Tag: M.W:200-300

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. 2941-48-2, Name is 2,5-Dichlorobenzothiazole, molecular formula is C7H3Cl2NS. In a Patent，once mentioned of 2941-48-2, Recommanded Product: 2,5-Dichlorobenzothiazole

The present invention relates to novel compounds of formula (I) that can be employed in the treatment, alleviation or prevention of a group of disorders and abnormalities associated with Tau (Tubulin associated unit) protein aggregates including, but not limited to, Neurofibrillary Tangles (NFTs), such as Alzheimer’s disease (AD).

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Recommanded Product: 2,5-Dichlorobenzothiazole. In my other articles, you can also check out more blogs about 2941-48-2

Reference：
Thiazole | C3H1708NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.80945-86-4, Name is 6-Bromo-2-chlorobenzothiazole, molecular formula is C7H3BrClNS. In a Article，once mentioned of 80945-86-4, Quality Control of: 6-Bromo-2-chlorobenzothiazole

A new reagent, ethyltriphenyl phosphonium tribromide (ETPPTB), has been synthesized and studied. Results show that the reagent is quite efficient for various reactions such as organic bominations, acylations, and isothiocyanate preparation. Copyright

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 80945-86-4 is helpful to your research., Quality Control of: 6-Bromo-2-chlorobenzothiazole

Reference：
Thiazole | C3H10947NS – PubChem,
Thiazole | chemical compound | Britannica

In an article, published in an article, once mentioned the application of 566169-93-5, Name is 2-(4-(Methylamino)phenyl)benzo[d]thiazol-6-ol,molecular formula is C14H12N2OS, is a conventional compound. this article was the specific content is as follows.Application In Synthesis of 2-(4-(Methylamino)phenyl)benzo[d]thiazol-6-ol

The Amyloid beta protein binding specificity to [be] high, high permeability of the blood-brain barrier, brain senile plaques in storage properties, whereas, in the remaining portion except the old brain plaques characteristic hardly boron carrier compound. [Solving means] a flavone derivatives, chromone derivatives, coumarin derivatives, orlon derivatives, chalcone derivative, benzothiazole derivative in the stilbene derivative, beta-Amyloid-associated disease or pathological -10 boron atom in each derivative compounds for boron neutron capture therapy applications to Amyloid protein. [Drawing] no (by machine translation)

Do you like my blog? If you like, you can also browse other articles about this kind. Application In Synthesis of 2-(4-(Methylamino)phenyl)benzo[d]thiazol-6-ol. Thanks for taking the time to read the blog about 566169-93-5

Reference：
Thiazole | C3H447NS – PubChem,
Thiazole | chemical compound | Britannica

566169-93-5, Name is 2-(4-(Methylamino)phenyl)benzo[d]thiazol-6-ol, molecular formula is C14H12N2OS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 566169-93-5, HPLC of Formula: C14H12N2OS

Two new fluorinated imidazo[1,2-a]pyridine derivatives, 6-(2′-fluoroethyl)-2-(4′-dimethylamino)phenylimidazo[1,2-a]pyridine (FEPIP) and 6-(3′-fluoropropyl)-2-(4′-dimethylamino)phenylimidazo[1,2-a]pyridine (FPPIP), were synthesized. The binding affinity for FEPIP and FPPIP to amyloid plaques in human AD cortical tissues was determined. Radiolabeling, in vitro film autoradiography, and micro-PET study were performed with [18F]FPPIP to determine its utility as a radioligand for amyloid plaque imaging in the brain of AD patients.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.HPLC of Formula: C14H12N2OS. In my other articles, you can also check out more blogs about 566169-93-5

Reference：
Thiazole | C3H420NS – PubChem,
Thiazole | chemical compound | Britannica

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. 69812-29-9, C6H7ClN2O3S2. A document type is Patent, introducing its new discovery., SDS of cas: 69812-29-9

The present invention relates to a novel class of sulfonamides which are aspartyl protease inhibitors. In one embodiment, this invention relates to a novel class of HIV aspartyl protease inhibitors characterized by specific structural and physicochemical features. This invention also relates to pharmaceutical compositions comprising these compounds. The compounds and pharmaceutical compositions of this invention are particularly well suited for inhibiting HIV-1 and HIV-2 protease activity and consequently, may be advantageously used as anti-viral agents against the HIV-1 and HIV-2 viruses. This invention also relates to methods for inhibiting the activity of HIV aspartyl protease using the compounds of this invention and methods for screening compounds for anti-HIV activity.

Interested yet? Keep reading other articles of 69812-29-9!, SDS of cas: 69812-29-9

Reference：
Thiazole | C3H1777NS – PubChem,
Thiazole | chemical compound | Britannica

144060-99-1, Name is 2-(4-Fluorophenyl)-4-methylthiazole-5-carboxylic acid, molecular formula is C11H8FNO2S, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 144060-99-1, Safety of 2-(4-Fluorophenyl)-4-methylthiazole-5-carboxylic acid

The invention relates to a novel 2-phenylthiazole-5-methanamide compound shown as a general formula I, a precursor, a stereo isomer and physiologically-acceptable salt thereof, a medicinal composition containing the compound, and an application of the compound as the aspect of medicine.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of 2-(4-Fluorophenyl)-4-methylthiazole-5-carboxylic acid. In my other articles, you can also check out more blogs about 144060-99-1

Reference：
Thiazole | C3H580NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.302964-02-9, Name is 2-Boc-Aminothiazole-5-carboxylic acid, molecular formula is C9H12N2O4S. In a Patent，once mentioned of 302964-02-9, SDS of cas: 302964-02-9

Compounds represented by Formula (I): or pharmaceutically acceptable salts thereof, are effective as NMDA NR2B antagonists useful for relieving pain.

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.SDS of cas: 302964-02-9, you can also check out more blogs about302964-02-9

Reference：
Thiazole | C3H2391NS – PubChem,
Thiazole | chemical compound | Britannica

Synthetic Route of 73040-66-1, 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. 73040-66-1, C9H7ClN2S. A document type is Article, introducing its new discovery.

The authors describe the synthesis and characterization of two different five-member heterocycle derivatives (thiazole and thiadiazole) by several organic procedures. These compounds were characterized by FTIR, 1H NMR, and elemental analyses. Also, the authors attempt to study the inhibition effects of these derivatives to the corrosion of copper in nitric acid media by weight loss technique. The temperature factor affecting the inhibition efficiency of these derivatives is discussed. Also, the inhibition efficiency depended on the changing substituents on the molecules. It was found from the results that the thiadiazole inhibitors have inhibition efficiency more than thiazole inhibitors.

If you are hungry for even more, make sure to check my other article about 73040-66-1. Synthetic Route of 73040-66-1

Reference：
Thiazole | C3H5965NS – PubChem,
Thiazole | chemical compound | Britannica

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.5331-91-9, Name is 5-Chlorobenzo[d]thiazole-2(3H)-thione, molecular formula is C7H4ClNS2. In a Article，once mentioned of 5331-91-9, Recommanded Product: 5331-91-9

The basic objective of this investigation is to explore potential metallo-organic antimicrobial agents based on silver?heterocyclic-2-thiones. In this respect, a series of silver(I) halide complexes with imidazolidine-2-thiones (L-NR, R = H, Me, Et, Prn, Bun, Ph), namely, mononuclear [AgX(L-NR)(PPh3)2] (X, R: Cl, Bu, 1; Br, Ph, 7); [AgX(L-NR)3] (Br, Bu, 5; Br, Prn, 8) and halogen bridged dinuclear [Ag2(mu-X)2(L-NR)2(PPh3)2] (Cl, Bun, 2; Cl, Ph, 3; Cl, Prn, 4; Br, Ph, 6) have been synthesized and characterized using modern techniques. The thio-ligands are terminally S-bonded in all the complexes. The in vitro antimicrobial potential and biosafety evaluation of the above complexes as well as that of previously reported analogous silver complexes has been studied against Gram positive bacteria, namely, Staphylococcus aureus (MTCC 740) and Methicillin resistant Staphylococcus aureus (MRSA), Gram negative bacteria Klebsiella pneumoniae (MTCC 109), Salmonella typhimurium (MTCC 98) and a yeast Candida albicans (MTCC 227). Most of the complexes tested have shown significant antimicrobial activity with low values of minimum inhibitory concentration (MIC). Significantly, the activity against MRSA is an important outcome of this investigation. Among complexes tested for their cytotoxicity using MTT [3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyl tetrazolium bromide] assay, some complexes showed low cellular toxicity with high percent cell viability. A dinuclear complex [Ag2(mu-Cl)2(L-NPh)2(PPh3)2] 3 with 93.3% cell viability emerges the most important candidate for further investigations.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 5331-91-9 is helpful to your research., Recommanded Product: 5331-91-9

Reference：
Thiazole | C3H6292NS – PubChem,
Thiazole | chemical compound | Britannica

16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS, belongs to thiazole compound, is a common compound. In a patnet, once mentioned the new application about 16112-21-3, HPLC of Formula: C14H11NS

A one-pot synthesis of 2-arylbenzothiazoles from the reaction of 2-aminothiophenol and aromatic aldehydes catalyzed by 1,3-dibromo-5,5- dimethylhydantoin is reported.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.HPLC of Formula: C14H11NS. In my other articles, you can also check out more blogs about 16112-21-3

Reference：
Thiazole | C3H843NS – PubChem,
Thiazole | chemical compound | Britannica