11 Results for "

PTPN2 inhibitor

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "PTPN2 inhibitor" in MCE Product Catalog:

7
7 Cited Publications
Cat. No.: HY-145923
CAS No.: 2489404-97-7
Purity:  99.38%
Synonyms: ABBV-CLS-484
Target:  

Phosphatase STAT JAK

Research Areas:  

Cancer

Osunprotafib (ABBV-CLS-484) is an orally active and selective active site PTPN1 (IC50: 2.5 nM) and PTPN2(IC50: 1.8 nM) inhibitor. Osunprotafib has 6-8-fold weaker activity on PTPN9 and no detectable activity on SHP-1 or SHP-2. Osunprotafib increases the sensitivity of human cancer cell lines to IFNγ. Osunprotafib generates robust anti-tumor immunity by enhancing JAK-STAT signalling and reducing T cell dysfunction .
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Cat. No.: HY-153446
CAS No.: 2407610-46-0
Purity:  99.30%
Synonyms: PTPN2/1-IN-1
Target:  

Phosphatase

Research Areas:  

Cancer

Tegeprotafib (PTPN2/1-IN-1) (Compound 124) is an orally active PTPN1 and PTPN2 inhibitor with IC50s of 4.4 nM and 1-10 nM against PTPN2 and PTP1B, respectively .
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Cat. No.: HY-162428
CAS No.: 3032920-59-2
Target:  

Phosphatase

Research Areas:  

Cancer

PTPN2/1-IN-3 (compound 4) is a modified, orally active PTPN2/N1 inhibitor based on ABBV-CLS-484 (HY-145923). PTPN2/1-IN-3 has anti-tumor effects, inhibiting PTPN2 with an IC50 of 9.3 nM and having an oral bioavailability of 93% in mice .
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Cat. No.: HY-178716
CAS No.: 3093350-55-8
Target:  

Phosphatase IFNAR STAT JAK

Research Areas:  

Cancer

PTPN2/1-IN-4 (Compound WS35) is an orally active, dual-functional inhibitor of PTPN1 and PTPN2 with IC50s of 12.8 and 5.8 nM for PTPN1 and PTPN2, respectively. PTPN2/1-IN-4 modulates the IFNγ-JAK-STAT signaling pathway and significantly augments CD8+ T-cell tumor infiltration. PTPN2/1-IN-4 has potent anticancer activity, robustly inhibiting tumor growth both as a monotherapy and in combination with an anti-PD-1 antibody in B16-OVA syngeneic mouse models .
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Cat. No.: HY-145923B
CAS No.: 2986745-48-4
Synonyms: ABBV-CLS-484 hydrochloride
Target:  

Phosphatase

Research Areas:  

Inflammation/Immunology Cancer

Osunprotafib (ABBV-CLS-484) hydrochloride is an orally active and selective active site PTPN1 (IC50: 2.5 nM) and PTPN2(IC50: 1.8 nM) inhibitor. Osunprotafib hydrochloride has 6-8-fold weaker activity on PTPN9 and no detectable activity on SHP-1 or SHP-2. Osunprotafib hydrochloride increases the sensitivity of human cancer cell lines to IFNγ. Osunprotafib hydrochloride generates robust anti-tumor immunity by enhancing JAK-STAT signalling and reducing T cell dysfunction .
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Cat. No.: HY-163596
CAS No.: 3033936-66-9
Target:  

Phosphatase

Research Areas:  

Cancer

PTPN2-IN-1 (compound 4) is a PTPN2 inhibitor with the IC50 ≤5 μM. PTPN2-IN-1 inhibits cell growth of B16F10 .
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Cat. No.: HY-179380
CAS No.: 3093350-44-5
Target:  

Phosphatase IFNAR JAK STAT

Research Areas:  

Cancer

PTPN2-IN-2 is a potent and orally active PTPN2 inhibitor (IC50 = 7.05 nM) that enhances the IFN-γ signaling pathway. PTPN2-IN-2 inhibits PTP1B with an IC50 of 9.88 nM. PTPN2-IN-2 inhibits tumor growth, promotes the activation and infiltration of tumor immune cells in a B16-OVA mouse model. PTPN2-IN-2 can be used for the research of melanoma .
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Cat. No.: HY-156608
CAS No.: 2948340-59-6
Target:  

Phosphatase

Research Areas:  

Cancer

Anticancer agent 144 (compound 444) is a dual PTPN2/PTP1B inhibitor with IC50 values <2.5 nM. Anticancer agent 144 can be used in cancer research .
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Cat. No.: HY-156607
CAS No.: 2948339-38-4
Target:  

Phosphatase

Research Areas:  

Cancer

Anticancer agent 143 (compound 369) is a dual PTPN2/PTP1B inhibitor with IC50 values <2.5 nM. Anticancer agent 143 can be used in cancer research .
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Cat. No.: HY-181255
CAS No.: 3112461-52-3
Target:  

Phosphatase

Research Areas:  

Cancer

PTPN2-IN-3 (example 52) is a PTPN2 inhibitor that can be used in tumor research .
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Cat. No.: HY-183937A
Target:  

PROTACs Phosphatase STAT

Research Areas:  

Cancer

PD-305 is a selective PTPN2 PROTAC degrader, with DC50 values of 0.25 nM and 5.11 nM against PTPN2 and PTPN1, respectively. PD-305 enhances IFN-γ-induced STAT1 phosphorylation, inhibits the proliferation of IFN-γ-stimulated colorectal cancer cells, promotes CD8 + T cell activation, enhances the tumor-killing activity of T cells, and suppresses tumor growth in mouse models. PD-305 can be used for the research of colorectal cancer .
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