173240-66-9 Usage
Description
[(3S)-oxolan-3-yl] N-[(2S,3S)-4-[(2S)-2-benzyl-4-[(2S)-4-[(1R)-1-carbamoyl-2-phenyl-ethyl]-2-(2-methylpropyl)-3-oxo-1H-pyrrol-2-yl]-3-oxo-1H-pyrrol-2-yl]-3-hydroxy-1-phenyl-butan-2-yl]carbamate is a complex organic molecule with a unique arrangement of functional groups and stereochemistry. It features an oxolan-3-yl group, a carbamate group, multiple pyrrol-2-yl groups, a benzyl group, a phenyl group, and a hydroxy group. The presence of these groups and the chiral center in the molecule contribute to its overall structure and properties.
Uses
1. Used in Pharmaceutical Industry:
[(3S)-oxolan-3-yl] N-[(2S,3S)-4-[(2S)-2-benzyl-4-[(2S)-4-[(1R)-1-carbamoyl-2-phenyl-ethyl]-2-(2-methylpropyl)-3-oxo-1H-pyrrol-2-yl]-3-oxo-1H-pyrrol-2-yl]-3-hydroxy-1-phenyl-butan-2-yl]carbamate is used as a potential therapeutic agent for various medical conditions due to its complex structure and multiple functional groups.
2. Used in Chemical Research:
[(3S)-oxolan-3-yl] N-[(2S,3S)-4-[(2S)-2-benzyl-4-[(2S)-4-[(1R)-1-carba moyl-2-phenyl-ethyl]-2-(2-methylpropyl)-3-oxo-1H-pyrrol-2-yl]-3-oxo-1H -pyrrol-2-yl]-3-hydroxy-1-phenyl-butan-2-yl]carbamate can be utilized in chemical research for studying the effects of different functional groups and stereochemistry on the molecule's properties and reactivity. It can also be used as a starting material for the synthesis of other complex organic molecules.
3. Used in Material Science:
The unique structure and properties of [(3S)-oxolan-3-yl] N-[(2S,3S)-4-[(2S)-2-benzyl-4-[(2S)-4-[(1R)-1-carbamoyl-2-phenyl-ethyl]-2-(2-methylpropyl)-3-oxo-1H-pyrrol-2-yl]-3-oxo-1H-pyrrol-2-yl]-3-hydroxy-1-phenyl-butan-2-yl]carbamate make it a candidate for the development of new materials with specific properties, such as novel polymers or coatings.
4. Used in Drug Delivery Systems:
Similar to gallotannin, this complex molecule could potentially be employed in drug delivery systems to improve the delivery, bioavailability, and therapeutic outcomes of various drugs. The development of novel organic and metallic nanoparticles as carriers for this compound could enhance its applications in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 173240-66-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,2,4 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 173240-66:
(8*1)+(7*7)+(6*3)+(5*2)+(4*4)+(3*0)+(2*6)+(1*6)=119
119 % 10 = 9
So 173240-66-9 is a valid CAS Registry Number.
InChI:InChI=1/C43H50N4O7/c1-28(2)22-43(38(49)34(25-46-43)33(40(44)51)20-29-12-6-3-7-13-29)35-26-45-42(39(35)50,23-31-16-10-5-11-17-31)24-37(48)36(21-30-14-8-4-9-15-30)47-41(52)54-32-18-19-53-27-32/h3-17,25-26,28,32-33,36-37,45-46,48H,18-24,27H2,1-2H3,(H2,44,51)(H,47,52)/t32-,33+,36-,37-,42-,43-/m0/s1
173240-66-9Relevant articles and documents
Pyrrolinone-based HIV protease inhibitors. Design, synthesis, and antiviral activity: Evidence for improved transport
Smith III, Amos B.,Hirschmann, Ralph,Pasternak, Alexander,Guzman, Mark C.,Yokoyama, Akihisa,Sprengeler, Paul A.,Darke, Paul L.,Emini, Emilio A.,Schleif, William A.
, p. 11113 - 11123 (2007/10/03)
Pyrrolinone-based peptidomimetics, the first mimics of β-strands, are potent inhibitors of HIV-1 protease. Importantly, the bis(pyrrolinones) described herein proved to be more active in cellular antiviral assays compared with an analogous peptide-derived
