quinoline-3-carboxamide and Neoplasms

quinoline-3-carboxamide has been researched along with Neoplasms* in 2 studies

Reviews

1 review(s) available for quinoline-3-carboxamide and Neoplasms

ArticleYear
Progress in the development of kynurenine and quinoline-3-carboxamide-derived drugs.
    Expert opinion on investigational drugs, 2020, Volume: 29, Issue:11

    The diverse neuro- and immunomodulatory effects of kynurenine pathway (KP) enzymes and metabolites exert offer possibilities for intervention in diseases such as autoimmunity, neurodegeneration, and neoplastic processes.. This review focuses on data obtained from the preclinical and clinical use of a KP metabolite analog and structurally related compounds. 4-Cl-KYN has completed clinical trials in depression without success. However, the good safety data give hope for further trials in suicide prevention, neuropathic pain, and dyskinesia. Quinoline-3-carboxamide derivatives laquinimod, paquinimod, and tasquinimod show structural similarities to kynurenines. Laquinimod and paquinimod show promising results in the treatment of autoimmune diseases, tasquinimod is considered primarily as an anti-cancer drug. Data available until 31 May 2020 at Clinicaltrials.gov and PubMed have been reviewed.

    Topics: Animals; Antineoplastic Agents; Autoimmune Diseases; Drug Development; Humans; Kynurenine; Neoplasms; Neurodegenerative Diseases; Quinolines

2020

Other Studies

1 other study(ies) available for quinoline-3-carboxamide and Neoplasms

ArticleYear
Synthesis and cytotoxicity of thieno[2,3-b]quinoline-2-carboxamide and cycloalkyl[b]thieno[3,2-e]pyridine-2-carboxamide derivatives.
    Bioorganic & medicinal chemistry, 2016, Mar-01, Volume: 24, Issue:5

    Seventy nine derivatives of thieno[2,3-b]quinolines, tetrahydrothieno[2,3-b]quinoline, dihydrocyclopenta[b]thieno[3,2-e]pyridine, cyclohepta[b]thieno[3,2-e]pyridine and hexahydrocycloocta[b]thieno[3,2-e]pyridine were either synthesized or obtained commercially and tested for their antiproliferative activity against HCT116, MDA-MB-468 and MDA-MB-231 human cancer cell lines. The most potent eight compounds were active against all cell lines with IC50 values in the 80-250nM range. In general hexahydrocycloocta[b]thieno[3,2-e]pyridines were most active with increasing activity observed as larger cycloalkyl rings were fused to the pyridine ring.

    Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Drug Screening Assays, Antitumor; Humans; Neoplasms; Quinolines; Structure-Activity Relationship; Thienopyridines

2016