3,8-Dihydroxy-6-(hydroxymethyl)-1,2,5-trimethoxyanthracene-9,10-dione

Details

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Internal ID 04ef1d2a-15c2-4398-9a8e-b3de8d0c1737
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 3,8-dihydroxy-6-(hydroxymethyl)-1,2,5-trimethoxyanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O8/c1-24-16-7(6-19)4-9(20)12-13(16)14(22)8-5-10(21)17(25-2)18(26-3)11(8)15(12)23/h4-5,19-21H,6H2,1-3H3
InChI Key RZTYULFUADBMOI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O8
Molecular Weight 360.30 g/mol
Exact Mass 360.08451746 g/mol
Topological Polar Surface Area (TPSA) 123.00 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,8-Dihydroxy-6-(hydroxymethyl)-1,2,5-trimethoxyanthracene-9,10-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9589 95.89%
Caco-2 + 0.6137 61.37%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7772 77.72%
OATP2B1 inhibitior - 0.7115 71.15%
OATP1B1 inhibitior + 0.8649 86.49%
OATP1B3 inhibitior + 0.8046 80.46%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7207 72.07%
P-glycoprotein inhibitior - 0.8131 81.31%
P-glycoprotein substrate - 0.9108 91.08%
CYP3A4 substrate + 0.5061 50.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7944 79.44%
CYP3A4 inhibition - 0.7002 70.02%
CYP2C9 inhibition + 0.5531 55.31%
CYP2C19 inhibition - 0.5240 52.40%
CYP2D6 inhibition - 0.8538 85.38%
CYP1A2 inhibition + 0.8206 82.06%
CYP2C8 inhibition - 0.8212 82.12%
CYP inhibitory promiscuity + 0.5201 52.01%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8863 88.63%
Carcinogenicity (trinary) Non-required 0.6675 66.75%
Eye corrosion - 0.9901 99.01%
Eye irritation + 0.6388 63.88%
Skin irritation - 0.8048 80.48%
Skin corrosion - 0.9672 96.72%
Ames mutagenesis + 0.7346 73.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5753 57.53%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5017 50.17%
skin sensitisation - 0.8570 85.70%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.4778 47.78%
Acute Oral Toxicity (c) III 0.5801 58.01%
Estrogen receptor binding + 0.9174 91.74%
Androgen receptor binding - 0.6100 61.00%
Thyroid receptor binding - 0.5464 54.64%
Glucocorticoid receptor binding + 0.8784 87.84%
Aromatase binding + 0.8182 81.82%
PPAR gamma + 0.6435 64.35%
Honey bee toxicity - 0.8966 89.66%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9548 95.48%

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 98.18% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.81% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.77% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 88.51% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.79% 94.00%
CHEMBL4208 P20618 Proteasome component C5 86.78% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.85% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.44% 99.15%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.61% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.89% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.71% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.54% 85.14%
CHEMBL2535 P11166 Glucose transporter 81.35% 98.75%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.11% 86.92%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.79% 96.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.69% 91.71%

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.
Chamaecrista greggii

Cross-Links

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PubChem 101676232
LOTUS LTS0168200
wikiData Q105248596