ID: ALA3350644

Max Phase: Preclinical

Molecular Formula: C12H20N5O13P3

Molecular Weight: 535.24

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=C1C(=O)NC(=O)N([C@H]2C[C@H](N=[N+]=[N-])[C@@H](COCP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)C1C

Standard InChI:  InChI=1S/C12H20N5O13P3/c1-6-7(2)17(12(19)14-11(6)18)10-3-8(15-16-13)9(28-10)4-27-5-31(20,21)29-33(25,26)30-32(22,23)24/h7-10H,1,3-5H2,2H3,(H,20,21)(H,25,26)(H,14,18,19)(H2,22,23,24)/t7?,8-,9+,10+/m0/s1

Standard InChI Key:  UVIUBXKVDCKKBS-HCZOVWHVSA-N

Associated Targets(non-human)

Murine leukemia virus 47 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Human immunodeficiency virus type 1 reverse transcriptase 18245 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: 535.24Molecular Weight (Monoisotopic): 535.0270AlogP: 0.66#Rotatable Bonds: 10
Polar Surface Area: 267.22Molecular Species: ACIDHBA: 10HBD: 5
#RO5 Violations: 1HBA (Lipinski): 18HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: -10.24CX Basic pKa: CX LogP: -1.37CX LogD: -8.66
Aromatic Rings: 0Heavy Atoms: 33QED Weighted: 0.08Np Likeness Score: 1.04

References

1. Jie L, Van Aerschot A, Balzarini J, Janssen G, Busson R, Hoogmartens J, De Clercq E, Herdewijn P..  (1990)  5'-O-phosphonomethyl-2',3'-dideoxynucleosides: synthesis and anti-HIV activity.,  33  (9): [PMID:1697345] [10.1021/jm00171a023]

Source