(2S,4E,6E)-12-pyridin-3-yldodeca-4,6-dien-2-ol

Details

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Internal ID c55bd399-776e-4816-82bc-98338d3f657c
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name (2S,4E,6E)-12-pyridin-3-yldodeca-4,6-dien-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H25NO/c1-16(19)11-8-6-4-2-3-5-7-9-12-17-13-10-14-18-15-17/h2,4,6,8,10,13-16,19H,3,5,7,9,11-12H2,1H3/b4-2+,8-6+/t16-/m0/s1
InChI Key KVTVYOVSAHMPHK-LOHDTLGXSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H25NO
Molecular Weight 259.40 g/mol
Exact Mass 259.193614421 g/mol
Topological Polar Surface Area (TPSA) 33.10 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.07
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,4E,6E)-12-pyridin-3-yldodeca-4,6-dien-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.8545 85.45%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Plasma membrane 0.4939 49.39%
OATP2B1 inhibitior - 0.8627 86.27%
OATP1B1 inhibitior + 0.8874 88.74%
OATP1B3 inhibitior + 0.9520 95.20%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6856 68.56%
P-glycoprotein inhibitior - 0.8825 88.25%
P-glycoprotein substrate - 0.7694 76.94%
CYP3A4 substrate - 0.5502 55.02%
CYP2C9 substrate - 0.6219 62.19%
CYP2D6 substrate - 0.7401 74.01%
CYP3A4 inhibition + 0.5738 57.38%
CYP2C9 inhibition - 0.6843 68.43%
CYP2C19 inhibition - 0.6208 62.08%
CYP2D6 inhibition - 0.8843 88.43%
CYP1A2 inhibition + 0.5512 55.12%
CYP2C8 inhibition + 0.4523 45.23%
CYP inhibitory promiscuity - 0.7659 76.59%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.6733 67.33%
Eye corrosion - 0.8049 80.49%
Eye irritation - 0.9298 92.98%
Skin irritation + 0.6903 69.03%
Skin corrosion - 0.8422 84.22%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4074 40.74%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.5942 59.42%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity - 0.5069 50.69%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.8956 89.56%
Acute Oral Toxicity (c) III 0.7052 70.52%
Estrogen receptor binding - 0.6058 60.58%
Androgen receptor binding - 0.7874 78.74%
Thyroid receptor binding + 0.6035 60.35%
Glucocorticoid receptor binding - 0.5846 58.46%
Aromatase binding - 0.6115 61.15%
PPAR gamma + 0.6269 62.69%
Honey bee toxicity - 0.9501 95.01%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5463 54.63%
Fish aquatic toxicity - 0.8012 80.12%

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 97.89% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.72% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.08% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 91.02% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.47% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 87.60% 87.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.13% 86.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.83% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.29% 91.11%
CHEMBL1781 P11387 DNA topoisomerase I 81.98% 97.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.23% 92.88%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.18% 93.81%
CHEMBL2996 Q05655 Protein kinase C delta 80.79% 97.79%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 80.18% 92.95%

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 10061128
LOTUS LTS0161632
wikiData Q104402083