1235280-35-9 Usage
General Description
(R)-N-Acetyl-6-Chloro-Trp-OMe is a chemical compound consisting of a modified form of the amino acid tryptophan. It contains an acetyl group and a chloro group attached to the tryptophan molecule. (R)-N-Acetyl-6-Chloro-Trp-OMe is often used in research and pharmaceutical applications, particularly in the study of bioactive peptides and the development of new drugs. It may have potential therapeutic properties due to its ability to interact with biological systems and influence various cellular processes. The specific functions and potential applications of (R)-N-Acetyl-6-Chloro-Trp-OMe continue to be investigated in various scientific studies.
Check Digit Verification of cas no
The CAS Registry Mumber 1235280-35-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,5,2,8 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1235280-35:
(9*1)+(8*2)+(7*3)+(6*5)+(5*2)+(4*8)+(3*0)+(2*3)+(1*5)=129
129 % 10 = 9
So 1235280-35-9 is a valid CAS Registry Number.
1235280-35-9Relevant articles and documents
A fast and direct iodide-catalyzed oxidative 2-selenylation of tryptophan
Gao, Yu-Ting,Liu, Shao-Dong,Cheng, Liang,Liu, Li
supporting information, p. 3504 - 3507 (2021/04/12)
A metal-free 2-selenylation of tryptophan derivatives is reported, where the use of iodide as the catalyst and oxone as the oxidant is key to obtain high yields. Various functional groups within the di-seleny and the indole ring are tolerated, and no racemization is generally observed.
Synthesis and biological evaluation of novel tryptoline derivatives as indoleamine 2,3-dioxygenase (IDO) inhibitors
Tanaka, Minoru,Li, Xin,Hikawa, Hidemasa,Suzuki, Takafumi,Tsutsumi, Katsuhiko,Sato, Masashi,Takikawa, Osamu,Suzuki, Hideharu,Yokoyama, Yuusaku
, p. 1159 - 1165 (2013/03/14)
Indoleamine 2,3-dioxygenase (IDO) plays a significant role in several disorders such as Alzheimer's disease, age-related cataracts and tumors. A series of novel tryptoline derivatives were synthesized and evaluated for their inhibitory activity against ID
