Benzeneacetic acid, 2-hydroxy-alpha-oxo-, methyl ester

Details

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Internal ID a75d786d-f21d-4c58-87cb-87465299a400
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoyl derivatives
IUPAC Name methyl 2-(2-hydroxyphenyl)-2-oxoacetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H8O4/c1-13-9(12)8(11)6-4-2-3-5-7(6)10/h2-5,10H,1H3
InChI Key YXZAANSFGURKCL-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O4
Molecular Weight 180.16 g/mol
Exact Mass 180.04225873 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.20
Atomic LogP (AlogP) 0.75
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Methyl 2-(2-hydroxyphenyl)-2-oxo-acetate
Benzeneacetic acid, 2-hydroxy-alpha-oxo-, methyl ester
methyl 2-(2-hydroxyphenyl)-2-oxoacetate
Methyl (2-hydroxyphenyl)glycoxylate
SCHEMBL6747775
Methyl 2-Hydroxyphenylglyoxylate
DTXSID30955630
YXZAANSFGURKCL-UHFFFAOYSA-N
Methyl (2-hydroxyphenyl)(oxo)acetate

2D Structure

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2D Structure of Benzeneacetic acid, 2-hydroxy-alpha-oxo-, methyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9737 97.37%
Caco-2 - 0.6545 65.45%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.8949 89.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9779 97.79%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9357 93.57%
P-glycoprotein inhibitior - 0.9784 97.84%
P-glycoprotein substrate - 0.9672 96.72%
CYP3A4 substrate - 0.6550 65.50%
CYP2C9 substrate - 0.8157 81.57%
CYP2D6 substrate - 0.8607 86.07%
CYP3A4 inhibition - 0.9754 97.54%
CYP2C9 inhibition - 0.9582 95.82%
CYP2C19 inhibition - 0.9618 96.18%
CYP2D6 inhibition - 0.9613 96.13%
CYP1A2 inhibition - 0.8797 87.97%
CYP2C8 inhibition - 0.8274 82.74%
CYP inhibitory promiscuity - 0.9670 96.70%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6784 67.84%
Carcinogenicity (trinary) Non-required 0.6700 67.00%
Eye corrosion + 0.5110 51.10%
Eye irritation + 0.9956 99.56%
Skin irritation + 0.7035 70.35%
Skin corrosion - 0.8876 88.76%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8627 86.27%
Micronuclear + 0.7207 72.07%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8837 88.37%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.6343 63.43%
Acute Oral Toxicity (c) II 0.5026 50.26%
Estrogen receptor binding - 0.7946 79.46%
Androgen receptor binding - 0.5998 59.98%
Thyroid receptor binding - 0.7529 75.29%
Glucocorticoid receptor binding - 0.9215 92.15%
Aromatase binding - 0.8336 83.36%
PPAR gamma - 0.8352 83.52%
Honey bee toxicity - 0.9523 95.23%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9113 91.13%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.40% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.06% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.95% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.88% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.88% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 85.44% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.89% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.68% 99.23%
CHEMBL2321614 Q9NPC2 Potassium channel subfamily K member 9 80.21% 80.00%

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.
Ferula communis

Cross-Links

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PubChem 182159
LOTUS LTS0027150
wikiData Q82935310