PREAUSTINOID A1

ID: ALA1911629

Max Phase: Preclinical

Molecular Formula: C26H36O7

Molecular Weight: 460.57

Molecule Type: Small molecule

Associated Items:

Representations

Synonyms (1): Preaustinoid A1
Synonyms from Alternative Forms(1):

    Canonical SMILES:  C=C1[C@@]2(C)C[C@H]3[C@]4(C)CCC(=O)OC(C)(C)[C@@H]4CC[C@]3(C)[C@]1(C(=O)OC)C(=O)[C@@](C)(O)C2=O

    Standard InChI:  InChI=1S/C26H36O7/c1-14-23(5)13-16-22(4)11-10-17(27)33-21(2,3)15(22)9-12-24(16,6)26(14,20(30)32-8)19(29)25(7,31)18(23)28/h15-16,31H,1,9-13H2,2-8H3/t15-,16-,22+,23+,24-,25-,26-/m0/s1

    Standard InChI Key:  XBLDTXYFLHSWHN-OJXUJTMOSA-N

    Associated Targets(Human)

    CASP1 Tchem Caspase-1 (6235 Activities)
    Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
    IL1B Tclin Interleukin-1 beta (9 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: 460.57Molecular Weight (Monoisotopic): 460.2461AlogP: 3.17#Rotatable Bonds: 1
    Polar Surface Area: 106.97Molecular Species: NEUTRALHBA: 7HBD: 1
    #RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
    CX Acidic pKa: 11.48CX Basic pKa: CX LogP: 3.74CX LogD: 3.74
    Aromatic Rings: 0Heavy Atoms: 33QED Weighted: 0.36Np Likeness Score: 2.71

    References

    1. Stierle DB, Stierle AA, Patacini B, McIntyre K, Girtsman T, Bolstad E..  (2011)  Berkeleyones and related meroterpenes from a deep water acid mine waste fungus that inhibit the production of interleukin 1-β from induced inflammasomes.,  74  (10): [PMID:21916432] [10.1021/np2003066]

    Source