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ID: ALA3616998
Max Phase: Preclinical
Molecular Formula: C14H13NO3
Molecular Weight: 243.26
Molecule Type: Small molecule
Associated Items:
ID: ALA3616998
Max Phase: Preclinical
Molecular Formula: C14H13NO3
Molecular Weight: 243.26
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=C(NCc1ccc(O)c(O)c1)c1ccccc1
Standard InChI: InChI=1S/C14H13NO3/c16-12-7-6-10(8-13(12)17)9-15-14(18)11-4-2-1-3-5-11/h1-8,16-17H,9H2,(H,15,18)
Standard InChI Key: LSJYCBNGIFOQTK-UHFFFAOYSA-N
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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: 243.26 | Molecular Weight (Monoisotopic): 243.0895 | AlogP: 2.03 | #Rotatable Bonds: 3 |
Polar Surface Area: 69.56 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 9.25 | CX Basic pKa: | CX LogP: 2.16 | CX LogD: 2.16 |
Aromatic Rings: 2 | Heavy Atoms: 18 | QED Weighted: 0.72 | Np Likeness Score: -0.47 |
1. Chapman TM, Gillen KJ, Wallace C, Lee MT, Bakrania P, Khurana P, Coombs PJ, Stennett L, Fox S, Bureau EA, Brownlees J, Melton DW, Saxty B.. (2015) Catechols and 3-hydroxypyridones as inhibitors of the DNA repair complex ERCC1-XPF., 25 (19): [PMID:26318993] [10.1016/j.bmcl.2015.08.031] |
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