38 results on '"Sun, Chengzao"'
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2. Cyclic Peptide Linker Design and Optimization by Molecular Dynamics Simulations
3. Development of ProTx-II Analogues as Highly Selective Peptide Blockers of Nav1.7 for the Treatment of Pain
4. Guiding Chemically Synthesized Peptide Drug Lead Optimization by Derisking Mast Cell Degranulation-Related Toxicities of a NaV1.7 Peptide Inhibitor
5. Guiding Chemically Synthesized Peptide Drug Lead Optimization by Derisking Mast Cell Degranulation-Related Toxicities of a NaV1.7 Peptide Inhibitor.
6. Phage-display selection of a human single-chain F (sub v) antibody highly specific for melonoma and breast cancer cells using a chemoenzymatically synthesized G (sub M3) - carbohydrate antigen
7. Enabling ScFvs as multi-drug carriers: A dendritic approach
8. Native chemical ligation derived method for recombinant peptide/protein C-terminal amidation
9. CHAPTER 14. From Spider Toxins to Therapeutics—Developing Selective Nav1.7 Peptide Inhibitors for Pain
10. Bifunctional PEGylated Exenatide-Amylinomimetic Hybrids to Treat Metabolic Disorders: An Example of Long-Acting Dual Hormonal Therapeutics
11. Mixed aggregates containing n-butyl-, sec-butyl-, or tert-butyllithium and a chiral lithium amide derived from N-isopropyl-O-methyl valinol
12. Improved Glucose Control and Reduced Body Weight in Rodents with Dual Mechanism of Action Peptide Hybrids
13. Synthesis, Characterization, and Reaction of a Ketone-Derived 1,4-Dienolate Compound
14. Prevention of Drug-Induced Memory Impairment by Immunopharmacotherapy
15. Characterization of a Chiral Enolate Aggregate and Observation of 6Li−1H Scalar Coupling
16. Analysis of an Asymmetric Addition with a 2:1 Mixed Lithium Amide/n-Butyllithium Aggregate
17. Aggregation Studies of Complexes Containing a Chiral Lithium Amide and n-Butyllithium
18. A Sulfated, Phosphorylated 7 kDa Secreted Peptide Characterized by Direct Analysis of Cell Culture Media
19. Kinase-mediated trapping of bi-functional conjugates of paclitaxel or vinblastine with thymidine in cancer cells
20. Targeting Cell-Impermeable Prodrug Activation to Tumor Microenvironment Eradicates Multiple Drug-Resistant Neoplasms
21. The design, synthesis, and evaluation of two universal doxorubicin-linkers: Preparation of conjugates that retain topoisomerase II activity
22. A facile route to paclitaxel C-10 carbamates
23. Enzymatic Incorporation of an Antibody-Activated Blue Fluorophore into DNA
24. A Human Single-Chain Antibody Specific for Integrin α3β1 Capable of Cell Internalization and Delivery of Antitumor Agents
25. Solid-Phase Synthesis of Anandamide Analogues
26. Synthesis and Biological Validation of a Ubiquitous Quorum-Sensing Molecule
27. Phage-Display Selection of a Human Single-Chain Fv Antibody Highly Specific for Melanoma and Breast Cancer Cells Using a Chemoenzymatically Synthesized GM3−Carbohydrate Antigen
28. Syntheses of dendritic linkers containing chlorambucil residues for the preparation of antibody–multidrug immunoconjugates
29. Mixed Aggregates: Lithium Enolate of 3-Pentanone and a Chiral Lithium Amide
30. Bifunctional PEGylated Exenatide-AmylinomimeticHybridsto Treat Metabolic Disorders: An Example of Long-Acting Dual HormonalTherapeutics.
31. A Human Single-Chain Antibody Specific for Integrin α3β1 Capable of Cell Internalization and Delivery of Antitumor Agents
32. Development of ProTx-II Analogues as Highly Selective Peptide Blockers of Na v 1.7 for the Treatment of Pain.
33. Synthesis, characterization, and reaction of a ketone-derived 1,4-dienolate compound.
34. Characterization of a chiral enolate aggregate and observation of 6Li-1H scalar coupling.
35. A human single-chain antibody specific for integrin alpha3beta1 capable of cell internalization and delivery of antitumor agents.
36. Synthesis and biological validation of a ubiquitous quorum-sensing molecule.
37. Overexpression of legumain in tumors is significant for invasion/metastasis and a candidate enzymatic target for prodrug therapy.
38. Phage-display selection of a human single-chain fv antibody highly specific for melanoma and breast cancer cells using a chemoenzymatically synthesized G(M3)-carbohydrate antigen.
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