(5R,8R,9S,10R,12S)-1beta-(Tigloyloxy)-4alpha,19:15,16-diepoxy-6alpha,12-dihydroxy-18-acetoxycleroda-13-ene-15-one

Details

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Internal ID b376396d-dcbd-4f62-a5fd-c8a52cbe3d14
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name [(1R,4R,4aR,5S,7R,8S,8aR)-4a-(acetyloxymethyl)-5-hydroxy-8-[(2S)-2-hydroxy-2-(5-oxo-2H-furan-3-yl)ethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] (E)-2-methylbut-2-enoate
SMILES (Canonical) CC=C(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3O)C)(C)CC(C4=CC(=O)OC4)O)COC(=O)C
SMILES (Isomeric) C/C=C(\C)/C(=O)O[C@@H]1CC[C@]2(CO2)[C@]3([C@H]1[C@@]([C@@H](C[C@@H]3O)C)(C)C[C@@H](C4=CC(=O)OC4)O)COC(=O)C
InChI InChI=1S/C27H38O9/c1-6-15(2)24(32)36-20-7-8-26(13-35-26)27(14-34-17(4)28)21(30)9-16(3)25(5,23(20)27)11-19(29)18-10-22(31)33-12-18/h6,10,16,19-21,23,29-30H,7-9,11-14H2,1-5H3/b15-6+/t16-,19+,20-,21+,23-,25+,26+,27-/m1/s1
InChI Key BPMCHJRJBOHQAU-YWFRBXFRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H38O9
Molecular Weight 506.60 g/mol
Exact Mass 506.25158279 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5R,8R,9S,10R,12S)-1beta-(Tigloyloxy)-4alpha,19:15,16-diepoxy-6alpha,12-dihydroxy-18-acetoxycleroda-13-ene-15-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9740 97.40%
Caco-2 - 0.6845 68.45%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8183 81.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8636 86.36%
OATP1B3 inhibitior + 0.9555 95.55%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6271 62.71%
BSEP inhibitior + 0.9690 96.90%
P-glycoprotein inhibitior + 0.7416 74.16%
P-glycoprotein substrate + 0.6631 66.31%
CYP3A4 substrate + 0.7032 70.32%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8932 89.32%
CYP3A4 inhibition - 0.6326 63.26%
CYP2C9 inhibition - 0.7921 79.21%
CYP2C19 inhibition - 0.8904 89.04%
CYP2D6 inhibition - 0.9405 94.05%
CYP1A2 inhibition - 0.8592 85.92%
CYP2C8 inhibition + 0.5245 52.45%
CYP inhibitory promiscuity - 0.8927 89.27%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.4501 45.01%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9406 94.06%
Skin irritation - 0.5165 51.65%
Skin corrosion - 0.9383 93.83%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6839 68.39%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5601 56.01%
skin sensitisation - 0.8901 89.01%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.4892 48.92%
Acute Oral Toxicity (c) I 0.5979 59.79%
Estrogen receptor binding + 0.8634 86.34%
Androgen receptor binding + 0.7370 73.70%
Thyroid receptor binding - 0.5240 52.40%
Glucocorticoid receptor binding + 0.8350 83.50%
Aromatase binding + 0.8113 81.13%
PPAR gamma + 0.5961 59.61%
Honey bee toxicity - 0.6099 60.99%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9900 99.00%

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 99.00% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.04% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.49% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.97% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.38% 90.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.16% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.65% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.19% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.33% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.89% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.71% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.75% 82.69%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 86.10% 91.07%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.40% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.30% 99.23%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.77% 97.28%
CHEMBL340 P08684 Cytochrome P450 3A4 82.01% 91.19%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.97% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.88% 86.33%
CHEMBL5028 O14672 ADAM10 81.49% 97.50%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 81.41% 91.65%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.29% 94.23%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.65% 94.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.04% 94.62%

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.
Ajuga decumbens

Cross-Links

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PubChem 24881997
LOTUS LTS0117935
wikiData Q104943097