CADIOLIDE G

ID: ALA2204155

Max Phase: Preclinical

Molecular Formula: C25H16Br4O6

Molecular Weight: 732.01

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): Cadiolide G
Synonyms from Alternative Forms(1):

    Canonical SMILES:  COc1c(Br)cc([C@H](O)C2=C(c3ccc(O)c(Br)c3)/C(=C/c3ccc(O)c(Br)c3)OC2=O)cc1Br

    Standard InChI:  InChI=1S/C25H16Br4O6/c1-34-24-16(28)9-13(10-17(24)29)23(32)22-21(12-3-5-19(31)15(27)8-12)20(35-25(22)33)7-11-2-4-18(30)14(26)6-11/h2-10,23,30-32H,1H3/b20-7-/t23-/m0/s1

    Standard InChI Key:  YPRPNGIQHRPLSH-QVARGSHZSA-N

    Associated Targets(Human)

    A549 127892 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    K562 73714 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Associated Targets(non-human)

    Isocitrate lyase 219 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Escherichia coli 133304 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Proteus hauseri 146 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Salmonella enterica 1497 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Kocuria rhizophila 337 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Bacillus spizizenii 1898 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Staphylococcus aureus 210822 Activities

    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

    Candida albicans 78123 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: 732.01Molecular Weight (Monoisotopic): 727.7680AlogP: 7.24#Rotatable Bonds: 5
    Polar Surface Area: 96.22Molecular Species: NEUTRALHBA: 6HBD: 3
    #RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
    CX Acidic pKa: 7.51CX Basic pKa: CX LogP: 7.09CX LogD: 6.80
    Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.24Np Likeness Score: 0.86

    References

    1. Won TH, Jeon JE, Kim SH, Lee SH, Rho BJ, Oh DC, Oh KB, Shin J..  (2012)  Brominated aromatic furanones and related esters from the ascidian Synoicum sp.,  75  (12): [PMID:23145909] [10.1021/np3005562]
    2. Ahn CH, Won TH, Kim H, Shin J, Oh KB..  (2013)  Inhibition of Candida albicans isocitrate lyase activity by cadiolides and synoilides from the ascidian Synoicum sp.,  23  (14): [PMID:23747224] [10.1016/j.bmcl.2013.05.051]

    Source