What is the Z-PRO-VAL-OH?

Z-PRO-VAL-OH is , while it's Molecular Formula is C18H24 N2 O5. Used in Pharmaceutical Industry: Z-PRO-VAL-OH is used as a building block for peptides and proteins for its role in protein synthesis and structural stability, which is crucial for the development of new drugs and therapeutic agents. Used in Biomedical Research: Z-PRO-VAL-OH is used as a research tool for studying protein synthesis, structural stability, and the mechanisms of action of various biological processes, contributing to the advancement of biomedical knowledge. Used in Anti-inflammatory Applications: Z-PRO-VAL-OH is used as an anti-inflammatory agent for its potential to regulate immune responses and reduce inflammation, offering a promising therapeutic option for various inflammatory conditions. Used in Drug Development: Z-PRO-VAL-OH is used in the development of new drugs and therapeutic agents, leveraging its properties as a building block for peptides and proteins to create novel treatments for various diseases and disorders.

What is the CAS number for Z-PRO-VAL-OH?

The CAS number of Z-PRO-VAL-OH is 21285-27-8.

What is Z-PRO-VAL-OH (21285-27-8) used for?

Z-PRO-VAL-OH, a derivative of the amino acid proline, is a non-proteinogenic amino acid that is not commonly found in proteins but plays various biological roles. It is known for its ability to act as a building block for peptides and proteins, contributing to protein synthesis and structural stability. Furthermore, Z-PRO-VAL-OH has been studied for its potential therapeutic applications, including anti-inflammatory properties and immune response regulation, making it a versatile and important molecule with promising biomedical uses.InChI:InChI=1/C18H24N2O5/c1-12(2)15(17(22)23)19-16(21)14-9-6-10-20(14)18(24)25-11-13-7-4-3-5-8-13/h3-5,7-8,12,14-15H,6,9-11H2,1-2H3,(H,19,21)(H,22,23)

What is the Z-PRO-VAL-OH?

Z-PRO-VAL-OH is , while it's Molecular Formula is C18H24 N2 O5. Used in Pharmaceutical Industry: Z-PRO-VAL-OH is used as a building block for peptides and proteins for its role in protein synthesis and structural stability, which is crucial for the development of new drugs and therapeutic agents. Used in Biomedical Research: Z-PRO-VAL-OH is used as a research tool for studying protein synthesis, structural stability, and the mechanisms of action of various biological processes, contributing to the advancement of biomedical knowledge. Used in Anti-inflammatory Applications: Z-PRO-VAL-OH is used as an anti-inflammatory agent for its potential to regulate immune responses and reduce inflammation, offering a promising therapeutic option for various inflammatory conditions. Used in Drug Development: Z-PRO-VAL-OH is used in the development of new drugs and therapeutic agents, leveraging its properties as a building block for peptides and proteins to create novel treatments for various diseases and disorders.

What is the CAS number for Z-PRO-VAL-OH?

The CAS number of Z-PRO-VAL-OH is 21285-27-8.

What is Z-PRO-VAL-OH (21285-27-8) used for?

Z-PRO-VAL-OH, a derivative of the amino acid proline, is a non-proteinogenic amino acid that is not commonly found in proteins but plays various biological roles. It is known for its ability to act as a building block for peptides and proteins, contributing to protein synthesis and structural stability. Furthermore, Z-PRO-VAL-OH has been studied for its potential therapeutic applications, including anti-inflammatory properties and immune response regulation, making it a versatile and important molecule with promising biomedical uses.InChI:InChI=1/C18H24N2O5/c1-12(2)15(17(22)23)19-16(21)14-9-6-10-20(14)18(24)25-11-13-7-4-3-5-8-13/h3-5,7-8,12,14-15H,6,9-11H2,1-2H3,(H,19,21)(H,22,23)

Z-PRO-VAL-OH

Factory supply good quality Z-PRO-VAL-OH 21285-27-8 with stock

Molecular Formula: C18H24 N2 O5
Molecular Weight: 348.399
Vapor Pressure: 1.27E-14mmHg at 25°C
Boiling Point: 587°Cat760mmHg
Flash Point: 308.8°C
PSA： 95.94000
Density: 1.246g/cm³
LogP: 2.34180

Z-PRO-VAL-OH(Cas 21285-27-8) Usage

General Description

Z-PRO-VAL-OH is a chemical compound that belongs to the family of amino acids, specifically a derivative of proline. It is classified as a non-proteinogenic amino acid, meaning it is not commonly found in proteins but has various biological roles. Z-PRO-VAL-OH is known for its ability to act as a building block for peptides and proteins, playing a crucial role in protein synthesis and structural stability. Additionally, this compound has been studied for its potential therapeutic applications, such as its anti-inflammatory properties and ability to regulate immune responses. Overall, Z-PRO-VAL-OH is a versatile and important molecule with promising biomedical uses.

InChI:InChI=1/C18H24N2O5/c1-12(2)15(17(22)23)19-16(21)14-9-6-10-20(14)18(24)25-11-13-7-4-3-5-8-13/h3-5,7-8,12,14-15H,6,9-11H2,1-2H3,(H,19,21)(H,22,23)

21285-27-8 Relevant articles

Synthesis of dipeptides from N-hydroxy-3-azaspiro[5,5]undecane-2,4-dione activated α-amino acids

Nowshuddin, Shaik,Ram Reddy

scheme or table, p. 22 - 25 (2011/04/18)

A simple two step procedure for the synt...

Synthesis of proline-derived dipeptides and their catalytic enantioselective direct aldol reactions: Catalyst, solvent, additive and temperature effects

Chen,Sung,Sung, Kuangsen

experimental part, p. 839 - 845 (2010/08/06)

A series of dipeptides of l-proline-l-am...

Efficient peptide coupling involving sterically hindered amino acids

Katritzky, Alan R.,Todadze, Ekaterina,Angrish, Parul,Draghici, Bogdan

, p. 5794 - 5801 (2008/02/09)

(Chemical Equation Presented) Hindered a...

An Effective Water-Free Aprotic System for Dissolving Free Amino Acids

Raydnov, M. G.,Klimenko, L. V.,Mitin, Yu. V.

, p. 283 - 287 (2007/10/03)

An effective water-free system was propo...

21285-27-8 Process route

: 886981-23-3
benzyl (2S)-2-(1H-1,2,3-benzotriazol-1-ylcarbonyl)tetrahydro-1H-pyrrole-1-carboxylate

: 72-18-4,25609-85-2,7004-03-7,921-10-8
L-valine

: 21285-27-8
(2S)-2-[({(2S)-1-[(benzyloxy)carbonyl]tetrahydro-1H-pyrrol-2-yl}carbonyl)amino]-3-methylbutanoic acid

Conditions

Conditions	Yield
With triethylamine; In water; acetonitrile; at 20 ℃; for 1h;	95%

: 72-18-4,25609-85-2,7004-03-7,921-10-8
L-valine

: Z-Pro-OBt

: 21285-27-8
(2S)-2-[({(2S)-1-[(benzyloxy)carbonyl]tetrahydro-1H-pyrrol-2-yl}carbonyl)amino]-3-methylbutanoic acid

Conditions

Conditions	Yield
Z-Pro-OBt; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h; L-valine; With sodium perchlorate; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 1h;	85%

21285-27-8 Upstream products

2874-20-6
benzyloxycarbonyl-L-prolin-L-valin methyl ester
26061-29-0
(S)-benzyl 2-((S)-1-tert-butoxy-3-methyl-1-oxobutan-2-ylcarbamoyl)pyrrolidine-1-carboxylate
99909-22-5
Z-Pro-Val-OBzl
72-18-4
L-valine

21285-27-8 Downstream products

52899-09-9
N -L-prolyl-L-valine
67545-92-0
(S )-2-((S )-4-isopropyl-5-oxo-4,5-dihydro-oxazol-2-yl)-pyrrolidine-1-carboxylic acid benzyl ester
51782-86-6
Z-Pro-Val-Pro-OCH₃
28334-65-8
Z-S-Pro-S-Val-S-Pro-OtBu