The influence of catalyst in reaction 13599-22-9

There is still a lot of research devoted to this compound(SMILES:OC(=O)C1=NN(C(=C1)C1=CC=CC=C1)C1=CC=CC=C1)Application of 13599-22-9, and with the development of science, more effects of this compound(13599-22-9) can be discovered.

Application of 13599-22-9. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 1,5-Diphenyl-1H-pyrazole-3-carboxylic acid, is researched, Molecular C16H12N2O2, CAS is 13599-22-9, about Bcl-2/MDM2 Dual Inhibitors Based on Universal Pyramid-Like α-Helical Mimetics. Author is Wang, Ziqian; Song, Ting; Feng, Yingang; Guo, Zongwei; Fan, Yudan; Xu, Wenjie; Liu, Lu; Wang, Anhui; Zhang, Zhichao.

No α-helical mimetic that exhibits Bcl-2/MDM2 dual inhibition has been rationally designed due to the different helicities of the α-helixes at their binding interfaces. Herein, the authors extracted a one-turn α-helix-mimicking ortho-triarene unit from o-phenylene foldamers. Linking benzamide substrates with a rotatable C-N bond, the authors constructed a novel semirigid pyramid-like scaffold that could support its two-turn α-helix mimicry without aromatic stacking interactions and could adopt the different dihedral angles of the key residues of p53 and BH3-only peptides. On the basis of this universal scaffold, a series of substituent groups were installed to capture the key residues of both p53TAD and BimBH3 and balance the differences of the bulks between them. Identified by FP, ITC, and NMR spectroscopy, compound I that directly binds to Mcl-1, Bcl-2, and MDM2 with balanced submicromolar affinities was obtained. Cell-based experiments demonstrated its antitumor ability through Bcl-2/MDM2 dual inhibition simultaneously.

There is still a lot of research devoted to this compound(SMILES:OC(=O)C1=NN(C(=C1)C1=CC=CC=C1)C1=CC=CC=C1)Application of 13599-22-9, and with the development of science, more effects of this compound(13599-22-9) can be discovered.

Reference:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem