28 Results for "

PA-1

" in MedChemExpress (MCE) Product Catalog:
Products (28)

28 Results for "PA-1" in MCE Product Catalog:

Cat. No.: HY-P10352A
Target:  

Bacterial

Research Areas:  

Infection

Pediocin PA-1 TFA is a class IIa bacteriocin that specifically binds to membrane proteins of susceptible Gram-positive bacteria (such as Listeria monocytogenes) to form voltage-independent hydrophilic pores, leading to dissipation of proton motive force, ATP depletion and cell death. Pediocin PA-1 TFA shows no significant activity against intact Gram-negative bacteria, strains carrying immunity genes and obligate anaerobic commensal gut microbiota, and its bactericidal function depends on the integrity of disulfide bonds, with activity lost upon reduction. Pediocin PA-1 TFA can be used not only as a food biopreservative but also for research on listeriosis [1] .
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Cat. No.: HY-P10352
CAS No.: 111745-56-3
Target:  

Bacterial

Research Areas:  

Infection

Pediocin PA 1 is a class IIa bacteriocin that specifically binds to membrane proteins of susceptible Gram-positive bacteria (such as Listeria monocytogenes) to form voltage-independent hydrophilic pores, leading to dissipation of proton motive force, ATP depletion and cell death. Pediocin PA 1 shows no significant activity against intact Gram-negative bacteria, strains carrying immunity genes and obligate anaerobic commensal gut microbiota, and its bactericidal function depends on the integrity of disulfide bonds, with activity lost upon reduction. Pediocin PA 1 can be used not only as a food biopreservative but also for research on listeriosis [1] .
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Cat. No.: HY-134174A
CAS No.: 169437-35-8
Purity:  ≥99.0%
Synonyms: 16:0-18:1 PA
1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphate sodium (16:0-18:1 PA) is a phospholipid with activities in regulating biological membrane fluidity and participating in cell signal transduction. 1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphate sodium can be used to study the effects on the activity of chloroplast envelope monogalactosyldiacylglycerol (MGDG) synthase. 1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphate sodium plays an important role in cell membrane integrity and function.
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Cat. No.: HY-W725309
CAS No.: 384833-24-3
Synonyms: 1-Stearoyl-2-oleoyl-sn-glycero-3-phosphate sodium
18:0-18:1 PA (1-Stearoyl-2-oleoyl-sn-glycero-3-phosphate) sodium is an anionic lipid [1].
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Cat. No.: HY-128850S1
CAS No.: 875654-27-6
Synonyms: N-Acetylmannosamine-13C; ManNAc-13C
N-Acetyl-D-mannosamine- 13C is the 13C labeled N-Acetyl-D-mannosamine. N-Acetyl-D-mannosamine (ManNAc) is an essential precursor of N-acetylneuraminic acid (NeuAc), the specific monomer of bacterial capsular polysialic acid (PA)
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Cat. No.: HY-125667
CAS No.: 1620951-72-5
Synonyms: Photoamiloride-1
Target:  

Sodium Channel

Research Areas:  

Metabolic Disease

PA1 is a photoswitchable epithelial sodium channel (ENaC) blocker. PA1 can switch to cis-PA1 at 400nm and trans-PA1 at 500nm. PA1 inhibits δ/αENaC, αβγENaC, and δβγENaC, with IC50 values of 4.3nM, 90 nM, and 390 nM, respectively [1].
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Cat. No.: HY-N9130
CAS No.: 480-82-0
Indicine (Compound 3) is an alkaloid. Indicine can reduce pyrrolizine alkaloids (PA) .
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Cat. No.: HY-145486
CAS No.: 799268-65-8
Synonyms: 20:4 Lyso PA
Target:  

Liposome

Research Areas:  

Neurological Disease

1-Arachidonoyl-sn-glycerol 3-phosphate ammonium (20:4 Lyso PA) is a phospholipid and an LPA derived from arachidonic acid. The concentration of 1-Arachidonoyl-sn-glycerol 3-phosphate ammonium in plasma is significantly correlated with the age of onset of cocaine use and the duration of abstinence. 1-Arachidonoyl-sn-glycerol 3-phosphate ammonium can be used in the research of biomarkers for cocaine use disorder (CUD) [1].
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Cat. No.: HY-143407
CAS No.: 2882094-29-1
Target:  

FAK

Research Areas:  

Cancer

FAK-IN-3 (Compound 36) is a potent inhibitor of focal adhesion kinase (FAK). FAK-IN-3 not only decreases migration and invasion of PA-1 cells, but also reduces expression of MMP-2 and MMP-9. FAK-IN-3 inhibits tumor growth and metastasis, and no obvious adverse effects. FAK-IN-3 has the potential for the research of ovarian cancer [1].
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Cat. No.: HY-P991311

Target:  

LPL Receptor Wnt

Research Areas:  

Cancer

GSK3178022 is a human IgG1 monoclonal antibody (mAb) targeting LRP6. GSK3178022 inhibits the expression of WNT target genes SP5 and AXIN2. GSK3178022 has antitumor activity in the RSPO fusion model of colorectal cancer. Recommended isotype control: Human IgG1 kappa, Isotype Control (HY-P99001) [1].
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Cat. No.: HY-177782
Research Areas:  

Cancer

SB1349 is a molecular glucose degrading agent that targets the Lin28 protein. SB1349 can effectively induce proteasome dependent degradation of Lin28A and Lin28B. SB1349 can increase the level of mature let-7 miRNA, downregulate the oncogenes targeted by let-7, and effectively induce the differentiation of neuroblastoma cells. SB1349 can be used for cancer research [1].
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Cat. No.: HY-177497
CAS No.: 2852050-29-2
Research Areas:  

Cancer

SKLB-03220 is a selective and orally active EZH2 covalent inhibitor with an IC50 of 1.72 nM for EZH2 MUT. SKLB-03220 exhibits weak activities against other tested histone methyltransferases (HMTs) and kinases. SKLB-03220 displays noteworthy potency against ovarian cancer cell lines and induces cell apoptosis. SKLB-03220 significantly inhibits tumor growth in PA-1 xenograft model. SKLB-03220 can be used for the study of ovarian cancer [1].
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Cat. No.: HY-175459
Target:  

PROTACs FAK

Research Areas:  

Inflammation/Immunology Cancer

PROTAC FAK degrader 3 is a selective FAK PROTAC degrader (DC50 = 1.08 nM). PROTAC FAK degrader 3 induces FAK degradation dependent on the ubiquitin-proteasome system and its binding to FAK and CRBN. PROTAC FAK degrader 3 upregulates MHC-I gene transcription and tumor cell surface expression by inhibiting the non-catalytic activity of FAK, leading to increased antigen presentation and activation of cytotoxic CD8 T cells. PROTAC FAK degrader 3 enhances in vivo anti-tumor activity by promoting MHC-I expression and enhancing T cell activation. PROTAC FAK degrader 3 can be used in cancer research targeting FAK degradation in ovarian cancer, hepatocellular carcinoma, and other cancers [1].
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Cat. No.: HY-128850S5
Synonyms: N-Acetylmannosamine-15N; ManNAc-15N
N-Acetyl-D-mannosamine- 15N is the 15N labeled N-Acetyl-D-mannosamine. N-Acetyl-D-mannosamine (ManNAc) is an essential precursor of N-acetylneuraminic acid (NeuAc), the specific monomer of bacterial capsular polysialic acid (PA)
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Cat. No.: HY-W747907
CAS No.: 4753-19-9
Synonyms: β-Pyracin
4-Pyridoxolactone (β-Pyracin) is a critical substrate in vitamin B6 degradation pathway I, primarily involved in the vitamin B6 metabolic process mediated by soil microorganisms. 4-Pyridoxolactone serves as the specific substrate for 4-pyridoxolactonase, undergoing a zinc-dependent lactone-ring hydrolysis reaction catalyzed by this enzyme to generate 4-pyridoxic acid (4PA) .
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Cat. No.: HY-N15109
CAS No.: 336625-36-6
Phoenistatin is a substance that increases the expression of genes. 3 nM-1000 μM of Phoenistatin causes more than 3 times the gene expression of the PA1-1 promoter [1].
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Cat. No.: HY-RS09978
Research Areas:  

Others

PAGR1 Human Pre-designed siRNA Set A contains three designed siRNAs for PAGR1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-169246
Target:  

CDK Apoptosis

Research Areas:  

Cancer

CDK2-IN-32 (Compound 5g) is a selective CDK2 inhibitor with an IC50 of 0.21 μM. CDK2-IN-32 shows cytotoxicity against Vero cells with an IC50 of 28.52 μM [1].
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Cat. No.: HY-176488
CAS No.: 2034334-74-0
Research Areas:  

Cancer

Y-99 is a PORCN inhibitor with an IC50 of 155.4 nM against the Wnt/β-catenin signaling pathway. Y-99 inhibits the expression of p-LRP6, β-catenin, and c-Myc [1].
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Cat. No.: HY-131574
CAS No.: 31701-88-9
Heliosupine N-oxide, Heliosupin metabolite, inhibits muscarinic acetylcholine receptor (mAChR) with the IC50 of 350 μM. Heliosupine N-oxide is a pyrrolizidine alkaloid (PA) .
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