Fmoc-L-Cysteine

Name: Fmoc-L-Cysteine | 135248-89-4
Brand: US-CATO
SKU: S57CPTD788295_100_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD788295_100_MG

Vendor: US-CATO

Product Information

Product Name

Fmoc-L-Cysteine

Brand Name

US-CATO

Product Number

CPTD788295

CAS

135248-89-4

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

11024349

IUPAC Name

(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-sulfanylpropanoic acid

InChI Key

RMTDKXQYAKLQKF-INIZCTEOSA-N

SMILES

C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC@@H(CS)C(=O)O

References Data Source From Pubchem

Designing supramolecular catalytic systems for mammalian synthetic metabolism

Publication Name: Nature Reviews Materials

Publication Date: 2025-04-29

DOI: 10.1038/s41578-025-00801-6

Upstream Proteolysis by Ste24 does not Require a C-Terminal Methyl Ester as Revealed Using 33-Residue a-Factor Precursor Peptide Substrates Synthesized via Epimerization-Free Methods

Publication Name: International Journal of Peptide Research and Therapeutics

Publication Date: 2025-01-06

DOI: 10.1007/s10989-024-10677-9

Double Conjugation Using Mercapto-Acryloyl and Alkyne-Azide Reactions for the Synthesis of Branched Multiantigenic Vaccine Candidates

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2021

DOI: 10.1007/978-1-0716-1617-8_13

Amino Acids Bearing Aromatic or Heteroaromatic Substituents as a New Class of Ligands for the Lysosomal Sialic Acid Transporter Sialin

Publication Name: Journal of Medicinal Chemistry

Publication Date: 2020-07-01

DOI: 10.1021/acs.jmedchem.9b02119

Chemical proteomics reveals new targets of cysteine sulfinic acid reductase

Publication Name: Nature Chemical Biology

Publication Date: 2018-09-03

DOI: 10.1038/s41589-018-0116-2

Fmoc-L-Cysteine

Product Information

General Information

References Data Source From Pubchem

Designing supramolecular catalytic systems for mammalian synthetic metabolism

Upstream Proteolysis by Ste24 does not Require a C-Terminal Methyl Ester as Revealed Using 33-Residue a-Factor Precursor Peptide Substrates Synthesized via Epimerization-Free Methods

Double Conjugation Using Mercapto-Acryloyl and Alkyne-Azide Reactions for the Synthesis of Branched Multiantigenic Vaccine Candidates

Amino Acids Bearing Aromatic or Heteroaromatic Substituents as a New Class of Ligands for the Lysosomal Sialic Acid Transporter Sialin

Chemical proteomics reveals new targets of cysteine sulfinic acid reductase

Fmoc-L-Cysteine

s-(Trifluoromethyl)-l-homocysteine

D-Cysteine hydrochloride

S-Propargylcysteine

D-Cysteine

L-Cysteine (hydrochloride)

S-Methyl-L-cysteine

L-Homocysteine thiolactone (hydrochloride)

L-Cysteine methyl ester (hydrochloride)

About Us

Popular Searches

Contact

#title#

Features
Availability:
Price
Options
Actions

Fmoc-L-Cysteine

Product Information

General Information

References Data Source From Pubchem

Designing supramolecular catalytic systems for mammalian synthetic metabolism

Upstream Proteolysis by Ste24 does not Require a C-Terminal Methyl Ester as Revealed Using 33-Residue a-Factor Precursor Peptide Substrates Synthesized via Epimerization-Free Methods

Double Conjugation Using Mercapto-Acryloyl and Alkyne-Azide Reactions for the Synthesis of Branched Multiantigenic Vaccine Candidates

Amino Acids Bearing Aromatic or Heteroaromatic Substituents as a New Class of Ligands for the Lysosomal Sialic Acid Transporter Sialin

Chemical proteomics reveals new targets of cysteine sulfinic acid reductase

Fmoc-L-Cysteine

Related Product

s-(Trifluoromethyl)-l-homocysteine

D-Cysteine hydrochloride

S-Propargylcysteine

D-Cysteine

L-Cysteine (hydrochloride)

S-Methyl-L-cysteine

L-Homocysteine thiolactone (hydrochloride)

L-Cysteine methyl ester (hydrochloride)

#title#

Login

Register