Pyrenochaetic acid G

Details

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Internal ID 0b2fbbbd-3b9d-4b09-84b3-265237a79bf9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 4-[(2S)-2-hydroxybutanoyl]-3-methoxy-5-methylbenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O5/c1-4-9(14)12(15)11-7(2)5-8(13(16)17)6-10(11)18-3/h5-6,9,14H,4H2,1-3H3,(H,16,17)/t9-/m0/s1
InChI Key DYNJXWQSYFQHGS-VIFPVBQESA-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 1.70
Atomic LogP (AlogP) 1.66
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Pyrenochaetic acid G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9728 97.28%
Caco-2 + 0.6024 60.24%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8397 83.97%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9325 93.25%
OATP1B3 inhibitior + 0.8886 88.86%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8109 81.09%
P-glycoprotein inhibitior - 0.9263 92.63%
P-glycoprotein substrate - 0.8480 84.80%
CYP3A4 substrate - 0.6363 63.63%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.8468 84.68%
CYP3A4 inhibition - 0.9409 94.09%
CYP2C9 inhibition - 0.9208 92.08%
CYP2C19 inhibition - 0.8795 87.95%
CYP2D6 inhibition - 0.8704 87.04%
CYP1A2 inhibition - 0.8763 87.63%
CYP2C8 inhibition - 0.6084 60.84%
CYP inhibitory promiscuity - 0.9615 96.15%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7347 73.47%
Carcinogenicity (trinary) Non-required 0.7290 72.90%
Eye corrosion - 0.9342 93.42%
Eye irritation + 0.8092 80.92%
Skin irritation - 0.7612 76.12%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7031 70.31%
Micronuclear + 0.5735 57.35%
Hepatotoxicity + 0.5535 55.35%
skin sensitisation - 0.8081 80.81%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.7791 77.91%
Acute Oral Toxicity (c) III 0.5552 55.52%
Estrogen receptor binding + 0.5717 57.17%
Androgen receptor binding - 0.6593 65.93%
Thyroid receptor binding - 0.6187 61.87%
Glucocorticoid receptor binding - 0.6982 69.82%
Aromatase binding - 0.8060 80.60%
PPAR gamma - 0.5955 59.55%
Honey bee toxicity - 0.9579 95.79%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.8452 84.52%
Fish aquatic toxicity + 0.8744 87.44%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.66% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 92.30% 97.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.89% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.87% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.44% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.90% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.69% 96.95%
CHEMBL2581 P07339 Cathepsin D 86.86% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.74% 95.56%
CHEMBL2535 P11166 Glucose transporter 86.55% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 85.72% 90.20%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.69% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.02% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 82.97% 94.73%
CHEMBL1811 P34995 Prostanoid EP1 receptor 81.36% 95.71%
CHEMBL4208 P20618 Proteasome component C5 80.47% 90.00%

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 139583183
LOTUS LTS0039877
wikiData Q75056229