25-O-ethylluffariellolide

Details

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Internal ID 8f4323d5-5c92-4584-bf14-6bbfeb692de3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 3-[(3E,7E)-4,8-dimethyl-10-(2,6,6-trimethylcyclohexen-1-yl)deca-3,7-dienyl]-2-ethoxy-2H-furan-5-one
SMILES (Canonical) CCOC1C(=CC(=O)O1)CCC=C(C)CCC=C(C)CCC2=C(CCCC2(C)C)C
SMILES (Isomeric) CCOC1C(=CC(=O)O1)CC/C=C(\C)/CC/C=C(\C)/CCC2=C(CCCC2(C)C)C
InChI InChI=1S/C27H42O3/c1-7-29-26-23(19-25(28)30-26)15-9-13-20(2)11-8-12-21(3)16-17-24-22(4)14-10-18-27(24,5)6/h12-13,19,26H,7-11,14-18H2,1-6H3/b20-13+,21-12+
InChI Key CFCUAIAPOSWTBK-KVDUHBSMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C27H42O3
Molecular Weight 414.60 g/mol
Exact Mass 414.31339520 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 6.90
Atomic LogP (AlogP) 7.59
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 11

Synonyms

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CHEMBL484033

2D Structure

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2D Structure of 25-O-ethylluffariellolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.6799 67.99%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6672 66.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7832 78.32%
OATP1B3 inhibitior + 0.9288 92.88%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.9662 96.62%
P-glycoprotein inhibitior + 0.8000 80.00%
P-glycoprotein substrate - 0.7137 71.37%
CYP3A4 substrate + 0.6593 65.93%
CYP2C9 substrate - 0.5989 59.89%
CYP2D6 substrate - 0.9013 90.13%
CYP3A4 inhibition - 0.7807 78.07%
CYP2C9 inhibition - 0.6064 60.64%
CYP2C19 inhibition - 0.5414 54.14%
CYP2D6 inhibition - 0.8739 87.39%
CYP1A2 inhibition - 0.5637 56.37%
CYP2C8 inhibition + 0.4604 46.04%
CYP inhibitory promiscuity + 0.5881 58.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5126 51.26%
Eye corrosion - 0.9644 96.44%
Eye irritation - 0.9216 92.16%
Skin irritation - 0.6085 60.85%
Skin corrosion - 0.9671 96.71%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8444 84.44%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.6300 63.00%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.6464 64.64%
Estrogen receptor binding - 0.5285 52.85%
Androgen receptor binding + 0.5820 58.20%
Thyroid receptor binding + 0.6038 60.38%
Glucocorticoid receptor binding + 0.6323 63.23%
Aromatase binding + 0.5519 55.19%
PPAR gamma + 0.7190 71.90%
Honey bee toxicity - 0.7354 73.54%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5200 52.00%
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 97.84% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.78% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 92.68% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.42% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.78% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.74% 97.09%
CHEMBL2581 P07339 Cathepsin D 90.51% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.43% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.83% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.61% 94.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.54% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.22% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.60% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.51% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.09% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.70% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.74% 94.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.90% 95.50%

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.
There are no matching plants.

Cross-Links

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PubChem 21573066
LOTUS LTS0054272
wikiData Q104956340