115006-86-5 Usage
Description
Cyclo(L-Leu-trans-4-hydroxy-L-Pro) is a cyclic dipeptide composed of the amino acids L-Leucine and trans-4-hydroxy-L-Proline. This chemical compound is recognized for its capacity to influence a range of biological processes, such as acting as an antioxidant and anti-inflammatory agent. Additionally, it has been investigated for its potential to enhance wound healing and tissue repair. The distinctive structure and properties of Cyclo(L-Leu-trans-4-hydroxy-L-Pro) render it a compelling subject for further exploration into its possible therapeutic uses in the fields of medicine and healthcare.
Uses
Used in Pharmaceutical Industry:
Cyclo(L-Leu-trans-4-hydroxy-L-Pro) is utilized as a therapeutic agent for its potential antioxidant and anti-inflammatory properties, which can be beneficial in treating various conditions that involve oxidative stress and inflammation.
Used in Wound Healing and Tissue Repair Applications:
In the healthcare sector, Cyclo(L-Leu-trans-4-hydroxy-L-Pro) is employed as a wound healing and tissue repair promoter, owing to its demonstrated capacity to enhance these processes, which is crucial for recovery from injuries and surgeries.
Used in Research and Development:
Cyclo(L-Leu-trans-4-hydroxy-L-Pro) serves as a subject of interest in research and development settings, where its unique structure and properties are further investigated to uncover additional therapeutic applications and optimize its use in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 115006-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,0 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115006-86:
(8*1)+(7*1)+(6*5)+(5*0)+(4*0)+(3*6)+(2*8)+(1*6)=85
85 % 10 = 5
So 115006-86-5 is a valid CAS Registry Number.
115006-86-5Relevant articles and documents
Enantiomerically pure piperazines via NaBH4/I2reduction of cyclic amides
Harish, Vagala,Periasamy, Mariappan
, p. 175 - 180 (2017/01/11)
Enantiomerically pure (3S,7R,8aS)-3-phenyloctahydropyrrolo[1,2-a]pyrazine-7-ol, (3S,7R,8aS)-3-methyl octahydropyrrolo[1,2-a]pyrazine-7-ol, (3S,7R,8aS)-3-isopropyloctahydropyrrolo[1,2-a]pyrazine-7-ol and (3S,7R,8aS)-3-isobutyloctahydropyrrolo[1,2-a]pyrazine-7-ol 16d were synthesized via preparation of the corresponding cyclic amides from enantiomerically pure L-proline and hydroxyproline derivatives followed by reduction using sodium borohydride-iodine.
