计算溶液所需的质量、体积或浓度。
活性类型 | 活性值-log(M) | 作用机制 | 期刊 | 参考文献(PubMed IDs) |
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货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
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C125175-5mg |
5mg |
现货 ![]() |
| |
C125175-25mg |
25mg |
现货 ![]() |
| |
C125175-100mg |
100mg |
现货 ![]() |
|
别名 | 克立咪唑 |
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英文别名 | SR-01000000057-6 | BSPBio_000273 | CCG-106577 | CS-1481 | Histakool | NCGC00015243-01 | NCGC00015243-07 | Oprea1_226569 | CLEMIZOLE [WHO-DD] | Prestwick1_000227 | Benzimidazole, 1-(p-chlorobenzyl)-2-(1-pyrrolidinylmethyl)- | Histacur | BRD-K04704168-003-1 |
规格或纯度 | Moligand™, ≥98% |
英文名称 | Clemizole |
生化机理 | 说明:IC50 值:8mM(NS4B)[1]盐酸氯咪唑是一种 H1 组胺受体拮抗剂。最近,研究人员发现盐酸氯咪唑可在体外抑制 NS4B 的 RNA 结合和丙型肝炎病毒(HCV)的复制:尽管效果显著,但盐酸氯咪唑的抗病毒效果一般(对 HCV 基因型 2a 克隆的 50% 有效浓度为 8 微摩尔)。氯咪唑与干扰素、利巴韦林或核苷类(NM283)和非核苷类(HCV796)HCV聚合酶抑制剂的组合具有相加作用[1]。啮齿动物和人类在氯咪唑代谢途径上的差异具有重要意义,因为研究发现人类的主要代谢产物具有协同抗 HCV 活性[2]:盐酸氯咪唑治疗受试者丙型肝炎的安全性和耐受性研究 |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
作用类型 | 通道阻滞剂 |
作用机制 | TRPC3 通道阻断剂;TRPC4 通道阻断剂;TRPC5 通道阻断剂;TRPC6 通道阻断剂 |
产品介绍 |
Clemizole是H1受体拮抗剂,还能抑制NS4B的RNA结合及HCV的复制。 Clemizole is a H1 histamine receptor antagonist.Recently, researchers have identified that clemizole hydrochloride can inhibit NS4B's RNA binding and hepatitis C virus (HCV) replication. |
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作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
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EC号 | 207-133-5 |
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分子类型 | 小分子 |
IUPAC Name | 1-[(4-chlorophenyl)methyl]-2-(pyrrolidin-1-ylmethyl)benzimidazole |
INCHI | InChI=1S/C19H20ClN3/c20-16-9-7-15(8-10-16)13-23-18-6-2-1-5-17(18)21-19(23)14-22-11-3-4-12-22/h1-2,5-10H,3-4,11-14H2 |
InChi Key | CJXAEXPPLWQRFR-UHFFFAOYSA-N |
Canonical SMILES | C1CCN(C1)CC2=NC3=CC=CC=C3N2CC4=CC=C(C=C4)Cl |
Isomeric SMILES | C1CCN(C1)CC2=NC3=CC=CC=C3N2CC4=CC=C(C=C4)Cl |
关联CAS | 442-52-4 |
PubChem CID | 2782 |
NSC Number | 46261 |
MeSH Entry Terms | clemizole |
分子量 | 325.84 |
溶解性 | 25°C: DMSO |
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分子量 | 325.800 g/mol |
XLogP3 | 4.000 |
氢键供体数Hydrogen Bond Donor Count | 0 |
氢键受体数Hydrogen Bond Acceptor Count | 2 |
可旋转键计数Rotatable Bond Count | 4 |
精确质量Exact Mass | 325.135 Da |
单同位素质量Monoisotopic Mass | 325.135 Da |
拓扑极表面积Topological Polar Surface Area | 21.100 Ų |
重原子数Heavy Atom Count | 23 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 377.000 |
同位素原子数Isotope Atom Count | 0 |
定义的原子立体中心计数Defined Atom Stereocenter Count | 0 |
未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
定义的键立体中心计数Defined Bond Stereocenter Count | 0 |
未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
所有立体化学键的总数The total count of all stereochemical bonds | 0 |
共价键合单元计数Covalently-Bonded Unit Count | 1 |
Purity(HPLC) | 98-100(%) |
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Appearance(C125175) | orange crystals or powder |
NMR spectrum | Conforms to Structure |
1. Richter JM, Schaefer M, Hill K. (2014) Clemizole hydrochloride is a novel and potent inhibitor of transient receptor potential channel TRPC5.. Mol Pharmacol, 86 (5): (514-21). [PMID:25140002] [10.1021/op500134e] |