3-Methyl-3-buten-1-yl cinnamate

Details

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Internal ID a72a2448-cb8f-46c4-87b7-980f3bef88a1
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid esters
IUPAC Name 3-methylbut-3-enyl 3-phenylprop-2-enoate
SMILES (Canonical) CC(=C)CCOC(=O)C=CC1=CC=CC=C1
SMILES (Isomeric) CC(=C)CCOC(=O)C=CC1=CC=CC=C1
InChI InChI=1S/C14H16O2/c1-12(2)10-11-16-14(15)9-8-13-6-4-3-5-7-13/h3-9H,1,10-11H2,2H3
InChI Key BJUYLTVRBQUZIH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H16O2
Molecular Weight 216.27 g/mol
Exact Mass 216.115029749 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.21
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 3-Methyl-3-buten-1-yl 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 + 0.9089 90.89%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5396 53.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9133 91.33%
OATP1B3 inhibitior + 0.9195 91.95%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6029 60.29%
P-glycoprotein inhibitior - 0.9621 96.21%
P-glycoprotein substrate - 0.9567 95.67%
CYP3A4 substrate - 0.5773 57.73%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.8720 87.20%
CYP3A4 inhibition - 0.8199 81.99%
CYP2C9 inhibition - 0.9018 90.18%
CYP2C19 inhibition - 0.5458 54.58%
CYP2D6 inhibition - 0.9020 90.20%
CYP1A2 inhibition + 0.5761 57.61%
CYP2C8 inhibition + 0.4872 48.72%
CYP inhibitory promiscuity - 0.5891 58.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7328 73.28%
Carcinogenicity (trinary) Non-required 0.5707 57.07%
Eye corrosion + 0.4724 47.24%
Eye irritation + 0.9055 90.55%
Skin irritation + 0.6641 66.41%
Skin corrosion - 0.9759 97.59%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4822 48.22%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.8318 83.18%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.6424 64.24%
Acute Oral Toxicity (c) III 0.8666 86.66%
Estrogen receptor binding - 0.7152 71.52%
Androgen receptor binding + 0.7328 73.28%
Thyroid receptor binding - 0.7219 72.19%
Glucocorticoid receptor binding - 0.7348 73.48%
Aromatase binding + 0.5951 59.51%
PPAR gamma - 0.8049 80.49%
Honey bee toxicity - 0.9264 92.64%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9892 98.92%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.69% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.82% 96.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 93.43% 94.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.14% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.49% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.46% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.09% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.99% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 86.95% 91.49%
CHEMBL5028 O14672 ADAM10 84.61% 97.50%
CHEMBL221 P23219 Cyclooxygenase-1 84.55% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 84.11% 94.73%

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.
Pandanus tectorius

Cross-Links

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PubChem 60077393
LOTUS LTS0139245
wikiData Q104937372