4-Hydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)oxybenzoic acid

Details

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Internal ID d5a51a9e-665e-466e-b47a-4f202fed1e0a
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenoxyacetic acid derivatives
IUPAC Name 4-hydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)oxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O6/c1-6(11(15)16-2)17-9-5-7(10(13)14)3-4-8(9)12/h3-5,12H,1H2,2H3,(H,13,14)
InChI Key NHKOSAMAYMOMMO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O6
Molecular Weight 238.19 g/mol
Exact Mass 238.04773803 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.16
H-Bond Acceptor 5
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 4-Hydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)oxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9742 97.42%
Caco-2 - 0.7216 72.16%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8440 84.40%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9667 96.67%
OATP1B3 inhibitior + 0.9638 96.38%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9401 94.01%
P-glycoprotein inhibitior - 0.9575 95.75%
P-glycoprotein substrate - 0.9161 91.61%
CYP3A4 substrate - 0.6517 65.17%
CYP2C9 substrate - 0.7853 78.53%
CYP2D6 substrate - 0.8821 88.21%
CYP3A4 inhibition - 0.9098 90.98%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition - 0.5858 58.58%
CYP2D6 inhibition - 0.9142 91.42%
CYP1A2 inhibition - 0.6604 66.04%
CYP2C8 inhibition + 0.5749 57.49%
CYP inhibitory promiscuity - 0.8619 86.19%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6890 68.90%
Carcinogenicity (trinary) Non-required 0.6201 62.01%
Eye corrosion - 0.8169 81.69%
Eye irritation + 0.9026 90.26%
Skin irritation + 0.5373 53.73%
Skin corrosion - 0.8656 86.56%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8535 85.35%
Micronuclear + 0.7700 77.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.6929 69.29%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5709 57.09%
Acute Oral Toxicity (c) IV 0.4676 46.76%
Estrogen receptor binding - 0.5456 54.56%
Androgen receptor binding - 0.7490 74.90%
Thyroid receptor binding - 0.6717 67.17%
Glucocorticoid receptor binding - 0.5306 53.06%
Aromatase binding - 0.6047 60.47%
PPAR gamma - 0.7336 73.36%
Honey bee toxicity - 0.9048 90.48%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.9900 99.00%

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 94.00% 91.11%
CHEMBL3194 P02766 Transthyretin 92.12% 90.71%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.72% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.13% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.56% 95.56%
CHEMBL4208 P20618 Proteasome component C5 88.54% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.69% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 83.87% 90.20%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.26% 81.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.34% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.27% 96.95%

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.
Aster indicus

Cross-Links

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PubChem 23727652
LOTUS LTS0231116
wikiData Q105179445