57 Results for "

PAc

" in MedChemExpress (MCE) Product Catalog:
Products (57)

57 Results for "PAc" in MCE Product Catalog:

Cat. No.: HY-D0651
CAS No.: 70210-06-9
Acid red 119 is an acid red dye that can be removed from aqueous solutions when polyaluminum chloride (PAC) and polyaluminum chloride sludge (PACS) are used as coagulants.
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Cat. No.: HY-178366
Target:  

Influenza Virus

Research Areas:  

Infection

PAC/NP-IN-1 (Compound 30) is a dual-target anti-influenza agent that specifically binds to nucleoprotein (NP) and the C-terminal domain of PA protein (PAc). PAC/NP-IN-1 inhibits influenza A virus A/WSN/33 (H1N1) (EC50 = 3.63 μM, IC50 = 3.08 μM). PAC/NP-IN-1 can be used for the study of influenza infection .
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Cat. No.: HY-RS09953
Research Areas:  

Others

PACC1 Human Pre-designed siRNA Set A contains three designed siRNAs for PACC1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-159632
PAR4 antagonist 6 (Compound 12) is a PAR4 antagonist, with IC50 values of 134 and 401 nM for hPAR4 (PAC1) and mPAR4 (PAC1), respectively .
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Cat. No.: HY-RS09955
Research Areas:  

Others

PACS1 Human Pre-designed siRNA Set A contains three designed siRNAs for PACS1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS09956
Research Areas:  

Others

PACS2 Human Pre-designed siRNA Set A contains three designed siRNAs for PACS2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-125690
CAS No.: 144118-26-3
Target:  

PACAP Receptor

Research Areas:  

Cancer

Thielocin B1 is a protein-protein interaction inhibitor of PAC3 homodimer .
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Cat. No.: HY-P1817
CAS No.: 144025-82-1
Target:  

PACAP Receptor

Research Areas:  

Cardiovascular Disease

PACAP-38 (16-38), human, mouse, rat is a peptide fragment encompassing the C-terminal 16-38 segment of PACAP (1-38), human, ovine, rat (HY-P0221). PACAP-38 (16-38), human, mouse, rat lacks the N-terminal 1-15 receptor activation core, but retains the ability to bind to the PAC/VPAC receptor family (PAC1/VPAC1/VPAC2 receptor). PACAP-38 (16-38), human, mouse, rat promotes histamine release and exerts a certain degree of hypotensive effect .
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Cat. No.: HY-119158
CAS No.: 1476847-58-1
VU0652925, an analog of BMS986120, is a PAR4 antagonist, with IC50 values of 43 pM and 39.2 pM for PAC1 and P-selectin, respectively. VU0652925 is able to suppress GPIIbIIIa activation .
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Cat. No.: HY-N16481
CAS No.: 347406-26-2
Parameritannin A-1 is a tetrameric proanthocyanidin (PAC) that can be isolated from the bark of Parameria laevigata Moldenke (Apocynaceae). Parameritannin A-1 is a COX-2 inhibitor. Parameritannin A-1 also inhibits the activity of phospholipase A2 (PLA2) .
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Cat. No.: HY-P11907
CAS No.: 678967-50-5
Target:  

Bacterial Fungal

Research Areas:  

Infection

Pac-525 is a tryptophan-rich cationic antibacterial peptide and membrane-disrupting agent. Pac-525 exhibits antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria, anaerobic bacteria, *Candida albicans* and *Fusarium solani*. Pac-525 interacts strongly with negatively charged phospholipid vesicles, induces vesicle dye release and disrupts microbial membranes. Pac-525 shows cytotoxicity against macrophages. Pac-525 can be used in studies related to bacterial and fungal infections .
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Cat. No.: HY-158968
CAS No.: 708287-29-0
Purity:  ≥98.0%
Target:  

MDM-2/p53

Research Areas:  

Cancer

MMs02943764 is a 1,2,4-triazole derivative with anticancer activity. MMs02943764 has significant antiproliferative effects on multiple cancer cell lines. PAC, a structural analog of MMs02943764, has significant cytotoxicity against the leukemia cell line K562 (IC50=35.264 μM), reduces the degradation of p53 by inhibiting Mdm2 and Pirh2, and induces K562 cell cycle arrest .
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Cat. No.: HY-180567
CAS No.: 3088543-72-7
Target:  

HIV Protease

Research Areas:  

Infection Inflammation/Immunology

PAC-Phe-Val is a potent HIV-1 protease inhibitor with an IC50 value of 33.10 nM. PAC-Phe-Val forms stable and strong interactions with critical active site residues, contributing to its high inhibitory potency. PAC-Phe-Val can be used for HIV/AIDS research .
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Cat. No.: HY-P0221A
Synonyms: Pituitary Adenylate Cyclase Activating Polypeptide 38 TFA
PACAP (1-38), human, ovine, rat TFA is a PAC1 receptor agonist. PACAP (1-38), human, ovine, rat TFA binds to PACAP type I receptor, PACAP type II receptor VIP1, and PACAP type II receptor VIP2 with IC50s of 4 nM, 2 nM, and 1 nM, respectively. PACAP (1-38), human, ovine, rat TFA increases the α-secretase activity. PACAP (1-38), human, ovine, rat TFA elevates cytosolic Ca 2+, increases proliferation and increases phosphorylation of extracellular regulates kinase (ERK) and the epidermal growth factor receptor (EGFR). PACAP (1-38), human, ovine, rat TFA demonstrates potent, efficacious, and sustained stimulatory effects on sympathetic neuronal NPY and catecholamine production. PACAP (1-38), human, ovine, rat TFA can be used for neurotrophic and neuroprotective research .
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Cat. No.: HY-182121
CAS No.: 173273-38-6
Research Areas:  

Others

Pac-2-amino-dA-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
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Cat. No.: HY-182175
CAS No.: 689283-85-0
Research Areas:  

Others

iPr-Pac-G-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
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Cat. No.: HY-W1121756
CAS No.: 150065-82-0
Research Areas:  

Others

DNA G(iPr-pac) amidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
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Cat. No.: HY-W1121757
CAS No.: 121058-86-4
Research Areas:  

Others

2'-OTBS A(pac) amidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
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Cat. No.: HY-182160
CAS No.: 128219-82-9
Target:  

Phosphoramidites

2'-OMe-Pac-A-CE phosphoramidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
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Cat. No.: HY-W1121755
CAS No.: 1402072-31-4
Research Areas:  

Others

2'-OMe G(iPr-pac) amidite is a phosphoramidite that can be used in the synthesis of oligonucleotides.
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