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关于此项目
经验公式(希尔记法):
C8H15N7O2S3
化学文摘社编号:
分子量:
337.45
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
Quality level:
产品名称
法莫替丁,
Quality Level
originator
Johnson & Johnson
SMILES string
N\C(N)=N\c1nc(CSCCC(=N)NS(N)(=O)=O)cs1
InChI
1S/C8H15N7O2S3/c9-6(15-20(12,16)17)1-2-18-3-5-4-19-8(13-5)14-7(10)11/h4H,1-3H2,(H2,9,15)(H2,12,16,17)(H4,10,11,13,14)
InChI key
XUFQPHANEAPEMJ-UHFFFAOYSA-N
Gene Information
human ... HRH2(3274)
Application
法莫替丁已用于测试其对HEK293膜中转染的人ether-a-go-go相关基因(hERG)结合的效应。它也被用于基于聚己内酯的药物递送研究。
Biochem/physiol Actions
法莫替丁对毒蕈碱和烟碱样受体无效。它竞争性地抑制胃酸的分泌,并引发粘膜损伤保护。
H2组胺受体拮抗剂;抗溃疡剂。
Features and Benefits
该化合物由 Johnson & Johnson 开发。想要浏览其他由制药公司开发的化合物以及已批准药物/候选药物清单, 请单击此处。
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存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Famotidine for the prevention of gastric and duodenal ulcers caused by nonsteroidal antiinflammatory drugs
Taha AS, et al.
The New England Journal of Medicine, 334(22), 1435-1439 (1996)
Polycaprolactone thin-film drug delivery systems: empirical and predictive models for device design
Schlesinger E, et al.
Materials Science and Engineering, C, 57, 232-239 (2015)
Makoto Anraku et al.
International journal of pharmaceutics, 487(1-2), 142-147 (2015-04-18)
An intermolecular complex formed from a 1:1 weight ratio of chitosan (CS, molecular weight 30 kDa) and sulfobutyl ether β-cyclodextrin (SBE-β-CyD, degree of substitution 7) was less soluble than either of the original components. The release of famotidine from tablets
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| F6889-1G | 04061833619087 |
| F6889-5G | 04061832090856 |
| F6889-500MG | 04061833619094 |