1.Analysis of Dimethyltryptamine in Captured Suspicious Substances:Three Case Reports.
Jin Lun XU ; Si Yang HE ; Di QIAO ; Zhang Jun GU ; Chen LIANG ; Chun Fang NI
Journal of Forensic Medicine 2021;37(4):524-526
Abstract.
N,N-Dimethyltryptamine
2.Studies on constituents of rootsanel leaves from Desmodium blandum and their cytotoxic activity against growth of several tumor cells.
Ning GAN ; Xin YANG ; Tian-Hua LI ; Ping HE
China Journal of Chinese Materia Medica 2008;33(18):2077-2080
OBJECTIVETo investigate the chemical constituents of Desmodium blandum and their cytotoxic activity against the growth of several tumor cells.
METHODVarious chromatographic techniques including silica gel, Sephadex LH-20 column chromatography were employed for the isolation and purification of the constituents. The structures of compounds were elucidated by spectral analyses (IR, UV, NMR, MS). Their cytotoxic activity was then studied.
RESULTEight compounds were isolated from the stems of D. blandum and identified as N, N-dimethyltryptamine (1), 5-methoxy-N, N-dimethyltryptamine (2), citrusinol (3), yukovanol (4), (Z)-1-(4-hydroxy-2, 3-dimethoxyphenyl)-3-(4-hydroxyphenyl) propene (5), (Z)-1-(3-hydroxy-2, 4-dimethoxy-phenyl)-3-(4-hydroxy-3-methoxy-phenyl) propene (6), methylprotocatechuate (7), katuranin (8).
CONCLUSIONAmong these compounds, compound 6 was isolated from D. blandum for the first time. In the MTT test, compounds 2 and 6 exhibit cytotoxic activities against the KB cell, and compounds 3 and 6 exhibit the same activities against the HepG2 cell.
Alkenes ; chemistry ; pharmacology ; Benzene Derivatives ; chemistry ; pharmacology ; Cell Line, Tumor ; Cell Proliferation ; drug effects ; Drugs, Chinese Herbal ; chemistry ; toxicity ; Fabaceae ; chemistry ; Humans ; Magnetic Resonance Spectroscopy ; Molecular Structure ; N,N-Dimethyltryptamine ; chemistry ; Plant Leaves ; chemistry ; Spectrometry, Mass, Electrospray Ionization ; Spectrophotometry, Infrared
3.Synthesis and biological effects of N-hydroxy-methyl-5-bromoisatine and derivatives
Pharmaceutical Journal 1999;282(10):4-5
By bromation of isatin 5-bromoisatin (I) was obtained. On boiling (I) with 4% formaldehyde solution for short period of time, a compound was isolated which has been characterized as N-hydroxymethyl-5-bromoisatin (II). By condensation of I with various H2N-B compounds, 6 derivatives (III-VIII) were formed. The structures of the obtained products were characterized by IR spectroscopy (II was characterized by MS, 1H.NMR). The synthesized compounds were tested for biological activities such as antibacterial and antifungal. Among these, two compounds (I, II) showed an antibacterial activity on 8 strains of bacteria. Compound VI showed an antibacterial activity on 3 strains of bacteria. Compound VI showed an antibacterial activity on 3 strains of bacteria.
Bufotenin
;
Anti-Bacterial Agents