Tetradec-6-en-8,10,12-triyn-3-ol

Details

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Internal ID a5a1de40-05e5-4645-a0a1-2ad0d9b6993b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name tetradec-6-en-8,10,12-triyn-3-ol
SMILES (Canonical) CCC(CCC=CC#CC#CC#CC)O
SMILES (Isomeric) CCC(CCC=CC#CC#CC#CC)O
InChI InChI=1S/C14H16O/c1-3-5-6-7-8-9-10-11-12-13-14(15)4-2/h10-11,14-15H,4,12-13H2,1-2H3
InChI Key FQCGENNZXNYXIL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O
Molecular Weight 200.28 g/mol
Exact Mass 200.120115130 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tetradec-6-en-8,10,12-triyn-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.5063 50.63%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.3914 39.14%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.8577 85.77%
OATP1B3 inhibitior + 0.9188 91.88%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9040 90.40%
P-glycoprotein inhibitior - 0.9587 95.87%
P-glycoprotein substrate - 0.8654 86.54%
CYP3A4 substrate - 0.5698 56.98%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7649 76.49%
CYP3A4 inhibition - 0.8735 87.35%
CYP2C9 inhibition - 0.8590 85.90%
CYP2C19 inhibition - 0.8580 85.80%
CYP2D6 inhibition - 0.9214 92.14%
CYP1A2 inhibition + 0.6526 65.26%
CYP2C8 inhibition - 0.9525 95.25%
CYP inhibitory promiscuity - 0.6931 69.31%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.6451 64.51%
Eye corrosion + 0.4777 47.77%
Eye irritation - 0.9469 94.69%
Skin irritation + 0.6780 67.80%
Skin corrosion - 0.8044 80.44%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4597 45.97%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5696 56.96%
skin sensitisation + 0.9284 92.84%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.9412 94.12%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.4508 45.08%
Acute Oral Toxicity (c) III 0.6832 68.32%
Estrogen receptor binding - 0.6671 66.71%
Androgen receptor binding - 0.6223 62.23%
Thyroid receptor binding - 0.5680 56.80%
Glucocorticoid receptor binding - 0.6701 67.01%
Aromatase binding - 0.5685 56.85%
PPAR gamma - 0.8238 82.38%
Honey bee toxicity - 0.8557 85.57%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.3771 37.71%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.50% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.29% 92.86%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 89.19% 98.75%
CHEMBL221 P23219 Cyclooxygenase-1 87.18% 90.17%
CHEMBL2581 P07339 Cathepsin D 85.46% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.06% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.59% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.44% 89.34%
CHEMBL206 P03372 Estrogen receptor alpha 81.10% 97.64%

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.
Artemisia vulgaris subsp. vulgaris

Cross-Links

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PubChem 162949434
LOTUS LTS0034278
wikiData Q104999520