The synthesis of precursors of labelled neuropeptides

DOI: 10.1002/recl.19831020505

Source and publish data:

Recueil des Travaux Chimiques des Pays-Bas p. 276 - 283 (1983)

Update date:2022-08-03

Topics:

Authors:

Van Nispen

Bijl Bijl

Hendrix Hendrix

Greven Greven

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1002/recl.19831020505

Full text of DOI:10.1002/recl.19831020505

Products guided by the article

Product name:Boc-Gly-Gly-Phe(I)-Met-OMe

Cas No:87325-43-7

R&D Labs maybe for 87325-43-7

Zhongshan Haihong Medicine Co., Ltd.

Contact:86-0760-86925778 （0）18824993998

Address:A7 building,lianyuan road Torch Hi-tech Industrial Development Zone
SuZhou Ascepion Pharmaceuticals, Inc.(expird)

Contact:0512-86881668

Address:Building C,68Xingqing Road,Suzhou,China.
HaiNan Periwinkle Pharmaceutical Co.,Ltd.

website:http://www.cchpharm.com/en/index.html

Contact:020-82208978

Address:Gongye road,Wuzhishan city,HaiNan province
Yangling Ciyuan biotech Co., Ltd.

Contact:86-15802970736

Address:2-1804, International Park Mansion, No.2, South Fengdeng Road, Lianhu District
Wuhan Benjamin Pharmaceutical Chemical Co.,Ltd

Contact:86-27-52341789

Address:Room 1518 B suite, optical valley time square, No 111 Guanshan Road, Hongshan District,Wuhan,Hubei Province,China.

Relevant to this article

Synthesis, base pairing properties and nuclease resistance of oligothymidylate analogs containing methoxyphosphoramidate internucleoside linkages

Doi:10.1080/15257779408013213
(1994)
Synthesis of fused triazolo-imidazole derivatives by sequential van Leusen/alkyne-azide cycloaddition reactions

Doi:10.1016/j.tetlet.2005.10.090
(2005)
Synthesis and biological evaluation of N-(7-indazolyl)benzenesulfonamide derivatives as potent cell cycle inhibitors

Doi:10.1016/j.bmc.2005.09.037
(2006)
Synthesis and antiviral evaluation of cyclic and acyclic 2-methyl-3-hydroxy-4-pyridinone nucleoside derivatives

Doi:10.1021/jm0504306
(2006)
Doi:10.1021/ja01190a059
(1948)
Bafilomycin analogue site-specifically fluorinated at the pharmacophore macrolactone ring has potent vacuolar-type ATPase inhibitory activity

Doi:10.1016/j.tetlet.2016.04.075
(2016)

Article Doi