Aristolochic acid I methyl ester

Details

Top
Internal ID b8e260af-3014-4223-a1cd-acc3c851dd0c
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name methyl 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate
SMILES (Canonical) COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC
SMILES (Isomeric) COC1=CC=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)OC
InChI InChI=1S/C18H13NO7/c1-23-13-5-3-4-9-10(13)6-12(19(21)22)15-11(18(20)24-2)7-14-17(16(9)15)26-8-25-14/h3-7H,8H2,1-2H3
InChI Key RZUABJWVTLHGHJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C18H13NO7
Molecular Weight 355.30 g/mol
Exact Mass 355.06920175 g/mol
Topological Polar Surface Area (TPSA) 99.80 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
Methyl aristolochate
1169-60-4
Aristolochic acid A methyl ester
Aristolochic acid, methyl ester
CCRIS 2993
NSC 87404
BRN 0347502
VQL974W6E6
aristolochic acid-I, methyl ester
methyl 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Aristolochic acid I methyl ester

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9735 97.35%
Caco-2 + 0.8400 84.00%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5206 52.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9278 92.78%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7625 76.25%
P-glycoprotein inhibitior - 0.5557 55.57%
P-glycoprotein substrate - 0.7078 70.78%
CYP3A4 substrate + 0.6442 64.42%
CYP2C9 substrate - 0.7858 78.58%
CYP2D6 substrate - 0.8493 84.93%
CYP3A4 inhibition - 0.6568 65.68%
CYP2C9 inhibition - 0.8138 81.38%
CYP2C19 inhibition - 0.7328 73.28%
CYP2D6 inhibition - 0.9118 91.18%
CYP1A2 inhibition + 0.9114 91.14%
CYP2C8 inhibition + 0.6668 66.68%
CYP inhibitory promiscuity + 0.7231 72.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.4364 43.64%
Eye corrosion - 0.9773 97.73%
Eye irritation - 0.7765 77.65%
Skin irritation - 0.7713 77.13%
Skin corrosion - 0.9477 94.77%
Ames mutagenesis + 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7813 78.13%
Micronuclear + 0.9800 98.00%
Hepatotoxicity + 0.6534 65.34%
skin sensitisation - 0.8644 86.44%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6370 63.70%
Acute Oral Toxicity (c) II 0.5627 56.27%
Estrogen receptor binding + 0.8948 89.48%
Androgen receptor binding + 0.6028 60.28%
Thyroid receptor binding + 0.6557 65.57%
Glucocorticoid receptor binding + 0.9195 91.95%
Aromatase binding + 0.6239 62.39%
PPAR gamma + 0.8601 86.01%
Honey bee toxicity - 0.8856 88.56%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9785 97.85%

Targets

Top

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.31% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.56% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 95.37% 94.80%
CHEMBL2535 P11166 Glucose transporter 95.28% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.67% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.52% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.74% 96.09%
CHEMBL240 Q12809 HERG 92.94% 89.76%
CHEMBL2581 P07339 Cathepsin D 92.80% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.87% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.92% 92.62%
CHEMBL1255126 O15151 Protein Mdm4 90.39% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.02% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.55% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.27% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.11% 89.00%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 83.58% 80.96%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.09% 99.23%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.41% 93.81%
CHEMBL5028 O14672 ADAM10 80.76% 97.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.51% 94.00%

Plants that contains it

Top
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 cucurbitifolia
Aristolochia kaempferi
Aristolochia manshuriensis
Aristolochia mollissima

Cross-Links

Top
PubChem 96709
NPASS NPC38961
LOTUS LTS0186276
wikiData Q83018053