Results 1 - 10 of 43 (Click here to explore results)

<

1

2

3

4

5

>

Synthesis and pharmacological profile of a series of 2,5-substituted-N,N-dimethyltryptamine derivatives as novel antagonists for the vascular 5-HT1B-like receptor. Gerard P. Moloney, Graeme R. Martin, Neil Mathews, Heather Hobbs, Susan Dodsworth, Pang Yih Sang, Cameron Knight, Miles Maxwell, Robert C. Glen , J. Chem. Soc., Perkin Trans. 1 , 1999 , 2713

Platinum-catalyzed cyclization reaction of alkynes: synthesis of azepino[3,4-b]indol-1-ones. Marina Gruit, Anahit Pews-Davtyan, Matthias Beller , Org. Biomol. Chem. , 2011 , 9 , 1148

Synthesis and serotonergic activity of a series of 2-(N-benzyl)carboxamido-5-substituted-N,N-dimethyltryptamine derivatives: novel antagonists for the vascular 5-HT1B-like receptors. Gerard P. Moloney, Graeme R. Martin, Neil Mathews, Heather Hobbs, Susan Dodsworth, Pang Yih Sang, Cameron Knight, Miles Maxwell, Robert C. Glen , J. Chem. Soc., Perkin Trans. 1 , 1999 , 2699

Reactivity of alkynylindole-2-carboxamides in [Pd]-catalysed C–H activation and phase transfer catalysis: formation of pyrrolo-diindolones vs. β-carbolinones. R. N. Prasad Tulichala, K. C. Kumara Swamy , Org. Biomol. Chem. , 2016 , 14 , 4519

Small molecule Hedgehog pathway antagonists. Trieu N. Trinh, Eileen A. McLaughlin, Christopher P. Gordon, Ilana R. Bernstein, Victoria J. Pye, Kate A. Redgrove, Adam McCluskey , Org. Biomol. Chem. , 2017 , 15 , 3046

Catalyst-free and multicomponent synthesis of 3-aminoalkylated indoles via a Mannich-type reaction: multitargeted anticancer, tyrosinase and α-glucosidase inhibitory activities. Thi-Kim-Chi Huynh, Kim-Khanh-Huy Ngo, Hoang-Phuc Nguyen, Hoai-Khanh Dang, Van-Trung Phung, Khac-Minh Thai, Thi-Kim-Dung Hoang , New J. Chem. , 2021 , 45 , 18183

Improved synthesis of 4-/6-substituted 2-carboxy-1H-indole-3-propionic acid derivatives and structure–activity relationships as GPR17 agonists. Younis Baqi, Samer Alshaibani, Kirsten Ritter, Aliaa Abdelrahman, Andreas Spinrath, Evi Kostenis, Christa E. Müller , Med. Chem. Commun. , 2014 , 5 , 86

Synthesis and in vitro pharmacological evaluation of indolyl carboxylic amide analogues as D3 dopamine receptor selective ligands. Zhude Tu, Shihong Li, Aixiao Li, Michelle Taylor, David Ho, Maninder Malik, Robert R. Luedtke, Robert H. Mach , Med. Chem. Commun. , 2013 , 4 , 1283

Design, synthesis, and biological evaluation of novel arylcarboxamide derivatives as anti-tubercular agents. Shahinda S. R. Alsayed, Shichun Lun, Giuseppe Luna, Chau Chun Beh, Alan D. Payne, Neil Foster, William R. Bishai, Hendra Gunosewoyo , RSC Adv. , 2020 , 10 , 7523

Molecular insights into Mmpl3 lead to the development of novel indole-2-carboxamides as antitubercular agents. Rajdeep Ray, Sumit Raosaheb Birangal, Fajeelath Fathima, Helena I. Boshoff, He Eun Forbes, Raghu Chandrashekhar Hariharapura, G. Gautham Shenoy , Mol. Syst. Des. Eng. , 2022 , 7 , 592