2-Methyl-6-(3,7,11-trimethyldodeca-2,6,10-trienyl)benzene-1,4-diol

Details

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Internal ID b6aa1699-3ef1-4006-a629-eb34f2633227
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2-methyl-6-(3,7,11-trimethyldodeca-2,6,10-trienyl)benzene-1,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H32O2/c1-16(2)8-6-9-17(3)10-7-11-18(4)12-13-20-15-21(23)14-19(5)22(20)24/h8,10,12,14-15,23-24H,6-7,9,11,13H2,1-5H3
InChI Key CMIAQOJJEOLRAQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O2
Molecular Weight 328.50 g/mol
Exact Mass 328.240230259 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 7.20
Atomic LogP (AlogP) 6.37
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Methyl-6-(3,7,11-trimethyldodeca-2,6,10-trienyl)benzene-1,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.6297 62.97%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8162 81.62%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.8914 89.14%
OATP1B3 inhibitior + 0.9168 91.68%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.8427 84.27%
P-glycoprotein inhibitior - 0.6790 67.90%
P-glycoprotein substrate - 0.9245 92.45%
CYP3A4 substrate - 0.5510 55.10%
CYP2C9 substrate - 0.7887 78.87%
CYP2D6 substrate + 0.3876 38.76%
CYP3A4 inhibition + 0.6903 69.03%
CYP2C9 inhibition + 0.5278 52.78%
CYP2C19 inhibition + 0.6199 61.99%
CYP2D6 inhibition - 0.7539 75.39%
CYP1A2 inhibition + 0.8353 83.53%
CYP2C8 inhibition - 0.6873 68.73%
CYP inhibitory promiscuity + 0.8054 80.54%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7139 71.39%
Carcinogenicity (trinary) Non-required 0.6806 68.06%
Eye corrosion - 0.9285 92.85%
Eye irritation - 0.6296 62.96%
Skin irritation - 0.6375 63.75%
Skin corrosion - 0.7649 76.49%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7976 79.76%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5625 56.25%
skin sensitisation + 0.7793 77.93%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.7071 70.71%
Acute Oral Toxicity (c) III 0.6035 60.35%
Estrogen receptor binding + 0.8206 82.06%
Androgen receptor binding + 0.6041 60.41%
Thyroid receptor binding + 0.6932 69.32%
Glucocorticoid receptor binding + 0.6567 65.67%
Aromatase binding + 0.6386 63.86%
PPAR gamma + 0.8980 89.80%
Honey bee toxicity - 0.9046 90.46%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7000 70.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.68% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 95.71% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 94.83% 94.73%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 92.20% 83.57%
CHEMBL2581 P07339 Cathepsin D 89.33% 98.95%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 88.84% 93.10%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.05% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.73% 99.17%
CHEMBL4208 P20618 Proteasome component C5 80.56% 90.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 74960803
LOTUS LTS0086257
wikiData Q104964604