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Chemical Structure
GYY 4137 [106740-09-4]
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AG-CR1-3513
CAS Number106740-09-4
Product group Chemicals
Estimated Purity>95%
Molecular Weight288.4 . 87.1
Overview
- SupplierAdipoGen Life Sciences
- Product NameGYY 4137
- Delivery Days Customer10
- CAS Number106740-09-4
- CertificationResearch Use Only
- Estimated Purity>95%
- Molecular FormulaC11H16NO2PS2 . C4H9NO
- Molecular Weight288.4 . 87.1
- Scientific DescriptionChemical. CAS: 106740-09-4. Formula: C11H16NO2PS2 . C4H9NO. MW: 288.4 . 87.1. Water-soluble, slow-releasing hydrogen sulfide (H2S) donor. Exhibits vasodilator and antihypertensive activity. Anti-inflammatory. Inhibits LPS-induced release of proinflammatory mediators (IL-1beta, IL-6, TNF-alpha, nitric oxide (NO) and PGE2) and increases the synthesis of the anti-inflammatory chemokine IL-10 through NF-kappaB, ATF-2 and HSP27 dependent pathways. Causes stomatal opening and reduces nitric oxide accumulation in plants. Oxidative stress-induced cell death inhibitor. Shows novel anti-cancer effects in vitro and in vivo. Anti-thrombotic via p-selectin dependent mechanism. - Water-soluble, slow-releasing hydrogen sulfide (H2S) donor [1]. Exhibits vasodilator and antihypertensive activity [1, 2, 4]. Anti-inflammatory [2, 3]. Inhibits LPS-induced release of proinflammatory mediators (IL-1beta, IL-6, TNF-alpha, nitric oxide (NO) and PGE2) and increases the synthesis of the anti-inflammatory chemokine IL-10 through NF-kappaB, ATF-2 and HSP27 dependent pathways [2, 3]. Causes stomatal opening and reduces nitric oxide accumulation in plants [5]. Oxidative stress-induced cell death inhibitor [6]. Shows novel anti-cancer effects in vitro and in vivo [7]. Anti-thrombotic via p-selectin dependent mechanism [8].
- SMILESC1COCC[NH2+]1.COC1=CC=C(C=C1)P([S-])(=S)N1CCOCC1
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC12352200