68360-22-5Relevant academic research and scientific papers
Synthesis and analysis of dihydrotetrabenazine derivatives as novel vesicular monoamine transporter 2 inhibitors
Du, Guangying,Tian, Jingwei,Wang, Hongbo,Wang, Wenyan,Yang, Yifei,Ye, Liang,Yu, Dawei,Zhang, Rui,Zhu, Xiaoyin,Zou, Fangxia
, (2021/07/31)
Vesicular monoamine transporter 2 (VMAT2) is essential for synaptic transmission of all biogenic amines in the brain including serotonin, norepinephrine, histamine, and dopamine (DA). Given its crucial role in the neurophysiology and pharmacology of the central nervous system, VMAT2 is recognized as an important therapeutic target for various neurological disorders such as tardive dyskinesia (TD). Here, a novel series of dihydrotetrabenazine derivative analogs were designed and synthesized to evaluate their effects on [3H]dihydrotetrabenazine (DTBZ) binding and [3H]DA uptake at VMAT2. Of these analogs, compound 13e showed a high binding affinity for VMAT2 (IC50 = 5.13 ± 0.16 nM) with excellent inhibition of [3H]DA uptake (IC50 = 6.04 ± 0.03 nM) in striatal synaptosomes. In human liver microsomes, 13e was more stable (T1/2 = 161.2 min) than other reported VMAT2 inhibitors such as DTBZ (T1/2 = 119.5 min). In addition, 13e effectively inhibited the spontaneous locomotor activity (percent inhibition at 3 μmol/kg = 64.7%) in Sprague-Dawley rats. Taken together, our results indicate that 13e might be a promising lead compound for the development of novel treatments of TD.
The synthesis of precursor of FP- (+) DTBZ
Wu, Caijiao,Li, Hui,Sun, Feiyang,Bao, Changshun,Bao, Xuefei,Chen, Guoliang
, p. 3218 - 3225 (2019/09/13)
A synthetic route to the precursor of FP- (+) DTBZ was disclosed, in which 3-hydroxy-4-methoxybenzaldehyde was employed as a starting material. In the method, the benzyl-protecting protocol and the in-situ Diels-Alder reaction made the procedure more practical because of the mild conditions for selectively deprotection and the accelerated reaction process.
Synthesizing method of 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline
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Paragraph 0031-0033; 0040-0047; 0063-0059; 0065-0068, (2019/08/07)
The invention discloses a synthesizing method of 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline in the field of medicine synthesizing. The synthesizing method includes: dissolving 3-benzyloxy-4- methoxy phenylethylamine or hydrochloride thereof in the mixed liquid of glacial acetic acid and trifluoroacetic acid to generate the 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline under the effect of hexamethylene tetramine in a closed-loop manner. The synthesizing method has the advantages that the 3-benzyloxy-4- methoxy phenylethylamine is subjected to one-step closed-loop reaction under the effect ofhexamethylene tetramine to prepare the target product, and the synthesizing route is short; the 3-benzyloxy-4- methoxy phenylethylamine and the 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline are purified in a recrystallization manner to prepare the hydrochloride of the 3-benzyloxy-4- methoxy phenylethylamine and the 6-benzyloxy-7-methoxy-3,4-dihydroisoquinoline, the purification operation is simple, and the obtained compound is stable in property and can be conveniently stored for a long time.
Synthesis and biological evaluation of a D-ring-contracted analogue of lamellarin D
Colligs, Vanessa,Hansen, Steven Peter,Imbri, Dennis,Seo, Ean-Jeong,Kadioglu, Onat,Efferth, Thomas,Opatz, Till
, p. 6137 - 6148 (2017/09/30)
A D-ring contracted analogue of the strongly cytotoxic marine pyrrole alkaloid lamellarin D was synthesized and investigated for its antiproliferative action towards a wild type and a multidrug resistant (MDR) cancer cell line. The compound was found to inhibit tumor cell growth at submicromolar concentrations and showed a lower relative resistance in the MDR cell line than the antitumor drug camptothecin to which lamellarin D shows cross resistance and with which lamellarin D shares the same binding site.
(+)-9-Benzyloxy-α-dihydrotetrabenazine as an important intermediate for the VMAT2 imaging agents: Absolute configuration and chiral recognition
Liu, Chunyi,Chen, Zhengping,Li, Xiaomin,Tang, Jie,Qin, Xiaofeng
, p. 215 - 223 (2013/08/22)
This article reports, for the first time, on the absolute configuration of (+)-9-benzyloxy-α-dihydrotetrabenazine (8), as determined from the perspective of X-ray crystallography. Compound 8 was prepared by a six-step reaction using 3-benzyloxy-4-methoxybenzaldehyde (1) as a starting material. The X-ray crystal diffraction structure of two compounds, racemic 9-benzyloxy-tetrabenazine (5) and the diastereomeric salt of compound 8, is also described for the first time in this article. The X-ray results and the chiral HPLC helped elucidate that compound 8 has an absolute configuration as 2R,3R,11bR. The crystal structure of racemic compound 5 contains two symmetry- independent molecules in the unit cell. Interestingly, while they are structural isomers, they are enantiomers, too, i.e., in solution, because they are not mirror images of each other in the crystal lattice. In order to elucidate the intermolecular interaction mechanism of the diastereomeric salt of compound 8, its crystal packing was investigated with regard to the weak interactions, such as salt bridge, OH.O and CH.O hydrogen bonds, and intermolecular CH.π interaction. The results showed that the carbonyl-assisted salt bridges and the OH.O hydrogen bonds formed polar columns in the crystal structure of the diastereomeric salt of compound 8, resembling butterflies with open wings as viewed along the c-axis. These polar columns were extended to three-dimensional network by intermolecular CH.O hydrogen bonds and intermolecular CH.π interactions. Chirality, 2013. 2013 Wiley Periodicals, Inc. Copyright
Ruthenium-catalysed Oxidation of Secondary Amines to Imines using t-Butyl Hydroperoxide
Murahashi, Shun-Ichi,Naota, Takeshi,Taki, Hiroshi
, p. 613 - 614 (2007/10/02)
The ruthenium-catalysed oxidation of secondary amines with t-butyl hydroperoxide under mild conditions affords the corresponding imines in high yields.
