| ID | 1736 |
| Name | Chelirubine |
| Pubchem ID | 161243 |
| KEGG ID | C06327 |
| Source | Bocconia cordata |
| Type | Natural |
| Function | Nematocidal |
| Drug Like Properties | Yes |
| Molecular Weight | 362.36 |
| Exact mass | 362.102848 |
| Molecular formula | C21H16NO5+ |
| XlogP | 4.4 |
| Topological Polar Surface Area | 50 |
| H-Bond Donor | 0 |
| H-Bond Acceptor | 5 |
| Rotational Bond Count | 1 |
| IUPAC Name | N/A |
| Structure | |
| SDF file | |
| MOL file | |
| PDB file | |
| Canonical SMILE | C[N+]1=CC2=C3C(=CC(=C2C4=C1C5=CC6=C(C=C5C=C4)OCO6)OC)OCO3 |
| Isomeric SMILE | N/A |
| Drugpedia | wiki |
| References | 1. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21 2. Source 3. Function 4. All Records |
| ID | 1737 |
| Name | Chelirubine |
| Pubchem ID | 161243 |
| KEGG ID | C06327 |
| Source | Dicranostigma lactucoides |
| Type | Natural |
| Function | Nematocidal |
| Drug Like Properties | Yes |
| Molecular Weight | 362.36 |
| Exact mass | 362.102848 |
| Molecular formula | C21H16NO5+ |
| XlogP | 4.4 |
| Topological Polar Surface Area | 50 |
| H-Bond Donor | 0 |
| H-Bond Acceptor | 5 |
| Rotational Bond Count | 1 |
| IUPAC Name | N/A |
| Structure | |
| SDF file | |
| MOL file | |
| PDB file | |
| Canonical SMILE | C[N+]1=CC2=C3C(=CC(=C2C4=C1C5=CC6=C(C=C5C=C4)OCO6)OC)OCO3 |
| Isomeric SMILE | N/A |
| Drugpedia | wiki |
| References | 1. Dostal,Fitoterapia,63,(1992),67 2. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21 3. Source 4. Function 5. All Records |
| ID | 1738 |
| Name | Chelirubine |
| Pubchem ID | 161243 |
| KEGG ID | C06327 |
| Source | Eschscholtzia californica |
| Type | Natural |
| Function | Nematocidal |
| Drug Like Properties | Yes |
| Molecular Weight | 362.36 |
| Exact mass | 362.102848 |
| Molecular formula | C21H16NO5+ |
| XlogP | 4.4 |
| Topological Polar Surface Area | 50 |
| H-Bond Donor | 0 |
| H-Bond Acceptor | 5 |
| Rotational Bond Count | 1 |
| IUPAC Name | N/A |
| Structure | |
| SDF file | |
| MOL file | |
| PDB file | |
| Canonical SMILE | C[N+]1=CC2=C3C(=CC(=C2C4=C1C5=CC6=C(C=C5C=C4)OCO6)OC)OCO3 |
| Isomeric SMILE | N/A |
| Drugpedia | wiki |
| References | 1. Tanahashi,J.Nat.Prod.,53,(1990),579 2. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21 3. Source 4. Function 5. All Records |
| ID | 1739 |
| Name | Chelirubine |
| Pubchem ID | 161243 |
| KEGG ID | C06327 |
| Source | Stylophorum lasiocarpum |
| Type | Natural |
| Function | Nematocidal |
| Drug Like Properties | Yes |
| Molecular Weight | 362.36 |
| Exact mass | 362.102848 |
| Molecular formula | C21H16NO5+ |
| XlogP | 4.4 |
| Topological Polar Surface Area | 50 |
| H-Bond Donor | 0 |
| H-Bond Acceptor | 5 |
| Rotational Bond Count | 1 |
| IUPAC Name | N/A |
| Structure | |
| SDF file | |
| MOL file | |
| PDB file | |
| Canonical SMILE | C[N+]1=CC2=C3C(=CC(=C2C4=C1C5=CC6=C(C=C5C=C4)OCO6)OC)OCO3 |
| Isomeric SMILE | N/A |
| Drugpedia | wiki |
| References | 1. Slavik,Collect.Czech.Chem.Commun.,56,(1991),1116 2. Harborne,Phytochemical Dictionary Second Edition,Taylor and Francis,(1999),Chapter21 3. Source 4. Function 5. All Records |