2-(Hydroxyimino)-3-Phenylpropanoic Acid

Details

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Internal ID a6eae9d1-4a35-43e5-ab00-3ac240a4e339
Taxonomy Phenylpropanoids and polyketides > Phenylpropanoic acids
IUPAC Name (2Z)-2-hydroxyimino-3-phenylpropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H9NO3/c11-9(12)8(10-13)6-7-4-2-1-3-5-7/h1-5,13H,6H2,(H,11,12)/b10-8-
InChI Key PNTMGOUAICFJQK-NTMALXAHSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C9H9NO3
Molecular Weight 179.17 g/mol
Exact Mass 179.058243149 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.14
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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3682-17-5
2-(Hydroxyimino)-3-phenylpropanoic acid
(2Z)-2-hydroxyimino-3-phenylpropanoic acid
CHEMBL3797778
2-hydroxyimino-3-phenylpropanoic acid
99033-96-2
99033-95-1
starbld0001138
Phenylpyruvic acid oxime
CHEBI:131386
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-(Hydroxyimino)-3-Phenylpropanoic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9165 91.65%
Caco-2 + 0.6957 69.57%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6710 67.10%
OATP2B1 inhibitior - 0.8700 87.00%
OATP1B1 inhibitior + 0.9344 93.44%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8796 87.96%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.9823 98.23%
CYP3A4 substrate - 0.7329 73.29%
CYP2C9 substrate - 0.5940 59.40%
CYP2D6 substrate - 0.8624 86.24%
CYP3A4 inhibition - 0.9404 94.04%
CYP2C9 inhibition - 0.9408 94.08%
CYP2C19 inhibition - 0.8017 80.17%
CYP2D6 inhibition - 0.8996 89.96%
CYP1A2 inhibition + 0.5099 50.99%
CYP2C8 inhibition - 0.8697 86.97%
CYP inhibitory promiscuity - 0.9670 96.70%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5888 58.88%
Carcinogenicity (trinary) Non-required 0.6189 61.89%
Eye corrosion - 0.9592 95.92%
Eye irritation + 0.9587 95.87%
Skin irritation + 0.4946 49.46%
Skin corrosion - 0.8576 85.76%
Ames mutagenesis - 0.5054 50.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7813 78.13%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.6306 63.06%
skin sensitisation - 0.7705 77.05%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7745 77.45%
Acute Oral Toxicity (c) III 0.7066 70.66%
Estrogen receptor binding - 0.8558 85.58%
Androgen receptor binding - 0.7787 77.87%
Thyroid receptor binding - 0.7401 74.01%
Glucocorticoid receptor binding - 0.6022 60.22%
Aromatase binding - 0.5602 56.02%
PPAR gamma + 0.5827 58.27%
Honey bee toxicity - 0.9721 97.21%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.6438 64.38%

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 92.90% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 92.09% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.84% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.30% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.62% 94.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.90% 95.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.22% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.07% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 6416112
LOTUS LTS0113481
wikiData Q104402516