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2. The HER2-directed antibody-drug conjugate DHES0815A in advanced and/or metastatic breast cancer: preclinical characterization and phase 1 trial results

3. Selective PROTAC-mediated degradation of SMARCA2 is efficacious in SMARCA4 mutant cancers

4. To Market, to Market—2020: Macromolecular Therapeutics

5. PROTACs Targeting BRM (SMARCA2) Afford Selective In Vivo Degradation over BRG1 (SMARCA4) and Are Active in BRG1 Mutant Xenograft Tumor Models

7. To Market, to Market—2018: Small Molecules

8. To Market, To Market--2017

10. Supplementary Data from Calicheamicin Antibody–Drug Conjugates with Improved Properties

11. Supplementary Data from An Anti–CD22-seco-CBI-Dimer Antibody–Drug Conjugate (ADC) for the Treatment of Non-Hodgkin Lymphoma That Provides a Longer Duration of Response than Auristatin-Based ADCs in Preclinical Models

12. Supplementary Table 1. Supplementary Figures 1 and 2. from Intratumoral Payload Concentration Correlates with the Activity of Antibody–Drug Conjugates

13. Cryo-EM reveals an unprecedented binding site for NaV1.7 inhibitors enabling rational design of potent hybrid inhibitors

14. PROTACs Targeting BRM (SMARCA2) Afford Selective In VivoDegradation over BRG1 (SMARCA4) and Are Active in BRG1 Mutant Xenograft Tumor Models

15. Author response: Cryo-EM reveals an unprecedented binding site for NaV1.7 inhibitors enabling rational design of potent hybrid inhibitors

16. CryoEM reveals unprecedented binding site for NaV1.7 inhibitors enabling rational design of potent hybrid inhibitors

17. To Market, To Market--2016

19. Structure-based optimization of hydroxylactam as potent, cell-active inhibitors of lactate dehydrogenase

27. Antibody-mediated delivery of chimeric protein degraders which target estrogen receptor alpha (ERα)

28. Calicheamicin Antibody–Drug Conjugates with Improved Properties

30. Antibody-Mediated Delivery of Chimeric BRD4 Degraders. Part 2: Improvement of In Vitro Antiproliferation Activity and In Vivo Antitumor Efficacy

31. Antibody-Mediated Delivery of Chimeric BRD4 Degraders. Part 1: Exploration of Antibody Linker, Payload Loading, and Payload Molecular Properties

32. An Anti–CD22-seco-CBI-Dimer Antibody–Drug Conjugate (ADC) for the Treatment of Non-Hodgkin Lymphoma That Provides a Longer Duration of Response than Auristatin-Based ADCs in Preclinical Models

33. Preclinical optimization of Ly6E-targeted ADCs for increased durability and efficacy of anti-tumor response

34. Synthesis of an optically active, bicyclic 2-pyridone dipeptide mimetic

35. Abstract 5687: Selective, chemically-induced degradation of BRM (SMARCA2) enables in vivo efficacy in BRG1 (SMARCA4)-deficient xenograft tumor models

36. Systematic Variation of Pyrrolobenzodiazepine (PBD)-Dimer Payload Physicochemical Properties Impacts Efficacy and Tolerability of the Corresponding Antibody–Drug Conjugates

37. Front Cover: Antibody Conjugation of a Chimeric BET Degrader Enables in vivo Activity (ChemMedChem 1/2020)

38. Improved translation of stability for conjugated antibodies using an in vitro whole blood assay

39. Niobium(III) and (IV) Halide Complexes

40. Formal, stereoselective synthesis of hydroxyethylene dipeptide isosteres utilizing pseudoephedrine amides

42. Spectroscopic and crystallographic characterization of (sigma 2-terpyridyl)Re(CO)3cl. 2D-NMR evidence for a linkage isomerization reaction

43. Studies on the thermal generation and reactivity of a class of (sigma, pi)-1,4-biradicals

45. Antibody Conjugation of a Chimeric BET Degrader Enables in vivo Activity

47. Catalytic Cleavage of Disulfide Bonds in Small Molecules and Linkers of Antibody–Drug Conjugates

49. Antibody–Drug Conjugates Derived from Cytotoxic seco-CBI-Dimer Payloads Are Highly Efficacious in Xenograft Models and Form Protein Adducts In Vivo

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