Mangiferin methyl ether

ID: ALA3233510

Chembl Id: CHEMBL3233510

Cas Number: 21794-66-1

PubChem CID: 5491388

Max Phase: Preclinical

Molecular Formula: C20H20O11

Molecular Weight: 436.37

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc2oc3cc(O)c(O)cc3c(=O)c2c(O)c1[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

Standard InChI:  InChI=1S/C20H20O11/c1-29-10-4-11-13(15(24)6-2-7(22)8(23)3-9(6)30-11)17(26)14(10)20-19(28)18(27)16(25)12(5-21)31-20/h2-4,12,16,18-23,25-28H,5H2,1H3/t12-,16-,18+,19-,20+/m1/s1

Standard InChI Key:  HDPSXKXQSOVYLL-PQSJUMPYSA-N

Alternative Forms

  1. Parent:

    ALA3233510

    Homomangiferin

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: 436.37Molecular Weight (Monoisotopic): 436.1006AlogP: -0.41#Rotatable Bonds: 3
Polar Surface Area: 190.28Molecular Species: NEUTRALHBA: 11HBD: 7
#RO5 Violations: 2HBA (Lipinski): 11HBD (Lipinski): 7#RO5 Violations (Lipinski): 2
CX Acidic pKa: 7.39CX Basic pKa: CX LogP: -0.22CX LogD: -0.56
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.21Np Likeness Score: 1.96

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