(2R,3R,4S,5S,6R)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3,6,8-trimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 51fb0387-d2ea-4185-8026-2f24f66312c4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2R,3R,4S,5S,6R)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3,6,8-trimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) COC1CC2=CC(=C(C(=C2C(C1COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)O)OC)OC)O)OC
SMILES (Isomeric) CO[C@H]1CC2=CC(=C(C(=C2[C@H]([C@H]1CO[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C4=CC(=C(C(=C4)OC)O)OC)OC)O)OC
InChI InChI=1S/C28H38O13/c1-35-15-6-13-9-18(38-4)24(32)27(39-5)21(13)20(12-7-16(36-2)22(30)17(8-12)37-3)14(15)11-40-28-26(34)25(33)23(31)19(10-29)41-28/h7-9,14-15,19-20,23,25-26,28-34H,6,10-11H2,1-5H3/t14-,15-,19+,20-,23+,25-,26+,28+/m0/s1
InChI Key QWTCAACIKHUTQX-NQIAMKCKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H38O13
Molecular Weight 582.60 g/mol
Exact Mass 582.23124126 g/mol
Topological Polar Surface Area (TPSA) 186.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.27
H-Bond Acceptor 13
H-Bond Donor 6
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,4S,5S,6R)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3,6,8-trimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5520 55.20%
Caco-2 - 0.8199 81.99%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5704 57.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8310 83.10%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6741 67.41%
P-glycoprotein inhibitior - 0.4925 49.25%
P-glycoprotein substrate - 0.6297 62.97%
CYP3A4 substrate + 0.6205 62.05%
CYP2C9 substrate - 0.8016 80.16%
CYP2D6 substrate - 0.7634 76.34%
CYP3A4 inhibition - 0.9159 91.59%
CYP2C9 inhibition - 0.8907 89.07%
CYP2C19 inhibition - 0.8360 83.60%
CYP2D6 inhibition - 0.9303 93.03%
CYP1A2 inhibition - 0.7697 76.97%
CYP2C8 inhibition + 0.5534 55.34%
CYP inhibitory promiscuity - 0.7215 72.15%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6864 68.64%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.9242 92.42%
Skin irritation - 0.8351 83.51%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.6454 64.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7295 72.95%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.9179 91.79%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.9039 90.39%
Acute Oral Toxicity (c) III 0.6543 65.43%
Estrogen receptor binding + 0.7880 78.80%
Androgen receptor binding + 0.6621 66.21%
Thyroid receptor binding + 0.5737 57.37%
Glucocorticoid receptor binding + 0.6280 62.80%
Aromatase binding + 0.5555 55.55%
PPAR gamma + 0.6302 63.02%
Honey bee toxicity - 0.7950 79.50%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9127 91.27%

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 99.47% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.85% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.22% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.75% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 91.08% 92.94%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 89.57% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.68% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.98% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.42% 86.33%
CHEMBL2581 P07339 Cathepsin D 86.18% 98.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.47% 89.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.45% 96.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.73% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.43% 92.62%
CHEMBL3401 O75469 Pregnane X receptor 83.86% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.94% 89.00%
CHEMBL249 P25103 Neurokinin 1 receptor 80.67% 99.17%

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.
Carissa carandas

Cross-Links

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PubChem 162853185
LOTUS LTS0240786
wikiData Q105229384