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Boc-Tyr-Leu-OBzl is a synthetic tripeptide compound composed of three amino acids: Boc (tert-butyloxycarbonyl) as a protecting group, Tyr (tyrosine), and Leu (leucine), linked by peptide bonds. The molecule also features an OBzl (benzyl ester) group at the C-terminus of leucine. The Boc group serves to prevent unwanted reactions during peptide synthesis, while Tyr and Leu are essential natural amino acids found in proteins. The OBzl group acts as a protective moiety in peptide synthesis and can be selectively removed under specific conditions. Boc-Tyr-Leu-OBzl is valuable in peptide chemistry and pharmaceutical research for its capacity to replicate natural peptide structures and influence biological processes.

72210-21-0

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72210-21-0 Usage

Uses

Used in Peptide Chemistry:
Boc-Tyr-Leu-OBzl is utilized as a building block in the synthesis of larger peptides and proteins. Its presence allows for the stepwise assembly of peptide chains, with the Boc protecting group ensuring the selective formation of peptide bonds without unwanted side reactions.
Used in Pharmaceutical Research:
In pharmaceutical research, Boc-Tyr-Leu-OBzl is employed as a template for the development of bioactive peptides. Its ability to mimic natural peptide structures makes it a promising candidate for the design of therapeutic agents targeting various biological pathways and diseases.
Used in Drug Delivery Systems:
Boc-Tyr-Leu-OBzl can be incorporated into drug delivery systems to improve the stability, solubility, and bioavailability of peptide-based drugs. The OBzl group can be strategically removed under specific conditions to release the active peptide in a controlled manner, enhancing the therapeutic efficacy and reducing potential side effects.
Used in Diagnostics:
Boc-Tyr-Leu-OBzl may also find applications in diagnostic assays, where it can serve as a specific binding partner or a recognition element for the detection of target molecules, such as enzymes, receptors, or other peptides.
Overall, Boc-Tyr-Leu-OBzl is a versatile compound with potential applications across various fields, including peptide chemistry, pharmaceutical research, drug delivery, and diagnostics, due to its unique structure and functional properties.

Check Digit Verification of cas no

The CAS Registry Mumber 72210-21-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,2,1 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72210-21:
(7*7)+(6*2)+(5*2)+(4*1)+(3*0)+(2*2)+(1*1)=80
80 % 10 = 0
So 72210-21-0 is a valid CAS Registry Number.

72210-21-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-Tyr-Leu-OBzl

1.2 Other means of identification

Product number -
Other names BOC-TYR-GLY-GLY-PHE-LEU-OH

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:72210-21-0 SDS

72210-21-0Downstream Products

72210-21-0Relevant academic research and scientific papers

Incorporation of fluoroprolines to proctolin: Study on the effect of a fluorine atom toward peptidic conformation

Kitamoto, Takamasa,Ozawa, Taeko,Abe, Megumi,Marubayashi, Shunsuke,Yamazaki, Takashi

, p. 286 - 293 (2008/12/22)

In spite of quite small steric perturbation, substitution of proline (Pro) in the target pentapeptide proctolin (Arg-Tyr-Leu-Pro-Thr) for (4R)- as well as (4S)-4-fluoroproline led to apparent alteration of the pyrrolidine ring structure which eventually r

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