Aristolochic acid IV

Details

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Internal ID 78b1688e-196a-46d8-8fd9-f8a6e1b6c8bb
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name 8,10-dimethoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
SMILES (Canonical) COC1=CC2=C3C(=C(C=C2C(=C1)OC)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O
SMILES (Isomeric) COC1=CC2=C3C(=C(C=C2C(=C1)OC)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O
InChI InChI=1S/C18H13NO8/c1-24-8-3-10-9(13(4-8)25-2)5-12(19(22)23)15-11(18(20)21)6-14-17(16(10)15)27-7-26-14/h3-6H,7H2,1-2H3,(H,20,21)
InChI Key GYBINMVKWZEICQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H13NO8
Molecular Weight 371.30 g/mol
Exact Mass 371.06411637 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.35
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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15918-62-4
O-Methylaristolochic acid D
6-Methoxyaristolochic acid D
BRN 1332635
Aristolochic acid IV(sub a) methyl ether
CHEMBL465004
8,10-dimethoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
2,3-Methylenedioxy-5,7-dimethoxy-10-nitrophenanthroic acid
8,10-Dimethoxy-6-nitrophenanthro(3,4-d)-1,3-dioxole-5-carboxylic acid
8,10-Dimethoxy-6-nitrophenanthro[3,4-d]-1,3-dioxole-5-carboxylic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Aristolochic acid IV

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9544 95.44%
Caco-2 + 0.7107 71.07%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.5190 51.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9180 91.80%
OATP1B3 inhibitior + 0.9378 93.78%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.8223 82.23%
P-glycoprotein inhibitior - 0.5818 58.18%
P-glycoprotein substrate - 0.8315 83.15%
CYP3A4 substrate + 0.5235 52.35%
CYP2C9 substrate - 0.7799 77.99%
CYP2D6 substrate - 0.8756 87.56%
CYP3A4 inhibition - 0.7327 73.27%
CYP2C9 inhibition - 0.8217 82.17%
CYP2C19 inhibition - 0.7824 78.24%
CYP2D6 inhibition - 0.9063 90.63%
CYP1A2 inhibition + 0.8544 85.44%
CYP2C8 inhibition - 0.5957 59.57%
CYP inhibitory promiscuity + 0.5118 51.18%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.4698 46.98%
Eye corrosion - 0.9805 98.05%
Eye irritation - 0.6693 66.93%
Skin irritation - 0.7716 77.16%
Skin corrosion - 0.9466 94.66%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7422 74.22%
Micronuclear + 0.9700 97.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8645 86.45%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6318 63.18%
Acute Oral Toxicity (c) II 0.5602 56.02%
Estrogen receptor binding + 0.8607 86.07%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.6971 69.71%
Glucocorticoid receptor binding + 0.9233 92.33%
Aromatase binding + 0.5319 53.19%
PPAR gamma + 0.9034 90.34%
Honey bee toxicity - 0.8887 88.87%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.9668 96.68%

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
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.07% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.86% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.84% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.37% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.96% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 92.34% 94.80%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.95% 92.62%
CHEMBL2535 P11166 Glucose transporter 87.86% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.59% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.15% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 86.55% 97.36%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.38% 96.00%
CHEMBL1255126 O15151 Protein Mdm4 85.97% 90.20%
CHEMBL4208 P20618 Proteasome component C5 84.67% 90.00%
CHEMBL2581 P07339 Cathepsin D 84.38% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.88% 89.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.37% 93.00%

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 auricularia
Aristolochia cucurbitifolia
Aristolochia debilis
Aristolochia manshuriensis
Aristolochia rigida
Aristolochia zollingeriana

Cross-Links

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PubChem 167493
NPASS NPC290227
LOTUS LTS0087118
wikiData Q83035782