93620-52-1 Usage
Uses
Used in Pharmaceutical Industry:
(3S)-3-[[(2S)-2-[[(2S)-2-acetamido-3-carboxy-propanoyl]amino]-3-methyl-butanoyl]amino]-3-[[(1S)-1-carboxyethyl]carbamoyl]propanoic acid is used as a potential drug candidate for the development of new therapeutic agents. Its unique structure and functional groups allow for specific interactions with biological targets, making it a promising candidate for the treatment of various diseases and conditions.
Used in Biochemical Research:
(3S)-3-[[(2S)-2-[[(2S)-2-acetamido-3-carboxy-propanoyl]amino]-3-methyl-butanoyl]amino]-3-[[(1S)-1-carboxyethyl]carbamoyl]propanoic acid is used as a research tool in biochemical studies. Its complex structure and functional groups enable it to be utilized in the investigation of various biological processes and interactions, contributing to a better understanding of molecular mechanisms and potential therapeutic targets.
Used in Drug Development:
(3S)-3-[[(2S)-2-[[(2S)-2-acetamido-3-carboxy-propanoyl]amino]-3-methyl-butanoyl]amino]-3-[[(1S)-1-carboxyethyl]carbamoyl]propanoic acid is used as a starting point for the development of new drugs. Its unique properties and potential for interaction with biological systems make it a valuable compound for the design and synthesis of novel therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 93620-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,2 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93620-52:
(7*9)+(6*3)+(5*6)+(4*2)+(3*0)+(2*5)+(1*2)=131
131 % 10 = 1
So 93620-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H28N4O10/c1-7(2)14(22-16(29)10(5-12(24)25)20-9(4)23)17(30)21-11(6-13(26)27)15(28)19-8(3)18(31)32/h7-8,10-11,14H,5-6H2,1-4H3,(H,19,28)(H,20,23)(H,21,30)(H,22,29)(H,24,25)(H,26,27)(H,31,32)/t8-,10-,11-,14-/m0/s1
93620-52-1Relevant academic research and scientific papers
Etudes des complexes metalliques de Ac-Asp-Val-Asp-Ala-OH par potentiometrie et resonance magnetique nucleaire du 1H
Asso, Marcel,Benlian, David,Asso, Liliane,Granier, Claude
, p. 2379 - 2384 (2007/10/02)
Formation constants for complexes between acetylaspartylvalylaspartylalanine (Ac-DVDA-OH) and a number of transition metal cations have been determined by potentiometric titrations.The 1H nmr spectra have been recorded in order to support the potentiometric results and to obtain information concerning the conformation of the detected species.The praseodymium induced shifts of most resonances are observed to be strongly dependent on pH.The Ca2+ complexes generate a different 1H nmr spectrum for the aspartyl resonances at neutral pH.These observations are shown to be consistent with stepwise binding of the Ca2+ or Pr3+ cations to the carboxylate of Ala C-terminus in acidic medium, and to the carboxylates of aspartyl residues in neutral pH.
