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ID: ALA610447
Max Phase: Preclinical
Molecular Formula: C22H23N5O4
Molecular Weight: 421.46
Molecule Type: Small molecule
Associated Items:
ID: ALA610447
Max Phase: Preclinical
Molecular Formula: C22H23N5O4
Molecular Weight: 421.46
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1ccc(/C=N/NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)c2ccc(OC)cc2)cc1
Standard InChI: InChI=1S/C22H23N5O4/c1-30-18-7-3-15(4-8-18)12-25-27-22(29)20(11-17-13-23-14-24-17)26-21(28)16-5-9-19(31-2)10-6-16/h3-10,12-14,20H,11H2,1-2H3,(H,23,24)(H,26,28)(H,27,29)/b25-12+/t20-/m0/s1
Standard InChI Key: DAEADLYMDBALSZ-GRMYTIJRSA-N
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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: 421.46 | Molecular Weight (Monoisotopic): 421.1750 | AlogP: 1.92 | #Rotatable Bonds: 9 |
Polar Surface Area: 117.70 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 9 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 11.65 | CX Basic pKa: 6.53 | CX LogP: 1.68 | CX LogD: 1.63 |
Aromatic Rings: 3 | Heavy Atoms: 31 | QED Weighted: 0.36 | Np Likeness Score: -0.90 |
1. Jin Y, Tan Z, He M, Tian B, Tang S, Hewlett I, Yang M.. (2010) SAR and molecular mechanism study of novel acylhydrazone compounds targeting HIV-1 CA., 18 (6): [PMID:20188575] [10.1016/j.bmc.2010.02.003] |
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