In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
October 23rd, 2009 | 23 | Yes |
Popular Name: benzyl-chloro-dimethyl-BLAH benzyl-chloro-dimethyl-BLAH
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) | 5.47 | 12.78 | -39.21 | 1 | 1 | 1 | 4 | 326.891 | 2 | ↓ |
Hi High (pH 8-9.5) | 5.47 | 10.94 | -2.57 | 0 | 1 | 0 | 3 | 325.883 | 2 | ↓ |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
SGMR1-1-E | Sigma Opioid Receptor (cluster #1 Of 6), Eukaryotic | Eukaryotes | 429 | 0.39 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
SGMR1_RAT | Q9R0C9 | Sigma Opioid Receptor, Rat | 381 | 0.39 | Binding ≤ 1μM |
SGMR1_HUMAN | Q99720 | Sigma Opioid Receptor, Human | 40.1 | 0.45 | Binding ≤ 1μM |
SGMR1_HUMAN | Q99720 | Sigma Opioid Receptor, Human | 40.1 | 0.45 | Binding ≤ 10μM |
SGMR1_RAT | Q9R0C9 | Sigma Opioid Receptor, Rat | 381 | 0.39 | Binding ≤ 10μM |