All Stories

  1. Six new diterpenoids from Croton laevigatus
  2. Dynamic tracking of pathogenic receptor expression of live cells using pyrenyl glycoanthraquinone-decorated graphene electrodes
  3. Probing disease-related proteins with fluorogenic composite materials
  4. Selective fluorogenic imaging of hepatocellular H2S by a galactosyl azidonaphthalimide probe
  5. Glycosylation enhances the aqueous sensitivity and lowers the cytotoxicity of a naphthalimide zinc ion fluorescence probe
  6. Correction: Glycosylation enhances the aqueous sensitivity and lowers the cytotoxicity of a naphthalimide zinc ion fluorescence probe
  7. Design, synthesis and biological evaluation of 4-anilinothieno[2,3-d]pyrimidine-based hydroxamic acid derivatives as novel histone deacetylase inhibitors
  8. Design, synthesis and biological evaluation of 4-fluoropyrrolidine-2-carbonitrile and octahydrocyclopenta[b]pyrrole-2-carbonitrile derivatives as dipeptidyl peptidase IV inhibitors
  9. Bioactive rearranged limonoids from the Chinese mangrove Xylocarpus granatum Koenig
  10. Guignardins A–F, spirodioxynaphthalenes from the endophytic fungus Guignardia sp. KcF8 as a new class of PTP1B and SIRT1 inhibitors
  11. Synthesis and biological evaluation of novel thiadiazole amides as potent Cdc25B and PTP1B inhibitors
  12. Hepatoma-selective imaging of heavy metal ions using a ‘clicked’ galactosylrhodamine probe
  13. Corrigendum to “4-Quinolone-3-carboxylic acids as cell-permeable inhibitors of protein tyrosine phosphatase 1B” [Bioorg. Med. Chem. 22 (2014) 3670–3683]
  14. Synthesis and structure–activity relationship of non-phosphorus-based fructose-1,6-bisphosphatase inhibitors: 2,5-Diphenyl-1,3,4-oxadiazoles
  15. Four Phragmalin Orthoesters from the Chinese Mangrove Xylocarpus granatum
  16. A ‘Clicked’ Tetrameric Hydroxamic Acid Glycopeptidomimetic Antagonizes Sugar-Lectin Interactions On The Cellular Level
  17. Identification of a new bis-amino acid glycoside selectively toxic to multiple myeloma cells
  18. Involvement of transcription factor XBP1s in the resistance of HDAC6 inhibitor Tubastatin A to superoxidation via acetylation-mediated proteasomal degradation
  19. 4-Quinolone-3-carboxylic acids as cell-permeable inhibitors of protein tyrosine phosphatase 1B
  20. Novel grayanane diterpenoids from Rhododendron principis
  21. Azoxystrobin, a mitochondrial complex III Qo site inhibitor, exerts beneficial metabolic effects in vivo and in vitro
  22. Hainanerectamines A–C, Alkaloids from the Hainan Sponge Hyrtios erecta
  23. Design, Synthesis and Biological Evaluation of Peptidyl Epoxyketone Proteasome Inhibitors Composed of β‐amino Acids
  24. Design, synthesis and biological evaluation of novel tripeptidyl epoxyketone derivatives constructed from β-amino acid as proteasome inhibitors
  25. Curcusone D, a novel ubiquitin–proteasome pathway inhibitor via ROS-induced DUB inhibition, is synergistic with bortezomib against multiple myeloma cell growth
  26. New triterpenoids with protein tyrosine phosphatase 1B inhibition from Cedrela odorata
  27. Target-Specific Imaging of Transmembrane Receptors Using Quinonyl Glycosides Functionalized Quantum Dots
  28. Discovery, synthesis, and structure–activity relationships of 20(S)-protopanaxadiol (PPD) derivatives as a novel class of AMPKα2β1γ1 activators
  29. Regio- and Diastereoselective Construction of α-Hydroxy-δ-amino Ester Derivatives via 1,4-Conjugate Addition of β,γ-Unsaturated N-Sulfonylimines
  30. Potent and Orally Efficacious Bisthiazole-Based Histone Deacetylase Inhibitors
  31. Fluorogenic Resveratrol-Confined Graphene Oxide For Economic and Rapid Detection Of Alzheimer’s Disease
  32. Synthesis and biological evaluation of novel bis-aromatic amides as novel PTP1B inhibitors
  33. Discovery of a novel inhibitor of NAD(P)+-dependent malic enzyme (ME2) by high-throughput screening
  34. Hepatic IRE1α regulates fasting-induced metabolic adaptive programs through the XBP1s–PPARα axis signalling
  35. Substitution Pattern Reverses the Fluorescence Response of Coumarin Glycoligands upon Coordination with Silver (I)
  36. Design, synthesis and biological evaluation of hetero-aromatic moieties substituted pyrrole-2-carbonitrile derivatives as dipeptidyl peptidase IV inhibitors
  37. Chaetoglobosin Y, a new cytochalasan from Chaetomium globosum
  38. Sarsolenane and Capnosane Diterpenes from the Hainan Soft Coral Sarcophyton trocheliophorum Marenzeller as PTP1B Inhibitors
  39. Design and synthesis of paracaseolide A analogues as selective protein tyrosine phosphatase 1B inhibitors
  40. Dysidaminones A–M, cytotoxic and NF-κB inhibitory sesquiterpene aminoquinones from the South China Sea sponge Dysidea fragilis
  41. Design, synthesis and biological evaluation of 4′-demethyl-4-deoxypodophyllotoxin derivatives as novel tubulin and histone deacetylase dual inhibitors
  42. Three pairs of variecolortide enantiomers from Eurotium sp. with caspase-3 inhibitory activity
  43. 1H-2,3-Dihydroperimidine Derivatives: A New Class of Potent Protein Tyrosine Phosphatase 1B Inhibitors
  44. Novel small-molecule AMPK activator orally exerts beneficial effects on diabetic db/db mice
  45. The discovery and optimization of novel dual inhibitors of topoisomerase ii and histone deacetylase
  46. Design, synthesis, and biological evaluation of novel 2-ethyl-5-phenylthiazole-4-carboxamide derivatives as protein tyrosine phosphatase 1B inhibitors with improved cellular efficacy
  47. Berberine combined with 2-deoxy-d-glucose synergistically enhances cancer cell proliferation inhibition via energy depletion and unfolded protein response disruption
  48. A specific cholesterol metabolic pathway is established in a subset of HCCs for tumor growth
  49. Design, synthesis and evaluation of 7-azaindazolyl-indolyl-maleimides as glycogen synthase kinase-3β (GSK-3β) inhibitors
  50. Discovery of pyrazole as C-terminus of selective BACE1 inhibitors
  51. The first synthesis of natural disulfide bruguiesulfurol and biological evaluation of its derivatives as a novel scaffold for PTP1B inhibitors
  52. Synthesis and biological evaluation of novel benzyl-substituted (S)-phenylalanine derivatives as potent dipeptidyl peptidase 4 inhibitors
  53. Cembrane diterpenoids from the soft coral Sarcophyton trocheliophorum Marenzeller as a new class of PTP1B inhibitors
  54. Novel Small-Molecule AMP-Activated Protein Kinase Allosteric Activator with Beneficial Effects in db/db Mice
  55. Sensors: Fluorogenic Probing of Specific Recognitions between Sugar Ligands and Glycoprotein Receptors on Cancer Cells by an Economic Graphene Nanocomposite (Adv. Mater. 30/2013)
  56. A novel chemical uncoupler ameliorates obesity and related phenotypes in mice with diet-induced obesity by modulating energy expenditure and food intake
  57. Capturing intercellular sugar-mediated ligand-receptor recognitions via a simple yet highly biospecific interfacial system
  58. ChemInform Abstract: Bioactive Polyhydroxylated Steroids from the Hainan Soft Coral Sinularia depressa Tixier‐Durivault
  59. The Design and Synthesis of a New Class of RTK/HDAC Dual-Targeted Inhibitors
  60. The discovery of colchicine-SAHA hybrids as a new class of antitumor agents
  61. Fluorogenic Probing of Specific Recognitions between Sugar Ligands and Glycoprotein Receptors on Cancer Cells by an Economic Graphene Nanocomposite
  62. Design and Synthesis of 4‐(2,4,5‐Trifluorophenyl)butane‐1,3‐diamines as Dipeptidyl Peptidase IV Inhibitors
  63. Synthesis and Biological Evaluation of 3-Benzisoxazolyl-4-indolylmaleimides as Potent, Selective Inhibitors of Glycogen Synthase Kinase-3β
  64. Synthesis and in vitro cytotoxic evaluation of novel $$N$$ -(3,4,5-trimethoxyphenyl)pyridin-2( $$1H$$ )-one derivatives
  65. Characterization of a novel curcumin analog P1 as potent inhibitor of the NF-κB signaling pathway with distinct mechanisms
  66. Design, Synthesis, and Evaluation of 3‐Aryl‐4‐pyrrolyl‐maleimides as Glycogen Synthase Kinase‐3β Inhibitors
  67. Development of Novel Alkene Oxindole Derivatives As Orally Efficacious AMP-Activated Protein Kinase Activators
  68. Astragaloside II triggers T cell activation through regulation of CD45 protein tyrosine phosphatase activity
  69. Design, Synthesis and Evaluation of 3-(2-Aminoheterocycle)-4-benzyloxyphenylbenzamide Derivatives as BACE-1 Inhibitors
  70. Novel Small-Molecule PGC-1α Transcriptional Regulator With Beneficial Effects on Diabetic db/db Mice
  71. New Azalomycin F Analogs from Mangrove Streptomyces sp. 211726 with Activity against Microbes and Cancer Cells
  72. Bioactive polyhydroxylated steroids from the Hainan soft coral Sinularia depressa Tixier-Durivault
  73. Revisit of a dipropargyl rhodamine probe reveals its alternative ion sensitivity in both a solution and live cells
  74. Microwave-Assisted Synthesis and Biological Activities of 3,6-Disubstituted-1,2,4-triazine Derivatives
  75. Synthesis and PTP1B Inhibitory Activity of ( E )-1-Substitutedphenyl-3-(4-(( E )-(2-(4-phenylthiazol-2-yl)hydrazono)methyl)phenyl)-prop-2-en-1-ones
  76. Unprecedented Diterpenoids as a PTP1B Inhibitor from the Hainan Soft Coral Sarcophyton trocheliophorum Marenzeller
  77. Fluevirosines A–C: A Biogenesis Inspired Example in the Discovery of New Bioactive Scaffolds from Flueggea virosa
  78. Synthesis and biological evaluation of 4,4-dimethyl lithocholic acid derivatives as novel inhibitors of protein tyrosine phosphatase 1B
  79. Discovery of di-indolinone as a novel scaffold for protein tyrosine phosphatase 1B inhibitors
  80. ChemInform Abstract: A Novel Class of Small‐Molecule Caspase‐3 Inhibitors Prepared by Multicomponent Reactions.
  81. ChemInform Abstract: Synthesis and Biological Evaluation of Novel Indolin‐2‐one Derivatives as Protein Tyrosine Phosphatase 1B Inhibitors.
  82. Design, Synthesis, Structure–Activity Relationships, and Docking Studies of 1‐(γ‐1,2,3‐Triazol Substituted Prolyl)‐(S)‐3,3‐Difluoropyrrolidines as a Novel Series of Potent and Selective Dipeptidyl Peptidase‐4 Inhibitors
  83. ChemInform Abstract: Design, Synthesis and Biological Activity Evaluation of 2‐Mercapto‐4(3H)‐quinazolinone Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B.
  84. Discovering Novel α‐aminoacyl‐Containing Proline Derivatives with Potent and Selective Inhibitory Activity Against Dipeptidyl Peptidase IV: Design, Synthesis, Biological Evaluation, and Molecular Modeling
  85. Synthesis and characterization of 5,7-dihydroxyflavanone derivatives as novel protein tyrosine phosphatase 1B inhibitors
  86. A Role for Protein Inhibitor of Activated STAT1 (PIAS1) in Lipogenic Regulation through SUMOylation-independent Suppression of Liver X Receptors
  87. BMS309403 Stimulates Glucose Uptake in Myotubes through Activation of AMP-Activated Protein Kinase
  88. ChemInform Abstract: Synthesis and Biological Evaluation of Oleanolic Acid Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B.
  89. New Azaphilones and Chlorinated Phenolic Glycosides from Chaetomium elatum with Caspase-3 Inhibitory Activity
  90. A novel class of small-molecule caspase-3 inhibitors prepared by multicomponent reactions
  91. Synthesis and Biological Evaluation of 2,4,6‐Trihydroxychalcone Derivatives as Novel Protein Tyrosine Phosphatase 1B Inhibitors
  92. CCLab—a multi-objective genetic algorithm based combinatorial library design software and an application for histone deacetylase inhibitor design
  93. Absolute configurations of integracins A, B, and 15′‐dehydroxy‐integracin B
  94. CuAAC Click Chemistry Accelerates the Discovery of Novel Chemical Scaffolds as Promising Protein Tyrosine Phosphatases Inhibitors
  95. Discovery and Optimization of 2,4-Diaminoquinazoline Derivatives as a New Class of Potent Dengue Virus Inhibitors
  96. The anomeric mixture of some O-galactolipid derivatives is more toxic against cancer cells than either anomer alone
  97. Discovery and Structural Modification of 1-Phenyl-3-(1-phenylethyl)urea Derivatives as Inhibitors of Complement
  98. Novel microtubule-targeted agent 6-chloro-4-(methoxyphenyl) coumarin induces G2-M arrest and apoptosis in HeLa cells
  99. Quantitative Proteomic Analysis of Membrane Proteins Involved in Astroglial Differentiation of Neural Stem Cells by SILAC Labeling Coupled with LC–MS/MS
  100. ChemInform Abstract: Click to a Focused Library of Benzyl 6‐Triazolo(hydroxy)benzoic Glucosides: Novel Construction of PTP1B Inhibitors on a Sugar Scaffold.
  101. Synthesis and Biological Evaluation of Oleanolic Acid Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B
  102. Design, Synthesis and Biological Activity Evaluation of 2-Mercapto-4(3H)-quinazolinone Derivatives as Novel Inhibitors of Protein Tyrosine Phosphatase 1B
  103. Design, Synthesis and Biological Activity Evaluation of 2,5-Diphenyl-1,3,4-oxadiazole Derivatives as Novel Inhibitors of Fructose-1,6-bisphosphatase
  104. Synthesis and Anti-tumor Activity Evaluation of Alkyl Heterocyclyl Disulfides
  105. Dysidavarones A–D, New Sesquiterpene Quinones from the Marine Sponge Dysidea avara
  106. 5′-AMP-activated protein kinase (AMPK) regulates progesterone receptor transcriptional activity in breast cancer cells
  107. Searching for the Multi-Target-Directed Ligands against Alzheimer’s disease: Discovery of quinoxaline-based hybrid compounds with AChE, H3R and BACE 1 inhibitory activities
  108. Synthesis of (Glycopyranosyl‐triazolyl)‐purines and Their Inhibitory Activities against Protein Tyrosine Phosphatase 1B (PTP1B)
  109. Structural insights into the homology and differences between mouse protein tyrosine phosphatase-sigma and human protein tyrosine phosphatase-sigma
  110. ChemInform Abstract: Synthesis of Triazole‐Linked Amino Acid‐Aryl C‐Glycoside Hybrids via Click Chemistry as Novel PTP1B Inhibitors.
  111. Diterpenes from the Hainan Soft Coral Lobophytum cristatum Tixier-Durivault
  112. PKA phosphorylation couples hepatic inositol-requiring enzyme 1α to glucagon signaling in glucose metabolism
  113. Discovering the distinct inhibitory effects between C4-epimeric glycosyl amino acids: new insight into the development of protein tyrosine phosphatase inhibitors
  114. Synthesis and biological evaluation of (±)-3-(2-(2-fluorobenzyloxy) naphthalen-6-yl)-2-aminopropanoic acid derivatives as novel PTP1B inhibitors
  115. Synthesis and Biological Evaluation of Novel Indolin-2-One Derivatives as Protein Tyrosine Phosphatase 1B Inhibitors
  116. Click to a focused library of benzyl 6-triazolo(hydroxy)benzoic glucosides: Novel construction of PTP1B inhibitors on a sugar scaffold
  117. Paracaseolide A, First α-Alkylbutenolide Dimer with an Unusual Tetraquinane Oxa-Cage Bislactone Skeleton from Chinese Mangrove Sonneratia paracaseolaris
  118. ChemInform Abstract: Benzamides and Quinazolines from a Mangrove Actinomycetes Streptomyces sp. (No. 061316) and Their Inhibiting Caspase‐3 Catalytic Activity in vitro
  119. A new staurosporine analog from ActinomycetesStreptomycessp. (172614)
  120. Synthesis and biological evaluation of piperamide analogues as HDAC inhibitors
  121. ChemInform Abstract: Monosaccharide as a Central Scaffold Toward the Construction of Salicylate‐Based Bidentate PTP1B Inhibitors via Click Chemistry.
  122. Facile fabrication of promising protein tyrosine phosphatase (PTP) inhibitor entities based on ‘clicked’ serine/threonine–monosaccharide hybrids
  123. Design, Synthesis, and Biological Evaluation of Ring‐Opened Bengamide Analogues
  124. Synthesis of novel 6-triazologlycolipids via click chemistry and their preliminary cytotoxicity assessments
  125. ChemInform Abstract: A Unique and Rapid Approach Toward the Efficient Development of Novel Protein Tyrosine Phosphatase (PTP) Inhibitors Based on “Clicked” Pseudo‐Glycopeptides.
  126. Synthesis of Triazole-Linked Amino Acid-Aryl C -Glycoside Hybrids via Click Chemistry as Novel PTP1B Inhibitors
  127. Structural and stereochemical studies of five new pregnane steroids from the stem bark of Toona ciliata var. pubescens
  128. Extraction and PTP1B inhibitory activity of bromophenols from the marine red alga Symphyocladia latiuscula
  129. ChemInform Abstract: Triazole‐Linked Benzylated Glucosyl, Galactosyl, and Mannosyl Monomers and Dimers as Novel Sugar Scaffold‐Based PTP1B Inhibitors.
  130. ChemInform Abstract: Microwave‐Accelerated Click Chemistry: Expeditious Synthesis of Novel Triazole‐Linked Salicylic β‐D‐O‐Glycosides with PTP1B Inhibitory Activity.
  131. Leucine Deprivation Increases Hepatic Insulin Sensitivity via GCN2/mTOR/S6K1 and AMPK Pathways
  132. Histone deacetylase inhibitor activity in royal jelly might facilitate caste switching in bees
  133. A unique and rapid approach toward the efficient development of novel protein tyrosine phosphatase (PTP) inhibitors based on ‘clicked’ pseudo-glycopeptides
  134. ‘Click’ to bidentate bis-triazolyl sugar derivatives with promising biological and optical features
  135. Discovery and structural modification of novel inhibitors of PTP1B inspired by the ACT fragment of scleritodermin A
  136. Protolimonoids and norlimonoids from the stem bark of Toona ciliata var. pubescens
  137. Microwave-assisted construction of triazole-linked amino acid–glucoside conjugates as novel PTP1B inhibitors
  138. Benzamides and Quinazolines from a Mangrove Actinomycetes Streptomyces sp. (No. 061316) and Their Inhibiting Caspase-3 Catalytic Activity in Vitro
  139. Application of p21 and klf2 reporter gene assays to identify selective histone deacetylase inhibitors for cancer therapy
  140. Preparation of triazole-linked glycosylated α-ketocarboxylic acid derivatives as new PTP1B inhibitors
  141. Cytotoxic Amide Alkaloids from Piper boehmeriaefolium
  142. Expeditious preparation of triazole-linked glycolipids via microwave accelerated click chemistry and their electrochemical and biological assessments
  143. Rubiyunnanins C–H, cytotoxic cyclic hexapeptides from Rubia yunnanensis inhibiting nitric oxide production and NF-κB activation
  144. Synthesis and antitumor evaluation of methyl spongoate analogs
  145. 1H and 13C assignments of two new macrocyclic lactones isolated from Streptomyces sp. 211726 and revised assignments of Azalomycins F3a, F4aand F5a
  146. Characterization and Online Detection of Surfactin Isomers Based on HPLC-MSn Analyses and Their Inhibitory Effects on the Overproduction of Nitric Oxide and the Release of TNF-α and IL-6 in LPS-Induced Macrophages
  147. Azalomycin F4a 2-ethylpentyl ester, a new macrocyclic lactone, from mangrove actinomycete Streptomyces sp. 211726
  148. Discovery of novel PTP1B inhibitors with antihyperglycemic activity
  149. 8,8-Dimethyldihydroberberine with improved bioavailability and oral efficacy on obese and diabetic mouse models
  150. Dual-target-directed 1,3-diphenylurea derivatives: BACE 1 inhibitor and metal chelator against Alzheimer’s disease
  151. Dammaranes from Gynostemma pentaphyllum and synthesis of their derivatives as inhibitors of protein tyrosine phosphatase 1B
  152. Discovery and structural optimization of pyrazole derivatives as novel inhibitors of Cdc25B
  153. Phenolic compounds from the leaves of Cyclocarya paliurus (Batal.) Ijinskaja and their inhibitory activity against PTP1B
  154. AMPK Activators as Novel Therapeutics for Type 2 Diabetes
  155. Design and synthesis of a highly selective fluorescent turn-on probe for thiol bioimaging in living cells
  156. Triazole-linked Benzylated Glucosyl, Galactosyl, and Mannosyl Monomers and Dimers as Novel Sugar Scaffold-based PTP1B Inhibitors
  157. Synthesis and biological evaluation of heterocyclic ring-substituted maslinic acid derivatives as novel inhibitors of protein tyrosine phosphatase 1B
  158. Synthesis of tanshinone IIA analogues and their inhibitory activities against Cdc25 phosphatases
  159. Correction: Hong, K. et al. Actinomycetes for Marine Drug Discovery Isolated from Mangrove Soils and Plants in China. Mar. Drugs 2009, 7, 24–44
  160. High-Throughput Assay for Modulators of Mitochondrial Membrane Potential Identifies a Novel Compound With Beneficial Effects on db/db Mice
  161. LGH00031, a novel ortho-quinonoid inhibitor of cell division cycle 25B, inhibits human cancer cells via ROS generation
  162. Synthesis and Biological Evaluation of C7‐Demethyl Largazole Analogues
  163. Diterpenoids from the Hainan Soft Coral Sinularia parva
  164. Synthesis and biological evaluation of novel 4-azaindolyl-indolyl-maleimides as glycogen synthase kinase-3β (GSK-3β) inhibitors
  165. Two New Unprecedented Acetonyl‐Bearing Sesquiterpenes from the Hainan Sponge Dysidea fragilis
  166. Design and Synthesis of Matrix Metalloprotease Photoaffinity Trimodular Probes
  167. High-throughput screening using pseudotyped lentiviral particles: A strategy for the identification of HIV-1 inhibitors in a cell-based assay
  168. Design, synthesis and biological evaluation of novel dual inhibitors of acetylcholinesterase and β-secretase
  169. Discovery of potent β-secretase (bace-1) inhibitors by the synthesis of isophthalamide-containing hybrids
  170. AMP-activated Protein Kinase Is Involved in Neural Stem Cell Growth Suppression and Cell Cycle Arrest by 5-Aminoimidazole-4-carboxamide-1- -D-ribofuranoside and Glucose Deprivation by Down-regulating Phospho-retinoblastoma Protein and Cyclin D
  171. Actinomycetes for Marine Drug Discovery Isolated from Mangrove Soils and Plants in China
  172. Identification of pharmacophore model, synthesis and biological evaluation of N-phenyl-1-arylamide and N-phenylbenzenesulfonamide derivatives as BACE 1 inhibitors
  173. Synthesis of (S)-, (R)-, and (rac)-2-amino-3,3-bis(4-fluorophenyl)propanoic acids and an evaluation of the DPP IV inhibitory activity of Denagliptin diastereomers
  174. Discovery and characterization of a novel inhibitor of CDC25B, LGH000451
  175. Isoquinoline-1,3,4-trione Derivatives Inactivate Caspase-3 by Generation of Reactive Oxygen Species
  176. Oleanolic acid and its derivatives: New inhibitor of protein tyrosine phosphatase 1B with cellular activities
  177. Illudalic acid as a potential LAR inhibitor: Synthesis, SAR, and preliminary studies on the mechanism of action
  178. Soluble Polymer-Supported Synthesis of 5-Arylidene Thiazolidinones and Pyrimidinones Using a Novel Traceless Linker Strategy
  179. Sesquiterpenes from the Hainan Sponge Dysidea septosa
  180. Berberine and Its More Biologically Available Derivative, Dihydroberberine, Inhibit Mitochondrial Respiratory Complex I
  181. Corosolic acid stimulates glucose uptake via enhancing insulin receptor phosphorylation
  182. Small Molecule Antagonizes Autoinhibition and Activates AMP-activated Protein Kinase in Cells
  183. Discovery of a novel competitive inhibitor of PTP1B by high-throughput screening
  184. AICAR Induces Astroglial Differentiation of Neural Stem Cells via Activating the JAK/STAT3 Pathway Independently of AMP-activated Protein Kinase
  185. Design, Synthesis, and Biological Evaluation of Caprolactam‐Modified Bengamide Analogues
  186. Growth inhibition and induction of early apoptosis by arenicolsterol A, a novel cytotoxic enolic sulphated sterol from the marine annelid,Arenicola cristata
  187. Anti-Helicobacter pyloriand Thrombin Inhibitory Components from Chinese Dragon’s Blood,Dracaena cochinchinensis
  188. Activity‐Based Protein Profiling for Type I Methionine Aminopeptidase by Using Photo‐Affinity Trimodular Probes
  189. Benzoquinones from Ardisia japonica with Inhibitory Activity towards Human Protein Tyrosine Phosphatase 1B (PTP1B)
  190. Quinoxalinylurea derivatives as a novel class of JSP-1 inhibitors
  191. Two New Coumarins from Fraxinus chinensis Rexb.
  192. Novel irreversible caspase-1 inhibitor attenuates the maturation of intracellular interleukin-1β
  193. Preparation of 6-Substituted Quinoxaline JSP-1 Inhibitors by Microwave Accelerated Nucleophilic Substitution
  194. Vascular development is disrupted by endothelial cell-specific expression of the anti-apoptotic protein Bcl-2
  195. Construction of a small peptide library related to inhibitor OM99-2 and its structure-activity relationship to ?-secretase
  196. Conserved  -Helix Acts as Autoinhibitory Sequence in AMP-activated Protein Kinase   Subunits
  197. Berberine-stimulated glucose uptake in L6 myotubes involves both AMPK and p38 MAPK
  198. Ursolic acid and its derivative inhibit protein tyrosine phosphatase 1B, enhancing insulin receptor phosphorylation and stimulating glucose uptake
  199. Synthesis of Miltirone Analogues as Inhibitors of Cdc25 Phosphatases.
  200. Design, synthesis, and evaluation of Leu∗Ala hydroxyethylene-based non-peptide β-secretase (BACE) inhibitors
  201. Design and synthesis of a biotin-tagged photoaffinity probe of paeoniflorin
  202. PTP1B inhibitors from Saussrurea Lappa
  203. O-methyl nakafuran-8 lactone, a new sesquiterpenoid from a hainan marine sponge Dysidea sp.
  204. Design, Synthesis, and Biological Evaluation of Isoquinoline-1,3,4-trione Derivatives as Potent Caspase-3 Inhibitors
  205. Daturametelins H, I, and J: Three New Withanolide Glycosides from Datura metel L.
  206. Identification of Potent Type I MetAP Inhibitors by Simple Bioisosteric Replacement. Part 1. Synthesis and Preliminary SAR Studies of Thiazole‐4‐carboxylic Acid Thiazol‐2‐ylamide Derivatives.
  207. Selective Inhibition of Matrix Metalloproteinase Isozymes and in Vivo Protection against Emphysema by Substituted γ-Keto Carboxylic Acids
  208. Discovery of novel inhibitor of human leukocyte common antigen-related phosphatase
  209. Identification of potent type I MetAPs inhibitors by simple bioisosteric replacement. Part 2: SAR studies of 5-heteroalkyl substituted TCAT derivatives
  210. Identification of potent type I MetAP inhibitors by simple bioisosteric replacement. Part 1: Synthesis and preliminary SAR studies of thiazole-4-carboxylic acid thiazol-2-ylamide derivatives
  211. Benzothiophenes containing a piperazine side chain as selective ligands for the estrogen receptor α and their bioactivities in vivo
  212. PTP1B inhibitors from Ardisia japonica
  213. Furostanoside from Asparagus filicinus
  214. Synthesis and biological evaluation of (±)-cryptotanshinone and its simplified analogues as potent CDC25 inhibitors
  215. Inhibitors of type I MetAPs containing pyridine-2-carboxylic acid thiazol-2-ylamide. Part 2: SAR studies on the pyridine ring 3-substituent
  216. Inhibitors of type I MetAPs containing pyridine-2-carboxylic acid thiazol-2-ylamide. Part 1: SAR studies on the determination of the key scaffold
  217. Design and synthesis of chromogenic thiopeptolide substrates as MetAPs active site probes
  218. Tetrahydroisoquinoline Based Sulfonamide Hydroxamates as Potent Matrix Metalloproteinase Inhibitors.
  219. Mutations at the S1 Sites of Methionine Aminopeptidases from Escherichia coli and Homo sapiens Reveal the Residues Critical for Substrate Specificity
  220. Tetrahydroisoquinoline based sulfonamide hydroxamates as potent matrix metalloproteinase inhibitors
  221. Specificity for inhibitors of metal-substituted methionine aminopeptidase
  222. Discovery and Structural Modification of Inhibitors of Methionine Aminopeptidases from Escherichia coli and Saccharomyces cerevisiae
  223. New Insights into the Function and Regulation of Endothelial Cell Apoptosis
  224. Natural PTP1B Inhibitors from broussonetia papyrifera