Date published: 2026-4-1

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DCL-1 Inhibitors

DCL-1 inhibitors are a class of compounds that specifically target and modulate the activity of the protein known as "Deleted in Colorectal Cancer-Like 1" (DCL-1). This protein is a member of the family of glycosyltransferases, enzymes that are responsible for adding sugar moieties to various substrates, which can include proteins, lipids, and carbohydrates. Glycosylation, the process these enzymes catalyze, plays a crucial role in a wide array of biological functions, including protein folding, stability, and cellular signaling. DCL-1 is involved in the addition of specific sugar chains to proteins, thus affecting their functional and structural properties. Alterations in its enzymatic activity can result in changes in cellular communication, growth, and response to environmental signals.

Inhibitors of DCL-1 are designed to interfere with the enzyme's ability to catalyze glycosylation. By binding to the active site or interacting with regulatory regions of the protein, these inhibitors prevent DCL-1 from attaching sugar residues to its substrates. The modulation of DCL-1 activity by these inhibitors provides valuable insights into the regulation of glycosylation and its broader impact on cellular and molecular processes. Inhibition of glycosyltransferase activity can lead to changes in protein stability, localization, and interaction with other biomolecules, making DCL-1 inhibitors an important tool for studying glycosylation-dependent mechanisms. Researchers utilize these inhibitors to probe the specific roles of DCL-1 in biological systems and to explore how variations in glycosylation patterns can influence cellular behavior and structural organization.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

DRB

53-85-0sc-200581
sc-200581A
sc-200581B
sc-200581C
10 mg
50 mg
100 mg
250 mg
$43.00
$189.00
$316.00
$663.00
6
(1)

5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole (DRB) inhibits RNA polymerase II, curtailing primary miRNA transcription and thus limiting DCL1 substrate availability.

(−)-Epigallocatechin Gallate

989-51-5sc-200802
sc-200802A
sc-200802B
sc-200802C
sc-200802D
sc-200802E
10 mg
50 mg
100 mg
500 mg
1 g
10 g
$43.00
$73.00
$126.00
$243.00
$530.00
$1259.00
11
(1)

Epigallocatechin gallate, found in green tea, demonstrates inhibitory potential towards Dicer, which may indirectly impact DCL1's activity in the RNAi pathway.

Kinetin riboside

4338-47-0sc-221789
sc-221789A
500 mg
5 g
$141.00
$694.00
(1)

It exhibits potential Dicer inhibitory activity, which in turn can modulate DCL1's function by impeding the RNAi pathway.

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
$110.00
$250.00
$936.00
$50.00
33
(2)

A flavonoid with potential inhibitory effects on Dicer. Its inhibition can influence DCL1's role within the RNAi pathway.

Chloroquine Sulphate

132-73-0sc-337629
25 mg
$224.00
2
(0)

Chloroquine disrupts endosomal pathways, potentially affecting the RNAi pathway and DCL1's role in dsRNA processing.

Cycloheximide

66-81-9sc-3508B
sc-3508
sc-3508A
100 mg
1 g
5 g
$41.00
$84.00
$275.00
127
(6)

An inhibitor of eukaryotic protein synthesis which may indirectly affect DCL1's protein levels and activity.

α-Amanitin

23109-05-9sc-202440
sc-202440A
1 mg
5 mg
$269.00
$1050.00
26
(2)

An RNA polymerase II inhibitor that can impact primary miRNA transcription, subsequently influencing DCL1 activity.

Suramin sodium

129-46-4sc-507209
sc-507209F
sc-507209A
sc-507209B
sc-507209C
sc-507209D
sc-507209E
50 mg
100 mg
250 mg
1 g
10 g
25 g
50 g
$152.00
$214.00
$728.00
$2601.00
$10965.00
$21838.00
$41096.00
5
(1)

An agent known to interfere with various cellular processes and may impact the RNAi pathway by affecting upstream factors, thereby influencing DCL1.

Actinomycin D

50-76-0sc-200906
sc-200906A
sc-200906B
sc-200906C
sc-200906D
5 mg
25 mg
100 mg
1 g
10 g
$74.00
$243.00
$731.00
$2572.00
$21848.00
53
(3)

A compound that intercalates into DNA and can inhibit RNA synthesis, thus indirectly influencing the RNAi pathway and DCL1 activity.