In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
October 31st, 2005 | 25 | Yes |
Type pH range | xlogP | Des A‑Pol Apolar desolvation (kcal/mol) | Des Pol Polar desolvation (kcal/mol) | H Don H-bond donors | H Acc H-bond acceptors | Chg Net charge | tPSA (Ų) | MWT Molecular weight (g/mol) | RB Rotatable bonds | DL |
---|---|---|---|---|---|---|---|---|---|---|
Ref Reference (pH 7) | 4.42 | 1.79 | -9.04 | 0 | 4 | 0 | 39 | 339.414 | 5 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CP1A2-1-E | Cytochrome P450 1A2 (cluster #1 Of 3), Eukaryotic | Eukaryotes | 1200 | 0.33 | ADME/T ≤ 10μM |
CP2C9-1-E | Cytochrome P450 2C9 (cluster #1 Of 3), Eukaryotic | Eukaryotes | 800 | 0.34 | ADME/T ≤ 10μM |
CP2CJ-1-E | Cytochrome P450 2C19 (cluster #1 Of 3), Eukaryotic | Eukaryotes | 5100 | 0.30 | ADME/T ≤ 10μM |
CP2D6-1-E | Cytochrome P450 2D6 (cluster #1 Of 3), Eukaryotic | Eukaryotes | 4400 | 0.30 | ADME/T ≤ 10μM |
CP3A4-2-E | Cytochrome P450 3A4 (cluster #2 Of 4), Eukaryotic | Eukaryotes | 6000 | 0.29 | ADME/T ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CP1A2_HUMAN | P05177 | Cytochrome P450 1A2, Human | 1200 | 0.33 | ADME/T ≤ 10μM |
CP2CJ_HUMAN | P33261 | Cytochrome P450 2C19, Human | 5100 | 0.30 | ADME/T ≤ 10μM |
CP2C9_HUMAN | P11712 | Cytochrome P450 2C9, Human | 800 | 0.34 | ADME/T ≤ 10μM |
CP2D6_HUMAN | P10635 | Cytochrome P450 2D6, Human | 4400 | 0.30 | ADME/T ≤ 10μM |
CP3A4_HUMAN | P08684 | Cytochrome P450 3A4, Human | 56.2341325 | 0.41 | ADME/T ≤ 10μM |
Description | Species |
---|---|
Aflatoxin activation and detoxification | |
Aromatic amines can be N-hydroxylated or N-dealkylated by CYP1A2 | |
CYP2E1 reactions | |
Fatty acids | |
Methylation | |
Miscellaneous substrates | |
Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) | |
Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) | |
Xenobiotics |