Methyl (z,e)-4-(geranyloxy)cinnamate

Details

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Internal ID 12cb1edd-f84f-46c9-8509-b7f17e3cf16b
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid esters
IUPAC Name methyl (Z)-3-[4-[(2E)-3,7-dimethylocta-2,6-dienoxy]phenyl]prop-2-enoate
SMILES (Canonical) CC(=CCCC(=CCOC1=CC=C(C=C1)C=CC(=O)OC)C)C
SMILES (Isomeric) CC(=CCC/C(=C/COC1=CC=C(C=C1)/C=C\C(=O)OC)/C)C
InChI InChI=1S/C20H26O3/c1-16(2)6-5-7-17(3)14-15-23-19-11-8-18(9-12-19)10-13-20(21)22-4/h6,8-14H,5,7,15H2,1-4H3/b13-10-,17-14+
InChI Key KSSYIBXTLHIBBX-ICMDQPEBSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O3
Molecular Weight 314.40 g/mol
Exact Mass 314.18819469 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.94
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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Methyl(Z)-4-(geranyloxy)cinnamate
methyl (z,e)-4-(geranyloxy)cinnamate

2D Structure

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2D Structure of Methyl (z,e)-4-(geranyloxy)cinnamate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9175 91.75%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8958 89.58%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.9362 93.62%
OATP1B3 inhibitior + 0.9280 92.80%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9354 93.54%
P-glycoprotein inhibitior - 0.4681 46.81%
P-glycoprotein substrate - 0.8874 88.74%
CYP3A4 substrate + 0.5385 53.85%
CYP2C9 substrate - 0.6023 60.23%
CYP2D6 substrate - 0.8492 84.92%
CYP3A4 inhibition - 0.7266 72.66%
CYP2C9 inhibition - 0.7188 71.88%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.8506 85.06%
CYP1A2 inhibition + 0.7007 70.07%
CYP2C8 inhibition - 0.6036 60.36%
CYP inhibitory promiscuity - 0.5768 57.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7871 78.71%
Carcinogenicity (trinary) Non-required 0.6002 60.02%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.7708 77.08%
Skin irritation - 0.8435 84.35%
Skin corrosion - 0.9918 99.18%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9356 93.56%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.6537 65.37%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6286 62.86%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.5533 55.33%
Acute Oral Toxicity (c) III 0.6027 60.27%
Estrogen receptor binding + 0.6903 69.03%
Androgen receptor binding + 0.8022 80.22%
Thyroid receptor binding + 0.5956 59.56%
Glucocorticoid receptor binding + 0.5789 57.89%
Aromatase binding + 0.5841 58.41%
PPAR gamma + 0.5915 59.15%
Honey bee toxicity - 0.9041 90.41%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL2039 P27338 Monoamine oxidase B 96.16% 92.51%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.02% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.48% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.62% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.56% 96.09%
CHEMBL4208 P20618 Proteasome component C5 93.24% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.98% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 90.70% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 90.67% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.94% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.90% 92.08%
CHEMBL2581 P07339 Cathepsin D 81.54% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.95% 95.56%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.93% 94.33%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.84% 89.34%

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.
Boronia megastigma
Helichrysum italicum
Jacaranda caucana

Cross-Links

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PubChem 71720677
NPASS NPC151530
LOTUS LTS0063886
wikiData Q105145576