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

Details

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Internal ID a87c44b1-eaf9-41cf-b62f-3c933776737f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name [(2S,3R,4S,5S,6R)-2-[[(1S,4aR,6S,7R,7aS)-6-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H32O11/c1-12-16(28)10-14-7-8-33-24(20(12)14)36-25-23(22(31)21(30)18(11-26)34-25)35-19(29)6-4-13-3-5-15(27)17(9-13)32-2/h3-9,12,14,16,18,20-28,30-31H,10-11H2,1-2H3/b6-4+/t12-,14-,16-,18+,20+,21+,22-,23+,24-,25-/m0/s1
InChI Key KWGAFQKENQSNHF-LFVRPZHJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H32O11
Molecular Weight 508.50 g/mol
Exact Mass 508.19446183 g/mol
Topological Polar Surface Area (TPSA) 164.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.28
H-Bond Acceptor 11
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 [(2S,3R,4S,5S,6R)-2-[[(1S,4aR,6S,7R,7aS)-6-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-1-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-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 + 0.7770 77.70%
Caco-2 - 0.8850 88.50%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.4729 47.29%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.8182 81.82%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6191 61.91%
P-glycoprotein inhibitior - 0.6193 61.93%
P-glycoprotein substrate - 0.5535 55.35%
CYP3A4 substrate + 0.6638 66.38%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8648 86.48%
CYP3A4 inhibition - 0.8431 84.31%
CYP2C9 inhibition - 0.9371 93.71%
CYP2C19 inhibition - 0.9192 91.92%
CYP2D6 inhibition - 0.8701 87.01%
CYP1A2 inhibition - 0.8192 81.92%
CYP2C8 inhibition + 0.6926 69.26%
CYP inhibitory promiscuity - 0.8073 80.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7020 70.20%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9464 94.64%
Skin irritation - 0.7620 76.20%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6910 69.10%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8421 84.21%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.9662 96.62%
Acute Oral Toxicity (c) III 0.5653 56.53%
Estrogen receptor binding + 0.7942 79.42%
Androgen receptor binding - 0.5334 53.34%
Thyroid receptor binding - 0.5119 51.19%
Glucocorticoid receptor binding - 0.4885 48.85%
Aromatase binding - 0.5579 55.79%
PPAR gamma + 0.6301 63.01%
Honey bee toxicity - 0.7727 77.27%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.8116 81.16%

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 99.61% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.54% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.48% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 96.01% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.61% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.60% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.03% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.01% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.71% 99.17%
CHEMBL4208 P20618 Proteasome component C5 90.66% 90.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 89.37% 89.62%
CHEMBL3194 P02766 Transthyretin 87.39% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 86.68% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.92% 86.92%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.73% 91.07%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.63% 95.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.56% 92.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.49% 96.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.31% 94.45%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.20% 97.21%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.13% 95.89%

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.
Chiococca alba
Eurycoma longifolia

Cross-Links

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PubChem 100982915
LOTUS LTS0190639
wikiData Q105343785