Benzeneacetate

Details

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Internal ID 842618c7-c026-4695-83d7-f7ff07645e63
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 2-phenylacetate
SMILES (Canonical) C1=CC=C(C=C1)CC(=O)[O-]
SMILES (Isomeric) C1=CC=C(C=C1)CC(=O)[O-]
InChI InChI=1S/C8H8O2/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)/p-1
InChI Key WLJVXDMOQOGPHL-UHFFFAOYSA-M
Popularity 807 references in papers

Physical and Chemical Properties

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Molecular Formula C8H7O2-
Molecular Weight 135.14 g/mol
Exact Mass 135.044604462 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 2.10
Atomic LogP (AlogP) -0.02
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2-phenylacetate
2-phenylethanoate
Benzeneacetate
BDBM36183
WLJVXDMOQOGPHL-UHFFFAOYSA-M
c0211
AKOS024258138
AB01275449-01
A804964
Q27103051

2D Structure

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2D Structure of Benzeneacetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9859 98.59%
Caco-2 + 0.9488 94.88%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.6348 63.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9553 95.53%
OATP1B3 inhibitior + 0.9606 96.06%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9210 92.10%
P-glycoprotein inhibitior - 0.9928 99.28%
P-glycoprotein substrate - 0.9936 99.36%
CYP3A4 substrate - 0.8009 80.09%
CYP2C9 substrate + 0.6165 61.65%
CYP2D6 substrate - 0.8579 85.79%
CYP3A4 inhibition - 0.9724 97.24%
CYP2C9 inhibition - 0.9457 94.57%
CYP2C19 inhibition - 0.9393 93.93%
CYP2D6 inhibition - 0.9265 92.65%
CYP1A2 inhibition - 0.6614 66.14%
CYP2C8 inhibition - 0.9158 91.58%
CYP inhibitory promiscuity - 0.9265 92.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5294 52.94%
Carcinogenicity (trinary) Non-required 0.7074 70.74%
Eye corrosion + 0.9421 94.21%
Eye irritation + 0.9971 99.71%
Skin irritation + 0.9599 95.99%
Skin corrosion + 0.7451 74.51%
Ames mutagenesis - 0.7570 75.70%
Human Ether-a-go-go-Related Gene inhibition - 0.8900 89.00%
Micronuclear - 0.8056 80.56%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.6263 62.63%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity - 0.6484 64.84%
Acute Oral Toxicity (c) III 0.8746 87.46%
Estrogen receptor binding - 0.9559 95.59%
Androgen receptor binding - 0.9136 91.36%
Thyroid receptor binding - 0.8583 85.83%
Glucocorticoid receptor binding - 0.8587 85.87%
Aromatase binding - 0.8691 86.91%
PPAR gamma - 0.5089 50.89%
Honey bee toxicity - 0.9823 98.23%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.7559 75.59%

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
CHEMBL2581 P07339 Cathepsin D 93.43% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.39% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 87.62% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.60% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.95% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.00% 86.33%

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.
Angelica sinensis
Artemisia capillaris
Bupleurum chinense
Chaenomeles sinensis
Taraxacum mongolicum
Vitex trifolia

Cross-Links

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PubChem 4409936
NPASS NPC47226