In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
October 27th, 2004 | 29 | Yes |
Popular Name: S 5192 S 5192
(S)-3-Methyl-2-phenyl-N-(1-phenylpropyl)-4-quinolinecarboxamide
3-methyl-2-phenyl-N-[(1S)-1-phenylpropyl]quinoline-4-carboxamide
4-Quinolinecarboxamide, 3-methyl-2-phenyl-N-((1S)-1-phenylpropyl)-
4-Quinolinecarboxamide, 3-methyl-2-phenyl-N-(1-phenylpropyl)-, (S)-
N-(alpha-ethylbenzyl)-3-methyl-2-phenylquinoline-4-carboxamide
None
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) | 5.19 | -0.41 | -10.22 | 1 | 3 | 0 | 41 | 380.491 | 5 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
NK2R-1-E | Neurokinin 2 Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 277 | 0.32 | Binding ≤ 10μM |
NK3R-1-E | Neurokinin 3 Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 6 | 0.40 | Binding ≤ 10μM |
NK3R-1-E | Neurokinin 3 Receptor (cluster #1 Of 1), Eukaryotic | Eukaryotes | 10 | 0.39 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
NK2R_HUMAN | P21452 | Neurokinin 2 Receptor, Human | 277 | 0.32 | Binding ≤ 1μM |
NK3R_HUMAN | P29371 | Neurokinin 3 Receptor, Human | 5.5 | 0.40 | Binding ≤ 1μM |
NK2R_HUMAN | P21452 | Neurokinin 2 Receptor, Human | 277 | 0.32 | Binding ≤ 10μM |
NK3R_HUMAN | P29371 | Neurokinin 3 Receptor, Human | 5.5 | 0.40 | Binding ≤ 10μM |
Description | Species |
---|---|
G alpha (q) signalling events | |
Tachykinin receptors bind tachykinins |