Madeirin

Details

Top
Internal ID ac4561c9-c151-419e-893e-fb31483f6fb5
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 1-hydroxy-4-methoxy-2-methylanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H12O4/c1-8-7-11(20-2)12-13(14(8)17)16(19)10-6-4-3-5-9(10)15(12)18/h3-7,17H,1-2H3
InChI Key ZCYWBTZIWLDHTK-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H12O4
Molecular Weight 268.26 g/mol
Exact Mass 268.07355886 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 3.40
Atomic LogP (AlogP) 2.48
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
SCHEMBL19341713

2D Structure

Top
2D Structure of Madeirin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.7388 73.88%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.8538 85.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9303 93.03%
OATP1B3 inhibitior + 0.9805 98.05%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.7394 73.94%
P-glycoprotein substrate - 0.9430 94.30%
CYP3A4 substrate - 0.5388 53.88%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7976 79.76%
CYP3A4 inhibition - 0.7839 78.39%
CYP2C9 inhibition - 0.7287 72.87%
CYP2C19 inhibition - 0.7525 75.25%
CYP2D6 inhibition - 0.8490 84.90%
CYP1A2 inhibition + 0.9504 95.04%
CYP2C8 inhibition - 0.7592 75.92%
CYP inhibitory promiscuity - 0.6782 67.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7929 79.29%
Carcinogenicity (trinary) Non-required 0.5626 56.26%
Eye corrosion - 0.9837 98.37%
Eye irritation + 0.9456 94.56%
Skin irritation - 0.6144 61.44%
Skin corrosion - 0.9770 97.70%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7624 76.24%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.9513 95.13%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5389 53.89%
Acute Oral Toxicity (c) II 0.7324 73.24%
Estrogen receptor binding + 0.8410 84.10%
Androgen receptor binding + 0.7329 73.29%
Thyroid receptor binding + 0.5634 56.34%
Glucocorticoid receptor binding + 0.9007 90.07%
Aromatase binding + 0.7308 73.08%
PPAR gamma + 0.7846 78.46%
Honey bee toxicity - 0.9070 90.70%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9825 98.25%

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
CHEMBL2581 P07339 Cathepsin D 97.50% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.24% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.71% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.70% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.43% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.44% 89.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.16% 96.67%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.64% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 84.72% 94.73%
CHEMBL1907 P15144 Aminopeptidase N 84.32% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.91% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.57% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.87% 99.23%
CHEMBL4208 P20618 Proteasome component C5 82.60% 90.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.33% 93.03%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 81.49% 98.21%

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.
There are no matching plants.

Cross-Links

Top
PubChem 12631819
LOTUS LTS0015431
wikiData Q105371867