Geranyl vinyl ether

Details

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Internal ID 46ad8948-f3ee-4d55-8f8c-355d65393090
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (2E)-1-ethenoxy-3,7-dimethylocta-2,6-diene
SMILES (Canonical) CC(=CCCC(=CCOC=C)C)C
SMILES (Isomeric) CC(=CCC/C(=C/COC=C)/C)C
InChI InChI=1S/C12H20O/c1-5-13-10-9-12(4)8-6-7-11(2)3/h5,7,9H,1,6,8,10H2,2-4H3/b12-9+
InChI Key YBKJFYRRNMFOPP-FMIVXFBMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H20O
Molecular Weight 180.29 g/mol
Exact Mass 180.151415257 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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SCHEMBL4610325
YBKJFYRRNMFOPP-FMIVXFBMSA-N
Vinyl[(2E)-3,7-dimethyl-2,6-octadienyl] ether
(2E)-3,7-Dimethyl-1-(vinyloxy)-2,6-octadiene #

2D Structure

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2D Structure of Geranyl vinyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.8438 84.38%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4363 43.63%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9425 94.25%
OATP1B3 inhibitior + 0.9278 92.78%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8250 82.50%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9616 96.16%
CYP3A4 substrate - 0.5793 57.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7289 72.89%
CYP3A4 inhibition - 0.9401 94.01%
CYP2C9 inhibition - 0.9078 90.78%
CYP2C19 inhibition - 0.8646 86.46%
CYP2D6 inhibition - 0.9377 93.77%
CYP1A2 inhibition - 0.8002 80.02%
CYP2C8 inhibition - 0.9269 92.69%
CYP inhibitory promiscuity - 0.6919 69.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.5075 50.75%
Eye corrosion + 0.6093 60.93%
Eye irritation + 0.9339 93.39%
Skin irritation + 0.8313 83.13%
Skin corrosion - 0.9827 98.27%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5336 53.36%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation + 0.8257 82.57%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6445 64.45%
Acute Oral Toxicity (c) III 0.9059 90.59%
Estrogen receptor binding - 0.9665 96.65%
Androgen receptor binding - 0.8408 84.08%
Thyroid receptor binding - 0.8737 87.37%
Glucocorticoid receptor binding - 0.8137 81.37%
Aromatase binding - 0.8567 85.67%
PPAR gamma - 0.8242 82.42%
Honey bee toxicity - 0.7886 78.86%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9916 99.16%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.37% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.15% 96.09%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 87.37% 83.57%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.53% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 85.49% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.87% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.70% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 81.56% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.66% 94.45%

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.
Citrus × aurantium
Citrus deliciosa
Elettaria cardamomum
Rhodiola crenulata

Cross-Links

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PubChem 5365842
NPASS NPC133097