Olivacine






Names

    • 6H-pyrido[4,3-b]carbazole, 1,5-dimethyl-
    • Olivacine
    • Q15425302
    • DTXSID10197511
    • guatambuinine
    • 1,5-dimethyl-6H-pyrido[4,3-b]carbazole
    • 5WSL5LL2C3
    • 1,5-Dimethyl-6H-pyrido(4,3-b)carbazole
    • Olivacin
    • CHEMBL306472
    • 6H-Pyrido[4, 1,5-dimethyl-
    • 484-49-1
    • InChI=1/C17H14N2/c1-10-12-7-8-18-11(2)14(12)9-15-13-5-3-4-6-16(13)19-17(10)15/h3-9,19H,1-2H
    • 6H-Pyrido(4,3-b)carbazole, 1,5-dimethyl-
    • OLIVACINE [MI]
    • NSC-70134
    • 1,5-dimethyl-2H-pyrido[4,3-b]carbazole
    • SCHEMBL613418
    • UNII-5WSL5LL2C3
    • SJ 2773
    • NSC70134
    • CHEBI:7767
    • NSC 70134
    • DB-051554
    • C09230

Attributes

  • Canonical SMILES

    CC1=C2C=CNC(=C2C=C3C1=NC4=CC=CC=C43)C

  • InChI

    InChI=1S/C17H14N2/c1-10-12-7-8-18-11(2)14(12)9-15-13-5-3-4-6-16(13)19-17(10)15/h3-9,18H,1-2H3

  • Molecule Class: Alkaloids
  • TPSA: 28.68
  • #RotBonds: 0
  • MW: 246.313
  • HBD: 1
  • HBA: 1
  • logP: 4.4861400000000025
  • Chemical Formula: C17H14N2


Species

    Species Place of Collection NCBI Taxonomy Voucher Specimen
    T. laeta Brazil 761076 WAG

External Databases


References

  • Two fast screening methods (GC-MS and TLC-ChEI assay) for rapid evaluation of potential anticholinesterasic indole alkaloids in complex mixtures. An Acad Bras Cienc, 2008 (PMID 18797794).

Compound-Protein Relationships


Compound Activities

    • Acetylbutyrylcholinesterase inhibitory

Predicted NMR Spectral Data


Predicted MS Fragmentation Pattern

    N.B.: It is recommended to zoom in on a specific area of an MS plot before hovering on a peak.

Predicted ADMET Properties

    Property Model Name Predicted Value
    Absorption Caco-2 (logPaap) -4.82
    Human Oral Bioavailability 20% Bioavailable
    Human Intestinal Absorption Absorbed
    Madin-Darby Canine Kidney -4.24
    Human Oral Bioavailability 50% Non-Bioavailable
    P-Glycoprotein Inhibitor Non-Inhibitor
    P-Glycoprotein Substrate Substrate
    Skin Permeability -2.33
    Distribution Blood-Brain Barrier (Central Nervous System) -2.23
    Blood-Brain Barrier Penetrable
    Fraction Unbound (Human) 1.36
    Plasma Protein Binding 78.98
    Steady State Volume of Distribution 0.94
    Metabolism Breast Cancer Resistance Protein Inhibitor
    CYP 1A2 Inhibitor Inhibitor
    CYP 1A2 substrate Substrate
    CYP 2C19 Inhibitor Inhibitor
    CYP 2C19 substrate Substrate
    CYP 2C9 Inhibitor Non-Inhibitor
    CYP 2C9 Substrate Substrate
    CYP 2D6 Inhibitor Inhibitor
    CYP 2D6 Substrate Substrate
    CYP 3A4 Inhibitor Inhibitor
    CYP 3A4 Substrate Non-Substrate
    OATP1B1 Non-Inhibitor
    OATP1B3 Non-Inhibitor
    Excretion Clearance 7.01
    Organic Cation Transporter 2 Inhibitor
    Half-Life of Drug Half-Life < 3hs
    Toxicity AMES Mutagenesis Toxic
    Avian Safe
    Bee Safe
    Bioconcentration Factor 1.38
    Biodegradation Safe
    Carcinogenesis Toxic
    Crustacean Toxic
    Liver Injury I Safe
    Eye Corrosion Safe
    Eye irritation Toxic
    Maximum Tolerated Dose -0.27
    Liver Injury II Toxic
    hERG Blockers Safe
    Daphnia Maga 4.72
    Micronucleos Toxic
    NR-AhR Toxic
    NR-AR Safe
    NR-AR-LBD Safe
    NR-Aromatase Safe
    NR-ER Safe
    NR-ER-LBD Safe
    NR-GR Safe
    NR-PPAR-gamma Safe
    NR-TR Safe
    T. Pyriformis 4.37
    Rat (Acute) 2.42
    Rat (Chronic Oral) 2.19
    Fathead Minnow 4.88
    Respiratory Disease Safe
    Skin Sensitisation Toxic
    SR-ATAD5 Safe
    SR-ARE Safe
    SR-HSE Safe
    SR-MMP Safe
    SR-p53 Toxic
    General Properties Boiling Point 450.55
    Hydration Free Energy -8.71
    Log(D) at pH=7.4 3.73
    Log(P) 4.63
    Log S -5.18
    Log(Vapor Pressure) -8.08
    Melting Point 298.17
    pKa Acid 12.45
    pKa Basic 7.82