3,4-dihydroxybenzoic anhydride

ID: ALA3233513

Chembl Id: CHEMBL3233513

PubChem CID: 25064624

Max Phase: Preclinical

Molecular Formula: C14H10O7

Molecular Weight: 290.23

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  O=C(OC(=O)c1ccc(O)c(O)c1)c1ccc(O)c(O)c1

Standard InChI:  InChI=1S/C14H10O7/c15-9-3-1-7(5-11(9)17)13(19)21-14(20)8-2-4-10(16)12(18)6-8/h1-6,15-18H

Standard InChI Key:  INZJGLGPSGHIGY-UHFFFAOYSA-N

Alternative Forms

Associated Targets(non-human)

NA Neuraminidase (32 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Genome polyprotein (177 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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: 290.23Molecular Weight (Monoisotopic): 290.0427AlogP: 1.51#Rotatable Bonds: 2
Polar Surface Area: 124.29Molecular Species: NEUTRALHBA: 7HBD: 4
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 4#RO5 Violations (Lipinski):
CX Acidic pKa: 8.18CX Basic pKa: CX LogP: 2.58CX LogD: 2.51
Aromatic Rings: 2Heavy Atoms: 21QED Weighted: 0.38Np Likeness Score: 0.37

References

1. Abdel-Mageed WM, Bayoumi SA, Chen C, Vavricka CJ, Li L, Malik A, Dai H, Song F, Wang L, Zhang J, Gao GF, Lv Y, Liu L, Liu X, Sayed HM, Zhang L..  (2014)  Benzophenone C-glucosides and gallotannins from mango tree stem bark with broad-spectrum anti-viral activity.,  22  (7): [PMID:24613627] [10.1016/j.bmc.2014.02.014]

Source