- A facile and efficient route to one-pot synthesis of new cyclophanes using vinamidinium salts
-
In this study, an efficient method for the synthesis of new cyclophanes (5a-f,6a-g) through the condensation of 1,4-phenylenedimethanamine (3) or 2,3,5,6-tetramethylbenzene-1,4-diamine (4) with 2-substituted vinamidiniums (2a-g) is described. The cyclopha
- Golzar, Nooshin,Mehranpour, Abdolmohammad,Nowrouzi, Najmeh
-
-
Read Online
- Synthetic utility of vilsmeier reagents: Formation of vinamidinium salts from acyl ureas
-
Attempted synthesis of uracil derivatives (2) from acyl ureas (1) resulted in the formation of vinamidinium salts (3) which can he hydrolysed to give dialdehydes.
- Selvi, Srinivasan,Perumal, Paramasivan T.
-
-
Read Online
- Synthesis of new metal-free 1,2,4,5,9,10,12,13-octaaza[16]annulene derivatives using the reaction of vinamidinium salts with thiocarbohydrazide
-
A new series of marcocyclic ligands, 1,2,4,5,9,10,12,13-octaaza[16]annulene derivatives were synthesized by using the condensation reaction of the correspondingly [2+2] 2-heteroaryl-substituted vinamidinium salts or phenyl vinamidinium salts and derivativ
- Sabet, Askar,Mehranpour, Abdolmohammad
-
p. 833 - 840
(2021/01/12)
-
- Preparation of 2,5-disubstituted pyrimidines from vinamidinium salts and synthesis of novel disulfane derivatives
-
Novel pyrimidine derivatives were prepared from the reaction of 2-substituted 1,3-bis(dimethylamino)-trimethinium salts with thiourea or guanidine in the presence of ethyl-diisopropylamine in ethanol at reflux, and also some 5-substituted pyrimidine-2-thi
- Rafiee Samani, Ziba,Mehranpour, Abdolmohammad,Hasaninejad, Alireza
-
supporting information
p. 2150 - 2156
(2020/03/10)
-
- S - Cis Diene Conformation: A New Bathochromic Shift Strategy for Near-Infrared Fluorescence Switchable Dye and the Imaging Applications
-
In this paper, we present a novel charge-free fluorescence-switchable near-infrared (IR) dye based on merocyanine for target specific imaging. In contrast to the typical bathochromic shift approach by extending π-conjugation, the bathochromic shift of our merocyanine dye to the near-IR region is due to an unusual S-cis diene conformer. This is the first example where a fluorescent dye adopts the stable S-cis conformation. In addition to the novel bathochromic shift mechanism, the dye exhibits fluorescence-switchable properties in response to polarity and viscosity. By incorporating a protein-specific ligand to the dye, the probes (for SNAP-tag and hCAII proteins) exhibited dramatic fluorescence increase (up to 300-fold) upon binding with its target protein. The large fluorescence enhancement, near-IR absorption/emission, and charge-free scaffold enabled no-wash and site-specific imaging of target proteins in living cells and in vivo with minimum background fluorescence. We believe that our unconventional approach for a near-IR dye with the S-cis diene conformation can lead to new strategies for the design of near-IR dyes.
- Chen, Hsiang-Jung,Chew, Chee Ying,Chang, En-Hao,Tu, Yu-Wei,Wei, Li-Yu,Wu, Bo-Han,Chen, Chien-Hung,Yang, Ya-Ting,Huang, Su-Chin,Chen, Jen-Kun,Chen, I-Chia,Tan, Kui-Thong
-
supporting information
p. 5224 - 5234
(2018/04/23)
-
- Design, synthesis and biological evaluation of some novel N-arylpyrazole derivatives bearing the sulfonamide moiety as cytotoxic agents
-
A series of novel N-arylpyrazole derivatives (4a–4l) bearing the sulfonamide moiety were synthesized by the condensation reaction of 1,3-dicarbonyl compounds with 4-hydrazinylbenzenesulfonamide. The structures of the obtained compounds were established on
- Duan, Xiaobo,Wang, Yingxing,Feng, Weipei,Yang, Yaxing,Li, Hongyan,Li, Shenghui,Yang, Xiaobing,Zhang, Jinchao,Wang, Shuxiang,Zhou, Guoqiang,Zhou, Chuanqi
-
p. 271 - 281
(2017/01/14)
-
- Synthesis, anticancer activity and DNA-binding properties of novel 4-pyrazolyl-1,8-naphthalimide derivatives
-
A novel series of 4-pyrazolyl-1,8-naphthalimide derivatives have been designed and facilely synthesized. For anticancer activity in vitro, most of the compounds were found to be more toxic against human mammary cancer cells (MCF-7) than human cervical car
- Li, Shenghui,Xu, Shengjie,Tang, Yonghe,Ding, Shan,Zhang, Jinchao,Wang, Shuxiang,Zhou, Guoqiang,Zhou, Chuanqi,Li, Xiaoliu
-
supporting information
p. 586 - 590
(2014/01/23)
-
- Synthesis and biological evaluation of some novel N-arylpyrazole derivatives as cytotoxic agents
-
A series of novel N-arylpyrazole derivatives, 5a-5i, were achieved from substituted phenylacetic acid via Vilsmeier-Haack reaction, hydrolysis, condensation, and aromatic substitution reaction. Their chemical structures were confirmed by 1H NMR
- Li, Shenghui,Xu, Shengjie,Ding, Shan,Zhang, Jinchao,Wang, Shuxiang,Li, Xiaoliu
-
p. 1459 - 1468
(2014/05/06)
-
- Regioselective synthesis of novel 4,5-diaryl functionalized 3,4-dihydropyrimidine-2(1H)-thiones via a non-Biginelli-type approach and evaluation of their in vitro anticancer activity
-
An easy and novel approach to synthesize 4,5-diaryl functionalized 3,4-dihydropyrimidine-2(1H)-thiones via addition of aryllithiums to 5-aryl substituted pyrimidine-2(1H)-thiones, which could be regarded as a method complementary to the most widely used Biginelli-type synthesis, is described. In the reaction of aryllithiums with N-(Me)Bn substituted pyrimidine-2(1H)-thiones a high degree of regioselectivity of addition, leading to 4-aryl adducts, was achieved. Selected compounds tested for their in vitro anticancer activity against four human cancer cell lines showed the greatest activity against breast cancer (MCF7). 1-Benzyl-4-(3-hydroxyphenyl)-5-phenyl substituted 3,4-dihydropyrimidine-2(1H)-thione (10g) exhibiting 10-fold more potent activity than the best known monastrol (MON) stands as a promising candidate for further scaffold and asymmetric synthesis. the Partner Organisations 2014.
- Sosnicki, Jacek G.,Struk, Lukasz,Kurzawski, Mateusz,Peruzynska, Magdalena,Maciejewska, Gabriela,Drozdzik, Marek
-
p. 3427 - 3440
(2014/05/20)
-
- Design, synthesis and structure-activity relationship studies of morpholino-1H-phenalene derivatives that antagonize Mcl-1/Bcl-2
-
We report herein characteristic studies of Mcl-1 and Bcl-2 dual inhibitors. It was found that a protruding carbonyl group forming hydrogen bond with R263 plays a predominant role compared with the hydrophobic group that occupies the p2 pocket. A series of dual inhibitors representing different parts of the morpholino-1H-phenalene were designed, synthesized and evaluated.
- Li, Xiangqian,Liang, Xiaomeng,Song, Ting,Su, Pengchen,Zhang, Zhichao
-
p. 5738 - 5746
(2015/02/02)
-
- Fragment-based design, synthesis, and biological evaluation of N-substituted-5-(4-isopropylthiophenol)-2-hydroxynicotinamide derivatives as novel Mcl-1 inhibitors
-
We have previously reported a nanomolar inhibitor of antiapoptotic Mcl-1 protein, 3-thiomorpholin-8-oxo-8H-acenaphtho [1,2-b] pyrrole-9-carbonitrile (S1). S1 plays its function by binding to the BH3 groove of Mcl-1. Basing on this spacial structural characteristic, we developed a novel class of Mcl-1 inhibitor using fragment-based drug discovery approach. By dissecting S1, we identified the compound 4 with a 2-hydroxypyridine core as the starting fragment. In the following molecular growth, we used the ligand efficiency evaluation and fit quality score to assess the fragments. A novel potent compound, N-benzyl-5-(4-isopropylthiophenol)-2-hydroxyl nicotinamide (12c), which binds Mcl-1 with an IC50 value of 54 nM was obtained. Compound 12c demonstrated a better aqueous solubility than S1.
- Zhang, Zhichao,Liu, Chengwu,Li, Xiangqian,Song, Ting,Wu, Zhiyong,Liang, Xiaomeng,Zhao, Yan,Shen, Xiaoyun,Chen, Hongbo
-
p. 410 - 420
(2013/04/10)
-
- PYRROLE ANTIFUNGAL AGENTS
-
The invention provides compounds of formula (I), and pharmaceutically and agriculturally acceptable salts thereof; wherein: R1, R2, R3, R4, R5, R6, A1, L1 and n are as defined herein. These compounds and their pharmaceutically acceptable salts are useful in prevention or treatment of a fungal disease. Compounds of formula (I), and agriculturally acceptable salts thereof, may also be used as agricultural fungicides.
- -
-
Page/Page column 102-103
(2009/12/05)
-
- Neurotoxicity studies with the monoamine oxidase B substrate 1-methyl-3-phenyl-3-pyrroline
-
The neurotoxic properties of the parkinsonian inducing agent 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) are dependent on its metabolic activation in a reaction catalyzed by centrally located monoamine oxidase B (MAO-B). This reaction ultimately l
- Ogunrombi, Modupe O.,Malan, Sarel F.,Terre'Blanche, Gisella,Castagnoli, Kay,Castagnoli Jr., Neal,Bergh, Jacobus J.,Petzer, Jacobus P.
-
p. 458 - 467
(2008/02/05)
-
- 5H-BENZO[4,5]CYCLOHEPTA[1,2-B]PYRIDINE NMDA/NR2B ANTAGONISTS
-
Benzo [4,5]cyclohepta[1,2-b]pyridines represented by Formula (I): or pharmaceutically acceptable salts thereof, are effective as NMDA NR2B antagonists useful for relieving pain.
- -
-
Page/Page column 30; 32
(2010/02/07)
-
- CONVERSION OF THIOACETAMIDES, ACETAMIDES, AND ACETONITRILES INTO TRIMETHINIUM SALTS UNDER VILSMEIER CONDITIONS
-
Thioacetamides and N-(3-aminothioacryloyl)formamidines can be transformed to trimethinium salts by the reaction with formamide chlorides.The same products are formed by a modified Vilsmeier-Haack-Arnold reaction of acetamides or acetonitriles.The latter t
- Liebscher, Juergen,Knoll, Alexander,Hartmann, Horst,Anders, Sabine
-
p. 761 - 765
(2007/10/02)
-
- Experiments towards the Preparation of 6-Hydroxy-, 6-Methoxy-, and 6-(Hydroxyphenyl)-2,3-dihydro-1,4-diazepinium Salts and 1,2-Dihydro-5-(hydroxyphenyl)-2-oxopyrimidinium Salts
-
The preparation of a number of 2,3-dihydro-6-(hydroxyphenyl)-1,4-diazepinium salts (11c-f) and of 1,2-dihydro-5-(hydroxyphenyl)-2-oxopyrimidinium salts (17a, b) from 3-(hydroxyphenyl)vinamidinium salts (10b,c) is described.Attempted preparation of a 3-(2-
- Lloyd, Douglas,Reichardt, Christian,Struthers, Margot
-
p. 1368 - 1379
(2007/10/02)
-
- Diazepines. Part 25. Preparation and Properties of 6-Aryl-2,3-dihydro-1,4-diazepinium Salts. Electronic Interaction between the Rings and Steric Inhibition thereof
-
A variety of 6-aryldihydrodiazepinium salts (including also 6-biphenyl-4-yl, 6-α-naphthyl, and 6-N-pyridyl) has been prepared, mostly by reactions of 1,2-diamines with 3-aryl-1,5-diazapentadienium salts.The electron-rich dihydrodiazepinium cation activates the 6-aryl substituent towards electrophilic attack, and halogenation and nitration take place at the p-position.Substituents vicinal to the ring junction in either the six- or seven-membered rings inhibit this reactivity, presumably by preventing coplanarity of the two rings; the 13C n.m.r. spectra of these vicinally substituted compounds also show the lowered electronic interactions between the rings.NN'-diphenyl and NN'-dibenzyl substituents also inhibit electrophilic substitution in the 6-phenyl ring.Solution in deuteriosulphuric acid generates a stable radical species.Nucleophiles (monoamines, diamines, sodium hydroxide) attack the 5- and 7-positions of the diazepine ring.The 13C n.m.r. and mass spectra of these compounds are discussed.
- Lloyd, Douglas,Tucker, Kanwaljit S.,Marshall, Donald R.
-
p. 726 - 735
(2007/10/02)
-