Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl-

Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl- Suppliers list
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CAS:1478711-48-6
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Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl- Basic information
Product Name:Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl-
Synonyms:Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl-;BMS-986141;4-(4-(((6-Methoxy-2-(2-methoxyimidazo[2,1-b][1,3,4]thiadiazol-6-yl)benzofuran-4-yl)oxy)methyl)thiazol-2-yl)-N,N-dimethylbenzamide
CAS:1478711-48-6
MF:C27H23N5O5S2
MW:561.63
EINECS:
Product Categories:
Mol File:1478711-48-6.mol
Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl- Structure
Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl- Chemical Properties
density 1.47±0.1 g/cm3(Predicted)
form Solid
pka0.52±0.50(Predicted)
color White to off-white
Safety Information
MSDS Information
Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl- Usage And Synthesis
UsesBMS-98614 is an orally active, selective thrombin receptor protease-activated receptor-4 (PAR-4) antagonist with an IC50 value of 0.4 nM. BMS-98614 has excellent antithrombotic effect[1][2].
in vivo

BMS-986141 (compound 49) shows a slight but significant prolongation of KBT (kidney bleeding time) and demonstrates excellent anti-thrombotic efficacy at 0.5 mg/kg in cynomolgus monkey[1][2].

Animal Model:Monkey arterial thrombosis (AT) and mesenteric bleeding time (MBT) models[2]
Dosage:0.05, 0.1, 0.5 mg/kg
Administration:p.o., 2 hours
Result:Inhibited PAR4-AP-induced platelet aggregation in human and monkey blood with IC50 of 1.8 and 1.3 nM, respectively.
Reduced the thrombus weight by 36%, 63% and 88% at concentrations of 0.05, 0.1 and 0.5 mg/kg, respectively in AT model.
Increased MBT by 1.2 times.
Animal Model:Rat, dog and monkey[1]
Dosage:0.5, 1, 2 mpk
Administration:i.v., 0.5 mpk, 10 min or p.o., 2 mpk for rat, 1 mpk for dog and monkey
Result:The pharmacokinetic parameters of BMS-986141 (compound 49)
Parametersratdogmonkey
t1/2(h)3.7 ± 0.41375 ± 12
CL (mL/min/kg)14.3 ± 0.48.512 ± 2
Vss(L/kg)2.7 ± 0.32.714 ± 5
F (%)312536
IC 50PAR4: .4 nM (IC50)
References[1] E Scott Priestley, et al. Discovery of Two Novel Antiplatelet Clinical Candidates (BMS-986120 and BMS-986141) That Antagonize Protease-Activated Receptor 4. J Med Chem. 2022 Jul 14;65(13):8843-8854. DOI:10.1021/acs.jmedchem.2c00359
[2] P Wong, et al. Favorable therapeutic index of an orally-active small-molecule antagonist of the platelet protease-activated receptor-4, BMS-986141, compared with the P2Y12 antagonist ticagrelor in cynomolgus monkeys. European Heart Journal, Volume 41, Issue Supplement_2, November 2020.
Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl- Preparation Products And Raw materials
Tag:Benzamide, 4-[4-[[[6-methoxy-2-(2-methoxyimidazo[2,1-b]-1,3,4-thiadiazol-6-yl)-4-benzofuranyl]oxy]methyl]-2-thiazolyl]-N,N-dimethyl-(1478711-48-6) Related Product Information

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