Parahigginic acid

Details

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Internal ID 254b024c-c911-414f-ad55-63aa4eeb46f3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-methoxy-4-[(3E)-6-methylhepta-3,5-dien-2-yl]benzoic acid
SMILES (Canonical) CC(C=CC=C(C)C)C1=C(C=C(C=C1)C(=O)O)OC
SMILES (Isomeric) CC(/C=C/C=C(C)C)C1=C(C=C(C=C1)C(=O)O)OC
InChI InChI=1S/C16H20O3/c1-11(2)6-5-7-12(3)14-9-8-13(16(17)18)10-15(14)19-4/h5-10,12H,1-4H3,(H,17,18)/b7-5+
InChI Key YEIOFTMZKDEMAB-FNORWQNLSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H20O3
Molecular Weight 260.33 g/mol
Exact Mass 260.14124450 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.02
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CHEMBL452228

2D Structure

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2D Structure of Parahigginic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.7584 75.84%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.9167 91.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9283 92.83%
OATP1B3 inhibitior + 0.9635 96.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5123 51.23%
P-glycoprotein inhibitior - 0.8292 82.92%
P-glycoprotein substrate - 0.8615 86.15%
CYP3A4 substrate - 0.5840 58.40%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.8776 87.76%
CYP3A4 inhibition - 0.8583 85.83%
CYP2C9 inhibition - 0.7848 78.48%
CYP2C19 inhibition - 0.5183 51.83%
CYP2D6 inhibition - 0.9263 92.63%
CYP1A2 inhibition - 0.5616 56.16%
CYP2C8 inhibition - 0.6166 61.66%
CYP inhibitory promiscuity - 0.5431 54.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6419 64.19%
Carcinogenicity (trinary) Non-required 0.6579 65.79%
Eye corrosion - 0.8645 86.45%
Eye irritation + 0.8817 88.17%
Skin irritation + 0.5366 53.66%
Skin corrosion - 0.9818 98.18%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4653 46.53%
Micronuclear - 0.5726 57.26%
Hepatotoxicity - 0.5175 51.75%
skin sensitisation - 0.7344 73.44%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.5729 57.29%
Acute Oral Toxicity (c) III 0.8044 80.44%
Estrogen receptor binding + 0.6745 67.45%
Androgen receptor binding - 0.8339 83.39%
Thyroid receptor binding - 0.5087 50.87%
Glucocorticoid receptor binding - 0.6253 62.53%
Aromatase binding + 0.6283 62.83%
PPAR gamma - 0.5802 58.02%
Honey bee toxicity - 0.8347 83.47%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7352 73.52%
Fish aquatic toxicity + 0.9867 98.67%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.40% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.67% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.05% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.86% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 89.03% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.69% 95.56%
CHEMBL3194 P02766 Transthyretin 87.76% 90.71%
CHEMBL2581 P07339 Cathepsin D 87.50% 98.95%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 86.90% 87.67%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.64% 97.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.50% 91.11%
CHEMBL2535 P11166 Glucose transporter 83.75% 98.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.27% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 81.52% 91.19%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.58% 100.00%

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.
There are no matching plants.

Cross-Links

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PubChem 10445326
LOTUS LTS0056581
wikiData Q105347270