Date published: 2025-9-10

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β-defensin 14 Inibidores

β-defensin 14 inhibitors are a class of chemical compounds designed to specifically target and inhibit the activity of β-defensin 14, a member of the defensin family of small, cysteine-rich antimicrobial peptides. β-defensin 14 plays an essential role in the innate immune system, contributing to the defense against pathogens such as bacteria, fungi, and viruses by disrupting their cell membranes. This peptide is known for its ability to bind to microbial cell surfaces, leading to membrane destabilization and the destruction of pathogens. Inhibitors of β-defensin 14 aim to block its antimicrobial activity, potentially affecting the peptide's ability to bind to microbial membranes or interact with specific components of the immune response.

The development of β-defensin 14 inhibitors involves a detailed understanding of the peptide's structure, particularly its β-sheet-rich conformation stabilized by disulfide bridges, which is essential for its function in binding to microbial surfaces. These inhibitors are designed to interact with key regions of the peptide, such as its positively charged surface or hydrophobic regions, which are critical for membrane binding and antimicrobial activity. Structural biology techniques, including molecular modeling and X-ray crystallography, are commonly employed to identify these critical regions and to design inhibitors that specifically bind to them, preventing β-defensin 14 from carrying out its membrane-disrupting functions. Achieving high specificity is crucial in this process, as β-defensin 14 shares structural and functional similarities with other members of the defensin family. These inhibitors are valuable tools for studying the detailed mechanisms of host-microbe interactions, shedding light on the complex dynamics of innate immune responses and the role of defensins in protecting against microbial invaders.

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Nome do ProdutoCAS #Numero de CatalogoQuantidadePrecoUso e aplicacaoNOTAS

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$149.00
$470.00
$620.00
$1199.00
$2090.00
33
(3)

A tricostatina A inibe as histonas desacetilases, reduzindo potencialmente a expressão de RIM-BP3B através da alteração da estrutura da cromatina.

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

Este inibidor da DNA metiltransferase pode diminuir a expressão de RIM-BP3B ao afetar os padrões de metilação dos genes.

Actinomycin D

50-76-0sc-200906
sc-200906A
sc-200906B
sc-200906C
sc-200906D
5 mg
25 mg
100 mg
1 g
10 g
$73.00
$238.00
$717.00
$2522.00
$21420.00
53
(3)

A actinomicina D liga-se ao ADN e interrompe a ação da RNA polimerase, reduzindo potencialmente a síntese do ARNm do RIM-BP3B.

α-Amanitin

23109-05-9sc-202440
sc-202440A
1 mg
5 mg
$260.00
$1029.00
26
(2)

A α-Amanitina inibe a RNA polimerase II, o que pode levar à diminuição da transcrição de RIM-BP3B.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$62.00
$155.00
$320.00
233
(4)

O sirolimus inibe o mTOR, que pode reduzir a expressão de RIM-BP3B ao afetar as vias de síntese proteica.

Cycloheximide

66-81-9sc-3508B
sc-3508
sc-3508A
100 mg
1 g
5 g
$40.00
$82.00
$256.00
127
(5)

A cicloheximida inibe a síntese proteica eucariótica, diminuindo potencialmente a produção de RIM-BP3B.

Chloroquine

54-05-7sc-507304
250 mg
$68.00
2
(0)

A cloroquina pode alcalinizar os lisossomas, interferindo potencialmente com as vias de degradação do ARNm do RIM-BP3B.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

O LY294002 é um inibidor da PI3K que pode levar à redução da expressão de RIM-BP3B ao afetar os sinais a jusante.

Mithramycin A

18378-89-7sc-200909
1 mg
$54.00
6
(1)

A mitramicina A liga-se ao ADN, diminuindo potencialmente a expressão de RIM-BP3B através da inibição da síntese de ARN.

2-Deoxy-D-glucose

154-17-6sc-202010
sc-202010A
1 g
5 g
$65.00
$210.00
26
(2)

Inibe a glicólise, reduzindo potencialmente a energia para a expressão de RIM-BP3B e outros processos celulares.