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经验公式(希尔记法):
C31H52N2O5S · HCl
化学文摘社编号:
分子量:
601.28
UNSPSC Code:
51101500
MDL number:
NACRES:
NA.21
Quality Segment
assay
≥96% (HPLC)
form
powder
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria
mode of action
protein synthesis | inhibits
shipped in
ambient
storage temp.
−20°C
SMILES string
CC(C)[C@@H](N)C(NCC(C)(C)SCC(O[C@H]1[C@](C)([C@@H]2C)[C@@]3([H])[C@@](CC2)(CCC3=O)[C@@H](C)[C@H](O)[C@](C)(C=C)C1)=O)=O.Cl
InChI
1S/C31H52N2O5S.ClH/c1-10-29(8)15-22(38-23(35)16-39-28(6,7)17-33-27(37)24(32)18(2)3)30(9)19(4)11-13-31(20(5)26(29)36)14-12-21(34)25(30)31;/h10,18-20,22,24-26,36H,1,11-17,32H2,2-9H3,(H,33,37);1H/t19-,20+,22-,24-,25+,26+,29-,30+,31+;/m1./s1
InChI key
MFBPRQKHDIVLOJ-AFFLPQGKSA-N
General description
Valnemulin Hydrochloride is an antibiotic which belongs to the class of compounds known as pleuromutilins. It is a semisynthetic derivative of the naturally occurring antibiotic tiamulin. Valnemulin Hydrochloride has activity against various Gram-positive and some Gram-negative bacteria, including Mycoplasma and some anaerobic bacteria, as well as the protozoan parasite Eimeria.
Biochem/physiol Actions
Valnemulin Hydrochloride inhibits bacterial protein synthesis by binding to the 50S subunit of the bacterial ribosome. More specifically, it binds to the peptidyl transferase center of the ribosome and interferes with the transfer of amino acids to growing polypeptide chains, leading to the inhibition of protein synthesis and bacterial death.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| SBR00094-20MG | 04065271975323 |
