Category: 94-41-7

Authors Keskin, S in WILEY published article about ANTIOXIDANT ACTIVITY; PHENOLIC COMPOSITION; TURKISH PROPOLIS in [Keskin, Saban] Bilecik Seyh Edebali Univ, Vocat Sch Hlth Serv, Bilecik, Turkey in 2020, Cited 24. COA of Formula: C15H12O. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7

Orange peel oil contains high amount of d-limonene which is reported to have antidiabetic activity. Propolis contains many biologically active compounds like phenolic acids, flavonoids and terpenes. Because of its rich phenolic composition, antidiabetic activity of propolis has also been shown in literature. Consumption of raw propolis is limited because of its resinous nature. It should be extracted to convert it into consumable form. Ethanol is the most used solvent for this purpose. Ethanol is the limiting factor for propolis consumption either for religious concerns or being harmful for human health. There is an increasing need for new, compatible and healthier solvents for propolis extraction. This is the first paper describing the extraction of propolis with orange peel oil. 1:10 (g/v) ratio was used for extraction. Orange peel oil (OPO), orange peel oil propolis extract (OPOPE) and ethanol propolis extract (EPE) were separately analysed by using GC-MS technique. Total phenolic content of oil and propolis extract was also carried out. Inhibition of alpha-amylase from barley malt with new extract was also reported. It was found that OPOPE was rich in volatile compounds of propolis, phenolic acid derivatives and free fatty acids. It was observed that OPOPE showed higher inhibition on alpha-amylase enzyme (IC50 0.196 mg/mL). It can be concluded that orange peel oil could be used as solvent for preparing propolis extract. Propolis extract obtained with orange peel oil could also be used as complementary medicine for the treatment of type 2 diabetes.

COA of Formula: C15H12O. Welcome to talk about 94-41-7, If you have any questions, you can contact Keskin, S or send Email.

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Recently I am researching about BIODIESEL PRODUCTION; PALLADIUM NANOPARTICLES; CONVENIENT SYNTHESIS; CONJUGATE ADDITION; EXTRACT; SOLVENT; BASE; ACID; OIL; NITRATE, Saw an article supported by the UGC, New DelhiUniversity Grants Commission, India. Published in SPRINGER INTERNATIONAL PUBLISHING AG in CHAM ,Authors: Talukdar, A; Deka, DC. The CAS is 94-41-7. Through research, I have a further understanding and discovery of Chalcone. Formula: C15H12O

Water hyacinth ash is found to be an efficient and reusable catalyst for the synthesis of beta-amino carbonyl/nitrile compounds by aza-Michael reaction of amines with alpha,beta-unsaturated compounds at room temperature under solvent free condition. Due to low cost of the catalyst, good activity, ease of handling and easy recovery with high yields of the products in short reaction time, easy workup procedure, mild reaction condition, the protocol is highly applicable in synthetic organic chemistry.

Formula: C15H12O. About Chalcone, If you have any questions, you can contact Talukdar, A; Deka, DC or concate me.

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Category: thiazolidines. I found the field of Chemistry; Science & Technology – Other Topics very interesting. Saw the article Pyrenediones as versatile photocatalysts for oxygenation reactions with in situ generation of hydrogen peroxide under visible light published in 2020.0, Reprint Addresses Huang, DJ (corresponding author), Natl Univ Singapore, Dept Chem, Food Sci & Technol Program, Singapore 117543, Singapore.; Wu, J (corresponding author), Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore.. The CAS is 94-41-7. Through research, I have a further understanding and discovery of Chalcone.

Pyrenediones (PYDs) are efficient photocatalysts for three oxygenation reactions: epoxidation of electron deficient olefins, oxidative hydroxylation of organoborons, and oxidation of sulfides via in situ generation of H2O2 under visible light irradiation, using oxygen as a terminal oxidant and IPA as a solvent and a hydrogen donor.

Welcome to talk about 94-41-7, If you have any questions, you can contact Zhang, YN; Yang, X; Tang, HD; Liang, D; Wu, J; Huang, DJ or send Email.. Category: thiazolidines

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Thiazolidine – Wikipedia,
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In 2019.0 J NAT MED-TOKYO published article about PHENOLIC CONSTITUENTS; MEDICINAL-PLANTS; LICORICE ROOT; ISOFLAVONOIDS; ANTIOXIDANT; COMPONENTS in [Cheng, Ming; Zhang, Hongmin; Sun, Yingjie; Li, Wei; Qiu, Feng] Tianjin Univ Tradit Chinese Med, Sch Chinese Mat Med, 312 Anshanxi Rd, Tianjin 300193, Peoples R China; [Cheng, Ming; Ding, Liqin; Zhang, Hongmin; Jiang, Benke; Sun, Yingjie; Cao, Shijie; Qiu, Feng] Tianjin Univ Tradit Chinese Med, Inst Tradit Chinese Med, Tianjin Key Lab TCM Chem & Anal, Tianjin, Peoples R China; [Li, Wei; Koike, Kazuo] Toho Univ, Fac Pharmaceut Sci, Miyama 2-2-1, Chiba 2748510, Japan; [Kan, Hongfeng; Jiang, Benke] Shenyang Pharmaceut Univ, Shenyang, Liaoning, Peoples R China in 2019.0, Cited 50.0. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7. Recommanded Product: Chalcone

Two new flavonoid glycosides, 2 ‘,4 ‘-dihydroxydihydrochalcone-4-O-beta-d-glucopyranoside (1) and medicarpin-3-O-beta-d-apiofuranosyl (1 -> 2)-beta-d-glucopyranoside (2), together with 34 known flavonoids were isolated from the 75% EtOH extract of the dried roots of Glycyrrhiza uralensis Fisch. Their structures were elucidated on the basis of spectroscopic analyses. The flavonoids were classified into ten sub-types, namely, dihydrochalcone (1), pterocarpans (2-4), flavones (5-6), flavanones (7-11), chalcones (12-15), retro-chalcones (16-18), isoflavans (19-21), isoflavones (22-28), 3-arylcoumarins (29-30), and coumestans (31-36). The isolated flavonoids were evaluated for in vitro hepatoprotective activity against d-galactosamine-induced toxicity in human hepatoma HepG2 cells.

Recommanded Product: Chalcone. Bye, fridends, I hope you can learn more about C15H12O, If you have any questions, you can browse other blog as well. See you lster.

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Thiazolidine – Wikipedia,
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I found the field of Biotechnology & Applied Microbiology; Research & Experimental Medicine very interesting. Saw the article Response of Soybean Root to Phosphorus Deficiency under Sucrose Feeding: Insight from Morphological and Metabolome Characterizations published in 2020.0. Name: Chalcone, Reprint Addresses Ao, X (corresponding author), Shenyang Agr Univ, Coll Agron, Shenyang 110866, Peoples R China.. The CAS is 94-41-7. Through research, I have a further understanding and discovery of Chalcone

Phosphorus (P) is one the least available essential plant macronutrients in soils that is a major constraint on plant growth. Soybean (Glycine max L.) production is often limited due to low P availability. The better management of P deficiency requires improvement of soybean’s P use efficiency. Sugars are implicated in P starvation responses, and a complete understanding of the role of sucrose together with P in coordinating P starvation responses is missing in soybean. This study explored global metabolomic changes in previously screened low-P-tolerant (Liaodou, L13) and low-P-sensitive (Tiefeng 3, T3) soybean genotypes by liquid chromatography coupled mass spectrometry. We also studied the root morphological response to sucrose application (1%) in P-starved soybean genotypes against normal P supply. Root morphology in L13 genotype has significantly improved P starvation responses as compared to the T3 genotype. Exogenous sucrose application greatly affected root length, root volume, and root surface area in L13 genotype while low-P-sensitive genotype, i.e., T3, only responded by increasing number of lateral roots. Root : shoot ratio increased after sucrose treatment regardless of P conditions, in both genotypes. T3 showed a relatively higher number of differentially accumulated metabolites between P-starved and normal P conditions as compared to L13 genotype. Common metabolites accumulated under the influence of sucrose were 5-O-methylembelin, D-glucuronic acid, and N-acetyl-L-phenylalanine. We have discussed the possible roles of the pathways associated with these metabolites. The differentially accumulated metabolites between both genotypes under the influence of sucrose are also discussed. These results are important to further explore the role of sucrose in the observed pathways. Especially, our results are relevant to formulate strategies for improving P efficiency of soybean genotypes with different P efficiencies.

Welcome to talk about 94-41-7, If you have any questions, you can contact Yang, A; Kong, LJ; Wang, H; Yao, XD; Xie, FT; Wang, HY; Ao, X or send Email.. Name: Chalcone

Reference:
Thiazolidine – Wikipedia,
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An article Antioxidative Activity of 1,3,5-Triazine Analogues Incorporating Aminobenzene Sulfonamide, Aminoalcohol/Phenol, Piperazine, Chalcone, or Stilbene Motifs WOS:000534617300018 published article about TRIAZINE DERIVATIVES; LIPID-PEROXIDATION; PROMISING SCAFFOLD; INCREASE SURVIVAL; RADIATION-THERAPY; CHEMOTHERAPY; NUTRIENTS; TAMOXIFEN; EFFICACY; CANCER in [Havrankova, Eva; Calkovska, Nikola; Padrtova, Tereza; Csollei, Jozef; Opatrilova, Radka] Univ Vet & Pharmaceut Sci, Dept Chem Drugs, Fac Pharm, Brno 61242, Czech Republic; [Pazdera, Pavel] Masaryk Univ, Dept Chem, Ctr Synth Sustainable Condit & Their Management, Fac Sci, Brno 62500, Czech Republic in 2020.0, Cited 49.0. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7. HPLC of Formula: C15H12O

A series of 1,3,5-triazine analogues, incorporating aminobenzene sulfonamide, aminoalcohol/ phenol, piperazine, chalcone, or stilbene structural motifs, were evaluated as potential antioxidants. The compounds were prepared by using step-by-step nucleophilic substitution of chlorine atoms in starting 2,4,6-trichloro-1,3,5-triazine. Reactions were catalyzed by Cu(I)-supported on a weakly acidic resin. The radical scavenging activity was determined in terms of %inhibition activity and EC50, using the ABTS method. Trolox and ascorbic acid (ASA) were used as standards. In the lowest concentration 1 X 10(-4) M, the %inhibition activity values at 0 min were comparable with both standards at least for 10 compounds. After 60 min, compounds 5, 6, 13, and 25 showed nearly twice %inhibition (73.44-87.09%) in comparison with the standards (Trolox = 41.49%; ASA = 31.07%). Values of EC50 at 60 min (17.16-27.78 mu M) were 5 times lower for compounds 5, 6, 13, and 25 than EC50 of both standards (trolox = 178.33 mu M; ASA = 147.47 mu M). Values of EC50 correlated with %inhibition activity. Based on these results, the presented 1,3,5-triazine analogues have a high potential in the treatment of illnesses caused or related to oxidative stress.

Welcome to talk about 94-41-7, If you have any questions, you can contact Havrankova, E; Calkovska, N; Padrtova, T; Csollei, J; Opatrilova, R; Pazdera, P or send Email.. HPLC of Formula: C15H12O

Reference:
Thiazolidine – Wikipedia,
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An article Acyl Radicals from alpha-Keto Acids Using a Carbonyl Photocatalyst: Photoredox-Catalyzed Synthesis of Ketones WOS:000569377600028 published article about C-H BONDS; OXOCARBOXYLIC ACIDS; MERGING PHOTOREDOX; ELECTRON-TRANSFER; CARBOXYLIC-ACIDS; ARYL HALIDES; LIGHT; METAL; ACYLATION; ALKENES in [Zhu, Da-Liang; Wu, Qi; Wang, Hao; Ren, Zhi-Gang; Li, Hong-Xi] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China; [Young, David James] Charles Darwin Univ, Coll Engn Informat Technol & Environm, Darwin, NT 0909, Australia in 2020.0, Cited 65.0. HPLC of Formula: C15H12O. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7

Acyl radicals have been generated from alpha-keto acids using inexpensive and commercially available 2-chloro-thioxanthen-9-one as the photoredox catalyst under visible light illumination. These reactive species added to olefins or coupled with aryl halides via a bipyridyl-stabilized Ni(II) catalyst, enabling easy access to a diverse range of ketones. This reliable, atom-economical, and eco-friendly protocol is compatible with a wide range of functional groups.

Welcome to talk about 94-41-7, If you have any questions, you can contact Zhu, DL; Wu, Q; Young, DJ; Wang, H; Ren, ZG; Li, HX or send Email.. HPLC of Formula: C15H12O

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In 2019.0 MEDCHEMCOMM published article about BIOLOGICAL EVALUATION; MOLECULAR DOCKING; CYCLOOXYGENASE-2 COX-2; SUBSTANCE-P; DERIVATIVES; DESIGN; RISK; PROSTAGLANDINS; DENATURATION; CELECOXIB in [Chandel, Priyanka; Singla, Nishu; Kumar, Anshul; Gill, Rupinder Kaur] ISF Coll Pharm, Dept Pharmaceut Chem, Moga 142001, Punjab, India; [Kumar, Anoop] ISF Coll Pharm, Dept Pharmacol, Moga 142001, Punjab, India; [Singh, Gagandeep] Indian Inst Technol Ropar, Dept Chem, Ropar 140001, Punjab, India in 2019.0, Cited 61.0. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7. COA of Formula: C15H12O

In the present work, coumarin based pyrazolines (7a-g) have been synthesized and investigated for their in vitro and in vivo anti-inflammatory potential. Amongst the synthesized compounds, compounds 7a, 7d and 7f exhibited significant in vitro anti-inflammatory activity as compared to the standard etoricoxib. Keeping this in mind, in vivo investigations were carried out via carrageenan induced inflammation and acetic acid induced writhing models in male Wistar rats and compound 7a was found to possess appreciable anti-inflammatory and analgesic potential. The mode of action of compound 7a was also investigated by using substance P as the biomarker, which shows promising results. Further, the selectivity of the most active compound 7a against the cyclooxygenase enzyme was supported by molecular docking studies which reveal that compound 7a has greater binding affinity towards COX-2 over COX-1 and 5-LOX enzymes. In silico ADME analysis of compound 7a confirms the drug-like characteristics and the in vivo acute toxicity study showed the safety of the compound even up to a 2000 mg kg(-1) dose. Thus, compound 7a was identified as an effective anti-inflammatory agent, and can be explored for further analgesic/anti-inflammatory drug design and development.

COA of Formula: C15H12O. Bye, fridends, I hope you can learn more about C15H12O, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com

COA of Formula: C15H12O. Recently I am researching about RING-CLOSING METATHESIS; RAY CRYSTAL-STRUCTURE; 1,2-AZABOROLYL COMPLEXES; MULTICOMPONENT REACTIONS; AZABOROLYL COMPLEXES; SANDWICH COMPLEXES; B-N; BORON; LIGAND; POLYMERIZATION, Saw an article supported by the Deutsche ForschungsgemeinschaftGerman Research Foundation (DFG). Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Li, J; Daniliuc, CG; Kartha, KK; Fernandez, G; Kehr, G; Erker, G. The CAS is 94-41-7. Through research, I have a further understanding and discovery of Chalcone

The (Fmes)BH2 center dot SMe2 reagent (7) reacts sequentially with an acetylene and, e.g., xylylisonitrile in a convenient three-component reaction to give a series of unprecedented dihydro-1,3-azaborole derivatives 16. The tolane-derived example 16a was deprotonated and used as a ligand in organometallic chemistry. Compounds 16 served as the starting materials for the straightforward synthesis of various dihydro-1,3-azaborinine derivatives by treatment with an isonitrile. Several diaryldihydro-1,3 azaboroles showed interesting photophysical properties such as aggregation-induced emission and high fluorescence quantum yields.

COA of Formula: C15H12O. Welcome to talk about 94-41-7, If you have any questions, you can contact Li, J; Daniliuc, CG; Kartha, KK; Fernandez, G; Kehr, G; Erker, G or send Email.

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Thiazolidine – Wikipedia,
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An article Rhodium-Catalyzed Cascade Annulation of Benzimidates and Nitroalkenes for the Synthesis of Difunctionalized Indenes WOS:000477402600001 published article about C-H ACTIVATION; ANTIDEPRESSANT ACTIVITY; DIRECTING GROUPS; BOND; RH; ALKYNES; ACIDS; 1H-INDAZOLES; QUINAZOLINES; INHIBITION in [Lv, Ningning; Liu, Yue; Liu, Zhanxiang; Zhang, Yuhong] Zhejiang Univ, ZJU NHU United R&D Ctr, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China; [Chen, Zhengkai] Zhejiang Sci Tech Univ, Dept Chem, Hangzhou 310018, Zhejiang, Peoples R China; [Zhang, Yuhong] Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China in 2019.0, Cited 79.0. Category: thiazolidines. The Name is Chalcone. Through research, I have a further understanding and discovery of 94-41-7

A facile and expeditious protocol for the synthesis of difunctionalized indenes from readily available benzimidates and nitroalkenes through rhodium-catalyzed C-H activation and cyclization is reported here. The transformation exhibits powerful reactivity, tolerates a large number of functional groups, and proceeds in moderate to high yields under an ambient atmosphere, providing a straightforward method to access structurally diverse and valuable difunctionalized indene derivatives.

Welcome to talk about 94-41-7, If you have any questions, you can contact Lv, NN; Chen, ZK; Liu, Y; Liu, ZX; Zhang, YH or send Email.. Category: thiazolidines

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,Thiazolidine – ScienceDirect.com