In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
November 5th, 2008 | 17 | Yes |
Popular Name: 1-(4-Fluorophenyl)-1,2,3,4-tetrahydroisoquinoline 1-(4-Fluorophenyl)-1,2,3,4-tetra…
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CAS Number: 120086-34-2
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) | 3.43 | 7.07 | -3.84 | 1 | 1 | 0 | 12 | 227.282 | 1 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
PCP-1-E | Lysosomal Pro-X Carboxypeptidase (cluster #1 Of 1), Eukaryotic | Eukaryotes | 4900 | 0.44 | Binding ≤ 10μM |
SGMR1-1-E | Sigma Opioid Receptor (cluster #1 Of 6), Eukaryotic | Eukaryotes | 1800 | 0.47 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
PCP_HUMAN | P42785 | Lysosomal Pro-X Carboxypeptidase, Human | 4900 | 0.44 | Binding ≤ 10μM |
SGMR1_RAT | Q9R0C9 | Sigma Opioid Receptor, Rat | 1800 | 0.47 | Binding ≤ 10μM |
Description | Species |
---|---|
Intrinsic Pathway |