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 …
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
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 …
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 …
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 …
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
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 …
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 …
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 …
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
A new series of novel 1-phenanthryl-tetrahydroisoquinoline derivatives were designed,
synthesized and biologically evaluated for their PAK4 inhibitory activities and anti …
synthesized and biologically evaluated for their PAK4 inhibitory activities and anti …
Improved safety and anti-glioblastoma efficacy of cat3-encapsulated smedds through metabolism modification
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 …
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 …
children. Our previous study showed that PF403 had a potent antitumor ability. In the present …