Date published: 2025-9-11

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β-defensin 14阻害剤

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.

関連項目

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製品名CAS #カタログ #数量価格引用文献レーティング

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)

トリコスタチンAはヒストン脱アセチル化酵素を阻害し、クロマチン構造を変化させることでRIM-BP3Bの発現を低下させる可能性がある。

5-Azacytidine

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

このDNAメチルトランスフェラーゼ阻害剤は、遺伝子のメチル化パターンに影響を与えることで、RIM-BP3Bの発現を減少させる可能性がある。

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)

アクチノマイシンDはDNAに結合し、RNAポリメラーゼの働きを止め、RIM-BP3B mRNAの合成を減少させる可能性がある。

α-Amanitin

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

α-アマニチンはRNAポリメラーゼIIを阻害し、RIM-BP3Bの転写を減少させる可能性がある。

Rapamycin

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

シロリムスはmTORを阻害し、タンパク質合成経路に影響を与えることによって、RIM-BP3Bの発現をダウンレギュレートする可能性がある。

Cycloheximide

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

シクロヘキシミドは真核生物のタンパク質合成を阻害し、RIM-BP3Bの産生を減少させる可能性がある。

Chloroquine

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

クロロキンはリソソームをアルカリ化し、RIM-BP3B mRNAの分解経路を阻害する可能性がある。

LY 294002

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

LY294002はPI3K阻害剤であり、下流のシグナルに影響を与えることでRIM-BP3Bの発現を低下させる可能性がある。

Mithramycin A

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

ミトラマイシンAはDNAに結合し、RNA合成を阻害することでRIM-BP3Bの発現を低下させる可能性がある。

2-Deoxy-D-glucose

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

解糖を阻害し、RIM-BP3Bの発現や他の細胞プロセスのエネルギーを減少させる可能性がある。