Methyl Aristolate

Details

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Internal ID 5977b295-875a-4341-b0fe-d3203cf75a85
Taxonomy Benzenoids > Phenanthrenes and derivatives
IUPAC Name methyl 8-methoxynaphtho[2,1-g][1,3]benzodioxole-5-carboxylate
SMILES (Canonical) COC1=CC=CC2=C1C=CC3=C2C4=C(C=C3C(=O)OC)OCO4
SMILES (Isomeric) COC1=CC=CC2=C1C=CC3=C2C4=C(C=C3C(=O)OC)OCO4
InChI InChI=1S/C18H14O5/c1-20-14-5-3-4-11-10(14)6-7-12-13(18(19)21-2)8-15-17(16(11)12)23-9-22-15/h3-8H,9H2,1-2H3
InChI Key LBBQPQFZUZOHTO-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O5
Molecular Weight 310.30 g/mol
Exact Mass 310.08412354 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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Aristolic acid methyl ester
35142-06-4
CCRIS 2994
DYZ33R9ED7
8-Methoxyphenanthro(3,4-d)-1,3-dioxole-5-carboxylic acid methyl ester
8-Methoxyphenanthro(3,4-d)-1,3-dioxole-5-carboxylic acid, methyl ester
Phenanthro(3,4-d)-1,3-dioxole-5-carboxylic acid, 8-methoxy-, methyl ester
UNII-DYZ33R9ED7
CHEMBL520680
DTXSID00188635
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methyl Aristolate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.9418 94.18%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7161 71.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9567 95.67%
OATP1B3 inhibitior + 0.8996 89.96%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.8163 81.63%
P-glycoprotein inhibitior - 0.4636 46.36%
P-glycoprotein substrate - 0.7569 75.69%
CYP3A4 substrate + 0.5843 58.43%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8009 80.09%
CYP3A4 inhibition + 0.9142 91.42%
CYP2C9 inhibition + 0.9441 94.41%
CYP2C19 inhibition + 0.9517 95.17%
CYP2D6 inhibition + 0.8759 87.59%
CYP1A2 inhibition + 0.8689 86.89%
CYP2C8 inhibition + 0.5227 52.27%
CYP inhibitory promiscuity + 0.9210 92.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Warning 0.4504 45.04%
Eye corrosion - 0.9641 96.41%
Eye irritation + 0.5914 59.14%
Skin irritation - 0.7465 74.65%
Skin corrosion - 0.9765 97.65%
Ames mutagenesis + 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4003 40.03%
Micronuclear + 0.7474 74.74%
Hepatotoxicity + 0.5065 50.65%
skin sensitisation - 0.5753 57.53%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.6991 69.91%
Acute Oral Toxicity (c) III 0.6486 64.86%
Estrogen receptor binding + 0.9224 92.24%
Androgen receptor binding + 0.6951 69.51%
Thyroid receptor binding + 0.6234 62.34%
Glucocorticoid receptor binding + 0.9021 90.21%
Aromatase binding + 0.7273 72.73%
PPAR gamma + 0.8058 80.58%
Honey bee toxicity - 0.8709 87.09%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9466 94.66%

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 98.69% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.00% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 95.99% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.42% 96.09%
CHEMBL2535 P11166 Glucose transporter 93.89% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.81% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.73% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.16% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.84% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.62% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.44% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.02% 89.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.02% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.54% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.52% 94.73%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.50% 97.14%
CHEMBL340 P08684 Cytochrome P450 3A4 81.05% 91.19%
CHEMBL5028 O14672 ADAM10 80.33% 97.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.18% 99.17%

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.
Aristolochia cucurbitifolia
Aristolochia indica
Aristolochia kaempferi
Aristolochia manshuriensis

Cross-Links

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PubChem 160246
NPASS NPC118332
LOTUS LTS0132864
wikiData Q83060447