ID: ALA49204

Max Phase: Preclinical

Molecular Formula: C11H12FN5O2

Molecular Weight: 265.25

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1ncnc2c1ncn2[C@@H]1C/C(=C/F)[C@@H](O)[C@H]1O

Standard InChI:  InChI=1S/C11H12FN5O2/c12-2-5-1-6(9(19)8(5)18)17-4-16-7-10(13)14-3-15-11(7)17/h2-4,6,8-9,18-19H,1H2,(H2,13,14,15)/b5-2-/t6-,8-,9+/m1/s1

Standard InChI Key:  KOUXHHRRBXETSM-XNWSGGPBSA-N

Associated Targets(non-human)

Adenosylhomocysteinase 70 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: 265.25Molecular Weight (Monoisotopic): 265.0975AlogP: -0.07#Rotatable Bonds: 1
Polar Surface Area: 110.08Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.13CX Basic pKa: 3.68CX LogP: -1.15CX LogD: -1.15
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.67Np Likeness Score: 0.51

References

1. Liu S, Wolfe MS, Yuan C, Ali SM, Borchardt RT.  (1992)  Synthesis and evaluation of 4-5-dehydro-5-fluoroaristeromycins as S-adenosyl-L-homocysteine (AdoHcy) hydrolase inhibitors,  (12): [10.1016/S0960-894X(00)80467-9]

Source