ID: ALA2335927

Max Phase: Preclinical

Molecular Formula: C7H10N8

Molecular Weight: 206.21

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1cnc2c(NC(=N)N)nc(N)nc21

Standard InChI:  InChI=1S/C7H10N8/c1-15-2-11-3-4(12-6(8)9)13-7(10)14-5(3)15/h2H,1H3,(H6,8,9,10,12,13,14)

Standard InChI Key:  KXVIRBDVITZEPK-UHFFFAOYSA-N

Associated Targets(Human)

Aurora kinase A/B 33 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MCF7 126967 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cyclin-dependent kinase 2/cyclin E1 1877 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cyclin-dependent kinase 1/cyclin B1 1887 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: 206.21Molecular Weight (Monoisotopic): 206.1028AlogP: -0.75#Rotatable Bonds: 1
Polar Surface Area: 131.52Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 8.16CX LogP: -0.65CX LogD: -1.47
Aromatic Rings: 2Heavy Atoms: 15QED Weighted: 0.36Np Likeness Score: -0.60

References

1. Dolečková I, Cesnek M, Dračinský M, Brynda J, Voller J, Janeba Z, Kryštof V..  (2013)  Synthesis and biological evaluation of guanidino analogues of roscovitine.,  62  [PMID:23399722] [10.1016/j.ejmech.2013.01.021]

Source