Use of a Compound for Inducing Differentiation of Mesenchymal Stem Cells into Cartilage Cells
a technology of mesenchymal stem cells and compounds, which is applied in the direction of heterocyclic compound active ingredients, drug compositions, skeletal/connective tissue cells, etc., can solve the problems of non-specifically relieving pain or an inflammatory response, affecting the regeneration or proliferation of chondrocytes, so as to achieve the effect of treating cartilage diseases
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Synthesis of Compound of Formula 1
Example 1
Preparation of (quinoline-8-sulfonic acid (4-hydroxy-phenyl)-amide
[0086]
[0087]The compound of Formula 3 (216 mg, 1.98 mmol) and triethylamine (550 ml, 3.96 mmol) were introduced into a 0.2 M tetrahydrofuran solution including the compound of Formula 2 (300 mg, 1.32 mmol) while stirring, and stirred for 12 hours. The resulting mixture was filtered with ethylacetate, and then concentrated under a reduced pressure. The obtained primary compound was purified using silica gel column chromatography (eluent: ethylacetate:methylene chloride:hexane=2:1:3) to obtain a title compound at a yield of 49% (194 mg).
[0088]1H-NMR (500 MHz, DMSO-d6) δ 9.46 (s, 1H), 9.19 (s, 1H), 9.15 (dd, J=4.2, 1.8 Hz, 1H), 8.53 (dd, J=8.4, 1.7 Hz, 1H), 8.25 (dd, J=8.2, 1.4 Hz, 1H), 8.21 (dd, J=7.3, 1.4 Hz, 1H), 7.74 (dd, J=8.3, 4.2 Hz, 1H), 7.68-7.63 (m, 1H), 6.75-6.70 (m, 2H), 6.53-6.41 (m, 2H)
examples 2 to 28
[0089]Compounds of Examples 2 to 28 were prepared in the same manner as in the preparation method described in Example 1. Chemical structures and physical properties of the prepared compounds are listed in the following Table 1 and Table 2.
TABLE 1CompoundIUPACExamplesNumberChemical StructureFormulaNomenclature 1A1942C15H12N2O3SQuinoline-8- sulfonic acid (4- hydroxy-phenyl)- amide 2A1943C19H14N2O3SQuinoline-8- sulfonic acid (7- hydroxy- naphthalen-1-yl)- amide 3A1944C16H12N2O5S2-Hydroxy-5- (quinoline-8- sulfonylamino)- benzoic acid 4A1948C17H19NO5S5-(4-Tert-butyl- benzenesulfonyl- amino)-2-hydroxy- benzoic acid 5A1949C22H17NO3SBiphenyl-4- sulfonic acid (5- hydroxy- naphthalen-1-yl)- amide 6A1950C17H15NO3SN-(4-hydroxy- naphthalen-1-yl)- 4-methyl- benzenesulfonamide 7A1880C16H13NO3SNaphthalene-2- sulfonic acid (4- hydroxyl- phenyl)-amide 8A1881C17H15NO3SN-(5-hydroxyl- naphthalen-1-yl)- 4-methyl- benzenesulfonamide 9A1882C17H15NO3SN-(7-hydroxyl- naphthalen-1-yl)- 4-methyl- benzenesulfon...
experimental example 1
Confirmation of Differentiation of Mesenchymal Stem Cells to Chondrocytes by Compound of Formula 1
[0090]Separation and Incubation of Human Fat-Derived Mesenchymal Stem Cells
[0091]60 cc of an expanding solution (obtained by adding 30 mL of 1% lidocaine, 30 mL of 0.5% bupivacaine, 10 mL of 4.2% sodium bicarbonate and 1 mg of epinephrine to 1 L of normal water for injection) was applied to the periphery of a navel under sterile conditions. Fats were suctioned using Mercedes 3 mm×9 cm Aspiration Luer Lock Cannula (Byron Medical, Tucson, Ariz.), and then instantly kept on ice. Since a lipoaspirate filtered through a 250 mm sieve included an anesthetic and a contaminant such as blood, the lipoaspirate was washed with phosphate buffered saline (PBS) to remove the anesthetic and the contaminant. Collagenase I (1 mg / mL; Worthington Biochemical Corp., Lakewood, N.J.) was added to the obtained fat tissues, stirred, and then kept at 37° C. for an hour. The suspended adipose tissues were centrif...
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