Aristolochic acid C

Details

Top
Internal ID b4ef69cb-dfda-4def-86d1-81f881b89ea1
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name 10-hydroxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
SMILES (Canonical) C1OC2=C(O1)C3=C4C=C(C=CC4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O
SMILES (Isomeric) C1OC2=C(O1)C3=C4C=C(C=CC4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O
InChI InChI=1S/C16H9NO7/c18-8-2-1-7-3-11(17(21)22)13-10(16(19)20)5-12-15(24-6-23-12)14(13)9(7)4-8/h1-5,18H,6H2,(H,19,20)
InChI Key NBFGYDJKTHENDP-UHFFFAOYSA-N
Popularity 11 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H9NO7
Molecular Weight 327.24 g/mol
Exact Mass 327.03790163 g/mol
Topological Polar Surface Area (TPSA) 122.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.03
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
4849-90-5
ARISTOLOCHICACIDC
Aristolochiac acid C
10-hydroxy-6-nitrophenanthro[3,4-d][1,3]dioxole-5-carboxylic acid
CHEMBL603494
Phenanthro[3,4-d]-1,3-dioxole-5-carboxylic acid, 10-hydroxy-6-nitro-
Phenanthro[3,4-d]-1,3-dioxole-5-carboxylicacid, 10-hydroxy-6-nitro-
10-hydroxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
Aristolochic Acid IIIa
C16H9NO7
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Aristolochic acid C

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9443 94.43%
Caco-2 - 0.6987 69.87%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6145 61.45%
OATP2B1 inhibitior - 0.7067 70.67%
OATP1B1 inhibitior + 0.8705 87.05%
OATP1B3 inhibitior + 0.9347 93.47%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5660 56.60%
P-glycoprotein inhibitior - 0.8680 86.80%
P-glycoprotein substrate - 0.8324 83.24%
CYP3A4 substrate - 0.5228 52.28%
CYP2C9 substrate - 0.7799 77.99%
CYP2D6 substrate - 0.8846 88.46%
CYP3A4 inhibition - 0.8728 87.28%
CYP2C9 inhibition - 0.9159 91.59%
CYP2C19 inhibition - 0.9344 93.44%
CYP2D6 inhibition - 0.9163 91.63%
CYP1A2 inhibition + 0.8321 83.21%
CYP2C8 inhibition + 0.5587 55.87%
CYP inhibitory promiscuity - 0.6933 69.33%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.6370 63.70%
Carcinogenicity (trinary) Non-required 0.4133 41.33%
Eye corrosion - 0.9782 97.82%
Eye irritation + 0.7753 77.53%
Skin irritation - 0.6330 63.30%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis + 0.8830 88.30%
Human Ether-a-go-go-Related Gene inhibition - 0.9208 92.08%
Micronuclear + 0.9600 96.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.8047 80.47%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5195 51.95%
Nephrotoxicity + 0.5114 51.14%
Acute Oral Toxicity (c) II 0.4566 45.66%
Estrogen receptor binding + 0.8219 82.19%
Androgen receptor binding + 0.7609 76.09%
Thyroid receptor binding + 0.6466 64.66%
Glucocorticoid receptor binding + 0.8528 85.28%
Aromatase binding - 0.5713 57.13%
PPAR gamma + 0.7974 79.74%
Honey bee toxicity - 0.9208 92.08%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9781 97.81%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL301 P24941 Cyclin-dependent kinase 2 30000 nM
IC50
PMID: 20097066

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.47% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.10% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.18% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.78% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.48% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.67% 99.23%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.99% 94.80%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.94% 96.77%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.55% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.41% 89.00%
CHEMBL1255126 O15151 Protein Mdm4 81.56% 90.20%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.87% 93.10%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.05% 93.81%

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 contorta
Aristolochia debilis
Aristolochia foveolata
Aristolochia kaempferi
Aristolochia manshuriensis
Aristolochia pubescens

Cross-Links

Top
PubChem 165274
NPASS NPC171882
ChEMBL CHEMBL603494
LOTUS LTS0091047
wikiData Q72443766