(3R,3aR,4aS,5S,8S,8aR,9aR)-3,5,8a-trimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a,4,4a,5,6,7,8,9,9a-decahydrobenzo[f][1]benzofuran-2-one

Details

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Internal ID 3967124b-d54b-47e7-b214-d5c7108382a4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Sesquiterpene lactones > Eudesmanolides, secoeudesmanolides, and derivatives
IUPAC Name (3R,3aR,4aS,5S,8S,8aR,9aR)-3,5,8a-trimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a,4,4a,5,6,7,8,9,9a-decahydrobenzo[f][1]benzofuran-2-one
SMILES (Canonical) CC1CCC(C2(C1CC3C(C(=O)OC3C2)C)C)OC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) C[C@H]1CC[C@@H]([C@]2([C@H]1C[C@@H]3[C@H](C(=O)O[C@@H]3C2)C)C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C21H34O8/c1-9-4-5-15(29-20-18(25)17(24)16(23)14(8-22)28-20)21(3)7-13-11(6-12(9)21)10(2)19(26)27-13/h9-18,20,22-25H,4-8H2,1-3H3/t9-,10+,11+,12-,13+,14+,15-,16+,17-,18+,20-,21+/m0/s1
InChI Key XVGMYRALTIXNHP-FWLLLMNZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H34O8
Molecular Weight 414.50 g/mol
Exact Mass 414.22536804 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.20
H-Bond Acceptor 8
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 (3R,3aR,4aS,5S,8S,8aR,9aR)-3,5,8a-trimethyl-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a,4,4a,5,6,7,8,9,9a-decahydrobenzo[f][1]benzofuran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5995 59.95%
Caco-2 - 0.7447 74.47%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.7974 79.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8875 88.75%
OATP1B3 inhibitior + 0.9275 92.75%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.7632 76.32%
P-glycoprotein inhibitior - 0.8243 82.43%
P-glycoprotein substrate - 0.7999 79.99%
CYP3A4 substrate + 0.6888 68.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8861 88.61%
CYP3A4 inhibition - 0.9280 92.80%
CYP2C9 inhibition - 0.9028 90.28%
CYP2C19 inhibition - 0.9174 91.74%
CYP2D6 inhibition - 0.9595 95.95%
CYP1A2 inhibition - 0.8921 89.21%
CYP2C8 inhibition - 0.6998 69.98%
CYP inhibitory promiscuity - 0.9332 93.32%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6679 66.79%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9809 98.09%
Skin irritation - 0.6234 62.34%
Skin corrosion - 0.9458 94.58%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5173 51.73%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.9431 94.31%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5656 56.56%
Acute Oral Toxicity (c) I 0.6210 62.10%
Estrogen receptor binding + 0.5947 59.47%
Androgen receptor binding + 0.5905 59.05%
Thyroid receptor binding + 0.5887 58.87%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.6385 63.85%
PPAR gamma + 0.5544 55.44%
Honey bee toxicity - 0.6951 69.51%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8950 89.50%

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 97.14% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.97% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.97% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.14% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.26% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.64% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.93% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 86.41% 92.50%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.63% 96.21%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.63% 86.33%
CHEMBL226 P30542 Adenosine A1 receptor 84.60% 95.93%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.06% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.83% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.77% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.74% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.40% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.22% 89.00%

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.
Saussurea parviflora

Cross-Links

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PubChem 162879907
LOTUS LTS0014308
wikiData Q105342867