Quality Level
form
liquid, ready-to-use solution
concentration
100 mg/mL in ethanol/water
solubility
H2O: 100 mg/mL, ethanol: 100 mg/mL
suitability
suitable for testing specifications (Bacteriostatic (cell type) E. Coli DH5a, result: pass)
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria
mode of action
cell wall synthesis | interferes
shipped in
wet ice
storage temp.
−20°C
SMILES string
CC1(C)S[C@@H]2[C@H](NC(=O)C(C(O)=O)c3ccccc3)C(=O)N2[C@H]1C(O)=O
InChI
1S/C17H18N2O6S/c1-17(2)11(16(24)25)19-13(21)10(14(19)26-17)18-12(20)9(15(22)23)8-6-4-3-5-7-8/h3-7,9-11,14H,1-2H3,(H,18,20)(H,22,23)(H,24,25)/t9?,10-,11+,14-/m1/s1
InChI key
FPPNZSSZRUTDAP-UWFZAAFLSA-N
General description
化学结构:β-内酰胺
Application
羧苄青霉素(Carbenicillin)可用于筛选氨苄青霉素抗性转化细胞。还可用于研究青霉素敏感的转肽酶在细胞壁生物合成中的作用。
Biochem/physiol Actions
Other Notes
保持容器密闭,并置于干燥通风处。打开后的容器必须小心重新密封并保持直立以防止泄漏。
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 3 - Resp. Sens. 1 - Skin Sens. 1
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
104.0 °F - closed cup
flash_point_c
40 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
A J Wright
Mayo Clinic proceedings, 74(3), 290-307 (1999-03-25)
The penicillin family of antibiotics remains an important part of our antimicrobial armamentarium. In general, these agents have bactericidal activity, excellent distribution throughout the body, low toxicity, and efficacy against infections caused by susceptible bacteria. The initial introduction of aqueous
Andrea Brenna et al.
AMB Express, 4, 43-43 (2014-06-21)
Agrobacterium tumefaciens-mediated transformation is a powerful tool for reverse genetics and functional genomic analysis in a wide variety of plants and fungi. Tuber spp. are ecologically important and gastronomically prized fungi ("truffles") with a cryptic life cycle, a subterranean habitat
G N Rolinson
The Journal of antimicrobial chemotherapy, 41(6), 589-603 (1998-08-01)
For more than 40 years the author has been involved in research in the field of beta-lactam antibiotics. Much of this work was concerned with the development of the semisynthetic penicillins, following the isolation of the penicillin nucleus, 6-aminopenicillanic acid.
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| C1613-1ML | 04061833467794 |

