TAK-700 (Orteronel)
Catalog No.
A4326
Human 17,20-lyase inhibitor
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TAK-700 (Orteronel) is a potent and highly selective human 17,20-lyase inhibitor with IC50 of 38 nM, exhibits >1000-fold selectivity over other CYPs (e.g. 11-hydroxylase and CYP3A4). Phase 3.
- 1. Guengerich FP, Wilkey CJ, et al. "Conformational selection dominates binding of steroids to human cytochrome P450 17A1." J Biol Chem. 2019 Jun 28;294(26):10028-10041. PMID:31072872
- 2. Gonzalez E, Guengerich FP. "Kinetic processivity of the two-step oxidations of progesterone and pregnenolone to androgens by human cytochrome P450 17A1." J Biol Chem. 2017 Jul 6. pii: jbc.M117.794917. PMID:28684414
- 3. F. Peter Guengerich,Martin Egli,et al."The Kinetic and Chemical Mechanisms of Human Cytochrome P450 17A1." Vanderbilt University. 2017 May.
Physical Appearance | A solid |
Storage | Store at -20°C |
M.Wt | 307.35 |
Cas No. | 426219-18-3 |
Formula | C18H17N3O2 |
Solubility | insoluble in H2O; ≥11.2 mg/mL in DMSO; ≥11.93 mg/mL in EtOH with ultrasonic |
Chemical Name | 6-(7-hydroxy-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-7-yl)-N-methyl-2-naphthamide |
SDF | Download SDF |
Canonical SMILES | O=C(NC)C1=CC=C2C(C=CC(C3(O)C4=CN=CN4CC3)=C2)=C1 |
Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
General tips | We do not recommend long-term storage for the solution, please use it up soon. |
Quality Control & MSDS
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Chemical structure

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Related Biological Data
