Cyclopeptidic inactivators for chymotrypsin-like proteinases

DOI: 10.1016/0223-5234(91)90119-8

Source and publish data:

European Journal of Medicinal Chemistry p. 699 - 707 (1991)

Update date:2022-08-04

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Authors:

Wakselman

Mazaleyrat

Xie Xie

Montagne

Vilain Vilain

Reboud-Ravaux

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Article abstract of DOI:10.1016/0223-5234(91)90119-8

Cyclopeptides containing a functionalized meta-aminobenzoic acid residue (m-aB[CH₂X] with X = OC₆H₅, OAc, Br, Cl) linked to a tetraglycyl-phenylalanyl sequence, have been synthesized in solution. A phenyl ether group has b

Full text of DOI:10.1016/0223-5234(91)90119-8

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Article Doi

Cyclopeptidic inactivators for chymotrypsin-like proteinases

DOI: 10.1016/0223-5234(91)90119-8

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0223-5234(91)90119-8

Full text of DOI:10.1016/0223-5234(91)90119-8

Products guided by the article

R&D Labs maybe for 129229-77-2

Relevant to this article

STRUCTURE OF PRODUCTS OF ADDITION OF THIOSEMICARBAZIDES AND THIOSEMICARBAZONES TO ACETYLENEDICARBOXYLIC ACID AND ITS DIMETHYL ESTER

Chemical Synthesis of a Bisphosphorylated Mannose-6-Phosphate N-Glycan and its Facile Monoconjugation with Human Carbonic Anhydrase II for in vivo Fluorescence Imaging

FeCl3 mediated arylidenation of carbohydrates

Building Blocks for Oligonucleotide Analogues with Dimethylene Sulfide, Sulfoxide, and Sulfone Groups Replacing Phosphodiester Linkages

Novel small molecule inhibitors targeting the "switch region" of bacterial RNAP: Structure-based optimization of a virtual screening hit

FeCl₃ mediated arylidenation of carbohydrates