Olivacine

Details

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Internal ID 7aadcec3-83a0-4cd0-b1eb-78e1b0333921
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Carbazoles
IUPAC Name 1,5-dimethyl-2H-pyrido[4,3-b]carbazole
SMILES (Canonical) CC1=C2C=CNC(=C2C=C3C1=NC4=CC=CC=C43)C
SMILES (Isomeric) 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
InChI Key WBGUTGOSUBJTJZ-UHFFFAOYSA-N
Popularity 45 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14N2
Molecular Weight 246.31 g/mol
Exact Mass 246.115698455 g/mol
Topological Polar Surface Area (TPSA) 24.40 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.49
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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484-49-1
Olivacin
1,5-dimethyl-6H-pyrido[4,3-b]carbazole
1,5-Dimethyl-6H-pyrido(4,3-b)carbazole
SJ 2773
NSC70134
5WSL5LL2C3
CHEBI:7767
NSC-70134
guatambuinine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Olivacine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5462 54.62%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.7389 73.89%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9304 93.04%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.7932 79.32%
P-glycoprotein inhibitior - 0.8484 84.84%
P-glycoprotein substrate - 0.7798 77.98%
CYP3A4 substrate - 0.5459 54.59%
CYP2C9 substrate - 0.8132 81.32%
CYP2D6 substrate - 0.7428 74.28%
CYP3A4 inhibition + 0.7959 79.59%
CYP2C9 inhibition - 0.8294 82.94%
CYP2C19 inhibition + 0.8326 83.26%
CYP2D6 inhibition + 0.8931 89.31%
CYP1A2 inhibition + 0.9107 91.07%
CYP2C8 inhibition + 0.6258 62.58%
CYP inhibitory promiscuity + 0.6189 61.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5765 57.65%
Eye corrosion - 0.9771 97.71%
Eye irritation + 0.6871 68.71%
Skin irritation + 0.5419 54.19%
Skin corrosion - 0.9414 94.14%
Ames mutagenesis + 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4728 47.28%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.7998 79.98%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.8030 80.30%
Acute Oral Toxicity (c) III 0.6056 60.56%
Estrogen receptor binding + 0.9743 97.43%
Androgen receptor binding + 0.6658 66.58%
Thyroid receptor binding + 0.8101 81.01%
Glucocorticoid receptor binding + 0.9149 91.49%
Aromatase binding + 0.9129 91.29%
PPAR gamma + 0.6747 67.47%
Honey bee toxicity - 0.9222 92.22%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity - 0.4744 47.44%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 94.19% 98.95%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 92.13% 89.44%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.71% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.19% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.87% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 86.85% 94.75%
CHEMBL2039 P27338 Monoamine oxidase B 85.69% 92.51%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.49% 85.14%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 84.52% 96.47%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.46% 92.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.35% 99.23%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.88% 96.25%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 83.56% 85.49%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.40% 93.99%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.03% 94.62%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.39% 93.81%
CHEMBL3401 O75469 Pregnane X receptor 82.23% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.99% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.87% 94.00%
CHEMBL3524 P56524 Histone deacetylase 4 80.68% 92.97%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Aspidosperma subincanum
Tabernaemontana catharinensis
Tabernaemontana cymosa
Tabernaemontana heterophylla

Cross-Links

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PubChem 96364
LOTUS LTS0064236
wikiData Q104250908