(3-Ethyl-3-hydroxy-2,4,6-trimethyl-5-oxocyclohexyl) 3-hydroxy-2,4-dimethyl-5-oxo-6-(3,5,6-trimethyl-4-oxopyran-2-yl)heptanoate

Details

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Internal ID 00d2415c-98a8-44a2-88bc-c21307394a5b
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name (3-ethyl-3-hydroxy-2,4,6-trimethyl-5-oxocyclohexyl) 3-hydroxy-2,4-dimethyl-5-oxo-6-(3,5,6-trimethyl-4-oxopyran-2-yl)heptanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H42O8/c1-11-28(34)18(8)24(32)16(6)26(19(28)9)36-27(33)17(7)23(31)13(3)22(30)15(5)25-14(4)21(29)12(2)20(10)35-25/h13,15-19,23,26,31,34H,11H2,1-10H3
InChI Key JNKMSCYJWSFNIT-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H42O8
Molecular Weight 506.60 g/mol
Exact Mass 506.28796829 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.41
H-Bond Acceptor 8
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 (3-Ethyl-3-hydroxy-2,4,6-trimethyl-5-oxocyclohexyl) 3-hydroxy-2,4-dimethyl-5-oxo-6-(3,5,6-trimethyl-4-oxopyran-2-yl)heptanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9753 97.53%
Caco-2 - 0.7032 70.32%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8050 80.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8497 84.97%
OATP1B3 inhibitior + 0.8982 89.82%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6409 64.09%
P-glycoprotein inhibitior + 0.6836 68.36%
P-glycoprotein substrate - 0.5833 58.33%
CYP3A4 substrate + 0.6144 61.44%
CYP2C9 substrate + 0.8134 81.34%
CYP2D6 substrate - 0.8690 86.90%
CYP3A4 inhibition - 0.8994 89.94%
CYP2C9 inhibition - 0.8250 82.50%
CYP2C19 inhibition - 0.8659 86.59%
CYP2D6 inhibition - 0.9385 93.85%
CYP1A2 inhibition - 0.8344 83.44%
CYP2C8 inhibition - 0.7132 71.32%
CYP inhibitory promiscuity - 0.8442 84.42%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8413 84.13%
Carcinogenicity (trinary) Non-required 0.6948 69.48%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.9185 91.85%
Skin irritation - 0.7648 76.48%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis - 0.5654 56.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.5223 52.23%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.8606 86.06%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6669 66.69%
Acute Oral Toxicity (c) III 0.6879 68.79%
Estrogen receptor binding + 0.7404 74.04%
Androgen receptor binding + 0.6836 68.36%
Thyroid receptor binding + 0.5217 52.17%
Glucocorticoid receptor binding + 0.6283 62.83%
Aromatase binding + 0.6171 61.71%
PPAR gamma + 0.6382 63.82%
Honey bee toxicity - 0.8179 81.79%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9444 94.44%

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
CHEMBL2581 P07339 Cathepsin D 95.08% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.79% 89.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.36% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.28% 91.11%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 87.01% 96.47%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.78% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.50% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.09% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.08% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 81.01% 97.29%
CHEMBL299 P17252 Protein kinase C alpha 80.79% 98.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.59% 99.23%

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 74051738
LOTUS LTS0184412
wikiData Q105131967