PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
23470610-16	2013	The amisulpiride-ECT combination appears to be a safe treatment option.	amisulpride	4-16	ECT	Homo sapiens	17-20
32164484-2	2021	The objective of this study was to determine the relationship between the sequential ubiquitination of lysine residues K284 to K214 in AKT and R-HSPA5 (the arginylated form of HSPA5), which contribute to the autophagic/lysosomal degradation of AKT when impaired proteasomal activity induces cellular stress.	amisulpride	127-131	thymoma viral proto-oncogene 1	Mus musculus	135-138
32164484-2	2021	The objective of this study was to determine the relationship between the sequential ubiquitination of lysine residues K284 to K214 in AKT and R-HSPA5 (the arginylated form of HSPA5), which contribute to the autophagic/lysosomal degradation of AKT when impaired proteasomal activity induces cellular stress.	amisulpride	127-131	thymoma viral proto-oncogene 1	Mus musculus	244-247
32164484-7	2021	MUL1 (mitochondrial ubiquitin ligase activator of NFKB 1) also played a vital role in the lysosomal degradation of AKT by sequentially ubiquitinating AKT residues K284 to K214 for R-HSPA5-mediated autophagy.	amisulpride	171-175	mitochondrial ubiquitin ligase activator of NFKB 1	Mus musculus	0-4
32164484-7	2021	MUL1 (mitochondrial ubiquitin ligase activator of NFKB 1) also played a vital role in the lysosomal degradation of AKT by sequentially ubiquitinating AKT residues K284 to K214 for R-HSPA5-mediated autophagy.	amisulpride	171-175	mitochondrial ubiquitin ligase activator of NFKB 1	Mus musculus	6-56
32164484-7	2021	MUL1 (mitochondrial ubiquitin ligase activator of NFKB 1) also played a vital role in the lysosomal degradation of AKT by sequentially ubiquitinating AKT residues K284 to K214 for R-HSPA5-mediated autophagy.	amisulpride	171-175	thymoma viral proto-oncogene 1	Mus musculus	115-118
32164484-7	2021	MUL1 (mitochondrial ubiquitin ligase activator of NFKB 1) also played a vital role in the lysosomal degradation of AKT by sequentially ubiquitinating AKT residues K284 to K214 for R-HSPA5-mediated autophagy.	amisulpride	171-175	thymoma viral proto-oncogene 1	Mus musculus	150-153
32164484-7	2021	MUL1 (mitochondrial ubiquitin ligase activator of NFKB 1) also played a vital role in the lysosomal degradation of AKT by sequentially ubiquitinating AKT residues K284 to K214 for R-HSPA5-mediated autophagy.	amisulpride	171-175	heat shock protein 5	Mus musculus	182-187
32164484-9	2021	These results suggest that MUL1-mediated sequential ubiquitination of K284 to K214 may serve as a novel mechanism by which AKT is designated for lysosomal degradation.	amisulpride	78-82	mitochondrial ubiquitin ligase activator of NFKB 1	Mus musculus	27-31
32164484-9	2021	These results suggest that MUL1-mediated sequential ubiquitination of K284 to K214 may serve as a novel mechanism by which AKT is designated for lysosomal degradation.	amisulpride	78-82	thymoma viral proto-oncogene 1	Mus musculus	123-126
31687648-9	2019	Moreover, peripheral administration of the dopamine D2 receptor antagonist amisulpride to diabetic mice restored trabecular bone structure to near normal and partially reversed downregulation of LOX.	amisulpride	75-86	dopamine receptor D2	Mus musculus	43-63
31687648-9	2019	Moreover, peripheral administration of the dopamine D2 receptor antagonist amisulpride to diabetic mice restored trabecular bone structure to near normal and partially reversed downregulation of LOX.	amisulpride	75-86	lysyl oxidase	Mus musculus	195-198
32002948-3	2018	METHODS: The present study examines the differential effects of time-dependent treatment with haloperidol, olanzapine and amisulpride (20 muM) on VEGF and MAPK mRNA expression and VEGF level, using the T98 cell line as an example of nerve cells.	amisulpride	122-133	vascular endothelial growth factor A	Homo sapiens	146-150
23660595-3	2013	We mutated 3 amino acids (K214 and R282 in the calreticulin interaction site and C406 in the isomerase catalytic site), which are important for Pdia3"s ER chaperone function, and examined their role in responses to 1alpha,25(OH)2D3.	amisulpride	26-30	protein disulfide isomerase associated 3	Mus musculus	144-149