Category: benzofurans

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 767291-67-8, is researched, Molecular C20H42N2, about Synthesis and application of a new pseudo C2-symmetric tertiary diamine for the enantioselective addition of MeLi to aromatic imines, the main research direction is enantioselective addition methyllithium aromatic imine diamine ligand.Computed Properties of C20H42N2.

A new tertiary pseudo C2-sym. diamine derived from (1S,2S)-(+)-pseudoephedrine was synthesized and tested in the enantioselective addition of methyllithium on different aromatic imines. A comparative study with a similar C2-sym. ligand derived from the cyclohexane diamine showed better reactivity and enantioselectivity up to 91%.

Compounds in my other articles are similar to this one((1S,2S)-N1,N2-Bis(3,3-dimethylbutyl)-N1,N2-dimethylcyclohexane-1,2-diamine)Computed Properties of C20H42N2, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Reference of (R)-Ethyl 4-chloro-3-hydroxybutanoate. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: (R)-Ethyl 4-chloro-3-hydroxybutanoate, is researched, Molecular C6H11ClO3, CAS is 90866-33-4, about Development of Saccharomyces cerevisiae reductase YOL151W mutants suitable for chiral alcohol synthesis using an NADH cofactor regeneration system. Author is Yoon, Shin Ah; Jung, Jihye; Park, Seongsoon; Kim, Hyung Kwoun.

The aldo-keto reductases catalyze reduction reactions using various aliphatic and aromatic aldehydes/ketones. Most reductases require NADPH exclusively as their cofactors. However, NADPH is much more expensive and unstable than NADH. In this study, we attempted to change the five amino acid residues that interact with the 2′-phosphate group of the adenosine ribose of NADPH. These residues were selected based on a docking model of the YOL151W reductase and were substituted with other amino acids to develop NADH-utilizing enzymes. Ten mutants were constructed by site-directed mutagenesis and expressed in Escherichia coli. Among them, four mutants showed higher reductase activities than wild-type when using the NADH cofactor. Anal. of the kinetic parameters for the wild type and mutants indicated that the kcat/Km value of the Asn9Glu mutant toward NADH increased 3-fold. A docking model was used to show that the carboxyl group of Glu 9 of the mutant formed an addnl. hydrogen bond with the 2′-hydroxyl group of adenosine ribose. The Asn9Glu mutant was able to produce (R)-ethyl-4-chloro-3-hydroxyl butenoate rapidly when using the NADH regeneration system.

Although many compounds look similar to this compound(90866-33-4)Reference of (R)-Ethyl 4-chloro-3-hydroxybutanoate, numerous studies have shown that this compound(SMILES:O=C(OCC)C[C@@H](O)CCl), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: (R)-Ethyl 4-chloro-3-hydroxybutanoate, is researched, Molecular C6H11ClO3, CAS is 90866-33-4, about Stereochemical control of yeast reductions. 5. Characterization of the oxidoreductases involved in the reduction of β-keto esters.COA of Formula: C6H11ClO3.

Three β-keto reductases, purified to homogeneity from the cytosolic fraction of bakers’ yeast, were capable of actively reducing 4-chloroacetoacetic esters to yield corresponding carbinolic products of high optical purity [>0.97 enantiomeric excess (ee)]. All of them utilized NADPH preferentially as the coenzyme. One of these enzymes (mol. weight = 2,400,000) possessed phys. and chem. properties reminiscent of fatty acid synthetase and reduced β-keto esters to yield carbinols of D-configuration. Although the natural substrates for the other 2 enzymes have not yet been defined, they were readily resolved on a hydroxylapatite column. The faster moving protein (D-enzyme) had a mol. weight of 38,000 and reduced β-keto esters to yield D-carbinolic products, whereas L-enzyme (mol. weight = 74,000) afforded L-carbinols. Because mammalian L-3-hydroxyacyl-CoA dehydrogenase (EC 1.1.1.35) in the presence of NADH reduced 4-chloroacetoacetic esters to (R)-4-chloro-3-hydroxybutanoates of high ee (>0.97), this reductase activity was carefully searched for in bakers’ yeast. Whereas mitochondrial fractions of bakers’ yeast actively reduced acetoacetyl-CoA, only a trace of this reductase activity was detectable. This observation indicated that L-3-hydroxyacyl-CoA dehydrogenases of different species have marked differences in substrate specificities. To gain an insight into the influence of the ester substituent on the enantioselective reduction of γ-chloro-β-keto esters by intact bakers’ yeast, the kcat (turnover number) and Km for the 3 enzymes on various 4-chloroacetoacetic esters were measured.

In some applications, this compound(90866-33-4)COA of Formula: C6H11ClO3 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Reference of Bis(2,5-dioxopyrrolidin-1-yl) O,O’-ethane-1,2-diyl disuccinate. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: Bis(2,5-dioxopyrrolidin-1-yl) O,O’-ethane-1,2-diyl disuccinate, is researched, Molecular C18H20N2O12, CAS is 70539-42-3, about Polyaspartamide-Doxorubicin Conjugate as Potential Prodrug for Anticancer Therapy. Author is Di Meo, Chiara; Cilurzo, Felisa; Licciardi, Mariano; Scialabba, Cinzia; Sabia, Rocchina; Paolino, Donatella; Capitani, Donatella; Fresta, Massimo; Giammona, Gaetano; Villani, Claudio; Matricardi, Pietro.

The purpose of this study was to synthesize a new polymeric prodrug based on α,β-poly(N-2-hydroxyethyl)(2-aminoethylcarbamate)-d,l-aspartamide copolymer bearing amine groups in the side chain (PHEA-EDA), covalently linked to the anticancer drug doxorubicin and to test its potential application in anticancer therapy. The drug was previously derivatized with a biocompatible and hydrophilic linker, leading to a doxorubicin derivative highly reactive with amino groups of PHEA-EDA. The PHEA-EDA-DOXO prodrug was characterized in terms of chem. stability. The pharmacokinetics, biodistribution and cytotoxicity of the product was investigated in vitro and in vivo on human breast cancer MCF-7 and T47D cell lines and NOD-SCID mice bearing a MCF-7 human breast carcinoma xenograft. Data collected were compared to those obtained using free doxorubicin. The final polymeric product is water soluble and easily hydrolysable in vivo, due to the presence of ester and amide bonds along the spacer between the drug and the polymeric backbone. In vitro tests showed a retarded cytotoxic effect on tumor cells, whereas a significant improvement of the in vivo antitumor activity of PHEA-EDA-DOXO and a survival advantage of the treated NOD-SCID mice was evidenced, compared to that of free doxorubicin. The features of the PHEA-EDA-DOXO provide a potential protection of the drug from the plasmatic enzymic degradation and clearance, an improvement of the blood pharmacokinetic parameters and a suitable body biodistribution. The data collected support the promising rationale of the proposed macromol. prodrug PHEA-EDA-DOXO for further potential development and application in the treatment of solid cancer diseases.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Analysis of near-neighbor contacts in bacteriophage T4 wedges and hubless baseplates by using a cleavable chemical cross-linker, published in 1989-06-30, which mentions a compound: 70539-42-3, Name is Bis(2,5-dioxopyrrolidin-1-yl) O,O’-ethane-1,2-diyl disuccinate, Molecular C18H20N2O12, Product Details of 70539-42-3.

Although bacteriophage T4 baseplate morphogenesis has been analyzed in some detail, there is little information available on the spatial arrangement and associations of its 150 subunits. Therefore, anal. of its near-neighbor interactions by using the cleavable chem. cross-linker ethylene glycobis(succinimidylsuccinate) was carried out. The cross-linked complexes that have been identified in the one-sixth arms or wedges and also in baseplatelike structures called rings are described which consist of 6 wedges but lack the central hub, both of which are purified from T4 gene 5–infected cells. Thirty different complexes were identified, of which about half contain multimers of a single species and half contain 2 different species. In general, the complexes reflect and support the assembly pathway derived by Y. Kikuchi and J. King (1975 ), but broaden its scope to include such complexes as gp25-gp53, gp25-gp48, and gp48-gp53, which locate the gp48 binding site over the inner edge of the ring but outside the central hub. The data also supports the view that wedges are assembled from the outer edge inward toward the central hub. Wedge-wedge contact in rings was mediated primarily by gp12 and gp9, the absence of which dramatically destabilized the ring ↔ wedge equilibrium in favor of wedges. Although no heterologous complexes containing gp9 were identified, gp12 contacts unique to rings were observed with both gp10 and gp11.

In some applications, this compound(70539-42-3)Product Details of 70539-42-3 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 1260795-42-3, is researched, Molecular C9H7BrO3, about Synthesis of 3-Benzylphthalide Derivatives by Using a TDAE Strategy, the main research direction is benzylphthalide preparation; nitrobenzyl chloride tetrakisdimethylaminoethylene formylbenzoate nucleophilic addition.Safety of Methyl 4-bromo-2-formylbenzoate.

A one-pot synthesis of new 3-benzylphthalide derivatives I (X = CH, N; R1 = 4-NO2, 3-OMe-4-NO2, 2-NO2-4-C6H4, etc.; R2 = 4-CN, 5-Cl, 4-COOMe, etc.) was developed by using a strategy based on tetrakis(dimethylamino)ethylene (TDAE). The reactions in the presence of TDAE of substituted benzyl chlorides with Me 2-formylbenzoate or of substituted methyl-2-formylbenzoates with 4-nitrobenzyl chloride furnished the corresponding isobenzofuran-1(3H)-one products in moderate to good yields.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Epoxy compounds usually have stronger nucleophilic ability, because the alkyl group on the oxygen atom makes the bond angle smaller, which makes the lone pair of electrons react more dissimilarly with the electron-deficient system. Compound: Bis(2,5-dioxopyrrolidin-1-yl) O,O’-ethane-1,2-diyl disuccinate, is researched, Molecular C18H20N2O12, CAS is 70539-42-3, about The GCN4 leucine zipper can functionally substitute for the heat shock transcription factor’s trimerization domain.COA of Formula: C18H20N2O12.

The heat shock transcription factor (HSF) is the only known sequence-specific, homotrimeric DNA-binding protein. HSF binds to a DNA recognition site called a heat shock element (HSE), which contains varying numbers of nGAAn units (“”GAA boxes””) arranged in inverted repeats. To investigate the role of trimerization on HSF’s DNA-binding properties, the authors replaced the trimerization domain, which self-assembles to form a three-stranded α-helical coiled coil, with the GCN4 leucine zipper, which forms a two-stranded α-helical coiled coil. Surprisingly, this substitution did not effect the ability of HSF to function in vivo. Biochem. studies of an HSF-leucine zipper chimera in comparison to an HSF truncation show that the HSF-leucine zipper chimera, though dimeric in solution and dimeric when bound to a two-box HSE, forms a trimeric complex when bound to a three-box HSE. The ability to form trimers depends on the presence of three contiguous GAA boxes present in inverted repeats. The proximity of the leucine zippers due to the orientation of the binding sites suggests that the leucine zippers might be forming a three-stranded coiled coil and several experiments lend support to this model. The ability of the leucine zipper to change oligomeric states in context might explain why the leucine zipper can replace the trimerization domain of HSF in vivo.

In some applications, this compound(70539-42-3)COA of Formula: C18H20N2O12 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 90866-33-4, is researched, SMILESS is O=C(OCC)C[C@@H](O)CCl, Molecular C6H11ClO3Journal, Article, Research Support, Non-U.S. Gov’t, Journal of Organic Chemistry called High Enantioselectivity and Broad Substrate Specificity of a Carbonyl Reductase: Toward a Versatile Biocatalyst, Author is Ema, Tadashi; Moriya, Hiroyuki; Kofukuda, Toru; Ishida, Tomomasa; Maehara, Kentaro; Utaka, Masanori; Sakai, Takashi, the main research direction is ketone stereoselective reduction carbonyl reductase bakers yeast; alc stereoselective preparation enzymic reduction ketone.Application In Synthesis of (R)-Ethyl 4-chloro-3-hydroxybutanoate.

A carbonyl reductase isolated from bakers’ yeast shows high stereoselectivity and chemoselectivity in the reduction of carbonyl compounds in the presence of an ester group or a second carbonyl group. The results are compared with those obtained with whole cell reduction with bakers’ yeast.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Cagnon, J. R.; Marsaioli, A. J.; Riatto, V. B.; Pilli, R. A.; Manfio, G. P.; Eguchi, S. Y. researched the compound: (R)-Ethyl 4-chloro-3-hydroxybutanoate( cas:90866-33-4 ).SDS of cas: 90866-33-4.They published the article 《Microbial screening for the enantiospecific production of alkyl esters of 4-chloro-3-hydroxybutanoic acid》 about this compound( cas:90866-33-4 ) in Chemosphere. Keywords: Rhodotorula stereoselective reduction chlorohydroxybutanoate ester; Cunninghamella stereoselective reduction chlorohydroxybutanoate ester; stereoselective reduction chlorohydroxybutanoate ester fermentation. We’ll tell you more about this compound (cas:90866-33-4).

This article describes preliminary screening results of yeasts and fungi isolated from exotic environments like the Atlantic rain forest, the roots of Araucaria angustifolia, and a guava tree. Rhodotorula glutinis CCT 2182 and Cunninghamella echinulata CCT 4259 revealed high enantioselective reductase activities for the production of alkyl esters of (R)- and (S)-4-chloro-3-hydroxybutanoic acid, resp.

In some applications, this compound(90866-33-4)SDS of cas: 90866-33-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: Silver(I) trifluoromethanesulfonate, is researched, Molecular CAgF3O3S, CAS is 2923-28-6, about Sulfonate improves water solubility and cell selective toxicity and alters the lysozyme binding activity of half sandwich Rh(III) complexes, the main research direction is rhodium half sandwich pyridylbenzimidazole complex sulfonate substituted preparation fungicide.Product Details of 2923-28-6.

Introduction of the propyl-sulfonic acid group at N1 of the coordinated 1-R-2-(2-pyridyl)benzimidazole ligand (R-PyBzIm, R = Et, HO3SCH2CH2CH2) in [RhCl(η5-C5Me5)(R-PyBzIm)][OTf] gives rise to a water-soluble complex, which can bind to the model protein lysozyme via non-covalent interactions. The complex shows selective moderate toxicity against Cryptococcus neoformans (MIC = 21.6-43.3μM) and exhibits no cytotoxicity to healthy HEK293 cells.

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Reference:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem