Detail Information
P450 Protein:
| P450 Symbol | Cyp2b1 |
| Protein Name | Cytochrome P450 2B1 |
| Uniprot ID | P00176 |
| EC Number | 1.14.14.1 |
| Gene ID | 24300 |
| Species | Rattus norvegicus |
| Txid | 10116 |
| P450 Protein Structure |
Model Confidence (pLDDT)
Very high (>90)
High (90 > 70)
Low (70 > 50)
Very low (<50)
|
| Subcellular Location | |
| Protein Sequence | GO |
Reaction Scheme:
| Chemical Conversion | C12H16 → C12H16O |
| Reaction Type | Oxidation |
| Chemical Bond | CH |
| Solvents | Methanol, Water |
| Conditions | 30 min, pH 7.4, 37°C |
| Transformations | 1. Hydroxylation at an Aliphatic Carbon |
Cyp2b1
Substrate Information:
| Substrate Name | rel-[(1R,2S)-2-(1-Methylethyl)cyclopropyl]benzene |
| Substrate Chemical Formula | C12H16 |
| Substrate Smiles | C=1C=CC(=CC1)C2CC2C(C)C |
| Substrate Structure |
Product Information:
| Product Name | rel-(1R,2R)-alpha,alpha-Dimethyl-2-phenylcyclopropanemethanol |
| Product Chemical Formula | C12H16O |
| Product CAS Number | 71804-64-3 |
| Product Smiles | OC(C)(C)C1CC1C=2C=CC=CC2 |
| Product Structure |
References:
| Title: | Hypersensitive Mechanistic Probe Studies of Cytochrome P450-Catalyzed Hydroxylation Reactions. Implications for the Cationic Pathway |
| DOI: | https://doi.org/10.1021/ja981157i |
| Journal: | Journal of the American Chemical Society (1998) |
| Year: | 1998/7/24 |