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(S)-Benzyl 3-amino butylcarbamate, with the molecular formula C12H18N2O2, is a carbamate compound derived from the amino acid L-lysine. It has demonstrated potential pharmacological effects and is under investigation for its medicinal properties. (S)-benzyl 3-aMinobutylcarbaMate has shown promise as an anti-cancer agent and is also being researched for its potential in treating neurological conditions, such as Alzheimer's disease. Furthermore, it has been studied for its potential as a prodrug, which can be converted into an active pharmaceutical agent within the body. (S)-Benzyl 3-amino butylcarbamate holds the potential to become a significant compound for future drug development and research.

1187927-77-0

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1187927-77-0 Usage

Uses

Used in Pharmaceutical Industry:
(S)-Benzyl 3-amino butylcarbamate is used as a potential anti-cancer agent for its pharmacological effects. It is being studied for its ability to target and treat various types of cancer, offering a promising avenue for cancer therapy.
Used in Neurological Applications:
In the field of neurology, (S)-benzyl 3-amino butylcarbamate is used as a potential treatment for neurological conditions such as Alzheimer's disease. Its pharmacological properties are being investigated for their ability to address the underlying causes and symptoms of the disease.
Used as a Prodrug:
(S)-Benzyl 3-amino butylcarbamate is also used as a prodrug, which means it can be converted into an active pharmaceutical agent within the body. This characteristic allows for the development of new drug therapies that can be more effectively delivered and utilized by the body.

Check Digit Verification of cas no

The CAS Registry Mumber 1187927-77-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,9,2 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1187927-77:
(9*1)+(8*1)+(7*8)+(6*7)+(5*9)+(4*2)+(3*7)+(2*7)+(1*7)=210
210 % 10 = 0
So 1187927-77-0 is a valid CAS Registry Number.

1187927-77-0Downstream Products

1187927-77-0Relevant articles and documents

Unforeseen Possibilities to Investigate the Regulation of Polyamine Metabolism Revealed by Novel C-Methylated Spermine Derivatives

Khomutov, Maxim,Hyv?nen, Mervi T.,Simonian, Alina,Formanovsky, Andrey A.,Mikhura, Irina V.,Chizhov, Alexander O.,Kochetkov, Sergey N.,Alhonen, Leena,Veps?l?inen, Jouko,Kein?nen, Tuomo A.,Khomutov, Alex R.

, p. 11335 - 11347 (2019)

The biogenic polyamines, spermine (Spm) and spermidine, are organic polycations present in millimolar concentrations in all eukaryotic cells participating in the regulation of vital cellular functions including proliferation and differentiation. The desig

Synthesis of (3R,10R)- and (3S,10S)-Diastereomers of 3,10-Dimethylspermine

Chizhov, A. O.,Hyv?nen, M. T.,Kein?nen, T. A.,Khomutov, A. R.,Khomutov, M. A.,Kochetkov, S. N.,Ryzhov, I. M.,Salikhov, A. I.,Veps?l?inen, J.

, p. 1061 - 1066 (2020/12/30)

Abstract: A simple and practical 10-step synthesis is reported for previously unknown diastereomers of C?methylated spermine (Spm) analogue, 1,12-diamino-3,10-dimethyl-4,9-diazadodecane (3,10-Me2Spm), starting from commercially available enanti

Enantioselective synthesis of (R)- and (S)-3-methylspermidines

Khomutov,Keinanen,Hyvonen,Weisell,Vepsalainen,Alhonen,Kochetkov,Khomutov

, p. 548 - 553 (2015/10/12)

Earlier unknown enantiomerically pure (R)- and (S)-1,8-diamino-3-methyl-4-azaoctane's (3-MeSpd's) were synthesized within 11 steps with high overall yields and optical purity starting from commercially available R- and S-isomers of N-Boc-2-aminopropanol-1

SUBSTITUTED FUSED[1,2]IMIDAZO[4,5-C] RING COMPOUNDS AND METHODS

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Page/Page column 113, (2008/06/13)

[1,2]Imidazo[4,5-c] ring compounds (e.g., imidazo[4,5-c]quinolines, imidazo[4,5-c]naphthyridines, and imidazo[4,5-c]pyridines) substituted with a fused ring containing an oxygen and/or nitrogen atom attached at the 1- and/or 2-position, pharmaceutical compositions containing the compounds, intermediates, methods of making the compounds, and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.

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