9-Hydroxy-8-methoxy-6-nitro-phenanthrol[3,4-D][1,3]dioxole-5-carboxylic acid

Details

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Internal ID 4ba31db1-099e-46f3-a0cd-f666b2e54072
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name 9-hydroxy-8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylic acid
SMILES (Canonical) COC1=C(C=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O
SMILES (Isomeric) COC1=C(C=CC2=C3C(=C(C=C21)[N+](=O)[O-])C(=CC4=C3OCO4)C(=O)O)O
InChI InChI=1S/C17H11NO8/c1-24-15-8-4-10(18(22)23)13-9(17(20)21)5-12-16(26-6-25-12)14(13)7(8)2-3-11(15)19/h2-5,19H,6H2,1H3,(H,20,21)
InChI Key UCLGCTLOEZZSLA-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C17H11NO8
Molecular Weight 357.30 g/mol
Exact Mass 357.04846631 g/mol
Topological Polar Surface Area (TPSA) 131.00 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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7-hydroxy aristolochic acid A
Phenanthro[3,4-d]-1,3-dioxole-5-carboxylicacid, 9-hydroxy-8-methoxy-6-nitro-
7-hydroxy aristolochic A
CHEMBL600828
9-HYDROXY-8-METHOXY-6-NITRO-PHENANTHROL[3,4-D][1,3]DIOXOLE-5-CARBOXYLIC ACID
Aristolochic acid Va
1fv0
SCHEMBL4557492
HY-N2012
BDBM50306859
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 9-Hydroxy-8-methoxy-6-nitro-phenanthrol[3,4-D][1,3]dioxole-5-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9297 92.97%
Caco-2 + 0.5684 56.84%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5657 56.57%
OATP2B1 inhibitior - 0.7172 71.72%
OATP1B1 inhibitior + 0.9315 93.15%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.4787 47.87%
P-glycoprotein inhibitior - 0.8711 87.11%
P-glycoprotein substrate - 0.8565 85.65%
CYP3A4 substrate + 0.5312 53.12%
CYP2C9 substrate - 0.7819 78.19%
CYP2D6 substrate - 0.8707 87.07%
CYP3A4 inhibition - 0.8396 83.96%
CYP2C9 inhibition - 0.7711 77.11%
CYP2C19 inhibition - 0.8010 80.10%
CYP2D6 inhibition - 0.9052 90.52%
CYP1A2 inhibition + 0.7787 77.87%
CYP2C8 inhibition + 0.5339 53.39%
CYP inhibitory promiscuity + 0.6013 60.13%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6113 61.13%
Carcinogenicity (trinary) Non-required 0.4341 43.41%
Eye corrosion - 0.9806 98.06%
Eye irritation - 0.6225 62.25%
Skin irritation - 0.7581 75.81%
Skin corrosion - 0.9450 94.50%
Ames mutagenesis + 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7785 77.85%
Micronuclear + 0.9600 96.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.8630 86.30%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5219 52.19%
Acute Oral Toxicity (c) II 0.4714 47.14%
Estrogen receptor binding + 0.8375 83.75%
Androgen receptor binding + 0.5764 57.64%
Thyroid receptor binding + 0.5948 59.48%
Glucocorticoid receptor binding + 0.8869 88.69%
Aromatase binding - 0.4916 49.16%
PPAR gamma + 0.8090 80.90%
Honey bee toxicity - 0.8981 89.81%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9784 97.84%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL301 P24941 Cyclin-dependent kinase 2 25000 nM
IC50
PMID: 20097066

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.16% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.37% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.05% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.93% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 93.74% 94.80%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.44% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.41% 98.95%
CHEMBL2535 P11166 Glucose transporter 88.65% 98.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.36% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.92% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.91% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.14% 99.23%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.54% 92.62%

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 contorta
Aristolochia cucurbitifolia
Aristolochia debilis
Aristolochia foveolata
Aristolochia pubescens

Cross-Links

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PubChem 1941
NPASS NPC91234
ChEMBL CHEMBL600828
LOTUS LTS0136451
wikiData Q27093597