Cyclohexene, 1-(3-ethoxy-1-propenyl)-, (Z)-

Details

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Internal ID 0d9a6ead-c3c7-4473-b5a0-9461add8c3d3
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name 1-[(Z)-3-ethoxyprop-1-enyl]cyclohexene
SMILES (Canonical) CCOCC=CC1=CCCCC1
SMILES (Isomeric) CCOC/C=C\C1=CCCCC1
InChI InChI=1S/C11H18O/c1-2-12-10-6-9-11-7-4-3-5-8-11/h6-7,9H,2-5,8,10H2,1H3/b9-6-
InChI Key DRWNUSMKXPQONR-TWGQIWQCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O
Molecular Weight 166.26 g/mol
Exact Mass 166.135765193 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.08
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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51149-78-1
Cyclohexene, 1-(3-ethoxy-1-propenyl)-, (Z)-
Cyclohexene, (Z)-
DTXSID20418385
DRWNUSMKXPQONR-TWGQIWQCSA-N
NSC-244925
1-[(Z)-3-Ethoxy-1-propenyl]-1-cyclohexene
1-[(1Z)-3-Ethoxy-1-propenyl]-1-cyclohexene #

2D Structure

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2D Structure of Cyclohexene, 1-(3-ethoxy-1-propenyl)-, (Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.9762 97.62%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.4826 48.26%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.8426 84.26%
OATP1B3 inhibitior + 0.9430 94.30%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5462 54.62%
P-glycoprotein inhibitior - 0.9804 98.04%
P-glycoprotein substrate - 0.9578 95.78%
CYP3A4 substrate - 0.6011 60.11%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.7504 75.04%
CYP3A4 inhibition - 0.9614 96.14%
CYP2C9 inhibition - 0.9024 90.24%
CYP2C19 inhibition - 0.7763 77.63%
CYP2D6 inhibition - 0.9100 91.00%
CYP1A2 inhibition - 0.6192 61.92%
CYP2C8 inhibition - 0.8346 83.46%
CYP inhibitory promiscuity - 0.5280 52.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.4891 48.91%
Eye corrosion + 0.7097 70.97%
Eye irritation + 0.9861 98.61%
Skin irritation - 0.6066 60.66%
Skin corrosion - 0.9838 98.38%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5964 59.64%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5322 53.22%
skin sensitisation + 0.8574 85.74%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.6196 61.96%
Acute Oral Toxicity (c) III 0.8713 87.13%
Estrogen receptor binding - 0.8262 82.62%
Androgen receptor binding - 0.8073 80.73%
Thyroid receptor binding - 0.6924 69.24%
Glucocorticoid receptor binding - 0.6956 69.56%
Aromatase binding - 0.8302 83.02%
PPAR gamma - 0.6131 61.31%
Honey bee toxicity - 0.9095 90.95%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9655 96.55%

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
CHEMBL2581 P07339 Cathepsin D 90.70% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.11% 91.11%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.39% 91.71%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.79% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.54% 93.99%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.73% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.89% 94.73%
CHEMBL230 P35354 Cyclooxygenase-2 83.70% 89.63%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.23% 96.00%
CHEMBL4208 P20618 Proteasome component C5 81.86% 90.00%

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.
Schisandra chinensis
Tetradium ruticarpum

Cross-Links

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PubChem 5358347
NPASS NPC13730