ID: ALA2368584

Max Phase: Preclinical

Molecular Formula: C12H16N4O3

Molecular Weight: 264.29

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1nc(N)c2ccn([C@H]3C[C@H](O)[C@@H](CO)O3)c2n1

Standard InChI:  InChI=1S/C12H16N4O3/c1-6-14-11(13)7-2-3-16(12(7)15-6)10-4-8(18)9(5-17)19-10/h2-3,8-10,17-18H,4-5H2,1H3,(H2,13,14,15)/t8-,9+,10+/m0/s1

Standard InChI Key:  LDNDODQBCHXFEA-IVZWLZJFSA-N

Associated Targets(non-human)

Human respirovirus 3 1674 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Measles morbillivirus 693 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vaccinia virus 4609 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Human alphaherpesvirus 2 4932 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: 264.29Molecular Weight (Monoisotopic): 264.1222AlogP: -0.04#Rotatable Bonds: 2
Polar Surface Area: 106.42Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.89CX Basic pKa: 7.56CX LogP: -0.01CX LogD: -0.39
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.70Np Likeness Score: 0.51

References

1. Cottam HB, Kazimierczuk Z, Geary S, McKernan PA, Revankar GR, Robins RK..  (1985)  Synthesis and biological activity of certain 6-substituted and 2,6-disubstituted 2'-deoxytubercidins prepared via the stereospecific sodium salt glycosylation procedure.,  28  (10): [PMID:2995666] [10.1021/jm00148a015]

Source