ID: ALA5274515

Max Phase: Preclinical

Molecular Formula: C24H28O3

Molecular Weight: 364.49

Associated Items:

Representations

Canonical SMILES:  CC1(C)CCC[C@]2(C)Oc3cc(/C=C/c4ccc(O)cc4)cc(O)c3C[C@H]12

Standard InChI:  InChI=1S/C24H28O3/c1-23(2)11-4-12-24(3)22(23)15-19-20(26)13-17(14-21(19)27-24)6-5-16-7-9-18(25)10-8-16/h5-10,13-14,22,25-26H,4,11-12,15H2,1-3H3/b6-5+/t22-,24+/m1/s1

Standard InChI Key:  NVDNWXIJCXLGEI-LWZQCQJSSA-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: 5.79#Rotatable Bonds: 2
Polar Surface Area: 49.69Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.78CX Basic pKa: CX LogP: 6.19CX LogD: 6.17
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.66Np Likeness Score: 2.03

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