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Merck
CN

ROAMP

Roche

氨苄西林

95% (from N), solubility: (Soluble in aqueous solutions)

别名:

氨苄西林, D-(−)-α-氨苄青霉素

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关于此项目

经验公式(希尔记法):
C16H19N3O4S
化学文摘社编号:
分子量:
349.40
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
1090925
MDL number:
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产品名称

氨苄西林, 95% (from N), solubility: (Soluble in aqueous solutions)

SMILES string

[H][C@]12SC(C)(C)[C@@H](N1C(=O)[C@H]2NC(=O)[C@H](N)c3ccccc3)C(O)=O

InChI

1S/C16H19N3O4S/c1-16(2)11(15(22)23)19-13(21)10(14(19)24-16)18-12(20)9(17)8-6-4-3-5-7-8/h3-7,9-11,14H,17H2,1-2H3,(H,18,20)(H,22,23)/t9-,10-,11+,14-/m1/s1

InChI key

AVKUERGKIZMTKX-NJBDSQKTSA-N

description

C16H18N3O4SNa (Formula)

assay

95% (from N)

mol wt

Mr 371.4

packaging

pkg of 5 g (10835242001)
pkg of 50 g (10835269001)

manufacturer/tradename

Roche

mp

208 °C (dec.) (lit.)

solubility

soluble (Soluble in aqueous solutions)

shipped in

wet ice

storage temp.

2-8°C

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Application

氨苄青霉素已被用于选择带有质粒的耐药菌落的基因克隆策略。仅用于生命科学研究。不用于诊断操作。

Biochem/physiol Actions

β-内酰胺可被β-内酰胺酶失活。因此,氨苄青霉素是与β-内酰胺酶抑制剂一起使用的。
作用机制:氨苄西林是一种半合成的青霉素和ß-内酰胺抗生素,其通过灭活位于细菌的细胞膜内表面的转肽酶从而抑制细菌细胞壁合成。

耐药性机制:ß-内酰胺酶切开氨苄青霉素的ß-内酰胺环,使其失去活性。

抗菌谱:对革兰氏阳性菌(类似于苄青霉素)和革兰氏阴性菌(类似于四环素和氯霉素)均有效。

General description

6-[D(-)-α-氨基苯基乙酰胺基]-青霉烷酸
溶解度:可溶于水溶液
内容物:钠盐

Other Notes

仅用于生命科学研究。不可用于诊断。

法规信息

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分析证书(COA)

Lot/Batch Number

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