Piperonylic acid

Details

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Internal ID 156471c8-8ffc-4cfe-8b93-43775b318be2
Taxonomy Organoheterocyclic compounds > Benzodioxoles
IUPAC Name 1,3-benzodioxole-5-carboxylic acid
SMILES (Canonical) C1OC2=C(O1)C=C(C=C2)C(=O)O
SMILES (Isomeric) C1OC2=C(O1)C=C(C=C2)C(=O)O
InChI InChI=1S/C8H6O4/c9-8(10)5-1-2-6-7(3-5)12-4-11-6/h1-3H,4H2,(H,9,10)
InChI Key VDVJGIYXDVPQLP-UHFFFAOYSA-N
Popularity 103 references in papers

Physical and Chemical Properties

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Molecular Formula C8H6O4
Molecular Weight 166.13 g/mol
Exact Mass 166.02660867 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.40
Atomic LogP (AlogP) 1.11
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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94-53-1
1,3-Benzodioxole-5-carboxylic acid
Benzo[d][1,3]dioxole-5-carboxylic acid
Heliotropic acid
3,4-Methylenedioxybenzoic acid
Protocatechuic acid methylene ether
benzo[1,3]dioxole-5-carboxylic acid
3,4-(Methylenedioxy)benzoic acid
2H-1,3-Benzodioxole-5-Carboxylic Acid
5-Benzodioxolecarboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Piperonylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.7921 79.21%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7605 76.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9744 97.44%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9395 93.95%
P-glycoprotein inhibitior - 0.9774 97.74%
P-glycoprotein substrate - 0.9958 99.58%
CYP3A4 substrate - 0.8079 80.79%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8832 88.32%
CYP3A4 inhibition - 0.6500 65.00%
CYP2C9 inhibition - 0.9104 91.04%
CYP2C19 inhibition - 0.9300 93.00%
CYP2D6 inhibition - 0.9232 92.32%
CYP1A2 inhibition + 0.9433 94.33%
CYP2C8 inhibition - 0.9427 94.27%
CYP inhibitory promiscuity - 0.7782 77.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Warning 0.4687 46.87%
Eye corrosion - 0.9157 91.57%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.7103 71.03%
Skin corrosion - 0.8371 83.71%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8334 83.34%
Micronuclear + 0.5295 52.95%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.6360 63.60%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.6031 60.31%
Acute Oral Toxicity (c) III 0.7528 75.28%
Estrogen receptor binding - 0.5942 59.42%
Androgen receptor binding - 0.5374 53.74%
Thyroid receptor binding - 0.7338 73.38%
Glucocorticoid receptor binding - 0.8086 80.86%
Aromatase binding - 0.7456 74.56%
PPAR gamma - 0.5139 51.39%
Honey bee toxicity - 0.9810 98.10%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.8552 85.52%
Fish aquatic toxicity + 0.7858 78.58%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 19952.6 nM
Potency
via CMAUP
CHEMBL4040 P28482 MAP kinase ERK2 39810.7 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.79% 87.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.07% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 91.97% 94.80%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.71% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.55% 91.11%
CHEMBL4208 P20618 Proteasome component C5 88.58% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.89% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 85.58% 81.11%
CHEMBL3194 P02766 Transthyretin 84.24% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 83.07% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.02% 99.17%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 81.13% 93.24%

Cross-Links

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PubChem 7196
NPASS NPC45404
ChEMBL CHEMBL573781
LOTUS LTS0038535
wikiData Q27185967