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Orteronel
Cat. No.:
OB0225WX-2400
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
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Product Overview
Description:
Orteronel is a potent human 17,20-lyase inhibitor (IC50: 38 nM) that functions as an androgen biosynthesis blocker with 1000-fold selectivity over other CYP enzymes.
Synonym:
TAK-700; 426219-18-3; 6-(7-hydroxy-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-7-yl)-N-methyl-2-naphthamide; TAK-700 (Orteronel); Orteronel (racemate); TAK700; Orteronel (racemic); 6-(7-hydroxy-5,6-dihydropyrrolo[1,2-c]imidazol-7-yl)-N-methylnaphthalene-2-carboxamide; TAK 700 racemate; (R)-6-(7-hydroxy-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-7-yl)-N-methyl-2-naphthamide; 6-{7-hydroxy-5H,6H,7H-pyrrolo[1,2-c]imidazol-7-yl}-N-methylnaphthalene-2-carboxamide; Oteronel; 6-[7-hydroxy-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-7-yl]-N-methyl-2-naphthamide; TAK-700; Orteronel; TAK-700 (racemate); Orteronel (TAK-700)
CAS No.:
426219-18-3
Compound CID:
9883029
Formula:
C18H17N3O2
Formula Weight:
307.35
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
Orteronel is used in endocrine research as a selective inhibitor of 17,20-lyase (CYP17A1) to investigate the suppression of androgen biosynthesis in models of castration-resistant prostate cancer.
Library Information
Target:
CYP17; P450
Receptor:
CYP17A1
Pathways:
Metabolism
Plate Number:
L6700-01
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
61 mg/mL; 198.47 mM
ALogP:
1.075
HBA_Count:
2
HBD_Count:
1
Rotatable Bond:
2





