1,5-Dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dione

Details

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Internal ID e51a67ce-8f68-496f-bfb6-f3fb5121b265
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 1,5-dihydroxy-2,3,8-trimethoxy-6-methylanthracene-9,10-dione
SMILES (Canonical) CC1=CC(=C2C(=C1O)C(=O)C3=CC(=C(C(=C3C2=O)O)OC)OC)OC
SMILES (Isomeric) CC1=CC(=C2C(=C1O)C(=O)C3=CC(=C(C(=C3C2=O)O)OC)OC)OC
InChI InChI=1S/C18H16O7/c1-7-5-9(23-2)12-13(14(7)19)15(20)8-6-10(24-3)18(25-4)17(22)11(8)16(12)21/h5-6,19,22H,1-4H3
InChI Key BPLIUXMVBQOPEU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H16O7
Molecular Weight 344.30 g/mol
Exact Mass 344.08960285 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,5-Dihydroxy-2,3,8-trimethoxy-6-methylanthracene-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 + 0.9863 98.63%
Caco-2 + 0.7214 72.14%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.8104 81.04%
OATP2B1 inhibitior - 0.7150 71.50%
OATP1B1 inhibitior + 0.9238 92.38%
OATP1B3 inhibitior + 0.7963 79.63%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6446 64.46%
P-glycoprotein inhibitior - 0.7458 74.58%
P-glycoprotein substrate - 0.9230 92.30%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7976 79.76%
CYP3A4 inhibition - 0.8430 84.30%
CYP2C9 inhibition - 0.8526 85.26%
CYP2C19 inhibition - 0.8521 85.21%
CYP2D6 inhibition - 0.8259 82.59%
CYP1A2 inhibition + 0.8940 89.40%
CYP2C8 inhibition - 0.5976 59.76%
CYP inhibitory promiscuity - 0.7081 70.81%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8895 88.95%
Carcinogenicity (trinary) Non-required 0.5451 54.51%
Eye corrosion - 0.9852 98.52%
Eye irritation + 0.8163 81.63%
Skin irritation - 0.6817 68.17%
Skin corrosion - 0.9632 96.32%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7607 76.07%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.5305 53.05%
skin sensitisation - 0.9215 92.15%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.5509 55.09%
Acute Oral Toxicity (c) II 0.5649 56.49%
Estrogen receptor binding + 0.8460 84.60%
Androgen receptor binding - 0.6003 60.03%
Thyroid receptor binding + 0.5991 59.91%
Glucocorticoid receptor binding + 0.7837 78.37%
Aromatase binding + 0.6174 61.74%
PPAR gamma + 0.6488 64.88%
Honey bee toxicity - 0.9208 92.08%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9782 97.82%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.91% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.96% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.19% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.43% 94.00%
CHEMBL2581 P07339 Cathepsin D 89.89% 98.95%
CHEMBL2535 P11166 Glucose transporter 87.88% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.77% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.34% 99.15%
CHEMBL4208 P20618 Proteasome component C5 84.72% 90.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.40% 96.21%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.33% 96.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.65% 92.68%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.06% 99.23%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 81.40% 95.70%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.05% 96.67%

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
Echinacea purpurea

Cross-Links

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PubChem 15118839
LOTUS LTS0025668
wikiData Q105264910