Aristoloside

Details

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Internal ID fe360623-f2a5-447b-a55c-40cea31a3974
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name 8-methoxy-6-nitro-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
SMILES (Canonical) COC1=CC(=CC2=C3C(=C(C=C12)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)OC5C(C(C(C(O5)CO)O)O)O
SMILES (Isomeric) COC1=CC(=CC2=C3C(=C(C=C12)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O
InChI InChI=1S/C23H21NO13/c1-33-13-3-8(36-23-20(28)19(27)18(26)15(6-25)37-23)2-10-9(13)4-12(24(31)32)16-11(22(29)30)5-14-21(17(10)16)35-7-34-14/h2-5,15,18-20,23,25-28H,6-7H2,1H3,(H,29,30)/t15-,18-,19+,20-,23-/m1/s1
InChI Key GMKHAVDYTAXBIY-BSTKLLGTSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C23H21NO13
Molecular Weight 519.40 g/mol
Exact Mass 519.10128972 g/mol
Topological Polar Surface Area (TPSA) 210.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 0.52
H-Bond Acceptor 12
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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84014-70-0
8-methoxy-6-nitro-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
DTXSID001004297
10-(Hexopyranosyloxy)-8-methoxy-6-nitro-2H-phenanthro[3,4-d][1,3]dioxole-5-carboxylato
Phenanthro(3,4-d)-1,3-dioxole-5-carboxylic acid, 10-(beta-D-glucopyranosyloxy)-8-methoxy-6-nitro-

2D Structure

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2D Structure of Aristoloside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5791 57.91%
Caco-2 - 0.8598 85.98%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Nucleus 0.4361 43.61%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.8940 89.40%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8971 89.71%
P-glycoprotein inhibitior - 0.5547 55.47%
P-glycoprotein substrate - 0.6447 64.47%
CYP3A4 substrate + 0.6258 62.58%
CYP2C9 substrate - 0.7952 79.52%
CYP2D6 substrate - 0.8652 86.52%
CYP3A4 inhibition - 0.8934 89.34%
CYP2C9 inhibition - 0.7445 74.45%
CYP2C19 inhibition - 0.7067 70.67%
CYP2D6 inhibition - 0.8481 84.81%
CYP1A2 inhibition - 0.5384 53.84%
CYP2C8 inhibition + 0.5214 52.14%
CYP inhibitory promiscuity - 0.6723 67.23%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.5087 50.87%
Eye corrosion - 0.9817 98.17%
Eye irritation - 0.9327 93.27%
Skin irritation - 0.7759 77.59%
Skin corrosion - 0.9307 93.07%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5167 51.67%
Micronuclear + 0.9700 97.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.8493 84.93%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.5582 55.82%
Acute Oral Toxicity (c) III 0.5721 57.21%
Estrogen receptor binding + 0.7533 75.33%
Androgen receptor binding - 0.5457 54.57%
Thyroid receptor binding + 0.5821 58.21%
Glucocorticoid receptor binding + 0.7428 74.28%
Aromatase binding - 0.5514 55.14%
PPAR gamma + 0.6636 66.36%
Honey bee toxicity - 0.7749 77.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.8647 86.47%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.46% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.10% 96.77%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 94.99% 94.80%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.95% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.81% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.01% 94.45%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.86% 97.36%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.04% 96.00%
CHEMBL2581 P07339 Cathepsin D 91.91% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.76% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.33% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.94% 95.56%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.77% 96.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.23% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.22% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.65% 95.89%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 82.93% 94.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.64% 93.00%
CHEMBL1255126 O15151 Protein Mdm4 82.04% 90.20%
CHEMBL4208 P20618 Proteasome component C5 80.60% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.00% 94.00%

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 argentina
Aristolochia manshuriensis
Aristolochia tuberosa

Cross-Links

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PubChem 128576
NPASS NPC261836
LOTUS LTS0084916
wikiData Q82999227