[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (3aS,5Z,10Z,11aR)-10-methyl-3-methylidene-2-oxo-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylate

Details

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Internal ID b0a0b3e7-7e7d-4d9c-808a-d3c2b437ed29
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Germacranolides and derivatives
IUPAC Name [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (3aS,5Z,10Z,11aR)-10-methyl-3-methylidene-2-oxo-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylate
SMILES (Canonical) CC1=CC2C(CC=C(CCC1)C(=O)OC3C(C(C(C(O3)CO)O)O)O)C(=C)C(=O)O2
SMILES (Isomeric) C/C/1=C/[C@@H]2[C@@H](C/C=C(/CCC1)\C(=O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C(=C)C(=O)O2
InChI InChI=1S/C21H28O9/c1-10-4-3-5-12(6-7-13-11(2)19(26)28-14(13)8-10)20(27)30-21-18(25)17(24)16(23)15(9-22)29-21/h6,8,13-18,21-25H,2-5,7,9H2,1H3/b10-8-,12-6-/t13-,14+,15+,16+,17-,18+,21-/m0/s1
InChI Key FMUGLSYMLSBAHS-BLQBGWNPSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H28O9
Molecular Weight 424.40 g/mol
Exact Mass 424.17333247 g/mol
Topological Polar Surface Area (TPSA) 143.00 Ų
XlogP 0.50
Atomic LogP (AlogP) -0.13
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (3aS,5Z,10Z,11aR)-10-methyl-3-methylidene-2-oxo-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7102 71.02%
Caco-2 - 0.8268 82.68%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.8370 83.70%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8213 82.13%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8016 80.16%
P-glycoprotein inhibitior - 0.7413 74.13%
P-glycoprotein substrate - 0.8350 83.50%
CYP3A4 substrate + 0.6475 64.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8743 87.43%
CYP3A4 inhibition - 0.8732 87.32%
CYP2C9 inhibition - 0.8817 88.17%
CYP2C19 inhibition - 0.8722 87.22%
CYP2D6 inhibition - 0.9159 91.59%
CYP1A2 inhibition - 0.7262 72.62%
CYP2C8 inhibition + 0.4493 44.93%
CYP inhibitory promiscuity - 0.9194 91.94%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7053 70.53%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.9708 97.08%
Skin irritation - 0.6377 63.77%
Skin corrosion - 0.9382 93.82%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7514 75.14%
Micronuclear - 0.8900 89.00%
Hepatotoxicity - 0.6639 66.39%
skin sensitisation - 0.8929 89.29%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.8154 81.54%
Acute Oral Toxicity (c) III 0.5013 50.13%
Estrogen receptor binding + 0.7186 71.86%
Androgen receptor binding + 0.5454 54.54%
Thyroid receptor binding - 0.7001 70.01%
Glucocorticoid receptor binding - 0.5245 52.45%
Aromatase binding - 0.5607 56.07%
PPAR gamma + 0.5435 54.35%
Honey bee toxicity - 0.7950 79.50%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9751 97.51%

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 96.44% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 93.58% 83.82%
CHEMBL2581 P07339 Cathepsin D 93.50% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.71% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 89.83% 94.73%
CHEMBL3714130 P46095 G-protein coupled receptor 6 89.65% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.47% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.53% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.97% 97.09%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 86.84% 91.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.81% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 86.00% 97.79%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.62% 94.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.52% 96.61%
CHEMBL5255 O00206 Toll-like receptor 4 84.24% 92.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.43% 93.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.74% 89.00%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 80.52% 96.37%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.45% 95.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.27% 99.23%

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.
Taraxacum platycarpum subsp. hondoense
Taraxacum udum

Cross-Links

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PubChem 162852856
LOTUS LTS0011798
wikiData Q104998049