In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
November 8th, 2004 | 25 | No |
Popular Name: N-[(Z)-(1-amyl-2-keto-indolin-3-ylidene)amino]benzamide N-[(Z)-(1-amyl-2-keto-indolin-3-…
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) | 4.34 | 9.87 | -13.55 | 1 | 5 | 0 | 63 | 335.407 | 6 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CNR1-2-E | Cannabinoid CB1 Receptor (cluster #2 Of 2), Eukaryotic | Eukaryotes | 314 | 0.36 | Functional ≤ 10μM |
CNR2-1-E | Cannabinoid CB2 Receptor (cluster #1 Of 2), Eukaryotic | Eukaryotes | 240 | 0.37 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
CNR1_HUMAN | P21554 | Cannabinoid CB1 Receptor, Human | 314.1 | 0.36 | Functional ≤ 10μM |
CNR2_HUMAN | P34972 | Cannabinoid CB2 Receptor, Human | 240 | 0.37 | Functional ≤ 10μM |
Description | Species |
---|---|
Class A/1 (Rhodopsin-like receptors) | |
G alpha (i) signalling events |