ID: ALA4277156

Max Phase: Preclinical

Molecular Formula: C27H23NO7

Molecular Weight: 473.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(/C=C/C(=O)c2ccc(OCC(=O)Nc3ccc4c(c3)COC4=O)cc2)cc1OC

Standard InChI:  InChI=1S/C27H23NO7/c1-32-24-12-4-17(13-25(24)33-2)3-11-23(29)18-5-8-21(9-6-18)34-16-26(30)28-20-7-10-22-19(14-20)15-35-27(22)31/h3-14H,15-16H2,1-2H3,(H,28,30)/b11-3+

Standard InChI Key:  WEWVPFRDDBNWDX-QDEBKDIKSA-N

Associated Targets(Human)

IMPDH2 Tclin Inosine-5'-monophosphate dehydrogenase 2 (1326 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCG2 Tchem ATP-binding cassette sub-family G member 2 (4927 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: 473.48Molecular Weight (Monoisotopic): 473.1475AlogP: 4.29#Rotatable Bonds: 9
Polar Surface Area: 100.16Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.17CX Basic pKa: CX LogP: 3.88CX LogD: 3.88
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.28Np Likeness Score: -0.54

References

1. Shah CP, Kharkar PS..  (2018)  Discovery of novel human inosine 5'-monophosphate dehydrogenase 2 (hIMPDH2) inhibitors as potential anticancer agents.,  158  [PMID:30223117] [10.1016/j.ejmech.2018.09.016]
2. Silbermann K, Shah CP, Sahu NU, Juvale K, Stefan SM, Kharkar PS, Wiese M..  (2019)  Novel chalcone and flavone derivatives as selective and dual inhibitors of the transport proteins ABCB1 and ABCG2.,  164  [PMID:30594677] [10.1016/j.ejmech.2018.12.019]

Source