ID: ALA2313858

Max Phase: Preclinical

Molecular Formula: C35H50O9

Molecular Weight: 614.78

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCCCCC(=O)O[C@H]1c2cc(OC)c(OC)c(OC)c2-c2c(cc3c(c2OC)OCO3)C[C@H](C)[C@]1(C)O

Standard InChI:  InChI=1S/C35H50O9/c1-8-9-10-11-12-13-14-15-16-17-27(36)44-34-24-20-25(38-4)30(39-5)33(41-7)29(24)28-23(18-22(2)35(34,3)37)19-26-31(32(28)40-6)43-21-42-26/h19-20,22,34,37H,8-18,21H2,1-7H3/t22-,34-,35-/m0/s1

Standard InChI Key:  VOPUILLVARXVAT-LUXASXKVSA-N

Associated Targets(Human)

DNA-binding protein inhibitor ID-1 18 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: 614.78Molecular Weight (Monoisotopic): 614.3455AlogP: 7.57#Rotatable Bonds: 15
Polar Surface Area: 101.91Molecular Species: NEUTRALHBA: 9HBD: 1
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 13.67CX Basic pKa: CX LogP: 7.55CX LogD: 7.55
Aromatic Rings: 2Heavy Atoms: 44QED Weighted: 0.16Np Likeness Score: 1.62

References

1. Liu HW, Yu XZ, Padula D, Pescitelli G, Lin ZW, Wang F, Ding K, Lei M, Gao JM..  (2013)  Lignans from Schisandra sphenathera Rehd. et Wils. and semisynthetic schisantherin A analogues: absolute configuration, and their estrogenic and anti-proliferative activity.,  59  [PMID:23237974] [10.1016/j.ejmech.2012.11.003]

Source