489446-42-6Relevant articles and documents
Design, synthesis and biological evaluation of PSMA/hepsin-targeted heterobivalent ligands
Subedi, Milan,Minn, Il,Chen, Jianbo,Kim, YunHye,Ok, Kiwon,Jung, Yong Woo,Pomper, Martin G.,Byun, Youngjoo
, p. 208 - 218 (2016)
Cell surface biomarkers such as prostate-specific membrane antigen (PSMA) and hepsin have received considerable attention as targets for imaging prostate cancer (PCa) due to their high cell surface expression in such tumors and easy access for imaging pro
Synthesis method of 4-amino methylphenylboronic acid hydrochloride
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Paragraph 0020; 0022; 0024; 0026; 0028; 0030, (2021/04/28)
The invention discloses a synthesis method of 4-amino methylphenylboronic acid hydrochloride, and belongs to the field of organic synthesis. According to the method, 4-formyl phenylboronic acid is used as an initial raw material and is condensed with tert-butyl carbamate, and the 4-amino methylphenylboronic acid hydrochloride is generated through three steps of reactions of reduction and Boc removal. According to the method, imine is synthesized through condensation with 4-formyl phenylboronic acid, then sodium borohydride is reduced, and finally deprotection and salification are carried out, so that direct high-pressure hydrogenation in literatures is avoided, the yield is obviously increased, and meanwhile, the process reproducibility is good.
QUINOXALINE COMPOUNDS AND USES THEREOF
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Paragraph 00273, (2015/11/09)
This invention provides compounds of formula I and subsets thereof: wherein T, J, R, R4, Rq, o, RA, and RB and subsets thereof are as described in the specification. The compounds are inhibitors of NAMPT and are thus useful for treating cancer, inflammatory conditions, or T-cell mediated autoimmune disease.
Compounds with medicinal effects due to interaction with the glucocorticoid receptor
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Page/Page column 17, (2010/11/27)
The invention provides for compounds having the structure according to the formula I
Small molecule thienopyrimidine-based protein tyrosine kinase inhibitors
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Page/Page column 40, (2010/02/15)
Various thienopyrimidine-based analog compounds are able to selectively inhibit the Src family of tyrosine kinases. These compounds are useful in the treatment of various diseases including hyperproliferative diseases, hematologic diseases, osteoporosis, neurological diseases, autoimmune diseases, allergic/immunological diseases, or viral infections.