When did you first realize you had a special interest and talent in103-26-4

Product Details of 103-26-4. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Verma, A; Grams, RJ; Rastatter, BP; Santos, WL or concate me.

Product Details of 103-26-4. I found the field of Chemistry very interesting. Saw the article Semireduction of alkynoic acids via a transition metal-free alpha borylation-protodeborylation sequence published in 2019.0, Reprint Addresses Santos, WL (corresponding author), Virginia Tech, Dept Chem, Blacksburg, VA 24061 USA.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate.

A method for the semi-reduction of alkynoic acids through an alpha-borylation and subsequent protodeborylation mechanism has been developed. The transition metal-free protocol is achieved through the activation of bis(pinacolato)diboron by an in situ generated carboxylate moiety yielding aryl acrylic acids. Our studies demonstrate an unprecedented dual role for the carboxylate anion that involves the activation of the diboron reagent and a directing effect in the alpha-borylation. (C) 2019 Elsevier Ltd. All rights reserved.

Product Details of 103-26-4. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Verma, A; Grams, RJ; Rastatter, BP; Santos, WL or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Awesome and Easy Science Experiments about Methyl 3-phenyl-2-propenoate

Application In Synthesis of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Evtushok, VE; Vorob’ev, AY or concate me.

Application In Synthesis of Methyl 3-phenyl-2-propenoate. I found the field of Chemistry very interesting. Saw the article Synthesis of pyrazolo- and [1,2,4]triazolo-[1,5-a]quinolin-9-ols by cycloaddition to 8-hydroxyquinoline N-imide published in 2019.0, Reprint Addresses Vorob’ev, AY (corresponding author), Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, 9 Akad Lavrentieva Ave, Novosibirsk 630090, Russia.; Vorob’ev, AY (corresponding author), Novosibirsk State Univ, 1 Pirogova St, Novosibirsk 630090, Russia.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate.

The reaction of 1-amino-8-hydroxyquinolinium mesitylenesulfonate with alkenes and alkynes containing electron-withdrawing substituents was performed in MeCN-K2C?(3) system and gave the respective 9-hydroxypyrazolo[1,5-a]quinolines. The reaction with acetonitrile and aromatic nitriles in aqueous 2 N K?H solution gave the respective 2-substituted 9-hydroxy[1,2,4]triazolo[1,5-a]quinolines.

Application In Synthesis of Methyl 3-phenyl-2-propenoate. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Evtushok, VE; Vorob’ev, AY or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An update on the compound challenge: C10H10O2

Category: esters-buliding-blocks. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Younessi-Hamzekhanlu, M; Sanjari, S; Dejahang, A; Karkaj, ES; Nojadeh, MS; Gonenc, TM; Ozturk, M or concate me.

Category: esters-buliding-blocks. Authors Younessi-Hamzekhanlu, M; Sanjari, S; Dejahang, A; Karkaj, ES; Nojadeh, MS; Gonenc, TM; Ozturk, M in TAYLOR & FRANCIS LTD published article about in [Younessi-Hamzekhanlu, Mehdi; Nojadeh, Mohsen Sabzi] Univ Tabriz, Ahar Fac Agr & Nat Resources, Dept Forestry & Med Plants, Ahar, Iran; [Sanjari, Sepideh] AREEO, Agr Biotechnol Res Inst, Dept Syst Biol, Karaj, Iran; [Dejahang, Ata] Itasadra Biotechnol Co, Nazari Business Grp, R&D Sect, Qazvin, Iran; [Karkaj, Esmaeil Sheidai] Urmia Univ, Agr & Nat Resources Fac, Dept Range & Watershed Management, Orumiyeh, Iran; [Gonenc, Tuba Mert] Izmir Katip Celebi Univ, Fac Pharm, Dept Pharmacognosy, Izmir, Turkey; [Ozturk, Munir] Ege Univ, Bot Dept, Izmir, Turkey; [Ozturk, Munir] Ege Univ, Ctr Environm Studies, Izmir, Turkey in 2020.0, Cited 59.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Artemisia fragrans is an aromatic and perennial herb with green silver leaves and yellow flowers, widely distributed in Iran, Azerbaijan, Russia and Turkey. The plant and its essential oil (EO) are used in traditional medicine and have economic value. In this study, the composition, antibacterial and antioxidant activities of 16 A. fragrans essential oil samples collected from different habitats in Iran were analyzed. A total of 85 compounds were detected using GC-MS analysis, the major constituents being camphor (9.91-34.44 %), alpha-thujone (19.22-42.63 %) and 1,8-cineole (12.57-31.87 %). Davanone D, alpha-cadinol, verbenene, ortho-oci-men were detected in the analysis as the new components for this species and are first reported by us. Anti-bacterial activity and minimum inhibitory and bactericidal concentrations of EOs were tested on Escherichia coli, Klebsiella pneumonia and Proteus vulgaris (Gram-negative strains) Staphylococcus aureus, Staphylococ-cus epidermidis and Bacillus subtilis (Gram-positive strains). The EOs showed better inhibitory effects against Gram-negative strains compared to Gram-positive ones. Among the EOs, E7 (IC50 = 9.1 mu g/mL) population showed the highest radical scavenging capacity, which was equal to the positive control (butylated hyroxytoluene). The quantitative and qualitative variability of the studied EOs and their antibacterial and antioxidant activities may be recommended for pharmacological and cosmetic industries.

Category: esters-buliding-blocks. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Younessi-Hamzekhanlu, M; Sanjari, S; Dejahang, A; Karkaj, ES; Nojadeh, MS; Gonenc, TM; Ozturk, M or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Extracurricular laboratory: Synthetic route of Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Shahamat, Z; Nemati, F; Elhampour, A or concate me.. COA of Formula: C10H10O2

COA of Formula: C10H10O2. In 2020.0 J POROUS MAT published article about CONJUGATED MICROPOROUS POLYMER; HETEROGENEOUS CATALYST; EFFICIENT CATALYST; ORGANIC POLYMERS; NANOPARTICLES; COMPLEX; HYDROGENATION; NANOCATALYST; SILICA; PD in [Shahamat, Zahra; Nemati, Firouzeh; Elhampour, Ali] Semnan Univ, Dept Chem, Semnan, Iran in 2020.0, Cited 59.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

The paper describes synthesis of a novel mesoporous and magnetically regenerated heterogeneous nanocatalyst with high catalytic activity. The synthesis strategy includes a one-step polycondensation reaction of melamine, formaldehyde and FeCl3 center dot 6H(2)O in a simple and sustainable manner and followed by immobilization of Pd(II) on it. Formation and properties of nanocomposite were characterized by different techniques; the results were illustrated good surface area and a well-defined mesopore structure. Also the palladium-catalyzed C-C bond formation between aryl halides and olefins was selected to survey the activity of the synthesized nanocatalyst. Central Composite Design (CCD) strategy was used to predict the optimum synthesis conditions and identify the remarkable and effective factors including temperature, period of the reaction and amount of catalyst. These results were also verified experimentally. In order to minimize systematic error, the experimental runs as a randomized fashion were accomplished.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Shahamat, Z; Nemati, F; Elhampour, A or concate me.. COA of Formula: C10H10O2

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Properties and Exciting Facts About Methyl 3-phenyl-2-propenoate

SDS of cas: 103-26-4. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Perez-Castillo, Y; Lima, TC; Ferreira, AR; Silva, CR; Campos, RS; Neto, JBA; Magalhaes, HIF; Cavalcanti, BC; Junior, HVN; de Sousa, DP or concate me.

SDS of cas: 103-26-4. In 2020 BIOMED RES INT published article about ANTIFUNGAL ACTIVITY; PHENOLIC-COMPOUNDS; CANDIDA; ANTIBACTERIAL; EXTRACT; ESTERS; AMIDES in [Perez-Castillo, Yunierkis] Univ Amer, Escuela Ciencias Fis & Matemat, Quito, Ecuador; [Lima, Tamires C.] Univ Fed Sergipe, Dept Pharm, BR-49100000 Sao Cristovao, Sergipe, Brazil; [Ferreira, Alana R.; Magalhaes, Hemerson I. F.; de Sousa, Damiao P.] Univ Fed Paraiba, Dept Pharmaceut Sci, BR-58051970 Joao Pessoa, Paraiba, Brazil; [Silva, Cecilia R.; Campos, Rosana S.; Neto, Joao B. A.; Junior, Helio V. N.] Univ Fed Ceara, Sch Pharm, Dept Clin & Toxicol Anal, Lab Bioprospect & Expt Yeast, Fortaleza, Ceara, Brazil; [Cavalcanti, Bruno C.] Univ Fed Ceara, Dept Physiol & Pharmacol, Fortaleza, Ceara, Brazil in 2020, Cited 56. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4.

Over the last decade, there has been a dramatic increase in the prevalence and gravity of systemic fungal diseases. This study aimed therefore at evaluating the antifungal potential of ester derivatives of benzoic and cinnamic acids from three Candida species. The compounds were prepared via Fischer esterification, and the antifungal assay was performed by the microdilution method in 96-well microplates for determining the minimal inhibitory concentrations (MICs). The findings of the antifungal tests revealed that the analogue compound methyl ferulate, methyl o-coumarate, and methyl biphenyl-3-carboxylate displayed an interesting antifungal activity against all Candida strains tested, with MIC values of 31.25-62.5, 62.5-125, and 62.5 mu g/ml, respectively. A preliminary Structure-Activity Relationship study of benzoic and cinnamic acid derivatives has led to the recognition of some important structural requirements for antifungal activity. The results of molecular docking indicate that the presence of the enoate moiety along with hydroxyl and one methoxy substitution in the phenyl ring has a positive effect on the bioactivity of compound 7 against Candida albicans. These observations further support the hypothesis that the antifungal activity of compound 7 could be due to its binding to multiple targets, specifically to QR, TS, and ST-PK. Additional experiments are required in the future to test this hypothesis and to propose novel compounds with improved antifungal activity.

SDS of cas: 103-26-4. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Perez-Castillo, Y; Lima, TC; Ferreira, AR; Silva, CR; Campos, RS; Neto, JBA; Magalhaes, HIF; Cavalcanti, BC; Junior, HVN; de Sousa, DP or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

What Kind of Chemistry Facts Are We Going to Learn About Methyl 3-phenyl-2-propenoate

Category: esters-buliding-blocks. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Sable, V; Shah, J; Sharma, A; Kapdi, AR or concate me.

Authors Sable, V; Shah, J; Sharma, A; Kapdi, AR in WILEY-V C H VERLAG GMBH published article about AEROBIC OXIDATIVE ESTERIFICATION; LIGAND-FREE PALLADIUM; CARBOXYLIC-ACIDS; CATALYZED SYNTHESIS; TERMINAL ALKYNES; HIGHLY EFFICIENT; HECK REACTION; ALDEHYDES; NANOPARTICLES; ESTERS in [Sable, Vaibhav; Shah, Jagrut; Sharma, Anuja; Kapdi, Anant R.] Inst Chem Technol, Dept Chem, Nathalal Parekh Rd, Mumbai 400019, Maharashtra, India in 2019.0, Cited 85.0. Category: esters-buliding-blocks. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Palladium colloids obtained from the degradation of Hermann-Beller palladacycle proved to be an efficient catalytic system in combination with silver oxide as a selective oxidant for the oxidative esterification of differently substituted benzyl alcohols in MeOH as solvent. Excellent reactivity exhibited by the catalytic system also allowed the alcoholic coupling partner to be changed from MeOH to a wide range of alcohols having diverse functionalities. The mildness of the developed protocol also made it possible to employ propargyl alcohol as the coupling partner without any observation of any interference of the terminal alkyne. Selective oxidative coupling of a primary alcoholic functional group over secondary in the case of glycols and glycerols was also made possible using the developed catalyst system. To test the relevancy of Pd/Ag combined catalysis mixed Pd/Ag colloids were synthesized, characterized by TEM, XRD and XPS and applied to oxidative-esterification successfully.

Category: esters-buliding-blocks. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Sable, V; Shah, J; Sharma, A; Kapdi, AR or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Top Picks: new discover of Methyl 3-phenyl-2-propenoate

Category: esters-buliding-blocks. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Ghaffari, B; Mendes-Burak, J; Chan, KW; Coperet, C or concate me.

An article Silica-Supported Mn-II Sites as Efficient Catalysts for Carbonyl Hydroboration, Hydrosilylation, and Transesterification WOS:000489670500001 published article about PHASE SELECTIVE HYDROGENATION; MOLECULAR PRECURSOR; ENANTIOSELECTIVE EPOXIDATION; SUBSTRATE SCOPE; MANGANESE; CHEMISTRY; KETONES; ACTIVATION; ALDEHYDES; NICKEL in [Ghaffari, Behnaz; Mendes-Burak, Jorge; Chan, Ka Wing; Coperet, Christophe] Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Vladimir Prelog Weg 1-5, CH-8093 Zurich, Switzerland in 2019.0, Cited 72.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Category: esters-buliding-blocks

Manganese, the third most abundant transition-metal element after iron and titanium, has recently been demonstrated to be an effective homogeneous catalyst in numerous reactions. Herein, the preparation of silica-supported Mni(II) sites is reported using Surface Organometallic Chemistry (SOMC), combined with tailored thermolytic molecular precursors approach based on Mn-2[OSi(OtBu)(3)](4) and ZMn{N(SiMe3)(2)}(2)THF. These supported Mn-II sites, free of organic ligands, efficiently catalyze numerous reactions: hydroboration and hydrosilylation of ketones and aldehydes as well as the transesterification of industrially relevant substrates.

Category: esters-buliding-blocks. About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Ghaffari, B; Mendes-Burak, J; Chan, KW; Coperet, C or concate me.

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

The Absolute Best Science Experiment for Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Shahamat, Z; Nemati, F; Elhampour, A or concate me.. Formula: C10H10O2

Formula: C10H10O2. I found the field of Chemistry; Materials Science very interesting. Saw the article Palladium (II) anchored on a magnetic mesoporous polymelamine-formaldehyde as new catalyst for Heck coupling reaction: optimization of reaction using response surface methodology published in 2020.0, Reprint Addresses Nemati, F (corresponding author), Semnan Univ, Dept Chem, Semnan, Iran.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate.

The paper describes synthesis of a novel mesoporous and magnetically regenerated heterogeneous nanocatalyst with high catalytic activity. The synthesis strategy includes a one-step polycondensation reaction of melamine, formaldehyde and FeCl3 center dot 6H(2)O in a simple and sustainable manner and followed by immobilization of Pd(II) on it. Formation and properties of nanocomposite were characterized by different techniques; the results were illustrated good surface area and a well-defined mesopore structure. Also the palladium-catalyzed C-C bond formation between aryl halides and olefins was selected to survey the activity of the synthesized nanocatalyst. Central Composite Design (CCD) strategy was used to predict the optimum synthesis conditions and identify the remarkable and effective factors including temperature, period of the reaction and amount of catalyst. These results were also verified experimentally. In order to minimize systematic error, the experimental runs as a randomized fashion were accomplished.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Shahamat, Z; Nemati, F; Elhampour, A or concate me.. Formula: C10H10O2

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Awesome and Easy Science Experiments about Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Zhang, JW; Wang, Y; Feng, YX; Du, SS; Jia, LM or concate me.. Quality Control of Methyl 3-phenyl-2-propenoate

In 2021.0 J ESSENT OIL BEAR PL published article about CALLOSOBRUCHUS-CHINENSIS L.; INSECTICIDAL ACTIVITIES; CHEMICAL-COMPOSITION; SITOPHILUS-ORYZAE; DERMATOPHAGOIDES-FARINAE; BOTANICAL INSECTICIDES; CONSTITUENTS; BIOACTIVITIES; ANTIOXIDANT; GROWTH in [Zhang, Jiawei; Jia, Liming] Beijing Forestry Univ, Key Lab Silviculture & Conservat, Minist Educ, 35,Tsinghua East Rd, Beijing 100083, Peoples R China; [Wang, Yang; Feng, Yixi; Du, Shushan] Beijing Normal Univ, Fac Geog Sci, Beijing Key Lab Tradit Chinese Med Protect & Util, 19 Xinjiekouwai St, Beijing 100875, Peoples R China; [Jia, Liming] Beijing Forestry Univ, Natl Energy R&D Ctr Nonfood Biomass, 35,Tsinghua East Rd, Beijing 100083, Peoples R China in 2021.0, Cited 56.0. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4. Quality Control of Methyl 3-phenyl-2-propenoate

Synthetic insecticides, a traditional tool to avoid the reduction of stored-product due to insects, have emerged a serious of hazards to the environment for years, therefore, botanicals have entered people’s vision. This work aimed to present the essential oil composition of Melaleuca bracteata, and the contact as well as repellent activities against three stored-product insects, i.e. Lasioderma serricorne (Coleoptera: Ptinidae), Tribolium castaneum (Coleoptera: Tenebrionidae), and Sitophilus oryzae (Coleoptera: Curculionidae). For determining the composition, the analysis was performed by GC/FID and GC/MS. Among 11 identified compounds, the principal compounds were methyl eugenol (88.52 %) and methyl cinnamate (7.90 %). The essential oil demonstrated contact toxicity against L. serricorne, T. castaneum, and S. oryzae which LD50 values were 3.2, 22.6, and 20.4 mu g/adult, respectively. Methyl cinnamate was more effective than methyl eugenol. The repellent activity indicated that essential oil and major compositions of M. bracteata were effective against L. serricorne and T. castaneum, but no use for S. oryzae. In the contact assay, L. serricorne showed more sensitivity, however, in repellency assay, T. castaneum was susceptible. We seek to provide a new application of the popular ornamental plant, M. bracteata, and offer an alternative material to botanical insecticides development.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Zhang, JW; Wang, Y; Feng, YX; Du, SS; Jia, LM or concate me.. Quality Control of Methyl 3-phenyl-2-propenoate

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

The Shocking Revelation of Methyl 3-phenyl-2-propenoate

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Huang, Q; Zhang, FY; Liu, S; Jiang, YP; Ouyang, DS or concate me.. Safety of Methyl 3-phenyl-2-propenoate

I found the field of Research & Experimental Medicine; Pharmacology & Pharmacy very interesting. Saw the article Systematic investigation of the pharmacological mechanism for renal protection by the leaves of Eucommia ulmoides Oliver using UPLC-Q-TOF/ MS combined with network pharmacology analysis published in 2021.0. Safety of Methyl 3-phenyl-2-propenoate, Reprint Addresses Jiang, YP (corresponding author), Cent South Univ, Xiangya Hosp, Dept Pharm, Changsha 410008, Hunan, Peoples R China.; Ouyang, DS (corresponding author), Cent South Univ, Xiangya Hosp, Dept Clin Pharmacol, Changsha 410008, Hunan, Peoples R China.. The CAS is 103-26-4. Through research, I have a further understanding and discovery of Methyl 3-phenyl-2-propenoate

Bark is the traditional medicinal component of Eucommia ulmoides Oliver (E. ulmoides). However, the demand for E. ulmoides medicinal materials seriously limits their sustainability. To alleviate resource constraints, the bioactivity of E. ulmoides leaves and its pharmacodynamic basis were investigated. In the present study, extracts of E. ulmoides leaves were found to display potential renal protective properties in rat glomerular mesangial (HBZY-1) cells treated with high levels of glucose, suggesting that they possess potential factors capable of treating diabetic nephropathy. Ultra-performance liquid chromatography tandem quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) was used to comprehensively characterize the chemical components of E. ulmoides leaves. A total of 83 possible chemical components, including 12 iridoids, 13 flavonoids, 14 lignans, 20 phenylpropanoids, 14 phenolic acids, and 10 additional components, were identified in E. ulmoides leaves. Network pharmacology was used for a preliminary exploration of the potential mechanism of action of renal protection afforded by E. ulmoides leaves towards diabetic nephropathy. The network pharmacology results were verified using a series of biological experiments. The present study provided the basis for the comprehensive development and utilization of E. ulmoides leaves and the discovery of potential drugs.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Huang, Q; Zhang, FY; Liu, S; Jiang, YP; Ouyang, DS or concate me.. Safety of Methyl 3-phenyl-2-propenoate

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics