N-Oxydiethylenebenzothiazole-2-sulfenamide

CAS: 102-77-2

Ref. 3D-FO41005

Produktinformation

• Name: N-Oxydiethylenebenzothiazole-2-sulfenamide
• Synonyme: 2(4-Morpholinyl-Thio)-Benzothiazole, 2-(4-Morpholinothiobenzothiazole, 2-(4-Morpholinylmercapto)Benzothiazole, 2-(4-Morpholinylsulfanyl)-1,3-Benzothiazole, 2-(4-Morpholinylthio)Benzothiazole, 2-(Morpholin-4-Ylsulfanyl)-1,3-Benzothiazole, 2-(Morpholinothio)-Benzothiazol, 2-(Morpholinothio)Benzothiazole, 2-(Morpholinthio)-Benzothiazole, 2-Benzothiazolesulfenamide, N-Morpholinyl-, 2-Benzothiazolesulfenemorpholide, 2-Benzothiazolesulfenic acid morpholide, 2-Benzothiazolyl N-morpholino sulfide, 2-Benzothiazolyl-N-morpholinosulfide, 2-Benzothiazolylsufenylmorpholine, 2-Benzothiazolylsulfenyl Morpholine, 2-Benzothiazolylsulfenylmorpholine, 2-Benzothiazyl-N-Morpholine Disulfide, 4-(2-Benzothiazolylthio)-Morpholin, 4-(2-Benzothiazolylthio)morpholine, Accel NS, Accelerator MBS, Accelerator Mf, Accelerator Mor, Accelerator NOBS, Accelerator NS, Accelerator Nobs(Mbs,Mor), Accelns, Acelerator NOBS, Amax No 1, Benzothiazole, 2-(4-Morpholinylthio)-, Benzothiazole, 2-(Morpholinothio, Cure-rite OBTS, Delac MOR, Mbs 80, Meramid M, Morpholine, 4-(2-benzothiazolylthio)-, N,N-(Oxydiethylene)benzothiazole-2-sulfenamide, N-(1,3-benzothiazol-2-ylsulfanyl)morpholin-2-amine, N-(Oxidiethylene)-2-benzothiazolyl sulfenamide, N-(Oxydiethylene)-Benzothiazole-2-Sufenamide, N-Morpholino-2-benzothiazolylsulfenamide, N-Oxydiethyl-2-Benzthiazolsulfenamid, N-Oxydiethyl-2-benzothiazolesulfenamide, N-Oxydiethylene-2-Benzothiazole Sulfonamide, N-Oxydiethylene-2-benzothiazolylsulfenamide, NOBS Special, NSC 70078, Nobs, Nocceler MSA, Nocceler MSA-G, Pilcure MOR, Rhenogran MBS 80, Rubber Accelerator MBS, Rubber Accelerator NOBS, Sanceler NOB, Santocure MBS, Santocure MOR, Soxinol NBS, Sulfenamide M, Sulfenax MOR, Vulcafor BSM, Vulcafor MBS, Vulkacit MOZ, Vulkacit MOZ/LG

Beschreibung

N-Oxydiethylenebenzothiazole-2-sulfenamide is a sealant that has been shown to be effective in vitro against malignant cells. It reacts with the cell nuclei and prevents the production of DNA by interfering with the formation of disulfide bonds. In vivo studies have shown that N-oxydiethylenebenzothiazole-2-sulfenamide is not absorbed into the bloodstream and can be used as an agent for sealing brain lesions. This drug has also been shown to inhibit epidermal growth factor (EGF) and reduce glioma growth in animal models. N-Oxydiethylenebenzothiazole-2-sulfenamide may also have antiangiogenic effects, which may account for its inhibition of EGF.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 252.36 g/mol
• Formel: C₁₁H₁₂N₂OS₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C11H12N2OS2/c1-2-4-10-9(3-1)12-11(15-10)16-13-5-7-14-8-6-13/h1-4H,5-8H2
• InChI Key: InChIKey=MHKLKWCYGIBEQF-UHFFFAOYSA-N
• SMILES: c1ccc2sc(SN3CCOCC3)nc2c1