Madagascarin

Details

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Internal ID 2135f765-a3cc-4c97-904a-061a50108a98
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 1,3,8-trihydroxy-6-methyl-2-(1,6,8-trihydroxy-3-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione
SMILES (Canonical) CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)O)C4=C(C5=C(C=C4C)C(=O)C6=C(C5=O)C(=CC(=C6)O)O)O)O
SMILES (Isomeric) CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)O)C4=C(C5=C(C=C4C)C(=O)C6=C(C5=O)C(=CC(=C6)O)O)O)O
InChI InChI=1S/C30H18O10/c1-9-3-12-20(16(32)4-9)28(38)23-15(25(12)35)8-18(34)24(30(23)40)19-10(2)5-13-22(27(19)37)29(39)21-14(26(13)36)6-11(31)7-17(21)33/h3-8,31-34,37,40H,1-2H3
InChI Key DKDXVSSXDBKLAU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H18O10
Molecular Weight 538.50 g/mol
Exact Mass 538.08999677 g/mol
Topological Polar Surface Area (TPSA) 190.00 Ų
XlogP 5.10
Atomic LogP (AlogP) 3.75
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 1

Synonyms

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36506-89-5

2D Structure

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2D Structure of Madagascarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 - 0.7756 77.56%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8713 87.13%
OATP2B1 inhibitior + 0.5811 58.11%
OATP1B1 inhibitior + 0.8992 89.92%
OATP1B3 inhibitior - 0.2567 25.67%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.6920 69.20%
P-glycoprotein inhibitior - 0.4588 45.88%
P-glycoprotein substrate - 0.9398 93.98%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8237 82.37%
CYP3A4 inhibition - 0.6127 61.27%
CYP2C9 inhibition + 0.8747 87.47%
CYP2C19 inhibition - 0.5559 55.59%
CYP2D6 inhibition - 0.7736 77.36%
CYP1A2 inhibition + 0.8462 84.62%
CYP2C8 inhibition - 0.7105 71.05%
CYP inhibitory promiscuity + 0.5427 54.27%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8396 83.96%
Carcinogenicity (trinary) Non-required 0.6508 65.08%
Eye corrosion - 0.9936 99.36%
Eye irritation - 0.7322 73.22%
Skin irritation - 0.5199 51.99%
Skin corrosion - 0.8603 86.03%
Ames mutagenesis + 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8233 82.33%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.7305 73.05%
skin sensitisation - 0.8385 83.85%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6936 69.36%
Acute Oral Toxicity (c) III 0.7612 76.12%
Estrogen receptor binding + 0.7683 76.83%
Androgen receptor binding + 0.5639 56.39%
Thyroid receptor binding - 0.5784 57.84%
Glucocorticoid receptor binding + 0.6198 61.98%
Aromatase binding - 0.6408 64.08%
PPAR gamma + 0.6857 68.57%
Honey bee toxicity - 0.9171 91.71%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9911 99.11%

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
CHEMBL1951 P21397 Monoamine oxidase A 96.55% 91.49%
CHEMBL2581 P07339 Cathepsin D 96.50% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.23% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.17% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.84% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.95% 99.23%
CHEMBL4208 P20618 Proteasome component C5 90.53% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.26% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 88.11% 94.73%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.96% 96.12%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.57% 96.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.08% 94.00%
CHEMBL2073 P07947 Tyrosine-protein kinase YES 82.25% 83.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.21% 90.71%

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.
Harungana madagascariensis
Senna siamea

Cross-Links

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PubChem 12312660
LOTUS LTS0195082
wikiData Q104983095