A93607
4-氮杂苯并咪唑
99%
别名:
1H-咪唑并[4,5-b]吡啶
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关于此项目
经验公式（希尔记法）:
C6H5N3
化学文摘社编号:
分子量:
119.12
PubChem Substance ID:
eCl@ss:
32151902
UNSPSC Code:
12352100
NACRES:
NA.22
EC Number:
205-987-3
MDL number:
Assay:
99%
Form:
powder
InChI key
GAMYYCRTACQSBR-UHFFFAOYSA-N
InChI
1S/C6H5N3/c1-2-5-6(7-3-1)9-4-8-5/h1-4H,(H,7,8,9)
SMILES string
c1cnc2nc[nH]c2c1
assay
99%
form
powder
mp
148-151 °C (lit.)
Quality Level
Noemi Cowan et al.
Antimicrobial agents and chemotherapy, 60(10), 6127-6133 (2016-08-03)
The current treatments against Trichuris trichiura, albendazole and mebendazole, are only poorly efficacious. Therefore, combination chemotherapy was recommended for treating soil-transmitted helminthiasis. Albendazole-mebendazole and albendazole-oxantel pamoate have shown promising results in clinical trials. However, in vitro and in vivo drug
E Nicolaï et al.
Journal of medicinal chemistry, 36(9), 1175-1187 (1993-04-30)
A series of 1-benzylbenzimidazole and 3-benzylimidazo[4,5-b]pyridine substituted in the 2-position by an alkanoic or mercaptoalkanoic acid chain was synthesized for evaluation as potential thromboxane A2/prostaglandin H2 (TXA2/PGH2) receptor antagonists. The affinity of each compound for washed human platelet TXA2/PGH2 receptors
Teodora Ivanova et al.
ChemMedChem, 12(23), 1953-1968 (2017-10-24)
The proprotein convertase furin is a potential target for drug design, especially for the inhibition of furin-dependent virus replication. All effective synthetic furin inhibitors identified thus far are multibasic compounds; the highest potency was found for our previously developed inhibitor
Ping Lan et al.
European journal of medicinal chemistry, 46(1), 77-94 (2010-11-26)
3D-QSAR and docking studies were performed on sixty imidazo[4,5-b]pyridine derivatives as Aurora A kinase inhibitors. The CoMFA and CoMSIA models using forthy-eight molecules in the training set, gave r(cv)(2) values of 0.774 and 0.800, r(2) values of 0.975 and 0.977
Dorte Renneberg et al.
Journal of the American Chemical Society, 125(19), 5707-5716 (2003-05-08)
The DNA binding properties of fused heterocycles imidazo[4,5-b]pyridine (Ip) and hydroxybenzimidazole (Hz) paired with pyrrole (Py) in eight-ring hairpin polyamides are reported. The recognition profile of Ip/Py and Hz/Py pairs were compared to the five-membered ring pairs Im/Py and Hp/Py
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