ACETOXYFIMBROLIDE

ID: ALA498428

Max Phase: Preclinical

Molecular Formula: C11H12Br2O4

Molecular Weight: 368.02

Molecule Type: Small molecule

Associated Items:

Representations

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

    Canonical SMILES:  CCC[C@@H](OC(C)=O)C1=C(Br)/C(=C\Br)OC1=O

    Standard InChI:  InChI=1S/C11H12Br2O4/c1-3-4-7(16-6(2)14)9-10(13)8(5-12)17-11(9)15/h5,7H,3-4H2,1-2H3/b8-5+/t7-/m1/s1

    Standard InChI Key:  ZHKRZTOJPXQAJI-KBUNYLKBSA-N

    Associated Targets(non-human)

    Staphylococcus aureus (210822 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    Enterococcus faecium (13803 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    Candida albicans (78123 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    Escherichia coli (133304 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    Micrococcus luteus (7463 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    Bacillus subtilis (32866 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    Penicillium oxalicum (133 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: 368.02Molecular Weight (Monoisotopic): 365.9102AlogP: 3.16#Rotatable Bonds: 4
    Polar Surface Area: 52.60Molecular Species: NEUTRALHBA: 4HBD: 0
    #RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
    CX Acidic pKa: CX Basic pKa: CX LogP: 2.58CX LogD: 2.58
    Aromatic Rings: 0Heavy Atoms: 17QED Weighted: 0.72Np Likeness Score: 2.16

    References

    1. Wright AD, de Nys R, Angerhofer CK, Pezzuto JM, Gurrath M..  (2006)  Biological activities and 3D QSAR studies of a series of Delisea pulchra (cf. fimbriata) derived natural products.,  69  (8): [PMID:16933872] [10.1021/np050510c]
    2. Ankisetty S, Nandiraju S, Win H, Park YC, Amsler CD, McClintock JB, Baker JA, Diyabalanage TK, Pasaribu A, Singh MP, Maiese WM, Walsh RD, Zaworotko MJ, Baker BJ..  (2004)  Chemical investigation of predator-deterred macroalgae from the Antarctic peninsula.,  67  (8): [PMID:15332845] [10.1021/np049965c]

    Source