Workshop Advances on Cysteine Protecting Groups

Workshop Advances on Cysteine Protecting Groups

Published on 09/12/2021

You missed our workshop featuring Prof. Dr. Fernando Albericio (University of KwaZulu-Natal & University of Barcelona)? Any further questions? Please get in contact via info@iris-biotech.de

Highlights


  • General Introduction (Dr. Markus Weishaupt; Project Manager; Iris Biotech)
  • Expert Talk (Prof. Dr. Fernando Albericio; University of KwaZulu-Natal & University of Barcelona)
  • Q&A

Speakers

Karin Rustler Dr. Karin Rustler Chair
(Project Manager at Iris Biotech)
Fernando Albericio Prof. Dr. Fernando Albericio Special Guest
(Professor at University of KwaZulu-Natal and University of Barcelona)
Markus Weishaupt Dr. Markus Weishaupt Internal Speaker
(Project Manager at Iris Biotech)

Recording

Presentation Prof. Dr. Fernando Albericio

 

Download presentation
 

Related brochure

 

Download brochure
 

Related posts

 

PotM: SIT – A New Cysteine Protecting Group
The new disulfide-based protecting group sec-isoamyl mercaptan (SIT) is fully compatible with Fmoc- and Boc-SPPS and can easily be removed reductively upon addition of dithiothreitol.
Read more

 

 

Photocleavable Cys Protecting Group
FThis oNv (2-Nitroveratryl) is the latest addition to our repertoire of cysteine protecting groups. It opens new possibilities of orthogonality to the existing strategies for disulfide bridge formation.
Read more

 

 

Nitrodibenzofuran (NDBF) based Photocleavable Protecting Groups
Nitrodibenzofuran (NDBF) is a photocleavable side chain protecting group that can be removed by photolysis upon irradiation with UV-light or – especially for in vivo applications – by two-photon excitation using near infrared light.
Read more

 

 

Product of the Month: Fmoc-L-Cys(Allocam)-OH for 1-Step On-Resin Disulfide Bond Formation
The Allocam protecting group allows for selective deprotection and disulfide bond formation on-resin in one step.
Read more

 

 

Msbh, a Safety Catch Cysteine Protecting Group for the Synthesis of Cyclic Peptides
The regioselective formation of multiple disulfide bonds is often a synthetic challenge. We now offer an innovative safety-catch Cys protecting group that allows selective deprotection of the sulfhydryl group and is a valuable addition to the peptide chemist’s toolbox.
Read more

Related products

 

Fmoc-L-Cys(Msbh)-OH

Chemical name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-(4,4'-dimethylsulfinylbenzhydryl)-L-cysteine
Product code: FAA4155
Formula: C33H31NO6S3
MW: 633,80 g/mol

Go to product

 

 

Fmoc-L-Cys(Phacm)-OH

Chemical name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-Phenylacetylaminomethyl)-L-cysteine
Product code: FAA6910
Formula: C27H26N2O5S
MW: 490,57 g/mol

Go to product

 

 

Fmoc-L-Cys(Thp)-OH

Chemical name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-tetrahydropyranyl-L-cysteine
Product code: FAA4160
Formula: C23H25NO5S
MW: 427,15 g/mol

Go to product

 

 

Fmoc-L-Cys(SIT)-OH

Chemical name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-(sec-isoamyl mercaptan)-L-cysteine
Product code: FAA8495
Formula: C23H27NO4S2
MW: 445,59 g/mol

Go to product

 

 

Fmoc-L-Cys(Dpm)-OH

Chemical name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-diphenylmethyl-L-cysteine
Product code: FAA3190
Formula: C31H27NO4S
MW: 509,62 g/mol

Go to product

 

 

H-L-Cys(MDNPE)-OH

Chemical name: 1-[4',5'-(methylenedioxy)-2'-nitrophenyl]ethyl]-L-cysteine
Product code: HAA9270
Formula: C12H14N2O6S
MW: 314,31 g/mol

Go to product

 

 

Fmoc-L-Cys(NDBF)-OH

Chemical name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-(1-(3-nitro-dibenzofuran-2-yl)-ethyl)-L-cysteine
Product code: FAA8420
Formula: C32H26N2O7S
MW: 582,62 g/mol

Go to product

 

 

Fmoc-L-Cys(oNv)-OH

Chemical name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-S-(2-nitroveratryl)-L-cysteine
Product code: FAA3970
Formula: C27H26N2O8S
MW: 538,57 g/mol

Go to product