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

Details

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Internal ID 14347dff-d79f-4b17-a125-13927fda20b2
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 3,8-dihydroxy-1,2,5-trimethoxy-6-methylanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H16O7/c1-7-5-9(19)12-13(16(7)23-2)14(21)8-6-10(20)17(24-3)18(25-4)11(8)15(12)22/h5-6,19-20H,1-4H3
InChI Key KIKUHBMDBVOXFZ-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 3.00
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 3,8-Dihydroxy-1,2,5-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 + 0.6800 68.00%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8104 81.04%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9248 92.48%
OATP1B3 inhibitior + 0.7963 79.63%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7872 78.72%
P-glycoprotein inhibitior - 0.7170 71.70%
P-glycoprotein substrate - 0.9456 94.56%
CYP3A4 substrate - 0.5295 52.95%
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 - 0.8208 82.08%
CYP inhibitory promiscuity - 0.7081 70.81%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8895 88.95%
Carcinogenicity (trinary) Non-required 0.5451 54.51%
Eye corrosion - 0.9852 98.52%
Eye irritation + 0.8433 84.33%
Skin irritation - 0.6817 68.17%
Skin corrosion - 0.9632 96.32%
Ames mutagenesis + 0.6756 67.56%
Human Ether-a-go-go-Related Gene inhibition - 0.6468 64.68%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.9215 92.15%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5156 51.56%
Acute Oral Toxicity (c) II 0.5649 56.49%
Estrogen receptor binding + 0.8678 86.78%
Androgen receptor binding - 0.6512 65.12%
Thyroid receptor binding + 0.5266 52.66%
Glucocorticoid receptor binding + 0.7702 77.02%
Aromatase binding + 0.6685 66.85%
PPAR gamma + 0.5271 52.71%
Honey bee toxicity - 0.9049 90.49%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6100 61.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.30% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.52% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.76% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.76% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.63% 99.23%
CHEMBL4208 P20618 Proteasome component C5 86.96% 90.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.55% 93.40%
CHEMBL1951 P21397 Monoamine oxidase A 86.43% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.23% 94.00%
CHEMBL2535 P11166 Glucose transporter 84.22% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.97% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.70% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.13% 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

Cross-Links

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PubChem 101676226
LOTUS LTS0040217
wikiData Q105141576