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G protein-coupled receptors (GPCRs)
Leukotriene receptors
CP105696 , CAS No.158081-99-3, Antagonist of BLT 1 receptor

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CP105696 , CAS No.158081-99-3, Antagonist of BLT 1 receptor

Moligand™

CAS#: 158081-99-3
Formula: C₂₈H₂₈O₄
Molecular Weight: 428.52
PubChem CID: 9867257

Item Number

C609562

Grouped product items
SKU	Size	Availability	Price	Qty
C609562-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,334.90
C609562-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$2,001.90

View related series

BLT1 receptor Antagonist

Basic Description

Synonyms	CP-105696\|158081-99-3\|Pfizer 105696\|CP 105696\|CP-105,696\|CP105696\|1-(3-(4-phenylbenzyl)-4-hydroxychroman-7-yl)cyclopentane-1-carboxylic acid\|CHEMBL51770\|Z7354TW4BM\|DTXSID7047308\|Cyclopentanecarboxylic acid, 1-((3S,4R)-3-((1,1'-biphenyl)-4-ylmethyl)-3,4-di
Specifications & Purity	Moligand™
Grade	Moligand™
Action Type	ANTAGONIST
Mechanism of action	Antagonist of BLT 1 receptor

Associated Targets

PTGS2 Tclin Prostaglandin G/H synthase 2 0 Activities

Discover Target: PTGS2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

LTB4R Tchem Leukotriene B4 receptor 1 4 Activities

Discover Target: LTB4R

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

LTB4R2 Tchem Leukotriene B4 receptor 2 0 Activities

Discover Target: LTB4R2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	1-[(3S,4R)-4-hydroxy-3-[(4-phenylphenyl)methyl]-3,4-dihydro-2H-chromen-7-yl]cyclopentane-1-carboxylic acid
INCHI	InChI=1S/C28H28O4/c29-26-22(16-19-8-10-21(11-9-19)20-6-2-1-3-7-20)18-32-25-17-23(12-13-24(25)26)28(27(30)31)14-4-5-15-28/h1-3,6-13,17,22,26,29H,4-5,14-16,18H2,(H,30,31)/t22-,26+/m0/s1
InChi Key	KMNLXCBYBKHKSK-BKMJKUGQSA-N
Canonical SMILES	C1CCC(C1)(C2=CC3=C(C=C2)C(C(CO3)CC4=CC=C(C=C4)C5=CC=CC=C5)O)C(=O)O
Isomeric SMILES	C1CCC(C1)(C2=CC3=C(C=C2)[C@@H]([C@H](CO3)CC4=CC=C(C=C4)C5=CC=CC=C5)O)C(=O)O
PubChem CID	9867257
Molecular Weight	428.52

Database links

CAS Registry No.	158081-99-3
PubChem CID	9867257
ChEMBL Ligand	CHEMBL51770
GPCRdb Ligand	CP105696

Certificates

Certificate of Analysis(COA)

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Safety and Hazards(GHS)

RIDADR	NONHforallmodesoftransport

References

1. Uddin M, Seumois G, Lau LC, Rytila P, Davies DE, Djukanovic R. (2008) Enhancement of neutrophil function by the bronchial epithelium stimulated by epidermal growth factor.. Eur Respir J, 31 (4): (714-24). [PMID:18094008]

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