CYTOTOXIC PEPTIDES AND ANTIBODY DRUG CONJUGATES THEREOF
申请人:PFIZER INC.
公开号:US20130129753A1
公开(公告)日:2013-05-23
The present invention is directed to cytotoxic pentapeptides, to antibody drug conjugates thereof, and to methods for using the same to treat cancer.
本发明涉及细胞毒性五肽,其抗体药物偶联物,以及使用它们治疗癌症的方法。
[EN] MACROCYCLIC COMPOUNDS FOR MODULATING IL-17<br/>[FR] COMPOSÉS MACROCYCLIQUES POUR UNE MODULATION D'IL-17
申请人:ENSEMBLE THERAPEUTICS CORP
公开号:WO2013116682A1
公开(公告)日:2013-08-08
The invention relates generally to macrocyclic compounds of formula I and their therapeutic use. More particularly, the invention relates to macrocyclic compounds that modulate the activity of IL-17 and/or are useful in the treatment of medical conditions, such as inflammatory diseases and other IL-17-associated disorders.
Activation of aliphatic carbon–carbon bonds of esters and amides by rhodium(II) porphyrin
作者:Lirong Zhang、Kin Shing Chan
DOI:10.1016/j.jorganchem.2007.01.012
日期:2007.4
Aliphatic carbon–carbon bonds of esters and amides were activated successfully with rhodium(II) porphyrin radical to give rhodium(III) porphyrin alkyls in moderate yields.
酯和酰胺的脂族碳-碳键已被铑(II)卟啉自由基成功激活,从而以中等收率得到了铑(III)卟啉烷基。
BIFUNCTIONAL CYTOTOXIC AGENTS CONTAINING THE CTI PHARMACOPHORE
申请人:Pfizer Inc.
公开号:US20160271270A1
公开(公告)日:2016-09-22
The present invention is directed to novel bifunctional CTI-CTI and CBI-CTI dimers of the formula:
F
1
-L
1
-T-L
2
-F
2
where F
1
, L
1
, T, L
2
and F
2
are as defined herein, useful for the treatment for proliferative diseases, where the inventive dimers can function as stand-alone drugs, payloads in antibody-drug-conjugates (ADCs), and linker-payload compounds useful in connection with the production or administration of such ADCs; and to compositions including the aforementioned dimers, linker-payloads and ADCs, and methods for using these dimers, linker-payloads and ADCs, to treat pathological conditions including cancer.
Ti-direct, powerful, stereoselective aldol-type additions of esters and thioesters to carbonyl compounds: application to the synthesis and evaluation of lactone analogs of jasmone perfumes
thiophenyl esters or thioaryl esters with aldehydes and ketones was performed (total 46 examples). The present method is advantageous from atom-economical and cost-effective viewpoints; good to excellent yields, moderate to good syn-selectivity, substrate variations, reagent availability, and simple procedures. Utilizing the present reaction as the key step, an efficient short synthesis of three lactone