Triazoles -| Page 288 of 762

Extended knowledge of C2H4N4

Category: Triazoles. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Ye, YJ; Nikovics, K; To, A; Lepiniec, L; Fedosejevs, ET; Van Doren, SR; Baud, S; Thelen, JJ or concate me.

Authors Ye, YJ; Nikovics, K; To, A; Lepiniec, L; Fedosejevs, ET; Van Doren, SR; Baud, S; Thelen, JJ in NATURE RESEARCH published article about CARRIER PROTEIN; ARABIDOPSIS; SPINACH; LIGHT; BIOSYNTHESIS; WRINKLED1; COENZYME; PHOSPHORYLATION; ACCUMULATION; GENES in [Ye, Yajin; Fedosejevs, Eric T.; Van Doren, Steven R.; Thelen, Jay J.] Univ Missouri, Christopher S Bond Life Sci Ctr, Dept Biochem, 1201 E Rollins, Columbia, MO 65211 USA; [Nikovics, Krisztina; To, Alexandra; Lepiniec, Loic; Baud, Sebastien] Univ Paris Saclay, AgroParisTech, Inst Jean Pierre Bourgin, INRAE,CNRS, F-78000 Versailles, France in 2020.0, Cited 60.0. Category: Triazoles. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

In plants, light-dependent activation of de novo fatty acid synthesis (FAS) is partially mediated by acetyl-CoA carboxylase (ACCase), the first committed step for this pathway. However, it is not fully understood how plants control light-dependent FAS regulation to meet the cellular demand for acyl chains. We report here the identification of a gene family encoding for three small plastidial proteins of the envelope membrane that interact with the alpha-carboxyltransferase (alpha-CT) subunit of ACCase and participate in an original mechanism restraining FAS in the light. Light enhances the interaction between carboxyltransferase interactors (CTIs) and alpha-CT, which in turn attenuates carbon flux into FAS. Knockouts for CTI exhibit higher rates of FAS and marked increase in absolute triacylglycerol levels in leaves, more than 4-fold higher than in wild-type plants. Furthermore, WRINKLED1, a master transcriptional regulator of FAS, positively regulates CTI1 expression by direct binding to its promoter. This study reveals that in addition to light-dependent activation, envelope docking of ACCase permits fine-tuning of fatty acid supply during the plant life cycle.

Reference:
Article; Safari, Niloufar; Shirini, Farhad; Tajik, Hassan; Journal of Molecular Structure; vol. 1201; (2020);,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics

The Absolute Best Science Experiment for 61-82-5

Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Roner, MR; Carraher, CE; Miller, L; Mosca, F; Slawek, P; Haky, JE; Frank, J or concate me.

Safety of 1H-1,2,4-Triazol-5-amine. In 2020.0 J INORG ORGANOMET P published article about STRUCTURAL-CHARACTERIZATION; ANTICANCER; POLYESTERS; DIHALIDES; ABILITY; ABC/3TC in [Roner, Michael R.; Miller, Lindsey] Univ Texas Arlington, Dept Biol, Arlington, TX 76010 USA; [Carraher, Charles E., Jr.; Mosca, Francisca; Slawek, Paul; Haky, Jerome E.; Frank, Jessica] Florida Atlantic Univ, Dept Chem & Biochem, Boca Raton, FL 33431 USA in 2020.0, Cited 30.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

The ability to inhibit two important viruses is described. Two groups of polymers exhibited ability to totally inhibit the Zika virus. These polymers are derived from organotin dihalides and camphoric acid and lamivudine. This is the initial report of complete inhibition of the Zika virus by simple drugs. The ability to inhibit vaccinia virus is also reported. The inhibition of the vaccinia virus is shown by a number of organotin drugs including those also derived from lamivudine and camphoric acid and additional drugs derived from 3-amino-1,2,4-triazole, dicumarol, 4,6-diaminopyridine, alpha-cyano-4-hydroxcinnamic acid, and a variety of organotin polyethers including water soluble polymers derived from poly(ethylene glycol). All the drugs described in these studies are rapidly (< 30 s) synthesized using commercially available reactants at room temperature employing the interfacial reaction system that is employed industrially so that scale up to kilograms is relatively straight forward. Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Roner, MR; Carraher, CE; Miller, L; Mosca, F; Slawek, P; Haky, JE; Frank, J or concate me.

Top Picks: new discover of 61-82-5

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhao, Q; Hu, RS; Liu, D; Liu, X; Wang, J; Xiang, XH; Li, YY or concate me.. Safety of 1H-1,2,4-Triazol-5-amine

Authors Zhao, Q; Hu, RS; Liu, D; Liu, X; Wang, J; Xiang, XH; Li, YY in WILEY published article about GENE-EXPRESSION; STRESS-RESPONSE; ARABIDOPSIS; CATALASE; TOLERANCE; BINDING; PLANTS; FAMILY; HOMEOSTASIS; CAT2 in [Zhao, Qiang; Liu, Xin] Qingdao Agr Univ, Coll Hort, Qingdao, Peoples R China; [Hu, Ri-Sheng; Li, Yang-Yang] Hunan Tobacco Res Inst, Changsha, Hunan, Peoples R China; [Liu, Dan] Chinese Acad Agr Sci, Tobacco Res Inst, Qingdao, Shandong, Peoples R China; [Xiang, Xiao-Hua] Haikou Cigar Res Inst, Haikou, Hainan, Peoples R China in 2020.0, Cited 66.0. Safety of 1H-1,2,4-Triazol-5-amine. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Drought stress often limits plant growth and global crop yields. Catalase (CAT)-mediated hydrogen peroxide (H2O2) scavenging plays an important role in the adaptation of plant stress responses, but the transcriptional regulation of the CAT gene in response to drought stress is not well understood. Here, we isolated an APETALA2/ETHYLENE-RESPONSIVE FACTOR (AP2/ERF) domain-containing transcription factor (TF), NtERF172, which was strongly induced by drought, abscisic acid (ABA) and H2O2, from tobacco (Nicotiana tabacum) by yeast one-hybrid screening. NtERF172 localized to the nucleus and acted as a transcriptional activator. Chromatin immunoprecipitation, yeast one-hybrid assays, electrophoretic mobility shift assays and transient expression analysis assays showed that NtERF172 directly bound to the promoter region of the NtCAT gene and positively regulated its expression. Transgenic plants overexpressing NtERF172 displayed enhanced tolerance to drought stress, whereas suppression of NtERF172 decreased drought tolerance. Under drought stress conditions, the NtERF172-overexpressed lines showed higher catalase activity and lower accumulation of H2O2 compared with wild-type (WT) plants, while the NtERF172-silenced plants showed the inverse correlation. Exogenous application of amino-1,2,4-triazole (3-AT), an irreversible CAT inhibitor, to the NtERF172-overexpression lines showed decreased catalase activity and drought tolerance, and increased levels of cellular H2O2. Knockdown of NtCAT in the NtERF172-overexpression lines displayed a more drought stress-sensitive phenotype than NtERF172-overexpression lines. We propose that NtERF172 acts as a positive factor in drought stress tolerance, at least in part through the regulation of CAT-mediated H2O2 homeostasis.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhao, Q; Hu, RS; Liu, D; Liu, X; Wang, J; Xiang, XH; Li, YY or concate me.. Safety of 1H-1,2,4-Triazol-5-amine

Extended knowledge of C2H4N4

Recommanded Product: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Althagafi, I; El-Metwaly, N; Farghaly, TA or concate me.

An article New Series of Thiazole Derivatives: Synthesis, Structural Elucidation, Antimicrobial Activity, Molecular Modeling and MOE Docking WOS:000469518100100 published article about BIOLOGICAL EVALUATION; BIS-THIAZOLES; ANTI-HCV; INHIBITORS; DESIGN; IDENTIFICATION; POTENT; AGENTS; THIADIAZOLES; COMPLEXES in [Althagafi, Ismail; El-Metwaly, Nashwa; Farghaly, Thoraya A.] Umm Al Qura Univ, Fac Sci Appl, Dept Chem, Mecca 21514, Saudi Arabia; [El-Metwaly, Nashwa] Mansoura Univ, Dept Chem, Fac Sci, Mansoura 002050, Egypt; [Farghaly, Thoraya A.] Cairo Univ, Dept Chem, Fac Sci, Giza 12613, Egypt in 2019.0, Cited 41.0. Recommanded Product: 61-82-5. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Based on the extensive biological activities of thiazole derivatives against different types of diseases, we are interested in the effective part of many natural compounds, so we synthesized a new series of compounds containing di-, tri- and tetrathiazole moieties. The formation of such derivatives proceeded via reaction of 2-bromo-1-(4-methyl-2-(methylamino)thiazol-5-yl)ethan-1-one with heterocyclic amines, o-aminothiophenol and thiosemicarbazone derivatives. The structure and mechanistic pathways for all products were discussed and proved based on spectral results, in addition to conformational studies. Our aim after the synthesis is to investigate their antimicrobial activity against various types of bacteria and fungi species. Preceeding such an investigation, a molecular docking study was carried out with selected conformers, as representative examples, against three pathogen-proteins. This preliminary stage could support the biological application. The potency of these compounds as antimicrobial agents has been evaluated. The results showed that derivatives which have di- and trithiazole rings displayed high activity that exceeds the used standard antibiotic.

Recommanded Product: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Althagafi, I; El-Metwaly, N; Farghaly, TA or concate me.

Awesome and Easy Science Experiments about 1H-1,2,4-Triazol-5-amine

Recommanded Product: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Drokin, RA; Tiufiakov, DV; Voinkov, EK; Slepukhin, PA; Ulomsky, EN; Esaulkova, YL; Volobueva, AS; Lantseva, KS; Misyurina, MA; Zarubaev, VV; Rusinov, VL or concate me.

An article Methods of Synthesis and Antiviral Activity of New 4-Alkyl-3-Nitro-1,4-Dihydroazolo[5,1-c][1,2,4]Triazin-4-ols WOS:000649250900005 published article about ETIOTROPIC THERAPY; INFLUENZA; PRECURSOR; ARVI in [Drokin, Roman A.; Tiufiakov, Dmitrii V.; Voinkov, Egor K.; Ulomsky, Evgeny N.; Rusinov, Vladimir L.] Ural Fed Univ, 19 Mira St, Ekaterinburg 620002, Russia; [Slepukhin, Pavel A.; Ulomsky, Evgeny N.; Rusinov, Vladimir L.] Russian Acad Sci, Postovsky Inst Organ Synth, Ural Branch, 22-20 Sofyi Kovalevskoi St, Ekaterinburg 620108, Russia; [Esaulkova, Yana L.; Volobueva, Alexandrina S.; Misyurina, Mariya A.; Zarubaev, Vladimir V.] St Petersburg Pasteur Res Inst Epidemiol & Microb, 14 Mira St, St Petersburg 197101, Russia; [Lantseva, Kristina S.] St Petersburg State Univ, 7-9 Univ Embankment, St Petersburg 199034, Russia in 2021.0, Cited 26.0. Recommanded Product: 61-82-5. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

An azo coupling reaction of alpha-nitro ketones with 5-diazoazoles was used to obtain 4-alkyl-3-nitro-1,4-dihydroazolo[5,1-c][1,2,4]triazines, which were characterized with respect to their antiviral activity against influenza and Coxsackie B3 viruses.

Let`s talk about compound :1H-1,2,4-Triazol-5-amine

Computed Properties of C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Fares, IMZ; Mekky, AEM; Elwahy, AHM; Abdelhamid, IA or concate me.

Computed Properties of C2H4N4. Recently I am researching about LIGHT-EMITTING-DIODES; CELL-CYCLE ARREST; QUINAZOLINE DERIVATIVES; STEREOSELECTIVE-SYNTHESIS; BIOLOGICAL EVALUATION; ONE-POT; DESIGN; DOCKING; HETEROCYCLES; INHIBITORS, Saw an article supported by the . Published in TAYLOR & FRANCIS INC in PHILADELPHIA ,Authors: Fares, IMZ; Mekky, AEM; Elwahy, AHM; Abdelhamid, IA. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

A novel series of bis(tetrahydro[1,2,4]triazolo[5,1-b]quinazolin-8-ones) and bis(tetrahydrobenzo[4,5]imidazo[2,1-b]quinazolinones) containing amide linkages were regionselectively prepared via a three-component reaction of bis(aldehydes) with dimedone and 3-amino-1,2,4-triazole (or 2-aminobenzimidazole) under conventional heating as well as under microwave irradiation.

Computed Properties of C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Fares, IMZ; Mekky, AEM; Elwahy, AHM; Abdelhamid, IA or concate me.

Search for chemical structures by a sketch :1H-1,2,4-Triazol-5-amine

Safety of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Suzuki, S; Hasegawa, A; Uebori, M; Shinomiya, M; Yoshida, Y; Ookubo, K; Takino, M; Hasegawa, H; Takazawa, M; Takemine, S or concate me.

Safety of 1H-1,2,4-Triazol-5-amine. Authors Suzuki, S; Hasegawa, A; Uebori, M; Shinomiya, M; Yoshida, Y; Ookubo, K; Takino, M; Hasegawa, H; Takazawa, M; Takemine, S in WILEY published article about in [Suzuki, Shigeru; Uebori, Michiko; Takazawa, Mari] Chubu Univ, Grad Sch Biosci & Biotechnol, 1200 Matsumoto, Kasugai, Aichi 4878501, Japan; [Hasegawa, Atsuko] Kanagawa Environm Res Ctr, Environm Conservat Div, 1-3-39,Shinomiya, Hiratsuka, Kanagawa 2540014, Japan; [Shinomiya, Miho] Saitama Prefectural Univ, Sch Hlth & Social Serv, 820 Sannomiya, Koshigaya 3438540, Japan; [Yoshida, Yasuko] Sumica Chem Anal Serv Ltd, Environm Hlth & Safety Div, Bunkyo Ku, Sumitomo Fudosan Hongo Bldg 9F,22-5,Hongo 3 Chome, Tokyo 1130033, Japan; [Ookubo, Kaori] Saga Prefectural Inst Publ Hlth & Pharmaceut Res, Phys & Chem Res & Investigate Div, 1-20 Hacchonawatemachi, Saga 8490925, Japan; [Takino, Masahiko] Agilent Technol Japan Ltd, Chromatog & Mass Spectrometry Div, 9-1 Takakura Machi, Hachioji, Tokyo 1920033, Japan; [Hasegawa, Hitomi] Nagoya City Environm Sci Res Inst, Water Qual Div, Minami Ku, 5-16-8 Toyoda, Nagoya, Aichi 4570841, Japan; [Takazawa, Mari] Publ Works Res Inst, Water Environm Res Grp, 1-6 Minamihara, Tsukuba, Ibaraki, Japan; [Takemine, Shusuke] Ctr Environm Sci Saitama, Chem Subst Team, 914 Oaza Kamitanadare,Kisai Machi, Kazo, Saitama 3470115, Japan in 2021.0, Cited 41.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Despite the increasing detection of emerging substances in the environment, the identity of most are left unknown due to the lack of efficient identification methods. We developed a non-target analysis method for identifying unknown substances in the environment by liquid chromatography/high-resolution mass spectrometry (LC/HRMS) with a product ion and neutral loss database (PNDB). The present analysis describes an elucidation method with elemental compositions of the molecules, product ions, and corresponding neutral losses of the unknown substance: (1) with the molecular formula, possible molecular structures are retrieved from two chemical structure databases (PubChem and ChemSpider); then (2) with the elemental compositions of product ions and neutral losses, possible partial structures are retrieved from the PNDB; and finally, (3) molecular structures that match the possible partial structures are listed in order of number of hits. A molecular structure with a higher number of hits is more similar to the structure of the analyzed substance. The performance of the non-target method was evaluated by simulated analysis of 150 LC/HRMS spectra registered in MassBank. First, all substances of the same mass data (41/41) and 68% (39/57) of the mass data of the same substances not registered in the PNDB were elucidated. It was demonstrated that 14% (7/52) and 31% (16/52) of the substances with no mass spectral data registered in the PNDB were obtained at the first and within the fifth place, respectively. Owing to the fact that 10 of the total hits occurred in product ions and neutral losses, almost 50% of the substances evaluated with this method were placed at the top 4 positions in the similarity ranking. Importantly, the proposed method is effective for analyzing mass spectral data that has not been registered in the PNDB and thus is expected to be used for a variety of non-target analyses.

Downstream Synthetic Route Of 61-82-5

Recommanded Product: 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Liu, J; Wei, YH; Bao, FL; Li, GX; Liu, HY; Wang, HY or concate me.

Recently I am researching about COORDINATION POLYMERS; CRYSTAL-STRUCTURES; UNITS; SEPARATION; CH4; CO2; PERFORMANCE; STABILITY; TOPOLOGY; LIGANDS, Saw an article supported by the Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX18_2109]; Natural Science Foundation of Jiangsu Normal University, China [17XLR044]. Published in PERGAMON-ELSEVIER SCIENCE LTD in OXFORD ,Authors: Liu, J; Wei, YH; Bao, FL; Li, GX; Liu, HY; Wang, HY. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. Recommanded Product: 1H-1,2,4-Triazol-5-amine

Two metal-organic frameworks, [Zn-2(atrz)(2)(bpdc)]center dot 0.5H(2)O (1) and [Zn-2(mtrz)(2)(azdc)]center dot DMA center dot CH3OH center dot H2O (2), with 3-substitued 1,2,4-triazole (Hatrz = 3-amino-1,2,4-triazole, Hmtrz = 3-methyl-1,2,4-triazole) have been constructed. Both MOFs possess 3D self-penetrated frameworks featuring Zn-triazolate layers pillared by dicarboxylate ligands (H(2)bdc = 1,4-benzenedicarboxylate, H(2)azdc = azobenzene-4,4′-dicarboxylate). In particular, 2 exhibits a rare rob network with the dimeric Zn-triazolate as the 6-connected nodes, which resulted from the synergistic effects of both 3-substitued group of triazolate and size-alterable dicarboxylate pillar on the final frameworks. Detailed structural analysis of 1 and 2 and its comparison with commonly observed pcu net in pillared-layer structure has been presented. Pore-size tuning and functionalities have also been achieved related to diverse molecular length of pillars. 2 with long pillar displays suitable pore size, and consequently, demonstrates selective CO2 uptake and efficient dyes adsorption in aqueous solution based on size-exclusion effect. (C) 2019 Elsevier Ltd. All rights reserved.

Recommanded Product: 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Liu, J; Wei, YH; Bao, FL; Li, GX; Liu, HY; Wang, HY or concate me.

Brief introduction of C2H4N4

SDS of cas: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Goncharova, OA; Kuznetsov, DS; Andreev, NN; Kuznetsov, YI; Andreeva, NP or concate me.

Goncharova, OA; Kuznetsov, DS; Andreev, NN; Kuznetsov, YI; Andreeva, NP in [Goncharova, O. A.; Kuznetsov, D. S.; Andreev, N. N.; Kuznetsov, Yu, I; Andreeva, N. P.] Russian Acad Sci, Frumkin Inst Phys Chem & Electrochem, Moscow 119071, Russia published Chamber Inhibitors of Corrosion of AMg6 Aluminum Alloy in 2020.0, Cited 17.0. SDS of cas: 61-82-5. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Using a set of physicochemical (ellipsometry and contact angle measurements), electrochemical (potentiometric anode polarization and electrochemical impedance spectroscopy), and corrosion (periodic moisture condensation test) methods, the properties of adsorption films formed on the AMg6 aluminum alloy surface by the chamber method in vapors of some amines of heterocyclic compounds, carboxylic acids, and their salts are studied. It is established that the use of the studied compounds in the chamber processing of the alloy increases-though not effectively enough-its corrosion resistance in a humid atmosphere. The most promising inhibitors are carboxylic acids themselves; the optimum temperature for surface treatment with them is 140 degrees C. One-hour treatment of steel with pairs of oleic, neodecanoic acid, and carboxylic acid A at this temperature gives rise to the formation of nanoscale adsorption films on the AMg6 alloy, which slightly hydrophilize the surface, but possess a protective aftereffect. Apparently, further improvement of chamber protection methods of the AMg6 alloy should consist in the selection of synergists for chamber corrosion inhibitors of the carboxylate type.

SDS of cas: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Goncharova, OA; Kuznetsov, DS; Andreev, NN; Kuznetsov, YI; Andreeva, NP or concate me.

You Should Know Something about C2H4N4

Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhang, PD; Wu, XQ; He, T; Xie, LH; Chen, Q; Li, JR or concate me.

In 2020.0 CHEM COMMUN published article about PROPANE in [Li, Jian-Rong] Beijing Univ Technol, Beijing Key Lab Green Catalysis & Separat, Coll Environm & Energy Engn, Beijing 100124, Peoples R China; Beijing Univ Technol, Dept Chem & Chem Engn, Coll Environm & Energy Engn, Beijing 100124, Peoples R China in 2020.0, Cited 31.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. Formula: C2H4N4

The selective adsorption/separation of C-2 hydrocarbons has been realized in a flexible-robust MOF, Zn-2(Atz)(2)Ox. Owing to the distinctive guest-dependent multistep adsorption behaviors and suitable guest-framework interactions, this MOF shows outstanding separation performance for C2H2/C2H4 mixtures in a wide range of temperature confirmed by a column breakthrough experiment.

Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhang, PD; Wu, XQ; He, T; Xie, LH; Chen, Q; Li, JR or concate me.