ID: ALA3589321

Max Phase: Preclinical

Molecular Formula: C22H27N5O2S

Molecular Weight: 425.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCN1C(=S)N2CCCC2c2c(N3CCOCC3)nc(-c3ccc(OC)cc3)nc21

Standard InChI:  InChI=1S/C22H27N5O2S/c1-3-26-21-18(17-5-4-10-27(17)22(26)30)20(25-11-13-29-14-12-25)23-19(24-21)15-6-8-16(28-2)9-7-15/h6-9,17H,3-5,10-14H2,1-2H3

Standard InChI Key:  MLUMXMVEGLESPK-UHFFFAOYSA-N

Associated Targets(Human)

PIK3CB Tchem PI3-kinase p110-beta subunit (4044 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIK3CG Tclin PI3-kinase p110-gamma subunit (5411 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIK3CD Tclin PI3-kinase p110-delta subunit (6699 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PIK3C2B Tchem Phosphatidylinositol-4-phosphate 3-kinase C2 domain-containing beta polypeptide (438 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HeLa (62764 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SK-OV-3 (52876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

PIK3CA PI3-kinase p110-alpha subunit (51 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: 425.56Molecular Weight (Monoisotopic): 425.1885AlogP: 3.25#Rotatable Bonds: 4
Polar Surface Area: 53.96Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.27CX LogP: 4.09CX LogD: 4.09
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.69Np Likeness Score: -1.17

References

1. Ibrahim MA, Abou-Seri SM, Hanna MM, Abdalla MM, El Sayed NA..  (2015)  Design, synthesis and biological evaluation of novel condensed pyrrolo[1,2-c]pyrimidines featuring morpholine moiety as PI3Kα inhibitors.,  99  [PMID:26037808] [10.1016/j.ejmech.2015.05.036]

Source