1-Hydroxy-3-methyl-6-methoxy-8-(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyloxy)-9,10-anthraquinone

Details

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Internal ID 13df4e9b-36e2-4b05-b13a-294b3763eb6a
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 1-hydroxy-6-methoxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione
SMILES (Canonical) CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC
SMILES (Isomeric) CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO[C@H]5[C@@H]([C@H]([C@@H](CO5)O)O)O)O)O)O)OC
InChI InChI=1S/C27H30O14/c1-9-3-11-17(13(28)4-9)22(33)18-12(19(11)30)5-10(37-2)6-15(18)40-27-25(36)23(34)21(32)16(41-27)8-39-26-24(35)20(31)14(29)7-38-26/h3-6,14,16,20-21,23-29,31-32,34-36H,7-8H2,1-2H3/t14-,16-,20+,21-,23+,24-,25-,26+,27-/m1/s1
InChI Key AQAWTXYLEGFATL-FTBGQRARSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H30O14
Molecular Weight 578.50 g/mol
Exact Mass 578.16355563 g/mol
Topological Polar Surface Area (TPSA) 222.00 Ų
XlogP -0.80
Atomic LogP (AlogP) -1.87
H-Bond Acceptor 14
H-Bond Donor 7
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Hydroxy-3-methyl-6-methoxy-8-(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyloxy)-9,10-anthraquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6230 62.30%
Caco-2 - 0.8807 88.07%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.5173 51.73%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.8892 88.92%
OATP1B3 inhibitior + 0.9610 96.10%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.4792 47.92%
P-glycoprotein inhibitior - 0.5940 59.40%
P-glycoprotein substrate - 0.7050 70.50%
CYP3A4 substrate + 0.6473 64.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8452 84.52%
CYP3A4 inhibition - 0.9141 91.41%
CYP2C9 inhibition - 0.9389 93.89%
CYP2C19 inhibition - 0.9255 92.55%
CYP2D6 inhibition - 0.9223 92.23%
CYP1A2 inhibition - 0.8624 86.24%
CYP2C8 inhibition - 0.6239 62.39%
CYP inhibitory promiscuity - 0.9512 95.12%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7126 71.26%
Eye corrosion - 0.9906 99.06%
Eye irritation - 0.9249 92.49%
Skin irritation - 0.8566 85.66%
Skin corrosion - 0.9596 95.96%
Ames mutagenesis + 0.7372 73.72%
Human Ether-a-go-go-Related Gene inhibition + 0.6502 65.02%
Micronuclear + 0.5474 54.74%
Hepatotoxicity - 0.6587 65.87%
skin sensitisation - 0.8966 89.66%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6915 69.15%
Acute Oral Toxicity (c) III 0.7034 70.34%
Estrogen receptor binding + 0.8448 84.48%
Androgen receptor binding - 0.5300 53.00%
Thyroid receptor binding - 0.5156 51.56%
Glucocorticoid receptor binding + 0.5416 54.16%
Aromatase binding + 0.6103 61.03%
PPAR gamma + 0.7326 73.26%
Honey bee toxicity - 0.8101 81.01%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.8630 86.30%

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 98.96% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.76% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 96.22% 95.93%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.04% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.77% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.95% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.71% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.87% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.23% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 90.95% 94.73%
CHEMBL4208 P20618 Proteasome component C5 90.86% 90.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.65% 96.77%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.37% 99.15%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.93% 96.21%
CHEMBL4581 P52732 Kinesin-like protein 1 86.06% 93.18%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.39% 86.92%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.38% 97.36%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.13% 95.89%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 84.13% 96.90%
CHEMBL1951 P21397 Monoamine oxidase A 83.30% 91.49%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.04% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.88% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.75% 91.07%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.52% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.66% 96.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.54% 97.14%

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.
Cirsium oligophyllum
Dalbergia hupeana
Rhamnus pallasii

Cross-Links

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PubChem 101870821
NPASS NPC260225
LOTUS LTS0125988
wikiData Q104916690