Aristolodione

Details

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Internal ID 242288c7-11ab-44e6-b38e-72aa3d35dce5
Taxonomy Alkaloids and derivatives > Aporphines > 4,5-dioxoaporphines
IUPAC Name 15-hydroxy-16-methoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,8,13,15-heptaene-11,12-dione
SMILES (Canonical) CN1C2=CC3=CC=CC=C3C4=C2C(=CC(=C4OC)O)C(=O)C1=O
SMILES (Isomeric) CN1C2=CC3=CC=CC=C3C4=C2C(=CC(=C4OC)O)C(=O)C1=O
InChI InChI=1S/C18H13NO4/c1-19-12-7-9-5-3-4-6-10(9)15-14(12)11(16(21)18(19)22)8-13(20)17(15)23-2/h3-8,20H,1-2H3
InChI Key JGDZUWXHWYXMSD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H13NO4
Molecular Weight 307.30 g/mol
Exact Mass 307.08445790 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.87
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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109771-09-7
Piperadione
DTXSID30149032
CHEBI:174938
AKOS040736344
15-hydroxy-16-methoxy-10-methyl-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,8,13(17),14-heptaene-11,12-dione
15-hydroxy-16-methoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,8,13,15-heptaene-11,12-dione

2D Structure

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2D Structure of Aristolodione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8104 81.04%
Caco-2 + 0.8506 85.06%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5099 50.99%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9090 90.90%
OATP1B3 inhibitior + 0.9561 95.61%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9564 95.64%
BSEP inhibitior - 0.5994 59.94%
P-glycoprotein inhibitior - 0.8088 80.88%
P-glycoprotein substrate - 0.9175 91.75%
CYP3A4 substrate + 0.5705 57.05%
CYP2C9 substrate - 0.7979 79.79%
CYP2D6 substrate - 0.8470 84.70%
CYP3A4 inhibition - 0.7989 79.89%
CYP2C9 inhibition - 0.8521 85.21%
CYP2C19 inhibition - 0.9218 92.18%
CYP2D6 inhibition - 0.9483 94.83%
CYP1A2 inhibition + 0.6659 66.59%
CYP2C8 inhibition - 0.6977 69.77%
CYP inhibitory promiscuity - 0.7304 73.04%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5717 57.17%
Eye corrosion - 0.9926 99.26%
Eye irritation - 0.7941 79.41%
Skin irritation - 0.8149 81.49%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis + 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7196 71.96%
Micronuclear + 0.7559 75.59%
Hepatotoxicity + 0.5304 53.04%
skin sensitisation - 0.9453 94.53%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6076 60.76%
Nephrotoxicity - 0.7588 75.88%
Acute Oral Toxicity (c) III 0.7571 75.71%
Estrogen receptor binding + 0.8803 88.03%
Androgen receptor binding + 0.6445 64.45%
Thyroid receptor binding - 0.5182 51.82%
Glucocorticoid receptor binding + 0.8315 83.15%
Aromatase binding + 0.8639 86.39%
PPAR gamma - 0.4919 49.19%
Honey bee toxicity - 0.9266 92.66%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.6981 69.81%

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 98.38% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.36% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.57% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.53% 94.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 92.55% 80.78%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.25% 99.23%
CHEMBL214 P08908 Serotonin 1a (5-HT1a) receptor 89.68% 92.83%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.62% 99.15%
CHEMBL2535 P11166 Glucose transporter 88.98% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.76% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.80% 96.67%
CHEMBL2056 P21728 Dopamine D1 receptor 87.65% 91.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.10% 96.09%
CHEMBL4208 P20618 Proteasome component C5 84.43% 90.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.00% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.85% 89.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 81.63% 85.94%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.51% 82.69%
CHEMBL1907 P15144 Aminopeptidase N 80.82% 93.31%

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 chilensis
Aristolochia kaempferi
Piper longum

Cross-Links

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PubChem 184116
LOTUS LTS0118685
wikiData Q83014703