product name product origin purity grade use product code C.A.S. number MDL EINECS ID PubChem NACRES formula molecular molecular weight assay (unspecified) quality level sensitivity & storage solubility appearance (color) form general description x x x x applications x x x x x x x x x x x x x x notes x shelf lifex packaging/transport certifications
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Suramin Hexasodium Salt , ACS - sterilized 100% made in European Union (according to USP, EUP, ECHA-REACH) >99.99+% min. (raw virgin matter, ultra-pure) lab. / tech / pharma / bio-research EA61707 129-46-4 MFCD00210217 204-949-3 24277738 NA.25 C51H34N6Na6O23S6 1429.16 >99.99% to <101.5% 200 store in cool place; keep container tightly closed in a dry and well-ventilated place *5 °C/25 °C in water and saline (turbidity) <15% (H2O >10 mg/ml); sparingly soluble in 95% bethanol white to pale cream powder Suramin is a antiparasitic drug , which blocks endothelial cell proliferation and increases tyrosine phosphorylation of many signalling proteins; associated with urticaria, paresthesias, vomitino and neurologic toxicity; is used also to treat trypanosomiasis and onchocerciasis; to functions as an heparanase inhibitor and also exhibits anti-AIDS (acquired immunodeficiency syndrome) property ; also studied for the treatment of autism . Suramin Sodium salt has been used : - as a potent blocker of rat P2Y2 purinergic receptor ; - to study it's effects on short circuit current (lsc) acress strial marginal cells ; - to show it's effects on initial burst of glial activity ; - to assess it's neuroprotective potential in rats ; - as a purinoceptor inhibitor, to explore the mechanism of action of extracellular adenosine - triphosphate (eATP) . Suramin Sodium has been observed as a potent inhibitor of melanoma HPA (heparanase) and tumor cell metastasis; inhibition of NAD+-dependent deacetylase SIRT1 with an IC50 of 2.6 ?M along with SIRT5 has also been observed; Suramin Sodium has been recorded to antagonize EDG-3 (S1P3) selectively; Suramin Sodium is an inhibitor of A cyclase, FGF-1, FGF-2, IL-1, IL-4, PDGF, PC-PLD, PKC, SH-PTP, TERT, TGF beta 1, Topo I, Topo II and VEGF ; it is used as a G protein uncoupler and inhibitor of PDGF, EGF, TGF-β, SIRT1 and SIRT5; it also blocks calmodulin binding to recognition sites and G protein coupling to G protein-coupled receptors; increases open probability of ryanodine receptor (RyR) channels ; anticancer and antiviral agent store in cool place ; keep container tightly closed in a dry and well-ventilated place *(1) ; keep away from strong oxidizing agents *(1) ; 2 (two) years from production date (sealed package), * shipped in ambient (1) . special for chemicals transport (according to IATA / ADR / ECHA-REACH rules / int.l laws). C.O.A., MSDS, GMP, API, USP, EUP, ECHA-REACH, ORIGIN, etc... (originals will be delivered with good , and copies after confirmed order )
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