6-(9-chloro-4-(4-fluorophenyl)-5H-chromeno[4,3-b]pyridin-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-3-ol

ID: ALA1774938

Chembl Id: CHEMBL1774938

PubChem CID: 53237234

Max Phase: Preclinical

Molecular Formula: C26H18ClFN2O3

Molecular Weight: 460.89

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  OC1COc2ccc(-c3cc(-c4ccc(F)cc4)c4c(n3)-c3cc(Cl)ccc3OC4)cc2N1

Standard InChI:  InChI=1S/C26H18ClFN2O3/c27-16-4-8-23-19(10-16)26-20(12-32-23)18(14-1-5-17(28)6-2-14)11-21(30-26)15-3-7-24-22(9-15)29-25(31)13-33-24/h1-11,25,29,31H,12-13H2

Standard InChI Key:  NVLFLIGMWAYTNM-UHFFFAOYSA-N

Associated Targets(non-human)

OPG116 Uracil-DNA glycosylase (82 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vaccinia virus (4609 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BSC-1 (357 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 460.89Molecular Weight (Monoisotopic): 460.0990AlogP: 5.89#Rotatable Bonds: 2
Polar Surface Area: 63.61Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 10.96CX Basic pKa: 2.99CX LogP: 5.59CX LogD: 5.59
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.39Np Likeness Score: -0.57

References

1. Nuth M, Huang L, Saw YL, Schormann N, Chattopadhyay D, Ricciardi RP..  (2011)  Identification of inhibitors that block vaccinia virus infection by targeting the DNA synthesis processivity factor D4.,  54  (9): [PMID:21438571] [10.1021/jm101554k]

Source