ID: ALA4572031

Max Phase: Preclinical

Molecular Formula: C15H16N4O4

Molecular Weight: 316.32

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(NCc1ccccc1)c1c(NC2CC2)[nH]c(=O)n(O)c1=O

Standard InChI:  InChI=1S/C15H16N4O4/c20-13(16-8-9-4-2-1-3-5-9)11-12(17-10-6-7-10)18-15(22)19(23)14(11)21/h1-5,10,17,23H,6-8H2,(H,16,20)(H,18,22)

Standard InChI Key:  HYNAOOYWCMQTPT-UHFFFAOYSA-N

Associated Targets(Human)

CEM-SS 2428 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human immunodeficiency virus 1 70413 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Human immunodeficiency virus type 1 integrase 9041 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Properties

Molecular Weight: 316.32Molecular Weight (Monoisotopic): 316.1172AlogP: 0.28#Rotatable Bonds: 5
Polar Surface Area: 116.22Molecular Species: ACIDHBA: 6HBD: 4
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 5.37CX Basic pKa: CX LogP: 0.27CX LogD: -1.61
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.59Np Likeness Score: -0.80

References

1. Wu B, Tang J, Wilson DJ, Huber AD, Casey MC, Ji J, Kankanala J, Xie J, Sarafianos SG, Wang Z..  (2016)  3-Hydroxypyrimidine-2,4-dione-5-N-benzylcarboxamides Potently Inhibit HIV-1 Integrase and RNase H.,  59  (13): [PMID:27283261] [10.1021/acs.jmedchem.6b00040]

Source