68802-93-7 Usage
Uses
Used in Biochemical Research:
(S)-2-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexanoylamino)-3-methyl-butyric acid is used as a research tool for studying the structure and function of natural peptides and proteins. Its unique arrangement of functional groups allows scientists to investigate various biological processes and interactions.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (S)-2-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexanoylamino)-3-methyl-butyric acid is used as a potential therapeutic agent. Its complex structure and functional groups make it a promising candidate for the development of new drugs and treatments, particularly for conditions that may be targeted by mimicking or modulating the action of specific peptides or proteins.
Used in Drug Development:
(S)-2-((S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-hexanoylamino)-3-methyl-butyric acid is utilized in the development of novel drugs due to its potential therapeutic properties. Its precise structure and functional groups can be tailored to target specific biological pathways or receptors, making it a valuable asset in the creation of new medications for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 68802-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,0 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68802-93:
(7*6)+(6*8)+(5*8)+(4*0)+(3*2)+(2*9)+(1*3)=157
157 % 10 = 7
So 68802-93-7 is a valid CAS Registry Number.
68802-93-7Relevant academic research and scientific papers
Bahadduri, Praveen M.,Ray, Abhijit,Khandelwal, Akash,Swaan, Peter W.
, p. 2555 - 2557 (2008)
We employed a computational approach to design and synthesize a series of fluorescently labeled hPEPT1 substrates. Five Alexa Fluor-350-labeled peptides were assessed for their in vitro inhibitory activity in hPEPT1-transfected CHO cells. At least four labeled peptides show potent inhibitory activity toward hPEPT1-mediated uptake of [3H]-GlySar and three compounds displayed a significant cellular uptake specifically mediated by hPEPT1.
