ID: ALA4098478

Max Phase: Preclinical

Molecular Formula: C26H28O6

Molecular Weight: 436.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=C1C(=O)O[C@@H]2C3=C(C)[C@@H](OC(=O)/C=C/c4ccccc4)CC3[C@](C)(OC(C)=O)CC[C@@H]12

Standard InChI:  InChI=1S/C26H28O6/c1-15-19-12-13-26(4,32-17(3)27)20-14-21(16(2)23(20)24(19)31-25(15)29)30-22(28)11-10-18-8-6-5-7-9-18/h5-11,19-21,24H,1,12-14H2,2-4H3/b11-10+/t19-,20?,21-,24-,26+/m0/s1

Standard InChI Key:  GEWNKOJBAOWRAB-WKSFWCIKSA-N

Associated Targets(Human)

Ubiquitin-conjugating enzyme E2 D3 121 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HepG2 196354 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

QGY-7703 248 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

SMMC-7721 5516 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: 436.50Molecular Weight (Monoisotopic): 436.1886AlogP: 4.16#Rotatable Bonds: 4
Polar Surface Area: 78.90Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.33CX LogD: 4.33
Aromatic Rings: 1Heavy Atoms: 32QED Weighted: 0.31Np Likeness Score: 2.45

References

1. Chen H, Wu G, Gao S, Guo R, Zhao Z, Yuan H, Liu S, Wu J, Lu X, Yuan X, Yu Z, Zu X, Xie N, Yang N, Hu Z, Sun Q, Zhang W..  (2017)  Discovery of Potent Small-Molecule Inhibitors of Ubiquitin-Conjugating Enzyme UbcH5c from α-Santonin Derivatives.,  60  (16): [PMID:28696694] [10.1021/acs.jmedchem.6b01829]
2. Chen H, Yang X, Yu Z, Cheng Z, Yuan H, Zhao Z, Wu G, Xie N, Yuan X, Sun Q, Zhang W..  (2018)  Synthesis and biological evaluation of α-santonin derivatives as anti-hepatoma agents.,  149  [PMID:29499490] [10.1016/j.ejmech.2018.02.073]

Source