ID: ALA5281149

Max Phase: Preclinical

Molecular Formula: C24H28O3

Molecular Weight: 364.49

Associated Items:

Representations

Canonical SMILES:  CC1=CCCC(C)(C)[C@H]1Cc1c(O)cc(/C=C/c2ccc(O)cc2)cc1O

Standard InChI:  InChI=1S/C24H28O3/c1-16-5-4-12-24(2,3)21(16)15-20-22(26)13-18(14-23(20)27)7-6-17-8-10-19(25)11-9-17/h5-11,13-14,21,25-27H,4,12,15H2,1-3H3/b7-6+/t21-/m0/s1

Standard InChI Key:  PFXULLDGLDNOOD-BXKJMJEDSA-N

Associated Targets(Human)

HT-29 80576 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MCF7 126967 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

CCRF-CEM 65223 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

NCI-H460 60772 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 364.49Molecular Weight (Monoisotopic): 364.2038AlogP: 5.90#Rotatable Bonds: 4
Polar Surface Area: 60.69Molecular Species: NEUTRALHBA: 3HBD: 3
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.67CX Basic pKa: CX LogP: 6.43CX LogD: 6.41
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.47Np Likeness Score: 1.77

References

1. Lin CT, Yang YH, Cheng JJ, Don MJ..  (2023)  Total Syntheses, Absolute Configurations, and Cytotoxicity Evaluation of Ugonstilbenes A, B, and C from the Rhizomes of Helminthostachys zeylanica.,  86  (2.0): [PMID:36691388] [10.1021/acs.jnatprod.2c00919]

Source