ID: ALA612171

Max Phase: Preclinical

Molecular Formula: C13H15N5O5

Molecular Weight: 321.29

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cn2c(O)c3ncn(C4O[C@H](CO)[C@@H](O)[C@H]4O)c3nc2n1

Standard InChI:  InChI=1S/C13H15N5O5/c1-5-2-17-11(22)7-10(16-13(17)15-5)18(4-14-7)12-9(21)8(20)6(3-19)23-12/h2,4,6,8-9,12,19-22H,3H2,1H3/t6-,8-,9-,12?/m1/s1

Standard InChI Key:  YYRYAERLJJQKDV-PUXKXDTASA-N

Associated Targets(Human)

HEL 6614 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: 321.29Molecular Weight (Monoisotopic): 321.1073AlogP: -1.30#Rotatable Bonds: 2
Polar Surface Area: 138.16Molecular Species: NEUTRALHBA: 10HBD: 4
#RO5 Violations: 0HBA (Lipinski): 10HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.63CX Basic pKa: 3.10CX LogP: -2.18CX LogD: -2.18
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.46Np Likeness Score: 0.47

References

1. Boryski J, Golankiewicz B, De Clercq E..  (1991)  Synthesis and antiviral activity of 3-substituted derivatives of 3,9-dihydro-9-oxo-5H-imidazo[1,2-a]purines, tricyclic analogues of acyclovir and ganciclovir.,  34  (8): [PMID:1652016] [10.1021/jm00112a010]

Source