Deca-2,8-dien-4,6-diynyl 2-methylbut-2-enoate

Details

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Internal ID ee8127e2-b1a3-45ff-be08-80415ae70239
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name deca-2,8-dien-4,6-diynyl 2-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O2/c1-4-6-7-8-9-10-11-12-13-17-15(16)14(3)5-2/h4-6,11-12H,13H2,1-3H3
InChI Key IIAPMVVOZXWYMK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O2
Molecular Weight 228.29 g/mol
Exact Mass 228.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Deca-2,8-dien-4,6-diynyl 2-methylbut-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 - 0.5829 58.29%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6416 64.16%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8702 87.02%
OATP1B3 inhibitior + 0.9385 93.85%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6728 67.28%
P-glycoprotein inhibitior - 0.9316 93.16%
P-glycoprotein substrate - 0.9364 93.64%
CYP3A4 substrate - 0.5189 51.89%
CYP2C9 substrate - 0.5942 59.42%
CYP2D6 substrate - 0.8824 88.24%
CYP3A4 inhibition - 0.8944 89.44%
CYP2C9 inhibition - 0.9031 90.31%
CYP2C19 inhibition - 0.8985 89.85%
CYP2D6 inhibition - 0.9394 93.94%
CYP1A2 inhibition - 0.7920 79.20%
CYP2C8 inhibition - 0.9163 91.63%
CYP inhibitory promiscuity - 0.5180 51.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5657 56.57%
Carcinogenicity (trinary) Non-required 0.5273 52.73%
Eye corrosion + 0.8658 86.58%
Eye irritation - 0.6294 62.94%
Skin irritation + 0.8124 81.24%
Skin corrosion - 0.7906 79.06%
Ames mutagenesis + 0.5163 51.63%
Human Ether-a-go-go-Related Gene inhibition - 0.4193 41.93%
Micronuclear - 0.8941 89.41%
Hepatotoxicity + 0.5928 59.28%
skin sensitisation + 0.7146 71.46%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.7646 76.46%
Acute Oral Toxicity (c) III 0.8168 81.68%
Estrogen receptor binding - 0.5234 52.34%
Androgen receptor binding - 0.7793 77.93%
Thyroid receptor binding - 0.5342 53.42%
Glucocorticoid receptor binding - 0.5329 53.29%
Aromatase binding + 0.6076 60.76%
PPAR gamma - 0.6473 64.73%
Honey bee toxicity - 0.7510 75.10%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6555 65.55%
Fish aquatic toxicity + 0.8718 87.18%

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 94.09% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.44% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.85% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.52% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.21% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.86% 96.00%

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.
Heterotheca subaxillaris

Cross-Links

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PubChem 162889053
LOTUS LTS0163358
wikiData Q105113353