AZ3451

  Cat. No.:  DC10879   Featured
Chemical Structure
2100284-59-9
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More than 5000 active chemicals with high quality for research!
Field of application
AZ3451 is a potent and selective allosteric antagonist of protease-activated receptor 2 (PAR2)
Cas No.: 2100284-59-9
Chemical Name: 2-(6-Bromanyl-1,3-Benzodioxol-5-Yl)-~{n}-(4-Cyanophenyl)-1-[(1~{s})-1-Cyclohexylethyl]benzimidazole-5-Carboxamide
Synonyms: 2-(6-Bromo-1,3-benzodioxol-5-yl)-N-(4-cyanophenyl)-1-[(1S)-1-cyclohexylethyl]-1H-benzimidazole-5-carboxamide;AZ3451;(S)-2-(6-bromobenzo[d][1,3]dioxol-5-yl)-N-(4-cyanophenyl)-1-(1-cyclohexylethyl)-1H-benzo[d]imidazole-5-carboxamide;AZ 3451;2-(6-Bromanyl-1,3-Benzodioxol-5-Yl)-~{n}-(4-Cyanophenyl)-1-[(1~{s})-1-Cyclohexylethyl]benzimidazole-5-Carboxamide;(S)-2-(6-Bromobenzo[d][1,3]dioxol-5-yl)-N-(4-cyanophenyl)-1-(1-cyclohexylethyl)-1Hbenzo[d]imidazole-5-carboxamide;GTPL9560;BDBM50274114;s9744;2-(6-Bromo-1,3-benzodioxol-
SMILES: BrC1=C([H])C2=C(C([H])=C1C1=NC3C([H])=C(C(N([H])C4C([H])=C([H])C(C#N)=C([H])C=4[H])=O)C([H])=C([H])C=3N1[C@@]([H])(C([H])([H])[H])C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H])OC([H])([H])O2
Formula: C30H27BrN4O3
M.Wt: 571.4644
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: AZ3451 is a protease-activated receptor-2 (PAR2) antagonist.
In Vitro: Antagonist AZ3451 binds to a remote allosteric site outside the helical bundle of the protease-activated receptor 2. AZ3451 is highly lipophilic, which coincides with the hydrophobic nature of the binding pocket within the membrane. Antagonist binding prevents structural rearrangements required for receptor activation and signalling[1].
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC8860 Vorapaxar Vorapaxar (SCH 530348) is a potent and orally active thrombin receptor (PAR-1) antagonist with Ki of 8.1 nM.
DC7197 ML 161 Inhibitor of protease-activated receptor 1 (PAR1)-mediated platelet activation (IC50 = 0.26 μM for the inhibition of platelet P-selectin expression on human platelets). Thought to act allosterically. Also inhibits thrombin-induced platelet activation.
DC11923 BMS-986120 BMS-986120 (BMS986120) is a potent, selective, orally bioavailable, and reversible PAR4 antagonist with Kd of 0.098 nM for human PAR4.
DC10879 AZ3451 AZ3451 is a potent and selective allosteric antagonist of protease-activated receptor 2 (PAR2)
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