Munjistin 1-methyl ether

Details

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Internal ID bd73a642-82d1-4aaa-8dc1-2400a0ae9ea4
Taxonomy Benzenoids > Anthracenes > Anthracenecarboxylic acids and derivatives > Anthracenecarboxylic acids
IUPAC Name 3-hydroxy-1-methoxy-9,10-dioxoanthracene-2-carboxylic acid
SMILES (Canonical) COC1=C2C(=CC(=C1C(=O)O)O)C(=O)C3=CC=CC=C3C2=O
SMILES (Isomeric) COC1=C2C(=CC(=C1C(=O)O)O)C(=O)C3=CC=CC=C3C2=O
InChI InChI=1S/C16H10O6/c1-22-15-11-9(6-10(17)12(15)16(20)21)13(18)7-4-2-3-5-8(7)14(11)19/h2-6,17H,1H3,(H,20,21)
InChI Key HOWXBCDFXNIUJX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H10O6
Molecular Weight 298.25 g/mol
Exact Mass 298.04773803 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Munjistin 1-methyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9734 97.34%
Caco-2 - 0.5971 59.71%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.8009 80.09%
OATP2B1 inhibitior - 0.7132 71.32%
OATP1B1 inhibitior + 0.9313 93.13%
OATP1B3 inhibitior + 0.9199 91.99%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8175 81.75%
P-glycoprotein inhibitior - 0.8428 84.28%
P-glycoprotein substrate - 0.9597 95.97%
CYP3A4 substrate - 0.5927 59.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8695 86.95%
CYP3A4 inhibition - 0.8576 85.76%
CYP2C9 inhibition + 0.5974 59.74%
CYP2C19 inhibition - 0.8924 89.24%
CYP2D6 inhibition - 0.8965 89.65%
CYP1A2 inhibition + 0.5765 57.65%
CYP2C8 inhibition - 0.7844 78.44%
CYP inhibitory promiscuity - 0.7368 73.68%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8323 83.23%
Carcinogenicity (trinary) Non-required 0.6107 61.07%
Eye corrosion - 0.9899 98.99%
Eye irritation + 0.9058 90.58%
Skin irritation - 0.5551 55.51%
Skin corrosion - 0.9131 91.31%
Ames mutagenesis - 0.5214 52.14%
Human Ether-a-go-go-Related Gene inhibition - 0.8207 82.07%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.9420 94.20%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.6063 60.63%
Acute Oral Toxicity (c) II 0.5647 56.47%
Estrogen receptor binding + 0.7801 78.01%
Androgen receptor binding + 0.6099 60.99%
Thyroid receptor binding - 0.6180 61.80%
Glucocorticoid receptor binding + 0.6197 61.97%
Aromatase binding - 0.5158 51.58%
PPAR gamma + 0.6457 64.57%
Honey bee toxicity - 0.9075 90.75%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9847 98.47%

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
CHEMBL2581 P07339 Cathepsin D 97.38% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.28% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.23% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.40% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.20% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.10% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.51% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.60% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.72% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 83.39% 91.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.31% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 82.25% 90.20%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.93% 93.56%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.27% 96.67%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.83% 95.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.41% 99.17%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.06% 94.08%

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.
Rhynchotechum vestitum
Rubia wallichiana

Cross-Links

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PubChem 101939212
NPASS NPC108234
LOTUS LTS0115891
wikiData Q105031566