Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5198285
Max Phase: Preclinical
Molecular Formula: C23H22N4O
Molecular Weight: 370.46
Associated Items:
ID: ALA5198285
Max Phase: Preclinical
Molecular Formula: C23H22N4O
Molecular Weight: 370.46
Associated Items:
Canonical SMILES: Cc1cccc(NC(=O)NCCc2cccc(-c3cnc4[nH]ccc4c3)c2)c1
Standard InChI: InChI=1S/C23H22N4O/c1-16-4-2-7-21(12-16)27-23(28)25-10-8-17-5-3-6-18(13-17)20-14-19-9-11-24-22(19)26-15-20/h2-7,9,11-15H,8,10H2,1H3,(H,24,26)(H2,25,27,28)
Standard InChI Key: NYTRCRVOIPGPHC-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: 370.46 | Molecular Weight (Monoisotopic): 370.1794 | AlogP: 4.90 | #Rotatable Bonds: 5 |
Polar Surface Area: 69.81 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 13.59 | CX Basic pKa: 3.13 | CX LogP: 4.52 | CX LogD: 4.52 |
Aromatic Rings: 4 | Heavy Atoms: 28 | QED Weighted: 0.47 | Np Likeness Score: -1.33 |
1. Zhang XX, Xiao Y, Yan YY, Wang YM, Jiang H, Wu L, Shi JB, Liu XH.. (2022) Discovery of the Novel 1H-Pyrrolo[2,3-b]pyridine Derivative as a Potent Type II CDK8 Inhibitor against Colorectal Cancer., 65 (18.0): [PMID:36068975] [10.1021/acs.jmedchem.2c00820] |
Source(1):