product line
BioReagent
form
powder
specific activity
~1,500 U/mg
technique(s)
cell culture | mammalian: suitable
solubility
H2O: 400 mg, clear, colorless to faintly yellow (Solvent: 400 mL plus 4 mL of H2O)
antibiotic activity spectrum
Gram-positive bacteria
mode of action
cell wall synthesis | interferes
SMILES string
[K+].CC1(C)S[C@@H]2[C@H](NC(=O)COc3ccccc3)C(=O)N2[C@H]1C([O-])=O
InChI
1S/C16H18N2O5S.K/c1-16(2)12(15(21)22)18-13(20)11(14(18)24-16)17-10(19)8-23-9-6-4-3-5-7-9;/h3-7,11-12,14H,8H2,1-2H3,(H,17,19)(H,21,22);/q;+1/p-1/t11-,12+,14-;/m1./s1
InChI key
HCTVWSOKIJULET-LQDWTQKMSA-M
General description
Chemical structure: β-lactam
Biochem/physiol Actions
Penicillin V inhibits the synthesis of bacterial cell walls by blocking cell wall peptidoglycan chain cross-linking. Used in cell culture in combination with streptomcyin and other antibiotics.
Other Notes
Keep container tightly closed in a dry and well-ventilated place.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Resp. Sens. 1 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Adel Ben Salem et al.
Bioorganic & medicinal chemistry, 19(24), 7534-7540 (2011-11-15)
Two well-known antibiotic heterocycles, the 'quinolone' nalidixic acid and the β-lactam penicillin V, active at different levels of the bacterial growth process, have been attached via an ether-ester junction to the p-tert-butylcalix[4]arene lower rim, in alternate position. The resulting hydrophobic
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