methyl (1S,4aS,5S,7aS)-1-[(2S,3R,4S,5R,6R)-6-[[(1S,4aS,5S,7aS)-5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carbonyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate

Details

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Internal ID 3fe5bb94-3894-4555-8c5d-4192dd48a11c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name methyl (1S,4aS,5S,7aS)-1-[(2S,3R,4S,5R,6R)-6-[[(1S,4aS,5S,7aS)-5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carbonyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H48O23S2/c1-51-30(47)14-9-53-32(20-12(4-16(39)22(14)20)7-55-36(49)61-2)60-35-29(46)27(44)25(42)19(58-35)11-52-31(48)15-10-54-33(59-34-28(45)26(43)24(41)18(6-38)57-34)21-13(5-17(40)23(15)21)8-56-37(50)62-3/h4-5,9-10,16-29,32-35,38-46H,6-8,11H2,1-3H3/t16-,17-,18+,19+,20+,21+,22-,23-,24-,25-,26-,27-,28+,29+,32-,33-,34-,35-/m0/s1
InChI Key YFSAIZBRNNXWIY-VEQZGKQOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C37H48O23S2
Molecular Weight 924.90 g/mol
Exact Mass 924.20278012 g/mol
Topological Polar Surface Area (TPSA) 393.00 Ų
XlogP -4.00
Atomic LogP (AlogP) -3.11
H-Bond Acceptor 25
H-Bond Donor 9
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (1S,4aS,5S,7aS)-1-[(2S,3R,4S,5R,6R)-6-[[(1S,4aS,5S,7aS)-5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carbonyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5000 50.00%
Caco-2 - 0.8746 87.46%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6386 63.86%
OATP2B1 inhibitior - 0.7259 72.59%
OATP1B1 inhibitior + 0.7747 77.47%
OATP1B3 inhibitior + 0.9302 93.02%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8974 89.74%
P-glycoprotein inhibitior + 0.7312 73.12%
P-glycoprotein substrate - 0.6587 65.87%
CYP3A4 substrate + 0.6498 64.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.8065 80.65%
CYP2C9 inhibition - 0.8316 83.16%
CYP2C19 inhibition - 0.7505 75.05%
CYP2D6 inhibition - 0.9000 90.00%
CYP1A2 inhibition - 0.8425 84.25%
CYP2C8 inhibition + 0.5638 56.38%
CYP inhibitory promiscuity - 0.7033 70.33%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6315 63.15%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.9069 90.69%
Skin irritation - 0.7713 77.13%
Skin corrosion - 0.9433 94.33%
Ames mutagenesis - 0.5837 58.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7375 73.75%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.8524 85.24%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.8437 84.37%
Acute Oral Toxicity (c) III 0.5399 53.99%
Estrogen receptor binding + 0.8112 81.12%
Androgen receptor binding + 0.6931 69.31%
Thyroid receptor binding + 0.5236 52.36%
Glucocorticoid receptor binding + 0.7258 72.58%
Aromatase binding + 0.5492 54.92%
PPAR gamma + 0.7727 77.27%
Honey bee toxicity - 0.6902 69.02%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.7937 79.37%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.53% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.63% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.40% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 90.87% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.06% 86.33%
CHEMBL226 P30542 Adenosine A1 receptor 81.44% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.32% 94.45%
CHEMBL5255 O00206 Toll-like receptor 4 81.06% 92.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.91% 94.33%

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.
Paederia foetida

Cross-Links

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PubChem 11968434
NPASS NPC55416