Kurosu, Michio’s team published research in Bioorganic & Medicinal Chemistry Letters in 16 | CAS: 901770-40-9

Bioorganic & Medicinal Chemistry Letters published new progress about 901770-40-9. 901770-40-9 belongs to imidazoles-derivatives, auxiliary class Other Aliphatic Heterocyclic,Benzene,Phenol,Amide, name is N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide, and the molecular formula is C16H21N3O3S, Product Details of C16H21N3O3S.

Kurosu, Michio published the artcileSmall-molecule microarrays: Development of novel linkers and an efficient detection method for bound proteins, Product Details of C16H21N3O3S, the publication is Bioorganic & Medicinal Chemistry Letters (2006), 16(13), 3392-3395, database is CAplus and MEDLINE.

Novel isocyanate and diazoketone linkers possessing polyoxypropylenediamine as a spacer for small-mol. microarray are developed. White light interferometry is introduced to detect bound proteins on the glass slides without using chem. modified proteins.

Bioorganic & Medicinal Chemistry Letters published new progress about 901770-40-9. 901770-40-9 belongs to imidazoles-derivatives, auxiliary class Other Aliphatic Heterocyclic,Benzene,Phenol,Amide, name is N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide, and the molecular formula is C16H21N3O3S, Product Details of C16H21N3O3S.

Referemce:
https://en.wikipedia.org/wiki/Imidazole,
Imidazole | C3H4N2 – PubChem

Ke, Mi’s team published research in Nature Communications in 12 | CAS: 901770-40-9

Nature Communications published new progress about 901770-40-9. 901770-40-9 belongs to imidazoles-derivatives, auxiliary class Other Aliphatic Heterocyclic,Benzene,Phenol,Amide, name is N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide, and the molecular formula is C16H21N3O3S, SDS of cas: 901770-40-9.

Ke, Mi published the artcileSpatiotemporal profiling of cytosolic signalling complexes in living cells by selective proximity proteomics, SDS of cas: 901770-40-9, the publication is Nature Communications (2021), 12(1), 71, database is CAplus and MEDLINE.

Signaling complexes are often organized in a spatiotemporal manner and on a minute timescale. Proximity labeling based on engineered ascorbate peroxidase APEX2 pioneered in situ capture of spatiotemporal membrane protein complexes in living cells, but its application to cytosolic proteins remains limited due to the high labeling background. Here, we develop proximity labeling probes with increased labeling selectivity. These probes, in combination with label-free quant. proteomics, allow exploring cytosolic protein assemblies such as phosphotyrosine-mediated protein complexes formed in response to minute-scale EGF stimulation. As proof-of-concept, we systematically profile the spatiotemporal interactome of the EGFR signaling component STS1. For STS1 core complexes, our proximity proteomics approach shows comparable performance to affinity purification-mass spectrometry-based temporal interactome profiling, while also capturing addnl.-especially endosomally-located-protein complexes. In summary, we provide a generic approach for exploring the interactome of mobile cytosolic proteins in living cells at a temporal resolution of minutes.

Nature Communications published new progress about 901770-40-9. 901770-40-9 belongs to imidazoles-derivatives, auxiliary class Other Aliphatic Heterocyclic,Benzene,Phenol,Amide, name is N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide, and the molecular formula is C16H21N3O3S, SDS of cas: 901770-40-9.

Referemce:
https://en.wikipedia.org/wiki/Imidazole,
Imidazole | C3H4N2 – PubChem

El Alaoui, Abdessamad’s team published research in Angewandte Chemie, International Edition in 46 | CAS: 901770-40-9

Angewandte Chemie, International Edition published new progress about 901770-40-9. 901770-40-9 belongs to imidazoles-derivatives, auxiliary class Other Aliphatic Heterocyclic,Benzene,Phenol,Amide, name is N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide, and the molecular formula is C16H21N3O3S, Safety of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide.

El Alaoui, Abdessamad published the artcileShiga toxin-mediated retrograde delivery of a topoisomerase I inhibitor prodrug, Safety of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide, the publication is Angewandte Chemie, International Edition (2007), 46(34), 6469-6472, database is CAplus and MEDLINE.

A retrograde strategy: An innovative cancer-cell delivery concept exploits the naturally evolved characteristics of the Shiga toxin B-subunit (STxB) for the intracellular activation of a newly synthesized prodrug at the level of the biosynthetic/secretory pathway. Retrograde prodrug targeting allows its slow release, which should sustain the presence of the active principle in dividing tumor cells.

Angewandte Chemie, International Edition published new progress about 901770-40-9. 901770-40-9 belongs to imidazoles-derivatives, auxiliary class Other Aliphatic Heterocyclic,Benzene,Phenol,Amide, name is N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide, and the molecular formula is C16H21N3O3S, Safety of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide.

Referemce:
https://en.wikipedia.org/wiki/Imidazole,
Imidazole | C3H4N2 – PubChem

Ke, Mi et al. published their research in Nature Communications in 2021 |CAS: 901770-40-9

The Article related to living cell cytosolic signalling complex selective proteomic spatiotemporal profiling, Placeholder for records without volume info and other aspects.Safety of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide

On December 31, 2021, Ke, Mi; Yuan, Xiao; He, An; Yu, Peiyuan; Chen, Wendong; Shi, Yu; Hunter, Tony; Zou, Peng; Tian, Ruijun published an article.Safety of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide The title of the article was Spatiotemporal profiling of cytosolic signalling complexes in living cells by selective proximity proteomics. And the article contained the following:

Signaling complexes are often organized in a spatiotemporal manner and on a minute timescale. Proximity labeling based on engineered ascorbate peroxidase APEX2 pioneered in situ capture of spatiotemporal membrane protein complexes in living cells, but its application to cytosolic proteins remains limited due to the high labeling background. Here, we develop proximity labeling probes with increased labeling selectivity. These probes, in combination with label-free quant. proteomics, allow exploring cytosolic protein assemblies such as phosphotyrosine-mediated protein complexes formed in response to minute-scale EGF stimulation. As proof-of-concept, we systematically profile the spatiotemporal interactome of the EGFR signaling component STS1. For STS1 core complexes, our proximity proteomics approach shows comparable performance to affinity purification-mass spectrometry-based temporal interactome profiling, while also capturing addnl.-especially endosomally-located-protein complexes. In summary, we provide a generic approach for exploring the interactome of mobile cytosolic proteins in living cells at a temporal resolution of minutes. The experimental process involved the reaction of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide(cas: 901770-40-9).Safety of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide

The Article related to living cell cytosolic signalling complex selective proteomic spatiotemporal profiling, Placeholder for records without volume info and other aspects.Safety of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Kurosu, Michio et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2006 |CAS: 901770-40-9

The Article related to microarray isocyanate diazoketone linker bound protein, Pharmacology: Methods and other aspects.Recommanded Product: 901770-40-9

On July 1, 2006, Kurosu, Michio; Mowers, Williams A. published an article.Recommanded Product: 901770-40-9 The title of the article was Small-molecule microarrays: Development of novel linkers and an efficient detection method for bound proteins. And the article contained the following:

Novel isocyanate and diazoketone linkers possessing polyoxypropylenediamine as a spacer for small-mol. microarray are developed. White light interferometry is introduced to detect bound proteins on the glass slides without using chem. modified proteins. The experimental process involved the reaction of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide(cas: 901770-40-9).Recommanded Product: 901770-40-9

The Article related to microarray isocyanate diazoketone linker bound protein, Pharmacology: Methods and other aspects.Recommanded Product: 901770-40-9

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

El Alaoui, Abdessamad et al. published their research in Angewandte Chemie, International Edition in 2007 |CAS: 901770-40-9

The Article related to shiga toxin retrograde delivery topoisomerase i inhibitor prodrug, Pharmaceuticals: Pharmaceutics and other aspects.Recommanded Product: 901770-40-9

On September 30, 2007, El Alaoui, Abdessamad; Schmidt, Frederic; Amessou, Mohamed; Sarr, Marianne; Decaudin, Didier; Florent, Jean-Claude; Johannes, Ludger published an article.Recommanded Product: 901770-40-9 The title of the article was Shiga toxin-mediated retrograde delivery of a topoisomerase I inhibitor prodrug. And the article contained the following:

A retrograde strategy: An innovative cancer-cell delivery concept exploits the naturally evolved characteristics of the Shiga toxin B-subunit (STxB) for the intracellular activation of a newly synthesized prodrug at the level of the biosynthetic/secretory pathway. Retrograde prodrug targeting allows its slow release, which should sustain the presence of the active principle in dividing tumor cells. The experimental process involved the reaction of N-(4-Hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide(cas: 901770-40-9).Recommanded Product: 901770-40-9

The Article related to shiga toxin retrograde delivery topoisomerase i inhibitor prodrug, Pharmaceuticals: Pharmaceutics and other aspects.Recommanded Product: 901770-40-9

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem