Nicotelline

Details

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Internal ID f45f174c-4831-4429-a5c5-547e4287fc97
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Bipyridines and oligopyridines
IUPAC Name 2,4-dipyridin-3-ylpyridine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H11N3/c1-3-13(10-16-6-1)12-5-8-18-15(9-12)14-4-2-7-17-11-14/h1-11H
InChI Key OILSPHJMIPYURT-UHFFFAOYSA-N
Popularity 56 references in papers

Physical and Chemical Properties

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Molecular Formula C15H11N3
Molecular Weight 233.27 g/mol
Exact Mass 233.095297364 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 2.00
Atomic LogP (AlogP) 3.21
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Nicotellin
3,2':4',3''-Terpyridine
2,4-dipyridin-3-ylpyridine
UNII-7AO144V8IZ
7AO144V8IZ
NICOTELLINE [MI]
DTXSID40197781
RefChem:165722
DTXCID00120272
494-04-2
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Nicotelline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.7566 75.66%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.7534 75.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9782 97.82%
OATP1B3 inhibitior + 0.9562 95.62%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.7155 71.55%
P-glycoprotein inhibitior - 0.9293 92.93%
P-glycoprotein substrate - 0.9625 96.25%
CYP3A4 substrate - 0.7384 73.84%
CYP2C9 substrate - 0.7983 79.83%
CYP2D6 substrate - 0.7591 75.91%
CYP3A4 inhibition - 0.7382 73.82%
CYP2C9 inhibition - 0.8448 84.48%
CYP2C19 inhibition - 0.8039 80.39%
CYP2D6 inhibition - 0.9087 90.87%
CYP1A2 inhibition + 0.9186 91.86%
CYP2C8 inhibition + 0.6674 66.74%
CYP inhibitory promiscuity + 0.7113 71.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.7109 71.09%
Eye corrosion - 0.9282 92.82%
Eye irritation + 0.8882 88.82%
Skin irritation + 0.7684 76.84%
Skin corrosion - 0.8388 83.88%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5081 50.81%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.6113 61.13%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.6578 65.78%
Acute Oral Toxicity (c) III 0.5712 57.12%
Estrogen receptor binding + 0.9792 97.92%
Androgen receptor binding - 0.6288 62.88%
Thyroid receptor binding + 0.7595 75.95%
Glucocorticoid receptor binding + 0.7026 70.26%
Aromatase binding + 0.9820 98.20%
PPAR gamma + 0.8578 85.78%
Honey bee toxicity - 0.8713 87.13%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.5378 53.78%

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
CHEMBL2243 O00519 Anandamide amidohydrolase 94.21% 97.53%
CHEMBL1951 P21397 Monoamine oxidase A 91.25% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.00% 86.33%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 89.13% 81.11%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.06% 93.65%
CHEMBL2581 P07339 Cathepsin D 84.06% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.65% 94.73%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 83.49% 96.00%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 82.78% 96.47%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.29% 97.36%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.24% 93.10%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.07% 94.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.55% 100.00%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 80.87% 95.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.85% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.58% 96.09%
CHEMBL2535 P11166 Glucose transporter 80.53% 98.75%
CHEMBL275 Q07343 Phosphodiesterase 4B 80.52% 98.18%

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.
Nicotiana tabacum

Cross-Links

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PubChem 68123
LOTUS LTS0113740
wikiData Q27266849