In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
October 25th, 2005 | 40 | No |
Popular Name: N-(3-chloro-4-BLAHylcarbonyl-phenyl)-2-phenyl-benzamide N-(3-chloro-4-BLAHylcarbonyl-phe…
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) | 6.81 | 1.53 | -49.15 | 2 | 5 | 1 | 53 | 549.094 | 4 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
V1AR-1-E | Vasopressin V1a Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 24 | 0.27 | Binding ≤ 10μM |
V2R-1-E | Vasopressin V2 Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 9 | 0.28 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
V1AR_HUMAN | P37288 | Vasopressin V1a Receptor, Human | 130 | 0.24 | Binding ≤ 1μM |
V2R_HUMAN | P30518 | Vasopressin V2 Receptor, Human | 4 | 0.29 | Binding ≤ 1μM |
V1AR_HUMAN | P37288 | Vasopressin V1a Receptor, Human | 130 | 0.24 | Binding ≤ 10μM |
V2R_HUMAN | P30518 | Vasopressin V2 Receptor, Human | 4 | 0.29 | Binding ≤ 10μM |
Description | Species |
---|---|
G alpha (q) signalling events | |
G alpha (s) signalling events | |
Vasopressin regulates renal water homeostasis via Aquaporins | |
Vasopressin-like receptors |