ID: ALA3808734

Max Phase: Preclinical

Molecular Formula: C25H27N7O6

Molecular Weight: 521.53

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  NC(=O)COc1cc(CNc2nc3c(N)ncnc3n2[C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)ccc1-c1ccccc1

Standard InChI:  InChI=1S/C25H27N7O6/c26-18(34)11-37-16-8-13(6-7-15(16)14-4-2-1-3-5-14)9-28-25-31-19-22(27)29-12-30-23(19)32(25)24-21(36)20(35)17(10-33)38-24/h1-8,12,17,20-21,24,33,35-36H,9-11H2,(H2,26,34)(H,28,31)(H2,27,29,30)/t17-,20-,21-,24-/m1/s1

Standard InChI Key:  XLLWHNLRPAWRFN-FGSUIDRYSA-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: 521.53Molecular Weight (Monoisotopic): 521.2023AlogP: 0.16#Rotatable Bonds: 9
Polar Surface Area: 203.89Molecular Species: NEUTRALHBA: 12HBD: 6
#RO5 Violations: 3HBA (Lipinski): 13HBD (Lipinski): 8#RO5 Violations (Lipinski): 3
CX Acidic pKa: 12.45CX Basic pKa: 4.47CX LogP: -0.05CX LogD: -0.05
Aromatic Rings: 4Heavy Atoms: 38QED Weighted: 0.18Np Likeness Score: -0.10

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