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3. Workflow for E3 Ligase Ligand Validation for PROTAC Development.

4. Discovery of the SMYD3 Inhibitor BAY-6035 Using Thermal Shift Assay (TSA)-Based High-Throughput Screening

5. Identifying palladium culprits in amine catalysis

7. Discovery and Characterization of BAY-184: A New Potent and Selective Acylsulfonamide-Benzofuran In Vivo-Active KAT6AB Inhibitor.

10. Targeting the aryl hydrocarbon receptor (AhR) with BAY 2416964: a selective small molecule inhibitor for cancer immunotherapy

15. The European Federation for Medicinal Chemistry and Chemical Biology (EFMC) Best Practice Initiative:Hit Generation

16. European Medicinal Chemistry Leaders in Industry (EMCL) – On the Status and Future of Medicinal Chemistry Research in Europe**

17. Identification and characterization of the new generation sGC stimulator BAY 1165747 (BAY‐747) designed for the treatment of resistant hypertension

18. New Generation of sGC Stimulators: Discovery of Imidazo[1,2-a]pyridine Carboxamide BAY 1165747 (BAY-747), a Long-Acting Soluble Guanylate Cyclase Stimulator for the Treatment of Resistant Hypertension

21. Target 2035 – an update on private sector contributions

23. Identification and characterization of the new generation soluble guanylate cyclase stimulator BAY‐747 designed for the treatment of resistant hypertension.

24. Target 2035 – update on the quest for a probe for every protein

25. sj-pdf-1-jbx-10.1177_24725552211019409 – Supplemental material for Discovery of the SMYD3 Inhibitor BAY-6035 Using Thermal Shift Assay (TSA)-Based High-Throughput Screening

27. The European Federation for Medicinal Chemistry and Chemical Biology (EFMC) Best Practice Initiative:Phenotypic Drug Discovery

28. The European Federation for Medicinal Chemistry and Chemical Biology (EFMC) Best Practice Initiative: Phenotypic Drug Discovery

29. Target 2035 – an update on private sector contributions

30. Amine-Catalysed Suzuki–Miyaura-Type Coupling? the Identification and Isolation of the Palladium Culprits.

31. Rational Design and Synthesis of Selective PRMT4 Inhibitors: A New Chemotype for Development of Cancer Therapeutics**

32. Rational Design and Synthesis of Selective PRMT4 Inhibitors: a New Chemotype for Development of Cancer Therapeutics

35. Abstract 1288: Blocking tumor-associated immune suppression with BAY-218, a novel, selective aryl hydrocarbon receptor (AhR) inhibitor

36. Target 2035 – update on the quest for a probe for every protein

37. Abstract 1646: Discovery and characterization of BAY-6035, a novel benzodiazepine-based SMYD3 inhibitor

38. Front Cover: Discovery of Molidustat (BAY 85-3934): A Small-Molecule Oral HIF-Prolyl Hydroxylase (HIF-PH) Inhibitor for the Treatment of Renal Anemia (ChemMedChem 10/2018)

39. Donated chemical probes for open science

40. Discovery of Molidustat (BAY 85-3934): A Small-Molecule Oral HIF-Prolyl Hydroxylase (HIF-PH) Inhibitor for the Treatment of Renal Anemia

42. Electronic and steric control of regioselectivities in Rh(I)-catalyzed (5+2) cycloadditions: experiment and theory

43. Author response: Donated chemical probes for open science

44. Isoform-Selective ATAD2 Chemical Probe with Novel Chemical Structure and Unusual Mode of Action

45. Abstract 5239: Probing the cancer epigenome: empowering target validation by open innovation

46. Abstract 5084: Potent and isoform-selective ATAD2 bromodomain inhibitor with unprecedented chemical structure and mode of action

47. Abstract 980: BAY-299, a novel chemical probe for in-depth analysis of the function of the bromodomain proteins BRPF2 and TAF1

48. Benzoisoquinolinediones as Potent and Selective Inhibitors of BRPF2 and TAF1/TAF1L Bromodomains

50. Discovery and Characterization of a Highly Potent and Selective Aminopyrazoline-Based in Vivo Probe (BAY-598) for the Protein Lysine Methyltransferase SMYD2

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