4-(3,7-Dimethylocta-2,6-dienoxy)-3-hydroxybenzoic acid

Details

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Internal ID b3edb20d-e9cf-48d8-b97b-b4859b9dd03f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 4-(3,7-dimethylocta-2,6-dienoxy)-3-hydroxybenzoic acid
SMILES (Canonical) CC(=CCCC(=CCOC1=C(C=C(C=C1)C(=O)O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCOC1=C(C=C(C=C1)C(=O)O)O)C)C
InChI InChI=1S/C17H22O4/c1-12(2)5-4-6-13(3)9-10-21-16-8-7-14(17(19)20)11-15(16)18/h5,7-9,11,18H,4,6,10H2,1-3H3,(H,19,20)
InChI Key WSNILKGNSNUWSJ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H22O4
Molecular Weight 290.40 g/mol
Exact Mass 290.15180918 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.16
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(3,7-Dimethylocta-2,6-dienoxy)-3-hydroxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9833 98.33%
Caco-2 + 0.5563 55.63%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.9347 93.47%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9390 93.90%
OATP1B3 inhibitior + 0.8969 89.69%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.5893 58.93%
P-glycoprotein inhibitior - 0.8866 88.66%
P-glycoprotein substrate - 0.9026 90.26%
CYP3A4 substrate - 0.5768 57.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8467 84.67%
CYP3A4 inhibition - 0.5656 56.56%
CYP2C9 inhibition + 0.6048 60.48%
CYP2C19 inhibition + 0.6483 64.83%
CYP2D6 inhibition - 0.6558 65.58%
CYP1A2 inhibition + 0.8707 87.07%
CYP2C8 inhibition + 0.5948 59.48%
CYP inhibitory promiscuity + 0.5057 50.57%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7650 76.50%
Carcinogenicity (trinary) Non-required 0.6800 68.00%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.5844 58.44%
Skin irritation - 0.7684 76.84%
Skin corrosion - 0.9772 97.72%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4212 42.12%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.5434 54.34%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.5863 58.63%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.4803 48.03%
Acute Oral Toxicity (c) III 0.5916 59.16%
Estrogen receptor binding + 0.7930 79.30%
Androgen receptor binding - 0.5286 52.86%
Thyroid receptor binding + 0.5392 53.92%
Glucocorticoid receptor binding + 0.5562 55.62%
Aromatase binding + 0.7629 76.29%
PPAR gamma + 0.7871 78.71%
Honey bee toxicity - 0.9395 93.95%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.64% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.05% 86.33%
CHEMBL3194 P02766 Transthyretin 93.44% 90.71%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.12% 92.08%
CHEMBL4208 P20618 Proteasome component C5 90.33% 90.00%
CHEMBL3401 O75469 Pregnane X receptor 90.32% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.80% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.63% 97.21%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.57% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.29% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.80% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.41% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.99% 96.95%
CHEMBL1255126 O15151 Protein Mdm4 82.46% 90.20%
CHEMBL1811 P34995 Prostanoid EP1 receptor 81.22% 95.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.45% 94.42%

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 crassinervium

Cross-Links

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PubChem 162820364
LOTUS LTS0188194
wikiData Q104200593