Koreenceine B

Details

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Internal ID 03e221ac-130f-4574-b2b5-d4db971f36b5
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Hydropyridines > Tetrahydropyridines
IUPAC Name 6-nonyl-2,3,4,5-tetrahydropyridine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H27N/c1-2-3-4-5-6-7-8-11-14-12-9-10-13-15-14/h2-13H2,1H3
InChI Key IWHRJHPJNJKAHJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H27N
Molecular Weight 209.37 g/mol
Exact Mass 209.214349865 g/mol
Topological Polar Surface Area (TPSA) 12.40 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.75
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Koreenceine B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9875 98.75%
Caco-2 + 0.9230 92.30%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5360 53.60%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.9565 95.65%
OATP1B3 inhibitior + 0.9473 94.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.7156 71.56%
P-glycoprotein inhibitior - 0.9682 96.82%
P-glycoprotein substrate - 0.7040 70.40%
CYP3A4 substrate - 0.5724 57.24%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7870 78.70%
CYP3A4 inhibition - 0.9676 96.76%
CYP2C9 inhibition - 0.8781 87.81%
CYP2C19 inhibition - 0.7961 79.61%
CYP2D6 inhibition - 0.6472 64.72%
CYP1A2 inhibition + 0.6194 61.94%
CYP2C8 inhibition - 0.9146 91.46%
CYP inhibitory promiscuity - 0.9155 91.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6884 68.84%
Eye corrosion + 0.8937 89.37%
Eye irritation + 0.9862 98.62%
Skin irritation + 0.6996 69.96%
Skin corrosion + 0.9375 93.75%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4856 48.56%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5185 51.85%
skin sensitisation - 0.5718 57.18%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.8215 82.15%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6815 68.15%
Acute Oral Toxicity (c) III 0.7368 73.68%
Estrogen receptor binding - 0.8823 88.23%
Androgen receptor binding - 0.8333 83.33%
Thyroid receptor binding - 0.7398 73.98%
Glucocorticoid receptor binding - 0.8179 81.79%
Aromatase binding - 0.8636 86.36%
PPAR gamma - 0.7967 79.67%
Honey bee toxicity - 0.9873 98.73%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.8232 82.32%
Fish aquatic toxicity + 0.6936 69.36%

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 96.79% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.95% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 93.73% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.68% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.33% 92.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.66% 100.00%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 89.48% 90.24%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.39% 95.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.39% 97.25%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 88.36% 92.68%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 86.49% 91.81%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.31% 99.17%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.76% 96.25%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.66% 90.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.58% 86.33%
CHEMBL2885 P07451 Carbonic anhydrase III 80.57% 87.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 137957808
LOTUS LTS0096378
wikiData Q105121646