Development and validation of a reverse phase HPLC method for SHetA2, a novel anti-cancer drug, in mouse biological samples-Reference-Cited by-同舟云学术

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Development and validation of a reverse phase HPLC method for SHetA2, a novel anti-cancer drug, in mouse biological samples

Published:2019-06 Issue: Volume:170 Page:124-131
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Kukut Hatipoglu Manolya,Mahjabeen Sanjida,Garcia-Contreras Lucila

Funder

Gynecological Oncology Drug Development Fund

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference27 articles.

1. Flexible heteroarotinoid (Flex-Het) SHetA2 inhibits angiogenesis in vitro and in vivo;Myers;Invest. New Drugs,2009

2. CAAT/enhancer binding protein homologous protein-dependent death receptor 5 induction is a major component of SHetA2-induced apoptosis in lung cancer cells;Lin;Cancer Res.,2008

3. Development of flexible-heteroarotinoids for kidney cancer;Liu;Mol. Cancer Ther.,2009

4. Flexible heteroarotinoids (Flex-Hets) exhibit improved therapeutic ratios as anti-cancer agents over retinoic acid receptor agonists;Benbrook;Invest. New Drugs,2005

5. Cyclin D1 degradation is sufficient to induce G1 cell cycle arrest despite constitutive expression of cyclin E2 in ovarian cancer cells;Masamha;Cancer Res.,2009

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2. Domino Synthetic Strategy for Tetrahydrothiopyran Derivatives from Benzaldehydes, 2-Acetylfuran/2-Acetylthiophene, and Sodium Sulfide;The Journal of Organic Chemistry;2020-06-12

3. Vaginal Suppositories Containing SHetA2 to Treat Cervical Dysplasia: Pharmacokinetics of Daily Doses and Preliminary Safety Profile;Journal of Pharmaceutical Sciences;2020-06

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