ID: ALA3809948

Max Phase: Preclinical

Molecular Formula: C22H23N7O4

Molecular Weight: 449.47

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1ncnc2c1nc(NCc1ccc(-c3ccccn3)cc1)n2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O

Standard InChI:  InChI=1S/C22H23N7O4/c23-19-16-20(27-11-26-19)29(21-18(32)17(31)15(10-30)33-21)22(28-16)25-9-12-4-6-13(7-5-12)14-3-1-2-8-24-14/h1-8,11,15,17-18,21,30-32H,9-10H2,(H,25,28)(H2,23,26,27)/t15-,17-,18-,21-/m1/s1

Standard InChI Key:  JROHPLSDNYWYPR-QTQZEZTPSA-N

Associated Targets(Human)

Sodium/nucleoside cotransporter 2 91 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Sodium/nucleoside cotransporter 2 36 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: 449.47Molecular Weight (Monoisotopic): 449.1812AlogP: 0.69#Rotatable Bonds: 6
Polar Surface Area: 164.46Molecular Species: NEUTRALHBA: 11HBD: 5
#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 6#RO5 Violations (Lipinski): 2
CX Acidic pKa: 12.45CX Basic pKa: 4.75CX LogP: 0.61CX LogD: 0.61
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.28Np Likeness Score: -0.12

References

1. Tatani K, Hiratochi M, Kikuchi N, Kuramochi Y, Watanabe S, Yamauchi Y, Itoh F, Isaji M, Shuto S..  (2016)  Identification of Adenine and Benzimidazole Nucleosides as Potent Human Concentrative Nucleoside Transporter 2 Inhibitors: Potential Treatment for Hyperuricemia and Gout.,  59  (8): [PMID:27007871] [10.1021/acs.jmedchem.5b01884]

Source