PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
12721421-2	2003	In the present work, nicrospheres based on chitosan matrix, which incorporated aminophenylboronic acid as a derivative, were prepared and characterized, aimed at developing a beta-amylase adsorption process.	3-aminobenzeneboronic acid	79-102	beta-amylase	Glycine max	175-187
34424676-2	2021	We have carefully surface engineered the PLGA nanoparticle using amino dextran-fluorescein (A-DexFl) and amino-phenyl boronic acid (A-PBA) to exploit the binding affinity of boronic acids with that of cis-1,2 diols of dextran/glucose.	3-aminobenzeneboronic acid	105-130	suppressor of cytokine signaling 1	Homo sapiens	201-206
34866797-3	2022	We report the fabrication of an electrochemical sensor based on a molecularly imprinted polymer synthetic receptor for the quantitative detection of SARS-CoV-2 spike protein subunit S1 (ncovS1), by harnessing the covalent interaction between 1,2-diols of the highly glycosylated protein and the boronic acid group of 3-aminophenylboronic acid (APBA).	3-aminobenzeneboronic acid	317-342	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	160-165
34866797-3	2022	We report the fabrication of an electrochemical sensor based on a molecularly imprinted polymer synthetic receptor for the quantitative detection of SARS-CoV-2 spike protein subunit S1 (ncovS1), by harnessing the covalent interaction between 1,2-diols of the highly glycosylated protein and the boronic acid group of 3-aminophenylboronic acid (APBA).	3-aminobenzeneboronic acid	344-348	surface glycoprotein	Severe acute respiratory syndrome coronavirus 2	160-165
34876636-0	2021	Author Correction: Insulin smart drug delivery nanoparticles of aminophenylboronic acid-POSS molecule at neutral pH.	3-aminobenzeneboronic acid	64-87	insulin	Homo sapiens	19-26
34750459-0	2021	Insulin smart drug delivery nanoparticles of aminophenylboronic acid-POSS molecule at neutral pH.	3-aminobenzeneboronic acid	45-68	insulin	Homo sapiens	0-7
34750459-2	2021	Here, a glucose-responsive continuous insulin delivery system is developed, where novel polyhedral oligosilsesquioxane (POSS) modified with 3-aminophenylboronic acid (APBA) were used to encapsulate insulin (insulin entrapment efficiency: 73.2%) to prepare a fast response, high stability, good distribution, and excellent biocompatible system.	3-aminobenzeneboronic acid	140-165	insulin	Homo sapiens	38-45
34750459-2	2021	Here, a glucose-responsive continuous insulin delivery system is developed, where novel polyhedral oligosilsesquioxane (POSS) modified with 3-aminophenylboronic acid (APBA) were used to encapsulate insulin (insulin entrapment efficiency: 73.2%) to prepare a fast response, high stability, good distribution, and excellent biocompatible system.	3-aminobenzeneboronic acid	140-165	insulin	Homo sapiens	198-205
34750459-2	2021	Here, a glucose-responsive continuous insulin delivery system is developed, where novel polyhedral oligosilsesquioxane (POSS) modified with 3-aminophenylboronic acid (APBA) were used to encapsulate insulin (insulin entrapment efficiency: 73.2%) to prepare a fast response, high stability, good distribution, and excellent biocompatible system.	3-aminobenzeneboronic acid	167-171	insulin	Homo sapiens	38-45
34750459-2	2021	Here, a glucose-responsive continuous insulin delivery system is developed, where novel polyhedral oligosilsesquioxane (POSS) modified with 3-aminophenylboronic acid (APBA) were used to encapsulate insulin (insulin entrapment efficiency: 73.2%) to prepare a fast response, high stability, good distribution, and excellent biocompatible system.	3-aminobenzeneboronic acid	167-171	insulin	Homo sapiens	198-205
34750459-3	2021	Due to the strong hydrophobicity of POSS, the POSS moiety is located at the core in aqueous solution and combines with the boronic group of APBA and the diol generated in PEG-insulin to form a nanomicelle structure, that is, nanoparticles naturally.	3-aminobenzeneboronic acid	140-144	insulin	Homo sapiens	175-182
34750459-8	2021	Circular dichroism (CD) spectroscopy analysis was performed to measure insulin activity by comparing secondary structures of insulin, PEG-Insulin, and POSS-APBA@insulin.	3-aminobenzeneboronic acid	156-160	insulin	Homo sapiens	71-78
34750459-8	2021	Circular dichroism (CD) spectroscopy analysis was performed to measure insulin activity by comparing secondary structures of insulin, PEG-Insulin, and POSS-APBA@insulin.	3-aminobenzeneboronic acid	156-160	insulin	Homo sapiens	161-168
34424676-2	2021	We have carefully surface engineered the PLGA nanoparticle using amino dextran-fluorescein (A-DexFl) and amino-phenyl boronic acid (A-PBA) to exploit the binding affinity of boronic acids with that of cis-1,2 diols of dextran/glucose.	3-aminobenzeneboronic acid	132-137	suppressor of cytokine signaling 1	Homo sapiens	201-206
34342310-1	2021	Herein, we designed a diversified sensing platform for d-penicillamine based on amino-functionalized Zr-based metal-organic frameworks (UiO-66-NH2 MOFs) and 3-aminophenylboronic acid (APBA)@Alizarin Red (ARS).	3-aminobenzeneboronic acid	157-182	RIEG2	Homo sapiens	204-207
34342310-1	2021	Herein, we designed a diversified sensing platform for d-penicillamine based on amino-functionalized Zr-based metal-organic frameworks (UiO-66-NH2 MOFs) and 3-aminophenylboronic acid (APBA)@Alizarin Red (ARS).	3-aminobenzeneboronic acid	184-188	RIEG2	Homo sapiens	204-207
34342310-2	2021	The boronic acid group of 3-aminophenylboronic acid could react with Alizarin Red to form an APBA@ARS complex with a yellow fluorescence emission at 580 nm and ultraviolet absorption at 435 nm.	3-aminobenzeneboronic acid	26-51	RIEG2	Homo sapiens	98-101
34342310-2	2021	The boronic acid group of 3-aminophenylboronic acid could react with Alizarin Red to form an APBA@ARS complex with a yellow fluorescence emission at 580 nm and ultraviolet absorption at 435 nm.	3-aminobenzeneboronic acid	93-97	RIEG2	Homo sapiens	98-101
34342310-3	2021	APBA@ARS can greatly quench the fluorescence of UiO-66-NH2 MOFs at 450 nm via fluorescence resonance energy transfer (FRET).	3-aminobenzeneboronic acid	0-4	RIEG2	Homo sapiens	5-8
34342310-4	2021	When copper ions were present in the reaction system of APBA and Alizarin Red, the copper ions could complex with Alizarin Red to prevent the generation of APBA@ARS, and the absorption of Cu@ARS at 530 nm occurred.	3-aminobenzeneboronic acid	56-60	RIEG2	Homo sapiens	161-164
34342310-4	2021	When copper ions were present in the reaction system of APBA and Alizarin Red, the copper ions could complex with Alizarin Red to prevent the generation of APBA@ARS, and the absorption of Cu@ARS at 530 nm occurred.	3-aminobenzeneboronic acid	56-60	RIEG2	Homo sapiens	191-194
34342310-4	2021	When copper ions were present in the reaction system of APBA and Alizarin Red, the copper ions could complex with Alizarin Red to prevent the generation of APBA@ARS, and the absorption of Cu@ARS at 530 nm occurred.	3-aminobenzeneboronic acid	156-160	RIEG2	Homo sapiens	161-164
34342310-5	2021	Thus, the absorbance of APBA@ARS at 435 nm declined, restoring the fluorescence of UiO-66-NH2 MOFs.	3-aminobenzeneboronic acid	24-28	RIEG2	Homo sapiens	29-32
34342310-6	2021	Nevertheless, when d-penicillamine and copper ions coexist in the APBA and Alizarin Red reaction system, the copper ions would complex with the sulfhydryl group of d-penicillamine and no longer hinder the generation of APBA@ARS, and the fluorescence of UiO-66-NH2 MOFs is quenched again.	3-aminobenzeneboronic acid	66-70	RIEG2	Homo sapiens	224-227
34342310-6	2021	Nevertheless, when d-penicillamine and copper ions coexist in the APBA and Alizarin Red reaction system, the copper ions would complex with the sulfhydryl group of d-penicillamine and no longer hinder the generation of APBA@ARS, and the fluorescence of UiO-66-NH2 MOFs is quenched again.	3-aminobenzeneboronic acid	219-223	RIEG2	Homo sapiens	224-227
34342310-7	2021	Meanwhile, the absorbance of APBA@ARS at 435 nm enhanced and the absorbance at 530 nm decreased.	3-aminobenzeneboronic acid	29-33	RIEG2	Homo sapiens	34-37
35396654-2	2022	In vitro studies have demonstrated that the carbapenemase activity of KPC-2 and MBL can be inhibited by 3-aminophenylboronic acid and ethylenediaminetetraacetic acid (EDTA), respectively.	3-aminobenzeneboronic acid	104-129	carbapenem-hydrolyzing beta-lactamase KPC-2	Klebsiella pneumoniae	70-75
3103690-4	1987	We now confirm the involvement of serine and histidine in catalysing the phospholipase A2 action of lecithin-cholesterol acyltransferase by demonstrating the inhibition of this activity by phenylboronic acid (Ki = 1.23 mM) and m-aminophenylboronic acid (Ki = 2.32 mM), inhibitors of known serine/histidine hydrolases.	3-aminobenzeneboronic acid	229-252	phospholipase A2 group IB	Homo sapiens	73-89
3103690-4	1987	We now confirm the involvement of serine and histidine in catalysing the phospholipase A2 action of lecithin-cholesterol acyltransferase by demonstrating the inhibition of this activity by phenylboronic acid (Ki = 1.23 mM) and m-aminophenylboronic acid (Ki = 2.32 mM), inhibitors of known serine/histidine hydrolases.	3-aminobenzeneboronic acid	229-252	lecithin-cholesterol acyltransferase	Homo sapiens	100-136
34044194-1	2021	High quantum yield 3-aminophenylboronic acid-functionalized nitrogen-doped carbon dots (GAAP-CDs) were fabricated using a simple hydrothermal route and used as a sensing probe for toxic hypochlorite (ClO-).	3-aminobenzeneboronic acid	19-44	transmembrane BAX inhibitor motif containing 4	Homo sapiens	88-92
27376198-2	2016	Herein, we fabricated bovine serum albumin (BSA) protected Cu NCs (BSA-Cu NCs) and further functionalized them with 3-aminophenylboronic acid (APBA) for selectively discerning glycoproteins.	3-aminobenzeneboronic acid	143-147	albumin	Homo sapiens	29-42
33230701-3	2021	Upon PBA-CaCO3 introduction, 3-aminophenylboronic acid labeled to CaCO3 microsphere specifically recognized with CEA glycoprotein based on sugar-boronic acid interaction to form a sandwiched complex.	3-aminobenzeneboronic acid	29-54	CEA cell adhesion molecule 3	Homo sapiens	113-116
33455181-2	2020	In this study, amino phenylboronic acid-modified carbon dots (APBA-CDs) were introduced as a new nanoparticle-based on gp120 targeting that inhibits HIV-1 entry processes.	3-aminobenzeneboronic acid	15-39	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	119-124
32486639-0	2020	3-Aminophenyl boronic acid-functionalized quantum dot-based ratiometric fluorescence sensor for the highly sensitive detection of tyrosinase activity.	3-aminobenzeneboronic acid	0-26	tyrosinase	Homo sapiens	130-140
32486639-1	2020	Using the commercially available and economical 6-hydroxycoumarin (6-HC) as the substrate, a dual-emission ratiometric fluorescence sensor was developed to detect tyrosinase (TYR) activity based on 3-aminophenyl boronic acid-functionalized quantum dots (APBA-QDs).	3-aminobenzeneboronic acid	198-224	tyrosinase	Homo sapiens	163-173
32486639-1	2020	Using the commercially available and economical 6-hydroxycoumarin (6-HC) as the substrate, a dual-emission ratiometric fluorescence sensor was developed to detect tyrosinase (TYR) activity based on 3-aminophenyl boronic acid-functionalized quantum dots (APBA-QDs).	3-aminobenzeneboronic acid	198-224	tyrosinase	Homo sapiens	175-178
28822313-2	2018	Glucose was introduced into the GIP composed of Nafion and polyurethane along with aminophenyl boronic acid (APBA), which was formed on the bimetal electrode formed on a screen-printed electrode.	3-aminobenzeneboronic acid	83-107	gastric inhibitory polypeptide	Homo sapiens	32-35
28822313-2	2018	Glucose was introduced into the GIP composed of Nafion and polyurethane along with aminophenyl boronic acid (APBA), which was formed on the bimetal electrode formed on a screen-printed electrode.	3-aminobenzeneboronic acid	109-113	gastric inhibitory polypeptide	Homo sapiens	32-35
27368987-5	2016	RESULTS: Boronic acid disk test using meropenem as substrate and 600 microg of 3- aminophenylboronic acid (APB) was the most sensitive method (83.33 %) for detection of OXA-48, while the most specific method was MHT (100 %).	3-aminobenzeneboronic acid	79-105	OXA-48	Klebsiella pneumoniae	169-175
27107145-2	2016	The linkage effect of fructose-1,6-bisphosphate (FBP), the substrate of aldolase, can be achieved via its strong binding to magnetic nanoparticles (MNPs)/aminophenylboronic acid (APBA) and the formation of phosphoramidate bond derived from its reaction with p-phenylenediamine (PDA) on the surface of electrode.	3-aminobenzeneboronic acid	154-177	fructose-bisphosphatase 1	Homo sapiens	49-52
27107145-2	2016	The linkage effect of fructose-1,6-bisphosphate (FBP), the substrate of aldolase, can be achieved via its strong binding to magnetic nanoparticles (MNPs)/aminophenylboronic acid (APBA) and the formation of phosphoramidate bond derived from its reaction with p-phenylenediamine (PDA) on the surface of electrode.	3-aminobenzeneboronic acid	179-183	fructose-bisphosphatase 1	Homo sapiens	49-52
27368987-5	2016	RESULTS: Boronic acid disk test using meropenem as substrate and 600 microg of 3- aminophenylboronic acid (APB) was the most sensitive method (83.33 %) for detection of OXA-48, while the most specific method was MHT (100 %).	3-aminobenzeneboronic acid	107-110	OXA-48	Klebsiella pneumoniae	169-175
26298641-2	2016	In order to selectively capture HbA1c in sample, carboxy-EG6-undecanethiol was self-assembled on a gold thin-film substrate, followed by covalent coupling of 3-aminophenyl boronic acid (3-APBA).	3-aminobenzeneboronic acid	158-184	hemoglobin subunit alpha 1	Homo sapiens	32-36
26298641-2	2016	In order to selectively capture HbA1c in sample, carboxy-EG6-undecanethiol was self-assembled on a gold thin-film substrate, followed by covalent coupling of 3-aminophenyl boronic acid (3-APBA).	3-aminobenzeneboronic acid	186-192	hemoglobin subunit alpha 1	Homo sapiens	32-36
26048656-0	2015	A reliable phenotypic assay for detection of ESBLs and AmpCs in MBL-producing gram-negative bacteria with the use of aminophenylboronic acid, dipicolinic acid and cloxacillin.	3-aminobenzeneboronic acid	117-140	mannose-binding lectin family member 3, pseudogene	Homo sapiens	64-67
25678041-6	2015	For application, the Mn-doped CdS QDs were coated on the surface of a glassy carbon electrode and functionalized with a cell surface carbohydrate-specific ligand (3-aminophenylboronic acid).	3-aminobenzeneboronic acid	163-188	CDP-diacylglycerol synthase 1	Homo sapiens	30-33
24280050-2	2014	First, 3-aminobenzeneboronic acid (APBA) was used as the functional monomer and cross-linking reagent, which was polymerized on the surface of silicate-coated magnetic iron oxide nanoparticles (Fe3O4@SiO2 NPs) in the presence of human immunoglobulin G (HIgG), as the template exhibiting the same Fc region but different Fab region to anti-HIV-1 after the addition of the initiator, ammonium persulfate.	3-aminobenzeneboronic acid	7-33	FA complementation group B	Homo sapiens	320-323
24021657-0	2014	Sensitive and visible detection of apoptotic cells on Annexin-V modified substrate using aminophenylboronic acid modified gold nanoparticles (APBA-GNPs) labeling.	3-aminobenzeneboronic acid	89-112	annexin A5	Homo sapiens	54-63
24201003-5	2014	Next, the cis-diol group of ribose sugar at the end of the miRNAs chain allowed 3-aminophenylboronic acid (APBA)/biotin-modified multifunctional AuNPs (denoted as APBA-biotin-AuNPs) to be attached through the formation of a boronate ester covalent bond, which facilitated the capture of streptavidin-conjugated alkaline phosphatase (SA-ALP) via the biotin-streptavidin interaction.	3-aminobenzeneboronic acid	80-105	alkaline phosphatase, placental	Homo sapiens	311-331
24201003-5	2014	Next, the cis-diol group of ribose sugar at the end of the miRNAs chain allowed 3-aminophenylboronic acid (APBA)/biotin-modified multifunctional AuNPs (denoted as APBA-biotin-AuNPs) to be attached through the formation of a boronate ester covalent bond, which facilitated the capture of streptavidin-conjugated alkaline phosphatase (SA-ALP) via the biotin-streptavidin interaction.	3-aminobenzeneboronic acid	107-111	alkaline phosphatase, placental	Homo sapiens	311-331
24201003-5	2014	Next, the cis-diol group of ribose sugar at the end of the miRNAs chain allowed 3-aminophenylboronic acid (APBA)/biotin-modified multifunctional AuNPs (denoted as APBA-biotin-AuNPs) to be attached through the formation of a boronate ester covalent bond, which facilitated the capture of streptavidin-conjugated alkaline phosphatase (SA-ALP) via the biotin-streptavidin interaction.	3-aminobenzeneboronic acid	163-167	alkaline phosphatase, placental	Homo sapiens	311-331
24696553-5	2014	Co-production of ESBL and AmpC beta-lactamase was identified by using amino-phenylboronic acid disk method.	3-aminobenzeneboronic acid	70-94	EsbL	Escherichia coli	17-21
22410481-2	2012	The immunoelectrode design involves the use of amino phenylboronic acid for the oriented immobilization of anti-ACTH antibodies onto screen-printed carbon modified electrode surfaces.	3-aminobenzeneboronic acid	47-71	proopiomelanocortin	Homo sapiens	112-116
22281682-5	2012	We found that aminophenylboronic acid (APBA)-functionalized pNIPAm-co-AAc microgels in an etalon respond to 3 mg/mL glucose concentrations by red shifting their reflectance peaks by 110 nm up to 150 nm.	3-aminobenzeneboronic acid	14-37	glycine-N-acyltransferase	Homo sapiens	70-73
22281682-5	2012	We found that aminophenylboronic acid (APBA)-functionalized pNIPAm-co-AAc microgels in an etalon respond to 3 mg/mL glucose concentrations by red shifting their reflectance peaks by 110 nm up to 150 nm.	3-aminobenzeneboronic acid	39-43	glycine-N-acyltransferase	Homo sapiens	70-73
22016687-6	2011	The KPC-2-producing isolate was negative to phenotypic extended-spectrum beta-lactamase (ESBL) and AmpC detection tests and positive to modified Hodge test and carbapenemase inhibition test with aminophenylboronic acid.	3-aminobenzeneboronic acid	195-218	carbapenem-hydrolyzing beta-lactamase KPC-2	Klebsiella pneumoniae	4-9
21268025-1	2011	To develop self-regulated insulin delivery system, the glucose-sensitive copolymers with a fraction of phenylboronic acid group were prepared by the coupling reaction of -COOH of N-(carboxyacyl) chitosan and -NH(2) of 3-aminophenylboronic acid.	3-aminobenzeneboronic acid	218-243	insulin	Homo sapiens	26-33
21111601-2	2011	A pi-conjugated molecularly imprinted polymer (MIP) with nanopatterns for T-2 toxin (T-2) was prepared on SPR chip by in situ electropolymerization of 3-aminophenylboronicacid (3-APBA) with T-2.	3-aminobenzeneboronic acid	151-175	solute carrier family 25 member 5	Homo sapiens	85-88
21111601-2	2011	A pi-conjugated molecularly imprinted polymer (MIP) with nanopatterns for T-2 toxin (T-2) was prepared on SPR chip by in situ electropolymerization of 3-aminophenylboronicacid (3-APBA) with T-2.	3-aminobenzeneboronic acid	151-175	solute carrier family 25 member 5	Homo sapiens	85-88
21111601-2	2011	A pi-conjugated molecularly imprinted polymer (MIP) with nanopatterns for T-2 toxin (T-2) was prepared on SPR chip by in situ electropolymerization of 3-aminophenylboronicacid (3-APBA) with T-2.	3-aminobenzeneboronic acid	177-183	solute carrier family 25 member 5	Homo sapiens	85-88
21111601-2	2011	A pi-conjugated molecularly imprinted polymer (MIP) with nanopatterns for T-2 toxin (T-2) was prepared on SPR chip by in situ electropolymerization of 3-aminophenylboronicacid (3-APBA) with T-2.	3-aminobenzeneboronic acid	177-183	solute carrier family 25 member 5	Homo sapiens	85-88
17204406-4	2007	Addition of 300 mg/L 3-aminophenylboronic acid (APB) reduced the minimum inhibitory concentration for 90% of the organisms (MIC(90)) of imipenem and meropenem eight- and four-fold, respectively, for the bla(CMY-2)- and bla(DHA-1)-positive isolates, confirming the role of these enzymes in resistance.	3-aminobenzeneboronic acid	21-46	TEM beta-lactamase	Klebsiella pneumoniae	203-206
17204406-4	2007	Addition of 300 mg/L 3-aminophenylboronic acid (APB) reduced the minimum inhibitory concentration for 90% of the organisms (MIC(90)) of imipenem and meropenem eight- and four-fold, respectively, for the bla(CMY-2)- and bla(DHA-1)-positive isolates, confirming the role of these enzymes in resistance.	3-aminobenzeneboronic acid	21-46	TEM beta-lactamase	Klebsiella pneumoniae	219-222
17204406-4	2007	Addition of 300 mg/L 3-aminophenylboronic acid (APB) reduced the minimum inhibitory concentration for 90% of the organisms (MIC(90)) of imipenem and meropenem eight- and four-fold, respectively, for the bla(CMY-2)- and bla(DHA-1)-positive isolates, confirming the role of these enzymes in resistance.	3-aminobenzeneboronic acid	48-51	TEM beta-lactamase	Klebsiella pneumoniae	203-206
17204406-4	2007	Addition of 300 mg/L 3-aminophenylboronic acid (APB) reduced the minimum inhibitory concentration for 90% of the organisms (MIC(90)) of imipenem and meropenem eight- and four-fold, respectively, for the bla(CMY-2)- and bla(DHA-1)-positive isolates, confirming the role of these enzymes in resistance.	3-aminobenzeneboronic acid	48-51	TEM beta-lactamase	Klebsiella pneumoniae	219-222
16165279-6	2005	Finally, attempt has been made in order to increase the sensitivity of the glycation assay through efficient enrichment of the glycated insulin on magnetic beads containing immobilized 3-aminophenylboronic acid (APBA) on their surface.	3-aminobenzeneboronic acid	185-210	insulin	Bos taurus	136-143
16165279-6	2005	Finally, attempt has been made in order to increase the sensitivity of the glycation assay through efficient enrichment of the glycated insulin on magnetic beads containing immobilized 3-aminophenylboronic acid (APBA) on their surface.	3-aminobenzeneboronic acid	212-216	insulin	Bos taurus	136-143