1-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carbonyl]oxyoxan-2-yl]oxy-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid

Details

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Internal ID 8c5c3154-a348-4415-9288-d62e54fd17b8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name 1-[4,5-dihydroxy-6-(hydroxymethyl)-3-[5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carbonyl]oxyoxan-2-yl]oxy-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid
SMILES (Canonical) CSC(=O)OCC1=CC(C2C1C(OC=C2C(=O)OC3C(C(C(OC3OC4C5C(C(C=C5CO)O)C(=CO4)C(=O)O)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)O
SMILES (Isomeric) CSC(=O)OCC1=CC(C2C1C(OC=C2C(=O)OC3C(C(C(OC3OC4C5C(C(C=C5CO)O)C(=CO4)C(=O)O)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)O
InChI InChI=1S/C34H44O22S/c1-57-34(48)51-7-11-3-15(39)21-13(9-50-31(19(11)21)55-32-26(44)24(42)22(40)16(5-36)52-32)29(47)54-27-25(43)23(41)17(6-37)53-33(27)56-30-18-10(4-35)2-14(38)20(18)12(8-49-30)28(45)46/h2-3,8-9,14-27,30-33,35-44H,4-7H2,1H3,(H,45,46)
InChI Key VGQBMHXNJUYFRO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H44O22S
Molecular Weight 836.80 g/mol
Exact Mass 836.20449420 g/mol
Topological Polar Surface Area (TPSA) 373.00 Ų
XlogP -5.30
Atomic LogP (AlogP) -4.71
H-Bond Acceptor 22
H-Bond Donor 11
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[5-hydroxy-7-(methylsulfanylcarbonyloxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carbonyl]oxyoxan-2-yl]oxy-5-hydroxy-7-(hydroxymethyl)-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5064 50.64%
Caco-2 - 0.8874 88.74%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.6663 66.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7517 75.17%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4747 47.47%
P-glycoprotein inhibitior + 0.6777 67.77%
P-glycoprotein substrate - 0.6481 64.81%
CYP3A4 substrate + 0.6437 64.37%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8753 87.53%
CYP3A4 inhibition - 0.8761 87.61%
CYP2C9 inhibition - 0.8078 80.78%
CYP2C19 inhibition - 0.7131 71.31%
CYP2D6 inhibition - 0.8899 88.99%
CYP1A2 inhibition - 0.8125 81.25%
CYP2C8 inhibition + 0.5839 58.39%
CYP inhibitory promiscuity - 0.6581 65.81%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6260 62.60%
Eye corrosion - 0.9849 98.49%
Eye irritation - 0.9086 90.86%
Skin irritation - 0.7833 78.33%
Skin corrosion - 0.9401 94.01%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7646 76.46%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.8527 85.27%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7499 74.99%
Acute Oral Toxicity (c) III 0.5129 51.29%
Estrogen receptor binding + 0.7889 78.89%
Androgen receptor binding + 0.6821 68.21%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.4761 47.61%
Aromatase binding - 0.4851 48.51%
PPAR gamma + 0.6943 69.43%
Honey bee toxicity - 0.6842 68.42%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6750 67.50%
Fish aquatic toxicity + 0.7514 75.14%

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 96.57% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.47% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.25% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 89.21% 94.73%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.24% 97.36%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.07% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 83.21% 92.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.23% 95.56%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 80.32% 96.09%
CHEMBL1811 P34995 Prostanoid EP1 receptor 80.19% 95.71%
CHEMBL2581 P07339 Cathepsin D 80.05% 98.95%

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 73820752
LOTUS LTS0009771
wikiData Q105285961