(2R,3S,4R)-4-(2,4-dihydroxyphenyl)-2-(3,4-dihydroxyphenyl)chroman-3,5,7-triol

ID: ALA1223840

Chembl Id: CHEMBL1223840

PubChem CID: 14009015

Max Phase: Preclinical

Molecular Formula: C21H18O8

Molecular Weight: 398.37

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  Oc1ccc([C@@H]2c3c(O)cc(O)cc3O[C@H](c3ccc(O)c(O)c3)[C@H]2O)c(O)c1

Standard InChI:  InChI=1S/C21H18O8/c22-10-2-3-12(14(25)6-10)18-19-16(27)7-11(23)8-17(19)29-21(20(18)28)9-1-4-13(24)15(26)5-9/h1-8,18,20-28H/t18-,20+,21-/m1/s1

Standard InChI Key:  HHTOABNBQKDYJW-HLAWJBBLSA-N

Associated Targets(Human)

RNASE1 Tchem Ribonuclease pancreatic (45 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

Calculated Properties

Molecular Weight: 398.37Molecular Weight (Monoisotopic): 398.1002AlogP: 2.55#Rotatable Bonds: 2
Polar Surface Area: 150.84Molecular Species: NEUTRALHBA: 8HBD: 7
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 7#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.79CX Basic pKa: CX LogP: 2.69CX LogD: 2.67
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.33Np Likeness Score: 1.96

References

1. Dutta S, Basak A, Dasgupta S..  (2010)  Synthesis and ribonuclease A inhibition activity of resorcinol and phloroglucinol derivatives of catechin and epicatechin: Importance of hydroxyl groups.,  18  (17): [PMID:20692173] [10.1016/j.bmc.2010.06.077]

Source