methyl (1S,2R,5R,7S,8S,9R)-8-[2-(furan-3-yl)-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.02,7]dodec-3-ene-3-carboxylate

Details

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Internal ID 03bfb067-0dfc-436b-800e-6dd1d3110814
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name methyl (1S,2R,5R,7S,8S,9R)-8-[2-(furan-3-yl)-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.02,7]dodec-3-ene-3-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H36O12/c1-26(9-16(12-4-5-36-11-12)37-25-22(32)21(31)20(30)17(10-28)38-25)14-8-19(39-24(14)34)27(2)15(23(33)35-3)6-13(29)7-18(26)27/h4-6,11,13-14,16-22,25,28-32H,7-10H2,1-3H3/t13-,14-,16?,17+,18-,19-,20+,21-,22+,25+,26+,27-/m0/s1
InChI Key GMZIBNWBLDPKAJ-KSABOFSBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H36O12
Molecular Weight 552.60 g/mol
Exact Mass 552.22067658 g/mol
Topological Polar Surface Area (TPSA) 185.00 Ų
XlogP -0.10
Atomic LogP (AlogP) -0.03
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (1S,2R,5R,7S,8S,9R)-8-[2-(furan-3-yl)-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-5-hydroxy-2,8-dimethyl-10-oxo-11-oxatricyclo[7.2.1.02,7]dodec-3-ene-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8703 87.03%
Caco-2 - 0.8365 83.65%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6331 63.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7509 75.09%
OATP1B3 inhibitior + 0.9518 95.18%
MATE1 inhibitior - 0.9212 92.12%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6109 61.09%
P-glycoprotein inhibitior - 0.4777 47.77%
P-glycoprotein substrate + 0.5702 57.02%
CYP3A4 substrate + 0.7126 71.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8844 88.44%
CYP3A4 inhibition - 0.6635 66.35%
CYP2C9 inhibition - 0.8629 86.29%
CYP2C19 inhibition - 0.8918 89.18%
CYP2D6 inhibition - 0.9390 93.90%
CYP1A2 inhibition - 0.8691 86.91%
CYP2C8 inhibition + 0.4464 44.64%
CYP inhibitory promiscuity - 0.9196 91.96%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6005 60.05%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9437 94.37%
Skin irritation - 0.6258 62.58%
Skin corrosion - 0.9431 94.31%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7277 72.77%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5867 58.67%
skin sensitisation - 0.8823 88.23%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6138 61.38%
Acute Oral Toxicity (c) I 0.5654 56.54%
Estrogen receptor binding + 0.7251 72.51%
Androgen receptor binding + 0.6734 67.34%
Thyroid receptor binding - 0.5654 56.54%
Glucocorticoid receptor binding + 0.6480 64.80%
Aromatase binding + 0.6366 63.66%
PPAR gamma + 0.5523 55.23%
Honey bee toxicity - 0.6378 63.78%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9809 98.09%

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 98.83% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.08% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 97.18% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.99% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.08% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.64% 94.00%
CHEMBL2581 P07339 Cathepsin D 85.46% 98.95%
CHEMBL3437 Q16853 Amine oxidase, copper containing 85.10% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.65% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 84.55% 97.25%
CHEMBL5255 O00206 Toll-like receptor 4 83.65% 92.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.45% 89.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.19% 91.07%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.13% 95.83%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.73% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.43% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.27% 92.62%
CHEMBL4072 P07858 Cathepsin B 81.24% 93.67%

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.
Tinospora crispa

Cross-Links

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PubChem 10602782
LOTUS LTS0049439
wikiData Q105012256