Auxarthrol D

Details

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Internal ID 6ef2560f-58ac-4a8b-8ef5-d8b81f686941
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name (1S,2R,3S,4aR,9aS)-1,2,3,8,9a-pentahydroxy-6-methoxy-3-methyl-1,2,4,4a-tetrahydroanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O8/c1-15(22)5-8-11(18)7-3-6(24-2)4-9(17)10(7)12(19)16(8,23)14(21)13(15)20/h3-4,8,13-14,17,20-23H,5H2,1-2H3/t8-,13+,14-,15-,16+/m0/s1
InChI Key FSGPMKCPPHVOJH-VLSJOBMHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H18O8
Molecular Weight 338.31 g/mol
Exact Mass 338.10016753 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP -1.00
Atomic LogP (AlogP) -1.00
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Auxarthrol D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9552 95.52%
Caco-2 - 0.7715 77.15%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5853 58.53%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9040 90.40%
OATP1B3 inhibitior + 0.9632 96.32%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8574 85.74%
P-glycoprotein inhibitior - 0.8960 89.60%
P-glycoprotein substrate - 0.8915 89.15%
CYP3A4 substrate + 0.5831 58.31%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8070 80.70%
CYP3A4 inhibition - 0.6095 60.95%
CYP2C9 inhibition - 0.9242 92.42%
CYP2C19 inhibition - 0.8854 88.54%
CYP2D6 inhibition - 0.8165 81.65%
CYP1A2 inhibition + 0.6886 68.86%
CYP2C8 inhibition - 0.7590 75.90%
CYP inhibitory promiscuity - 0.9489 94.89%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9032 90.32%
Carcinogenicity (trinary) Non-required 0.5455 54.55%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.8513 85.13%
Skin irritation - 0.6477 64.77%
Skin corrosion - 0.8532 85.32%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7579 75.79%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5399 53.99%
skin sensitisation - 0.8116 81.16%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.6268 62.68%
Acute Oral Toxicity (c) III 0.6127 61.27%
Estrogen receptor binding + 0.7628 76.28%
Androgen receptor binding + 0.6293 62.93%
Thyroid receptor binding - 0.5073 50.73%
Glucocorticoid receptor binding + 0.7705 77.05%
Aromatase binding - 0.5389 53.89%
PPAR gamma + 0.6480 64.80%
Honey bee toxicity - 0.9013 90.13%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9295 92.95%

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 98.81% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.31% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.96% 96.09%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 94.05% 92.68%
CHEMBL4208 P20618 Proteasome component C5 92.56% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.39% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.91% 85.14%
CHEMBL2581 P07339 Cathepsin D 91.27% 98.95%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.01% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.64% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.97% 93.99%
CHEMBL1951 P21397 Monoamine oxidase A 86.21% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.83% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.51% 94.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.02% 91.07%
CHEMBL340 P08684 Cytochrome P450 3A4 83.99% 91.19%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.88% 96.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.28% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.88% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 81.26% 94.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.56% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.47% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.11% 94.45%

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 146682981
LOTUS LTS0206831
wikiData Q105000628