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Macklin Inc compounds pbt2
Structures of <t>PBT2</t> (A) and PBT2 reduce the mRNA levels of TaSP and Tap104 (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.
Compounds Pbt2, supplied by Macklin 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/compounds pbt2/product/Macklin Inc
Average 86 stars, based on 1 article reviews
compounds pbt2 - by Bioz Stars, 2026-05
86/100 stars

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1) Product Images from "In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti"

Article Title: In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti

Journal: International Journal for Parasitology: Drugs and Drug Resistance

doi: 10.1016/j.ijpddr.2026.100646

Structures of PBT2 (A) and PBT2 reduce the mRNA levels of TaSP and Tap104 (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.
Figure Legend Snippet: Structures of PBT2 (A) and PBT2 reduce the mRNA levels of TaSP and Tap104 (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Techniques Used:

PBT2 reduces the schizont burden in T. annulata -infected cells. Representative immunofluorescence images of TaNM and TaXJS cells in each treatment group, schizont nuclei are shown in green and host cell nuclei in blue (A). Quantification of the number of schizonts per host cell in each treatment group (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.
Figure Legend Snippet: PBT2 reduces the schizont burden in T. annulata -infected cells. Representative immunofluorescence images of TaNM and TaXJS cells in each treatment group, schizont nuclei are shown in green and host cell nuclei in blue (A). Quantification of the number of schizonts per host cell in each treatment group (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Techniques Used: Infection, Immunofluorescence

PBT2 inhibits the proliferation of TaNM and TaXJS cells in vitro. The IC 50 values of PBT2 on TaNM and TaXJS cells (A). The cell viability of BoMac cells with different concentration of PBT2 (B). Colony formation assay demonstrated that PBT2 completely abolished clonogenic growth, representative images of colony formation are shown (C). Quantification of colony numbers before and after treatment with PBT2 or Bup (D). The values obtained were used to determine the IC 50 using nonlinear regression (curve fitting analysis) in GraphPad Prism software. Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.
Figure Legend Snippet: PBT2 inhibits the proliferation of TaNM and TaXJS cells in vitro. The IC 50 values of PBT2 on TaNM and TaXJS cells (A). The cell viability of BoMac cells with different concentration of PBT2 (B). Colony formation assay demonstrated that PBT2 completely abolished clonogenic growth, representative images of colony formation are shown (C). Quantification of colony numbers before and after treatment with PBT2 or Bup (D). The values obtained were used to determine the IC 50 using nonlinear regression (curve fitting analysis) in GraphPad Prism software. Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Techniques Used: In Vitro, Concentration Assay, Colony Assay, Software

Metal ion content in T. annulata schizonts following PBT2 treatment. Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by one-way ANOVA followed by Dunnett's multiple comparisons test.
Figure Legend Snippet: Metal ion content in T. annulata schizonts following PBT2 treatment. Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by one-way ANOVA followed by Dunnett's multiple comparisons test.

Techniques Used:

PBT2 disrupts redox homeostasis and reduces SOD activity in infected cells. ROS levels in TaNM cells following PBT2 treatment were quantified by flow cytometry, representative flow cytometry histograms are shown (A). Quantitative analysis of ROS levels (B). SOD activity in TaNM cells after PBT2 exposure, showing a significant reduction compared with untreated controls (C). Manganese supplementation partially rescued PBT2-induced growth inhibition in TaNM cells, indicating functional involvement of Mn depletion in redox imbalance (D). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗, P < 0.05; ∗∗, P < 0.005; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by one-way ANOVA followed by Tukey's multiple comparisons test.
Figure Legend Snippet: PBT2 disrupts redox homeostasis and reduces SOD activity in infected cells. ROS levels in TaNM cells following PBT2 treatment were quantified by flow cytometry, representative flow cytometry histograms are shown (A). Quantitative analysis of ROS levels (B). SOD activity in TaNM cells after PBT2 exposure, showing a significant reduction compared with untreated controls (C). Manganese supplementation partially rescued PBT2-induced growth inhibition in TaNM cells, indicating functional involvement of Mn depletion in redox imbalance (D). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗, P < 0.05; ∗∗, P < 0.005; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by one-way ANOVA followed by Tukey's multiple comparisons test.

Techniques Used: Activity Assay, Infection, Flow Cytometry, Inhibition, Functional Assay

The growth inhibition of PBT2 on B. microti in vivo. Parasitemia was calculated by counting infected RBCs among 2000 R BCs using Giemsa-stained thin blood smears. The arrow indicates 5 consecutive days of treatment. Error bars represent the SD of the mean from five independent biological replicates, ∗, P < 0.05 by two-way ANOVA followed by Dunnett's multiple comparisons test (A). Representative Giemsa-stained blood smear image obtained at peak parasitemia on the 8th day (B).
Figure Legend Snippet: The growth inhibition of PBT2 on B. microti in vivo. Parasitemia was calculated by counting infected RBCs among 2000 R BCs using Giemsa-stained thin blood smears. The arrow indicates 5 consecutive days of treatment. Error bars represent the SD of the mean from five independent biological replicates, ∗, P < 0.05 by two-way ANOVA followed by Dunnett's multiple comparisons test (A). Representative Giemsa-stained blood smear image obtained at peak parasitemia on the 8th day (B).

Techniques Used: Inhibition, In Vivo, Infection, Staining

Hematology profiles of PBT2-treated mice in vivo. The changes of RBCs (A), HGB (B), and HCT (C) in mice treated with PBT2 and DA. Error bars represent the SD of the mean from five independent biological replicates. Different colored asterisks indicate that the differences between the various groups are statistically significant. ∗, P < 0.05; ∗∗, P < 0.005; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.
Figure Legend Snippet: Hematology profiles of PBT2-treated mice in vivo. The changes of RBCs (A), HGB (B), and HCT (C) in mice treated with PBT2 and DA. Error bars represent the SD of the mean from five independent biological replicates. Different colored asterisks indicate that the differences between the various groups are statistically significant. ∗, P < 0.05; ∗∗, P < 0.005; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Techniques Used: In Vivo



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Structures of <t>PBT2</t> (A) and PBT2 reduce the mRNA levels of TaSP and Tap104 (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.
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Image Search Results


Structures of PBT2 (A) and PBT2 reduce the mRNA levels of TaSP and Tap104 (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Journal: International Journal for Parasitology: Drugs and Drug Resistance

Article Title: In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti

doi: 10.1016/j.ijpddr.2026.100646

Figure Lengend Snippet: Structures of PBT2 (A) and PBT2 reduce the mRNA levels of TaSP and Tap104 (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Article Snippet: The compounds PBT2 ( A), Bup and Diminazene aceturate (DA) were purchased from MedChemExpress (MCE) and stored as a 10 mM stock solution in DMSO (Macklin).

Techniques:

PBT2 reduces the schizont burden in T. annulata -infected cells. Representative immunofluorescence images of TaNM and TaXJS cells in each treatment group, schizont nuclei are shown in green and host cell nuclei in blue (A). Quantification of the number of schizonts per host cell in each treatment group (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Journal: International Journal for Parasitology: Drugs and Drug Resistance

Article Title: In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti

doi: 10.1016/j.ijpddr.2026.100646

Figure Lengend Snippet: PBT2 reduces the schizont burden in T. annulata -infected cells. Representative immunofluorescence images of TaNM and TaXJS cells in each treatment group, schizont nuclei are shown in green and host cell nuclei in blue (A). Quantification of the number of schizonts per host cell in each treatment group (B). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Article Snippet: The compounds PBT2 ( A), Bup and Diminazene aceturate (DA) were purchased from MedChemExpress (MCE) and stored as a 10 mM stock solution in DMSO (Macklin).

Techniques: Infection, Immunofluorescence

PBT2 inhibits the proliferation of TaNM and TaXJS cells in vitro. The IC 50 values of PBT2 on TaNM and TaXJS cells (A). The cell viability of BoMac cells with different concentration of PBT2 (B). Colony formation assay demonstrated that PBT2 completely abolished clonogenic growth, representative images of colony formation are shown (C). Quantification of colony numbers before and after treatment with PBT2 or Bup (D). The values obtained were used to determine the IC 50 using nonlinear regression (curve fitting analysis) in GraphPad Prism software. Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Journal: International Journal for Parasitology: Drugs and Drug Resistance

Article Title: In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti

doi: 10.1016/j.ijpddr.2026.100646

Figure Lengend Snippet: PBT2 inhibits the proliferation of TaNM and TaXJS cells in vitro. The IC 50 values of PBT2 on TaNM and TaXJS cells (A). The cell viability of BoMac cells with different concentration of PBT2 (B). Colony formation assay demonstrated that PBT2 completely abolished clonogenic growth, representative images of colony formation are shown (C). Quantification of colony numbers before and after treatment with PBT2 or Bup (D). The values obtained were used to determine the IC 50 using nonlinear regression (curve fitting analysis) in GraphPad Prism software. Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Article Snippet: The compounds PBT2 ( A), Bup and Diminazene aceturate (DA) were purchased from MedChemExpress (MCE) and stored as a 10 mM stock solution in DMSO (Macklin).

Techniques: In Vitro, Concentration Assay, Colony Assay, Software

Metal ion content in T. annulata schizonts following PBT2 treatment. Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by one-way ANOVA followed by Dunnett's multiple comparisons test.

Journal: International Journal for Parasitology: Drugs and Drug Resistance

Article Title: In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti

doi: 10.1016/j.ijpddr.2026.100646

Figure Lengend Snippet: Metal ion content in T. annulata schizonts following PBT2 treatment. Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by one-way ANOVA followed by Dunnett's multiple comparisons test.

Article Snippet: The compounds PBT2 ( A), Bup and Diminazene aceturate (DA) were purchased from MedChemExpress (MCE) and stored as a 10 mM stock solution in DMSO (Macklin).

Techniques:

PBT2 disrupts redox homeostasis and reduces SOD activity in infected cells. ROS levels in TaNM cells following PBT2 treatment were quantified by flow cytometry, representative flow cytometry histograms are shown (A). Quantitative analysis of ROS levels (B). SOD activity in TaNM cells after PBT2 exposure, showing a significant reduction compared with untreated controls (C). Manganese supplementation partially rescued PBT2-induced growth inhibition in TaNM cells, indicating functional involvement of Mn depletion in redox imbalance (D). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗, P < 0.05; ∗∗, P < 0.005; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by one-way ANOVA followed by Tukey's multiple comparisons test.

Journal: International Journal for Parasitology: Drugs and Drug Resistance

Article Title: In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti

doi: 10.1016/j.ijpddr.2026.100646

Figure Lengend Snippet: PBT2 disrupts redox homeostasis and reduces SOD activity in infected cells. ROS levels in TaNM cells following PBT2 treatment were quantified by flow cytometry, representative flow cytometry histograms are shown (A). Quantitative analysis of ROS levels (B). SOD activity in TaNM cells after PBT2 exposure, showing a significant reduction compared with untreated controls (C). Manganese supplementation partially rescued PBT2-induced growth inhibition in TaNM cells, indicating functional involvement of Mn depletion in redox imbalance (D). Error bars represent the SD of the mean from three independent biological replicates. ns, P > 0.05; ∗, P < 0.05; ∗∗, P < 0.005; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by one-way ANOVA followed by Tukey's multiple comparisons test.

Article Snippet: The compounds PBT2 ( A), Bup and Diminazene aceturate (DA) were purchased from MedChemExpress (MCE) and stored as a 10 mM stock solution in DMSO (Macklin).

Techniques: Activity Assay, Infection, Flow Cytometry, Inhibition, Functional Assay

The growth inhibition of PBT2 on B. microti in vivo. Parasitemia was calculated by counting infected RBCs among 2000 R BCs using Giemsa-stained thin blood smears. The arrow indicates 5 consecutive days of treatment. Error bars represent the SD of the mean from five independent biological replicates, ∗, P < 0.05 by two-way ANOVA followed by Dunnett's multiple comparisons test (A). Representative Giemsa-stained blood smear image obtained at peak parasitemia on the 8th day (B).

Journal: International Journal for Parasitology: Drugs and Drug Resistance

Article Title: In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti

doi: 10.1016/j.ijpddr.2026.100646

Figure Lengend Snippet: The growth inhibition of PBT2 on B. microti in vivo. Parasitemia was calculated by counting infected RBCs among 2000 R BCs using Giemsa-stained thin blood smears. The arrow indicates 5 consecutive days of treatment. Error bars represent the SD of the mean from five independent biological replicates, ∗, P < 0.05 by two-way ANOVA followed by Dunnett's multiple comparisons test (A). Representative Giemsa-stained blood smear image obtained at peak parasitemia on the 8th day (B).

Article Snippet: The compounds PBT2 ( A), Bup and Diminazene aceturate (DA) were purchased from MedChemExpress (MCE) and stored as a 10 mM stock solution in DMSO (Macklin).

Techniques: Inhibition, In Vivo, Infection, Staining

Hematology profiles of PBT2-treated mice in vivo. The changes of RBCs (A), HGB (B), and HCT (C) in mice treated with PBT2 and DA. Error bars represent the SD of the mean from five independent biological replicates. Different colored asterisks indicate that the differences between the various groups are statistically significant. ∗, P < 0.05; ∗∗, P < 0.005; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Journal: International Journal for Parasitology: Drugs and Drug Resistance

Article Title: In vitro and in vivo anti-piroplasm activity of PBT2 against Theileria annulata and Babesia microti

doi: 10.1016/j.ijpddr.2026.100646

Figure Lengend Snippet: Hematology profiles of PBT2-treated mice in vivo. The changes of RBCs (A), HGB (B), and HCT (C) in mice treated with PBT2 and DA. Error bars represent the SD of the mean from five independent biological replicates. Different colored asterisks indicate that the differences between the various groups are statistically significant. ∗, P < 0.05; ∗∗, P < 0.005; ∗∗∗, P < 0.001; ∗∗∗∗, P < 0.0001 by two-way ANOVA followed by Dunnett's multiple comparisons test.

Article Snippet: The compounds PBT2 ( A), Bup and Diminazene aceturate (DA) were purchased from MedChemExpress (MCE) and stored as a 10 mM stock solution in DMSO (Macklin).

Techniques: In Vivo