Tag: M.W=100-150

An article Synthesis of Novel Tetra-Substituted Pyrazole Derivatives from 2,3-Furandione WOS:000488560500006 published article about BIOLOGICAL EVALUATION; 1,3,5-TRISUBSTITUTED PYRAZOLES; ANTIMICROBIAL ACTIVITY; ONE-POT; DESIGN; FUNCTIONALIZATION; ACID in [Genc, Hasan; Tozlu, Israfil] Van Yuzuncu Yil Univ, Fac Educ, Dept Sci, TR-65080 Van, Turkey; [Tasdemir, Volkan] Van Yuzuncu Yil Univ, Sci Res & Applicat Ctr, TR-65080 Van, Turkey; [Ogun, Erdal] Van Yuzuncu Yil Univ, Biol Dept, Sci Fac, TR-65080 Van, Turkey in 2019.0, Cited 42.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8. Recommanded Product: 64-10-8

Synthesis of pyrazole-3-carboxylic acid was progressed via two different protocols, one of which is solid state. Pyrazole-3-carboxylic acid was converted into different derivatives such as ester, urea, amide and nitrile. The amide compound was converted to nitrile using SOCl2 and DMF. Solid state heating of carboxylic acid gave decarboxylated product. Cyclization of tetra-substituted pyrazole with hydrazines resulted in pyrazolopyridazinones. The antimicrobial activities of the synthesized pyrazole derivatives against Bacillus cereus, Escherichia coli, Micrococcus luteus, Staphylococcus aureus, and Saccharomyces cerevisiae were evaluated. One of the pyrazole derivatives which possess nitro group showed antimicrobial activity in only B. cereus, a Gram-positive bacteria, with an MIC of 128 mu g/mL.

Recommanded Product: 64-10-8. About 1-Phenylurea, If you have any questions, you can contact Genc, H; Tasdemir, V; Tozlu, I; Ogun, E or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

HPLC of Formula: C7H8N2O. In 2019 TETRAHEDRON LETT published article about RING-CLOSING METATHESIS; NITROGEN-HETEROCYCLES; OLEFIN METATHESIS; SEPTANOSIDES; PEPTIDES; LACTAMS; ANALOGS; BETA in [Novanna, Motakatla; Kannadasan, Sathananthan] Vellore Inst Technol, Sch Adv Sci, Dept Chem, Vellore 632014, Tamil Nadu, India; [Shanmugam, Ponnusamy] CSIR, Organ & Bioorgan Chem Div, Cent Leather Res Inst, Chennai 600020, Tamil Nadu, India in 2019, Cited 46. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

A facile and efficient method has been developed for the synthesis of (2)-6-allyl-1-phenyl-1,2,5,6tetrahydro-7H-benzo[b][1,5]-diazonin-7-one and (Z)-1,6-diphenyl-1,2,5,6-tetrahydro-7H-benzo[b][1,5]-diazonin-7-one from anthranilamide via N-arylation/N-allylation and from isatoic anhydride via ring opening/N-arylation/N-allylation followed by ring closing metathesis using Grubbs-II catalyst as a key step. Grubbs-II catalyst was found to be superior over Grubbs-I catalyst in terms of reaction time and yield of the product, and the routes developed were suitable to synthesize benzo fused nine membered nitrogen heterocycles. The requirement of diallylated substrates with protected amine and amide nitrogen is suitable for RCM has been established for the synthesis of diazoninone derivatives. (C) 2019 Elsevier Ltd. All rights reserved.

HPLC of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Novanna, M; Kannadasan, S; Shanmugam, P or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Quality Control of 1-Phenylurea. In 2019.0 J MED CHEM published article about ANDROGEN RECEPTOR; HISTONE H3; COACTIVATOR; CARM1; METHYLATION; DISCOVERY; TRANSCRIPTION; EXPRESSION in [Guo, Zuhao; Cao, Danyan; Chen, Danqi; Wang, Qi; Li, Yanlian; Li, Jian; Du, Zhiyan; Wang, Xin; Chen, Lin; Shen, Jingkang; Xiong, Bing] Chinese Acad Sci, Shanghai Inst Mat Med, Dept Med Chem, 555 Zuchongzhi Rd, Shanghai 201203, Peoples R China; [Zhang, Zhuqing; Yang, Hong; Xu, Xiaowei; Zheng, Xineng; Ding, Jian; Geng, Meiyu; Huang, Xun] Chinese Acad Sci, Shanghai Inst Mat Med, Div Antitumor Pharmacol, State Key Lab Drug Res, 555 Zuchongzhi Rd, Shanghai 201203, Peoples R China; [Zhang, Zhuqing; Xu, Xiaowei; Zheng, Xineng; Wang, Qi; Ding, Jian; Geng, Meiyu; Huang, Xun; Xiong, Bing] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China in 2019.0, Cited 46.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8.

PRMT4 is a type I protein arginine methyltransferase and plays important roles in various cellular processes. Overexpression of PRMT4 has been found to be involved in several types of cancers. Selective and in vivo effective PRMT4 inhibitors are needed for demonstrating PRMT4 as a promising therapeutic target. On the basis of compound 6, a weak dual PRMT4/6 inhibitor, we constructed a tetrahydroisoquinoline scaffold through a cut-and-sew scaffold hopping strategy. The subsequent SAR optimization efforts employed structure-based approach led to the identification of a novel PRMT4 inhibitor 49. Compound 49 exhibited prominently high potency and selectivity, moderate pharmacokinetic profiles, and good antitumor efficacy in acute myeloid leukemia xenograft model via oral administration, thus demonstrating this compound as a useful pharmacological tool for further target validation and drug development in cancer therapy.

Quality Control of 1-Phenylurea. About 1-Phenylurea, If you have any questions, you can contact Guo, ZH; Zhang, ZQ; Yang, H; Cao, DY; Xu, XW; Zheng, XN; Chen, DQ; Wang, Q; Li, YL; Li, J; Du, ZY; Wang, X; Chen, L; Ding, J; Shen, JK; Geng, MY; Huang, X; Xiong, B or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Recommanded Product: 2-Aminobenzamide. In 2020 J HETEROCYCLIC CHEM published article about AZIDE-ALKYNE CYCLOADDITION; ONE-POT SYNTHESIS; 1,3-DIPOLAR CYCLOADDITION; CATALYST; ANTIBACTERIAL; DENDRIMERS; CHEMISTRY; COPPER(I); ANALOGS in [Keivanloo, Ali; Bakherad, Mohammad; Mokhtarei, Lotfollah] Shahrood Univ Technol, Fac Chem, Shahrood 3619995161, Iran in 2020, Cited 42. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Water soluble sodium 4-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate ligand was used successfully for the preparation of 1,2,3-triazoles pharmacophore linked-quinazolinone scaffold. The reaction of ethyl 4-oxo-3,4-dihydroquinazoline-2-carboxylate and related amide compounds with propargyl bromide afforded ethyl 4-oxo-3-(prop-2-yn-1-yl)-3,4-dihydroquinazoline-2-carboxylate and its amide derivatives. The reaction of propargylated compounds with azides catalyzed by copper (II) salt, in the presence of Sodium 4-amino-5-hydroxy-7-sulfonaphthalene-2-sulfonate as a ligand in water produced novel 1,2,3-triazole pharmacophore linked-quinazolinone-4-one scaffold with high-to-excellent yields. The ligand assisted in the click reaction and reduced loading of copper salt to 2 mol%. Simplicity, short reaction times, use of water as green solvent, and low catalyst loading are the main advantages of this procedure.

Recommanded Product: 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Keivanloo, A; Bakherad, M; Mokhtarei, L or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Category: thiomorpholine. Authors Fernandez-Lobato, L; Lopez-Sanchez, Y; Blejman, G; Jurado, F; Moyano-Fuentes, J; Vera, D in ELSEVIER SCI LTD published article about in [Fernandez-Lobato, L.; Jurado, F.; Vera, D.] Univ Jaen, Escuela Politecn Super, Dept Elect Engn, Linares 23700, Spain; [Lopez-Sanchez, Y.] Univ Jaen, Dept Econ, Lab Anal & Innovat Tourism LAInnTUR, Jaen, Spain; [Blejman, G.] Circular Carbon GmbH, Madrid, Spain; [Moyano-Fuentes, J.] Univ Jaen, Escuela Politecn Super, Dept Business Org Mkt & Sociol, Linares 23700, Spain in 2021.0, Cited 57.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8

Spain is the first olive oil producer worldwide (representing around 45%), with more than 80% of its agricultural area dedicated to this crop. The goal of this study is to assess the environmental impact of the Spanish virgin olive oil production, attending to the farming and industrial phases. A Life Cycle Assessment (LCA) is conducted for 5 harvests in approximately 4.000 ha of olive grove in Jaen, the largest producer region of Spain. The type of farming is the most representative in Spain: conventional (non-organic), with a medium-low slope, extensive (100-150 trees per ha) and around 60% dryland orchards. The industrial phase is based on 2-phase extraction process and olive pomace valorization. The functional unit (FU) chosen for the comparative analysis is 1 kg of unpacked virgin olive oil under a perspective from cradle to gate. One of the most representative categories, climate change, places the average environmental impact in 2.43 kg CO2 eq/kg, while the range is between 1.93 and 3.00 kg CO2 eq/kg depending on the harvest. Huge differences between values are observed in the farming phase and they are mostly caused by the virgin olive oil yield of every harvest. The carbon sequestration analyses and the impact produced per FU ranges from 43.78% (for 15/16 harvest) to 46.36% (for 17/18). The impact hotspots detected in the farming phase, in terms of climate change potential, are the categories of plant protection products and herbicides (24.11% of the average value) and fertilizers (20.01%). However, the environmental impact of the industrial phase is relatively constant, with a value of 0.547-0.554 kg of CO2 equivalent. The 80.74% is caused by pomace valorization, which translated to the average whole value, represents the 18.56%. (C) 2020 Elsevier Ltd. All rights reserved.

Category: thiomorpholine. About 1-Phenylurea, If you have any questions, you can contact Fernandez-Lobato, L; Lopez-Sanchez, Y; Blejman, G; Jurado, F; Moyano-Fuentes, J; Vera, D or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Authors Romero, IA; van Dillewijn, P; Nesme, J; Sorensen, SJ; Romero, E in ELSEVIER published article about BIOREMEDIATION SYSTEMS; BACTERIAL COMMUNITY; INCP-1 PLASMIDS; DEGRADATION; DIURON; SOIL; BIODEGRADATION; MINERALIZATION; HYDROLASE; IMPACTS in [Aguilar Romero, Ines; van Dillewijn, Pieter; Romero, Esperanza] CSIC, EEZ, Dept Environm Protect, C Prof Albareda 1, E-18008 Granada, Spain; [Nesme, Joseph; Sorensen, Soren J.] Univ Copenhagen, Dept Biol, Sect Microbiol, DK-2100 Copenhagen, Denmark in 2019.0, Cited 44.0. SDS of cas: 64-10-8. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8

Despite certain limitations, bioaugmentation enhances the efficiency of bioremediation systems. In this study, three aqueous extracts (APE, ACE and APE) from aged residual biomixtures in three biopurification systems (BPSs) exposed to pesticides at a pilot scale were found to improve pesticide removal. The addition of ACEs and AVEs to solutions containing the model compound diuron increased removal rates 6- and 17-fold, respectively, as compared to APEs. These extracts also increased the removal of the metabolite 3,4-dichloroaniline, while AVEs, in particular, were found to remove all pesticides within 9 days. Three metabolites less hazardous than 3,4-dichloroaniline were identified by SPME/GC/MS. AVEs, which also enhance linuron removal in liquid media, were found to increase diuron removal 6-fold in BPSs. We observed an increase in the relative abundance of taxa, such as Chloroflexi, Acidobacteria, Gemmatimonadetes, Firmicutes, Deinococcus-Thermus and especially Proteobacteria (10%), in AV biomixtures, as well as an enrichment of gamma-proteobacteria and the actinobacterial genus Dokdonella in AVEs with respect to initial noncontaminated IV biomixture. We demonstrate that extracts containing a pollutant-acclimatized microbiome could be used as part of a bioaugmentation strategy to improve the functioning of on-farm BPSs and contaminated systems. (c) 2019 Elsevier B.V. All rights reserved.

SDS of cas: 64-10-8. About 1-Phenylurea, If you have any questions, you can contact Romero, IA; van Dillewijn, P; Nesme, J; Sorensen, SJ; Romero, E or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

In 2020 BIOORG MED CHEM LETT published article about POTENTIAL AGENTS; MEMORY; PHOSPHODIESTERASES; DYSFUNCTION in [Huang, Xian-Feng; Dong, Yan-Hua; Ke, Heng-Ming; Song, Guo-Qiang; Xu, De-Feng] Changzhou Univ, Sch Pharmaceut Engn & Life Sci, Changzhou 213164, Jiangsu, Peoples R China; [Huang, Xian-Feng; Dong, Yan-Hua; Ke, Heng-Ming; Song, Guo-Qiang; Xu, De-Feng] Changzhou Univ, Adv Catalysis Green Mfg Collaborat Innovat Ctr, Changzhou 213164, Jiangsu, Peoples R China; [Wang, Jin-Hui] Wenzhou Med Univ, Wenzhou 3 Clin Inst, Wenzhou Peoples Hosp, Wenzhou 325000, Zhejiang, Peoples R China in 2020, Cited 28. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Recommanded Product: 2-Aminobenzamide

A series of novel rutaecarpine derivatives were synthesized and subjected to pharmacological evaluation as PDE5 inhibitors. The structure-activity relationships were discussed and their binding conformation and simultaneous interaction mode were further clarified by the molecular docking studies. Among the 25 analogues, compound 8i exhibited most potent PDE5 inhibition with IC50 values about 0.086 mu M. Moreover, it also produced good effects against scopolamine-induced cognitive impairment in vivo. These results might bring significant instruction for further development of potential PDE5 inhibitors derived from rutaecarpine as a good candidate drug for the treatment of Alzheimer’s disease.

About 2-Aminobenzamide, If you have any questions, you can contact Huang, XF; Dong, YH; Wang, JH; Ke, HM; Song, GQ; Xu, DF or concate me.. Recommanded Product: 2-Aminobenzamide

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Application In Synthesis of 1-Phenylurea. I found the field of Chemistry; Science & Technology – Other Topics; Engineering very interesting. Saw the article Enhanced Surface Area, Graphene Quantum Dots, and Functional Groups for the Simple Acid-Treated Carbon Fiber Electrode of Flexible Fiber-Type Solid-State Supercapacitors without Active Materials published in 2020.0, Reprint Addresses Lin, LY (corresponding author), Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei 10608, Taiwan.; Lin, LY (corresponding author), Res Ctr Energy Conservat New Generat Residential, Taipei 10608, Taiwan.. The CAS is 64-10-8. Through research, I have a further understanding and discovery of 1-Phenylurea.

Flexible fiber-type solid-state supercapacitors (FSCs) are demanded for energy storage of wearable soft electronics. A flexible carbon fiber (CF) with high electrical conductivity and good energy storage ability can act as the current collector and the active material simultaneously. Improving the energy storage ability of the CF without depositing active materials is highly promising to avoid active materials from peeling off, especially under bending conditions. In this study, the CF is treated with acid mixtures containing different HNO3 to H2SO4 ratios. The roughened surface and the production of graphene quantum dots and functional groups are achieved for the acid-treated CF, especially for the CF treated with the acid mixtures. The largely enhanced specific capacitance (C-L) is first obtained for the optimized CF electrode (641.08 mF/cm at 5 mV/s) treated with the acid mixture containing the HNO3 to H2SO4 ratio of 1 to 3. The FSC also shows a maximum energy density of 16.57 mu W h/cm at the power density of 62.50 mu W/cm, as well as a C-L retention of 77% and Coulombic efficiency of 100% in 5000 times of a charge/discharge cycling process. Excellent flexibility is also attained for the FSC with no shape distortion of cyclic voltammetry curves measured under the bending angle of 180 degrees and with 1000 times of repeated bending. This work proposes a simple acid treatment to largely enhance the energy storage ability of pure CF electrodes. The bifunctional substance with current collecting and energy storing abilities is expected to be well developed in the future for applying on numerous efficient flexible energy storage devices.

Application In Synthesis of 1-Phenylurea. About 1-Phenylurea, If you have any questions, you can contact Hsiao, YJ; Lin, LY or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Synthesis, Crystal Structure, and Agricultural Antimicrobial Evaluation of Novel Quinazoline Thioether Derivatives Incorporating the 1,2,4-Triazolo[4,3-a]pyridine Moiety WOS:000492802400006 published article about BIOLOGICAL EVALUATION; INSECTICIDAL ACTIVITY; FUNGICIDAL ACTIVITIES; DESIGN; ANTIFUNGAL; SERIES; ORYZAE; BASE in [Fan, Zhijiang; Shi, Jun; Luo, Na; Ding, Muhan; Bao, Xiaoping] Guizhou Univ, Ctr Res & Dev Fine Chem, State Key Lab Breeding Base Green Pesticide & Agr, Key Lab Green Pesticide & Agr Bioengn,Minist Educ, Guiyang 550025, Guizhou, Peoples R China in 2019, Cited 46. Recommanded Product: 88-68-6. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

A total of 22 quinazoline thioether derivatives incorporating a 1,2,4-triazolo[4,3-a]pyridine moiety were designed, synthesized, and evaluated as antimicrobial agents in agriculture. Among these compounds, the chemical structure of compound 61 was further confirmed via single-crystal X-ray diffraction analysis. The bioassay results revealed that some of the compounds possessed noticeable in vitro antibacterial activities against the tested phytopathogenic bacteria. For example, compounds 6b and 6g had EC50 values as low as 10.0 and 24.7 mu g/mL against Xanthomonas axonopodis pv. citri (Xac), respectively, which were significantly better than that of the commercial agrobactericide bismerthiazol (56.9 mu g/mL). Particularly, compound 6b was also found to be capable of suppressing the pathogenic bacterium Xanthomonas oryzae pv. oryzae (Xoo) approximately 12-fold more potent than control bismerthiazol, in terms of their EC 50 values (7.2 versus 89.8 mu g/mL). Importantly, the most active compound 6b turned out to be one with the highest hydrophilicity and the lowest molecular weight within the series. In vivo bioassays further showed the application prospect of 6b as a promising plant bactericide for controlling Xoo. Additionally, in vitro antifungal activities of these compounds were also evaluated at the concentration of 50 mu g/mL. Overall, the present study demonstrated the potential of 1,2,4-triazolo[4,3-a]pyridine-bearing quinazoline thioether derivatives as efficient agricultural antibacterial agents for crop protection.

About 2-Aminobenzamide, If you have any questions, you can contact Fan, ZJ; Shi, J; Luo, N; Ding, MH; Bao, XP or concate me.. Recommanded Product: 88-68-6

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Recommanded Product: 64-10-8. In 2019.0 EUR J CANCER published article about BRAIN METASTASES; DOCETAXEL; PEMBROLIZUMAB; INHIBITORS in [Grossi, Francesco] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Med Oncol Unit, Milan, Italy; [Genova, Carlo] IRCCS Osped Policlin San Martino, Lung Canc Unit, Genoa, Italy; [Crino, Lucio; Delmonte, Angelo] Ist Sci Romagnolo Studio & Cura Tumori IRST IRCCS, Dept Med Oncol, Meldola, Italy; [Turci, Daniele] Osped S Maria Delle Croci, Med Oncol Unit, Ravenna, Italy; [Signorelli, Diego] Fdn IRCCS Ist Nazl Tumori, Dept Med Oncol, Milan, Italy; [Passaro, Antonio] European Inst Oncol IRCCS, IEO, Div Thorac Oncol, Milan, Italy; [Parra, Hector Soto] Azienda Osped Univ AOU Policlin Vittorio Emanuele, Dept Oncol, Catania, Italy; [Catino, Annamaria] IRCCS Ist Tumori Giovanni Paolo II, Med Oncol Unit, Patol Torac, Bari, Italy; [Landi, Lorenza] AUSL Romagna, Dept Hematol Oncol, Ravenna, Italy; [Gelsomino, Francesco] AOU Policlin St Orsola Malpighi, Oncol Unit, Bologna, Italy; [Tiseo, Marcello] Univ Parma, Dept Med & Surg, Parma, Italy; [Tiseo, Marcello] Azienda Osped Univ Parma, Oncol Med, Parma, Italy; [Puppo, Gianfranco] Osped Macerata, Pulmonol Unit, Macerata, Italy; [Roila, Fausto] Osped S Maria Misericordia, Med Oncol Unit, Perugia, Italy; [Ricciardi, Serena] Azienda Osped San Camillo Forlanini, Pulm Oncol Unit, Rome, Italy; [Tonini, Giuseppe] Univ Campus Biomed, Dept Oncol, Rome, Italy; [Cognetti, Francesco] Univ Roma La Sapienza, Ist Nazl Tumori Regina Elena, Med Oncol Unit, Rome, Italy; [Toschi, Luca] IRCCS Ist Clin Humanitas, Dept Hematol Oncol, Rozzano, Italy; [Tassinari, Davide] AUSL Romagna, Oncol Unit, Rimini, Italy; [Scoppola, Alessandro] Ist Dermopat Immacolata, Dept Med Oncol, Rome, Italy; [Giannarelli, Diana] Ist Nazl Tumori Regina Elena, BIostat, Rome, Italy; [Cortesi, Enrico] Policlin Umberto 1, Oncol Unit, Rome, Italy in 2019.0, Cited 19.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8.

Background: Nivolumab was the first immune checkpoint inhibitor approved for previously treated advanced nonesmall cell lung cancer (NSCLC). Before its introduction in the market, nivolumab was made available to NSCLC patients through an expanded access program (EAP). Here we present the Italian cohort of patients with non-squamous NSCLC enrolled in a worldwide nivolumab EAP, with subgroup analyses involving elderly patients, patients with central nervous system (CNS) metastases and patients receiving nivolumab beyond progression. Methods: Pretreated patients with advanced non-squamous NSCLC received nivolumab at 3 mg/kg every 2 weeks up to 24 months. Efficacy data (investigator-assessed tumour response, progression date and survival) and safety data were collected. Findings: 1588 patients were treated across 153 Italian centres. Overall response rate and disease control rate were 18% and 44%, respectively; median overall survival (OS) was 11.3 months (95% CI: 10.2-12.4). Elderly patients (>= 70 n = 522; >= 75 n = 232) achieved outcomes similar to the global study population; patients with CNS metastases (n = 409) had an OS of 8.6 months (95% CI: 6.4-10.8), and a 1-year OS rate of 43%. Nivolumab was administered beyond progression to 276 patients (26%), 57 of whom achieved subsequent disease control; the median OS of patients receiving nivolumab beyond progression was 16.2 months (95% CI: 14.0-18.4), while 1-year OS rate was 62%. Interpretation: To date, this is the largest clinical experience with nivolumab in a real-world setting. Our data support its use in clinical practice for pretreated non-squamous NSCLC, including patients with older age or CNS metastases. (C) 2019 Elsevier Ltd. All rights reserved.

Recommanded Product: 64-10-8. About 1-Phenylurea, If you have any questions, you can contact Grossi, F; Genova, C; Crino, L; Delmonte, A; Turci, D; Signorelli, D; Passaro, A; Parra, HS; Catino, A; Landi, L; Gelsomino, F; Tiseo, M; Puppo, G; Roila, F; Ricciardi, S; Tonini, G; Cognetti, F; Toschi, L; Tassinari, D; Scoppola, A; Giannarelli, D; Cortesi, E or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem