Human chorionic gonadotropin. V. Synthesis of a triacontapeptide corresponding to the C-terminal sequence 116-145 of the β-subunit of human chorionic gonadotropin (hCG)

DOI: 10.1248/cpb.28.2714

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2714 - 2719 (1980)

Update date:2022-08-02

Topics:

Authors:

Okada Okada

Iguchi Iguchi

Yagyu Yagyu

et al. et al.

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

Article abstract of DOI:10.1248/cpb.28.2714

Full text of DOI:10.1248/cpb.28.2714

NII-Electronic Library Service

Products guided by the article

Product name:Hydrazinecarboxylic acid, 2-(2-amino-3-hydroxy-1-oxopropyl)-, 1,1-dimethylethyl ester, (S)-

Cas No:52615-95-9

R&D Labs maybe for 52615-95-9

Suqian Ruixing Chemical Co., Ltd.

Contact:+86-527-80805666（总机）;84836008(销售)

Address:3 Jingsilu, Zone north, Hubin Xincheng Development Park, Suqian, China
Shijiazhuang Haitian Amino Acid Co., Ltd.

Contact:+86-311-88908111

Address:Shijiazhuang Hebei province,China
STAR SYNTHESIS CO.,LIMITED

Contact:+(852) 301-98033

Address:Flat C, 23/F, Lucky Plaza, 315-321 Lockhart Road, Wan Chai, Hong Kong
Nanjing Samwon International Limited

Contact:+86-25-84873444

Address:1108, BLDG B, New Century Plaza, No 1, South Taiping Rd.,
Jinan Yijialian Economic and Trade Development Co., Ltd.

Contact:+86 0531-66729596

Address:jinan

Relevant to this article

Remarkable catalytic effect of H⁺ in Michael-type additions of anilines to 3-butyn-2-one

Doi:10.1016/S0040-4020(01)00981-4
(2001)
Doi:10.1021/jo01062a617
(1961)
An enantioselective synthesis of the C₁-C₉ segment of antitumor macrolide peloruside A

Doi:10.1016/S0040-4039(03)00744-5
(2003)
Doi:10.1007/BF00502444
()
Synthesis of thiophene/phenylene co-oligomers. V [1]. Functionalization at molecular terminals toward optoelectronic device applications

Doi:10.1002/jhet.5570440417
(2007)
Oxazolo[4,5-b]pyridine-Based Piperazinamides as GSK-3β Inhibitors with Potential for Attenuating Inflammation and Suppression of Pro-Inflammatory Mediators

Doi:10.1002/ardp.201700022
(2017)

Article Doi