Application of abietane-type diterpenoid compound in preparation of drugs for preventing and/or treating thrombotic diseases
A technology for thrombotic diseases and compounds, applied in blood diseases, cardiovascular system diseases, active ingredients of hydroxyl compounds, etc., can solve the problems of high platelet reactivity, poor thrombosis inhibition effect, bleeding and other problems, and achieve significant antithrombotic activity, potential The effect of clinical application value
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Embodiment 1
[0048] Physicochemical properties, nuclear magnetic resonance spectrum carbon ( 13 C) and mass spectrometry data are as follows:
[0049] Compound 1:C 21 h 28 o 4 ; colorless crystals; 13 C NMR (150MHz, acetone-d 6 ):δ C 37.9 (CH 2 ,C-1),19.3(CH 2 ,C-2),43.2(CH 2 ,C-3),33.5(C,C-4),62.7(CH,C-5),201.0(C,C-6),130.1(CH,C-7),138.0(C,C-8) ,124.4(C,C-9),43.3(C,C-10),145.2(C,C-11),183.9(C,C-12),133.4(C,C-13),163.0(C, C-14),26.7(CH,C-15),21.8(CH 3 ,C-16),20.9(CH 3 ,C-17),33.5(CH 3 ,C-18),26.7(CH 3 ,C-19),19.3(CH 3 ,C-20),64.3(-OCH 3 ); EIMS m / z 344[M] + .
[0050] Compound 2:C 20 h 26 o 3 ; colorless crystals; 13 C NMR (150MHz, acetone-d 6 ):δ C 34.1 (CH 2 ,C-1),18.1(CH 2 ,C-2),38.5(CH 2 ,C-3),36.3(C,C-4),144.7(C,C-5),160.3(C,C-6),179.9(C,C-7),120.8(C,C-8) ,140.1(C,C-9),40.8(C,C-10),111.9(CH,C-11),155.5(C,C-12),135.1(C,C-13),125.4(CH, C-14),27.5(CH,C-15),22.5(CH 3 ,C-16),22.5(CH 3 ,C-17),35.6(CH 3 ,C-18),27.9(CH 3 ,C-19),28.5(CH 3 ,C-20); EIMS m / z 314...
Embodiment 2
[0061] The compound described in embodiment 1 is to the effect of rabbit platelet aggregation induced by arachidonic acid (AA):
[0062] 1. Solution preparation
[0063] AA solution: add the marked volume of pure water according to the instructions, fully dissolve the prepared AA solution with a concentration of 15mM, subpackage and refrigerate (-20°C) for later use;
[0064] Test sample (compound described in Example 1) solution or reference substance (aspirin) solution: use dimethyl sulfoxide (DMSO) preparation concentration to be the test sample mother solution or reference substance mother solution of 10mg / mL, then use DMSO was used to dilute and prepare the test sample solution or reference solution of the required concentration;
[0065] Ca-free 2+ Tyrode's solution (Ca 2+ free Tyrode's buffer): containing NaCl 137mM, KCl 2.68mM, MgSO 4 ·7H 2 O 0.2mM, NaH 2 PO 4 2H 2 O 0.42mM, NaHCO 3 11.9 mM, glucose 5.05mM, EGTA0.2 mM, pH 6.5;
[0066] Tyrode's buffer (0.25%...
Embodiment 3
[0087] Compound described in embodiment 1 is to FeCl 3 Inhibition of Induced Carotid Artery Thrombosis in Rats:
[0088] 1. Solution preparation
[0089] 50%FeCl 3 Solution: Dissolve ferric chloride solid with physiological saline to prepare FeCl with a concentration of 50% (W / V) 3 solution;
[0090] Dispensing vehicle: dissolve 2.5% CMC-Na (W / V) and 0.25% Tween80 (V / V) in normal saline;
[0091] Drug solution: after fully dissolving the compounds described in Example 1 with DMSO, dilute 10 times with the above-mentioned dispensing vehicle;
[0092] 2. FeCl 3 Induced carotid artery thrombosis experiment in rats
[0093] Instrument operation: After turning on the Transonic ultrasonic blood flow meter, set zero, calibrate, and complete the unit conversion (V----mL / min);
[0094] Animal model: rats were anesthetized by intraperitoneal injection of 10% chloral hydrate (350mg / kg), fixed, fixed in supine position, cut an incision along the middle of the neck, separated the ri...
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