count	source_label	source_id	relationship	target_label	target_id	entity_type	solr_id	publication_id	sentences
4		CHEBI:3652	inhibits	sec-butylamine	CHEBI:74526	Chemical	52577666-bc3f-11e5-8abe-001a4ae51246	10.1016/j.pestbp.2007.04.004	A similar observation was made by Rhodes that ALS inhibitor chlorsulfuron induced a rapid accumulation of 2-AB in higher plantL.
4		CHEBI:5869	activates	sec-butylamine	CHEBI:74526	Chemical	52577666-bc3f-11e5-8abe-001a4ae51246	10.1016/j.pestbp.2007.04.004	However, Shaner elicited opposite conclusion that growth inhibition following imazaquin treatment is not due to accumulation of 2-KB and/ or 2-AB in plants, though imazaquin significantly raised intracellular 2-KB concentration in his experiment, feeding 2-AB and 2-KB to maize plants increased 2-KB and 2-AB pools to much higher levels than those observed in imazaquin treated plants, yet such high pools of 2-KB and 2-AB in the plant had no significant effect on growth.
1	sec-butylamine	CHEBI:74526	activates		UNIPROT:P49441	Protein	1acb88e8-bbfb-11e5-9b9d-001a4ae51247	PMC2659391	Results and discussion ZOL and sec-butylamine induce IPP/DMAPP accumulation in J774·
1	sec-butylamine	CHEBI:74526	activates		UNIPROT:Q8NET8	Protein	fd3e7432-bc29-11e5-8abe-001a4ae51246	PMC3152771	"To further characterize the specificity of synoviocyte ""warm"" temperature response we monitored changes in [Ca2+]iduring prolonged exposure to 30 or 36°C in the presence or absence of 2-aminoethoxydiphenyl borate (2-AB) which activates and sensitizes TRPV3, but not TRPV4 [17,18]."
1	sec-butylamine	CHEBI:74526	activates		CHEBI:28875	Chemical	14d6ab4e-bbd7-11e5-9b9d-001a4ae51247	10.1016/j.molcatb.2011.02.012	Kinetics and enantioselectivity of sec-butylamine N-acylation The synthesis of myristic acid methylpropylamide catalyzed byC.
1	sec-butylamine	CHEBI:74526	activates		CHEBI:16057	Chemical	1acb88e8-bbfb-11e5-9b9d-001a4ae51247	PMC2659391	Results and discussion ZOL and sec-butylamine induce IPP/DMAPP accumulation in J774·
1	sec-butylamine	CHEBI:74526	activates		CHEBI:25750	Chemical	1c5a4f54-4fb1-11e8-ba45-001a4a160175	PMC5933716	Therefore, 2-AB, an aniline derivative, may accelerate the conversion of an oxime into its corresponding imine derivative.
1	sec-butylamine	CHEBI:74526	activates		CHEBI:3392	Chemical	6f1d5dfa-bc31-11e5-9b9d-001a4ae51247	PMC3788055	The metabolites 2-AB and 2-HB were identified during the growth of strain djl-11 on MBC, supporting previous studies of MBC catabolism byNocardioidessp.
1	sec-butylamine	CHEBI:74526	inhibits		GO:0000280	Phenotype	bd6450dc-c933-11ee-b346-0050569a791b	10.1016/j.chemosphere.2022.137723	One of the carbendazim degradation products is 2-amino-benzimidazole (2-AB) (Kiss and Virág, 2009), a kind of highly toxic substance, which could inhibit cell proliferation by blocking the processes of nuclear division (Yenjerla et al., 2009).
1	sec-butylamine	CHEBI:74526	inhibits		GO:0008283	Phenotype	bd6450dc-c933-11ee-b346-0050569a791b	10.1016/j.chemosphere.2022.137723	One of the carbendazim degradation products is 2-amino-benzimidazole (2-AB) (Kiss and Virág, 2009), a kind of highly toxic substance, which could inhibit cell proliferation by blocking the processes of nuclear division (Yenjerla et al., 2009).
1	sec-butylamine	CHEBI:74526	activates		GO:0009056	Phenotype	6f1d5dfa-bc31-11e5-9b9d-001a4ae51247	PMC3788055	The metabolites 2-AB and 2-HB were identified during the growth of strain djl-11 on MBC, supporting previous studies of MBC catabolism byNocardioidessp.
1		PF:PF08886	activates	sec-butylamine	CHEBI:74526	ProteinFamily	e2438cfa-3546-11e9-9cf0-001a4a160175	PMC5861832	4, the Glu–2-AB ligase activity catalyzed by wild-type GshA was inhibited by 50% in the presence of GSH.
1		UNIPROT:P48637	activates	sec-butylamine	CHEBI:74526	Protein	4daefebc-bc18-11e5-8abe-001a4ae51246	10.1016/j.yjmcc.2013.02.008	2-AB is metabolized to ophthalmate via γ-Glu-2-AB through a 2-step reaction and then catalyzed sequentially by γ-glutamylcysteine synthetase and glutathione synthetase[10].
1		UNIPROT:L0R6Q1	inhibits	sec-butylamine	CHEBI:74526	Protein	dd82716e-351e-11e8-9fbf-001a4a160176	28167211	Supplementary Fig. 4Supplementary Fig. 5N-glycan profiles of wild type and SLC35A4-deficient HepG2 cells.N-glycans were enzymatically released from glycoproteins produced by wild type and SLC35A4-deficient HepG2 cells, fluorescently labeled with 2-AB, purified and separated on the GlycoSep N column using HPLC.
