Benzyl tiglate

Details

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Internal ID 2594444b-86a1-4e36-b5b9-56da825f6d51
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzyloxycarbonyls
IUPAC Name benzyl (E)-2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OCC1=CC=CC=C1
SMILES (Isomeric) C/C=C(\C)/C(=O)OCC1=CC=CC=C1
InChI InChI=1S/C12H14O2/c1-3-10(2)12(13)14-9-11-7-5-4-6-8-11/h3-8H,9H2,1-2H3/b10-3+
InChI Key QRGSTISKDZCDHV-XCVCLJGOSA-N
Popularity 21 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O2
Molecular Weight 190.24 g/mol
Exact Mass 190.099379685 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.70
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Tiglic Acid Benzyl Ester
Benzyl trans-2,3-dimethylacrylate
Benzyl trans-2-methyl-2-butenoate
Benzyl 2-methylcrotonate
(E)-benzyl tiglate
Benzyl trans-2-methylcrotonate
FEMA No. 3330
2-Butenoic acid, 2-methyl-, phenylmethyl ester, (2E)-
2-Butenoic acid, 2-methyl-, phenylmethyl ester, (E)-
2-Butenoic acid, 2-methyl-, phenylmethyl ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Benzyl tiglate

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 + 0.8916 89.16%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7594 75.94%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9104 91.04%
OATP1B3 inhibitior + 0.9397 93.97%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5582 55.82%
P-glycoprotein inhibitior - 0.9810 98.10%
P-glycoprotein substrate - 0.9837 98.37%
CYP3A4 substrate - 0.6408 64.08%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.8841 88.41%
CYP3A4 inhibition - 0.9240 92.40%
CYP2C9 inhibition - 0.8942 89.42%
CYP2C19 inhibition - 0.8446 84.46%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition - 0.6048 60.48%
CYP2C8 inhibition - 0.7953 79.53%
CYP inhibitory promiscuity + 0.6452 64.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5184 51.84%
Carcinogenicity (trinary) Non-required 0.6667 66.67%
Eye corrosion - 0.6193 61.93%
Eye irritation + 0.8037 80.37%
Skin irritation + 0.5938 59.38%
Skin corrosion - 0.9826 98.26%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5830 58.30%
Micronuclear - 0.8441 84.41%
Hepatotoxicity + 0.5552 55.52%
skin sensitisation + 0.9293 92.93%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.5678 56.78%
Acute Oral Toxicity (c) III 0.9322 93.22%
Estrogen receptor binding - 0.8022 80.22%
Androgen receptor binding - 0.6577 65.77%
Thyroid receptor binding - 0.8320 83.20%
Glucocorticoid receptor binding - 0.7255 72.55%
Aromatase binding + 0.5719 57.19%
PPAR gamma - 0.8553 85.53%
Honey bee toxicity - 0.9096 90.96%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5855 58.55%
Fish aquatic toxicity + 0.9762 97.62%

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 94.96% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.11% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 93.39% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.47% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.71% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.99% 95.50%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.28% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.16% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 86.79% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.58% 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.
Cistus creticus
Lonicera japonica
Salvia sclarea
Syzygium aromaticum

Cross-Links

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PubChem 250096
NPASS NPC173443
LOTUS LTS0180584
wikiData Q27264164