(3S,6E,12E)-tetradeca-6,12-dien-8,10-diyn-3-ol

Details

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Internal ID 976d283e-e981-418d-9147-ec08d3519043
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (3S,6E,12E)-tetradeca-6,12-dien-8,10-diyn-3-ol
SMILES (Canonical) CCC(CCC=CC#CC#CC=CC)O
SMILES (Isomeric) CC[C@@H](CC/C=C/C#CC#C/C=C/C)O
InChI InChI=1S/C14H18O/c1-3-5-6-7-8-9-10-11-12-13-14(15)4-2/h3,5,10-11,14-15H,4,12-13H2,1-2H3/b5-3+,11-10+/t14-/m0/s1
InChI Key YVEIHDLHFDAKNB-RIUGAHHNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O
Molecular Weight 202.29 g/mol
Exact Mass 202.135765193 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.68
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 (3S,6E,12E)-tetradeca-6,12-dien-8,10-diyn-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 - 0.6169 61.69%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.3914 39.14%
OATP2B1 inhibitior - 0.8562 85.62%
OATP1B1 inhibitior + 0.8230 82.30%
OATP1B3 inhibitior + 0.9188 91.88%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7107 71.07%
P-glycoprotein inhibitior - 0.9516 95.16%
P-glycoprotein substrate - 0.8510 85.10%
CYP3A4 substrate - 0.5919 59.19%
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 - 0.9410 94.10%
CYP inhibitory promiscuity - 0.6931 69.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.6451 64.51%
Eye corrosion + 0.4777 47.77%
Eye irritation - 0.9594 95.94%
Skin irritation + 0.6780 67.80%
Skin corrosion - 0.8044 80.44%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4007 40.07%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5122 51.22%
skin sensitisation + 0.9284 92.84%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.9412 94.12%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.5741 57.41%
Acute Oral Toxicity (c) III 0.6832 68.32%
Estrogen receptor binding - 0.5328 53.28%
Androgen receptor binding - 0.6773 67.73%
Thyroid receptor binding - 0.5155 51.55%
Glucocorticoid receptor binding - 0.5356 53.56%
Aromatase binding - 0.5000 50.00%
PPAR gamma - 0.7380 73.80%
Honey bee toxicity - 0.8433 84.33%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7900 79.00%
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 91.78% 96.09%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 88.87% 98.75%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.34% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.70% 99.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.63% 97.25%
CHEMBL221 P23219 Cyclooxygenase-1 84.42% 90.17%
CHEMBL2581 P07339 Cathepsin D 83.87% 98.95%

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.
Cota tinctoria
Psorospermum febrifugum
Psorospermum glaberrimum
Psorospermum tenuifolium

Cross-Links

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PubChem 162956999
LOTUS LTS0227972
wikiData Q105348434