131980-29-5 Usage
Description
BOC-L-3-NITROPHENYLALANINE is a protected derivative of L-Phenylalanine, an essential amino acid that plays a crucial role in the synthesis of other important molecules such as L-tyrosine, L-DOPA, dopamine, norepinephrine, and epinephrine. The BOC-L-3-NITROPHENYLALANINE is specifically designed for use in the photocleavage of polypeptide backbones, making it a valuable tool in various research and industrial applications.
Uses
Used in Peptide Synthesis:
BOC-L-3-NITROPHENYLALANINE is used as a protected amino acid in peptide synthesis for the assembly of polypeptide chains. Its photocleavable property allows for the controlled release of the polypeptide backbone, which is essential in the development of novel therapeutic agents and drug delivery systems.
Used in Research Applications:
BOC-L-3-NITROPHENYLALANINE is used as a research tool in the study of protein structure, function, and dynamics. Its ability to undergo photocleavage enables researchers to investigate the effects of polypeptide backbone cleavage on protein stability, folding, and interactions with other biomolecules.
Used in Drug Development:
BOC-L-3-NITROPHENYLALANINE is used in the development of new drugs and therapeutic agents that target specific proteins or enzymes. Its photocleavable property allows for the design of drugs that can be activated or released upon exposure to light, providing a unique approach to drug delivery and targeting.
Used in Biochemical Assays:
BOC-L-3-NITROPHENYLALANINE is used as a substrate or probe in various biochemical assays to study enzyme activity, specificity, and kinetics. Its unique structure allows for the monitoring of enzyme-catalyzed reactions and the development of assays to evaluate the potency and selectivity of potential drug candidates.
Used in Chemical Synthesis:
BOC-L-3-NITROPHENYLALANINE is used as a building block in the synthesis of complex organic molecules and bioactive compounds. Its versatile chemical properties enable the development of novel synthetic routes and the creation of new molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 131980-29-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,9,8 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 131980-29:
(8*1)+(7*3)+(6*1)+(5*9)+(4*8)+(3*0)+(2*2)+(1*9)=125
125 % 10 = 5
So 131980-29-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2O6/c1-14(2,3)22-13(19)15-11(12(17)18)8-9-5-4-6-10(7-9)16(20)21/h4-7,11H,8H2,1-3H3,(H,15,19)(H,17,18)/t11-/m1/s1
131980-29-5Relevant articles and documents
Compounds and Methods for Inhibiting the Interaction of BCL Proteins with Binding Partners
-
Page/Page column 180, (2008/12/05)
The invention relates to isoxazolidine containing compounds that bind to bcl proteins and inhibit Bcl function. The compounds may be used for treating and modulating disorders associated with hyperproliferation, such as cancer.
Gonadotropin-Releasing Hormone Antagonists: Novel Members of the Azaline B Family
Rivier, Jean E.,Jiang, Guangcheng,Porter, John,Hoeger, Carl A.,Craig, A. Grey,et al.
, p. 2649 - 2662 (2007/10/03)
A series of antagonists of gonadotropin-releasing hormone (GnRH) homologous to azaline B (1, DCpa2, DPal3, Aph5(Atz), DAph6(Atz), ILys8, DAla10>GnRH) was synthesized, cha
