3,5-Bis(3-hydroxy-3-methylbut-1-enyl)-4-methoxybenzoic acid

Details

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Internal ID 490cbe9e-af94-4378-967f-acc028e743fb
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > P-methoxybenzoic acids and derivatives
IUPAC Name 3,5-bis(3-hydroxy-3-methylbut-1-enyl)-4-methoxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H24O5/c1-17(2,21)8-6-12-10-14(16(19)20)11-13(15(12)23-5)7-9-18(3,4)22/h6-11,21-22H,1-5H3,(H,19,20)
InChI Key VOQXHEPNITWNLF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H24O5
Molecular Weight 320.40 g/mol
Exact Mass 320.16237386 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.96
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,5-Bis(3-hydroxy-3-methylbut-1-enyl)-4-methoxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9871 98.71%
Caco-2 + 0.5316 53.16%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.9144 91.44%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.9139 91.39%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7551 75.51%
P-glycoprotein inhibitior - 0.7833 78.33%
P-glycoprotein substrate - 0.9689 96.89%
CYP3A4 substrate - 0.6287 62.87%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.8677 86.77%
CYP3A4 inhibition - 0.6812 68.12%
CYP2C9 inhibition - 0.6127 61.27%
CYP2C19 inhibition - 0.6699 66.99%
CYP2D6 inhibition - 0.9309 93.09%
CYP1A2 inhibition - 0.6960 69.60%
CYP2C8 inhibition - 0.7289 72.89%
CYP inhibitory promiscuity - 0.7586 75.86%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6891 68.91%
Carcinogenicity (trinary) Non-required 0.6123 61.23%
Eye corrosion - 0.8993 89.93%
Eye irritation + 0.9539 95.39%
Skin irritation - 0.6263 62.63%
Skin corrosion - 0.9509 95.09%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4321 43.21%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8287 82.87%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6613 66.13%
Acute Oral Toxicity (c) III 0.7070 70.70%
Estrogen receptor binding + 0.8855 88.55%
Androgen receptor binding - 0.6562 65.62%
Thyroid receptor binding + 0.6822 68.22%
Glucocorticoid receptor binding + 0.5975 59.75%
Aromatase binding + 0.6868 68.68%
PPAR gamma + 0.8103 81.03%
Honey bee toxicity - 0.9222 92.22%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity + 0.9857 98.57%

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 93.99% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.70% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.35% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.95% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.53% 91.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.90% 87.67%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%
CHEMBL2535 P11166 Glucose transporter 81.01% 98.75%
CHEMBL2581 P07339 Cathepsin D 80.42% 98.95%

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.
Piper hispidum

Cross-Links

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PubChem 68843065
LOTUS LTS0262252
wikiData Q105290360