methyl (2Z)-2-cyclohex-2-en-1-ylideneacetate

Details

Top
Internal ID 9aa6e1fb-7c00-4395-b909-2bb591eeb815
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Alpha,beta-unsaturated carboxylic esters > Enoate esters
IUPAC Name methyl (2Z)-2-cyclohex-2-en-1-ylideneacetate
SMILES (Canonical) COC(=O)C=C1CCCC=C1
SMILES (Isomeric) COC(=O)/C=C\1/CCCC=C1
InChI InChI=1S/C9H12O2/c1-11-9(10)7-8-5-3-2-4-6-8/h3,5,7H,2,4,6H2,1H3/b8-7+
InChI Key JREXMLWGPKSZOP-BQYQJAHWSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C9H12O2
Molecular Weight 152.19 g/mol
Exact Mass 152.083729621 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.83
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of methyl (2Z)-2-cyclohex-2-en-1-ylideneacetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.8467 84.67%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.5070 50.70%
OATP2B1 inhibitior - 0.8654 86.54%
OATP1B1 inhibitior + 0.9528 95.28%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8690 86.90%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9694 96.94%
CYP3A4 substrate - 0.5941 59.41%
CYP2C9 substrate - 0.5936 59.36%
CYP2D6 substrate - 0.8811 88.11%
CYP3A4 inhibition - 0.9679 96.79%
CYP2C9 inhibition - 0.9441 94.41%
CYP2C19 inhibition - 0.8968 89.68%
CYP2D6 inhibition - 0.9626 96.26%
CYP1A2 inhibition - 0.8331 83.31%
CYP2C8 inhibition - 0.9442 94.42%
CYP inhibitory promiscuity - 0.7858 78.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5867 58.67%
Carcinogenicity (trinary) Non-required 0.6564 65.64%
Eye corrosion + 0.8474 84.74%
Eye irritation + 0.9909 99.09%
Skin irritation + 0.5556 55.56%
Skin corrosion - 0.9821 98.21%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6622 66.22%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5642 56.42%
skin sensitisation + 0.8164 81.64%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.4829 48.29%
Acute Oral Toxicity (c) III 0.8602 86.02%
Estrogen receptor binding - 0.9303 93.03%
Androgen receptor binding - 0.5907 59.07%
Thyroid receptor binding - 0.8525 85.25%
Glucocorticoid receptor binding - 0.6854 68.54%
Aromatase binding - 0.9087 90.87%
PPAR gamma - 0.8033 80.33%
Honey bee toxicity - 0.9491 94.91%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8651 86.51%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 97.07% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.20% 91.11%
CHEMBL4208 P20618 Proteasome component C5 90.36% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.58% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.03% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.41% 94.45%
CHEMBL2581 P07339 Cathepsin D 82.34% 98.95%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 13425841
LOTUS LTS0177261
wikiData Q105133868