Prenyl benzoate

Details

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Internal ID 9ea05ccb-886d-423f-aecb-097f65e4139a
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name 3-methylbut-2-enyl benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O2/c1-10(2)8-9-14-12(13)11-6-4-3-5-7-11/h3-8H,9H2,1-2H3
InChI Key INVWRXWYYVMFQC-UHFFFAOYSA-N
Popularity 16 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 3.20
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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5205-11-8
3-Methyl-2-butenyl benzoate
3-Methylbut-2-enyl benzoate
Benzoic Acid 3-Methyl-2-butenyl Ester
3-methylbut-2-en-1-yl benzoate
2-BUTEN-1-OL, 3-METHYL-, BENZOATE
Benzoic acid, 3-methyl-2-butenyl ester
2-Buten-1-ol, 3-methyl-, 1-benzoate
O577ZIE86G
DTXSID8047131
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Prenyl benzoate

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 + 0.9531 95.31%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7886 78.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9563 95.63%
OATP1B3 inhibitior + 0.9321 93.21%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6538 65.38%
P-glycoprotein inhibitior - 0.9747 97.47%
P-glycoprotein substrate - 0.9806 98.06%
CYP3A4 substrate - 0.6834 68.34%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.8470 84.70%
CYP3A4 inhibition - 0.9557 95.57%
CYP2C9 inhibition - 0.8711 87.11%
CYP2C19 inhibition - 0.8009 80.09%
CYP2D6 inhibition - 0.8915 89.15%
CYP1A2 inhibition - 0.5607 56.07%
CYP2C8 inhibition - 0.7753 77.53%
CYP inhibitory promiscuity + 0.5408 54.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5484 54.84%
Carcinogenicity (trinary) Non-required 0.7260 72.60%
Eye corrosion - 0.6469 64.69%
Eye irritation + 0.9963 99.63%
Skin irritation + 0.7092 70.92%
Skin corrosion - 0.9534 95.34%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6788 67.88%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.8914 89.14%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.5908 59.08%
Acute Oral Toxicity (c) III 0.8513 85.13%
Estrogen receptor binding - 0.6938 69.38%
Androgen receptor binding - 0.7778 77.78%
Thyroid receptor binding - 0.7585 75.85%
Glucocorticoid receptor binding - 0.8544 85.44%
Aromatase binding - 0.6843 68.43%
PPAR gamma - 0.6868 68.68%
Honey bee toxicity - 0.9695 96.95%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7455 74.55%
Fish aquatic toxicity + 0.9911 99.11%

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
CHEMBL221 P23219 Cyclooxygenase-1 94.71% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.31% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.04% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 86.84% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.48% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.83% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.15% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.44% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.00% 95.50%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.27% 87.67%

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.
Croton eluteria

Cross-Links

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PubChem 21265
LOTUS LTS0111850
wikiData Q27285354