73684-59-0 Usage
Uses
Used in Pharmaceutical Industry:
N-tert-Butoxycarbonyl Acivicin is used as a protected form of Acivicin for the development of anti-cancer drugs. It offers enhanced stability and bioavailability, allowing for more effective delivery to cancer cells and improved therapeutic outcomes.
Used in Oncology Research:
N-tert-Butoxycarbonyl Acivicin is used as a research tool in oncology to study the mechanisms of action and potential applications of Acivicin in the treatment of various types of cancer. Its ability to cross the blood-brain barrier makes it particularly valuable for research into brain cancer and other malignancies that are difficult to target with conventional treatments.
Used in Drug Delivery Systems:
N-tert-Butoxycarbonyl Acivicin is used in the development of drug delivery systems to improve the efficacy and safety of Acivicin-based therapies. By protecting the active compound and enhancing its bioavailability, N-tert-Butoxycarbonyl Acivicin can help to overcome limitations associated with the direct use of Acivicin, such as poor solubility and potential side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 73684-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,8 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 73684-59:
(7*7)+(6*3)+(5*6)+(4*8)+(3*4)+(2*5)+(1*9)=160
160 % 10 = 0
So 73684-59-0 is a valid CAS Registry Number.
73684-59-0Relevant academic research and scientific papers
PRODRUGS OF GLUTAMINE ANALOGS
-
, (2018/08/26)
Prodrugs of glutamine analogs, such as prodrugs of acivicin, are disclosed.
A novel simplified synthesis of acivicin
Pinto, Andrea,Conti, Paola,Tamborini, Lucia,Micheli, Carlo De
experimental part, p. 508 - 511 (2009/07/18)
This report describes an efficient synthesis of the natural isomer of acivicin, which is the only one provided with a noteworthy biological activity. The present procedure allowed the synthesis of (+)-1 in just five steps with a 34% overall yield. Due to
