(3R,6E,12E)-tetradeca-6,12-dien-8,10-diyne-1,3,14-triol

Details

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Internal ID 20e3c216-f422-47b9-a6e3-4b2db8e6694a
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (3R,6E,12E)-tetradeca-6,12-dien-8,10-diyne-1,3,14-triol
SMILES (Canonical) C(CC(CCO)O)C=CC#CC#CC=CCO
SMILES (Isomeric) C(C[C@H](CCO)O)/C=C/C#CC#C/C=C/CO
InChI InChI=1S/C14H18O3/c15-12-9-7-5-3-1-2-4-6-8-10-14(17)11-13-16/h4,6-7,9,14-17H,8,10-13H2/b6-4+,9-7+/t14-/m1/s1
InChI Key UPFDCOQGBJSFPB-FCAQWLMHSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O3
Molecular Weight 234.29 g/mol
Exact Mass 234.125594432 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.62
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3R,6E,12E)-tetradeca-6,12-dien-8,10-diyne-1,3,14-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8018 80.18%
Caco-2 - 0.8223 82.23%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6799 67.99%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8995 89.95%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8088 80.88%
BSEP inhibitior - 0.8869 88.69%
P-glycoprotein inhibitior - 0.9499 94.99%
P-glycoprotein substrate - 0.8976 89.76%
CYP3A4 substrate - 0.5992 59.92%
CYP2C9 substrate - 0.8087 80.87%
CYP2D6 substrate - 0.7581 75.81%
CYP3A4 inhibition - 0.8618 86.18%
CYP2C9 inhibition - 0.8410 84.10%
CYP2C19 inhibition - 0.8134 81.34%
CYP2D6 inhibition - 0.9147 91.47%
CYP1A2 inhibition - 0.7288 72.88%
CYP2C8 inhibition - 0.9516 95.16%
CYP inhibitory promiscuity - 0.8009 80.09%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.6311 63.11%
Eye corrosion - 0.6918 69.18%
Eye irritation - 0.8787 87.87%
Skin irritation - 0.7003 70.03%
Skin corrosion - 0.9098 90.98%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4690 46.90%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5199 51.99%
skin sensitisation - 0.7972 79.72%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.5333 53.33%
Acute Oral Toxicity (c) III 0.4606 46.06%
Estrogen receptor binding - 0.4903 49.03%
Androgen receptor binding - 0.6371 63.71%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6920 69.20%
Aromatase binding + 0.5236 52.36%
PPAR gamma + 0.5523 55.23%
Honey bee toxicity - 0.7954 79.54%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.7980 79.80%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.78% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.03% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.20% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.84% 86.92%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.54% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 81.36% 87.45%

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.
Carthamus tinctorius

Cross-Links

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PubChem 162919827
LOTUS LTS0270379
wikiData Q105276761