Taipei Medical University

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Lin, P.-Y., Shi, S.-J., Shu, H.-L., Chen, H.-F., Lin, C.-C., Liu, P.-C., Wang, L.-F.
------>authors3_c=None
------>paper_class1=1
------>Impact_Factor=None
------>paper_class3=2
------>paper_class2=1
------>vol=28
------>confirm_bywho=chenctsu
------>insert_bywho=wanglf
------>Jurnal_Rank=None
------>authors4_c=None
------>comm_author=1
------>patent_EDate=None
------>authors5_c=None
------>publish_day=None
------>paper_class2Letter=None
------>page2=272
------>medlineContent=
------>unit=E0103
------>insert_date=20010425
------>iam=7
------>update_date=
------>author=???
------>change_event=5
------>ISSN=None
------>authors_c=None
------>score=500
------>journal_name=Bioorganic Chemistry
------>paper_name=A Simple Procedure for Preparation of N-Thiazolyl and N-Thiadiazolylcantharidinimides and Evaluation of Their Cytotoxicities against Human Hepatocellular Carcinoma Cells.
------>confirm_date=20020509
------>tch_id=062001
------>pmid=11133145
------>page1=266
------>fullAbstract=We made an effort to prepare effective cantharidinimides by heating the reactants 1 and 2a-j to 200 degrees C with toluene and triethylamine to provide 10 N-thiazolyl- and N-thiadiazolylcantharidinimides 3a-j in high yields of 48-91%. All of the synthetic compounds were tested for their capability to suppress growth of the human hepatocellular carcinoma cell lines, SK-Hep-1 and Hep 3B. The results showed that compound 3f was the most potent, and it was more cytotoxic than cantharidin. Copyright 2000 Academic Press.
------>tmu_sno=None
------>sno=3661
------>authors2=None
------>authors3=None
------>authors4=None
------>authors5=None
------>authors6=None
------>authors6_c=None
------>authors=Lin, P.-Y., Shi, S.-J., Shu, H.-L., Chen, H.-F., Lin, C.-C., Liu, P.-C., Wang, L.-F.
------>delete_flag=0
------>SCI_JNo=None
------>authors2_c=None
------>publish_area=None
------>updateTitle=A Simple Procedure for Preparation of N-Thiazolyl and N-Thiadiazolylcantharidinimides and Evaluation of Their Cytotoxicities against Human Hepatocellular Carcinoma Cells.
------>language=2
------>check_flag=
------>submit_date=
------>country=None
------>no=
------>patent_SDate=None
------>update_bywho=
------>publish_year=2000
------>submit_flag=
------>publish_month=None
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z