Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA156658
Max Phase: Preclinical
Molecular Formula: C19H22O5
Molecular Weight: 330.38
Molecule Type: Small molecule
Associated Items:
ID: ALA156658
Max Phase: Preclinical
Molecular Formula: C19H22O5
Molecular Weight: 330.38
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1cc(CCc2cccc(OC)c(=O)c2)cc(OC)c1OC
Standard InChI: InChI=1S/C19H22O5/c1-21-16-7-5-6-13(10-15(16)20)8-9-14-11-17(22-2)19(24-4)18(12-14)23-3/h5-7,10-12H,8-9H2,1-4H3
Standard InChI Key: PRYCTZPJGHQBNV-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 330.38 | Molecular Weight (Monoisotopic): 330.1467 | AlogP: 2.87 | #Rotatable Bonds: 7 |
Polar Surface Area: 53.99 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.99 | CX LogD: 2.99 |
Aromatic Rings: 2 | Heavy Atoms: 24 | QED Weighted: 0.78 | Np Likeness Score: 0.31 |
1. Andres C, Bernardo J, Yan Q, Hastie S, Macdonald T. (1993) Combretatroponeshybrids of combretastatin and colchicine. Synthesis and biochemical evaluation, 3 (4): [10.1016/S0960-894X(01)81230-0] |
Source(1):