Day: October 8, 2021

Wang, DC; Xin, YY; Li, XQ; Ning, HL; Wang, YD; Yao, DD; Zheng, YP; Meng, ZY; Yang, ZY; Pan, YT; Li, PP; Wang, HN; He, ZJ; Fan, WD in [Wang, Dechao; Xin, Yangyang; Li, Xiaoqian; Wang, Yudeng; Yao, Dongdong; Zheng, Yaping; Wang, Hongni; He, Zhongjie; Fan, Wendi] Northwestern Polytech Univ, Sch Chem & Chem Engn, Xian 710129, Peoples R China; [Ning, Hailong; Meng, Zhuoyue; Yang, Zhiyuan] Xian Univ Sci & Technol, Coll Chem & Chem Engn, Xian 710021, Peoples R China; [Pan, Yuting] Northwestern Polytech Univ, Queen Mary Univ London, Engn Sch, Xian 710129, Shaanxi, Peoples R China; [Li, Peipei] Xidian Univ, Sch Adv Mat & Nanotechnol, Xian 710071, Shaanxi, Peoples R China; [Yang, Zhiyuan] Minist Nat Resources, Key Lab Coal Resources Explorat & Comprehens Util, Xian 710021, Peoples R China published Transforming Metal-Organic Frameworks into Porous Liquids via a Covalent Linkage Strategy for CO2 Capture in 2021.0, Cited 74.0. 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.

Porous liquids (PLs), an emerging kind of liquid materials with permanent porosity, have attracted increasing attention in gas capture. However, directly turning metal-organic frameworks (MOFs) into PLs via a covalent linkage surface engineering strategy has not been reported. Additionally, challenges including reducing the cost and simplifying the preparation process are daunting. Herein, we proposed a general method to transform Universitetet i Oslo (UiO)-66-OH MOFs into PLs by surface engineering with organosilane (OS) and oligomer species via covalent bonding linkage. The oligomer species endow UiO-66OH with superior fluidity at room temperature. Meanwhile, the resulting PLs showed great potential in both CO2 adsorption and CO2/N-2 selective separation. The residual porosity of PLs was verified by diverse characterizations and molecular simulations. Besides, CO2 selective capture sites were determined by grand canonical Monte Carlo (GCMC) simulation. Furthermore, the universality of the covalent linkage surface engineering strategy was confirmed using different classes of oligomer species and another MOF (ZIF-8-bearing amino groups). Notably, this strategy can be extended to construct other PLs by taking advantages of the rich library of oligomer species, thus making PLs promising candidates for further applications in energy and environment-related fields, such as gas capture, separation, and catalysis.

Category: Triazoles. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Wang, DC; Xin, YY; Li, XQ; Ning, HL; Wang, YD; Yao, DD; Zheng, YP; Meng, ZY; Yang, ZY; Pan, YT; Li, PP; Wang, HN; He, ZJ; Fan, WD or concate me.

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

Authors Chhetri, S; Ghosh, S; Samanta, P; Murmu, NC; Kuila, T in WILEY-V C H VERLAG GMBH published article about FUNCTIONALIZED GRAPHENE; CORROSION PROTECTION; GRAPHITE OXIDE; ENHANCEMENT; RESISTANCE; NANOSHEETS; INHIBITORS; ZIRCONIA; DELIVERY; CATALYST in [Chhetri, Suman; Ghosh, Souvik; Samanta, Pranab; Murmu, Naresh Chandra; Kuila, Tapas] CSIR Cent Mech Enging Res Inst, Surface Engn & Tribol Div, Durgapur 713209, India; [Chhetri, Suman; Ghosh, Souvik; Samanta, Pranab; Murmu, Naresh Chandra; Kuila, Tapas] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India in 2019.0, Cited 41.0. Computed Properties of C2H4N4. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

The present study explores the synergistic effect of Fe3O4 and heteroatom doped reduced graphene oxide (rGO) nanohybrid on anti-corrosion performance of epoxy composite coating. In this connection, Fe3O4 nanoparticles were decorated over nitrogen doped rGO (Fe3O4-NRG) and characterized by Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, X-ray diffraction (XRD), X-ray Photoelectron spectroscopy (XPS), and Thermogravimetric analysis (TGA). This approach to modulating the surface properties of graphene and hence the interaction with polymer matrix were quite distinct from traditional surface functionlization or decoration in a sense that the doped nitrogen atom facilitate the growth of Fe3O4 particles and at the same time augmented the interaction of rGO with polymer matrix. The prepared nanohybrid was dispersed in epoxy matrix through mechanical mixing and coated over mild steel surface via spin coating technique. The potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) study revealed superior anti-corrosion performance of Fe3O4-NRG/epoxy coating in 3.5 wt% NaCl solution. The corrosion inhibition was found to improve by similar to 98.5% with 0.5 wt% loading of Fe3O4-NRG. We believe that this simple solvent free approach to prepare composite coating can be exploit for practical application and thus deserves special attention..

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Chhetri, S; Ghosh, S; Samanta, P; Murmu, NC; Kuila, T or concate me.. Computed Properties of C2H4N4

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

SDS of cas: 61-82-5. Authors Xu, XQ; Wu, P; Li, CY; Zhao, KY; Wang, CR; Deng, RP; Zhang, JL in AMER CHEMICAL SOC published article about in [Xu, Xiaoqing; Zhao, Keyong; Wang, Chiran; Deng, Renpan; Zhang, Jinli] Shihezi Univ, Key Lab Green Proc Chem Engn Xinjiang Bingtuan, Sch Chem & Chem Engn, Shihezi 832003, Peoples R China; [Wu, Peng] Soochow Univ, Sch Chem & Environm Engn, Suzhou 215123, Jiangsu, Peoples R China; [Li, Changyong] Univ Bremen, Ctr Appl Space Technol & Micrograv ZARM, D-28359 Bremen, Germany in 2021.0, Cited 59.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

In this work, amine-functionalized ZIF8 (i.e., ZIF8-A) was dispersed in n-heptanol (ZIF8-A/n-heptanol) to remove SO2. The effects of ZIF8-A proportion, SO2 concentration, and absorption and desorption temperatures on the removal of SO2 were systematically investigated. The experimental results showed that the activity of ZIF8-A on SO2 removal was enhanced after being dispersed in n-heptanol. The SO2 saturation capacity increased with increasing proportion of ZIF8-A and SO(2)concentration. The optimal temperatures for SO2 absorption and desorption were found to be 25 and 120 degrees C, respectively. Under the optimal experimental conditions (25 degrees C and 4% SO2), the SO2 saturation capacity was 589 mg/g. Five continuous absorption-desorption cycles suggested a good regeneration performance. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, ultraviolet analyses, and computational simulation indicated that SO2 mainly interacted with ZIF8-A via hydrogen bonds besides physical absorption. The simulation results further indicated that the enhanced SO2 adsorption performance of ZIF8-A when dispersed in n-heptanol was due to the lower self-diffusion coefficient and higher isosteric heat of SO2 molecules in ZIF8-A/nheptanol.

SDS of cas: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Xu, XQ; Wu, P; Li, CY; Zhao, KY; Wang, CR; Deng, RP; Zhang, JL or concate me.

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

Authors Holzel, T; Ganter, C in ELSEVIER SCIENCE SA published article about N-HETEROCYCLIC CARBENE; STABLE CARBENES; COMPLEXES; LIGANDS; CATALYSTS; VERSATILE; ACCESS in [Hoelzel, Torsten; Ganter, Christian] Heinrich Heine Univ Dusseldorf, Inst Anorgan Chem & Strukturchem, Univ Str 1, D-40225 Dusseldorf, Germany in 2020.0, Cited 76.0. COA of Formula: C2H4N4. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5

Methylation of 3-amino-1,2,4-triazole and 1-methyl-3-nitro-1,2,4-triazole provides access to three NHC-precursors. For the nitro compound only a monomethylation to the triazolium salt 3(OTf) is observed. The aminotriazole could be subsequently converted to mono- and dicationic carbene precursors 1I and 2(OTf)(2), respectively. The nitro group on NHC 3 leads to a decrease of donor strength and a slightly enhanced acceptor character as compared to a related NHC lacking the nitro group. The cationic NHC 2 is the poorest donor within the series and shows a TEP value of 2072 cm(-1). The properties of this species are dominated by its cationic nature while the influence of the NMe2 group is surprisingly small. X-ray diffraction studies suggest a guanidinium-like character for the NMe2 substituted compounds. (C) 2020 Elsevier B.V. All rights reserved.

COA of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Holzel, T; Ganter, C or concate me.

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

Recently I am researching about AGENTS; SAR; AMINOAZOLES; INHIBITORS, Saw an article supported by the V. N. Karazin Kharkiv National University [811H/12-17]. Published in TAYLOR & FRANCIS INC in PHILADELPHIA ,Authors: Kolosov, MA; Shvets, EH; Manuenkov, DA; Kulyk, OG; Mazepa, AV; Orlov, VD. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. Application In Synthesis of 1H-1,2,4-Triazol-5-amine

6-Functionalized 7-R-4,7-dihydro[1,2,4]azolo[1,5-a]pyrimidines (R = H or Me) were synthesized by Biginelli-like reaction of formaldehyde or acetaldehyde, aminoazoles, and corresponding beta-dicarbonyl precursor. Alkylation of the obtained compounds proceeds smoothly at position 4, while oxidation leads to 7-R-[1,2,4]azolo[1,5-a]pyrimidines formation. 6-Ethoxycarbonyl derivatives could be reduced to the corresponding alcohols by LiAlH4 and hydrolyzed to the acids. [GRAPHICS] .

Application In Synthesis of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Kolosov, MA; Shvets, EH; Manuenkov, DA; Kulyk, OG; Mazepa, AV; Orlov, VD or concate me.

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

Safety of 1H-1,2,4-Triazol-5-amine. In 2019.0 CHEM HETEROCYCL COM+ published article about ONE-POT SYNTHESIS; BUILDING-BLOCKS; HYDRAZINE; COMPLEXES; EFFICIENT; DERIVATIVES; LIGAND; YLIDE in [Kudyakova, Yulia S.; Slepukhin, Pavel A.; Burgart, Yanina V.; Saloutin, Victor I.; Bazhin, Denis N.] Russian Acad Sci, Ural Branch, Postovsky Inst Organ Synth, 22 S Kovalevskoi,20 Akad Skaya St, Ekaterinburg 620990, Russia; [Onoprienko, Aleksandra Ya.; Slepukhin, Pavel A.; Burgart, Yanina V.; Saloutin, Victor I.; Bazhin, Denis N.] Ural Fed Univ, 19 Mira St, Ekaterinburg 620002, Russia in 2019.0, Cited 53.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Five- and six-membered fluorine-containing azaheterocycles were synthesized based on available furan-3(2H)-ones, and the influence of the nature of the fluoroalkyl substituent on the direction of the chemical transformations by the action of N,N- and N,O-binucleophiles was revealed.

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 Kudyakova, YS; Onoprienko, AY; Slepukhin, PA; Burgart, YV; Saloutin, VI; Bazhin, DN or concate me.

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

Recently I am researching about ANABOLIC-STEROIDS; DECANOATE; HEALTH, Saw an article supported by the . SDS of cas: 61-82-5. Published in ELSEVIER in AMSTERDAM ,Authors: Iqbal, U; Choudhary, MI; Yousuf, S. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Co-crystals are emerging as members of supramolecular family having particular practical and fundamental significance for chemists, crystallographers, pharmaceutical scientists, and theoreticians. The presented study is focused to synthesize anti-cancer co-crystals of commercially available nandrolone (1), a synthetic anabolic-androgenic steroidal drug. Co-crystallization is done using economical and green grinding and reflux methods to obtain nandrolone (Nan): salicylic acid (Sal) and nandrolone (Nan): 3-amino-1,2,4-triazole (Triz) co-crystals, in 2:1 and 1:1 stoichiometric ratios, respectively. The structural analysis and characterization were carried out using single-crystal X-ray diffraction, and vibrational spectroscopy. Nandrolone (1) crystallizes in monoclinic P2(1) space group, while the co-crystal-I (Nan:Sal) and co-crystal-II (Nan:Triz), co-crystallized in the orthorhombic P2(1)2(1)2(1) space group. The intermolecular hydrogen bonds O-H center dot center dot center dot O, C-H center dot center dot center dot O, N-H center dot center dot center dot O, O-H center dot center dot center dot N, and N-H center dot center dot center dot N between the active pharmaceutical ingredient (nandrolone) and co-formers (salicylic acid, and 3-amino-1,2,4-triazole) stabilize the structures of cocrystals. In vibrational spectroscopy of co-crystal-I (Nan:Sal), the blue shifts in stretching frequencies of hydroxyl group from 3417.9 cm(-1) to 3427.8 cm(-1) further supported the hydrogen bond interactions between API and co-former. Similarly, in co-crystal-II (Nan:Triz) the NH2 stretching frequency from 3331.4- 3413.4 cm(-1) to 3312.7 cm(-1), supported the interaction of NH2 with API via intermolecular interaction. Nandrolone (1) and both co-crystals were found to be non-cytotoxic against 3T3 normal fibroblast cell line. Nandrolone (IC50 = 1.0 0.1 mu M), co-crystal-I (Nan:Sal) (IC50 = 1.6 +/- 0.3 mu M) and-II (Nan:Triz) (IC50 = 1.8 +/- 0.1 mu M) showed anti-cancer potential against cervical cancer HeLa cell line. While doxorubicin (IC50 = 1.2 +/- 0.2 mu M) was used as standard tested compound. SYNOPSIS Two new non-cytotoxic co-crystals of synthetic anabolic-androgenic steroidal drug nandrolone (Nan) with pharmaceutically acceptable salicylic acid (Sal), and triazole (Triz) were synthesized and their structures were elucidated using single-crystal X-ray diffraction, and vibrational spectroscopy. Quantitative analysis of -OH and -NH2 intermolecular interactions between API and co-former by Hirshfeld surface analysis further supported the role of various functionalities towards the stability of co-crystals. Both co-crystals were found to be non-cytotoxic against 3T3 normal fibroblast cell line. Co-crystal-I (Nan:Sal) and co-crystal-II (Nan:Triz) were found to be selectively active against HeLa cancer cell line (IC50 = 1.6 +/- 0.3 mu M), (IC50 = 1.8 +/- 0.1 mu M). (c) 2020 Elsevier B.V. All rights reserved.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Iqbal, U; Choudhary, MI; Yousuf, S or concate me.. SDS of cas: 61-82-5

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

An article A multifunctional therapeutic approach: Synthesis, biological evaluation, crystal structure and molecular docking of diversified 1H-pyrazolo[3,4-b]pyridine derivatives against Alzheimer’s disease WOS:000471089700002 published article about ACETYLCHOLINESTERASE; INHIBITORS; PROTOCOL; NEURODEGENERATION; DISCOVERY; PEPTIDES; AGENTS; DRUGS; SITE in [Umar, Tarana; Hoda, Nasimul] Jamia Millia Islamia, Dept Chem, New Delhi 110025, India; [Shalini, Shruti; Gusain, Siddharth; Seth, Prerna; Tiwari, Manisha] Univ Delhi, Dr BR Ambedkar Ctr Biomed Res, New Delhi 110007, India; [Raza, Md Kausar] Indian Inst Sci, Dept Inorgan & Phys Chem, Bangalore 560012, Karnataka, India; [Kumar, Jitendra] Sardar Vallabhbhai Patel Coll, Dept Chem, Bhabua 821101, Kaimur, India; [Kumar, Jitendra] VKSU, Ara 802301, Bihar, India in 2019.0, Cited 65.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. HPLC of Formula: C2H4N4

2-(piperazin-1-yl)-N-(1H-pyrazolo[3,4-b]pyridin-3-yl)acetamides are described as a new class of selective and potent acetylcholinesterase (AChE) inhibitors and amyloid beta aggregation inhibitors. Formation of synthesized compounds (P1-P9) was justified via H-1 NMR, C-13 NMR, mass spectra and single crystal X-Ray diffraction study. All compounds were evaluated for their acetylcholinesterase and butyrylcholinesterase inhibitory activity, inhibition of self-mediated A beta aggregation and Cu(II)-mediated A beta aggregation. Also, docking study carried out was in concordance with in vitro results. The most potent molecule amongst the derivatives exhibited excellent anti-AChE activity (IC50=4.8 nM). Kinetic study of P3 suggested it to be a mixed type inhibitor. In vitro study revealed that all the compounds are capable of inhibiting self-induced beta-amyloid (A beta) aggregation with the highest inhibition percentage to be 81.65%. Potency of P1 and P3 to inhibit self-induced A beta(1-)(42) aggregation was ascertained by TEM analysis. Compounds were also evaluated for their A beta disaggregation, antioxidation, metal-chelation activity. (C) 2019 Elsevier Masson SAS. All rights reserved.

HPLC of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Umar, T; Shalini, S; Raza, MK; Gusain, S; Kumar, J; Seth, P; Tiwari, M; Hoda, N or concate me.

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

Recently I am researching about MECHANICAL-PROPERTIES; COMPOSITE RESIN; THERMAL-DEGRADATION; FILLER MORPHOLOGY; FLEXURAL STRENGTH; WEAR; PARTICLES; MEMBRANES; FRACTION; BEHAVIOR, Saw an article supported by the . Safety of 1H-1,2,4-Triazol-5-amine. Published in SAGE PUBLICATIONS LTD in LONDON ,Authors: Yushau, US; Almofeez, L; Bozkurt, A. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

This article is focused on the preparation and characterization of functional nanosilica incorporated dental resins with better mechanical, cytotoxicity, sorption, and solubility properties. Silica nanoparticles were synthesized via Stober method and were functionalized with 3-amino-1,2,4-triazole. Dental nanocomposites were produced by embedding the functionalized nanosilica into bisphenol-A-glycidyl methacrylate/triethylene glycol dimethacrylate matrix to form B1-B6 series. This was achieved by mechanical mixing of the monomer (50:50 wt%), filler (10-60 wt%), initiator combination (CQ/EDMAB:O. 1 :0.4 wt%) and then followed by LED light curing (wavelength: 450-500 nm, power density:1000 mW cm(-2)) for 60 s. Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis techniques were used for characterization of the materials. Cytotoxicity tests were performed to evaluate cell viability and mechanical tests were done to check mechanical strength and stability of the materials. The mean sorption and solubility values of the materials were measured by making a series of experiments on different composite formulations.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Yushau, US; Almofeez, L; Bozkurt, A or concate me.. Safety of 1H-1,2,4-Triazol-5-amine

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

An article HbWRKY27, a group IIe WRKY transcription factor, positively regulates HbFPS1 expression in Hevea brasiliensis WOS:000596327900012 published article about FARNESYL DIPHOSPHATE SYNTHASE; ZINC-FINGER PROTEIN; ISOPRENOID BIOSYNTHESIS; MOLECULAR CHARACTERIZATION; MEVALONATE PATHWAY; IN-VITRO; GENE; CLONING; PLANT; EVOLUTION in [Qu, Long; Yin, Li-Yan] Hainan Univ, Sch Life & Pharmaceut Sci, Haikou 570228, Hainan, Peoples R China; [Qu, Long; Li, Hui-Liang; Guo, Dong; Wang, Ying; Zhu, Jia-Hong; Peng, Shi-Qing] Chinese Acad Trop Agr Sci, Inst Trop Biosci & Biotechnol, Minist Agr, Key Lab Biol & Genet Resources Trop Crops, 4 Xueyuan Rd, Haikou 571101, Hainan, Peoples R China in 2020.0, Cited 46.0. 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

Farnesyl pyrophosphate synthase (FPS) is a key enzyme that catalyzes the formation of farnesyl pyrophosphate, the main initiator for rubber chain initiation in Hevea brasiliensis Muell. Arg. The transcriptional regulatory mechanisms of the FPS gene still not well understood. Here, a WRKY transcription factor designated HbWRKY27 was obtained by screening the latex cDNA library applied the HbFPS1 promoter as bait. HbWRKY27 interacted with the HbFPS1 promoter was further identified by individual Y1H and EMSA assays. HbWRKY27 belongs to group IIe WRKY subfamily which contains a typical WRKY domain and C-X5-CX23-HXH motif. HbWRKY27 was localized to the nucleus. HbWRKY27 predominantly accumulated in latex. HbWRKY27 was up-regulated in latex by ethrel, salicylic acid, abscisic acid, and methyl jasmonate treatment. Transient expression of HbWRKY27 led to increasing the activity of the HbFPS1 promoter in tobacco plant, suggesting that HbWRKY27 positively regulates the HbFPS1 expression. Taken together, an upstream transcription factor of the key natural rubber biosynthesis gene HbFPS1 was identified and this study will provide novel transcriptional regulatory mechanisms of the FPS gene in Hevea brasiliensis.

Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Qu, L; Li, HL; Guo, D; Wang, Y; Zhu, JH; Yin, LY; Peng, SQ or concate me.

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