2,4,6,8-Tetramethyl-3,4-dihydroxydec-8(9)-enolide

Details

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Internal ID 10e2f29c-b212-4ffd-a577-6d26723be726
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name (3R,4R,5R,7S,9E)-4,5-dihydroxy-3,5,7,9-tetramethyl-1-oxacycloundec-9-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H24O4/c1-9-5-6-18-13(16)11(3)12(15)14(4,17)8-10(2)7-9/h5,10-12,15,17H,6-8H2,1-4H3/b9-5+/t10-,11+,12+,14+/m0/s1
InChI Key VAQCMXARBHDRBD-GZJDNEMJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H24O4
Molecular Weight 256.34 g/mol
Exact Mass 256.16745924 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.65
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,4,6,8-Tetramethyl-3,4-dihydroxydec-8(9)-enolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9503 95.03%
Caco-2 + 0.7796 77.96%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7104 71.04%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9342 93.42%
OATP1B3 inhibitior + 0.9518 95.18%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7181 71.81%
P-glycoprotein inhibitior - 0.9336 93.36%
P-glycoprotein substrate - 0.8176 81.76%
CYP3A4 substrate + 0.5259 52.59%
CYP2C9 substrate - 0.8070 80.70%
CYP2D6 substrate - 0.8701 87.01%
CYP3A4 inhibition - 0.8629 86.29%
CYP2C9 inhibition - 0.8726 87.26%
CYP2C19 inhibition - 0.8244 82.44%
CYP2D6 inhibition - 0.9414 94.14%
CYP1A2 inhibition - 0.7103 71.03%
CYP2C8 inhibition - 0.9815 98.15%
CYP inhibitory promiscuity - 0.9743 97.43%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5585 55.85%
Eye corrosion - 0.9850 98.50%
Eye irritation - 0.9506 95.06%
Skin irritation - 0.6009 60.09%
Skin corrosion - 0.9357 93.57%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7347 73.47%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.6648 66.48%
skin sensitisation - 0.7947 79.47%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.8399 83.99%
Acute Oral Toxicity (c) III 0.5355 53.55%
Estrogen receptor binding - 0.8199 81.99%
Androgen receptor binding - 0.5486 54.86%
Thyroid receptor binding - 0.6718 67.18%
Glucocorticoid receptor binding - 0.5835 58.35%
Aromatase binding - 0.7573 75.73%
PPAR gamma - 0.7535 75.35%
Honey bee toxicity - 0.8602 86.02%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9250 92.50%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.71% 95.56%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 92.31% 86.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.83% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.26% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.00% 85.14%
CHEMBL2581 P07339 Cathepsin D 89.84% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.72% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.70% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.25% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.56% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.17% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.96% 97.09%

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 139587619
LOTUS LTS0141400
wikiData Q77570439