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Results for “"Xiaochao Huang"”

7 results

Pt(IV) complexes conjugating with chalcone analogue as inhibitors of microtubule polymerization exhibited selective inhibition in human cancer cells

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Xiaochao Huang, Ri-Zhen Huang, Zhimei Wang, Lingxue Li et al.

Journal: European Journal of Medicinal ChemistryYear: 2018Citations: 51

Six novel of Pt(IV) complexes comprising chalcone analogues were synthesized and evaluated for anti-proliferative activity using MTT assay. In vitro evaluation revealed that all Pt(IV) complexes showed better and more potent activity against three human cancer cells including CDDP resistant cells th...

Health SciencesMedicineOncology
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Synthesis and pharmacological evaluation of dehydroabietic acid thiourea derivatives containing bisphosphonate moiety as an inducer of apoptosis

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Xiaochao Huang, Rizheng Huang, Zhi‐Xin Liao, Ying-Ming Pan et al.

Journal: European Journal of Medicinal ChemistryYear: 2015Citations: 47

A series of DHAA thiourea derivatives containing bisphosphonate moiety were designed and synthesized as potent antitumor agents. Structures of target molecules were confirmed using HR-MS, (1)H NMR and (13)C NMR and they exhibited potent anti-tumor activities against the SK-OV-3, BEL-7404, A549, HCT-...

Life SciencesBiochemistry, Genetics and Molecular BiologyMolecular BiologyOpen Access
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Pt(IV) prodrugs containing microtubule inhibitors displayed potent antitumor activity and ability to overcome cisplatin resistance

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Lingxue Li, Xiaochao Huang, Ri-Zhen Huang, Shaohua Gou et al.

Journal: European Journal of Medicinal ChemistryYear: 2018Citations: 37

It is well-known that cisplatin exhibited a broad spectrum of anticancer activities against many solid tumors, but its severe toxicity and drug resistance have largely limited wider clinical applications. Various strategies have been tried to discover new Pt (II) drugs with at least equal activity a...

Health SciencesMedicineOncology
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Discovery of dehydroabietic acid sulfonamide based derivatives as selective matrix metalloproteinases inactivators that inhibit cell migration and proliferation

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Ri-Zhen Huang, Gui-Bin Liang, Xiaochao Huang, Bin Zhang et al.

Journal: European Journal of Medicinal ChemistryYear: 2017Citations: 34

A series of dehydroabietic acid (DHAA) dipeptide derivatives containing the sulfonamide moiety were designed, synthesized and evaluated for inhibition of MMPs as well as the effects of in vitro cell migration. These compounds exhibited relatively good inhibition activity against MMPs with IC 50 valu...

Life SciencesBiochemistry, Genetics and Molecular BiologyCancer ResearchOpen Access
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Dual-targeting antitumor hybrids derived from Pt(IV) species and millepachine analogues

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Xiaochao Huang, Shixian Hua, Ri-Zhen Huang, Zhikun Liu et al.

Journal: European Journal of Medicinal ChemistryYear: 2018Citations: 33

Many strategies have been developed to circumvent the shortcomings of Pt(II)-based chemotherapy, but the inherent problems still have not been effectively resolved. Here we report a new series of dual-targeting Pt(IV) prodrugs, conjugates of millepachine analogues with the related Pt(IV) complexes d...

Health SciencesMedicineOncology
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Discovery of antitumor ursolic acid long-chain diamine derivatives as potent inhibitors of NF-κB

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Wei Jiang, Ri-Zhen Huang, Jing Zhang, Tong Guo et al.

Journal: Bioorganic ChemistryYear: 2018Citations: 21

A series of inhibitors of NF-κB based on ursolic acid (UA) derivatives containing long-chain diamine moieties were designed and synthesized as well as evaluated the antitumor effects. These compounds exhibited significant inhibitory activity to the NF-κB with IC50 values at micromolar concentrations...

Life SciencesBiochemistry, Genetics and Molecular BiologyMolecular Biology
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16-O-caffeoyl-16-hydroxylhexadecanoic acid, a medicinal plant-derived phenylpropanoid, induces apoptosis in human hepatocarcinoma cells through ROS-dependent endoplasmic reticulum stress

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Ri-Zhen Huang, Xiaochao Huang, Bin Zhang, Haiyang Jia et al.

Journal: PhytomedicineYear: 2018Citations: 18

Background Hepatocellular carcinoma (HCC) is the leading cause of cancer death, and novel chemotherapeutic drugs for treating HCC are urgently needed. 16-O-caffeoyl-16-hydroxylhexadecanoic acid (CHHA) is a new phenylpropanoid isolated by our group from Euphorbia nematocypha which is commonly used to...

Life SciencesBiochemistry, Genetics and Molecular BiologyMolecular Biology
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