PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19035590-0	2009	Selective benzylic and allylic alkylation of protic nucleophiles with sulfonamides through double Lewis acid catalyzed cleavage of sp3 carbon-nitrogen bonds.	Sulfonamides	70-82	Sp3 transcription factor	Homo sapiens	131-134	
32162518-5	2020	Thus, going from the sp3-hybrid lone pair in common sulfonamides to the sp-like lone pair in the smallest Paquette"s sultam resulted in an increase in S-N bond length by ca.	Sulfonamides	52-64	Sp3 transcription factor	Homo sapiens	21-24	
27897342-0	2017	Catalytic sp3 -sp3 Functionalisation of Sulfonamides: Late-Stage Modification of Drug-Like Molecules.	Sulfonamides	40-52	Sp3 transcription factor	Homo sapiens	10-13	
27897342-0	2017	Catalytic sp3 -sp3 Functionalisation of Sulfonamides: Late-Stage Modification of Drug-Like Molecules.	Sulfonamides	40-52	Sp3 transcription factor	Homo sapiens	15-18	
27897342-1	2017	A new application of Pd-catalysed allylation is reported that enables the synthesis of a range of branched sp3 -functionalised sulfonamides, a compound class for which few reported methods exist.	Sulfonamides	127-139	Sp3 transcription factor	Homo sapiens	107-110	
35441519-1	2022	A convenient "green" stereoretentive approach to sp3-enriched secondary sulfonamides bearing an asymmetric center at the alpha position to the sulfur atom is described.	Sulfonamides	72-84	Sp3 transcription factor	Homo sapiens	49-52