191736
Pargyline 盐酸盐
99%
别名:
N-甲基-N-2-丙炔基苄胺 盐酸盐, N-甲基-N-丙炔基苄胺 盐酸盐
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关于此项目
线性分子式:
C6H5CH2N(CH3)CH2C≡CH·HCl
化学文摘社编号:
分子量:
195.69
EC Number:
206-175-1
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
3699487
MDL number:
InChI key
BCXCABRDBBWWGY-UHFFFAOYSA-N
InChI
1S/C11H13N.ClH/c1-3-9-12(2)10-11-7-5-4-6-8-11;/h1,4-8H,9-10H2,2H3;1H
SMILES string
Cl[H].CN(CC#C)Cc1ccccc1
assay
99%
mp
160-163 °C (lit.)
Gene Information
human ... MAOA(4128), MAOB(4129)
Biochem/physiol Actions
选择性 MAO-B 抑制剂。
法规信息
新产品
此项目有
Masahiro Yoshida et al.
The Journal of organic chemistry, 78(4), 1687-1692 (2013-02-01)
The reaction of propargylic carbonates with 4-hydroxy-2-pyrones in the presence of a palladium catalyst is described. By the choice of the reaction temperature, two types of the substituted furo[3,2-c]pyran-4-one derivatives were regioselectively synthesized, respectively.
15N magnetic resonance hyperpolarization via the reaction of parahydrogen with 15N-propargylcholine.
Francesca Reineri et al.
Journal of the American Chemical Society, 134(27), 11146-11152 (2012-06-06)
(15)N-Propargylcholine has been synthesized and hydrogenated with para-H(2). Through the application of a field cycling procedure, parahydrogen spin order is transferred to the (15)N resonance. Among the different isomers formed upon hydrogenation of (15)N-propargylcholine, only the nontransposed derivative contributes to
Highly stereoselective synthesis of tertiary propargylic centers and their isomerization to enantiomerically enriched allenes.
José Luis García Ruano et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(32), 9775-9779 (2012-08-01)
Lavinia Boccia et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34(11), 15448-15461 (2020-09-29)
The LPBN (lateral parabrachial nucleus) plays an important role in feeding control. CGRP (calcitonin gene-related peptide) LPBN neurons activation mediates the anorectic effects of different gut-derived peptides, including amylin. Amylin and its long acting analog sCT (salmon calcitonin) exert their
Shauna N Vasilatos et al.
Carcinogenesis, 34(6), 1196-1207 (2013-01-29)
Our previous studies demonstrated that lysine-specific demethylase 1 (LSD1) and histone deacetylases (HDACs) closely interact in controlling growth of breast cancer cells. However, the underlying mechanisms are largely unknown. In this study, we showed that knockdown of LSD1 expression (LSD1-KD)
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