Day: October 28, 2021

Formula: C7H8N2O. 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.

Formula: C7H8N2O. 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

Li, WL; Yin, Y; Shuai, W; Xu, FJ; Yao, H; Liu, J; Cheng, KG; Xu, JY; Zhu, ZY; Xu, ST in [Li, Wenlong; Yin, Ying; Shuai, Wen; Xu, Feijie; Yao, Hong; Xu, Jinyi; Xu, Shengtao] China Pharmaceut Univ, State Key Lab Nat Med, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China; [Li, Wenlong; Yin, Ying; Shuai, Wen; Xu, Feijie; Yao, Hong; Xu, Jinyi; Xu, Shengtao] China Pharmaceut Univ, Dept Med Chem, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China; [Liu, Jie] China Pharmaceut Univ, Dept Organ Chem, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China; [Liu, Jie; Cheng, Keguang] Guangxi Normal Univ, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China; [Liu, Jie; Cheng, Keguang] Guangxi Normal Univ, Sch Chem & Pharm, Guilin 541004, Peoples R China; [Zhu, Zheying] Univ Nottingham, Sch Pharm, Div Mol Therapeut & Formulat, Univ Pk Campus, Nottingham NG7 2RD, England published Discovery of novel quinazolines as potential anti-tubulin agents occupying three zones of colchicine domain in 2019, Cited 26. COA of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

A series of novel quinazolines as tubulin inhibitors occupying three zones of colchicine domain have been designed and synthesized inspired by the recently disclosed crystal structure of verubulin analogue 6 with tubulin. Among the newly synthesized compounds, 19c showed noteworthy potency against K562, HepG2, KB, HCT-8 and MDB-MB-231 cancer cells. In vitro microtubule polymerization assays identified 19c as a potent tubulin assembly inhibitor, the binding mode of which with tubulin was confirmed by molecular modeling studies to occupy three zones of tubulin domain. Furthermore, 19c disrupted the intracellular microtubule network, caused G2/M phase arrest, induced cell apoptosis and depolarized mitochondria of K562 cells. 19c also reduced the cell migration and disrupted the capillary-like tube formation of human umbilical vein endothelial cells (HUVECs). Importantly, 19c significantly and dose dependently inhibited tumor growth in H22 liver cancer xenograft mouse model. All these results suggested that 19c deserves further research as a novel and potential anti-tubulin agent for the treatment of cancers.

COA of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Li, WL; Yin, Y; Shuai, W; Xu, FJ; Yao, H; Liu, J; Cheng, KG; Xu, JY; Zhu, ZY; Xu, ST or concate me.

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

SDS of cas: 99-61-6. Authors Koohestani, F; Sadjadi, S; Heravi, M in NATURE RESEARCH published article about in [Koohestani, Fatemeh; Sadjadi, Samahe] Iran Polymer & Petrochem Inst, Fac Petrochem, Gas Convers Dept, POB 14975-112, Tehran, Iran; [Heravi, Majid] Alzahra Univ, Sch Phys & Chem, Dept Chem, POB 1993891176, Tehran, Iran in 2021, Cited 35. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

Combining the encapsulating capability of cyclodextrin and instinctive features of bentonite clay, a versatile metal free catalyst has been developed that could promote various chemical reactions such as Knoevenagel condensation, synthesis of xanthan and octahydroquinazolinones in aqueous media under ultrasonic irradiation. To prepare the catalyst, bentonite was Cl-functionalized and then reacted with isatin and guanidine successively to furnish amino functionalized bentonite. The latter then reacted with tosylated cyclodextrin. The resultant catalytic composite was characterized via XRD, SEM, EDS, BET, elemental mapping analysis, TGA and FTIR. The catalytic activity tests approved excellent activity of the catalyst as well as broad substrate scope. Notably, the catalyst could be simply recovered and reused for several reaction runs. Moreover, the activity of the composite was superior to that of its components.

SDS of cas: 99-61-6. About 3-Nitrobenzaldehyde, If you have any questions, you can contact Koohestani, F; Sadjadi, S; Heravi, M or concate me.

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

Category: thiomorpholine. Authors Hsu, KL in CELL PRESS published article about in [Hsu, Ku-Lung] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA; [Hsu, Ku-Lung] Univ Virginia, Sch Med, Dept Pharmacol, Charlottesville, VA 22908 USA; [Hsu, Ku-Lung] Univ Virginia, Dept Mol Physiol & Biol Phys, Charlottesville, VA 22908 USA; [Hsu, Ku-Lung] Univ Virginia, Ctr Canc, Charlottesville, VA 22903 USA in 2021.0, Cited 10.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

In this issue of Cell Chemical Biology, Seneviratne et al. (2020) combine photoaffinity labeling and quantitative chemical proteomics to identify the molecular target of a lead compound discovered from a phenotypic drug screen. Their work showcase the power of coupling a photoreactive group to screening hits for rapid target deconvolution.

About Benzophenone, If you have any questions, you can contact Hsu, KL or concate me.. Category: thiomorpholine

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

Product Details of 104-21-2. Authors Roser, C; Toth, C; Renner, M; Herpel, E; Schirmacher, P in BMC published article about in [Roser, Christoph; Toth, Csaba; Renner, Marcus; Herpel, Esther; Schirmacher, Peter] Heidelberg Univ Hosp, Inst Pathol, Neuenheimer Feld 224, D-69120 Heidelberg, Germany; [Roser, Christoph] Heidelberg Univ Hosp, Dept Orthodont & Dentofacial Orthopaed, Neuenheimer Feld 400, D-69120 Heidelberg, Germany; [Herpel, Esther] Natl Ctr Tumor Dis NCT, Tissue Bank, Neuenheimer Feld 224, D-69120 Heidelberg, Germany; [Toth, Csaba] Trier MVZ Histol Cytol & Mol Diagnost, Max Planck Str 5, D-54296 Trier, Germany in 2021, Cited 53. The Name is 4-Methoxybenzyl acetate. Through research, I have a further understanding and discovery of 104-21-2

Background: Colorectal familial adenomatous polyposis (FAP) adenomas exhibit a uniform pathogenetic basis caused by a germline mutation in the adenomatous polyposis gene (APC), but the molecular changes leading to their development are incompletely understood. However, dysregulated apoptosis is known to substantially affect the development of colonic adenomas. One of the key regulatory proteins involved in apoptosis is apoptosis repressor with caspase recruitment domain (ARC). Methods: The expression of nuclear and cytoplasmic ARC in 212 adenomas from 80 patients was analyzed by immunohistochemistry. We also compared expression levels of ARC with the expression levels of p53, Bcl-2, COX-2, and MMR proteins. Statistical analyses were performed by Spearman’s rank correlation and linear regression test. Results: ARC was overexpressed in the nuclei and cytoplasm of most FAP adenomas investigated. Cytoplasmic ARC staining was moderately stronger (score 2) in 49.1% (n = 104/212) and substantially stronger (score 3) in 32.5% (n = 69/212) of adenomas compared to non-tumorous colorectal mucosa. In 18.4% (n = 39/212) of adenomas, cytoplasmic ARC staining was equivalent to that in non-tumorous mucosa. Nuclear expression of ARC in over 75% of cells was present in 30.7% (n = 65/212) of investigated adenomas, and nuclear expression in 10-75% of cells was detected in 62.7% (n = 133/212). ARC expression in under 10% of nuclei was found in 6.6% (n = 14/212) of adenomas. The correlation between nuclear ARC expression and cytoplasmic ARC expression was highly significant (p = 0.001). Moreover, nuclear ARC expression correlated positively with overexpression of Bcl-2, COX-2 p53 and beta-catenin. Cytoplasmic ARC also correlated with overexpression of Bcl-2. Sporadic MMR deficiency was detected in very few FAP adenomas and showed no correlation with nuclear or cytoplasmic ARC. Conclusions: Our results demonstrated that both cytoplasmic and nuclear ARC are overexpressed in FAP adenomas, thus in a homogenous collective. The highly significant correlation between nuclear ARC and nuclear beta-catenin suggested that ARC might be regulated by beta-catenin in FAP adenomas. Because of its further correlations with p53, Bcl-2, and COX-2, nuclear ARC might play a substantial role not only in carcinomas but also in precursor lesions.

Product Details of 104-21-2. About 4-Methoxybenzyl acetate, If you have any questions, you can contact Roser, C; Toth, C; Renner, M; Herpel, E; Schirmacher, P or concate me.

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

Safety of Anthrone. Authors Kaur, K; Mittal, SK; Kumar, SKA; Kumar, A; Kumar, S; Metters, JP; Banks, CE in MDPI published article about in [Kaur, Karamjeet; Mittal, Susheel K.] Thapar Inst Engn & Technol, Sch Chem & Biochem, Patiala 147001, Punjab, India; [Kumar, Ashok S. K.] VIT Univ, Sch Adv Sci, Vellore 632014, Tamil Nadu, India; [Kumar, Ashwani; Kumar, Subodh] GND Univ, Dept Chem, Amritsar 143005, Punjab, India; [Metters, Jonathan P.; Banks, Craig E.] Manchester Metropolitan Univ, Fac Sci & Engn, Sch Chem & Environm, Div Chem & Environm Sci, John Dalton Bldg,Chester St, Manchester M1 5GD, Lancs, England in 2021, Cited 33. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8

Voltammetric sensor using a symmetrical derivative of anthrone3 (1,7-diamino-3,9-dibutyl benzo[1,2,3-de:4,5,6-d’e’]diquinoline-2,8(3H,9H)-dione) (SPE-A) has been developed as a probe for Hg(II) ions. Performance of the probe as screen-printed electrode modified with the receptor (SPE-A) has been compared with anthrone3 in solution phase, using 1:1 water-acetonitrile solvent system. Anthrone3 displayed an electrochemically quasi-reversible nature in voltammograms with both the systems and is presented as a novel disposable voltammetric sensor for mercury ions. Upon interaction with cations, both the electrode systems showed sensitivity towards Hg2+ ions with a lower detection limit of 0.61 mu M. The magnitude of the voltammetric current with the SPE-A exhibited three times the current obtained with a bare glassy carbon electrode (GC). Kinetic performance of the SPE-A electrode is better than the GC electrode. The morphological studies indicate reusability of the electrodes.

Safety of Anthrone. About Anthrone, If you have any questions, you can contact Kaur, K; Mittal, SK; Kumar, SKA; Kumar, A; Kumar, S; Metters, JP; Banks, CE or concate me.

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

Wei, XW; Yuan, JM; Huang, WY; Chen, NY; Li, XJ; Pan, CX; Mo, DL; Su, GF in [Wei, Xin-Wei; Yuan, Jing-Mei; Chen, Nan-Ying; Li, Xiao-Juan; Pan, Cheng-Xue; Mo, Dong-Liang; Su, Gui-Fa] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China; [Huang, Wan-Yun] Guilin Med Univ, Dept Pharmacol, Guilin 541004, Peoples R China published 2-Styryl-4-aminoquinazoline derivatives as potent DNA-cleavage, p53-activation and in vivo effective anticancer agents in 2020, Cited 39. COA of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Forty-eight analogues of CP-31398, an antitumor agent modulated the mutant p53 gene were synthesized and their cytotoxicities against four cancer cell lines with different p-53 status including bladder cell 724 (w-p53), gastric cell MGC-803 (m-p53), prostate cell DU145 (m-p53), prostate cell PC-3 (null-p53), lung cell A549 (w-p53) and normal liver cell line HL-7702 (w-p53) were examined. (E)-2-(4-Nitrostyryl)-4-(3-dimethylaminopropyl)-aminoquinazoline (10ah) was identified as the most potent compound in anti-proliferation against MGC-803 cells, with IC50 lowed to 1.73 mu M, far potency than that of CP-31398. Molecular mechanism study revealed that 10ah and CP-31398 differ greatly in mechanism to exert their antitumor properties. 10ah could intercalate into DNA and resulted in significant DNA double-strand break 10ah-treatment in MGC-803 cells increased the expression of p53, phosphorylated p53 (p-p53), CDK4, p21 to cause cell cycle arrest at G2/M phase, significantly up-regulated the levels of pro-apoptosis proteins Bak, Bax, Bim while down-regulated the anti-apoptosis proteins Bcl-2, Bcl-xL and the levels of cyclin B1, fluctuated the intracellular reactive oxygen species (ROS), Ca2+ and mitochondria! membrane potential, activated Caspase-9 and Caspase-3 to induce apoptosis. 10ah also displayed potent anticancer efficiency against MGC-803 xenograft tumors models, with tumor growth inhibition (TGI) up to 61.8% at 20 mg/kg without obvious toxicity. (C) 2019 Elsevier Masson SAS. All rights reserved.

COA of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Wei, XW; Yuan, JM; Huang, WY; Chen, NY; Li, XJ; Pan, CX; Mo, DL; Su, GF or concate me.

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

An article Electrostatically Enhanced Sulfuric Acid: A Strong BrOnsted Acidic Catalyst for Multi-Component Reactions WOS:000468172400019 published article about ONE-POT SYNTHESIS; BIGINELLI REACTION; EFFICIENT SYNTHESIS; SOLID ACID; ACTIVATION; LIQUID in [Anzabi, Mohadese Yaghoobi; Yazdani, Hossein; Bazgir, Ayoob] Shahid Beheshti Univ, Dept Chem, GC, Tehran 1983963113, Iran in 2019, Cited 35. SDS of cas: 88-68-6. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

A new electrostatically enhanced sulfuric acid as a strong BrOnsted acidic catalyst has been developed for multi-component reactions. A positively charged center in the catalyst electrostatically activates it for acid-catalyzed multi-component reactions and afforded desired products in short reaction time and near room temperature in EtOH as a green solvent. [GRAPHICS] .

SDS of cas: 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Anzabi, MY; Yazdani, H; Bazgir, A or concate me.

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

COA of Formula: C7H8N2O. Parveen, I; Ahmed, N in [Parveen, Iram; Ahmed, Naseem] Indian Inst Technol Roorkee, Dept Chem, Roorkee 247667, Uttar Pradesh, India published A Route to Highly Functionalized Stereospecific trans -Aminated Aurones from 3-Bromoflavones with Aniline and N -Phenylurea via a Domino Aza-Michael Ring Opening and Cyclization Reactions in 2019.0, Cited 36.0. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8.

A facile cascade reaction is reported via aza-Michael addition, ring opening, and cyclization between 3-bromoflavone and aniline derivatives or N -phenylurea in the presence of KO t -Bu and CuI in DMF under mild reaction conditions. Products were obtained as stereospecific trans -aminated aurones in good to excellent yields (61-83%). Our protocol is operationally successful with ease, avoids the requirement of additives and ligands, and offers broad substrate scope.

About 1-Phenylurea, If you have any questions, you can contact Parveen, I; Ahmed, N or concate me.. COA of Formula: C7H8N2O

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

Name: Anthrone. Authors Das, S; Bhowmik, A; Sarkar, W; Mishra, A; Deb, I in AMER CHEMICAL SOC published article about in [Das, Sumit; Bhowmik, Arup; Sarkar, Writhabrata; Mishra, Aniket; Deb, Indubhusan] CSIR Indian Inst Chem Biol, Organ & Med Chem Div, Kolkata 700032, India; [Das, Sumit] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, Uttar Pradesh, India in 2021, Cited 75. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8

Activation of anthrone via benzylic deprotonation in the presence of triethylamine paves the way for the 1,2-addition reaction with imines to provide the desired functionalized anthrones in good to excellent yields under mild and operationally simple reaction conditions with a broad range of substrate scopes without using any external additives or toxic stoichiometric reagents.

Name: Anthrone. About Anthrone, If you have any questions, you can contact Das, S; Bhowmik, A; Sarkar, W; Mishra, A; Deb, I or concate me.

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