[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E)-3-[4-[(2S,3R,4S,5S,6R)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]prop-2-enoate

Details

Top
Internal ID b05fde40-11ff-418e-8dff-b973304af9ac
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid esters > O-cinnamoyl glycosides
IUPAC Name [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E)-3-[4-[(2S,3R,4S,5S,6R)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H34O16/c31-12-19-23(36)25(38)28(41)30(44-19)46-22(35)10-4-14-1-6-16(7-2-14)43-29-27(40)26(39)24(37)20(45-29)13-42-21(34)9-5-15-3-8-17(32)18(33)11-15/h1-11,19-20,23-33,36-41H,12-13H2/b9-5+,10-4+/t19-,20-,23-,24-,25+,26+,27-,28-,29-,30+/m1/s1
InChI Key HFIRFUKEPOQTLQ-KTFGOVRASA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C30H34O16
Molecular Weight 650.60 g/mol
Exact Mass 650.18468499 g/mol
Topological Polar Surface Area (TPSA) 262.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -2.10
H-Bond Acceptor 16
H-Bond Donor 9
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E)-3-[4-[(2S,3R,4S,5S,6R)-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]prop-2-enoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8264 82.64%
Caco-2 - 0.8820 88.20%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.5406 54.06%
OATP2B1 inhibitior - 0.7133 71.33%
OATP1B1 inhibitior + 0.9127 91.27%
OATP1B3 inhibitior + 0.9622 96.22%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6967 69.67%
P-glycoprotein inhibitior + 0.6648 66.48%
P-glycoprotein substrate - 0.9010 90.10%
CYP3A4 substrate + 0.5920 59.20%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8640 86.40%
CYP3A4 inhibition - 0.8666 86.66%
CYP2C9 inhibition - 0.8826 88.26%
CYP2C19 inhibition - 0.8950 89.50%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.9487 94.87%
CYP2C8 inhibition + 0.6158 61.58%
CYP inhibitory promiscuity - 0.8350 83.50%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.7039 70.39%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.9040 90.40%
Skin irritation - 0.8613 86.13%
Skin corrosion - 0.9589 95.89%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7988 79.88%
Micronuclear + 0.5133 51.33%
Hepatotoxicity - 0.9125 91.25%
skin sensitisation - 0.8212 82.12%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.9140 91.40%
Acute Oral Toxicity (c) III 0.5686 56.86%
Estrogen receptor binding + 0.6905 69.05%
Androgen receptor binding + 0.5468 54.68%
Thyroid receptor binding + 0.5178 51.78%
Glucocorticoid receptor binding + 0.5783 57.83%
Aromatase binding - 0.5257 52.57%
PPAR gamma + 0.6258 62.58%
Honey bee toxicity - 0.7609 76.09%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9032 90.32%

Targets

Top

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 99.76% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 95.99% 91.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.63% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.91% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.19% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.16% 97.09%
CHEMBL3194 P02766 Transthyretin 92.16% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.08% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.02% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.04% 99.15%
CHEMBL226 P30542 Adenosine A1 receptor 88.89% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.65% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.27% 94.73%
CHEMBL4208 P20618 Proteasome component C5 88.08% 90.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 87.55% 80.78%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.50% 86.92%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.28% 97.36%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.76% 95.50%

Plants that contains it

Top
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.
Clematis tashiroi

Cross-Links

Top
PubChem 122181706
LOTUS LTS0243588
wikiData Q105027351