315 Results for "

PTP

" in MedChemExpress (MCE) Product Catalog:
Products (315)

315 Results for "PTP" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-100625
CAS No.: 39674-97-0
Purity:  98.40%
BVT948 is a protein tyrosine phosphatase (PTP) inhibitor which can also inhibit several cytochrome P450 (P450) isoforms and lysine methyltransferase SETD8 (KMT5A).
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2
2 Cited Publications
Cat. No.: HY-120327
CAS No.: 1621673-53-7
Purity:  98.42%
Target:  

Phosphatase

KY-226 is a potent, selective, orally active and allosteric protein tyrosine phosphatase 1B (PTP1B) inhibitor with an IC50 of 0.25 μM, and without PPARγ agonist activity. KY-226 exerts anti-diabetic and anti-obesity effects by enhancing insulin and leptin signaling, respectively. KY-226 also protects neurons from cerebral ischemic injury .
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1
1 Cited Publications
Cat. No.: HY-W013478
CAS No.: 2632-13-5
Target:  

Phosphatase

Research Areas:  

Cancer

PTP inhibitor 1 is a protein tyrosine phosphatase (PTP) inhibitor, with anti-angiogenic effect .
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1
1 Cited Publications
Cat. No.: HY-15756
CAS No.: 765317-72-4
Purity:  99.55%
Target:  

Phosphatase

Research Areas:  

Metabolic Disease

PTP1B-IN-4 is a non-competitive allosteric inhibitor of the protein tyrosine phosphatase PTP1B, with an IC50 of 8 μM. PTP1B-IN-4 is potentail for the research of obesity and diabetes .
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1
1 Cited Publications
Cat. No.: HY-P5982
PTPσ Inhibitor, ISP is a PTPσ intracellular wedge domain mimetic peptide containing a TAT cell-penetrating domain, which acts as a PTPσ inhibitor. PTPσ Inhibitor, ISP binds to and inhibits PTPσ, thereby relieving CSPG-mediated axonal growth inhibition. PTPσ Inhibitor, ISP enhances CSPG degradation by promoting the secretion of Cathepsin B or MMP-2, and promotes DRG axonal growth, OPC migration and remyelination. PTPσ Inhibitor, ISP promotes nerve regeneration and improves sensory, motor and urinary functions in animal models of spinal cord injury, dorsal root injury and multiple sclerosis. PTPσ Inhibitor, ISP also increases the phosphorylation of ERK and AKT in colorectal cancer cells. PTPσ Inhibitor, ISP can be used in studies related to PTPσ/CSPG signaling, nerve regeneration, demyelinating diseases and RAS/ERK signaling .
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1
1 Cited Publications
Cat. No.: HY-112478
CAS No.: 329317-98-8
Purity:  99.90%
Target:  

Phosphatase SHP2

Research Areas:  

Cancer

PTP Inhibitor IV is a protein tyrosine phosphatase (PTP) inhibitor that competitively inhibits DUSP14 phosphatase activity with an 50 of 5.21 μM . PTP Inhibitor IV inhibits SHP-2, PTP1B, PTP-ε, PTP Meg-2, PTP-σ, PTP-β, and PTP-μ with 50s of 1.8 μM, 2.5 μM, 8.4 μM, 13 μM, 20 μM, 6.4 μM, and 6.7 μM, respectively .
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1
1 Cited Publications
Cat. No.: HY-P73685
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PTPN1; Protein-Tyrosine Phosphatase 1B; Prev. PTP1B; Protein Tyrosine Phosphatase, Placental; Tyrosine-Protein Phosphatase Non-Receptor Type 1; PTP-1B; Protein Tyrosine Phosphatase Non-Receptor Type 1; Tyrosine-Protein Phosphatase Non-Receptor Type
Species:  
Human
Source:  
E. coli
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1
1 Cited Publications
Cat. No.: HY-101964
CAS No.: 1051387-90-6
Purity:  98.01%
Target:  

SHP2 Phosphatase

Research Areas:  

Cancer

SPI-112 is a potent, selective and competitive SHP2 (PTPN11) inhibitor with IC50s of 1 μM, 18.3 μM and 14.5 μM for SHP2, protein tyrosine phosphatase (PTP) and PTP1B, respectively .
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1
1 Cited Publications
Cat. No.: HY-123846
CAS No.: 862975-18-6
Purity:  99.27%
Target:  

Phosphatase

Research Areas:  

Cardiovascular Disease

MLS-0437605 is a selective dual-specificity phosphatase 3 (DUSP3) inhibitor with an IC50 of 3.7 μM. MLS-0437605 is more selective for DUSP3 than DUSP22 and other protein tyrosine phosphatases (PTPs) .
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1
1 Cited Publications
Cat. No.: HY-111469
CAS No.: 888213-72-7
Purity:  99.14%
Target:  

Phosphatase

Research Areas:  

Metabolic Disease

CPT-157633, a difluoro-phosphonomethyl phenylalanine derivative, and is a PTP1B inhibitor. CPT-157633 prevents binge drinking-induced glucose intolerance .
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1
1 Cited Publications
Cat. No.: HY-N10002
CAS No.: 109163-69-1
Caffeoyltryptophan is a competitive PTP1B inhibitor, with an IC50 of 16.99 μM. Caffeoyltryptophan can also inhibit α-glucosidase, linoleic acid peroxidation and haemolysis. Caffeoyltryptophan can be used for the research of type 2 diabetes .
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1
1 Cited Publications
Cat. No.: HY-131901
CAS No.: 637-03-6
Purity:  99.32%
Synonyms: Oxophenylarsine; PhAsO; Arsenosobenzene
Research Areas:  

Others

Phenylarsine oxide (PAO), an inhibitor of endocytosis, inhibits PTPε with an IC50 of 18 μM. Phenylarsine oxide (PAO) inhibits oxygen consumption and decreases cellular ATP content overlap with those used to inhibit protein internalization .
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1
1 Cited Publications
Cat. No.: HY-141800
CAS No.: 354815-90-0
Purity:  99.32%
Target:  

Phosphatase

Research Areas:  

Others

MurA-IN-1 (compound 1a) is a PTPRR inhibitor, with IC50 values of 0.23 μM, 0.8 μM, 0.75 μM and 0.09 μM for PTP1B, PTPN5, PTPN7 and PTPRR, respectively . (A family of human MAPK-specific protein tyrosine phosphatases)
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1
1 Cited Publications
Cat. No.: HY-P71141
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: PTPN6; Protein-Tyrosine Phosphatase SHP-1; Protein Tyrosine Phosphatase Non-Receptor Type 6; Protein-Tyrosine Phosphatase 1C; PTP-1C; SH-PTP1; HCP; Tyrosine-Protein Phosphatase Non-Receptor Type; SHP-1; Hematopoietic Cell Phosphatase; HCPH; Protein-Tyrosi
Species:  
Human
Source:  
E. coli
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1
1 Cited Publications
Cat. No.: HY-P700618
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: PTPN11; Protein Tyrosine Phosphatase Non-Receptor Type 11 Isoform 1; Prev. NS1; Tyrosine-Protein Phosphatase Non-Receptor Type; SH-PTP2; Protein-Tyrosine-Phosphatase; PTP2C; Noonan Syndrome 1; BPTP3; CDNA, FLJ92431; SHP-2; PTPN11 Protein; SHP2; METCDS; SH
Species:  
Human
Source:  
E. coli
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1
1 Cited Publications
Cat. No.: HY-N0646
CAS No.: 29782-68-1
Silydianin is a flavonolignan. Silydianin can be obtained from Silybum marianum. Silydianin inhibits PTP1B with an IC50 of 17.38 μM. Silydianin inhibits both monophenolase and diphenolase of tyrosinase significantly, with IC50s of 2.6 μM and 16.5 μM, respectively. Silydianin induces Apoptosis and reduces cytokines (IL-4 and IL-5). Silymarin has antioxidant, cytoprotective and immunomodulatory effects. Silydianin has antitumor activity against prostate cancer. Silymarin can be used in allergic asthma research .
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Cat. No.: HY-P5247
Synonyms: PTP20
Palmitoyl tetrapeptide-20 (PTP20) is a biomimetic peptide agonist of α-MSH. Palmitoyl tetrapeptide-20 promotes hair pigmentation and delays hair graying by activating the MC1-R pathway (AC50: 0.16 nM), enhancing catalase activity to reduce H2O2 accumulation, and upregulating SIRT1 activity. Palmitoyl tetrapeptide-20 can be used in research on preventing hair loss and improving hair graying .
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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-164864
CAS No.: 3053413-58-1
Target:  

PROTACs STAT

Research Areas:  

Cancer

DU-14 (PTP1B/TC-PTP PROTAC) is a potent and selective PTP1B and TC-PTP dual PROTAC degrader. DU-14 (PTP1B/TC-PTP PROTAC) has the IC50 for PTP1B and TC-PTP phosphatase activity of 24.2 nM and 30.1 nM, respectively. DU-14 (PTP1B/TC-PTP PROTAC) enhances IFN-γ signaling, promotes T cell activation, and has anti-tumor activity .
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Cat. No.: HY-15133
CAS No.: 809272-64-8
Purity:  99.35%
Target:  

Phosphatase

Research Areas:  

Metabolic Disease Cancer

PTP1B-IN-3 is a potent and orally active PTP1B inhibitor with IC50s of 120 nM for both PTP1B and TCPTP. PTP1B-IN-3 has antidiabetic and anticancer effects .
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