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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C129234-10mg |
10mg |
现货 ![]() |
| |
C129234-250mg |
250mg |
期货 ![]() |
| |
C129234-1g |
1g |
期货 ![]() |
| |
C129234-5g |
5g |
期货 ![]() |
|
别名 | 坎地沙坦 | 坎地沙坦酯相关化合物G |
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英文别名 | candesartan | HTQMVQVXFRQIKW-UHFFFAOYSA-N | [3H]candesartan | CANDESARTAN CILEXETIL IMPURITY G [EP IMPURITY] | NCGC00167474-04 | C-266 | 1-[(2 inverted exclamation mark -(5-Tetrazolyl)-4-biphenylyl)methyl]-2-ethoxybenzimidazole-7-carboxylic Acid | BCPP000 |
规格或纯度 | Moligand™, ≥99% |
英文名称 | Candesartan |
生化机理 | 血管紧张素II受体1(AT1)拮抗剂(牛肾上腺皮质和兔主动脉的IC50值分别为1.12和2.86 nM)。在动物模型中表现出降压作用。candesartan cilexetil也可以作为前药获得。 |
储存温度 | 2-8°C储存 |
运输条件 | 冰袋运输 |
作用类型 | 拮抗剂 |
作用机制 | AT 1 受体拮抗剂 |
产品介绍 |
Candesartan 是angiotensin II(血管紧张素II)受体拮抗剂, IC50为0.26 nM。A selective angiotensin II receptor antagonist. Candesartan is an angiotensin II receptor antagonist with IC50 of 0.26 nM. Application: CAN may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by spectrophotometric and chromatography techniques.These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements. Candesartan is a selective AT1 (angiotensin II receptor 1) antagonist. Antagonism of angiotensin receptors inhibits vasoconstriction and the production of aldosterone, leading to a decrease in water and sodium concentration in blood plasma. Exhibits antihypertensive effects in animal models. Used in treatment of congestive heart failure, as antihypertensive. Candesartan does not affect cell viability or proliferation but increases the expression of VEGF and interleukin-8 in the cultured medium of KU-19-19 cells. Candesartan (0.1 nM) could reduce the maximal contractile response to angiostensin II by approximately 50%. |
ALogP | 4.1 |
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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 | 604-138-8 |
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分子类型 | 小分子 |
IUPAC Name | 2-ethoxy-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylic acid |
INCHI | InChI=1S/C24H20N6O3/c1-2-33-24-25-20-9-5-8-19(23(31)32)21(20)30(24)14-15-10-12-16(13-11-15)17-6-3-4-7-18(17)22-26-28-29-27-22/h3-13H,2,14H2,1H3,(H,31,32)(H,26,27,28,29) |
InChi Key | HTQMVQVXFRQIKW-UHFFFAOYSA-N |
Canonical SMILES | CCOC1=NC2=CC=CC(=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)C(=O)O |
Isomeric SMILES | CCOC1=NC2=CC=CC(=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)C(=O)O |
关联CAS | 139481-59-7 |
PubChem CID | 2541 |
NSC Number | 759858 |
MeSH Entry Terms | 2-ethoxy-1-((2'-(1H-tetrazol-5-yl)(1,1'-biphenyl)-4-yl)methyl)-1H-benzimidazole-7-carboxylic acid;2-ethoxy-7-carboxy-1-(2'-(1H-tetrazol-5-yl)biphenyl-4-yl)methylbenzimidazole;candesartan;CV 11974;CV-11974;CV11974 |
分子量 | 440.45 |
溶解性 | Soluble in ethyl acetate, methanol, water (<1 mg/ml at 25°C), DMSO (88 mg/ml at 25°C), and ethanol (1 mg/ml at 25°C) |
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凝固点 | 183-185°C |
分子量 | 440.500 g/mol |
XLogP3 | 4.100 |
氢键供体数Hydrogen Bond Donor Count | 2 |
氢键受体数Hydrogen Bond Acceptor Count | 7 |
可旋转键计数Rotatable Bond Count | 7 |
精确质量Exact Mass | 440.16 Da |
单同位素质量Monoisotopic Mass | 440.16 Da |
拓扑极表面积Topological Polar Surface Area | 119.000 Ų |
重原子数Heavy Atom Count | 33 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 660.000 |
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 | 99-100(%) |
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Appearance(C129234) | Powder |
NMR spectrum | Conforms to Structure |
¥402.90