(E)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-[3-methoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enamide

Details

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Internal ID 864fa1cc-6034-47a9-b094-b7e074add8cd
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (E)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-[3-methoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enamide
SMILES (Canonical) COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC)O
SMILES (Isomeric) COC1=C(C=CC(=C1)CCNC(=O)/C=C/C2=CC(=C(C=C2)O[C@H]3[C@@H]([C@H]([C@H]([C@H](O3)CO)O)O)O)OC)O
InChI InChI=1S/C25H31NO10/c1-33-18-11-15(3-6-16(18)28)9-10-26-21(29)8-5-14-4-7-17(19(12-14)34-2)35-25-24(32)23(31)22(30)20(13-27)36-25/h3-8,11-12,20,22-25,27-28,30-32H,9-10,13H2,1-2H3,(H,26,29)/b8-5+/t20-,22+,23+,24-,25-/m1/s1
InChI Key UYSRWDYTMGBBHP-IWAVKSQDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H31NO10
Molecular Weight 505.50 g/mol
Exact Mass 505.19479619 g/mol
Topological Polar Surface Area (TPSA) 167.00 Ų
XlogP 0.20
Atomic LogP (AlogP) -0.04
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 10

Synonyms

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(E)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-[3-methoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enamide
J3.611.852K

2D Structure

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2D Structure of (E)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-[3-methoxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5753 57.53%
Caco-2 - 0.8555 85.55%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.5421 54.21%
OATP2B1 inhibitior - 0.7107 71.07%
OATP1B1 inhibitior + 0.8664 86.64%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8712 87.12%
P-glycoprotein inhibitior - 0.4383 43.83%
P-glycoprotein substrate + 0.5084 50.84%
CYP3A4 substrate + 0.6450 64.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8437 84.37%
CYP3A4 inhibition - 0.8132 81.32%
CYP2C9 inhibition - 0.8497 84.97%
CYP2C19 inhibition - 0.9083 90.83%
CYP2D6 inhibition - 0.6536 65.36%
CYP1A2 inhibition - 0.8601 86.01%
CYP2C8 inhibition + 0.8775 87.75%
CYP inhibitory promiscuity - 0.8116 81.16%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7144 71.44%
Eye corrosion - 0.9915 99.15%
Eye irritation - 0.9538 95.38%
Skin irritation - 0.7801 78.01%
Skin corrosion - 0.9461 94.61%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6745 67.45%
Micronuclear + 0.6500 65.00%
Hepatotoxicity - 0.8500 85.00%
skin sensitisation - 0.8827 88.27%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.9341 93.41%
Acute Oral Toxicity (c) III 0.7531 75.31%
Estrogen receptor binding + 0.5590 55.90%
Androgen receptor binding + 0.6350 63.50%
Thyroid receptor binding + 0.5803 58.03%
Glucocorticoid receptor binding + 0.6253 62.53%
Aromatase binding - 0.6149 61.49%
PPAR gamma + 0.6230 62.30%
Honey bee toxicity - 0.7845 78.45%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.6968 69.68%

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 99.20% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.67% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.89% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 95.89% 96.00%
CHEMBL2581 P07339 Cathepsin D 95.81% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.99% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.11% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 88.52% 94.73%
CHEMBL1255126 O15151 Protein Mdm4 87.84% 90.20%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.79% 95.50%
CHEMBL4208 P20618 Proteasome component C5 84.87% 90.00%
CHEMBL3194 P02766 Transthyretin 84.41% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.31% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.13% 95.56%
CHEMBL2535 P11166 Glucose transporter 83.12% 98.75%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.52% 94.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.43% 90.71%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 82.22% 89.67%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.57% 96.90%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.16% 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.
Actaea dahurica
Cissampelos pareira
Cyclea barbata

Cross-Links

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PubChem 5318530
NPASS NPC239627