(2R,3R,4R,5R)-5-(2-amino-6-oxo-1H-purin-9(6H)-yl)-4-fluoro-3-hydroxy-2-(hydroxymethyl)tetrahydrofuran-2-carbonitrile

ID: ALA3425974

Chembl Id: CHEMBL3425974

PubChem CID: 136236459

Max Phase: Preclinical

Molecular Formula: C11H11FN6O4

Molecular Weight: 310.25

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  N#C[C@]1(CO)O[C@@H](n2cnc3c(=O)[nH]c(N)nc32)[C@H](F)[C@@H]1O

Standard InChI:  InChI=1S/C11H11FN6O4/c12-4-6(20)11(1-13,2-19)22-9(4)18-3-15-5-7(18)16-10(14)17-8(5)21/h3-4,6,9,19-20H,2H2,(H3,14,16,17,21)/t4-,6+,9-,11-/m1/s1

Standard InChI Key:  YJJFQCVGOBHMFP-RUQSRZACSA-N

Alternative Forms

  1. Parent:

    ALA3425974

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Associated Targets(Human)

POLRMT Tbio DNA-directed RNA polymerase, mitochondrial (57 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLG Tchem DNA polymerase subunit gamma-1/gamma-2 (16 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MT4 (17854 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

Calculated Properties

Molecular Weight: 310.25Molecular Weight (Monoisotopic): 310.0826AlogP: -1.82#Rotatable Bonds: 2
Polar Surface Area: 163.07Molecular Species: NEUTRALHBA: 9HBD: 4
#RO5 Violations: HBA (Lipinski): 10HBD (Lipinski): 5#RO5 Violations (Lipinski):
CX Acidic pKa: 10.15CX Basic pKa: 0.44CX LogP: -2.05CX LogD: -2.05
Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.50Np Likeness Score: 0.64

References

1. Clarke MO, Mackman R, Byun D, Hui H, Barauskas O, Birkus G, Chun BK, Doerffler E, Feng J, Karki K, Lee G, Perron M, Siegel D, Swaminathan S, Lee W..  (2015)  Discovery of β-D-2'-deoxy-2'-α-fluoro-4'-α-cyano-5-aza-7,9-dideaza adenosine as a potent nucleoside inhibitor of respiratory syncytial virus with excellent selectivity over mitochondrial RNA and DNA polymerases.,  25  (12): [PMID:25978965] [10.1016/j.bmcl.2015.04.073]

Source