Methyl 10-hydroxydec-2-ene-4,6,8-triynoate

Details

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Internal ID c5376b9a-baa6-44d4-a35e-e3a81adb2036
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name methyl 10-hydroxydec-2-en-4,6,8-triynoate
SMILES (Canonical) COC(=O)C=CC#CC#CC#CCO
SMILES (Isomeric) COC(=O)C=CC#CC#CC#CCO
InChI InChI=1S/C11H8O3/c1-14-11(13)9-7-5-3-2-4-6-8-10-12/h7,9,12H,10H2,1H3
InChI Key KMRVUUYYZYPPLL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H8O3
Molecular Weight 188.18 g/mol
Exact Mass 188.047344113 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.90
Atomic LogP (AlogP) -0.28
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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Methyl 10-hydroxydec-2-ene-4,6,8-triynoate
DTXSID50787854

2D Structure

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2D Structure of Methyl 10-hydroxydec-2-ene-4,6,8-triynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 - 0.7694 76.94%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7520 75.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9069 90.69%
OATP1B3 inhibitior + 0.9572 95.72%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9016 90.16%
P-glycoprotein inhibitior - 0.9718 97.18%
P-glycoprotein substrate - 0.9338 93.38%
CYP3A4 substrate - 0.5544 55.44%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.8737 87.37%
CYP3A4 inhibition - 0.9522 95.22%
CYP2C9 inhibition - 0.9350 93.50%
CYP2C19 inhibition - 0.9420 94.20%
CYP2D6 inhibition - 0.9714 97.14%
CYP1A2 inhibition - 0.8552 85.52%
CYP2C8 inhibition - 0.8833 88.33%
CYP inhibitory promiscuity - 0.9220 92.20%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5176 51.76%
Carcinogenicity (trinary) Non-required 0.6893 68.93%
Eye corrosion + 0.8883 88.83%
Eye irritation - 0.6956 69.56%
Skin irritation + 0.8079 80.79%
Skin corrosion + 0.9226 92.26%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7442 74.42%
Micronuclear - 0.9041 90.41%
Hepatotoxicity - 0.6038 60.38%
skin sensitisation + 0.4900 49.00%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.7122 71.22%
Acute Oral Toxicity (c) II 0.5256 52.56%
Estrogen receptor binding - 0.8628 86.28%
Androgen receptor binding - 0.7813 78.13%
Thyroid receptor binding - 0.5922 59.22%
Glucocorticoid receptor binding - 0.8308 83.08%
Aromatase binding - 0.5486 54.86%
PPAR gamma - 0.7584 75.84%
Honey bee toxicity - 0.8441 84.41%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.5521 55.21%

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 94.01% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.62% 94.45%
CHEMBL4040 P28482 MAP kinase ERK2 86.90% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.74% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.48% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.97% 96.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.82% 94.33%

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 71364379
LOTUS LTS0120186
wikiData Q82754632