Aristolochic acid E

Details

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Internal ID c9fd1891-b531-446d-8f87-71470d717aad
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name 8-hydroxy-9-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
SMILES (Canonical) COC1=C(C2=CC(=C3C(=CC4=C(C3=C2C=C1)OCO4)C(=O)O)[N+](=O)[O-])O
SMILES (Isomeric) COC1=C(C2=CC(=C3C(=CC4=C(C3=C2C=C1)OCO4)C(=O)O)[N+](=O)[O-])O
InChI InChI=1S/C17H11NO8/c1-24-11-3-2-7-8(15(11)19)4-10(18(22)23)13-9(17(20)21)5-12-16(14(7)13)26-6-25-12/h2-5,19H,6H2,1H3,(H,20,21)
InChI Key ZRCMNWRTDNPVFL-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H11NO8
Molecular Weight 357.30 g/mol
Exact Mass 357.04846631 g/mol
Topological Polar Surface Area (TPSA) 131.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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107259-48-3
7-Methoxy-8-hydroxyaristolochic acid
8-hydroxy-9-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
Phenanthro[4,3-d]-1,3-dioxole-5-carboxylicacid, 8-hydroxy-9-methoxy-6-nitro-
DTXSID40147983
FT-0662286
Phenanthro(3,4-d)-1,3-dioxole-5-carboxylic acid, 8-hydroxy-9-methoxy-6-nitro-

2D Structure

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2D Structure of Aristolochic acid E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9297 92.97%
Caco-2 + 0.5277 52.77%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.5657 56.57%
OATP2B1 inhibitior - 0.7164 71.64%
OATP1B1 inhibitior + 0.8994 89.94%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5846 58.46%
P-glycoprotein inhibitior - 0.8354 83.54%
P-glycoprotein substrate - 0.7847 78.47%
CYP3A4 substrate + 0.5512 55.12%
CYP2C9 substrate - 0.7819 78.19%
CYP2D6 substrate - 0.8707 87.07%
CYP3A4 inhibition - 0.8396 83.96%
CYP2C9 inhibition - 0.7711 77.11%
CYP2C19 inhibition - 0.8010 80.10%
CYP2D6 inhibition - 0.9052 90.52%
CYP1A2 inhibition + 0.7787 77.87%
CYP2C8 inhibition + 0.6460 64.60%
CYP inhibitory promiscuity + 0.6013 60.13%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6113 61.13%
Carcinogenicity (trinary) Non-required 0.4341 43.41%
Eye corrosion - 0.9806 98.06%
Eye irritation - 0.5405 54.05%
Skin irritation - 0.7581 75.81%
Skin corrosion - 0.9450 94.50%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7868 78.68%
Micronuclear + 0.9600 96.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.8630 86.30%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.5610 56.10%
Acute Oral Toxicity (c) II 0.4714 47.14%
Estrogen receptor binding + 0.8987 89.87%
Androgen receptor binding + 0.5746 57.46%
Thyroid receptor binding + 0.6115 61.15%
Glucocorticoid receptor binding + 0.8783 87.83%
Aromatase binding - 0.4834 48.34%
PPAR gamma + 0.7979 79.79%
Honey bee toxicity - 0.8977 89.77%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9784 97.84%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.97% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.46% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 94.84% 90.20%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.13% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.11% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.97% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.82% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.58% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.27% 89.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.59% 94.80%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.24% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.56% 99.17%
CHEMBL2535 P11166 Glucose transporter 84.82% 98.75%
CHEMBL3194 P02766 Transthyretin 83.66% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.26% 92.62%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.04% 94.42%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.10% 99.23%

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 contorta

Cross-Links

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PubChem 147113
NPASS NPC282685