6,8-dihydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-naphthalen-1-one

Details

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Internal ID ec673d56-e79c-4f8d-9418-40206b66bd13
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 6,8-dihydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-naphthalen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O9/c1-31-13-4-2-10(3-5-13)11-6-12-8-15(26)18(20(28)17(12)14(25)7-11)23-22(30)21(29)19(27)16(9-24)32-23/h2-5,7-8,16,19,21-24,26-30H,6,9H2,1H3/t16-,19-,21+,22-,23+/m1/s1
InChI Key UMZFQCHAQFPSIV-QJLVSEQISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O9
Molecular Weight 444.40 g/mol
Exact Mass 444.14203234 g/mol
Topological Polar Surface Area (TPSA) 157.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.44
H-Bond Acceptor 9
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,8-dihydroxy-3-(4-methoxyphenyl)-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-naphthalen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8587 85.87%
Caco-2 - 0.8775 87.75%
Blood Brain Barrier - 0.6879 68.79%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.5939 59.39%
OATP2B1 inhibitior - 0.5554 55.54%
OATP1B1 inhibitior + 0.8072 80.72%
OATP1B3 inhibitior + 0.9798 97.98%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.4833 48.33%
P-glycoprotein inhibitior - 0.6416 64.16%
P-glycoprotein substrate - 0.8156 81.56%
CYP3A4 substrate + 0.6521 65.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8222 82.22%
CYP3A4 inhibition - 0.7866 78.66%
CYP2C9 inhibition - 0.6325 63.25%
CYP2C19 inhibition - 0.5542 55.42%
CYP2D6 inhibition - 0.8443 84.43%
CYP1A2 inhibition + 0.5510 55.10%
CYP2C8 inhibition + 0.6050 60.50%
CYP inhibitory promiscuity + 0.7307 73.07%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7347 73.47%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.8693 86.93%
Skin irritation - 0.7987 79.87%
Skin corrosion - 0.9482 94.82%
Ames mutagenesis + 0.5599 55.99%
Human Ether-a-go-go-Related Gene inhibition - 0.3784 37.84%
Micronuclear + 0.6359 63.59%
Hepatotoxicity - 0.5948 59.48%
skin sensitisation - 0.8552 85.52%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8738 87.38%
Acute Oral Toxicity (c) III 0.5391 53.91%
Estrogen receptor binding + 0.8114 81.14%
Androgen receptor binding + 0.6600 66.00%
Thyroid receptor binding + 0.5204 52.04%
Glucocorticoid receptor binding + 0.6226 62.26%
Aromatase binding + 0.5935 59.35%
PPAR gamma + 0.7721 77.21%
Honey bee toxicity - 0.8444 84.44%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.8596 85.96%

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 99.78% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.64% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.60% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 93.99% 95.93%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.71% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.31% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.98% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.69% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.16% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.16% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.12% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.17% 95.89%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.57% 85.14%
CHEMBL4208 P20618 Proteasome component C5 89.06% 90.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.55% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.87% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 87.57% 86.92%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.60% 92.62%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.96% 96.21%
CHEMBL3820 P35557 Hexokinase type IV 82.60% 91.96%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.02% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 81.55% 94.73%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.93% 92.67%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.57% 95.89%

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.
Eutrema salsugineum

Cross-Links

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PubChem 162923908
LOTUS LTS0225320
wikiData Q105275841