In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
June 22nd, 2008 | 21 | Yes |
Popular Name: CAY10434 CAY10434
Find On: PubMed — Wikipedia — Google
CAS Numbers: 502656-68-0 , 769917-29-5
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) | 2.91 | 11.58 | -40.63 | 1 | 4 | 1 | 31 | 288.415 | 9 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CP4AB-1-E | Cytochrome P450 4A11 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 2 | 0.58 | Binding ≤ 10μM |
CP4F2-1-E | Cytochrome P450 4F2 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 2 | 0.58 | Binding ≤ 10μM |
CP1A2-1-E | Cytochrome P450 1A2 (cluster #1 Of 3), Eukaryotic | Eukaryotes | 800 | 0.41 | ADME/T ≤ 10μM |
CP2CJ-2-E | Cytochrome P450 2C19 (cluster #2 Of 3), Eukaryotic | Eukaryotes | 6220 | 0.35 | ADME/T ≤ 10μM |
CP2D6-2-E | Cytochrome P450 2D6 (cluster #2 Of 3), Eukaryotic | Eukaryotes | 410 | 0.43 | ADME/T ≤ 10μM |
CP3A4-2-E | Cytochrome P450 3A4 (cluster #2 Of 4), Eukaryotic | Eukaryotes | 4460 | 0.36 | ADME/T ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CP4AB_HUMAN | Q02928 | Cytochrome P450 4A11, Human | 2.2 | 0.58 | Binding ≤ 1μM |
CP4F2_HUMAN | P78329 | Cytochrome P450 4F2, Human | 2.2 | 0.58 | Binding ≤ 1μM |
CP4AB_HUMAN | Q02928 | Cytochrome P450 4A11, Human | 2.2 | 0.58 | Binding ≤ 10μM |
CP4F2_HUMAN | P78329 | Cytochrome P450 4F2, Human | 2.2 | 0.58 | Binding ≤ 10μM |
CP1A2_HUMAN | P05177 | Cytochrome P450 1A2, Human | 800 | 0.41 | ADME/T ≤ 10μM |
CP2CJ_HUMAN | P33261 | Cytochrome P450 2C19, Human | 6220 | 0.35 | ADME/T ≤ 10μM |
CP2D6_HUMAN | P10635 | Cytochrome P450 2D6, Human | 410 | 0.43 | ADME/T ≤ 10μM |
CP3A4_HUMAN | P08684 | Cytochrome P450 3A4, Human | 4460 | 0.36 | ADME/T ≤ 10μM |
Description | Species |
---|---|
Aflatoxin activation and detoxification | |
Aromatic amines can be N-hydroxylated or N-dealkylated by CYP1A2 | |
CYP2E1 reactions | |
Eicosanoids | |
Fatty acids | |
Methylation | |
Miscellaneous substrates | |
PPARA activates gene expression | |
Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) | |
Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) | |
Synthesis of Leukotrienes (LT) and Eoxins (EX) | |
Xenobiotics |
No pre-computed analogs available. Try a structural similarity search.