[1-Hydroxy-2-(2-hydroxyphenyl)-1-methoxy-2-oxoethyl] acetate

Details

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Internal ID da86ad7c-8385-4ff0-9844-f8795858e1a9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name [1-hydroxy-2-(2-hydroxyphenyl)-1-methoxy-2-oxoethyl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12O6/c1-7(12)17-11(15,16-2)10(14)8-5-3-4-6-9(8)13/h3-6,13,15H,1-2H3
InChI Key RRGYKMGILZUEMN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O6
Molecular Weight 240.21 g/mol
Exact Mass 240.06338810 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.43
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [1-Hydroxy-2-(2-hydroxyphenyl)-1-methoxy-2-oxoethyl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9274 92.74%
Caco-2 - 0.5742 57.42%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.9065 90.65%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9474 94.74%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8143 81.43%
P-glycoprotein inhibitior - 0.9140 91.40%
P-glycoprotein substrate - 0.9285 92.85%
CYP3A4 substrate - 0.5745 57.45%
CYP2C9 substrate - 0.5966 59.66%
CYP2D6 substrate - 0.8813 88.13%
CYP3A4 inhibition - 0.9621 96.21%
CYP2C9 inhibition - 0.9134 91.34%
CYP2C19 inhibition - 0.8191 81.91%
CYP2D6 inhibition - 0.9252 92.52%
CYP1A2 inhibition - 0.9157 91.57%
CYP2C8 inhibition - 0.6941 69.41%
CYP inhibitory promiscuity - 0.9554 95.54%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7244 72.44%
Carcinogenicity (trinary) Non-required 0.7202 72.02%
Eye corrosion - 0.8032 80.32%
Eye irritation - 0.5176 51.76%
Skin irritation - 0.5524 55.24%
Skin corrosion - 0.8774 87.74%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8468 84.68%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8403 84.03%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.6584 65.84%
Acute Oral Toxicity (c) II 0.5620 56.20%
Estrogen receptor binding - 0.6626 66.26%
Androgen receptor binding - 0.5811 58.11%
Thyroid receptor binding - 0.7180 71.80%
Glucocorticoid receptor binding - 0.7914 79.14%
Aromatase binding - 0.5875 58.75%
PPAR gamma - 0.5948 59.48%
Honey bee toxicity - 0.9389 93.89%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9525 95.25%

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 95.30% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.74% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.21% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.57% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.50% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.39% 86.33%
CHEMBL2535 P11166 Glucose transporter 85.37% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.57% 95.50%

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 hieronymi

Cross-Links

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PubChem 163192285
LOTUS LTS0149701
wikiData Q105244023