Carboxyatractyloside tripotassium
Based on 2 publication(s) in Google Scholar
Carboxyatractyloside tripotassium is a diterpenoid. Carboxyatractyloside tripotassium can be isolated from plants of the genus Xanthium. Carboxyatractyloside tripotassium is an ADP/ATP carrier inhibitor, inhibiting mitochondrial ADP/ATP transport. Carboxyatractyloside tripotassium promotes ROS production, induces Ca2+ release, and leads to mitochondrial dysfunction. Carboxyatractyloside tripotassium induces lethargy, weakness, and epileptic seizures in rats.
For research use only. We do not sell to patients.
- Purity: 99.97%
- CAS No.: 77228-71-8
- Formula: C31H43K3O18S2
- Molecular Weight:885.09
-
Storage:
-20°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
Publications Citing Use of MedChemExpress (MCE) Carboxyatractyloside tripotassium
More-
IP
-
Cell Proliferation/Viability Assay
-
Flow Cytometry
-
IHC
-
IF
All Calcium Channel Isoforms
More
Biological Activity
Carboxyatractyloside (10-25 μM; 48 h) tripotassium promotes cell death in primary mouse lung endothelial cells and exacerbates mitochondrial dysfunction, including mitochondrial depolarization, increased ROS generation, and MPT pore opening[2].
Carboxyatractyloside (2 μM) tripotassium induces Ca2+ release, mitochondrial swelling, and membrane potential collapse in aged rat liver mitochondria[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 77228-71-8
-
Appearance Solid
-
Molecular Weight 885.09
-
Formula C31H43K3O18S2
-
Color White to off-white
-
SMILES
C=C([C@H](CC1)C2)[C@H](O)[C@@]32CC[C@]4([H])[C@@](C(O)=O)(C(O[K])=O)C[C@@H](O[C@@H]5[C@H]([C@@H]([C@H]([C@H](CO)O5)OS(=O)(O[K])=O)OS(=O)(O[K])=O)OC(CC(C)C)=O)C[C@@]4(C)[C@@]31[H]
-
Synonyms
Gummiferin tripotassium
-
Structure Classification
-
Initial Source
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
-20°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
Publications (2)
-
Journal Impact Factor
-
Most Recent
-
Redox Biol
Redistribution of defective mitochondria-mediated dihydroorotate dehydrogenase imparts 5-fluorouracil resistance in colorectal cancer. [Abstract]2024 Jul:73:103207. PMID: 38805974 -
EMBO Mol Med
Conformational change of adenine nucleotide translocase-1 mediates cisplatin resistance induced by EBV-LMP1. [Abstract]2021 Dec 7;13(12):e14072. PMID: 34755470
Carboxyatractyloside tripotassium purchased from MedChemExpress. Usage Cited in: EMBO Mol Med. 2021 Dec 7;13(12):e14072. [Abstract]
Effect of inhibitors BKA and Carboxyatractyloside tripotassium (CATR) (5, 10, 20 nM) on ANT1‐VDAC1 binding in 293T cells.
Carboxyatractyloside tripotassium purchased from MedChemExpress. Usage Cited in: EMBO Mol Med. 2021 Dec 7;13(12):e14072. [Abstract]
CCK‐8 analysis of viability in HK1‐LMP1 cells treated for 24 h with Carboxyatractyloside tripotassium (CATR) (1 μM) alone, cisplatin (20 μM) alone, or cisplatin (20 μM) combined with CATR (1 μM).
Carboxyatractyloside tripotassium purchased from MedChemExpress. Usage Cited in: EMBO Mol Med. 2021 Dec 7;13(12):e14072. [Abstract]
Flow cytometry analysis of death of NPC cells treated for 24 h with CATR (1 μM) alone, Cisplatin (20 μM) alone, or Cisplatin (20 μM) combined with Carboxyatractyloside tripotassium (CATR) (1 μM).
Carboxyatractyloside tripotassium purchased from MedChemExpress. Usage Cited in: EMBO Mol Med. 2021 Dec 7;13(12):e14072. [Abstract]
Immunohistochemistry examination of the protein levels of Ki67 treated with Carboxyatractyloside tripotassium (CATR) (1 mg/kg, i.p.).
Carboxyatractyloside tripotassium purchased from MedChemExpress. Usage Cited in: EMBO Mol Med. 2021 Dec 7;13(12):e14072. [Abstract]
Apoptosis was analyzed by TUNEL assay treated with Carboxyatractyloside tripotassium (CATR) (1 μM).
Solvent & Solubility
H2O : ≥ 50 mg/mL (56.49 mM)
* "≥" means soluble, but saturation unknown.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Purity & Documentation
-
Data Sheet (283 KB)
-
SDS (480 KB)
- English - EN (480 KB)
- Français - FR (480 KB)
- Deutsch - DE (480 KB)
- Norwegian - NO (480 KB)
- Español - ES (480 KB)
- Swedish - SV (480 KB)
- Italian - IT (480 KB)
- Korean - KR (480 KB)
- Portuguese - PT (480 KB)
-
Handling Instructions (2659 KB)
References
[1]. Ri M, et al. Identification of Toyocamycin, an agent cytotoxic for multiple myeloma cells, as a potent inhibitor of ER stress-induced XBP1 mRNA splicing. Blood Cancer J. 2012 Jul;2(7):e79. [Content Brief]
[2]. Belosludtseva NV, et al. ANT-Mediated Inhibition of the Permeability Transition Pore Alleviates Palmitate-Induced Mitochondrial Dysfunction and Lipotoxicity. Biomolecules. 2024 Sep 15;14(9):1159. [Content Brief]
[3]. García N, et al. Cyclosporin A is unable to inhibit carboxyatractyloside-induced permeability transition in aged mitochondria. Comp Biochem Physiol C Toxicol Pharmacol. 2009 Apr;149(3):374-81. [Content Brief]
[4]. Luciani S, et al. Effects of carboxyatractyloside a structural analogue of atractyloside on mitochondrial oxidative phosphorylation. Life Sci II. 1971 Sep 8;10(17):961-8. [Content Brief]
[5]. Hatch RC, et al. Toxicologic study of carboxyatractyloside (active principle in cocklebur--Xanthium strumarium) in rats treated with enzyme inducers and inhibitors and glutathione precursor and depletor. Am J Vet Res. 1982 Jan;43(1):111-6. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| H2O | 1 mM | 1.1298 mL | 5.6491 mL | 11.2983 mL | 28.2457 mL |
| 5 mM | 0.2260 mL | 1.1298 mL | 2.2597 mL | 5.6491 mL | |
| 10 mM | 0.1130 mL | 0.5649 mL | 1.1298 mL | 2.8246 mL | |
| 15 mM | 0.0753 mL | 0.3766 mL | 0.7532 mL | 1.8830 mL | |
| 20 mM | 0.0565 mL | 0.2825 mL | 0.5649 mL | 1.4123 mL | |
| 25 mM | 0.0452 mL | 0.2260 mL | 0.4519 mL | 1.1298 mL | |
| 30 mM | 0.0377 mL | 0.1883 mL | 0.3766 mL | 0.9415 mL | |
| 40 mM | 0.0282 mL | 0.1412 mL | 0.2825 mL | 0.7061 mL | |
| 50 mM | 0.0226 mL | 0.1130 mL | 0.2260 mL | 0.5649 mL |
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.