Biologically active indolizidine alkaloids

J Zhang, SL Morris‐Natschke, D Ma… - Medicinal Research …, 2021 - Wiley Online Library
Indolizidine alkaloids are chemical constituents isolated from various marine and terrestrial
plants and animals, including but not limited to trees, fungi, ants, and frogs, with a myriad of …

A novel class of antimicrobial drugs selectively targets a Mycobacterium tuberculosis PE-PGRS protein

H Seo, S Kim, HA Mahmud, MI Islam, Y Yoon… - PLoS …, 2022 - journals.plos.org
The continued spread of drug-resistant tuberculosis is one of the most pressing and complex
challenges facing tuberculosis management worldwide. Therefore, developing a new class …

Improving the oral bioavailability of an anti-glioma prodrug CAT3 using novel solid lipid nanoparticles containing oleic acid-CAT3 conjugates

H Wang, L Li, J Ye, R Wang, R Wang, J Hu, Y Wang… - Pharmaceutics, 2020 - mdpi.com
13a-(S)-3-pivaloyloxyl-6, 7-dimethoxyphenanthro (9, 10-b)-indolizidine (CAT3) is a novel
oral anti-glioma pro-drug with a potent anti-tumor effect against temozolomide-resistant …

[图书][B] Cancer inhibitors from Chinese natural medicines

JP Xu - 2016 - taylorfrancis.com
Nature is an attractive source of therapeutic and preventive compounds, and with such
chemical diversity found in millions of species of plants, over 60% of currently used …

CAT3, a novel agent for medulloblastoma and glioblastoma treatment, inhibits tumor growth by disrupting the Hedgehog signaling pathway

J Chen, H Lv, J Hu, M Ji, N Xue, C Li, S Ma, Q Zhou… - Cancer Letters, 2016 - Elsevier
Medulloblastoma (MB) and glioblastoma (GBM) are the most prevalent malignant brain
tumors. The identification of novel therapeutic strategies is urgent for MB and GBM patients …

In vitro activity of (-)-deoxypergularinine, on its own and in combination with anti-tubercular drugs, against resistant strains of Mycobacterium tuberculosis

KW Nam, WS Jang, MA Jyoti, S Kim, BE Lee, HY Song - Phytomedicine, 2016 - Elsevier
Background The increasing incidence of multidrug-resistant tuberculosis (MDR-TB)
infections has created a need for new effective drugs that also target extensively drug …

A novel and practical synthesis of CAT3: a phenanthroindolizidine alkaloid with potential in treating glioblastoma

RB Wang, HN Lv, SS Zhu, XD Ren, S Xu, SG Ma… - RSC …, 2018 - pubs.rsc.org
CAT3, one of the (+)-deoxytylophorinine-based phenanthroindolizidine alkaloids, is a
promising therapeutic agent for the treatment of hedgehog (Hh)-driven glioblastoma and is …

Advances in the 1-phenanthryl-tetrahydroisoquinoline series of PAK4 inhibitors: potent agents restrain tumor cell growth and invasion

C Hao, X Li, S Song, B Guo, J Guo, J Zhang… - Organic & …, 2016 - pubs.rsc.org
A new series of novel 1-phenanthryl-tetrahydroisoquinoline derivatives were designed,
synthesized and biologically evaluated for their PAK4 inhibitory activities and anti …

Improved safety and anti-glioblastoma efficacy of cat3-encapsulated smedds through metabolism modification

H Wang, L Li, J Ye, W Dong, X Zhang, Y Xu, J Hu… - Molecules, 2021 - mdpi.com
13 a-(S)-3-pivaloyloxyl-6, 7-dimethoxyphenanthro (9, 10-b)-indolizidine (CAT3) is a novel
oral anti-glioma pro-drug with a potent anti-tumor effect against temozolomide-resistant …

The novel anti-neuroblastoma agent PF403, inhibits proliferation and invasion in vitro and in brain xenografts Corrigendum in/10.3892/ijo. 2022.5415

C Li, Y Li, H Lv, S Li, K Tang… - International …, 2015 - spandidos-publications.com
Neuroblastoma is the most common cancer in infants and the fourth most common cancer in
children. Our previous study showed that PF403 had a potent antitumor ability. In the present …