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
Workshop Advances on Cysteine Protecting Groups

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

 

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Related brochure

 

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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.
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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.
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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.
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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.
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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.
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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

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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

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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

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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

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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

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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

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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

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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

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