180 Results for "

PTP1B

" in MedChemExpress (MCE) Product Catalog:
Products (180)

180 Results for "PTP1B" in MCE Product Catalog:

27
27 Publications Verification
Cat. No.: HY-P9970
CAS No.: 170277-31-3
Synonyms: Avakine; CT-P13; SB2; TA-650
Infliximab (Avakine) is a chimeric monoclonal IgG1 antibody that specifically binds to TNF-α. Infliximab prevents the interaction of TNF-α with TNF-α receptor (TNFR1 and TNFR2). Infliximab has the potential for autoimmune, chronic inflammatory diseases and diabetic neuropathy research [1] .
The component ratio of this product is Active ingredient : Excipients = 9 : 47.
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10
10 Cited Publications
Cat. No.: HY-N0621
CAS No.: 480-16-0
Morin is an orally active plant-derived flavonoid. Morin inhibits ROS generation. Morin induces Apoptosis. Morin inhibits PTP1B (IC50 of 15 μM) and activates the insulin receptor. Morin has a detoxifying effect. Morin can be used in diabetes, leukemia, colon cancer, cervical cancer, Parkinson's disease and hypertension research [1] .
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9
9 Cited Publications
Cat. No.: HY-B0537
CAS No.: 100-33-4
Synonyms: MP-601205
Research Areas:  

Infection Cancer

Pentamidine (MP-601205) is an antimicrobial agent and interferes with DNA biosynthetics. Pentamidine inhibits parasite Leishmania infantum with an IC50 of 2.5 μM. Pentamidine is a potent and selective protein tyrosine phosphatases (PTPases) and phosphatase of regenerating liver (PRL) inhibitor. Pentamidine has the potential for Gambian trypanosomiasis, antimony-resistant leishmaniasis, and Pneumocystis carinii pneumonia treatment. Antitumor and antibacterial activities [1] .
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9
9 Cited Publications
Cat. No.: HY-B0537B
CAS No.: 140-64-7
Synonyms: MP-601205 isethionate
Research Areas:  

Infection Cancer

Pentamidine isethionate (MP-601205 isethionate) is an antimicrobial agent and interferes with DNA biosynthetics. Pentamidine isethionate inhibits parasite Leishmania infantum with an IC50 of 2.5 μM. Pentamidine isethionate is a potent and selective protein tyrosine phosphatases (PTPases) and phosphatase of regenerating liver (PRL) inhibitor. Pentamidine isethionate has the potential for Gambian trypanosomiasis, antimony-resistant leishmaniasis, and Pneumocystis carinii pneumonia treatment. Antitumor and antibacterial activities [1] .
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8
8 Cited Publications
Cat. No.: HY-12219A
CAS No.: 1309370-86-2
Purity:  99.67%
Synonyms: Trodusquemine lactate; Aminosterol-1436 lactate
Target:  

Phosphatase

Research Areas:  

Endocrinology

MSI-1436 lactate is a selective, non-competitive inhibitor of the enzyme protein-tyrosine phosphatase 1B (PTP1B), with an IC50 of 1 μM, 200-fold preference over TCPTP (IC50 of 224 μM).
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6
6 Cited Publications
Cat. No.: HY-10704
CAS No.: 612530-44-6
Purity:  99.65%
Synonyms: PTP1B inhibitor
PTP1B-IN-1 (Compound 7a) is a small molecule inhibitor of PTP1B with an IC50 value of 1.6 mM. It is often used as the mother core for derivatives of analogues [1] .
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6
6 Cited Publications
Cat. No.: HY-112368
CAS No.: 314291-83-3
Purity:  99.77%
Target:  

SHP2 SHP1 Phosphatase

Research Areas:  

Cardiovascular Disease Cancer

PHPS1 is a potent and selective Shp2 inhibitor with Kis of 0.73, 5.8, 10.7, 5.8, and 0.47 μM for Shp2, Shp2-R362K, Shp1, PTP1B, and PTP1B-Q, respectively [1].
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6
6 Cited Publications
Cat. No.: HY-125108
CAS No.: 1177131-02-0
Purity:  99.93%
Target:  

SHP2 SHP1 Phosphatase

Research Areas:  

Cardiovascular Disease Cancer

PHPS1 sodium is a potent and selective Shp2 inhibitor with Kis of 0.73, 5.8, 10.7, 5.8, and 0.47 μM for Shp2, Shp2-R362K, Shp1, PTP1B, and PTP1B-Q, respectively [1].
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5
5 Cited Publications
Cat. No.: HY-100462
CAS No.: 1919853-46-5
Purity:  99.80%
Target:  

Phosphatase

Research Areas:  

Metabolic Disease

PTP1B-IN-2 is a potent protein tyrosine phosphatase 1B (PTP1B) inhibitor with an IC50 of 50 nM.
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5
5 Cited Publications
Cat. No.: HY-N0374
CAS No.: 144506-14-9
Licochalcone C could inhibit α-glucosidase, with IC50s of <100 nM and 92.43 μM for α-glucosidase and protein tyrosine phosphatase 1B (PTP1B), respectively.
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5
5 Cited Publications
Cat. No.: HY-N1549
CAS No.: 529-55-5
Synonyms: Naringenin 7-0-glucoside
Prunin is a potent inhibitor of human enterovirus A71 (HEVA71). Prunin shows strong inhibitory activity against protein tyrosine phosphatase 1B (PTP1B), with an IC50 of 5.5 μM [1] .
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4
4 Cited Publications
Cat. No.: HY-109041
CAS No.: 1008510-37-9
Purity:  ≥98.0%
Synonyms: AKB-9778
Target:  

Phosphatase Tie

Research Areas:  

Inflammation/Immunology

Razuprotafib (AKB-9778) is a potent and selective inhibitor of the catalytic activity of VE-PTP (vascular endothelial protein tyrosine phosphatase) with an IC50of 17 pM. Razuprotafib promotes TIE2 activation, enhances ANG1-induced TIE2 activation, and stimulates phosphorylation of signaling molecules in the TIE2 pathway, including AKT, eNOS, and ERK. Razuprotafib inhibits the structurally related phosphatase PTP1B with an IC50 of 780 nM. Razuprotafib shows excellent selectivity for VE-PTP versus a variety of phosphatases, with the exception of HPTPη (IC50=36 pM) and HPTPγ (100 pM) [1].
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3
3 Cited Publications
Cat. No.: HY-N4185
CAS No.: 61153-77-3
Licoflavone A is an orally active PTP1B/VEGFR-2 inhibitor, with an IC50 of 54.5 μM against PTP1B, an IC50 of 14.36 μM and a Kd of 142.38 nM against human VEGFR-2. Licoflavone A blocks the PI3K/AKT and MEK/ERK signaling pathways. Licoflavone A induces G1 phase cell cycle arrest, apoptosis via the intrinsic mitochondrial pathway (apoptosis), and inhibits migration, invasion and epithelial-mesenchymal transition (EMT) of gastric cancer cells. Licoflavone A inhibits the proliferation of gastric cancer cells in vitro and in xenograft models. Licoflavone A reduces the expression levels of HIF-1α, GLUT1, LDHA, PKM2 and HK2 in hypoxic gastric cancer cells, decreases glucose uptake and suppresses glycolysis. Licoflavone A can be used in research related to gastric cancer, type 2 diabetes and obesity [1] .
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3
3 Cited Publications
Cat. No.: HY-136065
CAS No.: 42494-73-5
Purity:  ≥98.0%
bpV(phen), a insulin-mimetic agent, is a potent protein tyrosine phosphatase (PTP) and PTEN inhibitor with IC50s of 38 nM, 343 nM and 920 nM for PTEN, PTP-β and PTP-1B, respectively. bpV(phen) inhibits proliferation of the protozoan parasite Leishmania in vitro. bpV(phen) strongly induces the secretion of a large number of chemokines and pro-inflammatory cytokines, and it activates a Th1-type pathway (IL-12, IFNγ). bpV(phen) can also induce cell apoptosis, and has anti-angiogenic and anti-tumor activity [1] .
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3
3 Cited Publications
Cat. No.: HY-122818
CAS No.: 171202-16-7
Purity:  ≥98.0%
Synonyms: Bisperoxovanadium(phen) trihydrate
BpV(phen) trihydrate, a insulin-mimetic agent, is a potent protein tyrosine phosphatase (PTP) and PTEN inhibitor with IC50s of 38 nM, 343 nM and 920 nM for PTEN, PTP-β and PTP-1B, respectively. BpV(phen) trihydrate inhibits proliferation of the protozoan parasite Leishmania in vitro. bpV(phen) trihydrate strongly induces the secretion of a large number of chemokines and pro-inflammatory cytokines, and it activates a Th1-type pathway (IL-12, IFNγ). BpV(phen) trihydrate can also induce cell apoptosis, and has anti-angiogenic and anti-tumor activity [1] .
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2
2 Cited Publications
Cat. No.: HY-12312
CAS No.: 243966-09-8
Purity:  ≥98.0%
Target:  

Phosphatase

Research Areas:  

Metabolic Disease

TCS 401 is a selective inhibitor of protein tyrosine phosphatase 1B (PTP1B).
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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 [1] .
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2
2 Cited Publications
Cat. No.: HY-19383
CAS No.: 251303-04-5
Synonyms: PTP 112
Target:  

Phosphatase IKK PPAR

Research Areas:  

Metabolic Disease

Ertiprotafib is an inhibitor of PTP1B, IkB kinase β (IKK-β), and a dual PPARα and PPARβ agonist, with an IC50 of 1.6 μM for PTP1B, 400 nM for IKK-β, an EC50 of ~1 μM for PPARα/PPARβ.
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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 [1] .
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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 [1] .
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