3-Methoxy-5-pentyl-2-prenylphenol

Details

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Internal ID eadaa524-de0f-4183-b546-e07a61036c44
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 3-methoxy-2-(3-methylbut-2-enyl)-5-pentylphenol
SMILES (Canonical) CCCCCC1=CC(=C(C(=C1)OC)CC=C(C)C)O
SMILES (Isomeric) CCCCCC1=CC(=C(C(=C1)OC)CC=C(C)C)O
InChI InChI=1S/C17H26O2/c1-5-6-7-8-14-11-16(18)15(10-9-13(2)3)17(12-14)19-4/h9,11-12,18H,5-8,10H2,1-4H3
InChI Key FCNLMUQPSJEBQE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26O2
Molecular Weight 262.40 g/mol
Exact Mass 262.193280068 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 5.90
Atomic LogP (AlogP) 4.64
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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80489-92-5
orb1992402
AKOS040734326
3-methoxy-2-(3-methylbut-2-enyl)-5-pentylphenol

2D Structure

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2D Structure of 3-Methoxy-5-pentyl-2-prenylphenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.9565 95.65%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8103 81.03%
OATP2B1 inhibitior - 0.7124 71.24%
OATP1B1 inhibitior + 0.8180 81.80%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.5226 52.26%
P-glycoprotein inhibitior - 0.7153 71.53%
P-glycoprotein substrate - 0.6264 62.64%
CYP3A4 substrate + 0.5390 53.90%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate + 0.4334 43.34%
CYP3A4 inhibition - 0.5310 53.10%
CYP2C9 inhibition - 0.5518 55.18%
CYP2C19 inhibition + 0.6917 69.17%
CYP2D6 inhibition - 0.7699 76.99%
CYP1A2 inhibition + 0.7733 77.33%
CYP2C8 inhibition + 0.7693 76.93%
CYP inhibitory promiscuity + 0.8070 80.70%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7075 70.75%
Carcinogenicity (trinary) Non-required 0.6435 64.35%
Eye corrosion - 0.9501 95.01%
Eye irritation + 0.7313 73.13%
Skin irritation - 0.6659 66.59%
Skin corrosion - 0.8398 83.98%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7297 72.97%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5926 59.26%
skin sensitisation + 0.6348 63.48%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6485 64.85%
Acute Oral Toxicity (c) III 0.7177 71.77%
Estrogen receptor binding + 0.7842 78.42%
Androgen receptor binding + 0.5588 55.88%
Thyroid receptor binding + 0.5904 59.04%
Glucocorticoid receptor binding - 0.4791 47.91%
Aromatase binding + 0.5728 57.28%
PPAR gamma + 0.8627 86.27%
Honey bee toxicity - 0.9137 91.37%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.6178 61.78%
Fish aquatic toxicity + 0.9948 99.48%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.23% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.20% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.03% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.88% 99.17%
CHEMBL240 Q12809 HERG 94.86% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.74% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.25% 94.45%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 92.63% 95.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.89% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.29% 96.95%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 88.67% 92.68%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.80% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 86.55% 94.73%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.75% 97.21%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.75% 92.94%
CHEMBL2535 P11166 Glucose transporter 80.54% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.25% 96.00%

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.
Glycyrrhiza acanthocarpa

Cross-Links

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PubChem 51136386
LOTUS LTS0266978
wikiData Q104993236