Date published: 2025-10-23

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CARKD Inhibitoren

CARKD inhibitors are a class of chemical compounds that specifically target and inhibit the activity of CARKD, or CAR kinase domain-containing protein. CARKD is involved in cellular energy metabolism, particularly in the regulation of key metabolic pathways. It is associated with the phosphorylation of proteins that participate in metabolic control, including enzymes involved in the management of cellular energy stores such as ATP and NAD+. By inhibiting CARKD, these compounds interfere with its kinase activity, disrupting its ability to phosphorylate substrate proteins and thereby affecting the overall regulation of metabolic processes. This can lead to alterations in energy balance within the cell, impacting functions like biosynthesis, energy production, and catabolism.

The structure and action of CARKD inhibitors can vary, but they typically work by binding to the active site of the kinase domain, preventing CARKD from interacting with its target proteins or transferring phosphate groups. Some inhibitors may also modify the protein's conformation, blocking its ability to function in a normal enzymatic manner. Researchers utilize CARKD inhibitors to study the broader implications of metabolic regulation and how CARKD influences cellular energy homeostasis. Inhibiting CARKD provides valuable insights into the role of protein phosphorylation in metabolic pathways, particularly in processes like glycolysis, oxidative phosphorylation, and fatty acid metabolism. These inhibitors are crucial for understanding how energy regulation is coordinated at the molecular level and for exploring the network of signaling pathways that maintain cellular metabolic balance.

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ProduktCAS #Katalog #MengePreisReferenzenBewertung

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)

Interkaliert die DNA und hemmt die RNA-Polymerase, was die Transkription von Genen und Pseudogenen beeinträchtigt.

α-Amanitin

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

Hemmt die RNA-Polymerase II, was die Transkription von Pseudogenen, die von dieser Polymerase transkribiert werden, verringern könnte.

Rifampicin

13292-46-1sc-200910
sc-200910A
sc-200910B
sc-200910C
1 g
5 g
100 g
250 g
$95.00
$322.00
$663.00
$1438.00
6
(1)

Bindet an bakterielle RNA-Polymerase, kann aber in hohen Konzentrationen auch eukaryotische RNA-Polymerase beeinflussen.

Triptolide

38748-32-2sc-200122
sc-200122A
1 mg
5 mg
$88.00
$200.00
13
(1)

Ein Diterpen-Triepoxid, das die Transkriptionsaktivität der RNA-Polymerase I, II und III hemmt.

Cordycepin

73-03-0sc-203902
10 mg
$99.00
5
(1)

Kann aufgrund seiner adenosinähnlichen Struktur, der jedoch eine Hydroxylgruppe fehlt, die Verlängerung der RNA-Kette beenden.

DRB

53-85-0sc-200581
sc-200581A
sc-200581B
sc-200581C
10 mg
50 mg
100 mg
250 mg
$42.00
$185.00
$310.00
$650.00
6
(1)

Hemmt die Transkriptionsdehnung der RNA-Polymerase II.

Leptomycin B

87081-35-4sc-358688
sc-358688A
sc-358688B
50 µg
500 µg
2.5 mg
$105.00
$408.00
$1224.00
35
(2)

Hemmt den Export von RNA-Molekülen aus dem Zellkern, was möglicherweise die Verarbeitung pseudogener RNA beeinträchtigt.

Quercetin

117-39-5sc-206089
sc-206089A
sc-206089E
sc-206089C
sc-206089D
sc-206089B
100 mg
500 mg
100 g
250 g
1 kg
25 g
$11.00
$17.00
$108.00
$245.00
$918.00
$49.00
33
(2)

Ein Flavonoid mit entzündungshemmenden und antioxidativen Eigenschaften, das die Genexpression und die RNA-Stabilität modulieren kann.

Roscovitine

186692-46-6sc-24002
sc-24002A
1 mg
5 mg
$92.00
$260.00
42
(2)

Ein Cyclin-abhängiger Kinase-Inhibitor, der die Transkriptionsregulation beeinflussen könnte.

(±)-JQ1

1268524-69-1sc-472932
sc-472932A
5 mg
25 mg
$226.00
$846.00
1
(0)

Bromodomain-Inhibitor, der die Bindung von acetyliertem Histon unterbricht, was zu einer Veränderung der Chromatinstruktur und der Genexpression führen kann.