B9680
Bay u9773
≥98% (HPLC), oil
别名:
6(R)-(4-Carboxyphenylthio)-5(S)-hydroxy-7(E),9(E),11(E),14(Z)-eicosatetraenoic acid
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关于此项目
经验公式（希尔记法）:
C27H36O5S
化学文摘社编号:
分子量:
472.64
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
51111800
MDL number:
InChI
1S/C27H36O5S/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-25(24(28)15-14-17-26(29)30)33-23-20-18-22(19-21-23)27(31)32/h6-7,9-13,16,18-21,24-25,28H,2-5,8,14-15,17H2,1H3,(H,29,30)(H,31,32)/b7-6-,10-9-,12-11+,16-13+/t24-,25+/m0/s1
SMILES string
CCCCC\C=C/C/C=C\C=C\C=C\[C@@H](Sc1ccc(cc1)C(O)=O)[C@@H](O)CCCC(O)=O
InChI key
PKJINWOACFYDQN-RBVMPENBSA-N
assay
≥98% (HPLC)
form
oil
color
white
solubility
DMSO: >25 mg/mL, ethanol: >25 mg/mL
originator
Bayer
shipped in
dry ice
storage temp.
−70°C
Quality Level
Biochem/physiol Actions
Subtype-selective cysteinyl-leukotriene (Cys-Lt) antagonist.
Features and Benefits
This compound is featured on the Leukotriene Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Bayer. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
S Ravasi et al.
Molecular pharmacology, 57(6), 1182-1189 (2000-05-29)
We report the identification of a novel pharmacological profile for the leukotriene (LT)C(4) binding site we previously identified in human lung parenchyma (HLP). We used a series of classic cysteinyl-LT (CysLT)(1) receptor antagonists belonging to different chemical classes and the
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