Tag: M.W=100-150

An article Synthesis, Evaluation of Biological Activity, Docking and Molecular Dynamic Studies of Pyrimidine Derivatives WOS:000631153800007 published article about ANTICANCER AGENTS; INHIBITORS; CELECOXIB; DESIGN in [Boumi, Shahin; Moghimirad, Jafar; Amanlou, Massoud; Amini, Mohsen] Univ Tehran Med Sci, Inst Pharmaceut Sci TIPS, Drug Design & Dev Res Ctr, Dept Med Chem,Fac Pharm, Tehran, Iran; [Ostad, Seyed Nasser; Tavajohi, Shohreh] Univ Tehran Med Sci, Fac Pharm, Dept Toxicol & Pharmacol, Tehran, Iran; [Ostad, Seyed Nasser; Tavajohi, Shohreh] Univ Tehran Med Sci, Poisoning Res Ctr, Tehran, Iran in 2021, Cited 18. Safety of 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

The microtubule is composed of alpha beta-tubulin heterodimers and is an attractive target for the design of anticancer drugs. Over the years, various compounds have been developed and their effect on tubulin polymerization has been studied. Despite great efforts to make an effective drug, no drug has been introduced which inhibit colchicine binding site. In the current work, a series of pyrimidine derivatives were designed and synthesized. Furthermore, their cytotoxic activities were evaluated and molecular docking studies were performed. Twenty compounds of pyrimidine were synthesized in 2 different groups. In the first group, 4,6-diaryl pyrimidine was connected to the third aryl group via thiomethylene spacer. In the second group, this linker was substituted by S-CH2-triazole moiety. The cytotoxic activity of these compounds was evaluated against 4 different cell lines (HT-29, MCF-7, T47D, NIH3T3). Compounds 6d, 6m, 6p showed potent cytotoxic activity against MCF7 cancerous cell lines. Between these compounds, compound 6p did not show cytotoxic activity against NIH- 3T3 (normal cell) cell line. Docking studies show that these compounds occupy colchicine binding site in tubulin protein and probably their anticancer mechanism is inhibition of tubulin polymerization. Altogether, with respect to obtained results, it is attractive and beneficial to further investigation on pyrimidine scaffold as antimitotic agents. Attention to the selectivity index of 6p on MCF7 cell line could be valuable in design new chemical agents for the treatment of breast cancer.

Welcome to talk about 123-11-5, If you have any questions, you can contact Boumi, S; Moghimirad, J; Amanlou, M; Ostad, SN; Tavajohi, S; Amini, M or send Email.. Safety of 4-Methoxybenzaldehyde

Reference:
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

An article Silica-supported heterogeneous catalysts-mediated synthesis of chalcones as potent urease inhibitors: in vitro and molecular docking studies WOS:000505350200003 published article about ALPHA,BETA-UNSATURATED KETONES; DERIVATIVES; ANALOGS in [Sultan, Aeysha; Mehr-un-Nisa; Rehman, Mian Habib Ur] Univ Educ, Dept Chem, Faisalabad Campus, Faisalabad, Pakistan; [Shajahan, Shanavas] Periyar Univ, Dept Phys, Nano & Hybrid Mat Lab, Salem 636011, India; [Ahamad, Tansir; Alshehri, Saad M.] King Saud Univ, Coll Sci, Dept Chem, POB 2455, Riyadh 11451, Saudi Arabia; [Sajjad, Noreen] Univ Lahore, Dept Chem, Lahore, Pakistan; [Torun, Lokman] Yilditz Univ Engn & Technol, Dept Chem, Istanbul, Turkey; [Khalid, Muhammad] Khawaja Ghulam Fareed Univ Engn & Technol, Dept Chem, Rahim Yar Khan, Pakistan; [Acevedo, Roberto] Univ San Sebastian, Fac Ingn & Tecnol, Bellavista 7, Santiago 420524, Chile in 2020.0, Cited 43.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Recommanded Product: 4′-Hydroxyacetophenone

We herein report a facile and high yielding protocol for silica-supported heterogeneous catalysts-mediated synthesis of chalcones. A comparison of results of our synthesis with conventional synthetic protocols is also being offered to assess the efficiency of the prepared catalysts. Biological evaluation of the newly synthesized compounds as urease inhibitors was performed. Most of the compounds were found to have potent urease inhibition activity. The chalcone 3-(3-hydroxyphenyl)-1-phenylpropenone was found to be the most potent with percentage inhibition 86.17 +/- 0.89 and half maximal inhibitory concentration (IC50) value 11.51 +/- 0.03 mu M. The molecular docking study emphasized that the same congeners 3-(furan-2-yl)-1-(4-hydroxyphenyl)propenone, 3-(4-hydroxyphenyl)-1-(4-methoxyphenyl)propanone, and 3-[4-(dimethylamino)phenyl]-1-(p-tolyl)propenone showed very good inhibitory potential against urease and show a higher docking scores 5718, 5940, 5596 and an ACE of – 246.66, – 244.79, and – 243.06 kJ/mol, respectively than the control ligand.

Welcome to talk about 99-93-4, If you have any questions, you can contact Sultan, A; Shajahan, S; Ahamad, T; Alshehri, SM; Sajjad, N; Mehr-un-Nisa; Rehman, MHU; Torun, L; Khalid, M; Acevedo, R or send Email.. Recommanded Product: 4′-Hydroxyacetophenone

Reference:
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

Recently I am researching about DIVALENT LANTHANIDE DERIVATIVES; RADICAL CYCLIZATION CASCADES; ELECTRON-TRANSFER REDUCTION; SAMARIUM DIIODIDE; CARBONYL-COMPOUNDS; ORGANIC-SYNTHESIS; SMI2 REACTIONS; PROTON DONORS; SOLID-STATE; KETONES, Saw an article supported by the National Science FoundationNational Science Foundation (NSF) [CHE 1565741]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Maity, S; Flowers, RA. The CAS is 100-51-6. Through research, I have a further understanding and discovery of Benzyl Alcohol. HPLC of Formula: C7H8O

Samarium diiodide (SmI2) is one of the most widely used single electron reductants available to organic chemists because it is effective in reducing and coupling a wide range of functional groups. Despite the broad utility and application of SmI2 in synthesis, the reagent is used in stoichiometric amounts and has a high molecular weight, resulting in a large amount of material being used for reactions requiring one or more equivalents of electrons. few approaches to develop catalytic reactions have been designed, they are not widely used or require specialized conditions. As a consequence, general solutions to develop catalytic reactions of Sm(II) remain elusive. Herein, we report mechanistic studies on catalytic reactions of Sm(II) employing a terminal magnesium reductant and trimethylsilyl chloride in concert with a non coordinating proton donor source. Reactions using this approach permitted reductions with as little as 1 mol % Sm. Mechanistic studies provide strong evidence that during the reaction, SmI2 transforms into SmCl2, therefore broadening the scope of accessible reactions. Furthermore, this mechanistic approach enabled catalysis employing HMPA as a ligand, facilitating the development of catalytic Sm(II) 5-exo-trig ketyl olefin cyclization reactions. The initial work described herein will enable further development of both useful and user-friendly catalytic reactions, a long-standing, but elusive goal in Sm(II) chemistry.

HPLC of Formula: C7H8O. Bye, fridends, I hope you can learn more about C7H8O, If you have any questions, you can browse other blog as well. See you lster.

Reference:
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

Backlund, CM; Parhamifar, L; Minter, L; Tew, GN; Andresen, TL in [Backlund, Coralie M.; Tew, Gregory N.] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA; [Minter, Lisa; Tew, Gregory N.] Univ Massachusetts, Dept Mol & Cellular Biol, Amherst, MA 01003 USA; [Minter, Lisa; Tew, Gregory N.] Univ Massachusetts, Dept Vet & Anim Sci, Amherst, MA 01003 USA; [Parhamifar, Ladan; Andresen, Thomas L.] Tech Univ Denmark, Dept Hlth Technol, DK-2800 Lyngby, Denmark published Protein Transduction Domain Mimics Facilitate Rapid Antigen Delivery into Monocytes in 2019.0, Cited 37.0. Product Details of 100-51-6. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6.

Delivering peptides and proteins with intracellular function represents a promising avenue for therapeutics, but remains a challenge due to the selective permeability of the plasma membrane. The successful delivery of cytosolically active proteins would enable many opportunities, including improved vaccine development through major histocompatibility complex (MHC) class I antigen display. Extended research using cell-penetrating peptides (CPPs) has aimed to facilitate intracellular delivery of exogenous proteins with some success. A new class of polymer-based mimics termed protein transduction domain mimics (PTDMs), which maintain the positive charge and amphiphilic nature displayed by many CPPs, was developed using a poly-norbornene-based backbone. Herein, we use a previously characterized PTDM to investigate delivery of the model antigen SIINFEKL into leukocytes. Peptide delivery into over 90% of CD14+ monocytes was detected in less than 15 min with nominal inflammatory cytokine response and high cell viability. The co-delivery of a TLR9 agonist and antigen using the PTDM into antigen presenting cells in vitro showed presentation of SIINFEKL in association with MHC class I molecules, in addition to upregulation of classical differentiation markers revealing the ability of the PTDM to successfully deliver cargo intracellularly and show application in the field of immunotherapy.

Welcome to talk about 100-51-6, If you have any questions, you can contact Backlund, CM; Parhamifar, L; Minter, L; Tew, GN; Andresen, TL or send Email.. Product Details of 100-51-6

Reference:
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

An article Targeting Mechanoresponsive Proteins in Pancreatic Cancer: 4-Hydroxyacetophenone Blocks Dissemination and Invasion by Activating MYH14 WOS:000487699000013 published article about MYOSIN-II; CELL MECHANICS; EXPRESSION; CYTOKINESIS; METASTASIS; CARCINOMA; FILAMIN; ACTININ-4; STIFFNESS; PATHWAYS in [Surcel, Alexandra; Schiffhauer, Eric S.; Thomas, Dustin G.; DiNapoli, Kathleen T.; West-Foyle, Hoku; Iglesias, Pablo A.; Robinson, Douglas N.] Johns Hopkins Univ, Sch Med, Dept Cell Biol, Baltimore, MD USA; [Zhu, Qingfeng; Anders, Robert A.] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA; [DiNapoli, Kathleen T.; Iglesias, Pablo A.] Johns Hopkins Univ, Dept Elect & Comp Engn, Whiting Sch Engn, Baltimore, MD 21218 USA; [Herbig, Maik; Otto, Oliver; Jacobi, Angela; Kraeter, Martin; Plak, Katarzyna; Guck, Jochen] Tech Univ Dresden, Ctr Mol & Cellular Bioengineering, Biotechnol Ctr, Dresden, Germany; [Jaffee, Elizabeth M.] Johns Hopkins Univ, Sidney Kimmel Canc Ctr Johns Hopkins, Skip Viragh Pancreat Canc Ctr, Dept Oncol, Baltimore, MD USA; [Jaffee, Elizabeth M.] Johns Hopkins Univ, Bloomberg Kimmel Inst, Baltimore, MD USA; [Robinson, Douglas N.] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA; [Robinson, Douglas N.] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA; [Otto, Oliver] Ernst Moritz Arndt Univ Greifswald, Ctr Innovat Competence, Humoral Immune React Cardiovasc Dis Biomech, Greifswald, Germany in 2019.0, Cited 65.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Quality Control of 4′-Hydroxyacetophenone

Metastasis is complex, involving multiple genetic, epigenetic, biochemical, and physical changes in the cancer cell and its microenvironment. Cells with metastatic potential are often characterized by altered cellular contractility and deformability, lending them the flexibility to disseminate and navigate through different microenvironments. We demonstrate that mechanoresponsiveness is a hallmark of pancreatic cancer cells. Key mechanoresponsive proteins, those that accumulate in response to mechanical stress, specifically nonmuscle myosin IIA (MYH9) and IIC (MYH14), alpha-actinin 4, and filamin B, were highly expressed in pancreatic cancer as compared with healthy ductal epithelia. Their less responsive sister paralogs-myosin IIB (MYH10), alpha-actinin 1, and filamin A-had lower expression differential or disappeared with cancer progression. We demonstrate that proteins whose cellular contributions are often overlooked because of their low abundance can have profound impact on cell architecture, behavior, and mechanics. Here, the low abundant protein MYH14 promoted metastatic behavior and could be exploited with 4-hydroxyacetophenone (4-HAP), which increased MYH14 assembly, stiffening cells. As a result, 4-HAP decreased dissemination, induced cortical actin belts in spheroids, and slowed retrograde actin flow. 4-HAP also reduced liver metastases in human pancreatic cancer-bearing nude mice. Thus, increasing MYH14 assembly overwhelms the ability of cells to polarize and invade, suggesting targeting the mechanoresponsive proteins of the actin cytoskeleton as a new strategy to improve the survival of patients with pancreatic cancer. Significance: This study demonstrates that mechanoresponsive proteins become upregulated with pancreatic cancer progression and that this system of proteins can be pharmacologically targeted to inhibit the metastatic potential of pancreatic cancer cells.

Quality Control of 4′-Hydroxyacetophenone. Welcome to talk about 99-93-4, If you have any questions, you can contact Surcel, A; Schiffhauer, ES; Thomas, DG; Zhu, QF; DiNapoli, KT; Herbig, M; Otto, O; West-Foyle, H; Jacobi, A; Krater, M; Plak, K; Guck, J; Jaffee, EM; Iglesias, PA; Anders, RA; Robinson, DN or send Email.

Reference:
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

SDS of cas: 100-51-6. Boroujeni, KP; Tohidiyan, Z; Shahsanaei, H; Lorigooini, Z; Fadavi, A in [Boroujeni, Kaveh Parvanak; Shahsanaei, Hekmatollah] Shahrekord Univ, Dept Chem, POB 88186-34141, Shahrekord, Iran; [Tohidiyan, Zeinab] Islamic Azad Univ, Shahrekord Branch, Dept Chem, Shahrekord, Iran; [Lorigooini, Zahra] Shahrekord Univ Med Sci, Basic Hlth Sci Inst, Med Plants Res Ctr, Shahrekord, Iran; [Fadavi, Abdulhamid] Islamic Azad Univ, Marvdasht Branch, Dept Chem, Marvdasht, Iran published Silver and palladium nanoparticles anchored to the core-shell Fe3O4@SiO2@ Al2O3 for catalytic aerobic oxidation of alcohols and apoptotic induction on MCF-7 cells in 2020.0, Cited 33.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6.

Silver and palladium nanoparticles anchored to the core-shell Fe3O4@SiO2@Al2O3 were successfully synthesized based on MIL(Al)96 MOF. The nanocomposites, 15-20 nm in size, exhibited high catalytic activity for selective aerobic oxidation of alcohols (even aliphatic alcohols) to the corresponding carbonyl compounds at room temperature without addition of any other additives. In this regard, the Fe3O4@SiO2@Al2O3/Pd,Ag exhibited more catalytic activity than the others. The cytotoxic effect of nanocomposites was tested in-vitro against MCF-7 human breast cancer cells by MTT assay. The results showed that all synthesized nanocomposites will be promising and potential as anticancer agents, with sample Fe3O4@SiO2@Al2O3 being the most cytotoxic after 24 and 48 h. Also, the obtained nanocomposites could induce apoptosis in breast cancer cell line (MCF-7) and the ability of induce apoptosis was in the following order: Fe3O4@SiO2@Al2O3@Ag > Fe3O4@SiO2@Al2O3 > Fe3O4@SiO2@Al2O3@Pd,Ag > Fe3O4@SiO2@Al2O3@Pd.

SDS of cas: 100-51-6. About Benzyl Alcohol, If you have any questions, you can contact Boroujeni, KP; Tohidiyan, Z; Shahsanaei, H; Lorigooini, Z; Fadavi, A or concate me.

Reference:
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

SDS of cas: 150-19-6. Authors Jiao, LY; Ning, ZH; Yin, XM; Hong, Q; Liu, SS; Ma, XX in ELSEVIER published article about in [Jiao, Lin-Yu; Ning, Zi-Hui; Yin, Xiao-Mei; Hong, Qian; Ma, Xiao-Xun] Northwest Univ, Sch Chem Engn, Xian 710069, Shaanxi, Peoples R China; [Jiao, Lin-Yu; Ning, Zi-Hui; Yin, Xiao-Mei; Hong, Qian; Ma, Xiao-Xun] Northwest Univ, Collaborat Innovat Ctr Dev Energy & Chem Ind Nort, Shaanxi Res Ctr Engn Technol Clean Coal Convers,I, Minist Educ Adv Use Technol Shanbei Energy,Chem E, Xian 710069, Shaanxi, Peoples R China; [Liu, Shanshan] Shaanxi Univ Sci & Technol, Coll Chem & Chem Engn, Shaanxi Key Lab Chem Addit Ind, Xian 710021, Shaanxi, Peoples R China in 2021.0, Cited 34.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6

An efficient and convenient rhodium(III)-catalyzed chelation-assisted ortho-selective carbon-hydrogen bond alkylation of phenols treated with readily available diazocarbonyl compounds as the alkyl source has been described. Migratory carbene insertion represents the principal step to realize this carbenoid coupling transformation, giving rise to a broad rang of alkylated products and at the same time, releasing nitrogen gas as sole byproduct. This protocol offers exclusive regioselectivities, moderate to excellent chemical yields, and good functional group tolerance.

SDS of cas: 150-19-6. Bye, fridends, I hope you can learn more about C7H8O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
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

An article Nickel-catalyzed C3-alkylation of indoles with alcohols via a borrowing hydrogen strategy WOS:000651900200001 published article about C BOND FORMATION; ALPHA-ALKYLATION; UNACTIVATED AMIDES; KETONES; METHYLATION; ESTERS; ARYLACETONITRILES; FUNCTIONALIZATION; COMPLEXES; METHANOL in [Hu, Miao; Jiang, Yong; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan; Jin, Liqun] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310032, Peoples R China; [Jin, Liqun] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China in 2021, Cited 65. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6. Product Details of 100-51-6

An efficient method for the Ni-catalyzed C3-alkylation of indoles using readily available alcohols as the alkylating reagents has been developed. The alkylation was addressed with an air and moisture-stable binuclear nickel complex ligated by tetrahydroquinolin-8-one as the effective pre-catalyst. The newly developed transformation could accommodate a broad substrate scope including primary/secondary benzylic and aliphatic alcohols and substituted indoles. Mechanistic studies suggested that the reaction proceeds through a borrowing hydrogen pathway.

Welcome to talk about 100-51-6, If you have any questions, you can contact Hu, M; Jiang, Y; Sun, N; Hu, BX; Shen, ZL; Hu, XQ; Jin, LQ or send Email.. Product Details of 100-51-6

Reference:
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

In 2021 CHEM SCI published article about CROSS-COUPLING REACTIONS; NUCLEOPHILIC-SUBSTITUTION; BIOLOGICAL EVALUATION; WILLIAMSON SYNTHESIS; COPPER; CARBONYLATION; CYCLIZATION; EFFICIENT; CHEMISTRY; MACROCYCLIZATION in [Huang, Chaofan; Lin, Jie; Liu, Qi; Qin, Anni; Wang, Huanan; Wu, Guolin; Wu, Penglin; Yuan, Yuan; Zheng, Wei-Feng; Zheng, Yangguangyan; Ma, Shengming] Fudan Univ, Dept Chem, Res Ctr Mol Recognit & Synth, 220 Handan Lu, Shanghai 200433, Peoples R China; [Shi, Fuchun; Cui, Yifan; Li, Can; Xiao, Junzhe; Xu, Haibo; Zhai, Yizhan; Yu, Biao; Ma, Shengming] Chinese Acad Sci, State Key Lab Organometall Chem, Shanghai Inst Organ Chem, 345 Lingling Lu, Shanghai 200032, Peoples R China in 2021, Cited 84. The Name is Mequinol. Through research, I have a further understanding and discovery of 150-76-5. Safety of Mequinol

A palladium-catalyzed C-O bond formation reaction between phenols and allenylic carbonates to give 2,3-allenic aromatic ethers with decent to excellent yields under mild reaction conditions has been described. A variety of synthetically useful functional groups are tolerated and the synthetic utility of this method has been demonstrated through a series of transformations of the allene moiety. By applying this reaction as the key step, the total syntheses of naturally occurring allenic aromatic ethers, eucalyptene and terricollene A (first synthesis; 4.5 g gram scale), have been accomplished.

Bye, fridends, I hope you can learn more about C7H8O2, If you have any questions, you can browse other blog as well. See you lster.. Safety of Mequinol

Reference:
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

Recommanded Product: 100-51-6. Sanchez-Garcia, F; Mirzayeva, A; Roldan, A; Castro, R; Palacios, V; Garcia-Barroso, C; Duran-Guerrero, E in [Mirzayeva, Aytan; Castro, Remedios; Garcia-Barroso, Carmelo; Duran-Guerrero, Enrique] Univ Cadiz, Univ Inst Wine & Food Res IVAGRO CAIV, Fac Sci, Analyt Chem Dept, Agrifood Campus Int Excellence CeiA3, Cadiz, Spain; [Sanchez-Garcia, Fini; Roldan, Ana; Palacios, Victor] Univ Cadiz, Chem Engn & Food Technol Dept, Cadiz, Spain published Evolution of volatile compounds and sensory characteristics of edible green seaweed (Ulva rigida) during storage at different temperatures in 2019.0, Cited 28.0. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6.

BACKGROUND Edible seaweeds are one of the most important resources that currently exist for their multiple uses and applications. Like other food types, during their storage there are significant changes in sensory characteristics associated with loss of freshness and with production and/or degradation of their volatile compounds. In this study, multiple headspace sorptive extraction (MHSSE) coupled with gas chromatography/mass spectrometry (GC/MS) detection has been applied to an edible green seaweed (Ulva rigida) in order to determine the evolution of volatile compounds during storage for 12 days at 4 or 16 degrees C. RESULTS The existing analytical methodology has been updated and validated for 18 additional compounds. At the end, 41 volatile compounds from different chemical families were quantified. Aldehydes, carboxylic acids and esters were the main classes found in U. rigida. Analytical and sensory data were submitted for statistical analysis. During storage, most volatile compounds were only affected by the number of storage days (P < 0.05), with significant decreases as storage time increased. Sensory analysis revealed significant changes in the samples stored for longer times (8, 10 and 12 days), with a clear influence of the boiled vegetable descriptor. CONCLUSION In order to get a successful preservation of seaweeds and to maintain their marine character during storage, both temperature and time should be carefully controlled. (c) 2019 Society of Chemical Industry Welcome to talk about 100-51-6, If you have any questions, you can contact Sanchez-Garcia, F; Mirzayeva, A; Roldan, A; Castro, R; Palacios, V; Garcia-Barroso, C; Duran-Guerrero, E or send Email.. Recommanded Product: 100-51-6

Reference:
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