Day: February 7, 2023

Creating Coordination Mismatch in MOFs: Tuning from Pore Structure of the Derived Supported Catalysts to Their Catalytic Performance was written by Tang, Feiying;Wang, Liqiang;Zhang, Guangji;Zhang, Min;Liu, You-Nian. And the article was included in Industrial & Engineering Chemistry Research in 2019.Product Details of 4769-96-4 This article mentions the following:

A Ni-substituted ZIF-67 was used as a precursor to prepare hollow-porous-carbon (HPC)-supported catalysts. It was found that Ni²⁺ can partially substitute Co²⁺ to create “defected structure” within ZIF-67, and the secondary pore structure of the derived HPC can be facilely tuned by adjusting the ratio of Ni²⁺ to Co²⁺. Catalyst HPC-Ni-ZIF-1 with hierarchical secondary pore and the largest pore volume exhibits an excellent catalytic performance for the hydrogenation of nitro compounds to corresponding amino compounds In the experiment, the researchers used many compounds, for example, 6-Nitro-1H-indole (cas: 4769-96-4Product Details of 4769-96-4).

6-Nitro-1H-indole (cas: 4769-96-4) belongs to indole derivatives. The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Product Details of 4769-96-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

A facile synthesis of pyrrolo[2,3-j]phenanthridines via the cascade reaction of indoleanilines and aldehydes was written by Huang, Wen-Jun;Chen, Zhi-Peng;Liu, Li-Xia;Zhou, Yong-Gui;Wu, Bo;Jiang, Guo-Fang. And the article was included in Journal of Heterocyclic Chemistry in 2022.Category: indole-building-block This article mentions the following:

A facile method for the synthesis of pyrrolo[2,3-j]phenanthridines from indoleanilines and aldehydes in the presence of Broensted acid catalyst and benzoquinone oxidant were established. This approach featured excellent yields, high efficiency and a wide range of substrate scope. Mechanism studies exhibited that this reaction was a cascade process including acid-catalyzed condensation of indoleanilines with aldehydes, cyclization and oxidative aromatization. In the experiment, the researchers used many compounds, for example, 5-Bromo-2,3-dimethyl-1H-indole (cas: 4583-55-5Category: indole-building-block).

5-Bromo-2,3-dimethyl-1H-indole (cas: 4583-55-5) belongs to indole derivatives. The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.Category: indole-building-block

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Relation between electronic structure and auxin activity of chlorinated β-indolylacetic acids was written by Cocordano, Maurice;D’Amato, Franck;Turcat, Jean J.. And the article was included in Annales de la Faculte des Sciences de Marseille in 1970.Recommanded Product: 1912-45-4 This article mentions the following:

Five chlorinated β-indolylacetic acids (I) were prepared by the cyclization of ClC6H4NHN:CHCH2CH2CO2H in ethanolic H2SO4 followed by saponification The auxinic activity of I derivatives was in the order 6-Cl- > nonchlorinated > 6,7-Cl2 > 7-Cl > 5,7-Cl2. The electronic structure of I was calculated by LCAO method. I forms by, its CO2H group, a conjugated unstable complex with the protein of the cell. In the experiment, the researchers used many compounds, for example, 2-(5-Chloro-1H-indol-3-yl)acetic acid (cas: 1912-45-4Recommanded Product: 1912-45-4).

2-(5-Chloro-1H-indol-3-yl)acetic acid (cas: 1912-45-4) belongs to indole derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. Due to this activity, the indole ring system has become an important component or intermediate in the synthesis of heterocycles.Recommanded Product: 1912-45-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

The IR and Raman spectra of tetrabromophthalic anhydride, tetrabromophthalimide, N-d-tetrabromophthalimide and potassium tetrabromophthalimide was written by Hase, Y.. And the article was included in Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy in 1980.Quality Control of 4,5,6,7-Tetrabromoisoindoline-1,3-dione This article mentions the following:

The 180-4000-cm^-1 IR and 40-4000-cm^-1 Raman spectra of polycrystalline tetrabromophthalic anhydride, tetrabromophthalimide and its N-deuterio derivative, and K tetrabromophthalimide were recorded and the observed frequencies assigned on the basis of C_2ν mol. symmetry. A normal coordinate anal. was carried out and the carbonyl stretching vibrations were discussed in relation to the obtained force constants In the experiment, the researchers used many compounds, for example, 4,5,6,7-Tetrabromoisoindoline-1,3-dione (cas: 24407-32-7Quality Control of 4,5,6,7-Tetrabromoisoindoline-1,3-dione).

4,5,6,7-Tetrabromoisoindoline-1,3-dione (cas: 24407-32-7) belongs to indole derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Quality Control of 4,5,6,7-Tetrabromoisoindoline-1,3-dione

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

2,6-Disubstituted imidazo[2,1-b][1,3,4]thiadiazole derivatives as potent Staphylococcal biofilm inhibitors was written by Cascioferro, Stella;Parrino, Barbara;Petri, Giovanna Li;Cusimano, Maria Grazia;Schillaci, Domenico;Di Sarno, Veronica;Musella, Simona;Giovannetti, Elisa;Cirrincione, Girolamo;Diana, Patrizia. And the article was included in European Journal of Medicinal Chemistry in 2019.COA of Formula: C9H5BrN2 This article mentions the following:

A class of 36 new 2-(6-phenylimidazo[2,-1-b][1,3,4]thiadiazol-2-yl)-1H-indoles, compounds I [R = H, Cl, Br; R¹ = H, Me; R² = H, 3-MeO, 4F, etc.] was efficiently synthesized and evaluated for their anti-biofilm properties against the Gram-pos. bacterial reference strains Staphylococcus aureus ATCC 25923, S. aureus ATCC 6538 and Staphylococcus epidermidis ATCC 12228, and the Gram-neg. strains Pseudomonas aeruginosa ATCC 15442 and Escherichia coli ATCC 25922. Many of these new compounds, were able to inhibit biofilm formation of the tested Staphylococcal strains showing BIC₅₀ lower than 10 μg/mL. In particular, compounds I [R = H, R¹ = H, R² = 2,5-diMeO; R = H, R¹ = Me, R² = 3-MeO] showed remarkable anti-biofilm activity against S. aureus ATCC 25923 with BIC₅₀ values of 0.5 and 0.8 μg/mL, resp., whereas compound I [R = Cl, R¹ = H, R² = 2,5-diMeO] was the most potent against S. aureus ATCC 6538, with a BIC₅₀ of 0.3 μg/mL. Remarkably, these compounds showed effects in the early stages of the biofilm formation without affecting the mature biofilm of the same strains and the viability of the planktonic form. Their ability in counteracting a virulence factor (biofilm formation) without interfering with the bacterial growth in the free life form make them novel valuable anti-virulence agents. In the experiment, the researchers used many compounds, for example, 5-Bromo-3-cyanoindole (cas: 90271-86-6COA of Formula: C9H5BrN2).

5-Bromo-3-cyanoindole (cas: 90271-86-6) belongs to indole derivatives. The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.COA of Formula: C9H5BrN2

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Access to 3-alkylselenindoles by multicomponent reaction of indoles, selenium powder and unactivated alkyl halides under transition-metal-free conditions was written by Liu, Huan;Cai, Zhong-Jian;Ji, Shun-Jun. And the article was included in Chinese Chemical Letters in 2022.Formula: C8H6N2O2 This article mentions the following:

Herein, a convenient and efficient multicomponent reaction of indoles, selenium powder and unactivated alkyl halides is reported. This protocol provides a practical, and facile approach for the synthesis of 3-alkylselenindole derivatives The advantages of this strategy include mild and transition-metal-free conditions, broad functional group tolerance, the use of simple and easily accessible selenium powder and alkyl halides as coupling partners. More importantly, the reaction proceeded smoothly with a large scale (> 10 g, > 90% yield), which further highlighted the potential application of this selenation strategy. In the experiment, the researchers used many compounds, for example, 6-Nitro-1H-indole (cas: 4769-96-4Formula: C8H6N2O2).

6-Nitro-1H-indole (cas: 4769-96-4) belongs to indole derivatives. Indole is an important structural motif of various drugs, therapeutic leads besides its prevalence in numerous natural products, agrochemicals, perfumery, and dyes. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Formula: C8H6N2O2

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

New Arylthioindoles and Related Bioisosteres at the Sulfur Bridging Group. 4. Synthesis, Tubulin Polymerization, Cell Growth Inhibition, and Molecular Modeling Studies was written by La Regina, Giuseppe;Sarkar, Taradas;Bai, Ruoli;Edler, Michael C.;Saletti, Roberto;Coluccia, Antonio;Piscitelli, Francesco;Minelli, Lara;Gatti, Valerio;Mazzoccoli, Carmela;Palermo, Vanessa;Mazzoni, Cristina;Falcone, Claudio;Scovassi, Anna Ivana;Giansanti, Vincenzo;Campiglia, Pietro;Porta, Amalia;Maresca, Bruno;Hamel, Ernest;Brancale, Andrea;Novellino, Ettore;Silvestri, Romano. And the article was included in Journal of Medicinal Chemistry in 2009.HPLC of Formula: 210345-56-5 This article mentions the following:

A series of arylthioindoles, e.g., I (X = S, R¹ = H, CO₂Me, CO₂Et, R² = H, Cl, Br, OMe), the corresponding ketones I (X = CO) and diarylmethanes I (X = CH₂), as well as pyrrole II (Y = CH₂, CO, Z = CH, R³ = CO₂Et, R⁴ = R⁵ = H; etc.) and imidazole analogs II (Y = CO, Z = N, R³ = R⁵ = H, R⁴ = CO₂Et; etc.) were synthesized and their activity as tubulin polymerization and cancer cell growth inhibitors assessed. As growth inhibitors of MCF-7 cells, sulfur derivatives were superior or sometimes equivalent to the ketones, while methylene derivatives were substantially less effective. Indoles I (X = S, R¹ = H, R² = Br; X = S, CO, CH₂, R¹ = CO₂Me, R² = Br, OMe) showed ∼50% of inhibition on human HeLa and HCT116/chr3 cells at 0.5 μM, and these compounds inhibited the growth of HEK, M14, and U937 cells with IC₅₀‘s in the 78-220 nM range. While murine macrophage J744.1 cell growth was significantly less affected (20% at higher concentrations), four other non-transformed cell lines remained sensitive to these indoles. The effect of drug treatment on cell morphol. was examined by time-lapse microscopy. In a protocol set up to evaluate toxicity on the Saccharomyces cerevisiae BY4741 wild type strain, compounds I (X = S, R¹ = H, R² = Br) and II (Y = CH₂, Z = CH, R³ = CO₂H, R⁴ = R⁵ = H) strongly reduced cell growth, and I (X = CH₂, R¹ = CO₂Me, R² = Br; X = S, CO, R¹ = CO₂Me, R² = OMe) also showed significant inhibition. In the experiment, the researchers used many compounds, for example, Methyl 5-bromo-1H-indole-2-carboxylate (cas: 210345-56-5HPLC of Formula: 210345-56-5).

Methyl 5-bromo-1H-indole-2-carboxylate (cas: 210345-56-5) belongs to indole derivatives. In addition to tryptophan, indigo, and indoleacetic acid, numerous compounds obtainable from plant or animal sources contain the indole molecular structure. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.HPLC of Formula: 210345-56-5

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Reactions of imides with samarium(II) iodide was written by Brandukova, N. E.;Vygodskii, Ya. S.;Komarova, L. I.;Strelkova, T. V.. And the article was included in Izvestiya Akademii Nauk, Seriya Khimicheskaya in 1996.Category: indole-building-block This article mentions the following:

One of the carbonyl groups of N-phenylphthalimide is reduced by SmI₂ to a CHOH or CH₂ group at ∼20°. The reaction pathway depends mainly on the reactant ratio and the sequence of reactant addition to the reaction mixture Under similar conditions, both CO groups of N-acetylcaprolactam are reduced by SmI₂, whereas the CO group of ε-caprolactam is not reduced. In the experiment, the researchers used many compounds, for example, 2-Phenylisoindolin-1-one (cas: 5388-42-1Category: indole-building-block).

2-Phenylisoindolin-1-one (cas: 5388-42-1) belongs to indole derivatives. Indole, also called Benzopyrrole, a heterocyclic organic compound occurring in some flower oils, such as jasmine and orange blossom, in coal tar, and in fecal matter.Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.Category: indole-building-block

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Synthesis and antiproliferatory activities evaluation of multi-substituted isatin derivatives was written by Ding, Ying;Zhao, Lianbo;Fu, Ying;Hao, Lei;Fu, Yupeng;Yuan, Yuan;Yu, Peng;Teng, Yuou. And the article was included in Molecules in 2021.HPLC of Formula: 112656-95-8 This article mentions the following:

A series of multi-substituted isatin derivatives I (R¹ = H, F, Cl, Br, OMe; R² = F, Cl, Me, etc.) were synthesized using the powerful Sandmeyer reaction. Inhibition of proliferation activities of these derivatives against human leukemia cells (K562), human hepatocellular carcinoma cells (HepG2) and human colon carcinoma cells (HT-29) were evaluated in vitro using the MTT assay. Among the series, compound I (R¹ = F; R² = Br) exhibited strong antiproliferatory activities against K562, HepG2 and HT-29 cells with IC₅₀ values of 1.75, 3.20, and 4.17μM, resp. The morphol., growth inhibitory and apoptosic effects of compound I (R¹ = F; R² = Br) in K562 cells, wound healing effect in HepG2 cells, and tube formatting effect in matrix gel of HUVEC cells were evaluated consequently. All results indicated that compound I (R¹ = F; R² = Br) could be used as a potential antitumor agent in further investigations. In the experiment, the researchers used many compounds, for example, 7-Nitroindoline-2,3-dione (cas: 112656-95-8HPLC of Formula: 112656-95-8).

7-Nitroindoline-2,3-dione (cas: 112656-95-8) belongs to indole derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. More than 200 indole derivatives have already been marketed as drugs or are under advanced stages of clinical trials.HPLC of Formula: 112656-95-8

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Synthesis of indolizine derivatives containing eight-membered rings via a gold-catalyzed two-fold hydroarylation of diynes was written by Liu, Ruixing;Wang, Qiang;Wei, Yin;Shi, Min. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2018.SDS of cas: 4769-96-4 This article mentions the following:

A gold-catalyzed method for the construction of indolizines with eight-membered rings has been developed. The reaction proceeded through a two-fold hydroarylation with indole or pyrrole derivatives containing a 1,6-diyne using a tri(1-adamantyl)phosphine gold complex as the catalyst, affording 1,8-disubstituted indolizines in moderate to good yields in DCE at 80°. The potential usefulness of these indolizines as blue or green OLEDs has been also disclosed. In the experiment, the researchers used many compounds, for example, 6-Nitro-1H-indole (cas: 4769-96-4SDS of cas: 4769-96-4).

6-Nitro-1H-indole (cas: 4769-96-4) belongs to indole derivatives. The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades.Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.SDS of cas: 4769-96-4

Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles