Month: September 2022

Zhou, Quan-Cheng;Wang, Tian-Rui;Li, Hui;Chen, Lei;Xin, Jia-Jin;Guo, Shen;Sheng, Gui-Hua;You, Zhong-Lu published 《Synthesis, crystal structures and insulin-like activity of three new oxidovanadium(V) complexes with aroylhydrazone ligand》 in 2019. The article was appeared in 《Journal of Inorganic Biochemistry》. They have made some progress in their research.Quality Control of Methyl 3-methylbenzoate The article mentions the following:

Three new oxidovanadium(V) complexes were designed, synthesized and characterized by C, H, N elemental anal., single crystal x-ray diffraction,UV/visible and IR spectra. Complex 1: [VOL¹X] (H₂L¹ = (E)-N’-(2-hydroxybenzylidene)-3-methbenzohydrazide, HX = ethylmaltol = 2-ethyl-3-hydroxy-4-pyrone), Complex 2: [VOL²(CH₃O)(CH₃OH)], (H₂L² = C₁₆H₁₆N₂O₄ = (E)-N’-(2-hydroxybenzylidene)-3,5-dimethoxybenzohydrazide, CH₃OH = methanol), Complex 3: [VOL³X] (H₂L³ = (E)-N’-(3-ethoxy-2-hydroxybenzylidene)-3,5-dimethoxybenzohydrazide). The insulin-like activity of the three complexes was tested. Both normal and streptozotocin (STZ)-diabetic mice were administered intragastrically for two weeks. The complexes at doses of 10.0 and 5.0 mg V·kg^-1 can significantly decrease the blood glucose level in STZ-diabetic mice, and the blood glucose level in the treated normal mice was not altered. The lesions of kidney and liver caused by diabetes have varying degrees of improvement. To complete the study, the researchers used Methyl 3-methylbenzoate (cas: 99-36-5) .

Methyl 3-methylbenzoate (cas: 99-36-5) is a common ester. Esters are widespread in nature and are widely used in industry. Several billion kilograms of polyesters are produced industrially annually, important products being polyethylene terephthalate, acrylate esters, and cellulose acetate.Quality Control of Methyl 3-methylbenzoate

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Wu, Han;Sun, Yu;Wong, Wee Lin;Cui, Jiajia;Li, Jingyang;You, Xuefu;Yap, Lee Fah;Huang, Yu;Hong, Wei;Yang, Xinyi;Paterson, Ian C.;Wang, Hao published 《The development of a novel transforming growth factor-β (TGF-β) inhibitor that disrupts ligand-receptor interactions》 in 2020. The article was appeared in 《European Journal of Medicinal Chemistry》. They have made some progress in their research.SDS of cas: 99-36-5 The article mentions the following:

Transforming growth factor-β (TGF-β) plays an important role in regulating epithelial to mesenchymal transition (EMT) and the TGF-β signaling pathway is a potential target for therapeutic intervention in the development of many diseases, such as fibrosis and cancer. Most currently available inhibitors of TGF-β signaling function as TGF-β receptor I (TβR-I) kinase inhibitors, however, such kinase inhibitors often lack specificity. In the present study, we targeted the extracellular protein binding domain of the TGF-β receptor II (TβR-II) to interfere with the protein-protein interactions (PPIs) between TGF-β and its receptors. One compound, CJJ300, inhibited TGF-β signaling by disrupting the formation of the TGF-β-TβR-I-TβR-II signaling complex. Treatment of A549 cells with CJJ300 resulted in the inhibition of downstream signaling events such as the phosphorylation of key factors along the TGF-β pathway and the induction of EMT markers. Concomitant with these effects, CJJ300 significantly inhibited cell migration. The present study describes for the first time a designed mol. that can regulate TGF-β-induced signaling and EMT by interfering with the PPIs required for the formation of the TGF-β signaling complex. Therefore, CJJ300 can be an important lead compound with which to study TGF-β signaling and to design more potent TGF-β signaling antagonists. And Methyl 3-methylbenzoate (cas: 99-36-5) was used in the research process.

Methyl 3-methylbenzoate (cas: 99-36-5) is a common ester.Esters are common in organic chemistry and biological materials, and often have a pleasant characteristic, fruity odor. This leads to their extensive use in the fragrance and flavor industry. Ester bonds are also found in many polymers.SDS of cas: 99-36-5

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Xue, Rui;Cui, Er-Liang;Hu, Guo-Quan;Zhu, Ming-Qiang published 《The composition, physicochemical properties, antimicrobial and antioxidant activity of wood vinegar prepared by pyrolysis of Eucommia ulmoides Oliver branches under different refining methods and storage conditions》. The research results were published in《Industrial Crops and Products》 in 2022.HPLC of Formula: 106-02-5 The article conveys some information:

To enhance the quality of wood vinegar (WV), the WV prepared by pyrolyzing Eucommia ulmoides Oliver (EUO) branches at the temperature of 650°C were refined by using different physicochem. methods. The crude WV was refined by ultra-low freezing and thawing (WV_FT), charcoal adsorption (WV_CA), and activated carbon adsorption (WV_ACA), resp. Meanwhile, the chem. compositions, antimicrobial and antioxidant activity of the crude WV (WV_C), the WV (WV_S) prepared two years ago, and the photolysis WV (WV_P) were investigated. The results showed that the WV_FT obtained by ultra-low freezing and thawing method possessed better quality with pH of 3.45, d. of 1.045 g/cm³ , refractive index of 26.85% and total organic acid of 11.00%. It was also found that WV_FT had better inhibition rate of 83.33% against Bacterium prodigiosum, indication the excellent antibacterial activity. Moreover, WV_FT had significant effect on scavenging rate (98.72%) for hydroxyl radicals. This research could offer some references for the refining methods of WV, and the WV was expected to be a potential candidate for materials of antioxidant and antimicrobial. The experimental procedure involved many compounds, such as Oxacyclohexadecan-2-one (cas: 106-02-5) .

Oxacyclohexadecan-2-one(cas:106-02-5) is a natural product found in Lonicera japonica and Angelica archangelica.HPLC of Formula: 106-02-5 It is a macrocyclic lactone that can be used as a flavoring agent and fragrance ingredient due to its musk flavor/odor.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Njateng, Guy Sedar Singor;Du, Zhizhi;Gatsing, Donatien;Donfack, Arno Rusel Nanfack;Talla, Michel Feussi;Wabo, Hippolyte Kamdem;Tane, Pierre;Mouokeu, Raymond Simplice;Luo, Xiaodong;Kuiate, Jules-Roger published 《Antifungal properties of a new terpernoid saponin and other compounds from the stem bark of Polyscias fulva Hiern (Araliaceae)》. The research results were published in《BMC Complementary and Alternative Medicine》 in 2015.Safety of Methyl 2,4-dihydroxy-3,6-dimethylbenzoate The article conveys some information:

Background: In our previous studies, it was evident that the dichloromethane-methanol (1:1 volume/volume) stem barks extract of Polyscias fulva and fractions (Et acetate, n-butanol and residue) demonstrated interesting antidermatophytic activities. So, as a continuity of that, this work aimed at identifying active principles with antifungal properties from P. fulva that could be used as markers for possible standardization of this plant as phytomedicine. Methods: The Et acetate, n-butanol and residual fractions of the dichloromethane-methanol (1:1 volume/volume) stem bark extract of Polyscias fulva were further fractionated by column chromatog. and the structures of isolated compounds elucidated based on their spectroscopic data in comparison with existing literature information. Antifungal activity was assayed by broth microdilution techniques on yeasts and dermatophytes spores. Results: The fractionation of the crude dichloromethane-methanol (1:1 volume/volume) stem bark extract of Polyscias fulva led to the isolation of 10 known compounds (1 to 10) and one new saponin (11: 3-O-[α-L-rhamnopyranosyl (1-2)-α-L-arabinopyranosyl]-28-O-[α-L-4-O-acetyl-rhamnopyranosyl (1-4)-β-D-glucopyranosyl-(1-6)-β-D-glucopyranosyl]-hederagenin). Among these compounds, 3-O-α-L- arabinopyranosyl-hederagenin and 3-O-[α-L-rhamnopyranosyl (1-2)-α-L-arabinopyranosyl]-hederagenin were the most active on the tested fungi with MIC values ranging from 0.78 to 100 μg/mL against both yeasts and dermatophytes. Conclusion: The results of this work constitute a step forward in the possible development of an antidermatophytic phytomedicine from Polyscias fulva stem bark, the isolated compounds being possible markers for the standardisation. And Methyl 2,4-dihydroxy-3,6-dimethylbenzoate (cas: 4707-47-5) was used in the research process.

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate(4707-47-5) is used in biological study as role of androgens in inducing distinct response of epithelial-mesenchymal transition factors in human prostate cancer cells.Safety of Methyl 2,4-dihydroxy-3,6-dimethylbenzoate

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Sattenapally, Narsimha;Sharma, Jhanvi;Hou, Yuqing published 《Selective conversion of primary amides to esters promoted by KHSO₄》 in 2018. The article was appeared in 《ARKIVOC (Gainesville, FL, United States)》. They have made some progress in their research.Synthetic Route of C9H10O2 The article mentions the following:

Primary amides, either aliphatic or aromatic, were easily converted to the corresponding esters via reflux in lower primary alcs. in the presence of KHSO₄. Secondary amides led to complicated mixtures under analogous conditions, whereas tertiary amides were inert. Use of iso-Pr alc. resulted in the formation of product at slower rate and lower yield along with side products, whereas, use of tertiary alcs. did not give successful conversion and allyl and benzyl alc. provided complex mixtures And Methyl 3-methylbenzoate (cas: 99-36-5) was used in the research process.

Methyl 3-methylbenzoate (cas: 99-36-5) is a common ester.Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids.Synthetic Route of C9H10O2 Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Melais, Nedjma;Aribi-Zouioueche, Louisa;Riant, Olivier published 《The effect of the migrating group structure on enantioselectivity in lipase-catalyzed kinetic resolution of 1-phenylethanol》. The research results were published in《Comptes Rendus Chimie》 in 2016.SDS of cas: 93-92-5 The article conveys some information:

We have studied the effects of the acyl moiety on the enantioselectivity of three lipases: Candida antarctica B, Pseudomonas cepacia and Candida cylindracea, frequently used in kinetic resolutions by acylation or hydrolysis. The size of the acyl group was examined using various enol esters during the transesterification of 1-phenylethanol and the hydrolysis of the corresponding phenylethyl esters. C. antarctica-B lipase showed the highest selectivity in the transesterification of 1-phenylethanol with isopropenyl and vinyl acetate, vinyl decanoate, vinyl laurate, (E > 200). The esters 1-Ph -ethyl-acetate, decanoate and laurate are also hydrolyzed with high selectivities (E > 150) with CAL-B. The results can be correlated to the three-dimensional form of each lipase. The effect of the migrating group on the reactivity and selectivity of the lipases are discussed for both reactions. And 1-Phenylethyl acetate (cas: 93-92-5) was used in the research process.

1-Phenylethyl acetate(cas:93-92-5) is a carboxylic ester. SDS of cas: 93-92-5 It may be prepared by acetylation of methyl phenyl carbinol; from benzaldehyde by reacting with magnesium methyl bromide and subsequent acetylation; from 1-bromoethylbenzene and silver acetate in acetic acid.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Slavchev, Ivaylo;Ward, Jas. S.;Rissanen, Kari;Dobrikov, Georgi M.;Simeonov, Svilen published 《Base-promoted direct amidation of esters: beyond the current scope and practical applications》. The research results were published in《RSC Advances》 in 2022.Reference of Methyl 3-methylbenzoate The article conveys some information:

The base-promoted direct amidation of unactivated esters is among the most useful reactions for amide bond formation in contemporary organic chem. The intensive research in this area has led to the development of a number of new methods to achive this transformation. However, to date, the existing literature is more methodol. and in many instances lacks practical directions. Therefore, the full potential of this transformation is yet to be revealed by broadening the substrate scope. In a search for new practical applications of the amidation reaction, herein a comprehensive study of a number of base-promoted direct amidations that encompass a wide range of amines and esters is presented. Furthermore, authors applied their findings in the synthesis of phosphoramidates and several industrially relevant products. The experimental procedure involved many compounds, such as Methyl 3-methylbenzoate (cas: 99-36-5) .

Methyl 3-methylbenzoate (cas: 99-36-5) is a common ester.Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids.Reference of Methyl 3-methylbenzoate Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Synthetic Route of C9H10O2《Reactions of benzyltriphenylphosphonium salts under photoredox catalysis》 was published in 2021. The authors were Boldt, Andrew M.;Dickinson, Sidney I.;Ramirez, Jonathan R.;Benz-Weeden, Anna M.;Wilson, David S.;Stevenson, Susan M., and the article was included in《Organic & Biomolecular Chemistry》. The author mentioned the following in the article:

The development of benzyltriphenylphosphonium salts RCH₂P⁺(C₆H₅)₃X^– (R = 3-methylphenyl, 4-bromophenyl, 3,5-dimethylphenyl, etc.; X = Cl, Br) as alkyl radical precursors using photoredox catalysis is described. Depending on substituents, the benzylic radicals may couple to form C-C bonds or abstract a hydrogen atom to form C-H bonds. A natural product, brittonin A, was also synthesized using this method. The experimental procedure involved many compounds, such as Methyl 3-methylbenzoate (cas: 99-36-5) .

Methyl 3-methylbenzoate (cas: 99-36-5) is a common ester.Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids.Synthetic Route of C9H10O2 Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Formula: C15H28O2In 2020, Tahiri, Nabil;Fodran, Peter;Jayaraman, Dhineshkumar;Buter, Jeffrey;Witte, Martin D.;Ocampo, Tonatiuh A.;Moody, D. Branch;Van Rhijn, Ildiko;Minnaard, Adriaan J. published 《Total Synthesis of a Mycolic Acid from Mycobacterium tuberculosis》. 《Angewandte Chemie, International Edition》published the findings. The article contains the following contents:

In Mycobacterium tuberculosis, mycolic acids and their glycerol, glucose, and trehalose esters (“cord factor”) form the main part of the mycomembrane. Despite their first isolation almost a century ago, full stereochem. evaluation is lacking, as is a scalable synthesis required for accurate immunol., including vaccination, studies. Herein, we report an efficient, convergent, gram-scale synthesis of four stereo-isomers of a mycolic acid and its glucose ester. Binding to the antigen presenting protein CD1b and T cell activation studies are used to confirm the antigenicity of the synthetic material. The absolute stereochem. of the syn-methoxy Me moiety in natural material is evaluated by comparing its optical rotation with that of synthetic material. To complete the study, the researchers used Oxacyclohexadecan-2-one (cas: 106-02-5) .

Oxacyclohexadecan-2-one(cas:106-02-5) is a natural product found in Lonicera japonica and Angelica archangelica.Formula: C15H28O2 It is a macrocyclic lactone that can be used as a flavoring agent and fragrance ingredient due to its musk flavor/odor.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Carvalho da Silva, Romezio Alves;Marques de Mesquita, Bruna;Frota de Farias, Iolanda;Garcia do Nascimento, Patricia Georgiana;Gomes de Lemos, Telma Leda;Monte, Francisco Jose Queiroz published 《Enzymatic chemical transformations of aldehydes, ketones, esters and alcohols using plant fragments as the only biocatalyst: Ximenia americana grains》 in 2018. The article was appeared in 《Molecular Catalysis》. They have made some progress in their research.Electric Literature of C10H12O2 The article mentions the following:

The present study demonstrated the ability of Ximenia american as a biocatalyst in reduction, hydrolysis and esterification reactions. The reduction reactions of aldehydes and ketones, ester hydrolysis and esterification of alcs. were carried out with interesting results. Reduction of ketones afforded yields of 6-60% with ee in the range of 35->99% and that of aldehydes in yields of 51-99%. On the other hand, ester hydrolysis afforded yields of 58-98% with ee in the range 34-87%, while esterification of alcs. in 18-99% yields. Exptl. conditions for all reactions have been defined using standard substrates as indicated in results and discussion. Some of the products are the potential building blocks for the synthesis of mols. which are of pharmaceutical and agrochem. importance. To complete the study, the researchers used 1-Phenylethyl acetate (cas: 93-92-5) .

1-Phenylethyl acetate(cas:93-92-5) is a carboxylic ester. Electric Literature of C10H12O2 It may be prepared by acetylation of methyl phenyl carbinol; from 1-bromoethylbenzene and silver acetate in acetic acid; from benzaldehyde by reacting with magnesium methyl bromide and subsequent acetylation.

Reference:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics