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| Product | Description | |
|---|---|---|
| Sodium Adipate | Sodium Adipate. CAS No. 7486-38-6. Molecular formula: Na2C6H8O4. |  |
| CL-316243 | CL-316243 is a potent and highly selective β3-adrenoceptor agonist (EC50 = 3 nM) with > 10000-fold selective over β1 and β2 receptors. CL 316243 possesses anti-obesity and anti-diabetic effects due to increasing brown adipose tissue thermogenesis and metabolic rate, and consequently may be useful for treating obesity as well as non-insulin-dependent diabetes mellitus in obese persons, without causing excessive side effects. Synonyms: CL-316243; CL 316243; CL316243; 5-[(2R)-2-[[(2R)-2-(3-chlorophenyl)-2-hydroxyethyl]amino]propyl]-1,3-benzodioxole-2,2-dicarboxylate; 138908-40-4 (CL-316243 sodium). Grades: >98%. CAS No. 183720-02-7. Molecular formula: C20H20ClNNa2O7. Mole weight: 419.794. |  |
| Cloprostenol sodium | Cloprostenol sodium is a synthetic and water-soluble aryl-oxymethyl analog of prostaglandin F2&alpha. lt is also a potent inhibitor of rat adipose precursor differentiation in primary cultures. It has luteolytic effects and is used for the synchronization of estrus in cattle. It is also used for the treatment of infertility in sows and gilts. Uses: Luteolytic agents. Synonyms: ICI 80996; ICI-80996; ICI 80996; ICI 80,996; ICI-80,996; ICI 80,996; DL-Cloprostenol sodium; Estroplan; Estrumate;DL-Cloprostenol sodium;Estroplan;Estrumate;sodium (Z)-7-(2-((E)-4-(3-chlorophenoxy)-3-hydroxybut-1-en-1-yl)-3,5-dihydroxycyclopentyl)hept-5-enoate;5-Heptenoicacid,7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-butenyl]-3,5-. Grades: >98%. CAS No. 55028-72-3. Molecular formula: C22H28ClNaO6. Mole weight: 446.9. | |
| Docusate Sodium | Docusate Sodium (Dioctyl sulfosuccinate sodium salt) is one of the main components in stool softeners. Docusate Sodium is a sulfated surfactant and may inactivate viral pathogens by disrupting viral envelopes and/or denaturing/disassociating proteins. Docusate Sodium is effective in vitro against wild type and drug-resistant strains of HSV type 1 and 2. Docusate Sodium is an obesogen. Docusate Sodium with developmental exposure leads to increased adult adiposity, inflammation, metabolic disorder and dyslipidemia in offspring fed a standard diet in mice [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Dioctyl sulfosuccinate sodium salt. CAS No. 577-11-7. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B1268. |  |
| Humic acid sodium salt | Sodium humate is made from natural lignite or leonardite, appears in black powder, granule and flake, it has been widely used in animal feed additive, aquiculture, industry as well as agriculture. Uses: Humic acid sodium salt is suitable reagent used to study the hygroscopic growth of solid aerosol particles consisting of mixtures of ammonium sulfate, adipic acid and humic acid mixtures. it is suitable reagent used to study the phase transitions and hygroscopic growth of humic acid aerosols by fourier transform infra-red (ftir) spectroscopy and tandem differential mobility analysis (tdma). Group: Heterocyclic organic compound. CAS No. 68131-04-4. Molecular formula: C9H8Na2O4. Mole weight: 226.13696. ECNumber: 268-608-0. Catalog: ACM68131044. |  |
| Okadaic acid sodium salt (high purity) (Halochondrine A, CCRIS 3329, HSDB 7243, 9, 10-Deepithio-9, 10-dide hydroacanthifolicin) | Non-phorbol type tumor promoter. Reversible, potent and selective serine threonine protein phosphatase inhibitor. PP2A (IC50=0. 2-1nM), PP1 (IC50=3-15nM), PP2B (IC50=>1µM). Does not inhibit PP2C. Stimulates intracellular protein phosphorylation. Useful tool for studying cellular processes that are regulated by phosphorylation. Does not affect activity of acid phosphatase, alkaline phosphatase and tyrosine phosphatase. Mimics the effects of insulin. Activates atypical protein kinase C (zeta/lambda) in 3T3/L1 adipocytes. Enhances transmitter release at neuromuscular junctions. Apoptosis inhibitor. Induces apoptosis in human breast carcinoma cells (MB-231 and MCF-7) and in myeloid cells. Neurotoxic. Used to study various cellular processes including cell cycle, apoptosis, nitric oxide metabolism and calcium signaling. Stimulates cell motility, loss of stabilization of focal adhesions and a consequent loss of cytoskeletal organization. Group: Biochemicals. Alternative Names: Halochondrine A, CCRIS 3329, HSDB 7243, 9, 10-Deepithio-9, 10-dide hydroacanthifolicin. Grades: Highly Purified. CAS No. 209266-80-8. Pack Sizes: 25ug, 100ug. US Biological Life Sciences. |  Worldwide |
| Sodium Ascorbyl Phosphate | Sodium Ascorbyl Phosphate. Synonyms: L-Ascorbic acid 2-phosphate trisodium salt, Sodium L-ascorbyl-2-phosphate. CAS No. 66170-10-3. Pack Sizes: 100 g ,1 kg. Product ID: CDC10-0069. Molecular formula: C6H6O9Na3P. Category: Antioxidant Cosmetic Chemicals. Product Keywords: Cosmetic Ingredients; Antioxidant Cosmetic Chemicals; Sodium Ascorbyl Phosphate; CDC10-0069; 66170-10-3; C6H6O9Na3P; L-Ascorbic acid 2-phosphate trisodium salt, Sodium L-ascorbyl-2-phosphate; MFCD03095479; 66170-10-3. Purity: 0.99. Color: White to off-white. Physical State: Powder. Solubility: Acidic DMSO (Slightly), Water (Slightly). Quality Level: 200. Storage: Inert atmosphere,Room Temperature. Application: 2-Phospho-L-ascorbic acid trisodium salt has been used as medium supplement in Dulbecco's Modified Eagle Medium (DMEM) for adipose-derived stem cells, human mesenchymal stem cells and osteoblast cells. Boiling Point: N/A. Melting Point: 260 °C. Product Description: L-Ascorbic acid 2-phosphate trisodium salt, Sodium L-ascorbyl-2-phosphate. |  |
| Stavudine sodium | Stavudine sodium is a dideoxynucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV. Stavudine sodium is an analog of thymidine. It is phosphorylated by cellular kinases into active triphosphate. Stavudine sodium triphosphate inhibits the HIV reverse transcriptase by competing with natural substrate, thymidine triphosphate. It also causes termination of DNA synthesis by incorporating into it. Mice were treated for 2 weeks with stavudine d4T (500 mg/kg/day), L-carnitine (200 mg/kg/day) or both drugs concomitantly. Body fatness was assessed by dual energy X-ray absorptiometry, and investigations were performed in plasma, liver, muscle and WAT. D4T reduced the gain of body adiposity, WAT leptin, whole body FAO and plasma ketone bodies, and increased liver triglycerides and plasma aminotransferases with mild ultrastructural abnormalities in hepatocytes. Synonyms: Zerit sodium; d4T sodium. Grades: >98%. CAS No. 134624-73-0. Molecular formula: C10H11N2NaO4. Mole weight: 246.2. | |
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