ID: ALA1934137

Max Phase: Preclinical

Molecular Formula: C20H28O5

Molecular Weight: 348.44

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): 15,16-Dihydrosphaeropsidin A
Synonyms from Alternative Forms(1):

    Canonical SMILES:  CC[C@]1(C)C=C2C(=O)[C@@]3(O)OC(=O)[C@@]4(CCCC(C)(C)[C@H]34)[C@@]2(O)CC1

    Standard InChI:  InChI=1S/C20H28O5/c1-5-17(4)9-10-19(23)12(11-17)13(21)20(24)14-16(2,3)7-6-8-18(14,19)15(22)25-20/h11,14,23-24H,5-10H2,1-4H3/t14-,17-,18-,19+,20+/m0/s1

    Standard InChI Key:  UVVLWVQILXUIKL-SQWSIXGCSA-N

    Associated Targets(non-human)

    Xanthomonas oryzae pv. oryzae 79 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

    Properties

    Molecular Weight: 348.44Molecular Weight (Monoisotopic): 348.1937AlogP: 2.49#Rotatable Bonds: 1
    Polar Surface Area: 83.83Molecular Species: NEUTRALHBA: 5HBD: 2
    #RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
    CX Acidic pKa: 9.95CX Basic pKa: CX LogP: 3.42CX LogD: 3.42
    Aromatic Rings: 0Heavy Atoms: 25QED Weighted: 0.71Np Likeness Score: 3.06

    References

    1. Evidente A, Venturi V, Masi M, Degrassi G, Cimmino A, Maddau L, Andolfi A..  (2011)  In vitro antibacterial activity of sphaeropsidins and chemical derivatives toward Xanthomonas oryzae pv. oryzae, the causal agent of rice bacterial blight.,  74  (12): [PMID:22124378] [10.1021/np200625m]

    Source