| In ZINC since | Heavy atoms | Benign functionality |
|---|---|---|
| October 6th, 2004 | 25 | Yes |
Popular Name: Levopropoxyphene (BAN Levopropoxyphene (BAN
Find On: PubMed — Wikipedia — Google
CAS Numbers: 34427-79-7 , [72050-78-3]
1-benzyl-3-(dimethylamino)-2-methyl-1-phenylpropyl propanoate
INN); Levopropoxyphene Napsylate (USAN
USP); Levopropoxyphene Napsylate Anhydrous (FDA)
[(2S,3R)-4-(dimethylamino)-3-methyl-1,2-diphenylbutan-2-yl] propanoate hydrochloride
| 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) | 4.98 | 13.19 | -35.64 | 1 | 3 | 1 | 31 | 340.487 | 9 | ↓ |
| Note Type | Comments | Provided By |
|---|---|---|
| Molecular_Solubility | 5.517 | Bitter DB |
| PUBCHEM_PATENT_ID | EP0129284A2; EP0129285A2; EP0129285B1; EP0267617A1; EP0267617B1; EP0367746A2; EP0367746B1; EP0491076A1; EP0637448A1; EP0944601A1; EP0944604A1; EP0944620A1; EP0944621A1; EP0944622A1; EP0975627A1; EP0987997A1; EP1021204A2; EP1037887A1; US4028467; US4183939 | IBM Patent Data |
| Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
|---|---|---|---|---|---|
| KCNH2-5-E | HERG (cluster #5 Of 5), Eukaryotic | Eukaryotes | 2754 | 0.31 | Binding ≤ 10μM |
| Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
|---|---|---|---|---|---|
| KCNH2_HUMAN | Q12809 | HERG, Human | 2754.2287 | 0.31 | Binding ≤ 10μM |
| Description | Species |
|---|---|
| Voltage gated Potassium channels |