VESCALAGIN

ID: ALA607711

Max Phase: Preclinical

Molecular Formula: C41H26O26

Molecular Weight: 934.63

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): Vescalagin
Synonyms from Alternative Forms(1):

    Canonical SMILES:  O=C1OCC2OC(=O)c3cc(O)c(O)c(O)c3-c3c(O)c(O)c(O)c4c3C(=O)OC(C2OC(=O)c2cc(O)c(O)c(O)c2-c2c1cc(O)c(O)c2O)C1OC(=O)c2c-4c(O)c(O)c(O)c2C1O

    Standard InChI:  InChI=1S/C41H26O26/c42-8-1-5-12(24(48)21(8)45)13-6(2-9(43)22(46)25(13)49)39(60)65-34-11(4-63-37(5)58)64-38(59)7-3-10(44)23(47)26(50)14(7)15-18-16(28(52)32(56)27(15)51)17-19-20(30(54)33(57)29(17)53)31(55)35(66-41(19)62)36(34)67-40(18)61/h1-3,11,31,34-36,42-57H,4H2

    Standard InChI Key:  UDYKDZHZAKSYCO-UHFFFAOYSA-N

    Associated Targets(Human)

    TE-671 161 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    HCT-8 3484 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    A549 127892 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    KB 17409 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    HeLa 62764 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Blood 2950 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Associated Targets(non-human)

    Staphylococcus aureus 210822 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Candida albicans 78123 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Pseudomonas aeruginosa 123386 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

    Properties

    Molecular Weight: 934.63Molecular Weight (Monoisotopic): 934.0712AlogP: 1.32#Rotatable Bonds: 0
    Polar Surface Area: 455.18Molecular Species: NEUTRALHBA: 26HBD: 16
    #RO5 Violations: 3HBA (Lipinski): 26HBD (Lipinski): 16#RO5 Violations (Lipinski): 3
    CX Acidic pKa: 6.87CX Basic pKa: CX LogP: 2.03CX LogD: 1.03
    Aromatic Rings: 5Heavy Atoms: 67QED Weighted: 0.06Np Likeness Score: 0.99

    References

    1. König M, Scholz E, Hartmann R, Lehmann W, Rimpler H..  (1994)  Ellagitannins and complex tannins from Quercus petraea bark.,  57  (10): [PMID:7807126] [10.1021/np50112a010]
    2. Adamczeski M, Ni JX, Jaber H, Huang J, Kang R, Nakatsu T.  (1992)  A Novel Hydrolyzable Tannin and Related Compounds Isolated from the Leaf Surface of Chrysolepis sempervirens,  55  (4): [10.1021/np50082a024]
    3. Kashiwada Y, Nonaka G, Nishioka I, Chang JJ, Lee KH..  (1992)  Antitumor agents, 129. Tannins and related compounds as selective cytotoxic agents.,  55  (8): [PMID:1431932] [10.1021/np50086a002]
    4. Haslam E..  (1996)  Natural polyphenols (vegetable tannins) as drugs: possible modes of action.,  59  (2): [PMID:8991956] [10.1021/np960040+]

    Source