国产亚洲人成a在线v网站_日韩一区二区三区射精-百度_久久久精品人妻一区二区三区蜜桃_国产喷水1区2区3区咪咪爱av_a级无遮挡超级高清-在线观看

Welcome to LookChem.com Sign In|Join Free

CAS

  • or
(2R)-4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid is a peptide derivative with the molecular formula C29H27NO6. It features a unique structure that includes two carbonyl groups and an amino acid side chain, with a fluorenylmethoxy carbonyl and a phenylmethoxy carbonyl group attached. This chemical compound plays a significant role in the field of organic chemistry and biochemistry.

369611-58-5

Post Buying Request

369611-58-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • (2R)-2-{[(benzyloxy)carbonyl]amino}-4-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}butanoic acid

    Cas No: 369611-58-5

  • USD $ 1.9-2.9 / Gram

  • 100 Gram

  • 1000 Metric Ton/Month

  • Chemlyte Solutions
  • Contact Supplier
  • (2R)-4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid

    Cas No: 369611-58-5

  • USD $ 10.0-10.0 / Milligram

  • 1 Milligram

  • 100000000 Kilogram/Month

  • weifang yangxu group co.,ltd
  • Contact Supplier
  • N-α-Carbobenzoxy-N-γ-(9-fluorenylmethoxycarbonyl)-D-α,γ-diaminobutyric acid

    Cas No: 369611-58-5

  • No Data

  • No Data

  • No Data

  • BOC Sciences
  • Contact Supplier

369611-58-5 Usage

Uses

Used in Organic Chemistry:
(2R)-4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid is used as a protecting group for amino acids during peptide synthesis. It allows for selective deprotection and modification of the amino acid residues, which is crucial for the successful synthesis of complex peptide sequences.
Used in Biochemistry and Pharmaceutical Research:
In the field of biochemistry and pharmaceutical research, (2R)-4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid serves as an important tool for the synthesis of peptides and proteins. Its ability to protect and modify amino acid residues during peptide synthesis contributes to the development of novel therapeutic agents and the understanding of protein structure and function.
Used in the Synthesis of Peptides and Proteins:
(2R)-4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-[[(phenylmethoxy)carbonyl]amino]butanoic acid is used as a key component in the synthesis of peptides and proteins. Its presence enables chemists to create specific peptide sequences with desired properties, which can be further utilized in drug development, diagnostics, and therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 369611-58-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,9,6,1 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 369611-58:
(8*3)+(7*6)+(6*9)+(5*6)+(4*1)+(3*1)+(2*5)+(1*8)=175
175 % 10 = 5
So 369611-58-5 is a valid CAS Registry Number.

369611-58-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-2-(phenylmethoxymethylamino)butanoic acid

1.2 Other means of identification

Product number -
Other names (R)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(((benzyloxy)methyl)amino)butanoic acid

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:369611-58-5 SDS

369611-58-5Relevant articles and documents

A new peptidic somatostatin agonist with high affinity to all five somatostatin receptors.

Reubi, Jean Claude,Eisenwiener, Klaus-Peter,Rink, Hans,Waser, Beatrice,Maecke, Helmut R

, p. 45 - 49 (2007/10/03)

All commercially available somatostatin analogs for clinical use have a preference for some but not all somatostatin receptor subtypes. We describe here the synthesis and evaluation in binding and cAMP assays with cell lines stably transfected with sst(1)

Synthesis and evaluation of novel dipeptide-bound 1,2,4-thiadiazoles as irreversible inhibitors of guinea pig liver transglutaminase.

Marrano,de Macedo,Gagnon,Lapierre,Gravel,Keillor

, p. 3231 - 3241 (2007/10/03)

Herein we report the synthesis and evaluation of 14 novel peptides as potential irreversible inactivators of guinea pig liver transglutaminase (TGase). These peptides were designed to resemble Cbz-L-Gln-Gly, known to be a good TGase substrate, and to include a 1,2,4-thiadiazole group. The side chain length of the amino acid residue bearing the inhibitor group was also varied in order to permit investigation of this effect. Their inactivation rate constants were measured using a direct continuous spectrophotometric method and were found to vary between 0.330 to 0.89 microM(-1) min(-1).

Modification of receptor selectivity and functional activity of cyclic cholecystokinin analogues

Amblard, Muriel,Rodriguez, Marc,Lignon, Marie-Francoise,Galas, Marie-Christine,Bernad, Nicole,Aumelas, Andre,Martinez, Jean

, p. 171 - 180 (2007/10/03)

We reported earlier on the synthesis and biological activity at the CCK-B receptor of cyclized derivatives of CCK. These peptides, in which the positions 28 and 31 were replaced by lysine residues, were bridged by a succinyl moiety. To determine the importance of the nature and size of the cyclic structure, cyclic analogues were synthesized in which: (i) the lysine residues were replaced by ornithine and diaminobutyric acid and (ii) the succinic moiety was replaced by a malonic, adipic and glutaric moiety. They were tested For their ability to inhibit the specific binding of 125I-BH-CCK-8 to CCK receptors in rat pancreatic acini and guinea pig brain membranes. They were also evaluated for their ability to stimulate amylase secretion from rat pancreatic acini. The potency and selectivity of these analogues were compared with those obtained with CCK-4 and compound JIMV320, a potent and selective CCK-B receptor ligand synthesized earlier in our laboratory.

Metal Chelating Amino Acids in the Design of Peptides and Proteins. Synthesis of Nα-Fmoc/But Protected Amino Acids Incorporating Aminodiacetic Acid Moiety.

Kazmierski, Wieslaw M.

, p. 4493 - 4496 (2007/10/02)

The synthesis of Fmoc/But protected amino acid chelators 14, 15, 16 and 24 is described.With respect to their Boc/Bzl derivatives, the title compounds offer synthetic advantage: peptide Ac-Ada(1)-Ala3-Ada(1)-Ala4-Glu-Lys-NH2 was assembled by So

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 369611-58-5