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阿那曲唑

强效的芳香 化酶(CYP19)抑制剂
规格或纯度: ≥99%
  • CAS编号: 120511-73-1
  • 分子式: C17H19N5
  • 分子量: 293.37
  • PubChem编号: 2187
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货号 (SKU) 包装规格 是否现货 价格 数量
A126470-100mg 100mg 现货 Stock Image
A126470-500mg 500mg 现货 Stock Image
A126470-1g 1g 现货 Stock Image
A126470-5g 5g 现货 Stock Image
A126470-25g 25g 现货 Stock Image
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CYP19A1 Inhibitor

基本描述

规格或纯度 ≥99%
英文名称 Anastrozole
别名 阿那曲唑
英文别名 ICI-D1033;2;2"-[5-(1H-1;2;4-Triazol-1-ylmethyl)-1 3-Phenylene]bis(2-methyl-propiononitrile、 Arimidex;ZD1033 a,a,a′,a′-Tetramethyl-5-(1H-1,2,4-triazol-1-ylmethyl)-1,3-benzenediacetonitrile
生化机理 对肾上腺皮质激素合成没有明显作用的强效高选择性芳香化酶(CYP19)抑制剂(IC50 = 15 nM)。降低血浆雌激素水平,并在体内表现出抗肿瘤活性。口服有效。
储存温度 -20°C储存
运输条件 超低温冰袋运输
产品介绍

Anastrozole is known to inhibit the CYP19 enzyme (aromatase, IC50 = 15 nM) that converts androgens to estrogens. Anastrozole has been seen to reversibly bind to the CYP19 enzyme throμgh competitive inhibition.

Anastrozole is known to inhibit the CYP19 enzyme (aromatase, IC50 = 15 nM) that converts androgens to estrogens. Anastrozole has been seen to reversibly bind to the CYP19 enzyme through competitive inhibition.

名称和标识符

IUPAC Name 2-[3-(2-cyanopropan-2-yl)-5-(1,2,4-triazol-1-ylmethyl)phenyl]-2-methylpropanenitrile
INCHI InChI=1S/C17H19N5/c1-16(2,9-18)14-5-13(8-22-12-20-11-21-22)6-15(7-14)17(3,4)10-19/h5-7,11-12H,8H2,1-4H3
InChi Key YBBLVLTVTVSKRW-UHFFFAOYSA-N
Canonical SMILES CC(C)(C#N)C1=CC(=CC(=C1)CN2C=NC=N2)C(C)(C)C#N
分子式

C17H19N5

PubChem CID 2187
分子量 293.37

化学和物理性质

溶解性 溶于DMSO, 最高浓度 (mg/mL): 29.34, 最高浓度(mM): 100;溶于ethanol, 最高浓度 (mg/mL): 29.34, 最高浓度(mM): 100

安全信息

象形图
ghs06

Toxic

ghs08

Health Hazard

ghs07

Harmful

信号词 Danger
危险声明 H301: Toxic if swallowed
H351: Suspected of causing cancer
H302: Harmful if swallowed
H360: May damage fertility or the unborn child
预防措施声明 P280,P321,P405,P501,P264,P270,P330,P203,P301+P316,P301+P317,P318
WGK Germany 3
RTECS CZ1465000

靶标

Target ID 1362
名称 CYP19A1
缩写名 Aromatase
家族 CYP11, CYP17, CYP19, CYP20 and CYP21 families
基因和蛋白信息
Species Transmembrane Domains Amino Acids Chromosomal Location Gene Symbol Gene Name
Human 2 503 15q21.2 CYP19A1 cytochrome P450 family 19 subfamily A member 1
Mouse 1 503 9 29.49 cM Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1
Rat 2 508 8q24 Cyp19a1 cytochrome P450, family 19, subfamily a, polypeptide 1
Ensembl Gene ENSG00000137869 (Hs) , ENSMUSG00000032274 (Mm) , ENSRNOG00000000196 (Rn)
Entrez Gene 13075 (Mm) , 25147 (Rn) , 1588 (Hs)
OMIM 107910 (Hs)
Protein GI 13904860 (Hs) , 281182626 (Rn) , 6681099 (Mm)
UniProtKB P11511 (Hs) , P28649 (Mm) , P22443 (Rn)
Orphanet 120969 (Hs)
DrugBank Target P11511 (Hs)
ChEMBL Target CHEMBL1978 (Hs) , CHEMBL3859 (Rn)

关联配体

Ligand ID 5137
名称 anastrozole
别名 Arimidex®
类别 Synthetic organic
学名 2-[3-(1-cyano-1-methylethyl)-5-(1H-1,2,4-triazol-1-ylmethyl)phenyl]-2-methylpropanenitrile
生物活性评价 The sulfonamide class of antibacterial compounds are primarily bacteriostatic agents and have a broad spectrum of activity against both Gram-positive and Gram-negative species of bacteria (reviewed in ).
评价 Anastrozole decreases the amount of estrogens that the body makes by inhibiting the enzyme aromatase, which is responsible for converting androgens to estrogens in females.

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