PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24937183-0	2014	Synthesis and cytotoxic effect on cancer cell lines and macrophages of novel progesterone derivatives having an ester or a carbamate function at C-3 and C-17.	Carbamates	123-132	cytokine like 1	Homo sapiens	153-157	
24937183-2	2014	In the second series, both functional groups (ester and carbamate) are bound to C-17 on the pregn-4,6-diene-3,20-dione scaffold (13a-e and 14a-e).	Carbamates	56-65	cytokine like 1	Homo sapiens	80-84	
24937183-4	2014	The results from this study showed that steroid 14a, having a carbamate function at C-17, was the most potent against PC-3 cell line (96.6%) while 8c and 8e showed much higher cytotoxic activity (100%) for MCF-7 cell line.	Carbamates	62-71	cytokine like 1	Homo sapiens	84-88	
18582482-0	2008	Synthesis of novel C17 steroidal carbamates.	Carbamates	33-43	cytokine like 1	Homo sapiens	19-22	
18582482-2	2008	We have exploited the reaction of 1,1"-carbonylbis(2-methylimidazole) (CBMI) with several 17beta-hydroxy androstanes to synthesize a series of novel C17 steroidal carbamates.	Carbamates	163-173	cytokine like 1	Homo sapiens	149-152	
18582482-7	2008	The carbamate moiety at C17 allowed tight binding of the synthesized compounds to both wild-type (wt-) and mutated AR.	Carbamates	4-13	cytokine like 1	Homo sapiens	24-27	
17629476-0	2007	Steroids with a carbamate function at C-17, a novel class of inhibitors for human and hamster steroid 5alpha-reductase.	Carbamates	16-25	cytokine like 1	Homo sapiens	38-42