ATRACTYLOSIDE POTASSIUM SALT
ATRACTYLOSIDE POTASSIUM SALT Basic information
- Product Name:
- ATRACTYLOSIDE POTASSIUM SALT
- Synonyms:
-
- ATR, 2K
- ATRACTYLOSIDE, DIPOTASSIUM SALT
- ATRACTYLOSIDE, DIPOTASSIUM SALT, ATRACTYLIS GUMMIFERA
- ATRACTYLOSIDE POTASSIUM SALT
- 19-Norkaur-16-en-18-oic acid, 15-hydroxy-2-2-O-(3-methyl-1-oxobutyl)-3,4-di-O-sulfo-.beta.-D-glucopyranosyloxy-, dipotassium salt, (2.beta.,15.alpha.)-
- (2beta,15alpha)-15-Hydroxy-2-[[2-O-(3-methyl-1-oxobutyl)-3,4-di-O-sulfo-beta-D-glucopyranosyl]oxy]-19-norkaur-16-en-18-oic acid dipotassium salt
- 19-Norkaur-16-en-18-oicacid, 15-hydroxy-2-[[2-O-(3-Methyl-1-oxobutyl)-3,4-di-O-sulfo-b-D-glucopyranosyl]oxy]-,dipotassiuM salt, (2b,15a)- (9CI)
- Atractyloside dipotassium salt, >=98%
- CAS:
- 102130-43-8
- MF:
- C30H47KO16S2
- MW:
- 766.91
- Product Categories:
-
- reagent
- standard substance
- chemical reagent
- herbal extract
- pharmaceutical intermediate
- phytochemical
- reference standards from Chinese medicinal herbs (TCM).
- Cell Stress
- Mitochondrial Inhibitors
- Nitric Oxide and Cell Stress
- Mol File:
- 102130-43-8.mol
ATRACTYLOSIDE POTASSIUM SALT Chemical Properties
- Melting point:
- 234-238°C
- storage temp.
- Sealed in dry,2-8°C
- solubility
- H2O: 20 mg/mL
- form
- Solid
- color
- Pale Brown to Pale Beige
- Stability:
- Hygroscopic
- InChIKey
- VFOXXOVBJAYRTD-GYBHJGEKNA-N
MSDS
- Language:English Provider:SigmaAldrich
ATRACTYLOSIDE POTASSIUM SALT Usage And Synthesis
Description
Atractyloside is a natural heteroglucoside produced in some plants, including A. gummifera. Atractyloside prevents mitochondrial ATP synthesis by inhibiting ADP/ATP translocases, which are responsible for the exchange of adenine di- and triphosphates across the inner mitochondrial membrane.
Chemical Properties
White crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from Xanthium sibiricum, Atractylodes lancea, and Atractylodes macrocephala.
Uses
Atractyloside Dipotassium Salt is an inhibitor of ANT and apoptosis inducer.
in vivo
Atractyloside (2-4 mg/kg, i.p., 2 weeks before feeding duration ends) potassium salt protects mice against liver steatosis by activation of autophagy via ANT-AMPK-mTORC1 signaling pathway[13].
Atractyloside (50 mg/kg, i.p.) potassium salt produces a tubular nephrosis 180 min after its administration in male albino rats[14].
| Animal Model: | Male ICR wide-type (WT) mice (feed with a high-fat diet (HFD))[13] |
| Dosage: | 2, 4 mg/kg |
| Administration: | Intraperitoneal injection (i.p.), 2 weeks before the feeding duration ends |
| Result: | Reversed the changes of body weight, RW of liver and epididymal fat, and the serum AST level. Improved the NAFLD steatosis and decrease HFD-induced lipid accumulation in the liver. Decreased the protein expression of p-mTOR and the value of p-mTOR/mTOR. Increased the protein expression of LC3A/B-Ⅱ and ATG7. Increased amount of colocalization of LC3B and PLIN2. |
References
[1]. yamaguchi n, kagari t, kasai m. inhibition of the ryanodine receptor calcium channel in the sarcoplasmic reticulum of skeletal muscle by an adp/atp translocase inhibitor, atractyloside. biochem biophys res commun, 1999, 258(2): 247-251.
[2]. pick-kober kh, schneider f. proliferation, macromolecular synthesis and energy metabolism of in vitro grown ehrlich ascites tumor cells after inhibition of atp-adp translocation by atractyloside. eur j cell biol, 1984, 34(2): 323-329.
[3]. malekova l, kominkova v, ferko m, et al. bongkrekic acid and atractyloside inhibits chloride channels from mitochondrial membranes of rat heart. biochim biophys acta, 2007, 1767(1): 31-44.
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