ID: ALA486115

Max Phase: Preclinical

Molecular Formula: C25H24N8O6

Molecular Weight: 532.52

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1ncnc2c1ncn2CCn1cc(CO[C@@H]2Cc3c(O)cc(O)cc3O[C@@H]2c2ccc(O)c(O)c2)nn1

Standard InChI:  InChI=1S/C25H24N8O6/c26-24-22-25(28-11-27-24)32(12-29-22)3-4-33-9-14(30-31-33)10-38-21-8-16-18(36)6-15(34)7-20(16)39-23(21)13-1-2-17(35)19(37)5-13/h1-2,5-7,9,11-12,21,23,34-37H,3-4,8,10H2,(H2,26,27,28)/t21-,23-/m1/s1

Standard InChI Key:  JOCMPDOPUFZEHZ-FYYLOGMGSA-N

Associated Targets(Human)

Ribonuclease pancreatic 45 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: 532.52Molecular Weight (Monoisotopic): 532.1819AlogP: 1.78#Rotatable Bonds: 7
Polar Surface Area: 199.71Molecular Species: NEUTRALHBA: 14HBD: 5
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 6#RO5 Violations (Lipinski): 3
CX Acidic pKa: 9.00CX Basic pKa: 4.74CX LogP: 1.81CX LogD: 1.80
Aromatic Rings: 5Heavy Atoms: 39QED Weighted: 0.19Np Likeness Score: 0.45

References

1. Roy B, Dutta S, Choudhary A, Basak A, Dasgupta S..  (2008)  Design, synthesis and RNase A inhibition activity of catechin and epicatechin and nucleobase chimeric molecules.,  18  (20): [PMID:18829315] [10.1016/j.bmcl.2008.09.051]

Source