Ariskanin A

Details

Top
Internal ID 858d1ac6-5e0b-472a-bea2-e0572a5d758a
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name methyl 3,4-dimethoxy-10-nitrophenanthrene-1-carboxylate
SMILES (Canonical) COC1=C(C2=C(C(=C1)C(=O)OC)C(=CC3=CC=CC=C32)[N+](=O)[O-])OC
SMILES (Isomeric) COC1=C(C2=C(C(=C1)C(=O)OC)C(=CC3=CC=CC=C32)[N+](=O)[O-])OC
InChI InChI=1S/C18H15NO6/c1-23-14-9-12(18(20)25-3)15-13(19(21)22)8-10-6-4-5-7-11(10)16(15)17(14)24-2/h4-9H,1-3H3
InChI Key SJFUNPNDPBAPCB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C18H15NO6
Molecular Weight 341.30 g/mol
Exact Mass 341.08993720 g/mol
Topological Polar Surface Area (TPSA) 90.60 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.71
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Ariskanin A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9674 96.74%
Caco-2 + 0.8638 86.38%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.5264 52.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9126 91.26%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.7445 74.45%
P-glycoprotein inhibitior - 0.5877 58.77%
P-glycoprotein substrate - 0.8392 83.92%
CYP3A4 substrate + 0.5866 58.66%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8345 83.45%
CYP3A4 inhibition - 0.6824 68.24%
CYP2C9 inhibition - 0.6525 65.25%
CYP2C19 inhibition - 0.5064 50.64%
CYP2D6 inhibition - 0.9403 94.03%
CYP1A2 inhibition - 0.5622 56.22%
CYP2C8 inhibition + 0.7901 79.01%
CYP inhibitory promiscuity - 0.6298 62.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5335 53.35%
Carcinogenicity (trinary) Non-required 0.3851 38.51%
Eye corrosion - 0.9763 97.63%
Eye irritation - 0.6013 60.13%
Skin irritation - 0.8391 83.91%
Skin corrosion - 0.9674 96.74%
Ames mutagenesis + 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6900 69.00%
Micronuclear + 0.9700 97.00%
Hepatotoxicity + 0.6284 62.84%
skin sensitisation - 0.9314 93.14%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6203 62.03%
Acute Oral Toxicity (c) III 0.5570 55.70%
Estrogen receptor binding + 0.8902 89.02%
Androgen receptor binding + 0.6136 61.36%
Thyroid receptor binding + 0.5992 59.92%
Glucocorticoid receptor binding + 0.8734 87.34%
Aromatase binding + 0.5871 58.71%
PPAR gamma + 0.6814 68.14%
Honey bee toxicity - 0.9332 93.32%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9934 99.34%

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
CHEMBL240 Q12809 HERG 97.31% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.82% 86.33%
CHEMBL2535 P11166 Glucose transporter 93.99% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 93.23% 90.20%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.61% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.58% 99.17%
CHEMBL3902 P09211 Glutathione S-transferase Pi 90.03% 93.81%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.91% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.33% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.90% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.47% 96.00%
CHEMBL4208 P20618 Proteasome component C5 83.41% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.34% 94.00%
CHEMBL2581 P07339 Cathepsin D 83.25% 98.95%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 81.47% 96.47%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.74% 99.23%
CHEMBL4302 P08183 P-glycoprotein 1 80.59% 92.98%
CHEMBL3401 O75469 Pregnane X receptor 80.52% 94.73%

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.
Akebia quinata
Aristolochia debilis
Aristolochia manshuriensis
Aristolochia zollingeriana

Cross-Links

Top
PubChem 5320068
NPASS NPC206052
LOTUS LTS0250573
wikiData Q105254272