6,8-dihydroxy-3-(4-hydroxyphenyl)-5-[3-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4H-naphthalen-1-one

Details

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Internal ID e112c51a-5193-49b4-a529-81cbd14b2b4c
Taxonomy Benzenoids > Naphthalenes > Phenylnaphthalenes
IUPAC Name 6,8-dihydroxy-3-(4-hydroxyphenyl)-5-[3-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4H-naphthalen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H42O15/c1-13-23(38)26(41)28(43)31(45-13)47-30-17(14-4-6-15(35)7-5-14)10-18-16(19(36)11-20(37)22(18)25(30)40)8-9-33(2,3)48-32-29(44)27(42)24(39)21(12-34)46-32/h4-7,11,13,21,23-24,26-29,31-32,34-39,41-44H,8-10,12H2,1-3H3/t13-,21+,23-,24+,26+,27-,28+,29+,31-,32-/m0/s1
InChI Key HUUIECVKUUJRGR-JDBHOZPRSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H42O15
Molecular Weight 678.70 g/mol
Exact Mass 678.25237063 g/mol
Topological Polar Surface Area (TPSA) 256.00 Ų
XlogP 0.40
Atomic LogP (AlogP) -0.67
H-Bond Acceptor 15
H-Bond Donor 10
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,8-dihydroxy-3-(4-hydroxyphenyl)-5-[3-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-2-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-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 + 0.8939 89.39%
Caco-2 - 0.8880 88.80%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.8491 84.91%
OATP2B1 inhibitior - 0.7227 72.27%
OATP1B1 inhibitior + 0.8671 86.71%
OATP1B3 inhibitior + 0.7920 79.20%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7276 72.76%
BSEP inhibitior + 0.7875 78.75%
P-glycoprotein inhibitior + 0.6462 64.62%
P-glycoprotein substrate - 0.5232 52.32%
CYP3A4 substrate + 0.6650 66.50%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8549 85.49%
CYP3A4 inhibition - 0.9186 91.86%
CYP2C9 inhibition - 0.7677 76.77%
CYP2C19 inhibition - 0.7272 72.72%
CYP2D6 inhibition - 0.8902 89.02%
CYP1A2 inhibition - 0.6373 63.73%
CYP2C8 inhibition + 0.7722 77.22%
CYP inhibitory promiscuity - 0.7361 73.61%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7036 70.36%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9135 91.35%
Skin irritation - 0.7615 76.15%
Skin corrosion - 0.9494 94.94%
Ames mutagenesis + 0.5663 56.63%
Human Ether-a-go-go-Related Gene inhibition + 0.7434 74.34%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.6843 68.43%
skin sensitisation - 0.8962 89.62%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.8644 86.44%
Acute Oral Toxicity (c) III 0.4061 40.61%
Estrogen receptor binding + 0.8311 83.11%
Androgen receptor binding + 0.6514 65.14%
Thyroid receptor binding + 0.5434 54.34%
Glucocorticoid receptor binding + 0.6879 68.79%
Aromatase binding + 0.6465 64.65%
PPAR gamma + 0.7284 72.84%
Honey bee toxicity - 0.7123 71.23%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9965 99.65%

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 99.58% 91.11%
CHEMBL2581 P07339 Cathepsin D 99.32% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.82% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.19% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 94.16% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.03% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.67% 96.09%
CHEMBL1951 P21397 Monoamine oxidase A 91.40% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.33% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.81% 94.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.44% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.34% 95.89%
CHEMBL3714130 P46095 G-protein coupled receptor 6 87.85% 97.36%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.49% 99.17%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 86.58% 95.53%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.30% 99.15%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.57% 92.94%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.50% 97.14%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.43% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.22% 94.45%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.21% 95.78%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 81.13% 92.68%

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.
Epimedium brevicornu
Gelsemium elegans

Cross-Links

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PubChem 5316595
NPASS NPC273125