26 Results for "

P22

" in MedChemExpress (MCE) Product Catalog:
Products (26)

26 Results for "P22" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-137322
CAS No.: 1372206-64-8
Purity:  99.84%
THX-B is a potent and non-peptidic p75 NTR (neurotrophin receptor p75) antagonist. THX-B can be used in the research of diabetic kidney disease, neurodegenerative and inflammatory disorders .
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1
1 Cited Publications
Cat. No.: HY-P82103
Synonyms: BAP; Bap37; BCAP 37; D prohibitin; P22; Phb2; PNAS 141; Prohibitin 2

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-107586
CAS No.: 78860-34-1
Purity:  98.10%
Synonyms: DAQ B1; L-783281; Dimethylasterriquinone
Demethylasterriquinone B1 (DAQ B1; L-783281) is an orally active insulin receptor (insulin receptor) agonist and AKT activator. By activating AKT, Demethylasterriquinone B1 upregulates the expression and activity of eNOS to increase NO production, while downregulating the expression of the NADPH oxidase subunit p22phox to reduce oxidative stress and improve vascular endothelial dysfunction in hypertensive rats. Demethylasterriquinone B1 combind with an AKT inhibitor targets the insulin signaling pathway to activate two antiviral pathways, RNA interference and JAK/STAT, in mosquitoes, thereby reducing Zika virus infection .
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Cat. No.: HY-P99620
CAS No.: 1443004-15-6
Synonyms: CT-P22; CT120

Target:  

Influenza Virus

Research Areas:  

Infection

Firivumab (CT-P22; CT120) is a human IgG1 monoclonal influenza A virus hemagglutinin (Anti-IAV HA) antibody. Firivumab is capable of neutralizing H1N1, H5N1, H6N1, H6N2, H8N4, H8N8, H9N2 and H12N7. Firivumab shows protection against H1N1 virus in mice .
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Cat. No.: HY-P11040
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Peptide P2.2, a non-ribosomal peptide, is an antimicrobial peptide. Peptide P2.2 has potent antibacterial activity with MIC50s of 4 and 32 μM for V. parahaemolyticus and V. alginolyticus, respectively. Peptide P2.2 increases synergistic antibacterial effects with antibiotics (such as Ofloxacin (HY-B0125) and Linezolid (HY-10394)) with negligible hemolytic activity. Peptide P2.2 disrupts bacterial membranes and increases permeability by modulating proteins involved in the type VI and III secretion systems. Peptide P2.2 can be used for bacterial infections research .
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Cat. No.: HY-156425A
CAS No.: 2648709-80-0
Purity:  98.15%
Target:  

NADPH Oxidase

Research Areas:  

Inflammation/Immunology

NOX2-IN-2 diTFA (compound 33) is a potent NOX2 inhibitor targeting the p47phox-p22phox protein-protein interaction with a Ki of 0.24 μM. NOX2-IN-2 diTFA inhibits ROS production derived from NOX2 in cells .
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Cat. No.: HY-165116
CAS No.: 206059-98-5
Synonyms: 18:0p/22:6-PE; C18(Plasm)-22:6-PE; PE(P-18:0/22:6)
Target:  

Endogenous Metabolite

Research Areas:  

Others

1-1(Z)-Octadecenyl-2-docosahexaenoyl-sn-glycero-3-PE (18:0p/22:6-PE) is a lipid identified in rat brain tissue by mass spectrometry imaging with specific structural and distribution characteristics, and isomers of different fatty acid chains can be identified by improved methods.
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Cat. No.: HY-157695
CAS No.: 799268-64-7
Synonyms: C18(Plasm)-22:6-PC; PC(P-18:0/22:6); 18:0p/22:6-PC
Target:  

Endogenous Metabolite

Research Areas:  

Others

1-(1Z-Octadecenyl)-2-docosahexaenoyl-sn-glycero-3-phosphocholine (C18(Plasm)-22:6-PC) is a phospholipid identified in fish viscera by lipidomics strategy. It has different content and distribution in different fish species and can be used as an indicator of fish species differentiation.
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Cat. No.: HY-156425
CAS No.: 2648709-79-7
Target:  

NADPH Oxidase

Research Areas:  

Inflammation/Immunology

NOX2-IN-2 (compound 33) is a potent NOX2 inhibitor targeting the p47phox-p22phox protein-protein interaction with a Ki of 0.24 μM. NOX2-IN-2 inhibits ROS production derived from NOX2 in cells .
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Cat. No.: HY-N16527
CAS No.: 233690-85-2
7-O-Galloyl-D-sedoheptulose is an orally effective polyphenolic compound. 7-O-Galloyl-D-sedoheptulose lowers the serum levels of glucose, leptin, insulin, C-peptide, resistin, TNF-α, IL-6, and increases the serum level of adiponectin. 7-O-Galloyl-D-sedoheptulose significantly reduces the levels of ROS and lipid peroxidation products (TBARS) by down-regulating the protein expression of NADPH oxidase subunit Nox-4 and p22phox. 7-O-Galloyl-D-sedoheptulose down-regulates NF-κB and related pro-inflammatory factors (COX-2, iNOS), inhibits the phosphorylation of JNK and the activity of its downstream AP-1. 7-O-Galloyl-D-sedoheptulose reduces the expression of TGF-β1 and fibronectin, indicating its potential in anti-tissue fibrosis. 7-O-Galloyl-D-sedoheptulose can be used for the study of type 2 diabetes and its hepatic and pancreatic complications .
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Cat. No.: HY-172733S
CAS No.: 3052146-54-7
PRMT5-MTA-IN-3-d3 (compound P22) is the deuterium labeled PRMT5-MTA-IN-3 (HY-172733). PRMT5-MTA-IN-3-d3 is an orally active PRMT5-MTA inhibitor. PRMT5-MTA-IN-3-d3 has antiproliferative effects on HTC116-MTAP del and wild type colorectal cancer HCT-116 cell lines, with IC50 values of 6 nM and 961 nM, respectively. PRMT5-MTA-IN-3-d3 has anticancer effects, especially for MTAP-deficient tumors, such as non-small cell lung cancer (NSCLC), pancreatic cancer .
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Cat. No.: HY-P83017
Synonyms: DCNT22; DCTN22; Dctn3; dynactin 3 (P22); dynactin light chain; Dynactin subunit 3; P22

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P85054
Synonyms: BID; BH3-interacting domain death agonist; P22 BID; BID

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-RS02652
Research Areas:  

Others

CHP1 Human Pre-designed siRNA Set A contains three designed siRNAs for CHP1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P88591
Synonyms: CHP; P22; p24; Sid470p; SLC9A1BP

Host:  

Mouse

Application:  

IHC-P

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-RS10408
Research Areas:  

Others

PHB2 Human Pre-designed siRNA Set A contains three designed siRNAs for PHB2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P82103A
Synonyms: BAP; Bap37; BCAP 37; D prohibitin; P22; Phb2; PNAS 141; Prohibitin 2

Host:  

Rabbit

Application:  

WB, IHC-F, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P88591A
Synonyms: CHP; P22; p24; Sid470p; SLC9A1BP

Host:  

Mouse

Application:  

IHC-P

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P1331
CAS No.: 76622-26-9
Synonyms: Bovine adrenal medulla-22P
Target:  

Opioid Receptor

Research Areas:  

Neurological Disease

BAM-22P, a highly potent opioid peptide, is a potent opioid agonist.
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Cat. No.: HY-RS04082
Research Areas:  

Others

DYNC1H1 Human Pre-designed siRNA Set A contains three designed siRNAs for DYNC1H1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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