Tag: M.W:100-200

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 348-40-3, Name is 6-Fluorobenzo[d]thiazol-2-amine, Recommanded Product: 348-40-3.

A series of benzothiazole linked phenylpyridopyrimidinones (8a-g) and their diones (9a-g) have been designed, synthesized and evaluated for their anticancer activity. Among the series one of the conjugate 8b showed significant cytotoxicity against human cervical cancer cell line ME-180 with IC 50 value of 4.01 muM. This compound was tested on the cell cycle perturbations and DNA damage. Flow cytometry analysis revealed that the compound 8b showed drastic cell cycle perturbations due to concentration dependent increase in the sub-G0 phase in ME-180 cell line. DNA fragmentation and Hoechst staining reveals that this compound induced cell death by apoptosis. Further caspase-3 and loss of mitochondrial membrane potential suggested that the compound induces cell death by apoptosis.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Quality Control of: 6-Fluorobenzo[d]thiazol-2-amine. In my other articles, you can also check out more blogs about 348-40-3

Reference：
Thiazole | C3H10564NS – PubChem,
Thiazole | chemical compound | Britannica

Application of 440100-94-7, Children learn through play, and they learn more than adults might expect. Science experiments are a great way to spark their curiosity, get their minds active, and encourage them to do something that doesn’t involve a screen. 440100-94-7, C4HBrN2S. A document type is Patent, introducing its new discovery.

The present invention is related to a pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and a compound represented by the following structural formula: The present invention is also related a method of treating a subject with a disease which can be ameliorated by inhibition of poly(ADP-ribose)polymerase (PARP). The definitions of the variables are provided herein.

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Reference：
Thiazole | C3H2767NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 19952-47-7, Name is 2-Amino-4-chlorobenzothiazole, molecular formula is C7H5ClN2S. In a Article，once mentioned of 19952-47-7, COA of Formula: C7H5ClN2S

Structurally diverse annulated benzothiazoloquinazolines have been synthesized by an environmentally benign, efficient, and convenient synthesis involving three-component domino reaction of 2-aminobenzothiazoles, alpha-tetralone, and furan-2-carbaldehyde/p-methoxybenzaldehyde using an SO3H-functionalized halogen-free ionic liquid ([MIM(CH2)4SO3H][HSO4]) as a catalyst and a reaction medium.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.COA of Formula: C7H5ClN2S, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 19952-47-7, in my other articles.

Reference：
Thiazole | C3H9994NS – PubChem,
Thiazole | chemical compound | Britannica

Reference of 82294-70-0. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 82294-70-0, Name is 4-Methylthiazole-5-carbaldehyde

An enantioselective synthesis of alpha-methylene-beta-hydroxy carboxylic acid derivatives via a highly diastereoselective, one-pot syn-aldol and beta-elimination sequence utilizing the chiral beta-(phenylselenyl) propionyl imide 15 is described. This new method, which constitutes an alternative to the Baylis-Hillman reaction, has been applied to the synthesis of the C(15)-C(21) fragment of tedanolide C.

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Reference：
Thiazole | C3H5763NS – PubChem,
Thiazole | chemical compound | Britannica

Application of 20358-00-3. Let’s face it, organic chemistry can seem difficult to learn. Especially from a beginner’s point of view. Like 20358-00-3, Name is 2-Amino-5-chlorobenzothiazole. In a document type is Article, introducing its new discovery.

Several N-lactosylated aryl thioureas and benzothiazolyl thioureas have been prepared by the condensation of hepta-O-acetyl-beta-D-lactosyl isothiocyanate with aryl amines and 2-aminobenzothiazole/substituted benzothiazoles. Hepta-O-acetyl-beta-D-lactosyl isothiocyanate was prepared by the interaction of hepta-O-acetyl-alpha-D-lactosyl bromide and lead thiocyanate. The structures of these new N-lactosides have been established on the basis of IR, NMR, and mass spectral studies.

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Reference：
Thiazole | C3H2144NS – PubChem,
Thiazole | chemical compound | Britannica

Electric Literature of 61291-21-2. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 61291-21-2, Name is 5-Methylthiazole-2-carboxylic acid

New compounds containing [1,2,4]triazolo [1,5-a]pyridine (I), pyrazolo [1,5-a]pyridine (II), 1H-1,3-benzodiazole (III) and imidazo [1,2-a]pyrimidine (IV) backbones were designed and synthesized for PDE10A interaction. Among these compounds, 1H-1,3-benzodiazoles and imidazo [1,2-a]pyrimidines showed the highest affinity for PDE10A enzyme as well as good metabolic stability. Both classes of compounds were identified as selective and potent PDE10A enzyme inhibitors.

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Reference：
Thiazole | C3H6518NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 41731-23-1, Name is 2-Bromo-5-methylthiazole, molecular formula is C4H4BrNS. In a Patent，once mentioned of 41731-23-1, Computed Properties of C4H4BrNS

The present invention relates to a compound represented by formula (I) and pharmaceutically acceptable salts thereof are disclosed as useful for treating or preventing diabetes, hyperlipidemia, obesity, NASH, inflammation related disorders, and related diseases and conditions. The compounds are useful as agonists of the G-protein coupled receptor GPR120. Pharmaceutical compositions and methods of treatment are also included.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Computed Properties of C4H4BrNS. In my other articles, you can also check out more blogs about 41731-23-1

Reference：
Thiazole | C3H2570NS – PubChem,
Thiazole | chemical compound | Britannica

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 67899-00-7, Name is 2-Amino-4-methylthiazole-5-carboxylic acid, molecular formula is C5H6N2O2S. In a Patent，once mentioned of 67899-00-7, name: 2-Amino-4-methylthiazole-5-carboxylic acid

The present invention provides an amide compound represented by the formula (1): wherein R1 and R2 independently represent a hydrogen atom or a methyl group; and Cy1 represents a C3-C6 cycloalkyl group, said compound having excellent plant disease controlling effect.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.name: 2-Amino-4-methylthiazole-5-carboxylic acid, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 67899-00-7, in my other articles.

Reference：
Thiazole | C3H1981NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 14779-18-1, Name is 7-Methylbenzo[d]thiazol-2-amine,molecular formula is C8H8N2S, is a conventional compound. this article was the specific content is as follows.name: 7-Methylbenzo[d]thiazol-2-amine

A series of new benzo[d]thiazole-hydrazones analogues were synthesized and screened for their in vitro antibacterial and antifungal activities. The results revealed that compounds 13, 14, 15, 19, 20, 28 and 30 exhibited superior antibacterial potency compared to the reference drug chloramphenicol and rifampicin. Compounds 5, 9, 10, 11, 12, 28 and 30 were found to be good antifungal activity compared to the standard drug ketoconazole. A preliminary study of the structure-activity relationship (SAR) revealed that the antimicrobial activity depended on the effect of different substituents on the phenyl ring. The electron donating (OH and OCH3) groups presented in the analogues, increase the antibacterial activity (except compound 12), interestingly, while the electron withdrawing (Cl, NO2, F and Br) groups increase the antifungal activity (except compound 19 and 20). In addition, analogues containing thiophene (28) and indole (30) showed good antimicrobial activities. Whereas, aliphatic analogues (24?26) shown no activities in both bacterial and fungal stains even in high concentrations (100 mug/mL). Molecular docking studies were performed for all the synthesized compounds of which compounds 11, 19 and 20 showed the highest glide G-score.

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Reference：
Thiazole | C3H7438NS – PubChem,
Thiazole | chemical compound | Britannica

Related Products of 1603-91-4, An article , which mentions 1603-91-4, molecular formula is C4H6N2S. The compound – 4-Methylthiazol-2-amine played an important role in people’s production and life.

Substituted imidazo[2,1-b]thiazole compounds corresponding to formula I, a method for producing them, pharmaceutical compositions containing them, and the use thereof for regularing mGluR5 receptors, or for treating or inhibiting disorders or disease states at least partially mediated by mGluR5 receptor such as pain, anxiety attacks, drug or alcohol dependency, and others.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 1603-91-4, help many people in the next few years., Related Products of 1603-91-4

Reference：
Thiazole | C3H9707NS – PubChem,
Thiazole | chemical compound | Britannica