Pyrenochaetic acid E

Details

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Internal ID 1a74deb3-8d43-4558-8ad0-74f51ba4ebcb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 4-(4-hydroxybutanoyl)-3-methoxy-5-methylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O5/c1-8-6-9(13(16)17)7-11(18-2)12(8)10(15)4-3-5-14/h6-7,14H,3-5H2,1-2H3,(H,16,17)
InChI Key PWLXDKUWXOPAHE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O5
Molecular Weight 252.26 g/mol
Exact Mass 252.09977361 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.66
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pyrenochaetic acid E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9718 97.18%
Caco-2 + 0.6184 61.84%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.9139 91.39%
OATP2B1 inhibitior - 0.8566 85.66%
OATP1B1 inhibitior + 0.9218 92.18%
OATP1B3 inhibitior + 0.9346 93.46%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8765 87.65%
P-glycoprotein inhibitior - 0.9381 93.81%
P-glycoprotein substrate - 0.8122 81.22%
CYP3A4 substrate - 0.6100 61.00%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.8550 85.50%
CYP2C9 inhibition - 0.8366 83.66%
CYP2C19 inhibition - 0.8888 88.88%
CYP2D6 inhibition - 0.9381 93.81%
CYP1A2 inhibition - 0.6491 64.91%
CYP2C8 inhibition + 0.5472 54.72%
CYP inhibitory promiscuity - 0.9558 95.58%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7510 75.10%
Carcinogenicity (trinary) Non-required 0.7794 77.94%
Eye corrosion - 0.9819 98.19%
Eye irritation + 0.6790 67.90%
Skin irritation - 0.8067 80.67%
Skin corrosion - 0.9620 96.20%
Ames mutagenesis - 0.7723 77.23%
Human Ether-a-go-go-Related Gene inhibition - 0.7769 77.69%
Micronuclear - 0.7741 77.41%
Hepatotoxicity + 0.5409 54.09%
skin sensitisation - 0.8073 80.73%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.6773 67.73%
Acute Oral Toxicity (c) III 0.7587 75.87%
Estrogen receptor binding + 0.7096 70.96%
Androgen receptor binding - 0.7315 73.15%
Thyroid receptor binding - 0.7437 74.37%
Glucocorticoid receptor binding - 0.5252 52.52%
Aromatase binding - 0.5894 58.94%
PPAR gamma - 0.5494 54.94%
Honey bee toxicity - 0.9690 96.90%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.6731 67.31%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 94.05% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.57% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.66% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.00% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.99% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 87.45% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.03% 95.50%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.94% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.94% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 81.63% 94.73%
CHEMBL1811 P34995 Prostanoid EP1 receptor 80.25% 95.71%

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 139586432
LOTUS LTS0220974
wikiData Q77506432