ID: ALA4587942

Max Phase: Preclinical

Molecular Formula: C26H31NO5S2

Molecular Weight: 501.67

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1cc(/C=C/C(=O)c2ccc(OCCSC(=S)N3CCCCC3)cc2)cc(OC)c1OC

Standard InChI:  InChI=1S/C26H31NO5S2/c1-29-23-17-19(18-24(30-2)25(23)31-3)7-12-22(28)20-8-10-21(11-9-20)32-15-16-34-26(33)27-13-5-4-6-14-27/h7-12,17-18H,4-6,13-16H2,1-3H3/b12-7+

Standard InChI Key:  WWGCVAQXKSATTA-KPKJPENVSA-N

Associated Targets(Human)

SK-N-SH 1499 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

ECa-109 cell line 1254 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MGC-803 6426 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 501.67Molecular Weight (Monoisotopic): 501.1644AlogP: 5.49#Rotatable Bonds: 10
Polar Surface Area: 57.23Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 5.36CX LogD: 5.36
Aromatic Rings: 2Heavy Atoms: 34QED Weighted: 0.18Np Likeness Score: -0.58

References

1. Fu DJ, Zhang SY, Liu YC, Zhang L, Liu JJ, Song J, Zhao RH, Li F, Sun HH, Liu HM, Zhang YB..  (2016)  Design, synthesis and antiproliferative activity studies of novel dithiocarbamate-chalcone derivates.,  26  (16): [PMID:27423479] [10.1016/j.bmcl.2016.07.012]

Source