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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F156753-250mg |
250mg |
现货 ![]() |
| |
F156753-1g |
1g |
现货 ![]() |
| |
F156753-5g |
5g |
现货 ![]() |
|
别名 | 非那甾胺 | 非那雄胺 | N-叔丁基-3-氧代-4-氮杂-5α-雄甾-1-烯-17β-甲酰胺 |
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英文别名 | Finasteridum (INN-Latin) | HSDB 6793 | CS-1767 | 17beta-(N-tert-butylcarbamoyl)-4-aza-5 alpha-androst-1-en-3-one | MK 0906 | FINASTERIDE [JAN] | N-tert-Butyl-3-oxo-4-aza-5alpha-androst-1-en-17beta-carboxamide | (4aR,4bS,6aS,7S,9aS,9bS,11aR)-N-(1,1-dimethy |
规格或纯度 | Moligand™, ≥98% |
英文名称 | Finasteride |
生化机理 | 非那雄胺是一种合成的 4-azasteroid 抗雄激素化合物。它能特异性抑制 5α 还原酶 2,这种细胞内酶能将雄性激素睾酮转化为 5α 双氢睾酮(DHT)。非那雄胺在上皮细胞中抑制 5α 还原酶活性的 Ki 值为 10nM,明显低于在基质中的 Ki 值(Ki = 33nM)。非那雄胺是 5α 还原酶 1 的抑制剂,是 II 型 5α 还原酶抑制剂(II 型和 I 型的 IC 50 值分别为 11.3 和 313 nM)。缩小前列腺体积。抑制睾酮向双氢睾酮的转化。具有体内活性和口服活性。 |
应用 | An antiandrogen that inhibits 5α-Reductase 2 |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
作用类型 | 抑制剂 |
作用机制 | 类固醇 5-α-还原酶 2 抑制剂 |
备注 | 如果有可能,您尽量在使用的当天配置溶液,并在当天使用完它。但是,如果您需要预先配制储备溶液,我们建议您将溶液等份保存在-20°C的密封小瓶中。通常,它们最多可以使用一个月。在使用前和打开样品瓶之前,我们建议您让您的产品在室温下平衡至少1小时。需要更多关于溶解度,用法和处理的建议吗?请访问我们的常见问题(FAQ)页面以获取更多详细信息。 |
产品介绍 |
Finasteride是口服活性的睾酮5α-还原酶抑制剂,Ki为10 nM。An antiandrogen that inhibits 5α-Reductase 2 Finasteride is an orally active testosterone 5-alpha-reductase inhibitor (Ki= 10 nM). |
ALogP | 3 |
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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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PubChem SID | 504753695 |
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分子类型 | 小分子 |
IUPAC Name | (1S,3aS,3bS,5aR,9aR,9bS,11aS)-N-tert-butyl-9a,11a-dimethyl-7-oxo-1,2,3,3a,3b,4,5,5a,6,9b,10,11-dodecahydroindeno[5,4-f]quinoline-1-carboxamide |
INCHI | InChI=1S/C23H36N2O2/c1-21(2,3)25-20(27)17-8-7-15-14-6-9-18-23(5,13-11-19(26)24-18)16(14)10-12-22(15,17)4/h11,13-18H,6-10,12H2,1-5H3,(H,24,26)(H,25,27)/t14-,15-,16-,17+,18+,22-,23+/m0/s1 |
InChi Key | DBEPLOCGEIEOCV-WSBQPABSSA-N |
Canonical SMILES | CC12CCC3C(C1CCC2C(=O)NC(C)(C)C)CCC4C3(C=CC(=O)N4)C |
Isomeric SMILES | C[C@]12CC[C@H]3[C@H]([C@@H]1CC[C@@H]2C(=O)NC(C)(C)C)CC[C@@H]4[C@@]3(C=CC(=O)N4)C |
WGK Germany | 3 |
RTECS | CL5245000 |
PubChem CID | 57363 |
分子量 | 372.55 |
Reaxy-Rn | 4269024 |
溶解性 | Soluble in DMSO, ethanol, methanol, and chloroform. |
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熔点 | 253°C |
分子量 | 372.500 g/mol |
XLogP3 | 3.000 |
氢键供体数Hydrogen Bond Donor Count | 2 |
氢键受体数Hydrogen Bond Acceptor Count | 2 |
可旋转键计数Rotatable Bond Count | 2 |
精确质量Exact Mass | 372.278 Da |
单同位素质量Monoisotopic Mass | 372.278 Da |
拓扑极表面积Topological Polar Surface Area | 58.200 Ų |
重原子数Heavy Atom Count | 27 |
形式电荷Formal Charge | 0 |
复杂度Complexity | 678.000 |
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 | 7 |
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 |
象形图 | GHS08, GHS09, GHS07 |
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信号词 | Danger |
危险声明 |
H302: 吞食有害 H410: 对水生生物有剧毒并具有长期持续影响 H372: 通过长时间或反复暴露对器官造成损害 H360: 可能损害生育力或未出生的孩子 |
预防措施声明 |
P273: 避免释放到环境中。 P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。 P405: 密闭存放 P501: 将内容物/容器处理到。。。 P264: 处理后要彻底洗手。 P260: 不要吸入灰尘/烟雾/气体/雾/蒸汽/喷雾。 P270: 使用本产品时,请勿进食、饮水或吸烟。 P391: 收集溢出物 P330: 漱口 P203: 使用前,获取、阅读并遵守所有安全说明。 P301+P317: 如果被吞咽:请寻求医疗帮助。 P318: 如果暴露或担心,请就医。 P319: 如果你感到不适,请寻求医疗帮助。 |
WGK Germany | 3 |
RTECS | CL5245000 |
Reaxy-Rn | 4269024 |
Merck Index | 4082 |
个人防护装备 | dust mask type N95 (US), Eyeshields, Faceshields, Gloves |
Melting point | 250-254(℃) |
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Purity(HPLC) | 98-100(%) |
Appearance(F156753) | White to Off-White Powder |
Proton NMR spectrum | Conforms to Structure |
1. Yao Wang, Lili Liu, Cheng Cheng, Shuxuan Wang, Qirui Zhai, Yunyang Song, Ronghua Dai. (2023) Study on mechanism of Zishen Pill treating benign prostatic hyperplasia based on serum pharmacochemistry and network pharmacology. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 234 (115480). [PMID:37454501] [10.1016/j.jpba.2023.115480] |
2. Chi-Ming Liu, ZiChen Shao, XuZhou Chen, HanWu Chen, MengQiao Su, ZiWen Zhang, ZhengPing Wu, Peng Zhang, LiJie An, YinJie Jiang, Ai-Jun Ouyang. (2023) Neferine attenuates development of testosterone-induced benign prostatic hyperplasia in mice by regulating androgen and TGF-β/Smad signaling pathways. SAUDI PHARMACEUTICAL JOURNAL, 31 (1219). [PMID:37293563] [10.1016/j.jsps.2023.05.004] |
1. Yao Wang, Lili Liu, Cheng Cheng, Shuxuan Wang, Qirui Zhai, Yunyang Song, Ronghua Dai. (2023) Study on mechanism of Zishen Pill treating benign prostatic hyperplasia based on serum pharmacochemistry and network pharmacology. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 234 (115480). [PMID:37454501] [10.1016/j.jpba.2023.115480] |
2. Chi-Ming Liu, ZiChen Shao, XuZhou Chen, HanWu Chen, MengQiao Su, ZiWen Zhang, ZhengPing Wu, Peng Zhang, LiJie An, YinJie Jiang, Ai-Jun Ouyang. (2023) Neferine attenuates development of testosterone-induced benign prostatic hyperplasia in mice by regulating androgen and TGF-β/Smad signaling pathways. SAUDI PHARMACEUTICAL JOURNAL, 31 (1219). [PMID:37293563] [10.1016/j.jsps.2023.05.004] |