Triazoles

COA of Formula: C2H4N4. Zhang, HD; Lai, HS; Wu, XR; Li, GK; Hu, YF in [Zhang, Huadong; Lai, Huasheng; Wu, Xiangrong; Li, Gongke; Hu, Yufei] Sun Yat Sen Univ, Sch Chem, Guangzhou 510275, Peoples R China published CoFe2O4@HNTs/AuNPs Substrate for Rapid Magnetic Solid-Phase Extraction and Efficient SERS Detection of Complex Samples All-in-One in 2020.0, Cited 60.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Fast and accurate practical sample detection is a great challenge in on-site detection. Herein, we developed a CoFe2O4@HNTs/ AuNPs substrate for rapid and efficient magnetic solid-phase extraction (MSPE) surface-enhanced Raman scattering (SERS) detection of aromatic amines and nitrofuran in real samples all-in-one. Magnetic CoFe2O4 beads filled inside halloysite nanotubes (HNTs) can avoid aggregation of particles, endow the substrate with the rapid magnetic separation ability to simplify the pretreatment procedure, and reduce complex matrix interference. Meanwhile, outer surface AuNPs can generate electromagnetic enhancement and hot spots to amplify Raman signals of target molecules enriched/concentrated by HNTs. The CoFe2O4@HNTs/AuNPs substrate exhibited excellent SERS activity (high sensitivity, good reproducibility, and repeatability), pH stability (3.0-11.0), and good MSPE ability (fast magnetic enrichment/separation ability within 5 min). The CoFe2O4@HNTs/AuNPs MSPE SERS substrate can be applied for the determination of 4,4′-thioaniline and nitrofurantoin with a linear range of 0.054-21.7 mg/L and 0.05-1.0 mg/L, and the limits of detection were down to 0.026 mg/L and 0.014 mg/L, respectively. Furthermore, the enhancement factor (EF) of the substrate to 4,4′-thioaniline is up to 2.7 x 10(7). Besides, the substrate can realize practical SERS determination of trace 4,4-thioaniline in cosmetics and nitrofurantoin in fish feed and aquatic samples. The recoveries were varied from 71.6% to 103.6% for 4,4-thioaniline in hair dyes and 81.9% to 116.3% for nitrofurantoin in fish feed and aquatic samples, respectively. Such a robust and efficient MSPE SERS substrate possesses great potential in rapid detection (within 15 min) for a practical sample, and it also provides a methodology for the preparation of other HNTs-based composites.

COA of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhang, HD; Lai, HS; Wu, XR; Li, GK; Hu, YF 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

Quality Control of 1H-1,2,4-Triazol-5-amine. In 2020.0 CHEMISTRYSELECT published article about CARBOXYLIC-ACID DERIVATIVES; ANTITUMOR AGENTS; ANTIOXIDANT; INHIBITORS; DESIGN; POTENT in [Sompalle, Rajesh; Roopan, Selvaraj Mohana; Priya, Duraipandi Devi; Arunachalapandi, Murugan] Vellore Inst Technol, Sch Adv Sci, Dept Chem, Chem Heterocycles & Nat Prod Res Lab, Vellore 632014, Tamil Nadu, India; [Sompalle, Rajesh] Besant Theosoph Coll, Dept Chem, Chittoor 517325, Andhra Pradesh, India; [Suthindhiran, Krishnamurthy; Sarkar, Gargi] Vellore Inst Technol, Sch Biosci & Technol, Marine Biotechnol & Bioprod Lab, Vellore 632014, Tamil Nadu, India; [Ranjith, Malavika] Vellore Inst Technol, Sch Chem Engn, Vellore 632014, Tamil Nadu, India in 2020.0, Cited 45.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

Microwave synthetic methodologies were proposed for the preparation of positional isomeric dihydro-triazolo-pyrimido-acridines, 3a-j and 9a-h via friedlander synthesis using response surface methodology (RSM). The advantages of these methodologies over conventional methods are it provides good yields with short reaction times. Free radical scavenging and antifungal studies were performed for compounds 3a-j and 9a-h. The results of antioxidant assay revealed that compounds 3c, 3d and 9b exhibited excellent property whereas compounds 3a and 9a showed significant antifungal property against Aspergillus flavus (A.flavus) and Aspergillus niger (A. niger).

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Sompalle, R; Roopan, SM; Priya, DD; Suthindhiran, K; Sarkar, G; Ranjith, M; Arunachalapandi, M or concate me.. Quality Control 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

Authors Cardona, B; Rudel, RA in ELSEVIER IRELAND LTD published article about PRENATAL EXPOSURE; CANCER; CHEMICALS; ESTROGEN; ATRAZINE; RODENT; EPIDEMIOLOGY; ORGANIZATION; MALATHION; TOXICITY in [Cardona, Bethsaida; Rudel, Ruthann A.] Silent Spring Inst, Newton, MA 02460 USA in 2020.0, Cited 86.0. Recommanded Product: 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

Breast cancer risk from pesticides may be missed if effects on mammary gland are not assessed in toxicology studies required for registration. Using US EPA’s registration documents, we identified pesticides that cause mammary tumors or alter development, and evaluated how those findings were considered in risk assessment. Of 28 pesticides that produced mammary tumors, EPA’s risk assessment acknowledges those tumors for nine and dismisses the remaining cases. For five pesticides that alter mammary gland development, the implications for lactation and cancer risk are not assessed. Many of the mammary-active pesticides activate pathways related to endocrine disruption: altering steroid synthesis in H295R cells, activating nuclear receptors, or affecting xenobiotic metabolizing enzymes. Clearer guidelines based on breast cancer biology would strengthen assessment of mammary gland effects, including sensitive histology and hormone measures. Potential cancer risks from several common pesticides should be re-evaluated, including: malathion, triclopyr, atrazine, propylene oxide, and 3-iodo-2-propynyl butylcarbamate (IPBC).

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Cardona, B; Rudel, RA or concate me.. Recommanded Product: 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

Recently I am researching about METAL-ORGANIC FRAMEWORKS; HIGHLY EFFICIENT; CAPTURE; REMOVAL; MOFS; SORBENTS; HYDROGEN; ZR, Saw an article supported by the R&D Convergence Program of Ministry of Science, ICT and Future Planning, National Research Council of Science Technology [CRC-14-1-KRICT]; Korea Institute of Science and Technology (KIST)Korea Institute of Science & Technology (KIST) [2E28020]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Lee, YR; Do, XH; Cho, KY; Jeong, K; Baek, KY. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine. Category: Triazoles

The efficient removal of radioactive iodine (I-2) has drawn worldwide attention because of the severe effects of radiotoxicity on the environment and human health. As a result, efficient porous materials for the capture and safe storage of radioactive iodine are required. In this work, nanoscale zeolitic imidazolate framework-8 (ZIF-8) and its amino-functionalized ZIF-8 derivatives with 3-amino-1,2,4-triazole (Atz), denoted as ZIF8-A, were prepared via postsynthetic modification, and their performance for I-2 removal from n-hexane was investigated. The abundant amine functionalities in the ZIF8-A structure including the primary and secondary amine groups (-NH2 and -NH) and triazole-ring (-C=N-NH-) not only serve as effective adsorption sites but also form strong interactions with I-2 via electron transfer from the nitrogen atom of the ligand to I-2. The adsorption isotherms and the kinetics were well fitted by the Langmuir model and the pseudo-second-order kinetic model, respectively, suggesting a monolayer chemisorption process. ZIF8-A61 achieved an adsorption capacity of more than 870% compared to the pristine ZIF-8. Based on the experimental and computational results, a plausible mechanism for the adsorption of I-2 on ZIF8-A nanocrystals is proposed by considering the host-guest interactions, specifically, those between the amine functional groups and I-2. In addition, the reusability and structural stability of the adsorbents were investigated.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Lee, YR; Do, XH; Cho, KY; Jeong, K; Baek, KY or concate me.. Category: Triazoles

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

I found the field of Science & Technology – Other Topics very interesting. Saw the article Toxicological response of the model fungus Saccharomyces cerevisiae to different concentrations of commercial graphene nanoplatelets published in 2020.0. Quality Control of 1H-1,2,4-Triazol-5-amine, Reprint Addresses Tamayo-Ramos, JA (corresponding author), Univ Burgos, Int Res Ctr Crit Raw Mat ICCRAM, Plaza Misael Banuelos S-N, Burgos 09001, Spain.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

Graphene nanomaterials have attracted a great interest during the last years for different applications, but their possible impact on different biological systems remains unclear. Here, an assessment to understand the toxicity of commercial polycarboxylate functionalized graphene nanoplatelets (GN) on the unicellular fungal model Saccharomyces cerevisiae was performed. While cell proliferation was not negatively affected even in the presence of 800 mg L-1 of the nanomaterial for 24 hours, oxidative stress was induced at a lower concentration (160 mg L-1), after short exposure periods (2 and 4 hours). No DNA damage was observed under a comet assay analysis under the studied conditions. In addition, to pinpoint the molecular mechanisms behind the early oxidative damage induced by GN and to identify possible toxicity pathways, the transcriptome of S. cerevisiae exposed to 160 and 800 mg L-1 of GN was studied. Both GN concentrations induced expression changes in a common group of genes (337), many of them related to the fungal response to reduce the nanoparticles toxicity and to maintain cell homeostasis. Also, a high number of genes were only differentially expressed in the GN800 condition (3254), indicating that high GN concentrations can induce severe changes in the physiological state of the yeast.

Quality Control of 1H-1,2,4-Triazol-5-amine. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Suarez-Diez, M; Porras, S; Laguna-Teno, F; Schaap, PJ; Tamayo-Ramos, JA 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

An article Synthesis of C-beta-D-glucopyranosyl derivatives of some fused azoles for the inhibition of glycogen phosphorylase WOS:000455623300004 published article about GLUCOSE ANALOG INHIBITORS; BINDING; NUCLEOSIDES; IMIDAZOLES; REVEAL; MUSCLE in [Szennyes, Eszter; Bokor, Eva; Somsak, Laszlo] Univ Debrecen, Dept Organ Chem, POB 400, H-4002 Debrecen, Hungary; [Docsa, Tibor; Sipos, Adam] Univ Debrecen, Fac Med, Dept Med Chem, Egyet Ter 1, H-4032 Debrecen, Hungary in 2019.0, Cited 37.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. SDS of cas: 61-82-5

Annulated C-beta-D-glucopyranosyl heterocycles were synthesized and tested as inhibitors of glycogen phosphorylase. 2-(beta-D-Glucopyranosyl)-1H-imidazo[4,5-b] pyridine was formed by ring-closure of O-perbenzoylated C-beta-D-glucopyranosyl formic acid with 2,3-diaminopyridine in the presence of triphenylphosphite. Cyclisations of bromomethyl 2,3,4,6-tetra-O-benzoyl-beta-D-glucopyranosyl ketone with a set of 2-aminoheterocycles resulted in constitutionally reversed C-beta-D-glucopyranosyl imidazoles fused by pyridine, pyrimidine, thiazole, 1,3,4-thiadiazole, benzothiazole and benzimidazole. O-Debenzoylation of the above compounds was effected by standard transesterification to get the test compounds. The 1H-imidazo[4,5-b] pyridine proved to be a low micromolar inhibitor (K-i = 21.1 mu M) of rabbit muscle glycogen phosphorylase b, while the other heterocycles displayed weak or no inhibition against the same enzyme.

SDS of cas: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Szennyes, E; Bokor, E; Docsa, T; Sipos, A; Somsak, L 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

Recommanded Product: 61-82-5. Zhang, L; Zhang, F; Liu, FB; Shen, J; Wang, JX; Jiang, M; Zhang, DS; Yang, PF; Chen, Y; Song, SY in [Zhang, Liang; Liu, Fangbing; Song, Shiyong] Chinese Acad Sci, CAS Key Lab Plant Germplasm Enhancement & Special, Wuhan Bot Garden, Wuhan 430074, Hubei, Peoples R China; [Zhang, Liang; Liu, Fangbing] Univ Chinese Acad Sci, Beijing 100049, Peoples R China; [Zhang, Liang; Liu, Fangbing; Song, Shiyong] Chinese Acad Sci, Ctr Econ Bot, Core Bot Gardens, Wuhan 430074, Peoples R China; [Zhang, Fan; Shen, Jun; Wang, Jiaxuan; Jiang, Meng; Chen, Ying; Song, Shiyong] Zhejiang Univ, Inst Crop Sci, State Key Lab Rice Biol, Zhejiang Prov Key Lab Crop Genet Resources, Hangzhou 310058, Peoples R China; [Zhang, Dasheng] Chinese Acad Sci, Shanghai Chenshan Bot Garden, Shanghai Chenshan Plant Sci Res Ctr, Shanghai 201602, Peoples R China; [Yang, Pingfang] Hubei Univ, Sch Life Sci, State Key Lab Biocatalysis & Enzyme Engn, Wuhan 430062, Peoples R China published The lotus NnFTIP1 and NnFT1 regulate flowering time in Arabidopsis in 2021.0, Cited 40.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5.

In higher plants, floral signals are mainly collected and transduced to FLOWERING LOCUS T (FT) in Arabidopsis and its orthologues. The movement of FT from leaves to the shoot apical meristem (SAM) is partially mediated by FT-INTERACTING PROTEIN1 (FTIP1). Although the functions of OsFTIP1 in rice and DOFTIP1 in orchid in FT transport have also been investigated, the FTIP1 homologue in lotus (Nelumbo nucifera Gaertn.), a type of horticultural plant with high economic and cultural value, has not been isolated, and the mechanism of NnFT1 transport has not been explored. Here, we revealed that NnFTIP1 mediates the transport of NnFT1 in ectopic transgenic lines in Arabidopsis. Overexpression of NnFTIP1 in the ftip1-1 background rescued the late flowering phenotype of ftip1-1, indicating that NnFTIP1 has a conserved function as FTIP1. NnFTIP1 and NnFT1 share similar tissue expression patterns and subcellular localization. NnFTIP1 and NnFT1 interact both in vitro and in vivo. In addition, NnFTIP1 affects NnFT1 transport from leaves to the SAM. Furthermore, we found that NnUOF8, a MYB-like transcription factor, directly regulates the expression of NnFTIP1. Our results suggest that the functions of FTIP1 and FT are conserved during evolution in flowering plants.

Recommanded Product: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Zhang, L; Zhang, F; Liu, FB; Shen, J; Wang, JX; Jiang, M; Zhang, DS; Yang, PF; Chen, Y; Song, SY 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

I found the field of Chemistry very interesting. Saw the article Efficient Route for the Synthesis of Diverse Heteroannelated 5-Cyanopyridines published in 2021.0. Product Details of 61-82-5, Reprint Addresses Volochnyuk, DM; Ryabukhin, SV (corresponding author), Enamine Ltd, 78 Chervonotkatska Str, Kiev, Ukraine.; Volochnyuk, DM; Ryabukhin, SV (corresponding author), Taras Shevchenko Natl Univ Kyiv, 60 Volodymyrska Str, Kiev, Ukraine.; Volochnyuk, DM (corresponding author), Natl Acad Sci Ukraine, Inst Organ Chem, 5 Murmanska Str, Kiev, Ukraine.. The CAS is 61-82-5. Through research, I have a further understanding and discovery of 1H-1,2,4-Triazol-5-amine

The new efficient, convenient protocol for the synthesis of heteroannelated 3-cyanopyridines and pyrimidines starting from diverse aminoheterocycles and 3,3-dimethoxy-2-formylpropionitrile sodium salt was elaborated. The advantages and improvements of the procedure compared to previously known methods are shown. The scope and limitations of the method are determined. The impact of the structural features on regioselectivity are discussed. The preparativeness, scalability, and application scope of the elaborated protocol are demonstrated by the synthesis of five heteroannelated 3-cyanopyridines in quantities up to 100 grams.

About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Mityuk, AP; Hrebonkin, A; Lebed, PS; Grabchuk, GP; Volochnyuk, DM; Ryabukhin, SV or concate me.. Product Details of 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 Synthesis and Characterization of Novel Azole Functionalized Poly(glycidyl methacrylate)s for Antibacterial and Anticandidal Activity WOS:000504668300004 published article about ANTIMICROBIAL ACTIVITY; QUATERNARY AMMONIUM; CHITOSAN; AMINE; MODE in [Rehman, Suriya; Alsalem, Zainab H.] Imam Abdulrahman Bin Faisal Univ, IRMC, Epidem Dis Res Dept, POB 1982, Dammam 31441, Saudi Arabia; [Gunday, Seyda T.; Bozkurt, Ayhan] Imam Abdulrahman Bin Faisal Univ, IRMC, Dept Biophys, POB 1982, Dammam 31441, Saudi Arabia in 2019.0, Cited 35.0. 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

Background: Presently, rise in the infectious diseases and subsequent development of drug resistance, is a global threat to human health. However, much efforts are being made by scientists, to develop novel antimicrobials, and also to improve the efficacy of available drugs, in order to combat the life-threatening infections. Objective: Synthesis and characterization of azole functional polymer systems for antimicrobial applications. Materials and Methods: Poly(glycidyl methacrylate) (PGMA), was produced by free radical polymerization of the monomer, glycidyl methacrylate (GMA). Different azole functional PGMAs were produced, through chemical modification with imidazole (Im), 1H-1,2,4-triazole (Tri) and 3-amino-1,2,4-triazole (ATri), to get PGMA-Imi, PGMA-Tri and PGMA-ATri, respectively. The structure was confirmed by Fourier transform infrared spectroscopy (FT-IR), thermal properties were investigated by Thermogravimetric Analysis (TGA), and surface morphology was studied by scanning electron microscopy (SEM). Newly synthesized derivatives were further explored, for their antibacterial and anticandidal activities. Results: All the three synthesized and characterized derivatives, displayed a significant activity against the tested microorganisms. The minimum inhibitory concentration (MIC) and minimum bactericidal/fungicidal concentration (MBC/MFC), recorded against Staphylococcus aureus (S. aureus), was 0.5 &1mg/ml for PGMA-Imi, followed by PGMA-ATri & PGMA-Tri, respectively, followed by E. coli with, 1 & 2 mg/ml, 4 & 8 mg/ml, 4& 8 mg/ml, respectively, whereas the maximum MIC & MFC was recorded against C. albicans i.e., 8 & 16 mg/ml, 4 & 8 mg/ml ,4 & 8 mg/ml for PGMA-ATri, PGMA-Tri, PGMA-Imi, respectively. Conclusion: In the present work, we report on the state-of-the-art, azole functional polymer systems for antimicrobial applications. These findings suggest that the synthesized azole functional polymer films have antimicrobial properties, which could be potential candidates for coating applications in the biomedical and wastewater treatment field.

Recommanded Product: 61-82-5. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Rehman, S; Gunday, ST; Alsalem, ZH; Bozkurt, A 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

An article A Tetratricopeptide Repeat Protein Regulates Carotenoid Biosynthesis and Chromoplast Development in Monkeyflowers (Mimulus) WOS:000545741500024 published article about BOX TRANSCRIPTION FACTOR; TOMATO FRUITFULL HOMOLOGS; PHYTOENE SYNTHASE; MITOCHONDRIAL MORPHOLOGY; NEGATIVE REGULATOR; PETUNIA ENCODES; PLASTID NUMBER; GENES CPPDS2/4; PIGMENTATION; MUTANT in [Stanley, Lauren E.; Ding, Baoqing; Mou, Fengjuan; Hill, Connor; Yuan, Yao-Wu] Univ Connecticut, Dept Ecol & Evolutionary Biol, Storrs, CT 06269 USA; [Sun, Wei; Chen, Shilin] China Acad Chinese Med Sci, Inst Chinese Mat Med, Beijing 100700, Peoples R China; [Mou, Fengjuan] Southwest Forestry Univ, Fac Forestry, Kunming 650224, Yunnan, Peoples R China; [Yuan, Yao-Wu] Univ Connecticut, Inst Syst Genom, Storrs, CT 06269 USA in 2020.0, Cited 101.0. The Name is 1H-1,2,4-Triazol-5-amine. Through research, I have a further understanding and discovery of 61-82-5. COA of Formula: C2H4N4

Little is known about the factors regulating carotenoid biosynthesis in flowers. Here, we characterized the REDUCED CAROTENOID PIGMENTATION2 (RCP2) locus from two monkeyflower (Mimulus) species, the bumblebee-pollinated species Mimulus lewisii and the hummingbird-pollinated species Mimulus verbenaceus. We show that loss-of-function mutations of RCP2 cause drastic down-regulation of the entire carotenoid biosynthetic pathway. The causal gene underlying RCP2 encodes a tetratricopeptide repeat protein that is closely related to the Arabidopsis (Arabidopsis thaliana) REDUCED CHLOROPLAST COVERAGE proteins. RCP2 appears to regulate carotenoid biosynthesis independently of RCP1, a previously identified R2R3-MYB master regulator of carotenoid biosynthesis. We show that RCP2 is necessary and sufficient for chromoplast development and carotenoid accumulation in floral tissues. Simultaneous down-regulation of RCP2 and two closely related paralogs, RCP2-L1 and RCP2-L2, yielded plants with pale leaves deficient in chlorophyll and carotenoids and with reduced chloroplast compartment size. Finally, we demonstrate that M. verbenaceus is just as amenable to chemical mutagenesis and in planta transformation as the more extensively studied M. lewisii, making these two species an excellent platform for comparative developmental genetics studies of closely related species with dramatic phenotypic divergence.

COA of Formula: C2H4N4. About 1H-1,2,4-Triazol-5-amine, If you have any questions, you can contact Stanley, LE; Ding, BQ; Sun, W; Mou, FJ; Hill, C; Chen, SL; Yuan, YW 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