[(1S,2S,3aR,5S,5aR,6S,9R,9aR,10R,10aR)-1,3a,9-triacetyloxy-9a-(acetyloxymethyl)-5-hydroxy-2,5-dimethyl-4-oxo-6-prop-1-en-2-yl-1,2,3,5a,6,9,10,10a-octahydrobenzo[f]azulen-10-yl] butanoate

Details

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Internal ID 16031a3d-6f6f-4a47-8242-047412ebb181
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name [(1S,2S,3aR,5S,5aR,6S,9R,9aR,10R,10aR)-1,3a,9-triacetyloxy-9a-(acetyloxymethyl)-5-hydroxy-2,5-dimethyl-4-oxo-6-prop-1-en-2-yl-1,2,3,5a,6,9,10,10a-octahydrobenzo[f]azulen-10-yl] butanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H44O12/c1-10-11-24(37)43-28-25-26(42-20(7)35)17(4)14-32(25,44-21(8)36)29(38)30(9,39)27-22(16(2)3)12-13-23(41-19(6)34)31(27,28)15-40-18(5)33/h12-13,17,22-23,25-28,39H,2,10-11,14-15H2,1,3-9H3/t17-,22+,23+,25+,26-,27-,28+,30-,31+,32+/m0/s1
InChI Key YFFHHGUZDPXARY-NSFXRBBVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H44O12
Molecular Weight 620.70 g/mol
Exact Mass 620.28327683 g/mol
Topological Polar Surface Area (TPSA) 169.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.78
H-Bond Acceptor 12
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(1S,2S,3aR,5S,5aR,6S,9R,9aR,10R,10aR)-1,3a,9-triacetyloxy-9a-(acetyloxymethyl)-5-hydroxy-2,5-dimethyl-4-oxo-6-prop-1-en-2-yl-1,2,3,5a,6,9,10,10a-octahydrobenzo[f]azulen-10-yl] butanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 - 0.7617 76.17%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6737 67.37%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.8608 86.08%
OATP1B3 inhibitior + 0.9365 93.65%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.8868 88.68%
P-glycoprotein inhibitior + 0.7854 78.54%
P-glycoprotein substrate + 0.6810 68.10%
CYP3A4 substrate + 0.6827 68.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8827 88.27%
CYP3A4 inhibition - 0.7870 78.70%
CYP2C9 inhibition - 0.7490 74.90%
CYP2C19 inhibition - 0.8357 83.57%
CYP2D6 inhibition - 0.9115 91.15%
CYP1A2 inhibition - 0.7336 73.36%
CYP2C8 inhibition + 0.4729 47.29%
CYP inhibitory promiscuity - 0.8512 85.12%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5884 58.84%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.8896 88.96%
Skin irritation + 0.5955 59.55%
Skin corrosion - 0.9311 93.11%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3605 36.05%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5053 50.53%
skin sensitisation - 0.8067 80.67%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.6679 66.79%
Acute Oral Toxicity (c) III 0.6745 67.45%
Estrogen receptor binding + 0.7484 74.84%
Androgen receptor binding + 0.6896 68.96%
Thyroid receptor binding + 0.5437 54.37%
Glucocorticoid receptor binding + 0.7603 76.03%
Aromatase binding + 0.7049 70.49%
PPAR gamma + 0.6754 67.54%
Honey bee toxicity - 0.7019 70.19%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5718 57.18%
Fish aquatic toxicity + 0.9884 98.84%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.66% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.92% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.62% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 97.09% 91.49%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 94.43% 82.69%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.67% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.15% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.87% 85.14%
CHEMBL4040 P28482 MAP kinase ERK2 86.26% 83.82%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 85.62% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.48% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.45% 94.45%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.80% 94.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.79% 99.23%
CHEMBL230 P35354 Cyclooxygenase-2 83.29% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.88% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.28% 95.89%
CHEMBL5255 O00206 Toll-like receptor 4 81.13% 92.50%
CHEMBL2996 Q05655 Protein kinase C delta 80.37% 97.79%

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.
Euphorbia polycaulis

Cross-Links

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PubChem 11028523
LOTUS LTS0240924
wikiData Q105347561