(2R,3R,4R,5R,6S)-2-[[(1S,2S,3R)-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-methyloxane-3,4,5-triol

Details

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Internal ID 6e104844-d265-4844-a0e7-6ad54dc3f8c4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2R,3R,4R,5R,6S)-2-[[(1S,2S,3R)-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-methyloxane-3,4,5-triol
SMILES (Canonical) CC1C(C(C(C(O1)OCC2C(CC3=CC(=C(C=C3C2C4=CC(=C(C=C4)O)OC)O)OC)OC)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@H]2[C@@H](CC3=CC(=C(C=C3[C@@H]2C4=CC(=C(C=C4)O)OC)O)OC)OC)O)O)O
InChI InChI=1S/C26H34O10/c1-12-23(29)24(30)25(31)26(36-12)35-11-16-19(32-2)8-14-9-21(34-4)18(28)10-15(14)22(16)13-5-6-17(27)20(7-13)33-3/h5-7,9-10,12,16,19,22-31H,8,11H2,1-4H3/t12-,16-,19+,22-,23-,24+,25+,26+/m0/s1
InChI Key AVAZTTIAQSFWRK-JKPLZBKSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H34O10
Molecular Weight 506.50 g/mol
Exact Mass 506.21519728 g/mol
Topological Polar Surface Area (TPSA) 147.00 Ų
XlogP 1.30
Atomic LogP (AlogP) 1.28
H-Bond Acceptor 10
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 (2R,3R,4R,5R,6S)-2-[[(1S,2S,3R)-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]-6-methyloxane-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 + 0.6200 62.00%
Caco-2 - 0.7576 75.76%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6490 64.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8992 89.92%
OATP1B3 inhibitior + 0.8863 88.63%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5722 57.22%
P-glycoprotein inhibitior - 0.5623 56.23%
P-glycoprotein substrate - 0.5110 51.10%
CYP3A4 substrate + 0.6308 63.08%
CYP2C9 substrate - 0.7948 79.48%
CYP2D6 substrate - 0.7642 76.42%
CYP3A4 inhibition - 0.8510 85.10%
CYP2C9 inhibition - 0.8449 84.49%
CYP2C19 inhibition - 0.8195 81.95%
CYP2D6 inhibition - 0.8707 87.07%
CYP1A2 inhibition - 0.6885 68.85%
CYP2C8 inhibition + 0.6745 67.45%
CYP inhibitory promiscuity - 0.5239 52.39%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6894 68.94%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9378 93.78%
Skin irritation - 0.8271 82.71%
Skin corrosion - 0.9581 95.81%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6987 69.87%
Micronuclear + 0.5159 51.59%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.9100 91.00%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.8647 86.47%
Acute Oral Toxicity (c) III 0.6400 64.00%
Estrogen receptor binding + 0.7477 74.77%
Androgen receptor binding + 0.5459 54.59%
Thyroid receptor binding + 0.6694 66.94%
Glucocorticoid receptor binding + 0.6464 64.64%
Aromatase binding + 0.5243 52.43%
PPAR gamma + 0.5892 58.92%
Honey bee toxicity - 0.8363 83.63%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9553 95.53%

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 99.70% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.03% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.51% 85.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.25% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.08% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.99% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.40% 98.95%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 91.13% 89.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.35% 95.89%
CHEMBL3714130 P46095 G-protein coupled receptor 6 89.32% 97.36%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.45% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.36% 99.17%
CHEMBL4208 P20618 Proteasome component C5 86.24% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.88% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.39% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 84.13% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 83.42% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.97% 92.62%
CHEMBL2535 P11166 Glucose transporter 81.47% 98.75%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 81.38% 82.67%

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.
Chaenomeles sinensis
Mallotus peltatus
Scurrula atropurpurea

Cross-Links

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PubChem 157239638
LOTUS LTS0005713
wikiData Q104919288