Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5207545
Max Phase: Preclinical
Molecular Formula: C20H18N2O3
Molecular Weight: 334.38
Associated Items:
ID: ALA5207545
Max Phase: Preclinical
Molecular Formula: C20H18N2O3
Molecular Weight: 334.38
Associated Items:
Canonical SMILES: O=c1ccc2cc(OCCCCn3cnc4ccccc43)ccc2o1
Standard InChI: InChI=1S/C20H18N2O3/c23-20-10-7-15-13-16(8-9-19(15)25-20)24-12-4-3-11-22-14-21-17-5-1-2-6-18(17)22/h1-2,5-10,13-14H,3-4,11-12H2
Standard InChI Key: ZNODOKXMXCWWEQ-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: | 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: 334.38 | Molecular Weight (Monoisotopic): 334.1317 | AlogP: 4.00 | #Rotatable Bonds: 6 |
Polar Surface Area: 57.26 | 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: 5.37 | CX LogP: 3.51 | CX LogD: 3.51 |
Aromatic Rings: 4 | Heavy Atoms: 25 | QED Weighted: 0.39 | Np Likeness Score: -0.95 |
1. G AC, Gondru R, Li Y, Banothu J.. (2022) Coumarin-benzimidazole hybrids: A review of developments in medicinal chemistry., 227 [PMID:34715585] [10.1016/j.ejmech.2021.113921] |
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