(2-Methyl-4-propan-2-ylhexa-2,5-dienyl) acetate

Details

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Internal ID 5f865eee-d2ef-43bb-9a2d-ad0c0f82eeff
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name (2-methyl-4-propan-2-ylhexa-2,5-dienyl) acetate
SMILES (Canonical) CC(C)C(C=C)C=C(C)COC(=O)C
SMILES (Isomeric) CC(C)C(C=C)C=C(C)COC(=O)C
InChI InChI=1S/C12H20O2/c1-6-12(9(2)3)7-10(4)8-14-11(5)13/h6-7,9,12H,1,8H2,2-5H3
InChI Key TXJXQVRSITVNSI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O2
Molecular Weight 196.29 g/mol
Exact Mass 196.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.95
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2-Methyl-4-propan-2-ylhexa-2,5-dienyl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.6731 67.31%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6110 61.10%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.9341 93.41%
OATP1B3 inhibitior + 0.9193 91.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8400 84.00%
P-glycoprotein inhibitior - 0.9164 91.64%
P-glycoprotein substrate - 0.9400 94.00%
CYP3A4 substrate - 0.6031 60.31%
CYP2C9 substrate - 0.6131 61.31%
CYP2D6 substrate - 0.8882 88.82%
CYP3A4 inhibition - 0.9285 92.85%
CYP2C9 inhibition - 0.9054 90.54%
CYP2C19 inhibition - 0.8569 85.69%
CYP2D6 inhibition - 0.9316 93.16%
CYP1A2 inhibition - 0.8235 82.35%
CYP2C8 inhibition - 0.9437 94.37%
CYP inhibitory promiscuity - 0.7799 77.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5557 55.57%
Carcinogenicity (trinary) Non-required 0.5196 51.96%
Eye corrosion + 0.8926 89.26%
Eye irritation + 0.7296 72.96%
Skin irritation + 0.8734 87.34%
Skin corrosion - 0.9198 91.98%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4366 43.66%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.7723 77.23%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.7274 72.74%
Acute Oral Toxicity (c) IV 0.6716 67.16%
Estrogen receptor binding - 0.9355 93.55%
Androgen receptor binding - 0.8200 82.00%
Thyroid receptor binding - 0.7479 74.79%
Glucocorticoid receptor binding - 0.8837 88.37%
Aromatase binding - 0.7493 74.93%
PPAR gamma - 0.8403 84.03%
Honey bee toxicity - 0.6811 68.11%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8255 82.55%
Fish aquatic toxicity + 0.9841 98.41%

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 93.26% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.52% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.08% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.18% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.40% 94.73%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.40% 100.00%
CHEMBL340 P08684 Cytochrome P450 3A4 80.02% 91.19%

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.
Artemisia schimperi

Cross-Links

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PubChem 162916648
LOTUS LTS0092540
wikiData Q105266795