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2-Methylsulfanyl-benzothiazole-6-sulfonic acid ((2R,3S)-3-amino-2-hydroxy-4-phenyl-butyl)-isobutyl-amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

473739-27-4

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473739-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 473739-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,7,3 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 473739-27:
(8*4)+(7*7)+(6*3)+(5*7)+(4*3)+(3*9)+(2*2)+(1*7)=184
184 % 10 = 4
So 473739-27-4 is a valid CAS Registry Number.

473739-27-4Relevant academic research and scientific papers

Design and Development of Highly Potent HIV-1 Protease Inhibitors with a Crown-Like Oxotricyclic Core as the P2-Ligand To Combat Multidrug-Resistant HIV Variants

Ghosh, Arun K.,Rao, Kalapala Venkateswara,Nyalapatla, Prasanth R.,Osswald, Heather L.,Martyr, Cuthbert D.,Aoki, Manabu,Hayashi, Hironori,Agniswamy, Johnson,Wang, Yuan-Fang,Bulut, Haydar,Das, Debananda,Weber, Irene T.,Mitsuya, Hiroaki

, p. 4267 - 4278 (2017)

Design, synthesis, and evaluation of a new class of exceptionally potent HIV-1 protease inhibitors are reported. Inhibitor 5 displayed superior antiviral activity and drug-resistance profiles. In fact, this inhibitor showed several orders of magnitude improved antiviral activity over the FDA approved drug darunavir. This inhibitor incorporates an unprecedented 6-5-5 ring-fused crown-like tetrahydropyranofuran as the P2 ligand and an aminobenzothiazole as the P2′ ligand with the (R)-hydroxyethylsulfonamide isostere. The crown-like P2 ligand for this inhibitor has been synthesized efficiently in an optically active form using a chiral Diels-Alder catalyst providing a key intermediate in high enantiomeric purity. Two high resolution X-ray structures of inhibitor-bound HIV-1 protease revealed extensive interactions with the backbone atoms of HIV-1 protease and provided molecular insight into the binding properties of these new inhibitors.

Design of HIV-1 protease inhibitors active on multidrug-resistant virus

Surleraux, Dominique L. N. G.,De Kock, Herman A.,Verschueren, Wim G.,Pille, Geert M. E.,Maes, Louis J. R.,Peeters, Anik,Vendeville, Sandrine,De Meyer, Sandra,Azijn, Hilde,Pauwels, Rudi,De Bethune, Marie-Pierre,King, Nancy M.,Prabu-Jeyabalan, Moses,Schiffer, Celia A.,Wigerinck, Piet B. T. P.

, p. 1965 - 1973 (2007/10/03)

On the basis of structural data gathered during our ongoing HIV-1 protease inhibitors program, from which our clinical candidate TMC114 9 was selected, we have discovered new series of fused heteroaromatic sulfonamides. The further extension into the P2′

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