ID: ALA1770694

Max Phase: Preclinical

Molecular Formula: C19H36O8

Molecular Weight: 392.49

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): Iso-Dihydrodendranthemoside A
Synonyms from Alternative Forms(1):

    Canonical SMILES:  C[C@H](O)CC[C@@]1(O)[C@@H](C)C[C@H](O[C@H]2O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]2O)CC1(C)C

    Standard InChI:  InChI=1S/C19H36O8/c1-10-7-12(8-18(3,4)19(10,25)6-5-11(2)21)26-17-16(24)15(23)14(22)13(9-20)27-17/h10-17,20-25H,5-9H2,1-4H3/t10-,11-,12-,13-,14-,15+,16-,17-,19+/m0/s1

    Standard InChI Key:  ARLXZLBJVXNRGP-GFFWZXEVSA-N

    Associated Targets(non-human)

    Ribonuclease HI 16 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: 392.49Molecular Weight (Monoisotopic): 392.2410AlogP: -0.48#Rotatable Bonds: 6
    Polar Surface Area: 139.84Molecular Species: NEUTRALHBA: 8HBD: 6
    #RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 6#RO5 Violations (Lipinski): 1
    CX Acidic pKa: 12.21CX Basic pKa: CX LogP: -0.54CX LogD: -0.54
    Aromatic Rings: 0Heavy Atoms: 27QED Weighted: 0.36Np Likeness Score: 2.74

    References

    1. Kim JA, Yang SY, Wamiru A, McMahon JB, Le Grice SF, Beutler JA, Kim YH..  (2011)  New monoterpene glycosides and phenolic compounds from Distylium racemosum and their inhibitory activity against ribonuclease H.,  21  (10): [PMID:21489793] [10.1016/j.bmcl.2011.03.091]

    Source