ID: ALA5205354

Max Phase: Preclinical

Molecular Formula: C33H38O14S

Molecular Weight: 690.72

Associated Items:

Representations

Canonical SMILES:  CC(=O)OCC1=CC[C@@H]2C(C(=O)SCc3ccccc3)=CO[C@@H](O[C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]3OC(C)=O)[C@H]12

Standard InChI:  InChI=1S/C33H38O14S/c1-17(34)40-13-23-11-12-24-25(31(39)48-16-22-9-7-6-8-10-22)14-42-32(27(23)24)47-33-30(45-21(5)38)29(44-20(4)37)28(43-19(3)36)26(46-33)15-41-18(2)35/h6-11,14,24,26-30,32-33H,12-13,15-16H2,1-5H3/t24-,26-,27-,28-,29+,30-,32+,33+/m1/s1

Standard InChI Key:  HEOOAYJMBVNHFW-NAVWFSHISA-N

Associated Targets(non-human)

Xanthine dehydrogenase 2296 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: 690.72Molecular Weight (Monoisotopic): 690.1982AlogP: 2.91#Rotatable Bonds: 12
Polar Surface Area: 176.26Molecular Species: NEUTRALHBA: 15HBD: 0
#RO5 Violations: 2HBA (Lipinski): 14HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 2.37CX LogD: 2.37
Aromatic Rings: 1Heavy Atoms: 48QED Weighted: 0.18Np Likeness Score: 1.37

References

1. Chen JS, Wang MX, Wang MM, Zhang YK, Guo X, Chen YY, Zhang MQ, Sun JY, Liu YF, Liu C..  (2022)  Synthesis and biological evaluation of geniposide derivatives as inhibitors of hyperuricemia, inflammatory and fibrosis.,  237  [PMID:35468514] [10.1016/j.ejmech.2022.114379]

Source