Aristolochic acid d

Details

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Internal ID cd5fc293-1087-4ce1-8e63-b570ea92d6b8
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name 10-hydroxy-8-methoxy-6-nitronaphtho[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)O
SMILES (Isomeric) COC1=CC(=CC2=C3C(=C(C=C12)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O
InChI InChI=1S/C17H11NO8/c1-24-12-3-7(19)2-9-8(12)4-11(18(22)23)14-10(17(20)21)5-13-16(15(9)14)26-6-25-13/h2-5,19H,6H2,1H3,(H,20,21)
InChI Key PADIFGYTAXNCRK-UHFFFAOYSA-N
Popularity 11 references 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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17413-38-6
Aristolochic acid-D
Aristolochic acid Iva
aristolochic D
10-hydroxy-8-methoxy-6-nitrophenanthro[3,4-d][1,3]dioxole-5-carboxylic acid
CCRIS 2995
CHEMBL604748
10-hydroxy-8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
Phenanthro[3,4-d]-1,3-dioxole-5-carboxylic acid, 10-hydroxy-8-methoxy-6-nitro-
Aristolochicacidd
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 d

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9407 94.07%
Caco-2 + 0.5527 55.27%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.5289 52.89%
OATP2B1 inhibitior - 0.7191 71.91%
OATP1B1 inhibitior + 0.9012 90.12%
OATP1B3 inhibitior + 0.9426 94.26%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6139 61.39%
P-glycoprotein inhibitior - 0.7307 73.07%
P-glycoprotein substrate - 0.7961 79.61%
CYP3A4 substrate + 0.5449 54.49%
CYP2C9 substrate - 0.7819 78.19%
CYP2D6 substrate - 0.8707 87.07%
CYP3A4 inhibition - 0.7910 79.10%
CYP2C9 inhibition - 0.8597 85.97%
CYP2C19 inhibition - 0.8510 85.10%
CYP2D6 inhibition - 0.9045 90.45%
CYP1A2 inhibition + 0.8278 82.78%
CYP2C8 inhibition + 0.5649 56.49%
CYP inhibitory promiscuity + 0.5364 53.64%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6213 62.13%
Carcinogenicity (trinary) Non-required 0.4591 45.91%
Eye corrosion - 0.9805 98.05%
Eye irritation - 0.5933 59.33%
Skin irritation - 0.7502 75.02%
Skin corrosion - 0.9430 94.30%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8046 80.46%
Micronuclear + 0.9600 96.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8619 86.19%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.7218 72.18%
Acute Oral Toxicity (c) II 0.4932 49.32%
Estrogen receptor binding + 0.8386 83.86%
Androgen receptor binding + 0.5427 54.27%
Thyroid receptor binding + 0.6138 61.38%
Glucocorticoid receptor binding + 0.9079 90.79%
Aromatase binding - 0.5339 53.39%
PPAR gamma + 0.8363 83.63%
Honey bee toxicity - 0.8764 87.64%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9630 96.30%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL301 P24941 Cyclin-dependent kinase 2 25000 nM
IC50
PMID: 20097066

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.42% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.47% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.26% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.97% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.06% 95.56%
CHEMBL1255126 O15151 Protein Mdm4 92.20% 90.20%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.82% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.99% 99.17%
CHEMBL2535 P11166 Glucose transporter 89.36% 98.75%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.23% 94.80%
CHEMBL2581 P07339 Cathepsin D 89.08% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.87% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.77% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.45% 92.62%
CHEMBL3194 P02766 Transthyretin 81.69% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.40% 96.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.24% 94.42%

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
Aristolochia debilis
Aristolochia kaempferi
Aristolochia manshuriensis
Aristolochia mollissima
Aristolochia pubescens
Asarum heterotropoides
Asarum sieboldii

Cross-Links

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PubChem 161218
NPASS NPC240684
ChEMBL CHEMBL604748
LOTUS LTS0038957
wikiData Q83039509