7-Ethyl-10-hydroxyundec-7-ene-3,6-dione

Details

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Internal ID e3f250e4-36a5-4262-9772-c1b1ccff85c0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 7-ethyl-10-hydroxyundec-7-ene-3,6-dione
SMILES (Canonical) CCC(=O)CCC(=O)C(=CCC(C)O)CC
SMILES (Isomeric) CCC(=O)CCC(=O)C(=CCC(C)O)CC
InChI InChI=1S/C13H22O3/c1-4-11(7-6-10(3)14)13(16)9-8-12(15)5-2/h7,10,14H,4-6,8-9H2,1-3H3
InChI Key ORXJSCDQUTXZPA-UHFFFAOYSA-N
Popularity 1 reference 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-10-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 + 0.9931 99.31%
Caco-2 + 0.9316 93.16%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6587 65.87%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.9102 91.02%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8198 81.98%
P-glycoprotein inhibitior - 0.9516 95.16%
P-glycoprotein substrate - 0.9181 91.81%
CYP3A4 substrate - 0.6285 62.85%
CYP2C9 substrate - 0.7791 77.91%
CYP2D6 substrate - 0.8454 84.54%
CYP3A4 inhibition - 0.7219 72.19%
CYP2C9 inhibition - 0.8982 89.82%
CYP2C19 inhibition - 0.9046 90.46%
CYP2D6 inhibition - 0.9118 91.18%
CYP1A2 inhibition - 0.6652 66.52%
CYP2C8 inhibition - 0.9532 95.32%
CYP inhibitory promiscuity - 0.8823 88.23%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.7153 71.53%
Eye corrosion - 0.7220 72.20%
Eye irritation + 0.6549 65.49%
Skin irritation + 0.4898 48.98%
Skin corrosion - 0.9512 95.12%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6301 63.01%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5341 53.41%
skin sensitisation + 0.6007 60.07%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.9589 95.89%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.7304 73.04%
Acute Oral Toxicity (c) III 0.8217 82.17%
Estrogen receptor binding - 0.8354 83.54%
Androgen receptor binding - 0.7992 79.92%
Thyroid receptor binding - 0.6589 65.89%
Glucocorticoid receptor binding - 0.6412 64.12%
Aromatase binding - 0.8494 84.94%
PPAR gamma - 0.6400 64.00%
Honey bee toxicity - 0.9168 91.68%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.9456 94.56%

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 93.77% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.97% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.62% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.18% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.90% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.09% 97.25%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.66% 97.21%

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 162918265
LOTUS LTS0223439
wikiData Q104193688