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arl 67156 trisodium salt  (Tocris)


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    Structured Review

    Tocris arl 67156 trisodium salt
    Arl 67156 Trisodium Salt, supplied by Tocris, used in various techniques. Bioz Stars score: 94/100, based on 61 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/arl+67156/ARL+67156+trisodium+salt/pmc12629791-96-0-5
    Average 94 stars, based on 61 article reviews
    arl 67156 trisodium salt - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    other:

    Article Title: Pannexin 1: a novel regulator of acute hypoxic pulmonary vasoconstriction
    Article Snippet: Endogenous ecto-nucleotidases were inhibited by addition of ARL 67156 (300 mMol/L; Tocris; Bristol, UK).

    Article Title: The dualistic role of the purinergic P2Y12-receptor in an in vivo model of Parkinson's disease: Signalling pathway and novel therapeutic targets.
    Article Snippet: ARL 67156 (Cat. No. 1283) and PSB 0739 were from Tocris Biosciences, Bristol, UK (Cat. No. 3983) and FasudilHCl were from LC Laboratories, Woburn, MA, USA (Cat. No. F-4660).

    Article Title: The ATP-exporting channel Pannexin 1 promotes CD8 + T cell effector and memory responses
    Article Snippet: ARL-67156 , Tocris , Cat# 1283.

    Article Title: Microglia contribute to neuronal synchrony despite endogenous ATP-related phenotypic transformation in acute mouse brain slices
    Article Snippet: The same confocal setup was used in combination with a ×40 objective (CFI Apochromat Lambda S ×40/1.25 WI NA = 1.25 WD = 0.18 mm FOV (full) = 840 μm) to image ATP dynamics after ecto-ATPase blockade by ARL 67156 (Tocris; 10uM); 0.5 frame/s.

    Produced:

    Article Title: Compositions and methods for regulating blood pressure
    Article Snippet: ARL 67156 was purchased from Tocris, and 10Panx1 was produced by Genscript. .. ARL 67156 was purchased from Tocris, and 10Panx1 was produced by Genscript. ..

    Recombinant:

    Article Title: Compositions and methods for regulating leukocyte adhesion
    Article Snippet: .. Endogenous ecto-nucleotidases were inhibited by incubating EC monolayers with 300 μM ARL 67156 (Tocris) for 30 minutes at 37° C. Cells were then stimulated with recombinant human TNFα (R&D Systems). ..

    shRNA:

    Article Title: Extracellular Nucleotides and Histamine Suppress TLR3- and RIG-I-Mediated Release of Antiviral IFNs from Human Airway Epithelial Cells.
    Article Snippet: All experiments that used media for the stimulation phase utilized Lonza BEBM (CC-3171) media supplemented with Ca2+ to bring the total concentration up to 2mM. .. Pharmacological tools were as follows: UTP (Sigma U6875), SLIGKV-NH2 (Tocris 4153), ATP (Sigma A6419), Adenosine (Tocris 3624), AR-C 118925XX (Tocris 4890), histamine (Tocris 3545), BTP2 (Sigma 203890), cetirizine (Tocris 2577), YM-254890 (Cayman Chemical 29735), Gö 6983 (Tocris 2285), GF 109203X (Tocris 0741), PDBu (Tocris 4153), PMA (Tocris 1201), ruxolitinib (Tocris 7054), ARL 67156 (Tocris 1283), NECA (Tocris 1691), IFN-β (R & D systems 8499-IF), poly(I:C) (Invivogen tlrl-picw), 2,3 cGAMP (Invivogen tlrl-nacga23), ISD (Invivogen tlrl-isdn), 3p-hpRNA (Invivogen tlrl-hprna). shRNA knockdowns: On day 0, NHBE cells were thawed into T-25 flasks at approximately 25,000 cells/flask. ..



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    Tocris arl67156
    a A schematic diagram of ATP release from tanycytes and conversion of nucleotides by ectonucleotidases. ATP is released through Cx43 from tanycytes and is converted to ADP and AMP by ENTPD. AMP is converted to adenosine by NT5E. Adenosine is transported by ENT1 and is converted to inosine by ADA. b Relative expression levels of ectonucleotidases families and nucleoside transporters in A2/29 cells ( n = 6). c Relative intracellular and extracellular adenosine levels in si-scram and si- Tspo A2/29 cells ( n = 9 per group). d , f Relative intracellular and extracellular ATP levels in si-scram and si- Tspo A2/29 cells in the presence or absence of ENTPD inhibitor ( <t>ARL67156</t> , 0.1 mM) ( d ) or NT5E inhibitor (APCP, 0.1 mM) ( f ) for 3 h ( n = 9 per group). e, g – i Relative intracellular and extracellular adenosine levels in si-scram and si- Tspo A2/29 cells in the presence or absence of ARL67156 ( e ) APCP ( g ) ADA inhibitor (EHNA, 0.01 mM) ( h ) or ENT1 inhibitor (NBMPR, 0.01 mM) ( i ) for 3 h ( n = 9 per group). Data are mean ± s.e.m. or boxes indicating the interquartile range with whiskers, and dotted lines indicate that significance was calculated separately for each. Significance was determined by one-way ANOVA with Dunnett’s multiple-comparisons test (** P < 0.01, **** P < 0.0001) in b two-tailed unpaired Student’s t -test (*** P < 0.001) in c or otherwise by two-way ANOVA with Šidák’s multiple-comparisons test (** P < 0.01, *** P < 0.001, **** P < 0.0001). n.s., not significant.
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    a A schematic diagram of ATP release from tanycytes and conversion of nucleotides by ectonucleotidases. ATP is released through Cx43 from tanycytes and is converted to ADP and AMP by ENTPD. AMP is converted to adenosine by NT5E. Adenosine is transported by ENT1 and is converted to inosine by ADA. b Relative expression levels of ectonucleotidases families and nucleoside transporters in A2/29 cells ( n = 6). c Relative intracellular and extracellular adenosine levels in si-scram and si- Tspo A2/29 cells ( n = 9 per group). d , f Relative intracellular and extracellular ATP levels in si-scram and si- Tspo A2/29 cells in the presence or absence of ENTPD inhibitor ( <t>ARL67156</t> , 0.1 mM) ( d ) or NT5E inhibitor (APCP, 0.1 mM) ( f ) for 3 h ( n = 9 per group). e, g – i Relative intracellular and extracellular adenosine levels in si-scram and si- Tspo A2/29 cells in the presence or absence of ARL67156 ( e ) APCP ( g ) ADA inhibitor (EHNA, 0.01 mM) ( h ) or ENT1 inhibitor (NBMPR, 0.01 mM) ( i ) for 3 h ( n = 9 per group). Data are mean ± s.e.m. or boxes indicating the interquartile range with whiskers, and dotted lines indicate that significance was calculated separately for each. Significance was determined by one-way ANOVA with Dunnett’s multiple-comparisons test (** P < 0.01, **** P < 0.0001) in b two-tailed unpaired Student’s t -test (*** P < 0.001) in c or otherwise by two-way ANOVA with Šidák’s multiple-comparisons test (** P < 0.01, *** P < 0.001, **** P < 0.0001). n.s., not significant.
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    Image Search Results


    a A schematic diagram of ATP release from tanycytes and conversion of nucleotides by ectonucleotidases. ATP is released through Cx43 from tanycytes and is converted to ADP and AMP by ENTPD. AMP is converted to adenosine by NT5E. Adenosine is transported by ENT1 and is converted to inosine by ADA. b Relative expression levels of ectonucleotidases families and nucleoside transporters in A2/29 cells ( n = 6). c Relative intracellular and extracellular adenosine levels in si-scram and si- Tspo A2/29 cells ( n = 9 per group). d , f Relative intracellular and extracellular ATP levels in si-scram and si- Tspo A2/29 cells in the presence or absence of ENTPD inhibitor ( ARL67156 , 0.1 mM) ( d ) or NT5E inhibitor (APCP, 0.1 mM) ( f ) for 3 h ( n = 9 per group). e, g – i Relative intracellular and extracellular adenosine levels in si-scram and si- Tspo A2/29 cells in the presence or absence of ARL67156 ( e ) APCP ( g ) ADA inhibitor (EHNA, 0.01 mM) ( h ) or ENT1 inhibitor (NBMPR, 0.01 mM) ( i ) for 3 h ( n = 9 per group). Data are mean ± s.e.m. or boxes indicating the interquartile range with whiskers, and dotted lines indicate that significance was calculated separately for each. Significance was determined by one-way ANOVA with Dunnett’s multiple-comparisons test (** P < 0.01, **** P < 0.0001) in b two-tailed unpaired Student’s t -test (*** P < 0.001) in c or otherwise by two-way ANOVA with Šidák’s multiple-comparisons test (** P < 0.01, *** P < 0.001, **** P < 0.0001). n.s., not significant.

    Journal: Experimental & Molecular Medicine

    Article Title: Adenosine transmission from hypothalamic tanycytes to AGRP/NPY neurons regulates energy homeostasis

    doi: 10.1038/s12276-025-01449-6

    Figure Lengend Snippet: a A schematic diagram of ATP release from tanycytes and conversion of nucleotides by ectonucleotidases. ATP is released through Cx43 from tanycytes and is converted to ADP and AMP by ENTPD. AMP is converted to adenosine by NT5E. Adenosine is transported by ENT1 and is converted to inosine by ADA. b Relative expression levels of ectonucleotidases families and nucleoside transporters in A2/29 cells ( n = 6). c Relative intracellular and extracellular adenosine levels in si-scram and si- Tspo A2/29 cells ( n = 9 per group). d , f Relative intracellular and extracellular ATP levels in si-scram and si- Tspo A2/29 cells in the presence or absence of ENTPD inhibitor ( ARL67156 , 0.1 mM) ( d ) or NT5E inhibitor (APCP, 0.1 mM) ( f ) for 3 h ( n = 9 per group). e, g – i Relative intracellular and extracellular adenosine levels in si-scram and si- Tspo A2/29 cells in the presence or absence of ARL67156 ( e ) APCP ( g ) ADA inhibitor (EHNA, 0.01 mM) ( h ) or ENT1 inhibitor (NBMPR, 0.01 mM) ( i ) for 3 h ( n = 9 per group). Data are mean ± s.e.m. or boxes indicating the interquartile range with whiskers, and dotted lines indicate that significance was calculated separately for each. Significance was determined by one-way ANOVA with Dunnett’s multiple-comparisons test (** P < 0.01, **** P < 0.0001) in b two-tailed unpaired Student’s t -test (*** P < 0.001) in c or otherwise by two-way ANOVA with Šidák’s multiple-comparisons test (** P < 0.01, *** P < 0.001, **** P < 0.0001). n.s., not significant.

    Article Snippet: Tan Tspo WT and Tan Tspo cKO mice were implanted with a unilateral cannula (PlasticsOne) at the 3V (1.3 mm posterior, 0.0 mm medial, and 5.3 mm ventral to bregma) to inject ARL67156 (0.1 nmol; Tocris, 1283) or vehicle or with a bilateral cannula (PlasticsOne) at the ARC (1.3 mm posterior, ±0.5 mm lateral and 5.6 mm ventral to bregma) to inject DPCPX (0.4 nmol; Tocris, 0439) or vehicle.

    Techniques: Expressing, Two Tailed Test

    a , d , g , j Schematic illustrations of ARL67156 ( a ) APCP ( d ) EHNA ( g ) and NBMPR ( j ) treatments in the indirect coculture system. b , e , h , k Relative extracellular ATP or adenosine levels in si-scram or si- Tspo A2/29 cells indirectly cocultured with N41 cells in the presence or absence of ARL67156 ( b ) APCP ( e ) EHNA ( h ) or NBMPR ( k ) under 0.06 mM oleic acid (OL) treatment for 3 h ( n = 9 per group). c , f , i , l Relative mRNA levels of Agrp and Npy in N41 cells cocultured with si-scram or si- Tspo A2/29 cells in the presence or absence of ARL67156 ( c ), APCP ( f ) EHNA ( i ) or NBMPR ( l ) under OL treatment for 3 h ( n = 9 per group). Data are mean ± s.e.m. or boxes indicating the interquartile range with whiskers, and dotted linesindicate that significance was calculated separately for each. Significance was determined by two-way ANOVA with Šidák’s multiple-comparisons test (* P < 0.5, ** P < 0.01, *** P < 0.001, **** P < 0.0001; n.s., not significant).

    Journal: Experimental & Molecular Medicine

    Article Title: Adenosine transmission from hypothalamic tanycytes to AGRP/NPY neurons regulates energy homeostasis

    doi: 10.1038/s12276-025-01449-6

    Figure Lengend Snippet: a , d , g , j Schematic illustrations of ARL67156 ( a ) APCP ( d ) EHNA ( g ) and NBMPR ( j ) treatments in the indirect coculture system. b , e , h , k Relative extracellular ATP or adenosine levels in si-scram or si- Tspo A2/29 cells indirectly cocultured with N41 cells in the presence or absence of ARL67156 ( b ) APCP ( e ) EHNA ( h ) or NBMPR ( k ) under 0.06 mM oleic acid (OL) treatment for 3 h ( n = 9 per group). c , f , i , l Relative mRNA levels of Agrp and Npy in N41 cells cocultured with si-scram or si- Tspo A2/29 cells in the presence or absence of ARL67156 ( c ), APCP ( f ) EHNA ( i ) or NBMPR ( l ) under OL treatment for 3 h ( n = 9 per group). Data are mean ± s.e.m. or boxes indicating the interquartile range with whiskers, and dotted linesindicate that significance was calculated separately for each. Significance was determined by two-way ANOVA with Šidák’s multiple-comparisons test (* P < 0.5, ** P < 0.01, *** P < 0.001, **** P < 0.0001; n.s., not significant).

    Article Snippet: Tan Tspo WT and Tan Tspo cKO mice were implanted with a unilateral cannula (PlasticsOne) at the 3V (1.3 mm posterior, 0.0 mm medial, and 5.3 mm ventral to bregma) to inject ARL67156 (0.1 nmol; Tocris, 1283) or vehicle or with a bilateral cannula (PlasticsOne) at the ARC (1.3 mm posterior, ±0.5 mm lateral and 5.6 mm ventral to bregma) to inject DPCPX (0.4 nmol; Tocris, 0439) or vehicle.

    Techniques:

    a The schematic strategy and schedule of ARL67156 or Veh ICV injection into the 3V through an implanted cannula in Tan Tspo WT or Tan Tspo cKO mice. b , c Food intake ( b ) and body weight change ( c ) of Tan Tspo WT and Tan Tspo cKO mice for 24 h after ARL67156 (0.1 nmol) or Veh ICV injection and HFD feeding ( n = 6 per group). d Relative Agrp and Npy expression levels in Tan Tspo WT and Tan Tspo cKO mice 4 h after ARL67156 or Veh ICV injection and HFD feeding ( n = 6 per group). e Relative expression levels of adenosine receptors in the mouse hypothalamus ( n = 6). f Representative image of A1R (red) expressed on NPY neurons (green) in the hypothalamus and colocalization coefficients of A1R with NPY neurons ( n = 10). g Representative image of A2bR (red) expressed on NPY neurons (green) in the hypothalamus and colocalization coefficients of A2bR with NPY neurons ( n = 10). h The schematic strategy and schedule of A1R inhibitor (DPCPX) or Veh ICV injection into the ARC through an implanted cannula in Tan Tspo WT or Tan Tspo cKO mice. i , j Food intake ( i ) and body weight change ( j ) of Tan Tspo WT and Tan Tspo cKO mice for 24 h after DPCPX (0.4 nmol) or Veh ICV injection and HFD feeding ( n = 6 per group). k Relative Agrp and Npy expression levels in Tan Tspo WT and Tan Tspo cKO mice 4 h after DPCPX or Veh ICV injection and HFD feeding ( n = 6 per group). Scale bars, 20 μm ( f and g ). Data are mean ± s.e.m. or boxes indicating the interquartile range with whiskers, and dotted lines indicate that significance was calculated separately for each. Significance was determined by one-way ANOVA with Dunnett’s multiple-comparisons test (**** P < 0.0001; n.d., not detected) in e or otherwise by two-way ANOVA with Šidák’s multiple-comparisons test (* P < 0.5, ** P < 0.01, *** P < 0.001, **** P < 0.0001; n.s., not significant).

    Journal: Experimental & Molecular Medicine

    Article Title: Adenosine transmission from hypothalamic tanycytes to AGRP/NPY neurons regulates energy homeostasis

    doi: 10.1038/s12276-025-01449-6

    Figure Lengend Snippet: a The schematic strategy and schedule of ARL67156 or Veh ICV injection into the 3V through an implanted cannula in Tan Tspo WT or Tan Tspo cKO mice. b , c Food intake ( b ) and body weight change ( c ) of Tan Tspo WT and Tan Tspo cKO mice for 24 h after ARL67156 (0.1 nmol) or Veh ICV injection and HFD feeding ( n = 6 per group). d Relative Agrp and Npy expression levels in Tan Tspo WT and Tan Tspo cKO mice 4 h after ARL67156 or Veh ICV injection and HFD feeding ( n = 6 per group). e Relative expression levels of adenosine receptors in the mouse hypothalamus ( n = 6). f Representative image of A1R (red) expressed on NPY neurons (green) in the hypothalamus and colocalization coefficients of A1R with NPY neurons ( n = 10). g Representative image of A2bR (red) expressed on NPY neurons (green) in the hypothalamus and colocalization coefficients of A2bR with NPY neurons ( n = 10). h The schematic strategy and schedule of A1R inhibitor (DPCPX) or Veh ICV injection into the ARC through an implanted cannula in Tan Tspo WT or Tan Tspo cKO mice. i , j Food intake ( i ) and body weight change ( j ) of Tan Tspo WT and Tan Tspo cKO mice for 24 h after DPCPX (0.4 nmol) or Veh ICV injection and HFD feeding ( n = 6 per group). k Relative Agrp and Npy expression levels in Tan Tspo WT and Tan Tspo cKO mice 4 h after DPCPX or Veh ICV injection and HFD feeding ( n = 6 per group). Scale bars, 20 μm ( f and g ). Data are mean ± s.e.m. or boxes indicating the interquartile range with whiskers, and dotted lines indicate that significance was calculated separately for each. Significance was determined by one-way ANOVA with Dunnett’s multiple-comparisons test (**** P < 0.0001; n.d., not detected) in e or otherwise by two-way ANOVA with Šidák’s multiple-comparisons test (* P < 0.5, ** P < 0.01, *** P < 0.001, **** P < 0.0001; n.s., not significant).

    Article Snippet: Tan Tspo WT and Tan Tspo cKO mice were implanted with a unilateral cannula (PlasticsOne) at the 3V (1.3 mm posterior, 0.0 mm medial, and 5.3 mm ventral to bregma) to inject ARL67156 (0.1 nmol; Tocris, 1283) or vehicle or with a bilateral cannula (PlasticsOne) at the ARC (1.3 mm posterior, ±0.5 mm lateral and 5.6 mm ventral to bregma) to inject DPCPX (0.4 nmol; Tocris, 0439) or vehicle.

    Techniques: Injection, Expressing