Cyclotheonamide
WebThree new thrombin and trypsin inhibitors, cyclotheonamides C (3), D (4), and E (8) were isolated from the marine sponge Theonella swinhoei. Their structures were determined by spectral and chemical methods. ASJC Scopus subject areas Biochemistry Molecular Medicine Molecular Biology Pharmaceutical Science Drug Discovery Clinical Biochemistry WebA convergent approach using two key intermediates, segment A [a l-proline-l-α-hydroxy-β-homoarginine-d-phenylalanine (Pro-hArg-d-Phe) tripeptide] and segment B [a vinylogous …
Cyclotheonamide
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WebMay 27, 1993 · The macrocyclic peptide cyclotheonamide A (CtA), isolated from the marine sponge Theonella sp., represents an unusual class of serine protease inhibitor. A … WebCyclotheonamide A is a cyclic peptide isolated from the marine sponge Theonella. DrugBank. Cyclotheonamide A is a natural product found in …
WebCYCLOMETHICONE and CYCLOPENTASILOXANE, DECAMETHYL. Unacceptable. Unacceptable: EWG VERIFIED products cannot contain this ingredient. Cyclomethicone … WebFeb 19, 2010 · Structural modification at two positions is the key: Cyclotheonamide E4 unspecifically blocks trypsin-like serine proteases in a covalent fashion. We converted this compound into a reversibly binding, potent and selective β-tryptase inhibitor.
WebJan 3, 2024 · Entotheonella, cyclotheonamide A, and onnamide A within the pores, chambers, and exterior part of the yellow chemotype of the sponge . Collectively, these findings further support the hypothesis that Ca. Entotheonella locally produces these cytotoxic compounds in surface-accessible areas, possibly to protect the host sponge … WebOct 6, 2008 · The total synthesis of cyclotheonamide C (3), a macrocyclic pentapeptide incorporating an α‐keto homoarginine (k‐Arg) and a vinylogous dehydrotyrosine (V‐ΔTyr) …
WebNov 14, 1997 · The macrocyclic peptide cyclotheonamide A (CtA), isolated from the marine sponge Theonella sp., represents an unusual class of serine protease inhibitor. A complex of this inhibitor with human alpha …
WebJul 7, 1992 · Total synthesis of cyclotheonamide B, a facile route towards analogues 1995, Tetrahedron Letters Show abstract Topically resolved intramolecular CH-π interactions in phenylalanine derivatives 2009, Organic and Biomolecular Chemistry Cis-trans isomerization of organic molecules and biomolecules: Implications and applications … simplicity s9474WebAug 20, 2008 · Mastering unusual amino acids : The first total synthesis of the potent protease inhibitor cyclotheonamide C (see structure representation) has been achieved.The key features of the synthesis are a three‐component tandem procedure to create a masked α‐keto‐β‐arginine within a peptide chain, and the control of the … simplicity s9470WebCyclotheonamide A shows potent inhibitory activity against trypsin ( K =0.023 µM) and streptokinase ( K =0.035 µM) and moderate inhibitory activity against human α-thrombin … raymond dokpesi net worthWebAug 1, 1995 · Macrocyclic pentapeptide analogues (5–9) of the sponge natural product cyclotheonamide A (CtA, 3) were prepared by means of our convergent [3 + 2] synthetic protocol, in which a late-stage primary amine group is available for substitution (Maryanoff et al. Proc. Natl Acad. Sci. U.S.A. 1993, 90, 8048).These analogues, as well as CtA and … simplicity s9449WebSep 1, 1993 · The macrocyclic peptide cyclotheonamide A (CtA), isolated from the marine sponge Theonella sp., represents an unusual class of serine protease inhibitor. A complex of this inhibitor with human alpha-thrombin, a protease central to the bioregulation of thrombosis and hemostasis, was studied by x-ray crystallography. simplicity s9475WebCyclotheonamide E4 and E5, new potent tryptase inhibitors from an Ircinia species of sponge. Tryptase is a protease released from mast cells and is believed to … simplicity s9454WebFeb 19, 2010 · Structural modification at two positions is the key: Cyclotheonamide E4 unspecifically blocks trypsin-like serine proteases in a covalent fashion. We converted … simplicity s9395