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ChemicalBook--->CAS DataBase List--->405098-33-1

405098-33-1

405098-33-1 Structure

405098-33-1 Structure
IdentificationBack Directory
[Name]

N-[[4-(DIMETHYLAMINO)PHENYL]METHYL]-1,2,3,4-TETRAHYDRO-7-METHOXY-N-[4-(1-METHYLETHYL)PHENYL]-1-NAPHTHALENECARBOXAMIDE HYDROCHLORIDE
[CAS]

405098-33-1
[Synonyms]

W-54011
CS-2062
C5a Receptor Antagonist, W-54011
N-{[4-(diMethylaMino)phenyl]Methyl}-7-Methoxy-N-[4-(propan-2-yl)phenyl]-1,2,3,4-tetrahydronaphthalene-1-carboxaMide hydrochloride
N-[[4-(DIMETHYLAMINO)PHENYL]METHYL]-1,2,3,4-TETRAHYDRO-7-METHOXY-N-[4-(1-METHYLETHYL)PHENYL]-1-NAPHTHALENECARBOXAMIDE HYDROCHLORIDE
[Molecular Formula]

C30H37ClN2O2
[MDL Number]

MFCD06659046
[MOL File]

405098-33-1.mol
[Molecular Weight]

493.08
Questions And AnswerBack Directory
[Uses]

W 54011 is a potent orally active non-peptide C5a receptor antagonist.
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 30 mg/mL; DMSO: 30 mg/mL; Ethanol: 3 mg/mL
[form ]

White powder solid.
[color ]

White to light yellow
[Stability:]

Hygroscopic
Hazard InformationBack Directory
[Description]

W-54011 is an orally bioavailable, nonpeptide antagonist of complement component 5a receptor 1 (C5aR), also known as cluster of differentiation 88 (CD88). W-54011 inhibits 125I-rhC5a binding in neutrophils (Ki = 2.2 nM) and C5a-mediated intracellular Ca2+ mobilization (IC50 = 3.1 nM). W-54011 is selective and does not affect Ca2+ mobilization mediated by other G protein-coupled receptor (GPCR) ligands, N-Formyl-Met-Leu-Phe (fMLF; Item No. 21495), or IL-8 up to a concentration of 10 μM. It inhibits Ca2+ mobilization in neutrophils in humans, cynomolgus monkeys, and gerbils, but not in mice, rats, guinea pigs, rabbits, or dogs. At 10 nM, W-54011 also inhibits C5a-mediated migration and vessel formation of human microvascular endothelial cells (HMEC-1).
[storage]

Store at -20°C
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