✦ LIBER ✦

Synthesis and Biological Evaluation of Potent, Selective, Hexapeptide CCK-A Agonist Anorectic Agents

✍ Scribed by Pierson, M. Edward; Comstock, Jeanne M.; Simmons, Roy D.; Kaiser, Frederick; Julien, Ronald; Zongrone, John; Rosamond, James D.

Book ID: 125975618
Publisher: American Chemical Society
Year: 1997
Tongue: English
Weight: 218 KB
Volume: 40
Category: Article
ISSN: 0022-2623
DOI: 10.1021/jm970477u

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and biological activities of p

Synthesis and biological activities of peptidomimetic analogues of compound A71623, a potent and selective CCK-A receptor agonist

✍ Jean-Christophe Califano; Laurent Goullieux; Muriel Amblard; Jean-Alain Fehrentz 📂 Article 📅 1997 🏛 Springer Netherlands 🌐 English ⚖ 274 KB

Synthesis and biological activities of p

Synthesis and biological activities of peptidomimetic analogues of compound A71623, a potent and selective CCK-A receptor agonist

✍ Jean-Christophe Califano; Laurent Goullieux; Muriel Amblard; Jean-Alain Fehrentz 📂 Article 📅 1997 🏛 Springer Netherlands 🌐 English ⚖ 75 KB

Synthesis and Biological Evaluation of B

Synthesis and Biological Evaluation of Benzothiazole Derivatives as Potent Antitumor Agents.

✍ Yuichi Sugano; et al. et al. 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 9 KB 👁 2 views

Synthesis and biological evaluation of b

Synthesis and biological evaluation of baicalein derivatives as potent antitumor agents

✍ Luo, Rong; Wang, Jubo; Zhao, Li; Lu, Na; You, Qidong; Guo, Qinglong; Li, Zhiyu 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 1014 KB

Synthesis and biological evaluation of b

Synthesis and biological evaluation of benzothiazole derivatives as potent antitumor agents

✍ Masao Yoshida; Ichiro Hayakawa; Noriyuki Hayashi; Toshinori Agatsuma; Youko Oda; 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 259 KB

Synthesis and biological evaluation of b

Synthesis and biological evaluation of benzothiazole derivatives as potent antitumor agents

✍ Masao Yoshida; Ichiro Hayakawa; Noriyuki Hayashi; Toshinori Agatsuma; Youko Oda; 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 259 KB

Based on 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid[2-(cyclohexanecarbonylamino)benzothiazol-6-yl]amide (1), which shows selective cytotoxicity against tumorigenic cell lines, 2,6-dichloro-N-[2-(cyclopropanecarbonylamino)benzothiazol-6yl]benzamide (13b) was designed and synthesized as a biologic