ATCC
enterobacter cloacae strain atcc 13047 Enterobacter Cloacae Strain Atcc 13047, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/enterobacter cloacae strain atcc 13047/product/ATCC Average 93 stars, based on 1 article reviews
enterobacter cloacae strain atcc 13047 - by Bioz Stars,
2025-02
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Chem Impex International
oadc Oadc, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/oadc/product/Chem Impex International Average 95 stars, based on 1 article reviews
oadc - by Bioz Stars,
2025-02
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Cell Signaling Technology Inc
anti vimentin vim Anti Vimentin Vim, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/anti vimentin vim/product/Cell Signaling Technology Inc Average 93 stars, based on 1 article reviews
anti vimentin vim - by Bioz Stars,
2025-02
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ATCC
human macrophage line Human Macrophage Line, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/human macrophage line/product/ATCC Average 90 stars, based on 1 article reviews
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CEREP Inc
pgn 9856 ![]() Pgn 9856, supplied by CEREP Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/pgn 9856/product/CEREP Inc Average 86 stars, based on 1 article reviews
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Image Search Results

Journal: British Journal of Pharmacology
Article Title: The affinity, intrinsic activity and selectivity of a structurally novel EP 2 receptor agonist at human prostanoid receptors
doi: 10.1111/bph.14525
Figure Lengend Snippet: Structures of compounds used in these experiments: PGN‐9856, PGN‐9858, PGN‐9862 and PGN‐9863.
Article Snippet: Broad spectrum profiling of
Techniques:

Journal: British Journal of Pharmacology
Article Title: The affinity, intrinsic activity and selectivity of a structurally novel EP 2 receptor agonist at human prostanoid receptors
doi: 10.1111/bph.14525
Figure Lengend Snippet: Concentration‐dependent displacement of the binding of radiolabelled PGE 2 to human recombinant EP 2 receptors by PGN‐9856. Data are shown as mean ± SEM for n = 3–4 experiments.
Article Snippet: Broad spectrum profiling of
Techniques: Concentration Assay, Binding Assay, Recombinant

Journal: British Journal of Pharmacology
Article Title: The affinity, intrinsic activity and selectivity of a structurally novel EP 2 receptor agonist at human prostanoid receptors
doi: 10.1111/bph.14525
Figure Lengend Snippet: Agonist potency (cAMP response) of PGN‐9856, PGN‐9858, PGN ‐9862, PGN‐9863 and PGE 2 at human recombinant EP 2 receptors. Data are expressed relative to the response to 3 x 10 ‐8 M PGE 2 (set at 100%). Values shown are means ± SEM from 3 individual experiments.
Article Snippet: Broad spectrum profiling of
Techniques: Recombinant

Journal: British Journal of Pharmacology
Article Title: The affinity, intrinsic activity and selectivity of a structurally novel EP 2 receptor agonist at human prostanoid receptors
doi: 10.1111/bph.14525
Figure Lengend Snippet: (A) Effect of PGN‐9856, PGN‐9858, PGN‐9862, PGN‐9863 and the standard EP 2 receptor agonist, butaprost, on TNF‐α release from human LPS‐stimulated peripheral blood monocytes Data are mean ± SEM from 4–5 individual experiments. (B) Activity of PGN‐9856, PGN‐9858, PGN‐9862, PGN‐9863 and the standard EP 2 receptor agonist, butaprost, on IL‐2 release from in human lymphocytes stimulated by anti‐CD3 antibody. Data are mean ± SEM from 3–4 individual experiments.
Article Snippet: Broad spectrum profiling of
Techniques: Activity Assay

Journal: British Journal of Pharmacology
Article Title: The affinity, intrinsic activity and selectivity of a structurally novel EP 2 receptor agonist at human prostanoid receptors
doi: 10.1111/bph.14525
Figure Lengend Snippet: Comparison of the effects of PGN‐9856 and butaprost on inhibition of TNF‐α release in LPS‐stimulated whole blood. Basal release (no LPS) is indicated. Data are given as mean ± SEM from four donors.
Article Snippet: Broad spectrum profiling of
Techniques: Inhibition

Journal: British Journal of Pharmacology
Article Title: The affinity, intrinsic activity and selectivity of a structurally novel EP 2 receptor agonist at human prostanoid receptors
doi: 10.1111/bph.14525
Figure Lengend Snippet: (A) Inhibitory effects of PGN‐9856 ( n = 3) and the standard EP 2 receptor agonist butaprost ( n = 7) and DMSO vehicle control ( n = 7) on electrically stimulated human isolated non‐pregnant myometrium. Data shown are mean ± SEM % of the inhibition induced by sodium nitroprusside (SNP) 10 ‐4 M. (B) Original recordings of responses of human myometrial smooth muscle to electrical stimulation at 5 Hz for 10 sec every 100 sec and the inhibition of these responses produced by increasing cumulative concentrations of butaprost (upper trace) and PGN9856 (lower trace). Dots indicate approximately when drug concentrations were administered in 0.5 log unit increments at approximately 10 min intervals, beginning with 10 ‐9 M (‐9). Vertical bar indicates calibration of tension developed (g) for both traces.
Article Snippet: Broad spectrum profiling of
Techniques: Isolation, Inhibition, Produced

Journal: British Journal of Pharmacology
Article Title: The affinity, intrinsic activity and selectivity of a structurally novel EP 2 receptor agonist at human prostanoid receptors
doi: 10.1111/bph.14525
Figure Lengend Snippet: Comparison of the effects of PGN‐9856‐isopropyl ester (PGN‐9856i) and PF‐04217329 on the intraocular pressure of laser‐induced ocular hypertensive monkeys. PGN‐9856i produced a significant reduction in intraocular pressure at the 6, 24, and 48 h post‐dosing time points, compared to the immediate pre‐dosing time point (time 0). PF‐04217329 also produced identically significant reductions in IOP at all time points except at 48 h, when the effect on intraocular pressure had essentially returned to baseline and no statistically significant effect was apparent. Data are means ± SEM, n = 6.
Article Snippet: Broad spectrum profiling of
Techniques: Produced