[4,5-Dihydroxy-6-(hydroxymethyl)-2-[[6-(hydroxymethyl)-2-oxo-3,9-dioxatricyclo[5.3.1.04,11]undeca-1(10),5-dien-8-yl]oxy]oxan-3-yl] 5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate

Details

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Internal ID 821092ef-6a89-48bf-bd20-2556172746ab
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name [4,5-dihydroxy-6-(hydroxymethyl)-2-[[6-(hydroxymethyl)-2-oxo-3,9-dioxatricyclo[5.3.1.04,11]undeca-1(10),5-dien-8-yl]oxy]oxan-3-yl] 5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate
SMILES (Canonical) CSC(=O)OCC1=CC(C2C1C(OC=C2C(=O)OC3C(C(C(OC3OC4C5C6C(C=C5CO)OC(=O)C6=CO4)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O
SMILES (Isomeric) CSC(=O)OCC1=CC(C2C1C(OC=C2C(=O)OC3C(C(C(OC3OC4C5C6C(C=C5CO)OC(=O)C6=CO4)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O
InChI InChI=1S/C34H42O21S/c1-56-34(46)49-7-11-2-14(38)20-12(8-47-31(19(11)20)54-32-26(43)24(41)22(39)16(5-36)51-32)29(45)53-27-25(42)23(40)17(6-37)52-33(27)55-30-18-10(4-35)3-15-21(18)13(9-48-30)28(44)50-15/h2-3,8-9,14-27,30-33,35-43H,4-7H2,1H3
InChI Key WGKFNKQBTTUDPE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H42O21S
Molecular Weight 818.80 g/mol
Exact Mass 818.19392952 g/mol
Topological Polar Surface Area (TPSA) 342.00 Ų
XlogP -4.50
Atomic LogP (AlogP) -4.23
H-Bond Acceptor 22
H-Bond Donor 9
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [4,5-Dihydroxy-6-(hydroxymethyl)-2-[[6-(hydroxymethyl)-2-oxo-3,9-dioxatricyclo[5.3.1.04,11]undeca-1(10),5-dien-8-yl]oxy]oxan-3-yl] 5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-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 + 0.6438 64.38%
Caco-2 - 0.8894 88.94%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.7293 72.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7770 77.70%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6711 67.11%
P-glycoprotein inhibitior + 0.6745 67.45%
P-glycoprotein substrate - 0.5433 54.33%
CYP3A4 substrate + 0.6905 69.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8664 86.64%
CYP3A4 inhibition - 0.8432 84.32%
CYP2C9 inhibition - 0.7856 78.56%
CYP2C19 inhibition - 0.6968 69.68%
CYP2D6 inhibition - 0.8801 88.01%
CYP1A2 inhibition - 0.7928 79.28%
CYP2C8 inhibition + 0.6333 63.33%
CYP inhibitory promiscuity - 0.5984 59.84%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5411 54.11%
Eye corrosion - 0.9832 98.32%
Eye irritation - 0.9111 91.11%
Skin irritation - 0.7673 76.73%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.5637 56.37%
Human Ether-a-go-go-Related Gene inhibition + 0.7777 77.77%
Micronuclear - 0.5600 56.00%
Hepatotoxicity - 0.7321 73.21%
skin sensitisation - 0.8478 84.78%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.6855 68.55%
Acute Oral Toxicity (c) III 0.5363 53.63%
Estrogen receptor binding + 0.7953 79.53%
Androgen receptor binding + 0.6931 69.31%
Thyroid receptor binding - 0.5131 51.31%
Glucocorticoid receptor binding + 0.5650 56.50%
Aromatase binding + 0.5225 52.25%
PPAR gamma + 0.6861 68.61%
Honey bee toxicity - 0.6565 65.65%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8109 81.09%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.10% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.76% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 91.40% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.34% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 89.15% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.15% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.15% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.63% 94.00%
CHEMBL5255 O00206 Toll-like receptor 4 85.35% 92.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.77% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.15% 86.92%

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.
Saprosma scortechinii

Cross-Links

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PubChem 85344088
LOTUS LTS0069439
wikiData Q105304579