5,6,7,9-tetrahydroxy-2-methoxy-7-methyl-6,8-dihydro-5H-anthracene-1,4-dione

Details

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Internal ID 25e27dde-3b5e-4d3d-891f-2bb7c1a5330e
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 5,6,7,9-tetrahydroxy-2-methoxy-7-methyl-6,8-dihydro-5H-anthracene-1,4-dione
SMILES (Canonical) CC1(CC2=C(C3=C(C=C2C(C1O)O)C(=O)C=C(C3=O)OC)O)O
SMILES (Isomeric) CC1(CC2=C(C3=C(C=C2C(C1O)O)C(=O)C=C(C3=O)OC)O)O
InChI InChI=1S/C16H16O7/c1-16(22)5-8-6(13(19)15(16)21)3-7-9(17)4-10(23-2)14(20)11(7)12(8)18/h3-4,13,15,18-19,21-22H,5H2,1-2H3
InChI Key NRHMPEJAWNKHLC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O7
Molecular Weight 320.29 g/mol
Exact Mass 320.08960285 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.00
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,6,7,9-tetrahydroxy-2-methoxy-7-methyl-6,8-dihydro-5H-anthracene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9772 97.72%
Caco-2 - 0.7537 75.37%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5615 56.15%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.8843 88.43%
OATP1B3 inhibitior + 0.9656 96.56%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9338 93.38%
BSEP inhibitior - 0.6922 69.22%
P-glycoprotein inhibitior - 0.9104 91.04%
P-glycoprotein substrate - 0.7562 75.62%
CYP3A4 substrate + 0.6302 63.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8448 84.48%
CYP3A4 inhibition - 0.5704 57.04%
CYP2C9 inhibition - 0.7997 79.97%
CYP2C19 inhibition - 0.7639 76.39%
CYP2D6 inhibition - 0.7878 78.78%
CYP1A2 inhibition + 0.6513 65.13%
CYP2C8 inhibition - 0.6419 64.19%
CYP inhibitory promiscuity - 0.8520 85.20%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9175 91.75%
Carcinogenicity (trinary) Non-required 0.5473 54.73%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.7521 75.21%
Skin irritation - 0.6633 66.33%
Skin corrosion - 0.8828 88.28%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7752 77.52%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.5408 54.08%
skin sensitisation - 0.7209 72.09%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5955 59.55%
Acute Oral Toxicity (c) III 0.4668 46.68%
Estrogen receptor binding + 0.7766 77.66%
Androgen receptor binding - 0.5438 54.38%
Thyroid receptor binding - 0.7185 71.85%
Glucocorticoid receptor binding + 0.7591 75.91%
Aromatase binding + 0.5626 56.26%
PPAR gamma + 0.7381 73.81%
Honey bee toxicity - 0.8256 82.56%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9767 97.67%

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 99.38% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.66% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.56% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.56% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.16% 95.56%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 90.96% 92.68%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.43% 89.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.74% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.68% 97.25%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 88.41% 96.38%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.87% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.86% 86.33%
CHEMBL2535 P11166 Glucose transporter 87.55% 98.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.47% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 87.36% 92.94%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.85% 93.40%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.88% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.68% 94.45%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.30% 91.07%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.49% 96.67%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.05% 97.09%
CHEMBL1871 P10275 Androgen Receptor 80.18% 96.43%

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.
Taiwania cryptomerioides

Cross-Links

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PubChem 72501110
LOTUS LTS0067505
wikiData Q105365938