(1E,5Z,9E,12R,13S)-13-methoxy-1,5,9-trimethyl-12-(6-methylhepta-1,5-dien-2-yl)cyclotetradeca-1,5,9-triene

Details

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Internal ID 73cc56c8-5849-48e6-93e8-2a14a65c3c20
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name (1E,5Z,9E,12R,13S)-13-methoxy-1,5,9-trimethyl-12-(6-methylhepta-1,5-dien-2-yl)cyclotetradeca-1,5,9-triene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H42O/c1-20(2)11-8-16-24(6)25-18-17-22(4)14-9-12-21(3)13-10-15-23(5)19-26(25)27-7/h11-12,15,17,25-26H,6,8-10,13-14,16,18-19H2,1-5,7H3/b21-12-,22-17+,23-15+/t25-,26+/m1/s1
InChI Key FGDIMNAMJBFDNJ-RTYMIUGPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H42O
Molecular Weight 370.60 g/mol
Exact Mass 370.323565959 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 7.20
Atomic LogP (AlogP) 8.11
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1E,5Z,9E,12R,13S)-13-methoxy-1,5,9-trimethyl-12-(6-methylhepta-1,5-dien-2-yl)cyclotetradeca-1,5,9-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9949 99.49%
Caco-2 + 0.7831 78.31%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5011 50.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9348 93.48%
OATP1B3 inhibitior + 0.8455 84.55%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.6967 69.67%
P-glycoprotein inhibitior + 0.8461 84.61%
P-glycoprotein substrate - 0.7560 75.60%
CYP3A4 substrate + 0.5587 55.87%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7277 72.77%
CYP3A4 inhibition - 0.8062 80.62%
CYP2C9 inhibition - 0.8860 88.60%
CYP2C19 inhibition - 0.7369 73.69%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.6605 66.05%
CYP2C8 inhibition - 0.6326 63.26%
CYP inhibitory promiscuity - 0.7541 75.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7471 74.71%
Carcinogenicity (trinary) Non-required 0.6183 61.83%
Eye corrosion - 0.8728 87.28%
Eye irritation - 0.8482 84.82%
Skin irritation - 0.5391 53.91%
Skin corrosion - 0.9753 97.53%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9208 92.08%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5572 55.72%
skin sensitisation + 0.7249 72.49%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.6700 67.00%
Acute Oral Toxicity (c) III 0.8016 80.16%
Estrogen receptor binding - 0.5072 50.72%
Androgen receptor binding - 0.5808 58.08%
Thyroid receptor binding + 0.5530 55.30%
Glucocorticoid receptor binding - 0.4800 48.00%
Aromatase binding - 0.6044 60.44%
PPAR gamma + 0.6844 68.44%
Honey bee toxicity - 0.7357 73.57%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9737 97.37%

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 97.30% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.29% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.96% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.68% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.98% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.97% 94.73%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.43% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.89% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.58% 99.17%

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 163083230
LOTUS LTS0015934
wikiData Q104994829