Day: January 14, 2022

An article HDAC-Bax Multiple Ligands Enhance Bax-Dependent Apoptosis in HeLa Cells WOS:000585952100044 published article about HISTONE DEACETYLASE INHIBITOR; DRUG-COMBINATION; CERVICAL-CANCER; ACTIVATION; OLIGOMERIZATION; CHEMOTHERAPY; CHIDAMIDE; SYNERGY; BREAST; DEATH in [Liang, Tao; Zhou, Yi; Elhassan, Reham M.; Hou, Xuben; Yang, Xinying; Fang, Hao] Shandong Univ, Cheeloo Coll Med, Sch Pharmaceut Sci, Key Lab Chem Biol,Minist Educ,Dept Med Chem, Jinan 250012, Shandong, Peoples R China in 2020.0, Cited 40.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. SDS of cas: 99-93-4

Inspired by the synergistic effect of BTSA1 (a Bax activator) and SAHA (a histone deacetylase (HDAC) inhibitor) in HeLa cell growth suppression, a series of novel HDAC-Bax multiple ligands were designed rationally. Compound 23, which possesses similar HDAC inhibitory activity relative to SAHA and Bax affinity comparable to BTSA1, exhibits a superior growth suppression against HeLa cells, and its antiproliferative activities are 15-fold and 3-fold higher than BTSA1 and SAHA, respectively. The better antiproliferative activity and lower cytotoxicity of compound 23 indicated that our HDAC-Bax multiple ligand design strategy achieved success. Further studies suggested that compound 23 could enhance Bax-dependent apoptosis by upregulating Bax, followed by inducing the conformational activation of Bax. To our knowledge, we first report HDAC-Bax multiple ligands and demonstrate a new paradigm for the treatment of solid tumors by enhancing Bax-dependent apoptosis.

Bye, fridends, I hope you can learn more about C8H8O2, If you have any questions, you can browse other blog as well. See you lster.. SDS of cas: 99-93-4

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recommanded Product: 4-Methoxybenzaldehyde. Qin, XY; Meng, FT; Wang, MA; Tu, SJ; Hao, WJ; Wang, JY; Jiang, B in [Qin, Xiao-Yan; Meng, Fan-Tao; Tu, Shu-Jiang; Hao, Wen-Juan; Jiang, Bo] Jiangsu Normal Univ, Sch Chem & Mat Sci, Jiangsu Key Lab Green Synthet Chem Funct Mat, Xuzhou 221116, Jiangsu, Peoples R China; [Wang, Mian; Wang, Jianyi] Guangxi Univ, Med Coll, Nanning 530004, Peoples R China published Gold-Catalyzed Skeletal Rearrangement of Alkenes: Regioselective Synthesis of Skeletally Diverse Tricyclic Heterocycles and Mechanistic Investigations in 2021, Cited 90. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

Transition metal-catalyzed skeletal rearrangement reactions have rapid advances in organic community. Their development benefits synthetic methodologies by providing versatile and flexible approaches toward special molecular scaffolds with high selectivity. Herein, a gold-catalyzed skeletal rearrangement of alkenes with alkynyl bromides is reported, enabling direct and regioselective generation of more than 50 examples of skeletally diverse tricyclic heterocycles, namely, syn-tetrahydrocyclopenta[b]indoles and benzofuro[3,2-b]pyridines, with generally good yields. This protocol could tolerate terminal unactivated and internal activated alkenes under air conditions, which is hitherto unreported in gold catalysis and scarcely realized by other metal-catalyzed reactions, thus opening avenues for the regioselective assembly of heterocyclic systems with high efficiency. Aside from examining the scope of this skeletal rearrangement, mechanistic investigations to explain the regioselectivity of forming syn-tetrahydrocyclopenta[b]indoles and benzofuro[3,2-b]pyridines were conducted by systematic theoretical calculations.

Recommanded Product: 4-Methoxybenzaldehyde. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Qin, XY; Meng, FT; Wang, MA; Tu, SJ; Hao, WJ; Wang, JY; Jiang, B or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

COA of Formula: C8H8O2. In 2021 J ORG CHEM published article about STEREOSELECTIVE-SYNTHESIS; SYNTHETIC APPLICATIONS; ALPHA-CHLOROESTERS; CARBOLITHIATION; HALIDES in [Dejardin, Claire; Renou, Amaury; Maddaluno, Jacques; Durandetti, Muriel] Normandie Univ, UNIROUEN, INSA Rouen, CNRS,Lab COBRA UMR 6014 & FR 3038, F-76000 Rouen, France in 2021, Cited 42. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5.

An intramolecular carbometallation of a triple bond promoted by electrochemistry and mediated by nickel catalysis is described. This domino process transforms various aryl halides bearing a propargyl chain into substituted heterocycles in one single operation, with high stereoselectivities and in good to high yields. This reaction, characterized by a cyclic voltammetry set of experiments, proceeds following a syn-exo-dig cyclization process. When run at 80 degrees C, vinylbenzofuranes that are suitable substrates for cycloaddition reactions are obtained.

Welcome to talk about 123-11-5, If you have any questions, you can contact Dejardin, C; Renou, A; Maddaluno, J; Durandetti, M or send Email.. COA of Formula: C8H8O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Characterization and potential utilization of extracts and pyrolyzates from Jasminum nudiflorum Lindl. Bark WOS:000640934700009 published article about SECOIRIDOID GLUCOSIDES; ANTIBACTERIAL ACTIVITY; CHEMICAL-COMPOSITION; PYROLYSIS; PRODUCT; BIOMASS; MOLECULES; OIL; ANTIOXIDANT; COMPONENTS in [Gu, Haiping; Lam, Su Shiung; Yue, Xiaochen; Yang, Jun; Peng, Wanxi] Henan Agr Univ, Henan Prov Engn Res Ctr Biomass Value Added Prod, Zhengzhou 450002, Peoples R China; [Foong, Shin Ying; Lam, Su Shiung] Univ Malaysia Terengganu, Inst Trop Aquaculture & Fisheries Akuatrop, Pyrolysis Technol Res Grp, Terengganu 21030, Malaysia in 2021, Cited 75. The Name is (E)-2-Methylbut-2-enoic acid. Through research, I have a further understanding and discovery of 80-59-1. SDS of cas: 80-59-1

Utilization of lignocellulosic biomass is increasingly important. Jasminum nudiflorum Lindl. (JNL) is a widely cultivated landscape plant in China. To evaluate the chemical components, pyrolysis characteristics as well as the potential values of JNL bark for utilization, the components were extracted using methanol, ethanol, and benzene/ethanol (2:1, v/v) and pyrolyzed from room temperature to 300 ?C, respectively. Many components were detected in the extracts and the pyrolyzates of JNL bark and their chemical properties were analyzed. The compounds identified in the extracts and the pyrolyzates of JNL bark included acids, aldehydes, alcohols, esters, ketones, aromatics, saccharides, olefins, and nitrogen-containing compounds. Some of the identified compounds, such as urs-12-en-28-al, 3-(acetyloxy)-, (3.beta.)-, 5-hydroxymethylfurfural, and vanillin, are widely used in the medical, energy, and food industries. The pyrolysis of JNL bark using thermogravimetric (TG) analyzer showed the highest reaction rate occurred at between 200 and 300 ?C where the maximum mass loss was observed. According to the Coats-Redfern method, the calculated apparent activation energy (E) and pre-exponential factor (A) of the pyrolysis process of JNL bark were 52.04 kJ mol- 1 and 3.14 ? 105 min-1, respectively. This research provides information on the components and pyrolysis characteristics of JNL bark, which shows great potential for application in medical, food, and chemical industries.

SDS of cas: 80-59-1. Welcome to talk about 80-59-1, If you have any questions, you can contact Gu, HP; Foong, SY; Lam, SS; Yue, XC; Yang, J; Peng, WX or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Recently I am researching about CRYSTAL-STRUCTURES, Saw an article supported by the Scientific and Technological Research Council of Turkey (TUBITAK)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [112T746]; Hacettepe University Scientific Research Projects Coordination UnitHacettepe University [012D06301001, 1527]; Hacettepe University Technology Transfer CenterHacettepe University. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Salgin-Goksen, U; Telli, G; Erikci, A; Dedecengiz, E; Tel, BC; Kaynak, FB; Yelekci, K; Ucar, G; Gokhan-Kelekci, N. The CAS is 120-14-9. Through research, I have a further understanding and discovery of 3,4-Dimethoxybenzaldehyde. Recommanded Product: 3,4-Dimethoxybenzaldehyde

Thirty compounds having 1-[2-(5-substituted-2-benzoxazolinone-3-yl) acetyl]-3,5-disubstitutedphenyl-2-pyrazoline structure and nine compounds having N’-(1,3-disubstitutedphenylallylidene)-2-(5-substituted- 2-benzoxazolinone-3-yl)-acetohydrazide skeleton were synthesized and evaluated as monoamine oxidase (MAO) inhibitors. All of the compounds exhibited selective MAO-A inhibitor activity in the nanomolar or low micromolar range. The results of the molecular docking for hydrazone derivatives supported the in vitro results. Five compounds, 6 (0.008 mu M, Selectivity Index (SI): 9.70 x 10(-4)), 7 (0.009 mu M, SI: 4.55 x 10(-5)), 14 (0.001 mu M, SI: 8.00 x 10(-4)), 21 (0.009 mu M, SI: 1.37 x 10(-5)), and 42 (0.010 mu M, SI: 5.40 x 10(-6)), exhibiting the highest inhibition and selectivity toward hMAO-A and nontoxic to hepatocytes were assessed for antidepressant activity as acute and subchronic in mice. All of these five compounds showed significant antidepressant activity with subchronic administration consistent with the increase in the brain serotonin levels and the compounds crossed the blood-brain barrier according to parallel artificial membrane permeation assay. Compounds 14, 21, and 42 exhibited an ex vivo MAO-A profile, which is highly consistent with the in vitro data.

COA of Formula: C9H10O3. Bye, fridends, I hope you can learn more about C9H10O3, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Selective hydrogenolysis of lignin-derived aryl ethers over Co/C@N catalysts WOS:000510524900061 published article about METAL-ORGANIC FRAMEWORK; HYDRODEOXYGENATION; BIOMASS; COBALT; EFFICIENT; SPECTRA; BONDS; CYCLOHEXANOLS; CONVERSION; REDUCTION in [Song, Qing-Lu; Zhao, Yun-Peng; Wu, Fa-Peng; Li, Guo-Sheng; Fan, Xing; Cao, Jing-Pei; Wei, Xian-Yong] China Univ Min & Technol, Minist Educ, Key Lab Coal Proc & Efficient Utilizat, Xuzhou 221116, Jiangsu, Peoples R China; [Zhao, Yun-Peng] Taiyuan Univ Technol, Minist Sci & Technol, Training Base, State Key Lab Coal Sci & Technol Jointly Construc, Taiyuan 030024, Peoples R China; [Wang, Rui-Yu] China Univ Min & Technol, Low Carbon Energy Inst, Xuzhou 221008, Jiangsu, Peoples R China in 2020.0, Cited 50.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6. Quality Control of m-Methoxyphenol

Low aromaticity and a large number of oxygen-bridged bonds among the aromatic structural units of lignin make it possible to obtain chemicals directly. A novel Co/C@N catalyst with high activity towards hydrogenolysis of lignin-derived aryl ethers was synthesized according to the pyrolysis process of a predesigned ZIF-67. According to the results of characterization by powder X-ray diffraction (XRD), N-2 adsorption-desorption, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS), Co was reduced by the carbonized organic linker of ZIF-67, and N was doped into the carbon skeleton of the catalyst. The effects of holding time, temperature, and initial H-2 pressure on the catalytic performance of Co/C@N were evaluated in the selective hydrogenolysis of benzyl phenyl ether (BPE). BPE was completely converted and the selectivity of monomer reached to 98.2% under optimized reaction conditions. The C-alk-O bond in BPE was first dissociated to form toluene and phenol, and then phenol was rapidly hydrogenated to form cyclohexanol. Furthermore, the Co/C@N catalyst shows high activity for hydroprocessing and selective cleavage of other lignin-derived aryl ethers, including phenylethyl phenyl, diphenyl ether, dibenzyl ether, dinaphthalene ether, guaiacol, anisole and veratrole. (C) 2019 Elsevier Ltd. All rights reserved.

Bye, fridends, I hope you can learn more about C7H8O2, If you have any questions, you can browse other blog as well. See you lster.. Quality Control of m-Methoxyphenol

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Authors Kumar, A; Thallada, B in ROYAL SOC CHEMISTRY published article about FUEL-RANGE HYDROCARBONS; SELECTIVE HYDRODEOXYGENATION; PHASE HYDRODEOXYGENATION; AQUEOUS-PHASE; REACTION PATHWAYS; EFFICIENT; GUAIACOL; RU; HYDROGENATION; CYCLOHEXANOL in [Kumar, Adarsh; Thallada, Bhaskar] CSIR Indian Inst Petr IIP, Thermocatalyt Proc Area TPA, Mat Resource Efficiency Div MRED, Dehra Dun 248005, Uttarakhand, India; [Kumar, Adarsh; Thallada, Bhaskar] Acad Sci & Innovat Res AcSIR, Ghaziabad, Uttar Pradesh, India in 2021.0, Cited 61.0. Application In Synthesis of Mequinol. The Name is Mequinol. Through research, I have a further understanding and discovery of 150-76-5

The synthesis of efficient and engineered noble metal catalysts for selective conversion of waste renewable lignin to valuable chemical building blocks is crucial for the economic viability of current biorefineries. Motivated by the water effect in promoting catalytic activity, hydrous ruthenium oxide (HRO) incorporating acidic systems (H-ZSM5, HY zeolite, gamma-Al2O3, and SiO2) were investigated for selective hydrodeoxygenation of lignin-derived phenols in the aqueous phase. The results indicated that the hydrous form (surface bonded water molecules) of ruthenium and high acidity of the support promote the hydrogenolysis activity of the as-prepared catalysts and increase the yield of alkylated cyclohexanols. Among all catalysts, HRO@Y showed the best performance and afforded the highest selectivity to cyclohexanols. Intensive catalyst characterization demonstrated that in situ metal formation, a large number of acid sites, good metal dispersion, and high adsorption capacity of HRO@Y for polar fractions were responsible for the efficient activity. Water considerably improved the selective hydrodeoxygenation activity of the catalyst by promoting hydrogenation and demethoxylation and hindering dehydration.

About Mequinol, If you have any questions, you can contact Kumar, A; Thallada, B or concate me.. Application In Synthesis of Mequinol

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Effect of precursor pH on structural, magnetic and catalytic properties of CoFe2O4@SiO2 green nanocatalyst WOS:000605133500011 published article about COBALT FERRITE; HYDROTHERMAL SYNTHESIS; NANOPARTICLES; 5-ARYL-1,2,4-TRIAZOLIDINE-3-THIONES; CHEMISTRY; EFFICIENT; SPECTRA; ZNFE2O4; FACILE; FILMS in [Bardapurkar, Pranav P.; Arote, Sandeep A.; Pansambal, Shreyas S.] DJ Malpani Commerce & BN Sarda Sci Coll, SN Arts, Sangamner, Maharashtra, India; [Shewale, Sunil S.] Padmashri Vikhe Patil Coll Arts Sci & Commerce, Loni, Maharashtra, India; [Barde, Nilesh P.] Badrinarayan Barwale Mahavidyalaya, Jalna, Maharashtra, India in 2021, Cited 63. Name: 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Cobalt ferrite is a promising material for many therapeutic applications, photo-catalysis, gas detectors, high-density data storage, etc. Optimization of process parameters has a vital role in tailoring its properties. Present work reports effect of precursor pH on the properties of cobalt ferrite nanoparticles dispersed in silica. Crystallite size shows escalation from 16 to 18.5 nm with increase in pH. Many undesired phases were observed at lower precursor pH. Lattice parameter and particle size distribution showed significant impact of pH. Silica matrix showed momentous change in its structure giving a high porosity structure at pH 9. Magnetic parameters show effects due to gamma-Fe2O3 phase and pH. Effect on catalytic properties was investigated for the synthesis of 5-(4-chlorophenyl)-1,2,4-triazolidine-3-thione. Structural and morphological changes due to change in pH were found to enhance the catalytic yield considerably. Exquisiteness of the material as a catalyst is that it is magnetically separable and can be reused successively, making it an economic and green catalyst. [GRAPHICS] .

Welcome to talk about 123-11-5, If you have any questions, you can contact Bardapurkar, PP; Shewale, SS; Arote, SA; Pansambal, SS; Barde, NP or send Email.. SDS of cas: 123-11-5

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Computed Properties of C8H8O2. In 2019.0 FITOTERAPIA published article about ROOTS in [Kutluay, Vahap Murat; Saracoglu, Iclal] Hacettepe Univ, Fac Pharm, Dept Pharmacognosy, TR-06100 Ankara, Turkey; [Ishiuchi, Kan’ichiro; Makino, Toshiaki] Nagoya City Univ, Grad Sch Pharmaceut Sci, Dept Pharmacognosy, Nagoya, Aichi 4678603, Japan in 2019.0, Cited 25.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

The phytochemical studies on the aerial parts of Digitalis davisiana Heywood led to the isolation of three undescribed phenylethanoid glycosides named as digidavisoside A (5), digidavisoside B (7), and davisoside (8), along with 9 known compounds, ferruginoside B (1), isolugrandoside (2), lugrandoside (3), maxoside (4), 3 ””-O-methylmaxoside (6), trans-lamiuside E (9), digiciliside B (10), p-hydroxyacetophenone (11), and chrysoeriol (12). For the first time compound 11 was reported for Digitalis genus. The chemotaxonomical significance of these compounds in Plantaginaceae family was evaluated and 3′-O-glucosyl substituted phenylethanoid glycosides 4-8 and 10 were found to be chemotaxonomically important for the family. Cytotoxic activity of the aqueous fraction of the methanolic extract was also tested against HEp-2 (human larynx epidermoid carcinoma) and HepG2 (human hepatocellular carcinoma) cancer cell lines. The aqueous fraction showed stronger cytotoxicity on HEp-2 cells than on HepG2. Therefore, the cytotoxic activity of 1-4, 6, 7 and 9 were tested against HEp-2 and L929 (mouse fibroblast cell) cell lines. Other isolated compounds could not be tested due to their insufficient amount. The results were evaluated in the point of structure-activity relationships. IC50 values against HEp-2 cells were established in a range of 71.9-220 mu M. Maxoside (4), isolugrandoside (2) and lugrandoside (3) showed higher cytotoxicity against HEp.2 cell line than other isolated compounds.

Computed Properties of C8H8O2. Welcome to talk about 99-93-4, If you have any questions, you can contact Kutluay, VM; Ishiuchi, K; Makino, T; Saracoglu, I or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

In 2019.0 MOLECULES published article about TRANSITION-METAL-COMPLEXES; MOLECULAR DOCKING; RUTHENIUM(II) COMPLEXES; ANTICANCER ACTIVITY; CYTOTOXIC ACTIVITY; BINDING PROPERTIES; THERMAL-PROPERTIES; CRYSTAL-STRUCTURE; NI(II) COMPLEX; BSA-BINDING in [Li, Jiahe; Liu, Rongping; Jiang, Jinzhang; Liang, Xing; Huang, Ling; Ma, Zhen] Guangxi Univ, Sch Chem & Chem Engn, Nanning 530004, Guangxi, Peoples R China; [Li, Jiahe; Ma, Zhen] Univ Lisbon, Inst Super Tecn, Ctr Quim Estrutural, Av Rovisco Pais, P-1049001 Lisbon, Portugal; [Huang, Gang; Pan, Lixia] Guangxi Acad Sci, State Key Lab Nonfood Biomass & Enzyme Technol, Natl Engn Res Ctr Nonfood Biorefinery, Nanning 530004, Guangxi, Peoples R China; [Chen, Hailan] Guangxi Univ, Sch Anim Sci & Technol, Nanning 530004, Guangxi, Peoples R China in 2019.0, Cited 85.0. The Name is 3-Hydroxybenzaldehyde. Through research, I have a further understanding and discovery of 100-83-4. Category: indole-building-block

A series of ZnCl2 complexes (compounds 1-10) with 4′-(substituted-phenyl)-2,2′:6′,2 ”-terpyridine that bears hydrogen (L-1), p-methyl (L-2), p-methoxy (L-3), p-phenyl (L-4), p-tolyl (L-5), p-hydroxyl (L-6), m-hydroxyl (L-7), o-hydroxyl (L-8), p-carboxyl (L-9), or p-methylsulfonyl (L-10) were prepared and then characterized by H-1 NMR, electrospray mass-spectra (ESI-MS), IR, elemental analysis, and single crystal X-ray diffraction. In vitro cytotoxicity assay was used to monitor the antiproliferative activities against tumor cells. Absorption spectroscopy, fluorescence titration, circular dichroism spectroscopy, and molecular modeling studied the DNA interactions. All of the compounds display interesting photoluminescent properties and different maximal emission peaks due to the difference of the substituent groups. The cell viability studies indicate that the compounds have excellent antiproliferative activity against four human carcinoma cell lines, A549, Bel-7402, MCF-7, and Eca-109, with the lowest IC50 values of 0.33 (10), 0.66 (6), 0.37 (7), and 1.05 (7) mu M, respectively. The spectrophotometric results reveal that the compounds have strong affinity binding with DNA as intercalator and induce DNA conformational transition. Molecular docking studies indicate that the binding is contributed by the pi…pi stacking and hydrogen bonds, providing an order of nucleotide sequence binding selectivity as ATGC > ATAT > GCGC. These compounds intercalate into the base pairs of the DNA of the tumor cells to affect their replication and transcription, and the process is supposed to play an important role in the anticancer mechanism.

Welcome to talk about 100-83-4, If you have any questions, you can contact Li, JH; Liu, RP; Jiang, JZ; Liang, X; Huang, L; Huang, G; Chen, HL; Pan, LX; Ma, Z or send Email.. Category: indole-building-block

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles