Non-1-yn-5-en-9-aldehyde, 4-carbethoxy-

Details

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Internal ID 5622f9e6-7c11-4273-80b5-6ce289b62b8f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl (E)-7-oxo-2-prop-2-ynylhept-3-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O3/c1-3-8-11(12(14)15-4-2)9-6-5-7-10-13/h1,6,9-11H,4-5,7-8H2,2H3/b9-6+
InChI Key VIYRDRUEXDYGIG-RMKNXTFCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O3
Molecular Weight 208.25 g/mol
Exact Mass 208.109944368 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.72
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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VIYRDRUEXDYGIG-RMKNXTFCSA-N
Non-1-yn-5-en-9-aldehyde, 4-ethoxycarbonyl-
Ethyl (3E)-7-oxo-2-(2-propynyl)-3-heptenoate #

2D Structure

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2D Structure of Non-1-yn-5-en-9-aldehyde, 4-carbethoxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.5167 51.67%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7405 74.05%
OATP2B1 inhibitior - 0.8539 85.39%
OATP1B1 inhibitior + 0.8579 85.79%
OATP1B3 inhibitior + 0.9557 95.57%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8123 81.23%
P-glycoprotein inhibitior - 0.9529 95.29%
P-glycoprotein substrate - 0.9476 94.76%
CYP3A4 substrate - 0.5179 51.79%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8745 87.45%
CYP3A4 inhibition - 0.8674 86.74%
CYP2C9 inhibition - 0.8053 80.53%
CYP2C19 inhibition - 0.8551 85.51%
CYP2D6 inhibition - 0.9412 94.12%
CYP1A2 inhibition - 0.6293 62.93%
CYP2C8 inhibition - 0.8798 87.98%
CYP inhibitory promiscuity - 0.7765 77.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5966 59.66%
Carcinogenicity (trinary) Non-required 0.6408 64.08%
Eye corrosion + 0.9403 94.03%
Eye irritation - 0.9131 91.31%
Skin irritation + 0.6102 61.02%
Skin corrosion + 0.5657 56.57%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5734 57.34%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6073 60.73%
skin sensitisation + 0.5595 55.95%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5680 56.80%
Acute Oral Toxicity (c) III 0.4212 42.12%
Estrogen receptor binding - 0.7962 79.62%
Androgen receptor binding - 0.8290 82.90%
Thyroid receptor binding - 0.6941 69.41%
Glucocorticoid receptor binding - 0.6384 63.84%
Aromatase binding - 0.7604 76.04%
PPAR gamma - 0.6041 60.41%
Honey bee toxicity - 0.8554 85.54%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5345 53.45%
Fish aquatic toxicity + 0.8947 89.47%

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
CHEMBL230 P35354 Cyclooxygenase-2 91.19% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.22% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.82% 97.21%
CHEMBL221 P23219 Cyclooxygenase-1 89.03% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.42% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 87.36% 94.73%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 85.63% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.04% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.91% 96.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.52% 89.34%
CHEMBL2581 P07339 Cathepsin D 81.56% 98.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.53% 95.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.17% 94.33%

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.
Citrus × aurantium
Citrus × aurantium nothof. deliciosa

Cross-Links

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PubChem 5368199
NPASS NPC37051