Date published: 2025-10-10

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LOC100039560 Inhibitors

LOC100039560 inhibitors are a class of chemical compounds developed to target and inhibit the activity of the protein encoded by the gene LOC100039560. This gene is among those identified in genomic studies, notable for its unique expression profile, suggesting its involvement in specific cellular functions. While the full biological role of the protein encoded by LOC100039560 is not completely understood, it is believed to participate in distinct cellular pathways, as indicated by initial genomic and proteomic analyses. The development of inhibitors targeting this protein involves a thorough understanding of its molecular structure and how it functions within cellular systems. The primary aim of designing LOC100039560 inhibitors is to disrupt the functional activities of this protein, thus gaining insights into its role in cellular processes and potentially influencing these processes. This goal requires identifying critical sites or domains on the protein that are essential for its functionality and creating molecules that can effectively bind to and inhibit these sites.

The process of developing LOC100039560 inhibitors is complex and involves a multidisciplinary approach, incorporating biochemistry, molecular biology, and pharmacology. Researchers working on this initiative focus on determining the structural details of the LOC100039560 protein, using various advanced techniques to map its structure, particularly its functional domains. This structural understanding is crucial for the targeted design of inhibitors that are both specific to their target and effective in their action. The interaction between these inhibitors and the LOC100039560 protein is key to their efficacy. The inhibitors must bind to the protein in a manner that disrupts its ability to interact with other cellular components or perform its normal functions. Typically, this results in the formation of a complex between the inhibitor and specific regions on the protein, necessitating a highly accurate match in molecular structures. In addition to their binding properties, the design of LOC100039560 inhibitors also considers factors such as the compound's stability, solubility, and its ability to reach and interact effectively with the target site within biological systems. Researchers strive to optimize the pharmacokinetic properties of these inhibitors, ensuring they possess appropriate hydrophobic and hydrophilic characteristics and an optimal molecular size and shape for efficient interaction. The development of LOC100039560 inhibitors highlights the advanced level of current research in molecular targeting and underscores the complexities involved in designing inhibitors for proteins that are relatively uncharacterized but may play significant roles in biological processes.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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)

Binds to DNA and inhibits RNA polymerase, thus blocking RNA synthesis.

α-Amanitin

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

Inhibits RNA polymerase II, which is responsible for mRNA synthesis.

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)

Binds to bacterial RNA polymerase, inhibiting transcription initiation.

Cordycepin

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

Analog of adenosine that can terminate mRNA chain elongation.

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)

Inhibits RNA polymerase II transcription elongation.

Triptolide

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

Inhibits transcription by affecting the activity of RNA polymerase II.

Flavopiridol

146426-40-6sc-202157
sc-202157A
5 mg
25 mg
$78.00
$254.00
41
(3)

Inhibits cyclin-dependent kinases and can indirectly reduce transcription.

Camptothecin

7689-03-4sc-200871
sc-200871A
sc-200871B
50 mg
250 mg
100 mg
$57.00
$182.00
$92.00
21
(2)

Inhibits DNA topoisomerase I, causing DNA damage and affecting transcription.

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)

Inhibits exportin 1 (CRM1), preventing nuclear export of certain proteins and RNA.

Rocaglamide

84573-16-0sc-203241
sc-203241A
sc-203241B
sc-203241C
sc-203241D
100 µg
1 mg
5 mg
10 mg
25 mg
$270.00
$465.00
$1607.00
$2448.00
$5239.00
4
(1)

Inhibits initiation of translation and could downregulate protein synthesis.