Aristophyllide A

Details

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Internal ID 5e76103b-ce9a-4f42-9297-db0a0cbe2157
Taxonomy Benzenoids > Phenanthrenes and derivatives > Aristolochic acids and derivatives
IUPAC Name [(2S)-1-[(5R,6R)-5-ethenyl-5-methyl-6-(3-oxoprop-1-en-2-yl)cyclohexen-1-yl]propan-2-yl] 8-methoxy-6-nitronaphtho[2,1-g][1,3]benzodioxole-5-carboxylate
SMILES (Canonical) CC(CC1=CCCC(C1C(=C)C=O)(C)C=C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3
SMILES (Isomeric) C[C@@H](CC1=CCC[C@]([C@@H]1C(=C)C=O)(C)C=C)OC(=O)C2=CC3=C(C4=C5C=CC=C(C5=CC(=C24)[N+](=O)[O-])OC)OCO3
InChI InChI=1S/C32H31NO8/c1-6-32(4)12-8-9-20(29(32)18(2)16-34)13-19(3)41-31(35)23-15-26-30(40-17-39-26)28-21-10-7-11-25(38-5)22(21)14-24(27(23)28)33(36)37/h6-7,9-11,14-16,19,29H,1-2,8,12-13,17H2,3-5H3/t19-,29+,32-/m0/s1
InChI Key XXQZGCCUBVSBKJ-ZUECTMELSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C32H31NO8
Molecular Weight 557.60 g/mol
Exact Mass 557.20496695 g/mol
Topological Polar Surface Area (TPSA) 117.00 Ų
XlogP 7.10
Atomic LogP (AlogP) 6.86
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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CHEMBL449419

2D Structure

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2D Structure of Aristophyllide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9582 95.82%
Caco-2 - 0.8211 82.11%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5366 53.66%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8651 86.51%
OATP1B3 inhibitior + 0.9275 92.75%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9854 98.54%
P-glycoprotein inhibitior + 0.8778 87.78%
P-glycoprotein substrate + 0.6471 64.71%
CYP3A4 substrate + 0.7306 73.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8599 85.99%
CYP3A4 inhibition + 0.8160 81.60%
CYP2C9 inhibition - 0.6074 60.74%
CYP2C19 inhibition + 0.5511 55.11%
CYP2D6 inhibition - 0.8195 81.95%
CYP1A2 inhibition - 0.5494 54.94%
CYP2C8 inhibition + 0.8304 83.04%
CYP inhibitory promiscuity + 0.7851 78.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.4763 47.63%
Eye corrosion - 0.9796 97.96%
Eye irritation - 0.9250 92.50%
Skin irritation - 0.7743 77.43%
Skin corrosion - 0.9260 92.60%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4006 40.06%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.6274 62.74%
skin sensitisation - 0.8356 83.56%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5560 55.60%
Acute Oral Toxicity (c) III 0.5496 54.96%
Estrogen receptor binding + 0.8101 81.01%
Androgen receptor binding + 0.7352 73.52%
Thyroid receptor binding + 0.6543 65.43%
Glucocorticoid receptor binding + 0.8741 87.41%
Aromatase binding + 0.6544 65.44%
PPAR gamma + 0.7314 73.14%
Honey bee toxicity - 0.6572 65.72%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5355 53.55%
Fish aquatic toxicity + 1.0000 100.00%

Targets

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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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 99.46% 94.45%
CHEMBL240 Q12809 HERG 99.19% 89.76%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.62% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.36% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.19% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.08% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.07% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 96.20% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.33% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.70% 89.00%
CHEMBL2535 P11166 Glucose transporter 92.92% 98.75%
CHEMBL1255126 O15151 Protein Mdm4 92.37% 90.20%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 91.19% 85.30%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.72% 95.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.50% 96.00%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 88.62% 80.96%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 88.21% 94.80%
CHEMBL340 P08684 Cytochrome P450 3A4 87.64% 91.19%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 87.41% 92.88%
CHEMBL5028 O14672 ADAM10 87.04% 97.50%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.91% 90.24%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.32% 95.89%
CHEMBL3902 P09211 Glutathione S-transferase Pi 85.23% 93.81%
CHEMBL3401 O75469 Pregnane X receptor 84.92% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.53% 99.23%
CHEMBL2413 P32246 C-C chemokine receptor type 1 83.92% 89.50%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 83.90% 89.44%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.36% 97.14%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.72% 98.75%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.24% 100.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.58% 91.07%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.55% 99.17%

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 kaempferi
Aristolochia mollissima

Cross-Links

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PubChem 10840539
NPASS NPC256422
ChEMBL CHEMBL449419
LOTUS LTS0149061
wikiData Q105344171