Aristolochic acid Ia

Details

Top
Internal ID 0057d238-6533-4a1a-b54a-8af76f1862f1
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name 8-hydroxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
SMILES (Canonical) C1OC2=C(O1)C3=C4C=CC=C(C4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O
SMILES (Isomeric) C1OC2=C(O1)C3=C4C=CC=C(C4=CC(=C3C(=C2)C(=O)O)[N+](=O)[O-])O
InChI InChI=1S/C16H9NO7/c18-11-3-1-2-7-8(11)4-10(17(21)22)13-9(16(19)20)5-12-15(14(7)13)24-6-23-12/h1-5,18H,6H2,(H,19,20)
InChI Key LGZIKBZSCRORQN-UHFFFAOYSA-N
Popularity 1 reference 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
38965-71-8
CCRIS 2578
8-hydroxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
BRN 4563308
CHEMBL601026
8-Hydroxy-6-nitrophenanthro(3,4-d)-1,3-dioxolo-5-carboxylic acid
Phenanthro(3,4-d)-1,3-dioxole-5-carboxylic acid, 8-hydroxy-6-nitro-
8-hydroxy-6-nitrophenanthro[3,4-d][1,3]dioxole-5-carboxylic acid
starbld0023278
DTXSID60192258
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Aristolochic acid Ia

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9443 94.43%
Caco-2 - 0.6706 67.06%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.6145 61.45%
OATP2B1 inhibitior - 0.7130 71.30%
OATP1B1 inhibitior + 0.9228 92.28%
OATP1B3 inhibitior + 0.9347 93.47%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5472 54.72%
P-glycoprotein inhibitior - 0.8762 87.62%
P-glycoprotein substrate - 0.8953 89.53%
CYP3A4 substrate + 0.5112 51.12%
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 + 0.4547 45.47%
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 + 0.7124 71.24%
Skin irritation - 0.6330 63.30%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis + 0.9300 93.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9242 92.42%
Micronuclear + 0.9600 96.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.8047 80.47%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5195 51.95%
Nephrotoxicity - 0.5869 58.69%
Acute Oral Toxicity (c) II 0.4566 45.66%
Estrogen receptor binding + 0.8684 86.84%
Androgen receptor binding + 0.6488 64.88%
Thyroid receptor binding + 0.6630 66.30%
Glucocorticoid receptor binding + 0.8598 85.98%
Aromatase binding - 0.5056 50.56%
PPAR gamma + 0.8107 81.07%
Honey bee toxicity - 0.9261 92.61%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7700 77.00%
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 15000 nM
IC50
PMID: 20097066

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.09% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.64% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.37% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.46% 94.80%
CHEMBL2581 P07339 Cathepsin D 93.10% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.96% 86.33%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.44% 96.77%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.69% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.90% 99.23%
CHEMBL2535 P11166 Glucose transporter 87.59% 98.75%
CHEMBL3902 P09211 Glutathione S-transferase Pi 86.05% 93.81%
CHEMBL3401 O75469 Pregnane X receptor 85.54% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.20% 92.62%

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

Cross-Links

Top
PubChem 148297
NPASS NPC121510
ChEMBL CHEMBL601026