Day: October 8, 2021

SDS of cas: 99-61-6. Authors Thi, QGN; Le-Nhat-Thuy, G; Thi, TAD; Thi, PH; Tuan, AN; Thi, THN; Nguyen, TT; Ha, TN; Mai, HH; Nguyen, TV in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Quynh Giang Nguyen Thi; Giang Le-Nhat-Thuy; Tuyet Anh Dang Thi; Phuong Hoang Thi; Anh Nguyen Tuan; Thu Ha Nguyen Thi; Thanh Tra Nguyen; Thanh Nguyen Ha; Ha Hoang Mai; Tuyen Van Nguyen] Vietnam Acad Sci & Technol Vast, Inst Chem, 18 Hoang Quoc Viet, Hanoi, Vietnam; [Quynh Giang Nguyen Thi; Giang Le-Nhat-Thuy; Tuyet Anh Dang Thi; Ha Hoang Mai; Tuyen Van Nguyen] VAST, Grad Univ Sci & Technol, 18 Hoang Quoc Viet, Hanoi, Vietnam in 2021.0, Cited 32.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A series of novel podophyllotoxin-naphthoquinone compounds 5a-p were synthesized in good yields using microwave-assisted four-component reactions of 2-hydroxy-1,4-naphthoquinone, aromatic benzaldehydes, tetronic acid and ammonium acetate. All the synthesized compounds were fully characterized by spectral data and evaluated for their cytotoxicity activities against KB, HepG2, Lu1, MCF7, and non-cancerous Hek-293 cell lines. Among 16 new compounds screened, compounds 5a, 5d, 5h, and 5k displayed high potent inhibitory activities with IC50 < 40 nM against HepG2 and SK-Lu-1 cell lines, and showed lower toxicity for non-cancerous Hek-293 cell line, demonstrating the potential importance of these compounds in the development of potential anticancer agents. SDS of cas: 99-61-6. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Thi, QGN; Le-Nhat-Thuy, G; Thi, TAD; Thi, PH; Tuan, AN; Thi, THN; Nguyen, TT; Ha, TN; Mai, HH; Nguyen, TV or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Recently I am researching about RECYCLABLE CATALYST; N-METHYLIMIDAZOLE; ACID CATALYST; ACYLATION; 4-DIALKYLAMINOPYRIDINES; ANHYDRIDE; CELLULOSE; AMIDE; SCOPE, Saw an article supported by the Department of Science and Technology, IndiaDepartment of Science & Technology (India) [SERB/F/8435/2015-16]. Published in SPRINGER INTERNATIONAL PUBLISHING AG in CHAM ,Authors: Chaubey, SA; Mishra, R. The CAS is 104-21-2. Through research, I have a further understanding and discovery of 4-Methoxybenzyl acetate. Recommanded Product: 104-21-2

Herein, we report the synthesis of task-specific amino-functionalized imidazolium ionic liquid, acetate1-(2-tert-butoxycarbonylamino-ethyl)-3-methyl-3H-imidazol-1-ium; (Boc-NH-EMIM.OAc), as an efficient catalyst for the acetylation of alcohols, phenols, and amines in the presence of acetic anhydride (acetylating reagent). Remarkably, acetic anhydride in the presence of 10 mol% of catalyst (Boc-NH-EMIM.OAc) under solvent-free conditions showed excellent acetylation activity in shorter duration of time. On the basis of this, a general procedure for acetylation of alcohols, phenols, and amines has been developed. The ionic liquid (Boc-NH-EMIM.OAc) can be readily recovered and reused successfully up to four consecutive cycles without any significant loss of its catalytic activity. We have been able to show that this acetylating method has many advantages. It gives high yields, takes shorter time, and develops the possibility of benign environmental-friendly process.

About 4-Methoxybenzyl acetate, If you have any questions, you can contact Chaubey, SA; Mishra, R or concate me.. Recommanded Product: 104-21-2

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Recommanded Product: 88-68-6. Recently I am researching about RING-CLOSING METATHESIS; NITROGEN-HETEROCYCLES; OLEFIN METATHESIS; SEPTANOSIDES; PEPTIDES; LACTAMS; ANALOGS; BETA, Saw an article supported by the UGC (New Delhi)University Grants Commission, India; DST (New Delhi)Department of Science & Technology (India) [SB/EMEQ-044/2014]. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Novanna, M; Kannadasan, S; Shanmugam, P. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

A facile and efficient method has been developed for the synthesis of (2)-6-allyl-1-phenyl-1,2,5,6tetrahydro-7H-benzo[b][1,5]-diazonin-7-one and (Z)-1,6-diphenyl-1,2,5,6-tetrahydro-7H-benzo[b][1,5]-diazonin-7-one from anthranilamide via N-arylation/N-allylation and from isatoic anhydride via ring opening/N-arylation/N-allylation followed by ring closing metathesis using Grubbs-II catalyst as a key step. Grubbs-II catalyst was found to be superior over Grubbs-I catalyst in terms of reaction time and yield of the product, and the routes developed were suitable to synthesize benzo fused nine membered nitrogen heterocycles. The requirement of diallylated substrates with protected amine and amide nitrogen is suitable for RCM has been established for the synthesis of diazoninone derivatives. (C) 2019 Elsevier Ltd. All rights reserved.

Recommanded Product: 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Novanna, M; Kannadasan, S; Shanmugam, P or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Product Details of 90-44-8. Silva, RL; Demarque, DP; Dusi, RG; Sousa, JPB; Albernaz, LC; Espindola, LS in [Silva, Raquel L.; Demarque, Daniel P.; Dusi, Renata G.; Sousa, Joao Paulo B.; Albernaz, Lorena C.; Espindola, Laila S.] Univ Brasilia, Lab Farmacognosia, Campus Univ Darcy Ribeiro, BR-70910900 Brasilia, DF, Brazil published Residual Larvicidal Activity of Quinones againstAedes aegypti in 2020, Cited 36. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8.

The number of documented dengue cases has increased dramatically in recent years due to transmission through theAedes aegyptimosquito bite. Vector control remains the most effective measure to protect against this and other arboviral diseases including Zika, chikungunya and (urban) yellow fever, with an established vaccine only available for yellow fever. Although the quinone class shows potential as leading compounds for larvicide development, limited information restricts the development of optimized structures and/or formulations. Thus, in this contribution we investigated the larvicidal and pupicidal activity of three quinone compounds isolated from aConnarus suberosusroot wood ethyl acetate extract together with 28 quinones from other sources. Eight quinones demonstrated larvicidal activity, of which tectoquinone (4) proved to be the most active (LC(50)1.1 mu g/mL). The essential residual effect parameter of four of these quinones was evaluated in laboratory trials, with tectoquinone (4) and 2-ethylanthraquinone (7) presenting the most prolonged activity. In small-scale field residual tests, tectoquinone (4) caused 100% larvae mortality over 5 days, supporting its selection for formulation trials to develop a prototype larvicide to controlAe. aegypti.

About Anthrone, If you have any questions, you can contact Silva, RL; Demarque, DP; Dusi, RG; Sousa, JPB; Albernaz, LC; Espindola, LS or concate me.. Product Details of 90-44-8

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Formula: C7H8N2O. Fernandez, GA; Castro, EF; Rosas, RA; Fidalgo, DM; Adler, NS; Battini, L; de Marco, MEJ; Fabiani, M; Bruno, AM; Bollini, M; Cavallaro, LV in [Fernandez, Gabriela A.; Fidalgo, Daniela M.; Adler, Natalia S.; Battini, Leandro; Bollini, Mariela] Ctr Invest Bionanociencias CIBION, Lab Quim Med, Consejo Nacl Invest Cient Tecn CONICET, Buenos Aires, DF, Argentina; [Castro, Eliana F.] Ctr Invest Ciencias Vet & Agro, Inst Virol & Innovac Tecnol, Inst Nacl Tecnol Agropecuaria, Consejo Nacl Invest Cient & Tecn CONICET, Buenos Aires, DF, Argentina; [Castro, Eliana F.; Espana de Marco, Maria J.] Univ Buenos Aires, Fac Farm & Bioquim, Dept Microbiol Inmunol Biotecnol & Genet, Buenos Aires, DF, Argentina; [Rosas, Rocio A.; Fabiani, Matias; Cavallaro, Lucia V.] Univ Buenos Aires, Inst Invest Bacteriol & Virol Mol IBaViM, Dept Microbiol Inmunol Biotecnol & Genet, Catedra Virol,Fac Farm & Bioquim, Buenos Aires, DF, Argentina; [Rosas, Rocio A.; Fabiani, Matias] Consejo Nacl Invest Cient & Tecn CONICET, Buenos Aires, DF, Argentina; [Bruno, Ana M.] Univ Buenos Aires, Fac Farm & Bioquim, Dept Quim Organ, Buenos Aires, DF, Argentina published Design and Optimization of Quinazoline Derivatives: New Non-nucleoside Inhibitors of Bovine Viral Diarrhea Virus in 2020, Cited 54. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Bovine viral diarrhea virus (BVDV) belongs to the Pestivirus genus (Flaviviridae). In spite of the availability of vaccines, the virus is still causing substantial financial losses to the livestock industry. In this context, the use of antiviral agents could be an alternative strategy to control and reduce viral infections. The viral RNA-dependent RNA polymerase (RdRp) is essential for the replication of the viral genome and constitutes an attractive target for the identification of antiviral compounds. In a previous work, we have identified potential molecules that dock into an allosteric binding pocket of BVDV RdRp via a structure-based virtual screening approach. One of them, N-(2-morpholinoethyl)-2-phenylquinazolin-4-amine [1, 50% effective concentration (EC50) = 9.7 +/- 0.5 mu M], was selected to perform different chemical modifications. Among 24 derivatives synthesized, eight of them showed considerable antiviral activity. Molecular modeling of the most active compounds showed that they bind to a pocket located in the fingers and thumb domains in BVDV RdRp, which is different from that identified for other non-nucleoside inhibitors (NNIs) such as thiosemicarbazone (TSC). We selected compound 2-[4-(2-phenylquinazolin-4-yl)piperazin-1-yl]ethanol (1.9; EC50 = 1.7 +/- 0.4 mu M) for further analysis. Compound 1.9 was found to inhibit the in vitro replication of TSC-resistant BVDV variants, which carry the N264D mutation in the RdRp. In addition, 1.9 presented adequate solubility in different media and a high-stability profile in murine and bovine plasma.

Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Fernandez, GA; Castro, EF; Rosas, RA; Fidalgo, DM; Adler, NS; Battini, L; de Marco, MEJ; Fabiani, M; Bruno, AM; Bollini, M; Cavallaro, LV or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

SDS of cas: 119-61-9. Authors Wang, YY; Liu, M; Dong, L in ROYAL SOC CHEMISTRY published article about in [Wang, Ying-Ying; Liu, Man; Dong, Lin] Sichuan Univ, Sichuan Res Ctr Drug Precis Ind Technol, West China Sch Pharm, Key Lab Drug Targeting & Drug Delivery Syst,Educ, Chengdu 610041, Peoples R China in 2021.0, Cited 41.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

Highly selective activation of multiple sites of C-H bonds in a complex organic compound is a huge challenge. Herein, diverse novel fused polycyclic- and multi-substituted 2-oxyl naphthalene benzimidazole derivatives were selectively synthesized via Rh(iii)-catalyzed tandem C-H activation/cyclization. The efficient strategy for the construction of diverse annulation products was precisely controlled by changing the reaction conditions.

SDS of cas: 119-61-9. About Benzophenone, If you have any questions, you can contact Wang, YY; Liu, M; Dong, L or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Biotransformation of Benzoate to 2,4,6-Trihydroxybenzophenone by Engineered Escherichia coli WOS:000650680700001 published article about INHIBITORY NATURAL-PRODUCTS; BENZOPHENONE SYNTHASE; RHODOPSEUDOMONAS-PALUSTRIS; PRENYLATED BENZOPHENONES; ANTIBACTERIAL ACTIVITY; UNNATURAL FLAVONOIDS; MICROBIAL-PRODUCTION; CHALCONE SYNTHASE; BIOSYNTHESIS; XANTHONES in [Klamrak, Anuwatchakij; Nualkaew, Natsajee] Khon Kaen Univ, Fac Pharmaceut Sci, Khon Kaen 40002, Thailand; [Nabnueangsap, Jaran] Mahidol Univ, Salaya Cent Instrument Facil RSPG, Salaya, Nakhon Pathom 73170, Thailand in 2021.0, Cited 79.0. Category: thiomorpholine. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

The synthesis of natural products by E. coli is a challenging alternative method of environmentally friendly minimization of hazardous waste. Here, we establish a recombinant E. coli capable of transforming sodium benzoate into 2,4,6-trihydroxybenzophenone (2,4,6-TriHB), the intermediate of benzophenones and xanthones derivatives, based on the coexpression of benzoate-CoA ligase from Rhodopseudomonas palustris (BadA) and benzophenone synthase from Garcinia mangostana (GmBPS). It was found that the engineered E. coli accepted benzoate as the leading substrate for the formation of benzoyl CoA by the function of BadA and subsequently condensed, with the endogenous malonyl CoA by the catalytic function of BPS, into 2,4,6-TriHB. This metabolite was excreted into the culture medium and was detected by the high-resolution LC-ESI-QTOF-MS/MS. The structure was elucidated by in silico tools: Sirius 4.5 combined with CSI FingerID web service. The results suggested the potential of the new artificial pathway in E. coli to successfully catalyze the transformation of sodium benzoate into 2,4,6-TriHB. This system will lead to further syntheses of other benzophenone derivatives via the addition of various genes to catalyze for functional groups.

Category: thiomorpholine. About Benzophenone, If you have any questions, you can contact Klamrak, A; Nabnueangsap, J; Nualkaew, N or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Safety of 4-Methoxybenzyl acetate. In 2021 AUST J CHEM published article about VITAMIN-E in [Shahnavaz, Zohreh; Zaharani, Lia; Khaligh, Nader Ghaffari; Johan, Mohd Rafie] Univ Malaya, Inst Postgrad Studies, Nanotechnol & Catalysis Res Ctr, 3rd Floor,Block A, Kuala Lumpur 50603, Malaysia; [Mihankhah, Taraneh] Iran Univ Sci & Technol, Sch Civil Engn, Dept Water & Environm Engn, Environm Res Lab, Tehran 16765163, Iran in 2021, Cited 35. The Name is 4-Methoxybenzyl acetate. Through research, I have a further understanding and discovery of 104-21-2.

A new ionic liquid was synthesised, and its chemical structure was elucidated by FT-IR, 1D NMR, 2D NMR, and mass analyses. Some physical properties, thermal behaviour, and thermal stability of this ionic liquid were investigated. The formation of a two-protonic acid salt namely 4,4′-trimethylene-N,N’-dipiperidinium sulfate instead of 4,4′-trimethylene-N,N’-dipiperidinium hydrogensulfate was evidenced by NMR analyses. The catalytic activity of this ionic liquid was demonstrated in the esterification reaction of n-butanol and glacial acetic acid under different conditions. The desired acetate was obtained in 62-88% yield without using a Dean-Stark apparatus under optimal conditions of 10 mol-% of the ionic liquid, an alcohol to glacial acetic acid mole ratio of 1.3 : 1.0, a temperature of 75-100 degrees C, and a reaction time of 4 h. alpha-Tocopherol (alpha-TCP), a highly efficient form of vitamin E, was also treated with glacial acetic acid in the presence of the ionic liquid, and O-acetyl-alpha-tocopherol (Ac-TCP) was obtained in 88.4% yield. The separation of esters was conducted during workup without the utilisation of high-cost column chromatography. The residue and ionic liquid were used in subsequent runs after the extraction of desired products. The ionic liquid exhibited high catalytic activity even after five runs with no significant change in its chemical structure and catalytic efficiency.

Safety of 4-Methoxybenzyl acetate. About 4-Methoxybenzyl acetate, If you have any questions, you can contact Shahnavaz, Z; Zaharani, L; Khaligh, NG; Mihankhah, T; Johan, MR or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Authors Cadena-Cruz, JE; Guaman-Ortiz, LM; Romero-Benavides, JC; Bailon-Moscoso, N; Murillo-Sotomayor, KE; Ortiz-Guaman, NV; Heredia-Moya, J in BMC published article about SOLID ACID CATALYST; EFFICIENT; DERIVATIVES; APOPTOSIS; EDARAVONE; REGULATORS; AUTOPHAGY; PYRAZOLE; DFT in [Cadena-Cruz, Jose Eduardo] Univ Cent Ecuador, Fac Ciencias Quim, Quito, Ecuador; [Guaman-Ortiz, Luis M.; Bailon-Moscoso, Natalia; Murillo-Sotomayor, Kevin E.; Ortiz-Guaman, Nadia V.] Univ Tecn Particular Loja, Dept Ciencias Salud, San Cayetano Alto S-N, Loja 1101608, Ecuador; [Romero-Benavides, Juan Carlos] Univ Tecn Particular Loja, Dept Quim & Ciencias Exactas, San Cayetano Alto S-N, Loja 1101608, Ecuador; [Heredia-Moya, Jorge] Univ UTE, Fac Ciencias Salud Eugenio Espejo, Ctr Invest Biomed CENBIO, Quito 170527, Ecuador in 2021, Cited 51. Product Details of 99-61-6. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

Background Pyrazoles have attracted particular attention due to the diverse biological activities associated with this heterocyclic system, and some have been shown to be cytotoxic to several human cell lines. Several drugs currently on the market have this heterocycle as the key structural motif, and some have been approved for the treatment of different types of cancer. Results 4,4MODIFIER LETTER PRIME-(Arylmethylene)bis(1H-pyrazol-5-ols) derivatives 3a-q were synthetized by a three components reaction of 3-methyl-1-phenyl-5-pyrazolone (1) with various benzaldehydes 2 catalyzed by sodium acetate at room temperature. The structures of all synthesized compounds were characterized by physicochemical properties and spectral means (IR and NMR) and were evaluated for their radical scavenging activity by DPPH assay and tested in vitro on colorectal RKO carcinoma cells in order to determine their cytotoxic properties. All 4,4MODIFIER LETTER PRIME-(arylmethylene)bis(1H-pyrazol-5-ols) derivatives 3a-q were synthetized in high to excellent yield, and pure products were isolated by simple filtration. All compounds have good radical scavenging activity, and half of them are more active than ascorbic acid used as standard. Conclusion Several derivatives proved to be cytotoxic in the RKO cell line. In particular, compound 3i proved to be a very potent scavenger with an IC50 of 6.2 +/- 0.6 mu M and exhibited an IC50 of 9.9 +/- 1.1 mu M against RKO cell. Autophagy proteins were activated as a survival mechanism, whereas the predominant pathway of death was p53-mediated apoptosis.

Product Details of 99-61-6. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Cadena-Cruz, JE; Guaman-Ortiz, LM; Romero-Benavides, JC; Bailon-Moscoso, N; Murillo-Sotomayor, KE; Ortiz-Guaman, NV; Heredia-Moya, J or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Recently I am researching about COMPLETE GENOME SEQUENCE; NATURAL-PRODUCTS; ANTIBIOTIC PRODUCTION; SECONDARY METABOLISM; MASS-SPECTROMETRY; MOLECULAR NETWORKING; PATHOGENS; PLATFORM; STRESS; LINKS, Saw an article supported by the . Published in SPRINGER HEIDELBERG in HEIDELBERG ,Authors: Machushynets, NV; Wu, CS; Elsayed, SS; Hankemeier, T; van Wezel, GP. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide. Category: thiomorpholine

Actinobacteria are a major source of novel bioactive natural products. A challenge in the screening of these microorganisms lies in finding the favorable growth conditions for secondary metabolite production and dereplication of known molecules. Here, we report that Streptomyces sp. MBT27 produces 4-quinazolinone alkaloids in response to elevated levels of glycerol, whereby quinazolinones A (1) and B (2) form a new sub-class of this interesting family of natural products. Global Natural Product Social molecular networking (GNPS) resulted in a quinazolinone-related network that included anthranilic acid (3), anthranilamide (4), 4(3H)-quinazolinone (5), and 2,2-dimethyl-1,2-dihydroquinazolin-4(3H)-one (6). Actinomycins D (7) and X2 (8) were also identified in the extracts of Streptomyces sp. MBT27. The induction of quinazolinone production by glycerol combined with biosynthetic insights provide evidence that glycerol is integrated into the chemical scaffold. The unprecedented 1,4-dioxepane ring, that is spiro-fused into the quinazolinone backbone, is most likely formed by intermolecular etherification of two units of glycerol. Our work underlines the importance of varying the growth conditions for the discovery of novel natural products and for understanding their biosynthesis.

Category: thiomorpholine. About 2-Aminobenzamide, If you have any questions, you can contact Machushynets, NV; Wu, CS; Elsayed, SS; Hankemeier, T; van Wezel, GP or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem