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Merck
CN

T6514

Oleandomycin triacetate

别名:

Troleandomycin

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关于此项目

经验公式(希尔记法):
C41H67NO15
化学文摘社编号:
分子量:
813.97
UNSPSC Code:
51101500
EC Number:
220-392-9
Beilstein/REAXYS Number:
1418238
MDL number:
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mode of action

enzyme | inhibits, protein synthesis | interferes

SMILES string

CO[C@H]1C[C@@H](O[C@@H](C)[C@@H]1OC(C)=O)O[C@H]2[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3OC(C)=O)N(C)C)[C@@H](C)C[C@@]4(CO4)C(=O)[C@H](C)[C@@H](OC(C)=O)[C@@H](C)[C@@H](C)OC(=O)[C@@H]2C

General description

Chemical structure: macrolide


wgk

WGK 2

存储类别

13 - Non Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

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Soo H Bae et al.
The Journal of pharmacy and pharmacology, 61(12), 1637-1642 (2009-12-05)
It has been reported that hepatic cytochrome P450 (CYP)2C9 and CYP3A4 are responsible for the metabolism of sildenafil and formation of its metabolite, N-desmethylsildenafil, in humans. However, in-vivo studies in rats have not been reported. Sildenafil (20 mg/kg) was administered
Shobana Ganesan et al.
Toxicology and applied pharmacology, 241(1), 14-22 (2009-07-21)
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E Y Oh et al.
British journal of pharmacology, 151(1), 24-34 (2007-03-14)
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