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[(2R,3R,4R,5R,6S)-2-[[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]-4,5-dihydroxy-6-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Table of Contents

Details
Physical and Chemical Properties
Synonyms
2D Structure
3D Structure
ADMET Properties
Targets (proven and/or predicted)
Plants that contains it
Cross-Links

Details

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Internal ID ed5bf882-9b9d-4c37-a7ec-420eea7a4216
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name [(2R,3R,4R,5R,6S)-2-[[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]-4,5-dihydroxy-6-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C31H40O16/c1-13-23(36)26(39)28(46-21(35)6-4-14-3-5-17(34)19(9-14)41-2)31(43-13)44-18-10-15(11-32)22-16(18)7-8-42-29(22)47-30-27(40)25(38)24(37)20(12-33)45-30/h3-10,13,16,18,20,22-34,36-40H,11-12H2,1-2H3/b6-4+/t13-,16-,18+,20+,22+,23-,24+,25-,26+,27+,28+,29-,30-,31-/m0/s1
InChI Key JKLCTVDYVIZSMA-CXLKIWCRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H40O16
Molecular Weight 668.60 g/mol
Exact Mass 668.23163518 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP -1.80
Atomic LogP (AlogP) -1.97
H-Bond Acceptor 16
H-Bond Donor 8
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,3R,4R,5R,6S)-2-[[(1S,4aR,5S,7aS)-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-5-yl]oxy]-4,5-dihydroxy-6-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6784 67.84%
Caco-2 - 0.8933 89.33%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.5787 57.87%
OATP2B1 inhibitior - 0.8615 86.15%
OATP1B1 inhibitior + 0.8248 82.48%
OATP1B3 inhibitior + 0.9710 97.10%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.5879 58.79%
P-glycoprotein inhibitior - 0.4829 48.29%
P-glycoprotein substrate + 0.5638 56.38%
CYP3A4 substrate + 0.6822 68.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8696 86.96%
CYP3A4 inhibition - 0.8699 86.99%
CYP2C9 inhibition - 0.8350 83.50%
CYP2C19 inhibition - 0.6454 64.54%
CYP2D6 inhibition - 0.8471 84.71%
CYP1A2 inhibition - 0.8311 83.11%
CYP2C8 inhibition + 0.7377 73.77%
CYP inhibitory promiscuity + 0.5231 52.31%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6980 69.80%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.9215 92.15%
Skin irritation - 0.8010 80.10%
Skin corrosion - 0.9538 95.38%
Ames mutagenesis - 0.5437 54.37%
Human Ether-a-go-go-Related Gene inhibition - 0.3759 37.59%
Micronuclear + 0.5233 52.33%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8067 80.67%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.9400 94.00%
Acute Oral Toxicity (c) III 0.5747 57.47%
Estrogen receptor binding + 0.7845 78.45%
Androgen receptor binding + 0.5344 53.44%
Thyroid receptor binding - 0.4879 48.79%
Glucocorticoid receptor binding + 0.6653 66.53%
Aromatase binding - 0.5305 53.05%
PPAR gamma + 0.6424 64.24%
Honey bee toxicity - 0.6991 69.91%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5455 54.55%
Fish aquatic toxicity + 0.7948 79.48%

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 99.73% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.53% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.77% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.61% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.14% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.86% 95.56%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.61% 97.36%
CHEMBL3194 P02766 Transthyretin 91.65% 90.71%
CHEMBL1951 P21397 Monoamine oxidase A 89.73% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.62% 99.17%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.99% 80.78%
CHEMBL3401 O75469 Pregnane X receptor 85.48% 94.73%
CHEMBL4208 P20618 Proteasome component C5 84.78% 90.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.98% 86.92%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.70% 89.62%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.25% 92.94%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.17% 91.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.03% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.07% 97.09%

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.
Verbascum undulatum

Cross-Links

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PubChem 101713480
LOTUS LTS0127239
wikiData Q105130305