[5-Acetyloxy-6-(4,5-dihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)oxy-4-hydroxy-2-methyloxan-3-yl] acetate

Details

Top
Internal ID 3378ffa0-676e-4450-b26b-5077eec4e687
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name [5-acetyloxy-6-(4,5-dihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)oxy-4-hydroxy-2-methyloxan-3-yl] acetate
SMILES (Canonical) CC1C(C(C(C(O1)OC2=CC3=C(C(=C2)O)C(=O)C4=C(C3=O)C=C(C=C4O)C)OC(=O)C)O)OC(=O)C
SMILES (Isomeric) CC1C(C(C(C(O1)OC2=CC3=C(C(=C2)O)C(=O)C4=C(C3=O)C=C(C=C4O)C)OC(=O)C)O)OC(=O)C
InChI InChI=1S/C25H24O11/c1-9-5-14-18(16(28)6-9)21(31)19-15(20(14)30)7-13(8-17(19)29)36-25-24(35-12(4)27)22(32)23(10(2)33-25)34-11(3)26/h5-8,10,22-25,28-29,32H,1-4H3
InChI Key JSCVXZMYBMRSDK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C25H24O11
Molecular Weight 500.40 g/mol
Exact Mass 500.13186158 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.53
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of [5-Acetyloxy-6-(4,5-dihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)oxy-4-hydroxy-2-methyloxan-3-yl] acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9073 90.73%
Caco-2 - 0.7654 76.54%
Blood Brain Barrier - 0.8750 87.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7342 73.42%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.8964 89.64%
OATP1B3 inhibitior + 0.8421 84.21%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7653 76.53%
P-glycoprotein inhibitior + 0.7251 72.51%
P-glycoprotein substrate - 0.8411 84.11%
CYP3A4 substrate + 0.6147 61.47%
CYP2C9 substrate - 0.8177 81.77%
CYP2D6 substrate - 0.8814 88.14%
CYP3A4 inhibition - 0.9579 95.79%
CYP2C9 inhibition - 0.8971 89.71%
CYP2C19 inhibition - 0.9545 95.45%
CYP2D6 inhibition - 0.9564 95.64%
CYP1A2 inhibition + 0.6649 66.49%
CYP2C8 inhibition - 0.6805 68.05%
CYP inhibitory promiscuity - 0.8076 80.76%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6027 60.27%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.8820 88.20%
Skin irritation - 0.7413 74.13%
Skin corrosion - 0.9726 97.26%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4453 44.53%
Micronuclear + 0.8800 88.00%
Hepatotoxicity - 0.5072 50.72%
skin sensitisation - 0.9378 93.78%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.6492 64.92%
Acute Oral Toxicity (c) III 0.4710 47.10%
Estrogen receptor binding + 0.7840 78.40%
Androgen receptor binding - 0.4890 48.90%
Thyroid receptor binding - 0.5441 54.41%
Glucocorticoid receptor binding + 0.7559 75.59%
Aromatase binding - 0.5079 50.79%
PPAR gamma + 0.6173 61.73%
Honey bee toxicity - 0.7756 77.56%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5250 52.50%
Fish aquatic toxicity + 0.9734 97.34%

Targets

Top

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
CHEMBL1951 P21397 Monoamine oxidase A 99.02% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.10% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.04% 89.00%
CHEMBL2581 P07339 Cathepsin D 96.60% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.96% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.85% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 91.95% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.68% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.29% 96.09%
CHEMBL4208 P20618 Proteasome component C5 91.18% 90.00%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 90.35% 95.64%
CHEMBL340 P08684 Cytochrome P450 3A4 89.63% 91.19%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.13% 99.15%
CHEMBL3714130 P46095 G-protein coupled receptor 6 88.87% 97.36%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.80% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.95% 94.80%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.34% 96.21%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.78% 81.11%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.64% 97.21%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.88% 95.89%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 81.43% 85.00%
CHEMBL226 P30542 Adenosine A1 receptor 81.22% 95.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.13% 99.17%

Plants that contains it

Top
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.
Rhamnus prinoides

Cross-Links

Top
PubChem 56677946
LOTUS LTS0055214
wikiData Q105134277