Aristolamide

Details

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Internal ID 74aa2b11-59e2-4eff-b899-3c30dedbb84e
Taxonomy Benzenoids > Phenanthrenes and derivatives
IUPAC Name 8-methoxynaphtho[2,1-g][1,3]benzodioxole-5-carboxamide
SMILES (Canonical) COC1=CC=CC2=C1C=CC3=C2C4=C(C=C3C(=O)N)OCO4
SMILES (Isomeric) COC1=CC=CC2=C1C=CC3=C2C4=C(C=C3C(=O)N)OCO4
InChI InChI=1S/C17H13NO4/c1-20-13-4-2-3-10-9(13)5-6-11-12(17(18)19)7-14-16(15(10)11)22-8-21-14/h2-7H,8H2,1H3,(H2,18,19)
InChI Key WRICUAQTIAJGKC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H13NO4
Molecular Weight 295.29 g/mol
Exact Mass 295.08445790 g/mol
Topological Polar Surface Area (TPSA) 70.80 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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CHEMBL1684821

2D Structure

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2D Structure of Aristolamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9952 99.52%
Caco-2 + 0.8940 89.40%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4195 41.95%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9713 97.13%
OATP1B3 inhibitior + 0.9583 95.83%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7143 71.43%
P-glycoprotein inhibitior - 0.6923 69.23%
P-glycoprotein substrate - 0.7411 74.11%
CYP3A4 substrate + 0.5364 53.64%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8267 82.67%
CYP3A4 inhibition + 0.7924 79.24%
CYP2C9 inhibition + 0.6061 60.61%
CYP2C19 inhibition + 0.5110 51.10%
CYP2D6 inhibition - 0.6531 65.31%
CYP1A2 inhibition + 0.7995 79.95%
CYP2C8 inhibition - 0.5844 58.44%
CYP inhibitory promiscuity + 0.7309 73.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Warning 0.3663 36.63%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.6110 61.10%
Skin irritation - 0.7692 76.92%
Skin corrosion - 0.9591 95.91%
Ames mutagenesis + 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4722 47.22%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8186 81.86%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.5575 55.75%
Acute Oral Toxicity (c) III 0.5152 51.52%
Estrogen receptor binding + 0.8740 87.40%
Androgen receptor binding + 0.7522 75.22%
Thyroid receptor binding + 0.5855 58.55%
Glucocorticoid receptor binding + 0.8831 88.31%
Aromatase binding + 0.6505 65.05%
PPAR gamma + 0.7440 74.40%
Honey bee toxicity - 0.8686 86.86%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7256 72.56%

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 99.02% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.99% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.62% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.17% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.46% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.77% 86.33%
CHEMBL2535 P11166 Glucose transporter 92.68% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.71% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.49% 92.62%
CHEMBL3474 P14555 Phospholipase A2 group IIA 88.07% 94.05%
CHEMBL2581 P07339 Cathepsin D 86.92% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.40% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.76% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.55% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.52% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.80% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.21% 97.09%
CHEMBL1255126 O15151 Protein Mdm4 80.86% 90.20%

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 manshuriensis

Cross-Links

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PubChem 53320351
NPASS NPC77359