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F16 Hybrids Derived from Steviol or Isosteviol Are Accumulated in the Mitochondria of Tumor Cells and Overcome Drug Resistance

Molecules (Basel, Switzerland), 2024-01, Vol.29 (2), p.381

2024

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Synthesis of Rhodamine-Conjugated Lupane Type Triterpenes of Enhanced Cytotoxicity

Molecules (Basel, Switzerland), 2024-05, Vol.29 (10), p.2346

2024

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Synthesis and In Silico Docking Study towards M-Pro of Novel Heterocyclic Compounds Derived from Pyrazolopyrimidinone as Putative SARS-CoV-2 Inhibitors

Molecules (Basel, Switzerland), 2022-08, Vol.27 (16), p.5303

2022

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Rhodamine 101 Conjugates of Triterpenoic Amides Are of Comparable Cytotoxicity as Their Rhodamine B Analogs

Molecules (Basel, Switzerland), 2022-03, Vol.27 (7), p.2220

2022

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Synthesis and Enzymatic Evaluation of a Small Library of Substituted Phenylsulfonamido-Alkyl Sulfamates towards Carbonic Anhydrase II

Molecules (Basel, Switzerland), 2024-06, Vol.29 (13), p.3015

2024

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The Finally Rewarding Search for A Cytotoxic Isosteviol Derivative

Molecules (Basel, Switzerland), 2023-06, Vol.28 (13), p.4951

2023

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Developing an Amide-Spacered Triterpenoid Rhodamine Hybrid of Nano-Molar Cytotoxicity Combined with Excellent Tumor Cell/Non-Tumor Cell Selectivity

Molecules (Basel, Switzerland), 2023-09, Vol.28 (17), p.6404

2023

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Stereochemistry matters: Inhibition of carbonic anhydrase II by amino acid derived sulfamates depends on their absolute configuration

European journal of medicinal chemistry reports, 2024-08, Vol.11, p.100162, Article 100162

2024

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Synthesis and In Silico Docking of New Pyrazolo[4,3-e]pyrido[1,2-a]pyrimidine-based Cytotoxic Agents

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10258

2021

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Combination of Betulinic Acid Fragments and Carbonic Anhydrase Inhibitors-A New Drug Targeting Approach

Pharmaceutics, 2024-03, Vol.16 (3), p.401

2024

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Dehydroabietylamine-substituted trifluorobenzene sulfonamide rhodamine B hybrids as anticancer agents overcoming drug resistance

European journal of medicinal chemistry, 2024-10, Vol.276, p.116667, Article 116667

2024

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An asiatic acid derived trisulfamate acts as a nanomolar inhibitor of human carbonic anhydrase VA

Steroids, 2024-05, Vol.205, p.109381-109381, Article 109381

2024

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Asiatic acid as a leading structure for derivatives combining sub-nanomolar cytotoxicity, high selectivity, and the ability to overcome drug resistance in human preclinical tumor models

European journal of medicinal chemistry, 2023-03, Vol.250, p.115189-115189, Article 115189

2023

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Inhibitory properties of quinopimaric acid derivatives towards cholinesterases

Natural product research, 2023-10, p.1-9

2023

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Diethoxyphosphoryloxy‐oleanolic acid is a nanomolar‐inhibitor of butyrylcholinesterase

Chemical biology & drug design, 2024-03, Vol.103 (3), p.e14506-n/a

2024

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Acetylcholinesterase Inhibitory Activity of Modified Lupane, Oleanane, and Ursane A‐seco‐Triterpenoids

Chemistry & biodiversity, 2023-04, Vol.20 (4), p.e202300185-n/a

2023

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Isosteviol – A new scaffold for the synthesis of carbonic anhydrase II inhibitors

Results in Chemistry, 2024-01, Vol.7, p.101426, Article 101426

2024

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Arylsulfonamido-alkyl-sulfamates act as inhibitors of bovine carbonic anhydrase II

European journal of medicinal chemistry reports, 2024-12, Vol.12, p.100177, Article 100177

2024

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Synthesis and Exploitation of the Biological Profile of Novel Guanidino Xylofuranose Derivatives

ChemMedChem, 2022-07, Vol.17 (14), p.e202200180-n/a

2022

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Lupane acetates in small molecule drug hybrids: Probing their inhibitory activity for carbonic anhydrase II

European journal of medicinal chemistry reports, 2024-04, Vol.10, p.100139, Article 100139

2024

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An improved partial synthesis of corosolic acid and its conversion to highly cytotoxic mitocans

European journal of medicinal chemistry reports, 2022-12, Vol.6, p.100073, Article 100073

2022

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Dehydroabietylamine derived bistetrazoles from ultrasound-assisted pseudo-seven-component Ugi reactions act as efficient and selective inhibitors of cholinesterases

European journal of medicinal chemistry reports, 2024-04, Vol.10, p.100124, Article 100124

2024

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α-Glucosidase and cholinesterase inhibiting potential of a series of semisynthetic nitrogen triterpenic derivatives

Medicinal chemistry research, 2023-03, Vol.32 (3), p.485-494

2023

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Synthesis and cytotoxicity of diastereomeric benzylamides derived from maslinic acid, augustic acid and bredemolic acid

Results in Chemistry, 2023-01, Vol.5, p.100805, Article 100805

2023

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Stable triterpenoid iminium salts and their activity as inhibitors of butyrylcholinesterase

Journal of molecular structure, 2022-02, Vol.1249, p.131646, Article 131646

2022

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F16 Hybrids Derived from Steviol or Isosteviol Are Accumulated in the Mitochondria of Tumor Cells and Overcome Drug Resistance

Synthesis of Rhodamine-Conjugated Lupane Type Triterpenes of Enhanced Cytotoxicity

Synthesis and In Silico Docking Study towards M-Pro of Novel Heterocyclic Compounds Derived from Pyrazolopyrimidinone as Putative SARS-CoV-2 Inhibitors

Rhodamine 101 Conjugates of Triterpenoic Amides Are of Comparable Cytotoxicity as Their Rhodamine B Analogs

Synthesis and Enzymatic Evaluation of a Small Library of Substituted Phenylsulfonamido-Alkyl Sulfamates towards Carbonic Anhydrase II

The Finally Rewarding Search for A Cytotoxic Isosteviol Derivative

Developing an Amide-Spacered Triterpenoid Rhodamine Hybrid of Nano-Molar Cytotoxicity Combined with Excellent Tumor Cell/Non-Tumor Cell Selectivity

Stereochemistry matters: Inhibition of carbonic anhydrase II by amino acid derived sulfamates depends on their absolute configuration

Synthesis and In Silico Docking of New Pyrazolo[4,3-e]pyrido[1,2-a]pyrimidine-based Cytotoxic Agents

Combination of Betulinic Acid Fragments and Carbonic Anhydrase Inhibitors-A New Drug Targeting Approach

Dehydroabietylamine-substituted trifluorobenzene sulfonamide rhodamine B hybrids as anticancer agents overcoming drug resistance

An asiatic acid derived trisulfamate acts as a nanomolar inhibitor of human carbonic anhydrase VA

Asiatic acid as a leading structure for derivatives combining sub-nanomolar cytotoxicity, high selectivity, and the ability to overcome drug resistance in human preclinical tumor models

Inhibitory properties of quinopimaric acid derivatives towards cholinesterases

Diethoxyphosphoryloxy‐oleanolic acid is a nanomolar‐inhibitor of butyrylcholinesterase

Acetylcholinesterase Inhibitory Activity of Modified Lupane, Oleanane, and Ursane A‐seco‐Triterpenoids

Isosteviol – A new scaffold for the synthesis of carbonic anhydrase II inhibitors

Arylsulfonamido-alkyl-sulfamates act as inhibitors of bovine carbonic anhydrase II

Synthesis and Exploitation of the Biological Profile of Novel Guanidino Xylofuranose Derivatives

Lupane acetates in small molecule drug hybrids: Probing their inhibitory activity for carbonic anhydrase II

An improved partial synthesis of corosolic acid and its conversion to highly cytotoxic mitocans

Dehydroabietylamine derived bistetrazoles from ultrasound-assisted pseudo-seven-component Ugi reactions act as efficient and selective inhibitors of cholinesterases

α-Glucosidase and cholinesterase inhibiting potential of a series of semisynthetic nitrogen triterpenic derivatives

Synthesis and cytotoxicity of diastereomeric benzylamides derived from maslinic acid, augustic acid and bredemolic acid

Stable triterpenoid iminium salts and their activity as inhibitors of butyrylcholinesterase

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