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Benzoylglycyl-L-alanyl-L-proline

$595.00

Catalog Number: MDP0167 (20 mg)
Benzoylglycyl-L-alanyl-L-proline is a high quality Benzoylglycyl-L-alanyl-L-proline. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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Description

Benzoylglycyl-L-alanyl-L-proline
Catalog number: MDP0167
CAS Number: 194022-52-1
Sequence: Benzoylglycyl-L-alanyl-L-proline
Amount: 20 mg
Molecular Weight: 347.2 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20 °C
WARNING: For in vitro Research Use Only. NOT for use on humans or animals.
Grade: Biotechnology grade. All products are highly pure.

References:
1: Enalapril 2021 Aug 16. Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–.
2: Sidor NA, Velenosi TJ, Lajoie GA, Filler G, House AA, Weir MA, Thomson BK, Garg AX, Renaud JB, McDowell T, Knauer MJ, Tirona RG, Noble R, Selby N, Taal M, Urquhart BL. Investigation of N,N,N-Trimethyl-L-alanyl-L-proline Betaine (TMAP) as a Biomarker of Kidney Function ACS Omega. 2023 Apr 21;8(17):15160-15167.
3: Deutch CE. L-Proline nutrition and catabolism in Staphylococcus saprophyticus Antonie Van Leeuwenhoek. 2011 May;99(4):781-93.
4: Bull HG, Thornberry NA, Cordes MH, Patchett AA, Cordes EH. Inhibition of rabbit lung angiotensin-converting enzyme by N alpha-[(S)-1-carboxy-3-phenylpropyl]L-alanyl-L-proline and N alpha-[(S)-1-carboxy-3-phenylpropyl]L-lysyl-L-proline J Biol Chem. 1985 Mar 10;260(5):2952-62.
5: Velenosi TJ, Thomson BKA, Tonial NC, RaoPeters AAE, Mio MA, Lajoie GA, Garg AX, House AA, Urquhart BL. Untargeted metabolomics reveals N, N, N-trimethyl-L-alanyl-L-proline betaine (TMAP) as a novel biomarker of kidney function Sci Rep. 2019 May 2;9(1):6831.
6: Galardy RE, Grobelny D. N alpha-(diphenoxyphosphoryl)-L-alanyl-L-proline, N alpha-[bis (4-nitrophenoxy)phosphoryl]-L-alanyl-L-proline, and N alpha-[ (2-phenylethyl)phenoxyphosphoryl]-L-alanyl-L-proline: releasers of potent inhibitors of angiotensin converting enzyme at physiological pH and temperature J Med Chem. 1985 Oct;28(10):1422-7.
7: Mencel JJ, Regan JR, Barton J, Menard PR, Bruno JG, Calvo RR, Kornberg BE, Schwab A, Neiss ES, Suh JT. Angiotensin converting enzyme inhibitors. 10. Aryl sulfonamide substituted N-[1-carboxy-3-phenylpropyl]-L-alanyl-L-proline derivatives as novel antihypertensives J Med Chem. 1990 Jun;33(6):1606-15.
8: Fernekorn A, Fiehring C. [L-alanyl-L-proline-dipeptidase and glycyl-L-valine-depeptidase in malabsorption syndrome] Z Gesamte Inn Med. 1976 May 1;31(9):266-9.
9: Hanai R, Wada A. Analysis of the cis-trans isomerization kinetics of L-alanyl-L-proline by the elution-band relaxation method J Chromatogr. 1987 May 22;394(2):273-8.
10: Shibukawa M, Miyake A, Eda S, Saito S. Determination of the cis-trans isomerization barriers of L-alanyl-L-proline in aqueous solutions and at water/hydrophobic interfaces by on-line temperature-jump relaxation HPLC and dynamic on-column reaction HPLC Anal Chem. 2015 Sep 15;87(18):9280-7.

Products Related to Benzoylglycyl-L-alanyl-L-proline can be found at Peptides

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