Properties and Exciting Facts About 2-(Benzo[d]thiazol-2-yl)acetonitrile

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In an article, published in an article, once mentioned the application of 56278-50-3, Name is 2-(Benzo[d]thiazol-2-yl)acetonitrile,molecular formula is C9H6N2S, is a conventional compound. this article was the specific content is as follows.Application In Synthesis of 2-(Benzo[d]thiazol-2-yl)acetonitrile

The present invention relates to the 1 H-indazole-3-carboxamide compounds as glycogen synthase kinase 3 beta (GSK-3beta) inhibitors and to their use in the treatment of GSK-3beta-related disorders such as, for example, (i) insulin-resistance disorders; (ii) neurodegenerative diseases; (iii) mood disorders; (iv) schizophrenic disorders; (v) cancerous disorders; (vi) inflammation, (vii) osteoporosis, (viii) cardiac hypertrophy, (ix) epilepsies and (x) neuropathic pain.

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Reference:
Thiazole | C3H942NS – PubChem,
Thiazole | chemical compound | Britannica

The important role of 56278-50-3

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.COA of Formula: C9H6N2S, you can also check out more blogs about56278-50-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.56278-50-3, Name is 2-(Benzo[d]thiazol-2-yl)acetonitrile, molecular formula is C9H6N2S. In a Patent,once mentioned of 56278-50-3, COA of Formula: C9H6N2S

The invention belongs to the field of preparing chemical medicine, and in particular relates to indazole – carboxamide – pyridone derivatives and their preparation and use. The present invention has offered a kind of indazole – carboxamide – pyridone derivatives, the structure shown in formula I. The invention also provides the indazole – carboxamide – pyridone derivatives of the preparation method and use. The present invention provides indazole – carboxamide – pyridone derivatives, is in a large number of screening on the basis of the new compound, inhibits EZH2 activity, as an anti-tumor and autoimmune disease development and application provides new selection. (by machine translation)

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.COA of Formula: C9H6N2S, you can also check out more blogs about56278-50-3

Reference:
Thiazole | C3H947NS – PubChem,
Thiazole | chemical compound | Britannica

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In an article, published in an article, once mentioned the application of 56278-50-3, Name is 2-(Benzo[d]thiazol-2-yl)acetonitrile,molecular formula is C9H6N2S, is a conventional compound. this article was the specific content is as follows.Quality Control of: 2-(Benzo[d]thiazol-2-yl)acetonitrile

5-HETEROARYL SUBSTITUTED INDAZOLE-3-CARBOXAMIDES AND PREPARATION AND USE THEREOF

Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present disclosure concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., tendinopathy, dermatitis, psoriasis, morphea, ichthyosis, Raynaud’s syndrome, Darier’s disease, scleroderma, cancer, abnormal cellular proliferation, angiogenesis, Alzheimer’s disease, lung disease, and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as neurological conditions/disorders/diseases linked to overexpression of DYRK1A.

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Reference:
Thiazole | C3H954NS – PubChem,
Thiazole | chemical compound | Britannica

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Do you like my blog? If you like, you can also browse other articles about this kind. Application In Synthesis of 2-(Benzo[d]thiazol-2-yl)acetonitrile. Thanks for taking the time to read the blog about 56278-50-3

In an article, published in an article, once mentioned the application of 56278-50-3, Name is 2-(Benzo[d]thiazol-2-yl)acetonitrile,molecular formula is C9H6N2S, is a conventional compound. this article was the specific content is as follows.Application In Synthesis of 2-(Benzo[d]thiazol-2-yl)acetonitrile

THERAPEUTIC COMPOUNDS AND USES THEREOF

The present invention relates to compounds of formula (I): and to salts thereof, wherein A has any of the values defined in the specification, and compositions and uses thereof. The compounds are useful as inhibitors of CBP and/or EP300. Also included are pharmaceutical compositions comprising a compound of formula (I) or a pharmaceutically acceptable salt thereof, and methods of using such compounds and salts in the treatment of various CBP and/or EP300-mediated disorders.

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Reference:
Thiazole | C3H944NS – PubChem,
Thiazole | chemical compound | Britannica

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Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of 2-(Benzo[d]thiazol-2-yl)acetonitrile. In my other articles, you can also check out more blogs about 56278-50-3

56278-50-3, Name is 2-(Benzo[d]thiazol-2-yl)acetonitrile, molecular formula is C9H6N2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 56278-50-3, Safety of 2-(Benzo[d]thiazol-2-yl)acetonitrile

Complement Factor D inhibitors, pharmaceutical compositions, and uses thereof, as well as processes for their manufacture are provided. The compounds provided include Formula I, Formula II, Formula III, Formula IV, and Formula V, or a pharmaceutically acceptable salt, prodrug, isotopic analog, N-oxide, or isolated isomer thereof, optionally in a pharmaceutically acceptable composition. The inhibitors described herein target Factor D and inhibit or regulate the complement cascade.

Complement Factor D inhibitors, pharmaceutical compositions, and uses thereof, as well as processes for their manufacture are provided. The compounds provided include Formula I, Formula II, Formula III, Formula IV, and Formula V, or a pharmaceutically acceptable salt, prodrug, isotopic analog, N-oxide, or isolated isomer thereof, optionally in a pharmaceutically acceptable composition. The inhibitors described herein target Factor D and inhibit or regulate the complement cascade.

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Reference£º
Thiazole | C3H958NS – PubChem,
Thiazole | chemical compound | Britannica

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The present invention relates to substituted indazoles and related heterocycles. These compounds are useful for the prevention and/or treatment of hyperproliferative, inflammatory and degenerative disorders and diseases. Thus, this invention is also concerned with the use of the compounds of the present invention for the the prevention and/or treatment of hyperproliferative, inflammatory and degenerative disorders and diseases as well as pharmaceutical composition, medicaments and kits comprising the substituted indazoles and related heterocycles of the present invention and processes for manufacturing those compounds.

The present invention relates to substituted indazoles and related heterocycles. These compounds are useful for the prevention and/or treatment of hyperproliferative, inflammatory and degenerative disorders and diseases. Thus, this invention is also concerned with the use of the compounds of the present invention for the the prevention and/or treatment of hyperproliferative, inflammatory and degenerative disorders and diseases as well as pharmaceutical composition, medicaments and kits comprising the substituted indazoles and related heterocycles of the present invention and processes for manufacturing those compounds.

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Reference£º
Thiazole | C3H943NS – PubChem,
Thiazole | chemical compound | Britannica

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This invention relates to compounds, pharmaceutical compositions and methods for the treatment of a condition mediated by CB1 receptor activity in a mammalian subject including a human, which comprises administering to a mammal in need of such treatment a therapeutically effective amount of the compound of formula (I) wherein R1, R2 and R3 are as defined in this specification.

This invention relates to compounds, pharmaceutical compositions and methods for the treatment of a condition mediated by CB1 receptor activity in a mammalian subject including a human, which comprises administering to a mammal in need of such treatment a therapeutically effective amount of the compound of formula (I) wherein R1, R2 and R3 are as defined in this specification.

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Reference£º
Thiazole | C3H938NS – PubChem,
Thiazole | chemical compound | Britannica

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CBP and EP300 are highly homologous, bromodomain-containing transcription coactivators involved in numerous cellular pathways relevant to oncology. As part of our effort to explore the potential therapeutic implications of selectively targeting bromodomains, we set out to identify a CBP/EP300 bromodomain inhibitor that was potent both in vitro and in cellular target engagement assays and was selective over the other members of the bromodomain family. Reported here is a series of cell-potent and selective probes of the CBP/EP300 bromodomains, derived from the fragment screening hit 4-methyl-1,3,4,5-tetrahydro-2H-benzo[b][1,4]diazepin-2-one.

CBP and EP300 are highly homologous, bromodomain-containing transcription coactivators involved in numerous cellular pathways relevant to oncology. As part of our effort to explore the potential therapeutic implications of selectively targeting bromodomains, we set out to identify a CBP/EP300 bromodomain inhibitor that was potent both in vitro and in cellular target engagement assays and was selective over the other members of the bromodomain family. Reported here is a series of cell-potent and selective probes of the CBP/EP300 bromodomains, derived from the fragment screening hit 4-methyl-1,3,4,5-tetrahydro-2H-benzo[b][1,4]diazepin-2-one.

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Reference£º
Thiazole | C3H959NS – PubChem,
Thiazole | chemical compound | Britannica