7-Ethyl-9-hydroxyundec-7-ene-3,6-dione

Details

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Internal ID b2cb6aae-cbc9-4b74-944c-76d9603483c0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 7-ethyl-9-hydroxyundec-7-ene-3,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H22O3/c1-4-10(9-12(15)6-3)13(16)8-7-11(14)5-2/h9,12,15H,4-8H2,1-3H3
InChI Key KLMVGMFEHSXUMU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22O3
Molecular Weight 226.31 g/mol
Exact Mass 226.15689456 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 1.30
Atomic LogP (AlogP) 2.42
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Ethyl-9-hydroxyundec-7-ene-3,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9885 98.85%
Caco-2 + 0.9321 93.21%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7498 74.98%
OATP2B1 inhibitior - 0.8504 85.04%
OATP1B1 inhibitior + 0.8872 88.72%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7146 71.46%
P-glycoprotein inhibitior - 0.9397 93.97%
P-glycoprotein substrate - 0.9281 92.81%
CYP3A4 substrate - 0.6349 63.49%
CYP2C9 substrate - 0.7791 77.91%
CYP2D6 substrate - 0.8454 84.54%
CYP3A4 inhibition - 0.7293 72.93%
CYP2C9 inhibition - 0.8551 85.51%
CYP2C19 inhibition - 0.8728 87.28%
CYP2D6 inhibition - 0.8796 87.96%
CYP1A2 inhibition - 0.7013 70.13%
CYP2C8 inhibition - 0.9394 93.94%
CYP inhibitory promiscuity - 0.8250 82.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.7276 72.76%
Eye corrosion - 0.7281 72.81%
Eye irritation + 0.5764 57.64%
Skin irritation - 0.5140 51.40%
Skin corrosion - 0.9453 94.53%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5643 56.43%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5409 54.09%
skin sensitisation + 0.6201 62.01%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8922 89.22%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.6597 65.97%
Acute Oral Toxicity (c) III 0.7761 77.61%
Estrogen receptor binding - 0.7082 70.82%
Androgen receptor binding - 0.8128 81.28%
Thyroid receptor binding - 0.7827 78.27%
Glucocorticoid receptor binding - 0.7807 78.07%
Aromatase binding - 0.8478 84.78%
PPAR gamma - 0.7477 74.77%
Honey bee toxicity - 0.8904 89.04%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9007 90.07%

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 94.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.28% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.79% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.44% 96.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.24% 100.00%

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 162861724
LOTUS LTS0057764
wikiData Q104170396