2-Pentene, 1-ethoxy-4-methyl-, (Z)-

Details

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Internal ID 5a8a3870-12f1-4f7a-b7dc-32a0d3960307
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Dialkyl ethers
IUPAC Name (Z)-1-ethoxy-4-methylpent-2-ene
SMILES (Canonical) CCOCC=CC(C)C
SMILES (Isomeric) CCOC/C=C\C(C)C
InChI InChI=1S/C8H16O/c1-4-9-7-5-6-8(2)3/h5-6,8H,4,7H2,1-3H3/b6-5-
InChI Key XLTXOKDODGBUDF-WAYWQWQTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O
Molecular Weight 128.21 g/mol
Exact Mass 128.120115130 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.24
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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2-Pentene, 1-ethoxy-4-methyl-, (Z)-
51149-75-8
XLTXOKDODGBUDF-WAYWQWQTSA-N
(2Z)-1-Ethoxy-4-methyl-2-pentene #

2D Structure

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2D Structure of 2-Pentene, 1-ethoxy-4-methyl-, (Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.8409 84.09%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.6143 61.43%
OATP2B1 inhibitior - 0.8671 86.71%
OATP1B1 inhibitior + 0.8923 89.23%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7328 73.28%
P-glycoprotein inhibitior - 0.9840 98.40%
P-glycoprotein substrate - 0.9821 98.21%
CYP3A4 substrate - 0.6721 67.21%
CYP2C9 substrate - 0.7790 77.90%
CYP2D6 substrate - 0.7794 77.94%
CYP3A4 inhibition - 0.9889 98.89%
CYP2C9 inhibition - 0.9286 92.86%
CYP2C19 inhibition - 0.9164 91.64%
CYP2D6 inhibition - 0.9447 94.47%
CYP1A2 inhibition - 0.7385 73.85%
CYP2C8 inhibition - 0.9778 97.78%
CYP inhibitory promiscuity - 0.8346 83.46%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5225 52.25%
Eye corrosion + 0.7095 70.95%
Eye irritation + 0.9745 97.45%
Skin irritation + 0.7383 73.83%
Skin corrosion - 0.8946 89.46%
Ames mutagenesis - 0.5554 55.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7311 73.11%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5323 53.23%
skin sensitisation + 0.7830 78.30%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.6220 62.20%
Acute Oral Toxicity (c) III 0.9191 91.91%
Estrogen receptor binding - 0.9588 95.88%
Androgen receptor binding - 0.9206 92.06%
Thyroid receptor binding - 0.8174 81.74%
Glucocorticoid receptor binding - 0.7624 76.24%
Aromatase binding - 0.8987 89.87%
PPAR gamma - 0.8563 85.63%
Honey bee toxicity - 0.7916 79.16%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7512 75.12%

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 85.87% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.37% 96.00%
CHEMBL2885 P07451 Carbonic anhydrase III 83.78% 87.45%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.61% 94.45%
CHEMBL226 P30542 Adenosine A1 receptor 83.37% 95.93%
CHEMBL2581 P07339 Cathepsin D 83.09% 98.95%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 5365079
NPASS NPC23256