1-[1-Hydroxy-6-methoxy-3-methyl-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxynaphthalen-2-yl]ethanone

Details

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Internal ID ddf77d35-0bfd-4532-bf16-cbbc935d5774
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name 1-[1-hydroxy-6-methoxy-3-methyl-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxynaphthalen-2-yl]ethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H32O13/c1-9-4-11-5-12(34-3)6-14(17(11)20(30)16(9)10(2)26)37-25-23(33)21(31)19(29)15(38-25)8-36-24-22(32)18(28)13(27)7-35-24/h4-6,13,15,18-19,21-25,27-33H,7-8H2,1-3H3
InChI Key CAMBBKOLUMTIMN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H32O13
Molecular Weight 540.50 g/mol
Exact Mass 540.18429107 g/mol
Topological Polar Surface Area (TPSA) 205.00 Ų
XlogP -0.90
Atomic LogP (AlogP) -1.29
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-[1-Hydroxy-6-methoxy-3-methyl-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxynaphthalen-2-yl]ethanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5187 51.87%
Caco-2 - 0.8395 83.95%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.5499 54.99%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.8524 85.24%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6549 65.49%
P-glycoprotein inhibitior - 0.6582 65.82%
P-glycoprotein substrate - 0.5738 57.38%
CYP3A4 substrate + 0.6464 64.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8543 85.43%
CYP3A4 inhibition - 0.9524 95.24%
CYP2C9 inhibition - 0.9638 96.38%
CYP2C19 inhibition - 0.9380 93.80%
CYP2D6 inhibition - 0.9114 91.14%
CYP1A2 inhibition - 0.8567 85.67%
CYP2C8 inhibition + 0.5340 53.40%
CYP inhibitory promiscuity - 0.9232 92.32%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6946 69.46%
Eye corrosion - 0.9908 99.08%
Eye irritation - 0.9362 93.62%
Skin irritation - 0.8471 84.71%
Skin corrosion - 0.9654 96.54%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7586 75.86%
Micronuclear + 0.5474 54.74%
Hepatotoxicity - 0.7569 75.69%
skin sensitisation - 0.9045 90.45%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.9280 92.80%
Acute Oral Toxicity (c) III 0.7104 71.04%
Estrogen receptor binding + 0.8186 81.86%
Androgen receptor binding - 0.5763 57.63%
Thyroid receptor binding - 0.4875 48.75%
Glucocorticoid receptor binding - 0.5169 51.69%
Aromatase binding + 0.6619 66.19%
PPAR gamma + 0.6936 69.36%
Honey bee toxicity - 0.8361 83.61%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8158 81.58%

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 99.50% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.39% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.06% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.37% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.16% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 91.91% 94.73%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.37% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.72% 86.33%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.71% 97.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.74% 89.00%
CHEMBL4208 P20618 Proteasome component C5 86.69% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.07% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.48% 96.95%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.11% 95.50%
CHEMBL4581 P52732 Kinesin-like protein 1 84.03% 93.18%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.88% 95.56%
CHEMBL3714130 P46095 G-protein coupled receptor 6 82.79% 97.36%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.63% 89.62%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.02% 95.89%
CHEMBL220 P22303 Acetylcholinesterase 81.42% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.99% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.58% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 162888761
LOTUS LTS0186440
wikiData Q104951485