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GR 32191B

SIGMA/G5044 - ≥98% (HPLC), solid

Synonym: (4Z)-7-[(1R,2R,3S,5S)-5-([1,1′-Biphenyl]-4-ylmethoxy)-3-hydroxy-2-(1-piperidinyl)cyclopentyl]-4-heptenoic acid hydrochloride

CAS Number: 87248-13-3
Empirical Formula (Hill Notation): C30H40NO4Cl
Molecular Weight: 514.10
MDL Number: MFCD04113055
Linear Formula: C30H40NO4Cl
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-G5044-1MG 1 mg
 $226.00
1/EA		 Add To Favorites
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This image depicts G5044-1MG.

 

assay ≥98% (HPLC)
color off-white
form solid
InChI 1S/C30H39NO4.ClH/c32-27-21-28(35-22-23-15-17-25(18-16-23)24-11-5-3-6-12-24)26(13-7-1-2-8-14-29(33)34)30(27)31-19-9-4-10-20-31;/h1-3,5-6,11-12,15-18,26-28,30,32H,4,7-10,13-14,19-22H2,(H,33,34);1H/b2-1-;/t26-,27-,28-,30+;/m0./s1
InChI key ZYOBZRTZRQKKNC-UGNABIHOSA-N
mp 127-128 °C
originator GlaxoSmithKline
Quality Level 100 
shipped in wet ice
SMILES string Cl.O[C@H]1C[C@H](OCc2ccc(cc2)-c3ccccc3)[C@H](CCC=C/CCC(O)=O)[C@H]1N4CCCCC4
solubility H2O: ~16 mg/mL
storage temp. −20°C
Biochem/physiol Actions: Selective TP prostanoid receptor antagonist. Inhibits U-46619-induced contraction of guinea pig trachea with IC50=1.8 nM.
Features and Benefits: This compound is featured on the Prostanoid Receptors  page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here .
Features and Benefits: This compound was developed by GlaxoSmithKline . To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here .
Legal Information: Manufactured and sold under agreement from Glaxo­Smith­Kline
Packaging: 1, 5 mg in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
mp 127-128 °C
Storage Temp. −20°C
UNSPSC 12352200

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