ID: ALA3357923

Max Phase: Preclinical

Molecular Formula: C8H10N4O7

Molecular Weight: 274.19

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=c1[nH]c(=O)n(COC(CO)CO)c2no[n+]([O-])c12

Standard InChI:  InChI=1S/C8H10N4O7/c13-1-4(2-14)18-3-11-6-5(12(17)19-10-6)7(15)9-8(11)16/h4,13-14H,1-3H2,(H,9,15,16)

Standard InChI Key:  FRIMMAMRDWFWQN-UHFFFAOYSA-N

Associated Targets(Human)

WISH 126 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Vesicular stomatitis virus 4460 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

Properties

Molecular Weight: 274.19Molecular Weight (Monoisotopic): 274.0549AlogP: -3.36#Rotatable Bonds: 5
Polar Surface Area: 157.52Molecular Species: NEUTRALHBA: 9HBD: 3
#RO5 Violations: 0HBA (Lipinski): 11HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 7.04CX Basic pKa: CX LogP: -3.49CX LogD: -4.00
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.48Np Likeness Score: -0.17

References

1. Xu X, Wang J, Yao Q..  (2015)  Synthesis and quantitative structure-activity relationship (QSAR) analysis of some novel oxadiazolo[3,4-d]pyrimidine nucleosides derivatives as antiviral agents.,  25  (2): [PMID:25515560] [10.1016/j.bmcl.2014.11.065]

Source