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Acetic acid (3R,4R,5S,6S)-4,5-diacetoxy-6-methyl-2-phenylamino-tetrahydro-pyran-3-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

913057-17-7

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913057-17-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913057-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,0,5 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 913057-17:
(8*9)+(7*1)+(6*3)+(5*0)+(4*5)+(3*7)+(2*1)+(1*7)=147
147 % 10 = 7
So 913057-17-7 is a valid CAS Registry Number.

913057-17-7Relevant articles and documents

Synthesis of indirubin-N′-glycosides and their anti-proliferative activity against human cancer cell lines

Libnow, Stefanie,Methling, Karen,Hein, Martin,Michalik, Dirk,Harms, Manuela,Wende, Kristian,Flemming, Anke,Koeckerling, Martin,Reinke, Helmut,Bednarski, Patrick J.,Lalk, Michael,Langer, Peter

, p. 5570 - 5583 (2008)

The first indirubin-N′-glycosides were prepared based on reactions of isatin-N′-glycosides with indoxyls. The products show a significant anti-proliferative activity against various human cancer cell lines. Good results were observed for an indirubin-N′-mannoside which was shown to have medium to high anti-proliferative activity against all investigated cell lines. The highest activities and selectivities against the MCF-7 breast cancer cell line were observed for indirubin-N′-rhamnosides.

Synthesis and bioactivity of N-glycosylated 3-(2-oxo-2-arylethylidene)-indolin-2-ones

Kleeblatt, Dennis,Becker, Martin,Pl?tz, Michael,Sch?nherr, Madeleine,Villinger, Alexander,Hein, Martin,Eberle, Jürgen,Kunz, Manfred,Rahman, Qamar,Langer, Peter

, p. 20769 - 20782 (2015/03/30)

N-Glycosyl-3-alkylideneoxindoles, N-glycosylated 3-(2-oxo-2-arylethylidene)indolin-2-ones, were prepared by reaction of isatin-N-glycosides with substituted acetophenones. The biological activities of these new compounds revealed significant antitumor act

Synthesis and antiproliferative activity of N-glycosyl-3,3-diaryloxindoles

Kleeblatt, Dennis,Cordes, Christoph A.,Lebrenz, Philipp,Hein, Martin,Feist, Holger,Matin, Abdul,Raza, Rabia,Iqbal, Jamshed,Munshi, Omar,Rahman, Qamar,Villinger, Alexander,Langer, Peter

, p. 22828 - 22839 (2014/06/24)

N-Glycosylated 3,3-diaryloxindoles were prepared by Lewis acid catalyzed reaction of acetylated N-glycosylisatins with various benzene derivatives and subsequent deprotection. Some of the products showed antiproliferative activity against malignant cutane

Synthesis of N,N′-diglycosylated isoindigos

Kleeblatt, Dennis,Siyo, Baraa,Hein, Martin,Iaroshenko, Viktor O.,Iqbal, Jamshed,Villinger, Alexander,Langer, Peter

, p. 886 - 895 (2013/02/26)

The first N,N′-diglycosylated isoindigos were prepared by P(NEt 2)3-mediated dimerization of acetyl protected N-glycosyl-5-alkylisatins. Subsequent deacetylation yielded the corresponding deprotected N,N′-diglycosylated isoindigos. I

Synthesis and antiproliferative activity of selenoindirubins and selenoindirubin-N-glycosides

Erben, Friedrich,Kleeblatt, Dennis,Sonneck, Marcel,Hein, Martin,Feist, Holger,Fahrenwaldt, Thomas,Fischer, Christine,Matin, Abdul,Iqbal, Jamshed,Pl?tz, Michael,Eberle, Jürgen,Langer, Peter

, p. 3963 - 3978 (2013/07/11)

Selenoindirubins and selenoindirubin-N-glycosides were prepared by the reaction of isatins and isatin-N-glycosides with 3-acetoxy-benzo[b]selenophene, respectively. While selenoindirubin-N-glycosides have not been reported before, three non-glycosylated s

Synthesis of thia-analogous indirubin n-glycosides and their influence onmelanoma cell growth and apoptosis

Kunz, Manfred,Driller, Katrin M.,Hein, Martin,Libnow, Stephanie,Hohensee, Ina,Ramer, Robert,Hinz, Burkhard,Berger, Anja,Eberle, Juergen,Langer, Peter

scheme or table, p. 534 - 539 (2010/12/25)

Stopping cancer in its tracks Thia-analogues of indirubin-N-glycosides, prepared by condensation of N-glycosylisatines with thiaindane-3-one and subsequent deprotection, were tested for their activity against malignant melanoma cells. These indirubin-N-gl

First synthesis of oxa-analogous isoindigo-N-glycosides

Libnow, Stefanie,Hein, Martin,Langer, Peter

, p. 289 - 291 (2008/03/30)

Lactone-analogues of isoindigo-N-glycosides were prepared by condensation of N-glycosylisatines with 2-coumaranone and subsequent deprotection.

First synthesis of indirubin N-glycosides (red sugars)

Libnow, Stefanie,Hein, Martin,Michalik, Dirk,Langer, Peter

, p. 6907 - 6909 (2007/10/03)

The first indirubin N-glycosides were prepared by reaction of isatine N-glycosides with indoxyl acetate under basic conditions.

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