[(4R,4aR,5S,7S,8S,8aR)-8-[(1S)-1-acetyloxy-2-(5-oxo-2H-furan-3-yl)ethyl]-5-benzoyloxy-7-hydroxy-7,8-dimethylspiro[1,2,3,5,6,8a-hexahydronaphthalene-4,2'-oxirane]-4a-yl]methyl benzoate

Details

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Internal ID 386b4300-bd8f-4a3f-8e84-a29d88e1c7f2
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tetracarboxylic acids and derivatives
IUPAC Name [(4R,4aR,5S,7S,8S,8aR)-8-[(1S)-1-acetyloxy-2-(5-oxo-2H-furan-3-yl)ethyl]-5-benzoyloxy-7-hydroxy-7,8-dimethylspiro[1,2,3,5,6,8a-hexahydronaphthalene-4,2'-oxirane]-4a-yl]methyl benzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H40O10/c1-23(37)45-28(17-24-18-30(38)42-20-24)34(3)27-15-10-16-35(21-44-35)36(27,22-43-31(39)25-11-6-4-7-12-25)29(19-33(34,2)41)46-32(40)26-13-8-5-9-14-26/h4-9,11-14,18,27-29,41H,10,15-17,19-22H2,1-3H3/t27-,28+,29+,33+,34+,35+,36+/m1/s1
InChI Key WEMANRXAHPPLNI-HZXVDWMXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H40O10
Molecular Weight 632.70 g/mol
Exact Mass 632.26214747 g/mol
Topological Polar Surface Area (TPSA) 138.00 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.59
H-Bond Acceptor 10
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 [(4R,4aR,5S,7S,8S,8aR)-8-[(1S)-1-acetyloxy-2-(5-oxo-2H-furan-3-yl)ethyl]-5-benzoyloxy-7-hydroxy-7,8-dimethylspiro[1,2,3,5,6,8a-hexahydronaphthalene-4,2'-oxirane]-4a-yl]methyl benzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9754 97.54%
Caco-2 - 0.7965 79.65%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7912 79.12%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.8607 86.07%
OATP1B3 inhibitior + 0.9326 93.26%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.5771 57.71%
BSEP inhibitior + 0.9882 98.82%
P-glycoprotein inhibitior + 0.8849 88.49%
P-glycoprotein substrate + 0.5980 59.80%
CYP3A4 substrate + 0.7068 70.68%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8940 89.40%
CYP3A4 inhibition + 0.5690 56.90%
CYP2C9 inhibition - 0.7156 71.56%
CYP2C19 inhibition - 0.7589 75.89%
CYP2D6 inhibition - 0.9106 91.06%
CYP1A2 inhibition - 0.7385 73.85%
CYP2C8 inhibition + 0.6978 69.78%
CYP inhibitory promiscuity - 0.8311 83.11%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4437 44.37%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.9082 90.82%
Skin irritation - 0.5962 59.62%
Skin corrosion - 0.9386 93.86%
Ames mutagenesis - 0.6270 62.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8709 87.09%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.5067 50.67%
skin sensitisation - 0.8585 85.85%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.5483 54.83%
Acute Oral Toxicity (c) I 0.5783 57.83%
Estrogen receptor binding + 0.8382 83.82%
Androgen receptor binding + 0.7508 75.08%
Thyroid receptor binding + 0.5529 55.29%
Glucocorticoid receptor binding + 0.8041 80.41%
Aromatase binding + 0.6455 64.55%
PPAR gamma + 0.7011 70.11%
Honey bee toxicity - 0.7687 76.87%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5300 53.00%
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
CHEMBL2581 P07339 Cathepsin D 98.18% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 95.57% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.49% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.33% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 94.47% 90.17%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 93.72% 83.00%
CHEMBL240 Q12809 HERG 93.46% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.39% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.44% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.55% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.61% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.75% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.39% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.90% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.49% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.04% 97.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.38% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.73% 91.19%
CHEMBL2535 P11166 Glucose transporter 82.63% 98.75%
CHEMBL5028 O14672 ADAM10 82.49% 97.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.08% 93.04%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.58% 92.62%

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.
Scutellaria caucasica

Cross-Links

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PubChem 10604066
LOTUS LTS0041670
wikiData Q105303132