization.

[0074] In another preferred embodiment, the first solvent and the second solvent are the same or different, and are independently selected from the following groups: water, acetonitrile, tetrahydrofuran, methyl tert-butyl ether, 2-methyltetrahydrofuran, dichloromethane, N,N-dimethylformamide, N,N-dimethylacetamide, N,N-diethylformamide, dimethyl sulfoxide, ethyl acetate, isopropyl acetate, ketone solvents, alcohol solvents, or a combination thereof.

[0075] In another preferred embodiment, the ketone solvent is selected from the following group: acetone, 2-butanone, methyl isobutyl ketone, methyl tert-butyl ketone, 3-methyl-2-butanone, or a combination thereof.

[0076] In another preferred embodiment, the alcohol solvent is selected from the group consisting of methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, n-pentanol, or a combination thereof.

[0077] In the third aspect of the present invention, a composition is provided, comprising: (a) the crystal as described in the first aspect, and (b) a pharmaceutically acceptable excipient or carrier, or an excipient or carrier acceptable for health products, or an excipient or carrier acceptable for cosmetics, or an excipient or carrier acceptable for food.

[0078] In another preferred embodiment, the composition is selected from the following group: a pharmaceutical composition, a health product composition, a cosmetic composition, or a food composition.

[0079] In another preferred embodiment, the pharmaceutical composition comprises: (a) any one of the crystals described in the first aspect, and (b) a pharmaceutically acceptable excipient or carrier.

[0080] In another preferred embodiment, the dosage form of the pharmaceutical composition is selected from the following group: oral preparations, injection dosage forms, respiratory tract administration dosage forms, skin administration dosage forms, mucosal administration dosage forms, cavity administration dosage forms, etc.

[0081] In another preferred embodiment, the health care product composition comprises: (a) any one of the crystals described in the first aspect, and (b) an auxiliary material or carrier acceptable for health care products.

[0082] In another preferred embodiment, the cosmetic composition comprises: (a) any one of the crystals described in the first aspect, and (b) cosmetically acceptable excipients or carriers.

[0083] In another preferred embodiment, the cosmetic composition includes cosmetics selected from the following groups: skin cosmetics, hair cosmetics, beauty cosmetics, and special function cosmetics.

[0084] In another preferred embodiment, the food composition comprises: (a) any one of the crystals described in the first aspect, and (b) an auxiliary material or carrier acceptable to food.

[0085] In the fourth aspect of the present invention, there is provided a use of the crystal according to the first aspect for preparing medicines, health products, cosmetics or food additives.

[0086] In another preferred embodiment, the drug is used to protect the optic nerve, improve retinal damage, prevent / treat hair loss, prevent / improve cardiovascular and cerebrovascular diseases, inhibit renal tubular damage and aging, prevent liver fibrosis, improve fatty liver disease, improve dry eye symptoms, repair kidney damage, prevent diabetes / nephropathy, improve sarcopenia symptoms in the elderly, treat chronic inflammation, alleviate the condition of patients with polycystic ovary syndrome, prevent / delay glaucoma, reduce neuroinflammation, reduce the cardiac toxicity of anthracycline chemotherapy drugs, assist in cerebral infarction recovery, prevent and treat heart failure in the elderly, etc.

[0087] In another preferred embodiment, the health care products are used to slow down cell aging, delay reproductive aging in women, improve fertility, improve menopause, enhance male sexual function, improve sleep, relieve mood, increase energy, improve cardiovascular function, improve cardiovascular health, improve immunity, improve sub-health, prevent tumors, prevent Alzheimer's disease, etc.

[0088] In another preferred embodiment, the cosmetics are used to improve the function of damaged cells, improve skin quality / hair quality, prevent / treat skin photoaging, maintain skin softness and elasticity, delay skin aging, etc.

[0089] In another preferred embodiment, the food additive is used to improve appetite, improve digestive function, promote metabolism, promote hair / nail growth, etc., and improve nutritional value.

[0090] It should be understood that within the scope of the present invention, the above-mentioned technical features of the present invention and the technical features specifically described below (such as embodiments) can be combined with each other to form a new or preferred technical solution. Due to space limitations, they will not be described one by one here. BRIEF DESCRIPTION OF THE DRAWINGS

[0091] Figure 1 The XRPD pattern of NMNH calcium salt Form A is shown.

[0092] Figure 2 The XRPD pattern of NMNH calcium salt Form B is shown.

[0093] Figure 3 The XRPD pattern of NMNH calcium salt Form C is shown.

[0094] Figure 4 The XRPD pattern of NMNH calcium salt Form D is shown.

[0095] Figure 5 The XRPD pattern of NMNH calcium salt Form E is shown.

[0096] Figure 6 The NMNH calcium salt hydrate crystal forms A, B and C are shown. 1 H NMR spectrum.

[0097] Figure 7 The NMNH calcium salt ethanol-hydrate crystal form D is shown. 1 H NMR spectrum.

[0098] Figure 8 The NMNH calcium salt acetone-hydrate crystal form E is shown. 1 H NMR spectrum. DETAILED DESCRIPTION

[0099] The inventors have unexpectedly developed a specific salt of NMNH for the first time through extensive and in-depth research, and the salt is NMNH calcium salt. The present invention shows that the polymorphs of NMNH calcium salt have excellent stability. Compared with the NMNH disodium salt crystal form and amorphous form, the polymorphs of NMNH calcium salt (crystal form A, crystal form B, crystal form C, crystal form D, crystal form E) show long-term stability and anti-hygroscopicity, which are more conducive to long-term storage and market promotion. In addition, the polymorphs of the present invention meet the shelf life of the commodity and are suitable for pharmaceutical compositions, health products, cosmetics, food additives, etc. On this basis, the inventors have completed the present invention.

[0100] Terminology

[0101] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.

[0102] As used herein, n in the term "nH2O" refers to all possible values ​​between 0 and 6, including integers and non-integers; "H2O" is the chemical formula of water, representing water molecules or water. x in "xS" refers to all possible values ​​between 0 and 6, including integers and non-integers; "S" herein refers to organic solvent molecules, which can be any organic solvent.

[0103] As used herein, the term "about" when used in reference to a specific recited value means that the value may vary by no more than 1% from the specific value recited, for example, as used herein, the expression "about 100" includes 99 and 101 and all values ​​therebetween (e.g., 99.1, 99.2, 99.3, 99.4, etc.).

[0104] As used herein, the term "comprising" or "including (comprising)" may be open, semi-closed and closed. In other words, the term also includes "consisting essentially of" or "consisting of".

[0105] As used herein, the term "n or more 2θ values ​​selected from the following group" refers to any positive integer including n and greater than n (e.g., n, n+1, ...), wherein the upper limit Nup is the number of all 2θ peaks in the group. For example, "3 or more" includes not only 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, ... each positive integer of the upper limit Nup, but also includes "4 or more", "5 or more", "6 or more", etc.

[0106] NMNH calcium salt

[0107] As used herein, the terms "reduced β-nicotinamide mononucleotide calcium salt", "β-dihydronicotinamide mononucleotide calcium salt", "dihydronicotinamide mononucleotide calcium salt", "reduced nicotinamide mononucleotide calcium salt", "reduced NMN calcium salt", "NMNH calcium salt", "NMNH-Ca" are used interchangeably, all referring to the salt formed by reduced β-nicotinamide mononucleotide and calcium ions, the structure of which is shown in formula (I). It should be understood that the term includes amorphous, hydrates, solvates, solvent-hydrates and anhydrates.

[0108]

[0109] In the present invention, the preferred reduced NMNH calcium salt is a hydrate, and its structure is shown in formula (II):

[0110]

[0111] Polymorph

[0112] Solids exist in either amorphous or crystalline form. In the case of crystalline form, the molecules are positioned in a three-dimensional lattice. When a compound crystallizes from a solution or slurry, it can crystallize in different spatial lattice arrangements (a property known as "polymorphism"), forming crystals with different crystalline forms, which are known as "polymorphs". Different polymorphs of a given substance may differ from one another in one or more physical properties, such as solubility and dissolution rate, true specific gravity, crystal shape, packing mode, flowability and / or solid state stability.

[0113] Polymorphic forms of a compound can exhibit different melting points, hygroscopicity, stability, solubility, bioavailability, biological activity and flowability, which are important factors affecting drugability.

[0114] As used herein, "crystal", "crystal of the present invention" or "polymorph" are used interchangeably and refer to the crystal described in the first aspect of the present invention, whose crystal form is selected from the following group: form A, form B, form C, form D or form E.

[0115] crystallization

[0116] The solution can be manipulated so that the solubility limit of the target compound is exceeded, thereby completing production-scale crystallization. This can be accomplished in a variety of ways, for example, dissolving the compound at a relatively high temperature and then cooling the solution to below the saturation limit. Alternatively, the liquid volume can be reduced by boiling, atmospheric evaporation, vacuum drying, or by some other method. The solubility of the target compound can be reduced by adding an antisolvent or a solvent in which the compound has a low solubility or a mixture of such solvents. Another alternative is to adjust the pH value to reduce solubility. A detailed description of crystallization can be found in Crystallization, 3rd edition, JW Mullens, Butterworth-Heineman Ltd., 1993, ISBN0750611294.

[0117] If it is desired that salt formation and crystallization occur simultaneously, the addition of an appropriate acid or base may result in direct crystallization of the desired salt if the salt is less soluble in the reaction medium than the starting materials. Likewise, completion of the synthesis reaction in a medium in which the final desired form is less soluble than the reactants may result in direct crystallization of the final product.

[0118] Optimization of crystallization can include seeding the crystallization medium with crystals of the desired form. In addition, many crystallization methods use a combination of the above strategies. One implementation is to dissolve the target compound in a solvent at elevated temperature, followed by controlled addition of an appropriate volume of antisolvent to bring the system just below saturation levels. At this point, seeds of the desired form can be added (while maintaining the integrity of the seeds) and the system cooled to complete crystallization.

[0119] Solvate

[0120] During the contact between compound or drug molecules and solvent molecules, it is inevitable that the solvent molecules and compound molecules form a eutectic and remain in the solid material due to external and internal conditions. The substance formed after the compound and solvent crystallize is called a solvate. The types of solvents that easily form solvates with organic compounds include water, methanol, ethanol, benzene, ether, heterocyclic aromatic hydrocarbons, etc.

[0121] Hydrate

[0122] Hydrate is a special solvate. In the pharmaceutical industry, whether in the synthesis of raw materials, drug preparation, drug storage and drug activity evaluation, hydrate is worth discussing separately because of its particularity.

[0123] In the present invention, the crystals of the compound represented by formula (I) may be non-solvates or solvates; the crystal forms A, B and C of the crystals of the compound represented by formula (I) are all hydrates, the crystal form D is an ethanol-hydrate, and the crystal form E is an acetone-hydrate.

[0124] use

[0125] The present invention provides uses of NMNH calcium salt crystals (including crystal form A, crystal form B, crystal form C, crystal form D, and crystal form E): the crystals are highly efficient and broad-spectrum, and can be used in pharmaceutical compositions, health products, cosmetics, food additives, and the like.

[0126] Compared with the prior art, the present invention has the following beneficial effects:

[0127] (1) The crystals of the compound of formula (I) of the present invention (including crystal form A, crystal form B, crystal form C, crystal form D, and crystal form E) have better stability, lower hygroscopicity, and are more conducive to long-term storage and market promotion than the NMNH disodium salt crystal form and amorphous solid.

[0128] (2) The preparation method of the compound crystal of formula (I) (including crystal form A, crystal form B, crystal form C, crystal form D, and crystal form E) of the present invention is simple and suitable for industrial production.

[0129] (3) The crystals of the compound of formula (I) of the present invention (including crystal form A, crystal form B, crystal form C, crystal form D, and crystal form E) can be used in pharmaceutical compositions, health products, cosmetics, food additives, etc.

[0130] The present invention will be further described below in conjunction with specific examples. It should be understood that these examples are only used to illustrate the present invention and are not intended to limit the scope of the present invention. The experimental methods in the following examples without specifying specific conditions are usually based on conventional conditions or the conditions recommended by the manufacturer. Unless otherwise stated, percentages and parts are by weight.

[0131] Unless otherwise defined, all professional and scientific terms used herein have the same meaning as those familiar to those skilled in the art. In addition, any method and material similar or equivalent to the described content can be applied to the method of the present invention.

[0132] Test method:

[0133] XRPD (X-ray powder diffraction) pattern determination method: Bruker D2 Phaser X-ray powder diffractometer; radiation source

[0134] The measurement differences associated with such X-ray powder diffraction analysis results are caused by a variety of factors including: (a) errors in sample preparation (e.g., sample height), (b) instrument errors, (c) calibration differences, (d) operator errors (including errors that occur when determining peak positions), and (e) the nature of the material (e.g., preferred orientation errors). Calibration errors and sample height errors often result in displacements of all peaks in the same direction. When a flat support is used, small differences in sample height will result in large displacements of XRPD peak positions. Systematic studies have shown that sample height differences of 1 mm can result in peak displacements of up to 1° of 2θ. These displacements can be identified from the XRPD spectrum and can be eliminated by compensating for the displacements (applying the system calibration factor to all peak position values) or recalibrating the instrument. As described above, by applying the system calibration factor to make the peak positions consistent, measurement errors from different instruments can be corrected.

[0135] The following examples illustrate the invention without limiting the invention.

[0136] Example 1. Preparation of NMNH calcium salt aqueous solution

[0137] Add 1.7 kg β-NMN and 0.94 kg sodium dithionite to 10 liters of saturated sodium bicarbonate aqueous solution, stir at room temperature overnight, filter to obtain a clear solution, and adjust the pH of the clear solution to 3-4 with 37% hydrochloric acid. Desalt the solution by electrodialysis until the conductivity of the solution drops to 50-100 μS. Adjust the pH of the solution to 10 with calcium hydroxide; or add 0.57 kg calcium chloride and adjust the pH of the solution to 10 with sodium hydroxide; obtain an aqueous solution of NMNH calcium salt, containing about 1.71 kg NMNH calcium salt (the purity of the solution is 94.5% as measured by HPLC).

[0138] Example 2. Preparation of NMNH calcium salt form A

[0139] Take 500 ml of NMNH calcium salt aqueous solution and stir it in a 40-50°C oil bath, slowly add 2L of methanol, and the addition time is greater than 1 hour. After the addition is complete, stir at 40-50°C for 1-2 hours, filter, and dry at 40-50°C to obtain 79.5 g of NMNH calcium salt crystals. The obtained crystals are form A, with a yield of 84.2% and a purity of 99.83%.

[0140] The obtained solid was subjected to X-ray powder diffraction test, and the XRPD pattern of the obtained crystal form A was basically as follows: Figure 1 As shown, 1 HNMR spectrum Figure 6 The diffraction angle data are shown in Table 1 below, where the 2θ value error range is ±0.2°. Form A is a hydrate with a water content of 9.2%wt.

[0141] Table 1 XRPD data of Form A

[0142]

[0143]

[0144] Example 3. Preparation of NMNH calcium salt form B

[0145] Take 500 ml of NMNH calcium salt aqueous solution and stir it in an oil bath at 20-30°C, add 2 L of methanol at one time, stir at 20-30°C for 1-2 h, filter, and dry at 20-30°C to obtain 80.3 g of NMNH calcium salt crystals. The obtained crystals are form B, with a yield of 85.0% and a purity of 99.75%.

[0146] The obtained solid was subjected to X-ray powder diffraction test, and the XRPD pattern of the obtained crystal form B was basically as follows: Figure 2 As shown, 1 HNMR spectrum Figure 6 The diffraction angle data are shown in Table 2 below, where the 2θ value error range is ±0.2°. Form B is a hydrate with a water content of 13.3%wt.

[0147] Table 2 XRPD data of Form B

[0148]

[0149]

[0150] Example 4. Preparation of NMNH calcium salt form C

[0151] Take 500 ml of NMNH calcium salt aqueous solution and stir it in an oil bath at 20-30°C, slowly add 2 L of methanol, and the addition time is greater than 1 hour. After the addition is complete, stir for 1-2 hours, filter, and dry at 40-50°C to obtain 80.1 g of NMNH calcium salt crystals. The obtained crystals are form C, with a yield of 84.8% and a purity of 99.78%.

[0152] The obtained solid was subjected to X-ray powder diffraction test, and the XRPD pattern of the obtained crystal form C was basically as follows: Figure 3 As shown, 1 HNMR spectrum Figure 6 The diffraction angle data are shown in Table 3 below, where the 2θ value error range is ±0.2°. Form C is a hydrate with a water content of 9.5%wt.

[0153] Table 3 XRPD data of Form C

[0154]

[0155]

[0156] Example 5. Preparation of NMNH calcium salt form D

[0157] Take 500 ml of NMNH calcium salt aqueous solution and stir it in an oil bath at 20-30°C, slowly add 2 L of ethanol, and the addition time is greater than 1 hour. After the addition is complete, stir for 1-2 hours, filter, and dry at 30-40°C to obtain 80.7 g of NMNH calcium salt crystals. The obtained crystals are form D, with a yield of 85.5% and a purity of 99.64%.

[0158] The obtained solid was subjected to X-ray powder diffraction test, and the XRPD pattern of the obtained crystal form C was basically as follows: Figure 4 As shown, the diffraction angle data are basically as shown in Table 4 below, where the error range of the 2θ value is ±0.2°.

[0159] Form D is an ethanol-hydrate with a water content of 18.4% wt. 1 H NMR spectrum Figure 7 As shown, it is shown that each molecule of NMNH calcium salt contains approximately 0.33 ethanol molecules.

[0160] Table 4 XRPD data of Form D

[0161]

[0162] Example 6. Preparation of NMNH calcium salt form E

[0163] Take 500 ml of NMNH calcium salt aqueous solution and stir it in an oil bath at 20-30°C, slowly add 2 L of acetone, and the addition time is greater than 1 hour. After the addition is complete, stir for 1-2 hours, filter, and dry at 30-40°C to obtain 80.8 g of NMNH calcium salt crystals. The obtained crystals are form E, with a yield of 85.6% and a purity of 99.60%.

[0164] The obtained solid was subjected to X-ray powder diffraction test, and the XRPD pattern of the obtained crystal form C was basically as follows: Figure 5 As shown, the diffraction angle data are basically as shown in Table 5 below, where the error range of the 2θ value is ±0.2°.

[0165] Form E is acetone monohydrate, with a water content of 20.3% wt. 1 H NMR spectrum Figure 8 As shown, it is shown that each molecule of NMNH calcium salt contains approximately 0.33 acetone molecules.

[0166] Table 5 XRPD data of Form E

[0167]

[0168] Example 7. NMNH calcium salt crystal form A, crystal form B, crystal form C, crystal form D, crystal form E and NMNH disodium salt crystal form A, amorphous Comparison of stability and hygroscopicity of solids

[0169] The NMNH calcium salt crystal forms A, B, C, D and E were placed open in a stability test chamber at 25°C and 65% RH to examine their stability and hygroscopicity, and the data shown in Tables 6 and 7 were obtained.

[0170] Table 6 Comparison of stability of NMNH calcium salt crystal form A, crystal form B, crystal form C, crystal form D, crystal form E and NMNH disodium salt crystal form A, amorphous solid (25°C, 65% RH)

[0171]

[0172]

[0173] Table 7 Study on solid hygroscopicity of NMNH calcium salt crystal form A, crystal form B, crystal form C, crystal form D, and crystal form E (25°C, 65% RH)

[0174]

[0175] After being placed for 60 days, the purity and moisture content of NMNH calcium salt crystal forms A, B, C, D and E solids remain almost unchanged, that is, NMNH calcium salt crystal forms A, B, C, D and E solids can be placed in the open at 25°C and 65% RH for no less than 60 days and the purity and moisture content can remain stable.

[0176] According to WO2023160405 (A1), when NMNH disodium salt is stored in the air, both crystal forms B and C absorb water and transform into crystal form A. After saturation with water, the moisture content of crystal form A is 19%-30% (high water content), and the purity drops from 99.33% to 99.01% after 5 days. The amorphous solid of NMNH disodium salt is more unstable in the air. After being placed for 1 day, it absorbs water from powder to oil, and the purity drops from 99.30% to 99.02%.

[0177] It can be seen that the crystalline form and amorphous form of NMNH disodium salt are both unstable and easy to absorb water, which is extremely unfavorable for storage, cannot meet the shelf life of the product, and is difficult to market and promote. The stability and hygroscopicity resistance of NMNH calcium salt crystalline form A, crystalline form B, crystalline form C, crystalline form D, and crystalline form E are significantly improved, which is conducive to long-term continuous and stable storage and convenient for market promotion.

[0178] All documents mentioned in the present invention are cited as references in this application, just as each document is cited as reference individually. In addition, it should be understood that after reading the above teachings of the present invention, those skilled in the art can make various changes or modifications to the present invention, and these equivalent forms also fall within the scope defined by the claims attached to this application.

Claims

1. A reduced β-nicotinamide mononucleotide calcium salt crystal represented by formula (I), It is characterized in that The crystal is a crystalline form selected from the group consisting of crystalline form A, crystalline form B, crystalline form C, crystalline form D, or crystalline form E.

2. The crystal according to claim 1, characterized in that: The XRPD spectrum of the crystalline form A comprises 3 or more (e.g., 4, 5, 6, 7 or 8) 2θ values ​​selected from the group consisting of 6.9°±0.2°, 9.5°±0.2°, 12.6°±0.2°, 15.6°±0.2°, 17.9°±0.2°, 21.0°±0.2°, 21.8°±0.2°, 25.4°±0.2°; The XRPD spectrum of the crystalline form B comprises 3 or more (e.g., 4, 5, 6, 7 or 8) 2θ values ​​selected from the group consisting of 6.5°±0.2°, 8.1°±0.2°, 11.9°±0.2°, 13.1°±0.2°, 17.6°±0.2°, 21.4°±0.2°, 23.7°±0.2°, and 26.9°±0.2°; The XRPD spectrum of the crystalline form C includes 3 or more (such as 4, 5, 6, 7 or 8) 2θ values ​​selected from the following group: 6.2°±0.2°, 9.7°±0.2°, 12.4°±0.2°, 16.1°±0.2°, 17.1°±0.2°, 18.7°±0.2°, 20.8°±0.2°, and 26.6°±0.2°.

3. The crystal according to claim 1, characterized in that The crystalline form A also has one or more characteristics selected from the following group: 1) the XRPD spectrum of the crystalline form A comprises 6 or more 2θ values ​​selected from the group consisting of 6.9°±0.2°, 9.5°±0.2°, 12.6°±0.2°, 13.9°±0.2°, 14.4°±0.2°, 15.6°±0.2°, 16.7°±0.2°, 17.2°±0.2°, 17.9°±0.2°, 18.8°±0.2°, 21.0°±0.2°, 21.8°±0.2°, 23.1°±0.2°, 25.4°±0.2°, 26.5°±0.2°, 27.3°±0.2°, 28.1°±0.2°, 31.5°±0.2°, 32.8°±0.2°, and 35.6°±0.2°; 2) The XRPD pattern of the crystalline form A is substantially as shown in FIG1 ; 3) The crystal form A is a hydrate with a water content of 4%wt-13%wt; preferably, the crystal form A is a 1-3 hydrate.

4. The crystal according to claim 1, characterized in that The crystalline form B also has one or more characteristics selected from the following group: 1) The XRPD pattern of the crystalline form B comprises 6 or more 2θ values ​​selected from the group consisting of 6.5°±0.2°, 8.1°±0.2°, 11.9°±0.2°, 13.1°±0.2°, 13.5°±0.2°, 14.5°±0.2°, 17.6°±0.2°, 18.0°±0.2°, 18.9°±0.2°, 19.4°±0.2°, 19.7°±0.2°, 20.3°±0.2°, 21.4°±0.2°, 23.7°±0.2°, 24.3°±0.2°, 25.1°±0.2°, 26. 6.4°±0.2°, 26.9°±0.2°, 27.5°±0.2°, 28.7°±0.2°, 29.3°±0.2°, 30.5°±0.2°, 30.9°±0.2°, 31.6°±0.2°, 32.4°±0.2°, 32.9°±0.2°, 34.2°±0.2°, 35.0°±0.2°, 35.4°±0.2°, 36.7°±0.2°, 37.5°±0.2°, 37.9°±0.2°, 38.2°±0.2°, 38.9°±0.2°, 40.2°±0.2°; 2) The XRPD pattern of the crystalline form B is substantially as shown in FIG2 ; 3) The crystal form B is a hydrate with a water content of 4%wt-20%wt; preferably, the crystal form B is a 1-5 hydrate.

5. The crystal according to claim 1, characterized in that The crystalline form C also has one or more characteristics selected from the following group: 1) The XRPD spectrum of the crystalline form C comprises 6 or more 2θ values ​​selected from the group consisting of 6.2°±0.2°, 6.8°±0.2°, 9.7°±0.2°, 11.8°±0.2°, 12.4°±0.2°, 14.2°±0.2°, 15.5°±0.2°, 16.1°±0.2°, 17.1°±0.2°, 17.9°±0.2°, 18.7°±0.2°, 20.1°±0.2°, 20.8°±0.2°, 21.5°±0.2°, 22.9°±0.2°, 23.5°±0.2°, 24.1°±0.2°, 24.5°±0.2° .2°, 25.0°±0.2°, 25.8°±0.2°, 26.6°±0.2°, 27.3°±0.2°, 27.7°±0.2°, 28.3°±0.2°, 28.5°±0.2°, 29.7°±0.2°, 30.3°±0.2°, 30.8°±0.2°, 31.4°±0.2°, 32.8°±0.2°, 33.4°±0.2°, 34.4°±0.2°, 35.3°±0.2°, 36.0°±0.2°, 37.1°±0.2°, 38.0°±0.2°, 39.0°±0.2°, 39.8°±0.2°; 2) The XRPD pattern of the crystalline form C is substantially as shown in FIG3 ; 3) The crystal form C is a hydrate with a water content of 4%wt-13%wt; preferably, the crystal form C is a 1-3 hydrate.

6. The crystal according to claim 1, characterized in that The crystalline form D has one or more characteristics selected from the following group: 1) the XRPD spectrum of the crystalline form D comprises 3 or more 2θ values ​​selected from the group consisting of 7.0°±0.2°, 8.0°±0.2°, 12.0°±0.2°, 17.8°±0.2°, 20.2°±0.2°, and 26.9°±0.2°; 2) the XRPD spectrum of the crystalline form D further comprises one or more 2θ values ​​selected from the following group: 13.5°±0.2°, 14.2°±0.2°, 24.0°±0.2°; 3) the XRPD spectrum of the crystalline form D comprises 6 or more 2θ values ​​selected from the group consisting of 7.0°±0.2°, 8.0°±0.2°, 12.0°±0.2°, 13.5°±0.2°, 14.2°±0.2°, 15.7°±0.2°, 17.8°±0.2°, 19.2°±0.2°, 20.2°±0.2°, 23.5°±0.2°, 24.0°±0.2°, 24.5°±0.2°, 26.1°±0.2°, 26.9°±0.2°, 28.7°±0.2°, 30.5°±0.2°, and 33.8°±0.2°; 4) The XRPD pattern of the crystalline form D is substantially as shown in FIG4 ; 5) The crystal form D 1 The H NMR spectrum is essentially represented as in Figure 7 ; 6) The crystal form D is an ethanol-hydrate, containing about 0.2-0.5 ethanol and a water content of 16%wt-23%wt; preferably, the crystal form D is a 3-6 hydrate.

7. The crystal according to claim 1, characterized in that The crystalline form E has one or more characteristics selected from the following group: 1) the XRPD spectrum of the crystalline form E comprises 3 or more 2θ values ​​selected from the following group: 6.9°±0.2°, 8.0°±0.2°, 11.9°±0.2°, 17.8°±0.2°, 20.2°±0.2°, 26.9°±0.2°; 2) the XRPD spectrum of the crystalline form E further comprises one or more 2θ values ​​selected from the following group: 13.5°±0.2°, 14.2°±0.2°, 24.0°±0.2°; 3) the XRPD spectrum of the crystalline form E comprises 6 or more 2θ values ​​selected from the group consisting of 6.9°±0.2°, 8.0°±0.2°, 11.9°±0.2°, 13.5°±0.2°, 14.2°±0.2°, 15.7°±0.2°, 17.8°±0.2°, 18.8°±0.2°, 19.2°±0.2°, 20.2°±0.2°, 24.1°±0.2°, 26.0°±0.2°, 26.9°±0.2°, 28.7°±0.2°, 30.7°±0.2°, and 33.9°±0.2°; 4) The XRPD pattern of the crystalline form E is substantially as shown in FIG5 ; 5) The crystal form E 1 The H NMR spectrum is essentially represented as in Figure 8 ; 6) The crystal form E is an acetone monohydrate, containing about 0.2-0.5 acetone and a water content of 16%wt-23%wt; preferably, the crystal form E is a 3-6 hydrate.

8. A method for preparing the crystal according to claim 1, characterized in that: The method comprises the following steps: (I) Preparation of Form A: I-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent; I-2) adding a second solvent dropwise to the reduced β-nicotinamide mononucleotide calcium salt solution described in step I-1) at 40-50° C., filtering the crystals and drying at 40-50° C. to obtain a crystalline form A of the reduced β-nicotinamide mononucleotide calcium salt, wherein the first solvent is selected from water; the second solvent is selected from water, methanol, ethanol, n-propanol, isopropanol, acetone, acetonitrile, tetrahydrofuran, or a mixed solvent thereof; (II) Preparation of Form B: II-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent; II-2) adding a second solvent dropwise to the reduced β-nicotinamide mononucleotide calcium salt solution described in step II-1) at 20-30° C., filtering the crystals and drying at 20-30° C. to obtain reduced β-nicotinamide mononucleotide calcium salt crystalline form B, wherein the first solvent is selected from water; the second solvent is selected from water, methanol, or a mixed solvent thereof; (III) Preparation of Form C: III-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent; III-2) adding a second solvent to the reduced β-nicotinamide mononucleotide calcium salt solution of step III) at 20-30° C., filtering the crystals, and then drying at 40-50° C. to obtain reduced β-nicotinamide mononucleotide calcium salt crystalline form C, wherein the first solvent is selected from water; the second solvent is selected from water, methanol, or a mixed solvent thereof; (IV) Preparation of Form D: IV-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent; IV-2) adding a second solvent to the reduced β-nicotinamide mononucleotide calcium salt solution of step IV-1) at 20-30° C., filtering the crystals, and then drying at 30-40° C. to obtain a crystalline form D of the reduced β-nicotinamide mononucleotide calcium salt, wherein the first solvent is selected from water; and the second solvent is selected from water, ethanol, or a mixed solvent thereof; (V) Preparation of Form E: V-1) providing a solution containing reduced β-nicotinamide mononucleotide calcium salt in a first solvent; V-2) adding a second solvent dropwise to the reduced β-nicotinamide mononucleotide calcium salt solution described in step V-1) at 20-30° C., filtering the solution by crystallization, and then drying at 30-40° C. to obtain the reduced β-nicotinamide mononucleotide calcium salt crystalline form E, wherein the first solvent is selected from water; and the second solvent is selected from water, acetone, or a mixed solvent thereof.

9. A composition, characterized in that The composition comprises: (a) the crystal according to any one of claims 1 to 7, and (b) a pharmaceutically acceptable excipient or carrier, or an excipient or carrier acceptable for health products, or an excipient or carrier acceptable for cosmetics, or an excipient or carrier acceptable for food.

10. Use of the crystal according to any one of claims 1 to 7, characterized in that: Used for preparing medicines, health products, cosmetics or food additives.

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