4-Hexen-1-ol, 3-ethenyl-5-methyl-2-methylene-, 1-acetate

Details

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Internal ID 1cc9b6a1-cf28-4eaf-a732-381c4883db82
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name (3-ethenyl-5-methyl-2-methylidenehex-4-enyl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H18O2/c1-6-12(7-9(2)3)10(4)8-14-11(5)13/h6-7,12H,1,4,8H2,2-3,5H3
InChI Key OMXMXPLKVRQEIQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18O2
Molecular Weight 194.27 g/mol
Exact Mass 194.130679813 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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DTXSID801200011
4-Hexen-1-ol, 3-ethenyl-5-methyl-2-methylene-, 1-acetate
79507-87-2

2D Structure

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2D Structure of 4-Hexen-1-ol, 3-ethenyl-5-methyl-2-methylene-, 1-acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.5322 53.22%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.6755 67.55%
OATP2B1 inhibitior - 0.8572 85.72%
OATP1B1 inhibitior + 0.9529 95.29%
OATP1B3 inhibitior + 0.9326 93.26%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9224 92.24%
P-glycoprotein inhibitior - 0.9590 95.90%
P-glycoprotein substrate - 0.9636 96.36%
CYP3A4 substrate - 0.5842 58.42%
CYP2C9 substrate - 0.6131 61.31%
CYP2D6 substrate - 0.8882 88.82%
CYP3A4 inhibition - 0.9312 93.12%
CYP2C9 inhibition - 0.9141 91.41%
CYP2C19 inhibition - 0.8609 86.09%
CYP2D6 inhibition - 0.9368 93.68%
CYP1A2 inhibition - 0.8412 84.12%
CYP2C8 inhibition - 0.9171 91.71%
CYP inhibitory promiscuity - 0.7377 73.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5757 57.57%
Carcinogenicity (trinary) Non-required 0.6073 60.73%
Eye corrosion + 0.9132 91.32%
Eye irritation + 0.8985 89.85%
Skin irritation + 0.8898 88.98%
Skin corrosion - 0.9103 91.03%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5089 50.89%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.6920 69.20%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.6967 69.67%
Acute Oral Toxicity (c) IV 0.4362 43.62%
Estrogen receptor binding - 0.8869 88.69%
Androgen receptor binding - 0.8394 83.94%
Thyroid receptor binding - 0.8066 80.66%
Glucocorticoid receptor binding - 0.8481 84.81%
Aromatase binding - 0.7025 70.25%
PPAR gamma - 0.7227 72.27%
Honey bee toxicity - 0.7596 75.96%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity + 0.9672 96.72%

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 95.32% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.24% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.47% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.00% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 86.91% 91.19%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.05% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.81% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.28% 97.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.22% 91.11%

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 vulgaris

Cross-Links

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PubChem 101413630
LOTUS LTS0167382
wikiData Q105194544