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关于此项目
经验公式(希尔记法):
C8H10N2O3S
化学文摘社编号:
分子量:
214.24
NACRES:
NA.85
PubChem Substance ID:
UNSPSC Code:
51102829
EC Number:
244-870-1
MDL number:
form
powder or crystals
Quality Level
antibiotic activity spectrum
Gram-positive bacteria
mode of action
cell wall synthesis | interferes
storage temp.
2-8°C
SMILES string
CC1=C(N2[C@H](SC1)[C@H](N)C2=O)C(O)=O
InChI
1S/C8H10N2O3S/c1-3-2-14-7-4(9)6(11)10(7)5(3)8(12)13/h4,7H,2,9H2,1H3,(H,12,13)/t4-,7-/m1/s1
InChI key
NVIAYEIXYQCDAN-CLZZGJSISA-N
General description
化学结构:β-内酰胺
Application
7-氨基去乙酰氧基头孢烷酸用于头孢菌素的合成和生物转化研究。
Biochem/physiol Actions
7-ADCA是由产黄青霉菌产生的青霉素G生产的,涉及几个污染的化学步骤,然后使用青霉素酰化酶进行酶脱酰。
Other Notes
保存于密闭容器内,置于干燥通风处。
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hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Mutational analysis of a key residue in the substrate specificity of a cephalosporin acylase.
Linda G. Otten, Charles F. Sio, et al.
Chembiochem, 6, 820-825 (2004)
Linda G Otten et al.
The Journal of biological chemistry, 277(44), 42121-42127 (2002-08-29)
Using directed evolution, we have selected an adipyl acylase enzyme that can be used for a one-step bioconversion of adipyl-7-aminodesacetoxycephalosporanic acid (adipyl-7-ADCA) to 7-ADCA, an important compound for the synthesis of semisynthetic cephalosporins. The starting point for the directed evolution
A N Ivankin et al.
Prikladnaia biokhimiia i mikrobiologiia, 36(3), 303-306 (2000-06-27)
The use of peptide hydrolase (EC 3.4.13.1) from Xanthomonas rubrilineans for synthesis of the antibiotic cephalexin from 7-aminodesacetoxycephalosporanic acid was studied. The optimum conditions for production of cephalexin were determined, and the yield exceeded 80%. A method for monitoring the
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| A8398-5G | 04061833391549 |
| A8398-1G | 04061833391525 |
| A8398-250MG | 04061833391532 |