Koreenceine C

Details

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Internal ID e93cce54-a2af-4d1c-94a9-a73848d11a53
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Hydropyridines > Tetrahydropyridines
IUPAC Name 1-(2,3,4,5-tetrahydropyridin-6-yl)nonan-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H27NO/c1-2-3-4-5-6-10-14(16)12-13-9-7-8-11-15-13/h14,16H,2-12H2,1H3
InChI Key ODBVVAANIDRJBL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H27NO
Molecular Weight 225.37 g/mol
Exact Mass 225.209264485 g/mol
Topological Polar Surface Area (TPSA) 32.60 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.72
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Koreenceine C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.8714 87.14%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.5115 51.15%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9576 95.76%
OATP1B3 inhibitior + 0.9381 93.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.7140 71.40%
P-glycoprotein inhibitior - 0.9534 95.34%
P-glycoprotein substrate - 0.7592 75.92%
CYP3A4 substrate - 0.5418 54.18%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7622 76.22%
CYP3A4 inhibition - 0.9493 94.93%
CYP2C9 inhibition - 0.8891 88.91%
CYP2C19 inhibition - 0.9231 92.31%
CYP2D6 inhibition - 0.7295 72.95%
CYP1A2 inhibition - 0.7414 74.14%
CYP2C8 inhibition - 0.9420 94.20%
CYP inhibitory promiscuity - 0.9793 97.93%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6969 69.69%
Eye corrosion - 0.7227 72.27%
Eye irritation + 0.9535 95.35%
Skin irritation - 0.5136 51.36%
Skin corrosion + 0.5981 59.81%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4590 45.90%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5645 56.45%
skin sensitisation - 0.6666 66.66%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5394 53.94%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7244 72.44%
Acute Oral Toxicity (c) III 0.7584 75.84%
Estrogen receptor binding - 0.8464 84.64%
Androgen receptor binding - 0.7912 79.12%
Thyroid receptor binding - 0.6675 66.75%
Glucocorticoid receptor binding - 0.6937 69.37%
Aromatase binding - 0.8506 85.06%
PPAR gamma - 0.7270 72.70%
Honey bee toxicity - 0.9876 98.76%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.6252 62.52%
Fish aquatic toxicity - 0.7973 79.73%

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 98.57% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.91% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 94.28% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 93.00% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.38% 99.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 90.84% 91.81%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.33% 92.08%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.90% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.91% 97.25%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 86.92% 95.17%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.56% 90.08%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 85.57% 92.68%
CHEMBL4105838 Q96GG9 DCN1-like protein 1 85.20% 95.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.53% 93.99%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 84.32% 90.24%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.83% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.54% 93.56%

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 146683590
LOTUS LTS0175151
wikiData Q105189725