In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
October 4th, 2005 | 18 | Yes |
Popular Name: 7-Ethoxyresorufin 7-Ethoxyresorufin
Find On: PubMed — Wikipedia — Google
CAS Numbers: 5725-91-7 , [5725-91-7]
5725-91-7; 7-Ethoxyphenoxazone; 7-Ethoxyresorufin; C13630
7-Ethoxy-3H-phenoxazin-3-one, Ethoxyresorufin, O7-Ethylresorufin
7-Ethoxyphenoxazone; 7-Ethoxyresorufin; Ethoxyresorufin; Resorufin ethyl ether
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) | 3.05 | 0.44 | -10.66 | 0 | 4 | 0 | 52 | 241.246 | 2 | ↓ |
Note Type | Comments | Provided By |
---|---|---|
UniProt Database Links | CP2A8_MESAU; CP2F1_HUMAN | ChEBI |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CP1A2-1-E | Cytochrome P450 1A2 (cluster #1 Of 3), Eukaryotic | Eukaryotes | 500 | 0.49 | ADME/T ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CP1A2_HUMAN | P05177 | Cytochrome P450 1A2, Human | 500 | 0.49 | ADME/T ≤ 10μM |
Description | Species |
---|---|
Aflatoxin activation and detoxification | |
Aromatic amines can be N-hydroxylated or N-dealkylated by CYP1A2 | |
Methylation | |
Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) | |
Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) |