ID: ALA138980

Max Phase: Preclinical

Molecular Formula: C22H31N5O2S

Molecular Weight: 429.59

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc2ncnc(N3CCN(/C(S)=N\CC4CCCCC4)CC3)c2cc1OC

Standard InChI:  InChI=1S/C22H31N5O2S/c1-28-19-12-17-18(13-20(19)29-2)24-15-25-21(17)26-8-10-27(11-9-26)22(30)23-14-16-6-4-3-5-7-16/h12-13,15-16H,3-11,14H2,1-2H3,(H,23,30)

Standard InChI Key:  ZQEYGEXISSRFCI-UHFFFAOYSA-N

Associated Targets(Human)

Platelet-derived growth factor receptor 507 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: 429.59Molecular Weight (Monoisotopic): 429.2198AlogP: 3.64#Rotatable Bonds: 5
Polar Surface Area: 63.08Molecular Species: ZWITTERIONHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: 1.11CX Basic pKa: 14.20CX LogP: 5.01CX LogD: 5.01
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.44Np Likeness Score: -0.75

References

1. Matsuno K, Nakajima T, Ichimura M, Giese NA, Yu JC, Lokker NA, Ushiki J, Ide S, Oda S, Nomoto Y..  (2002)  Potent and selective inhibitors of PDGF receptor phosphorylation. 2. Synthesis, structure activity relationship, improvement of aqueous solubility, and biological effects of 4-[4-(N-substituted (thio)carbamoyl)-1-piperazinyl]-6,7-dimethoxyquinazoline derivatives.,  45  (20): [PMID:12238930] [10.1021/jm0201114]

Source