Welcome to LookChem.com Sign In|Join Free

CAS

  • or

112883-29-1

Post Buying Request

112883-29-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

112883-29-1 Usage

Description

FMOC-D-TYR-OH, also known as N-Fmoc-D-tyrosine, is an N-Fmoc-protected form of D-Tyrosine (T899970). D-Tyrosine is an unnatural isomer of L-Tyrosine (T899975) that possesses antimetabolic properties and is used as a chiral precursor for biosynthesized inhibitors. FMOC-D-TYR-OH is a white solid and is utilized in various applications due to its unique chemical properties and biological activities.

Uses

Used in Pharmaceutical Industry:
FMOC-D-TYR-OH is used as a chiral precursor for the synthesis of bioactive compounds with anti-inflammatory effects in humans. Its role in the pharmaceutical industry is crucial for developing new drugs that can help in managing inflammation-related conditions.
Used in Research and Development:
FMOC-D-TYR-OH is used as a research compound for studying the metabolic activity of Bacillus subtilis and its antimetabolic effects on rats. This application aids in understanding the underlying mechanisms of growth and development inhibition, which can be beneficial for developing new therapeutic strategies.
Used in Chemical Synthesis:
FMOC-D-TYR-OH is used as a protected amino acid in chemical synthesis, particularly in the synthesis of peptides and other biomolecules. Its N-Fmoc protection group allows for selective deprotection and coupling reactions, making it a valuable tool in the field of organic chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 112883-29-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,8 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112883-29:
(8*1)+(7*1)+(6*2)+(5*8)+(4*8)+(3*3)+(2*2)+(1*9)=121
121 % 10 = 1
So 112883-29-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H21NO5/c26-16-11-9-15(10-12-16)13-22(23(27)28)25-24(29)30-14-21-19-7-3-1-5-17(19)18-6-2-4-8-20(18)21/h1-12,21-22,26H,13-14H2,(H,25,29)(H,27,28)/t22-/m1/s1

112883-29-1SDS

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)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-hydroxyphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names 9-fluorenylmethyloxycarbonyl tyrosine

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:112883-29-1 SDS

112883-29-1Relevant articles and documents

Cerium oxide nanoparticle-mediated self-assembly of hybrid supramolecular hydrogels

Patil, Avinash J.,Kumar, Ravinash Krishna,Barron, Nicholas J.,Mann, Stephen

, p. 7934 - 7936 (2012)

Hybrid supramolecular hydrogels are prepared by non-enzymatic dephosphorylation of N-fluorenylmethyloxycarbonyl tyrosine-(O)-phosphate (FMOC-Tyr-P) using catalytic cerium oxide nanoparticles. The organic-inorganic hydrogels exhibit enhanced viscoelastic p

Toward the Rational Design of Galactosylated Glycoclusters That Target Pseudomonas aeruginosa Lectin A (LecA): Influence of Linker Arms That Lead to Low-Nanomolar Multivalent Ligands

Wang, Shuai,Dupin, Lucie,No?l, Mathieu,Carroux, Cindy J.,Renaud, Louis,Géhin, Thomas,Meyer, Albert,Souteyrand, Eliane,Vasseur, Jean-Jacques,Vergoten, Gérard,Chevolot, Yann,Morvan, Fran?ois,Vidal, Sébastien

, p. 11785 - 11794 (2016)

Anti-infectious strategies against pathogen infections can be achieved through antiadhesive strategies by using multivalent ligands of bacterial virulence factors. LecA and LecB are lectins of Pseudomonas aeruginosa implicated in biofilm formation. A series of 27 LecA-targeting glycoclusters have been synthesized. Nine aromatic galactose aglycons were investigated with three different linker arms that connect the central mannopyranoside core. A low-nanomolar (Kd=19 nm, microarray) ligand with a tyrosine-based linker arm could be identified in a structure–activity relationship study. Molecular modeling of the glycoclusters bound to the lectin tetramer was also used to rationalize the binding properties observed.

A Neutrophil-Inspired Supramolecular Nanogel for Magnetocaloric–Enzymatic Tandem Therapy

Chen, Mengwei,Cheng, Yu,Lesniak, Maciej S.,Mi, Yongli,Wang, Jingjing,Wang, Qigang,Wang, Xia,Wu, Chu,Wu, Jiaojiao,Wu, Qing,Zhang, Qi

, p. 3732 - 3738 (2020)

Neutrophils can responsively release reactive oxygen species (ROS) to actively combat infections by exogenous stimulus and cascade enzyme catalyzed bio-oxidation. A supramolecular nanogel is now used as an artificial neutrophil by enzymatic interfacial se

Synthesis and anticancer activities of proline-containing cyclic peptides and their linear analogs and congeners

Ghosh, Keshab Ch,Duttagupta, Indranil,Bose, Chandra,Banerjee, Priyanjalee,Gayen, Anuran Kumar,Sinha, Surajit

, p. 221 - 236 (2019)

A solution phase method was adopted for the synthesis of proline-containing cyclic pentapeptide 2 and total synthesis of naturally occurring cyclic heptapeptide Reniochalistatin B 3. For the synthesis of 3, both divergent and convergent strategies were used to improve the overall yield from 12 to 25%. Different N and C terminal modified linear analogs and congeners of 2 and 3 were synthesized. Both cyclic peptides 2 and 3 and their linear analogs/congeners were evaluated for anti-cancer activity against HeLa cell line, among which pentapeptide 2 h and hexapeptide 3n with N-terminal protected hexafluoroisopropyl carbamates (HFIPC) interestingly showed higher cytotoxicity with an IC50 of 2.73 and 4.3 μM, respectively compared to their Boc-protected analogs 2a (IC50 20 μM) and 3c (IC50 38.51 μM) and cyclic peptides 2 (>100 μM) and 3 (47 μM). These results were further validated by biological experiments such as colony formation and wound healing assays.

Enzyme Instructed Self-assembly of Naphthalimide-dipeptide: Spontaneous Transformation from Nanosphere to Nanotubular Structures that Induces Hydrogelation

Chakravarthy, Rajan Deepan,Lin, Hsin-Chieh,Mohammed, Mohiuddin

supporting information, (2020/08/03)

Understanding the structure-morphology relationships of self-assembled nanostructures is crucial for developing materials with the desired chemical and biological functions. Here, phosphate-based naphthalimide (NI) derivatives have been developed for the

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 112883-29-1