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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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W129766-250mg | 250mg | In stock | $286.90 | |
W129766-1g | 1g | In stock | $1,033.90 | |
W129766-5g | 5g | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $4,649.90 |
Selective PPARα agonist
Synonyms | Acidum pirinixicum [INN-Latin] | SB19568 | Wyeth 14,643 | Wyeth-14,643 | EX-A2258 | NSC 310038 | Tox21_300634 | HMS3402M22 | Acido pirinixico [INN-Spanish] | BML2-E12 | KBio2_004921 | NCGC00014702-03 | WY1 | 2-[4-chloro-6-(2,3-dimethylanilino)pyrimidin-2- |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | WY 14643 is a highly potent PPARα agonist. Peroxisome proliferator-activated receptors (PPARs) α, β, and γ are hormone receptors that induce the gene acyl-Coa and modulate the peroxisomal beta oxidation of fatty acids. WY 14643 has been shown to inhibit T |
Shipped In | Normal |
Grade | Moligand™ |
Action Type | AGONIST |
Mechanism of action | Agonist of Peroxisome proliferator-activated receptor-α |
Note | Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | WY 14643 (Pirinixic Acid) is a potent peroxisome proliferator and activator of PPARα with EC50 of 1.5 μM. |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 2-[4-chloro-6-(2,3-dimethylanilino)pyrimidin-2-yl]sulfanylacetic acid |
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INCHI | InChI=1S/C14H14ClN3O2S/c1-8-4-3-5-10(9(8)2)16-12-6-11(15)17-14(18-12)21-7-13(19)20/h3-6H,7H2,1-2H3,(H,19,20)(H,16,17,18) |
InChi Key | SZRPDCCEHVWOJX-UHFFFAOYSA-N |
Canonical SMILES | CC1=C(C(=CC=C1)NC2=CC(=NC(=N2)SCC(=O)O)Cl)C |
Isomeric SMILES | CC1=C(C(=CC=C1)NC2=CC(=NC(=N2)SCC(=O)O)Cl)C |
WGK Germany | 3 |
RTECS | AG2915000 |
PubChem CID | 5694 |
Molecular Weight | 323.8 |
Reaxy-Rn | 759945 |
PubChem CID | 5694 |
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ChEBI | CHEBI:32509 |
CAS Registry No. | 50892-23-4 |
ChEMBL Ligand | CHEMBL295416 |
BindingDB Ligand | 24566 |
Wikipedia | Pirinixic_acid |
NURSA Ligand | 10.1621/Q9I7FUAMIO |
RCSB PDB Ligand | WY1 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
K2116373 | Certificate of Analysis | Sep 13, 2023 | W129766 |
K2116374 | Certificate of Analysis | Sep 13, 2023 | W129766 |
J1509050 | Certificate of Analysis | May 11, 2023 | W129766 |
B2307155 | Certificate of Analysis | Feb 15, 2023 | W129766 |
Solubility | Soluble in DMSO (65 mg/ml at 25 °C), ethanol (52 mg/ml at 25 °C), DMF (~16.5 mg/ml), PBS (pH 7.2, ~0.04 mg/ml), and water (<1 mg/ml at 25 °C). |
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Melt Point(°C) | 155 °C |
Signal | Danger |
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Hazard Statements | H315:Causes skin irritation H319:Causes serious eye irritation H335:May cause respiratory irritation H302:Harmful if swallowed H350:May cause cancer |
Precautionary Statements | P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P201:Obtain special instructions before use. P308+P313:IF exposed or concerned: Get medical advice/attention. |
WGK Germany | 3 |
RTECS | AG2915000 |
Reaxy-Rn | 759945 |
1. Zhi-shen Xie, Jian-ping Zhao, Li-min Wu, Shuang Chu, Zheng-hao Cui, Yi-ran Sun, Hui Wang, Hui-fen Ma, Dong-rui Ma, Pan Wang, Xiao-wei Zhang, Zhen-qiang Zhang. (2023) Hederagenin improves Alzheimer's disease through PPARα/TFEB-mediated autophagy. PHYTOMEDICINE, 112 (154711). [PMID:36809694] [10.1016/j.phymed.2023.154711] |
1. Luo R et al.. (2020) Activation of PPARA-mediated autophagy reduces Alzheimer disease-like pathology and cognitive decline in a murine model.. Autophagy, 16 (52-69). [PMID:30898012] |
2. Huang Y et al.. (2020) Resveratrol protects against nonalcoholic fatty liver disease by improving lipid metabolism and redox homeostasis via the PPARa pathway.. Appl Physiol Nutr Metab, 45 (3): (227-239). [PMID:31173696] |
3. You J et al.. (2021) Role of Adiponectin-Notch pathway in cognitive dysfunction associated with depression and in the therapeutic effect of physical exercise.. Aging Cell, 20 (6): (e13387). [PMID:34053165] |
4. Zhi-shen Xie, Jian-ping Zhao, Li-min Wu, Shuang Chu, Zheng-hao Cui, Yi-ran Sun, Hui Wang, Hui-fen Ma, Dong-rui Ma, Pan Wang, Xiao-wei Zhang, Zhen-qiang Zhang. (2023) Hederagenin improves Alzheimer's disease through PPARα/TFEB-mediated autophagy. PHYTOMEDICINE, 112 (154711). [PMID:36809694] [10.1016/j.phymed.2023.154711] |