Date published: 2026-4-1

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RGD1564058 Inhibitors

RGD1564058 inhibitors represent a class of chemical compounds that exhibit a high specificity towards modulating the activity of molecular targets associated with RGD (arginine-glycine-aspartic acid) peptide interactions. These peptides are vital for cell adhesion processes, particularly those involving integrins, which are transmembrane receptors that facilitate cell-extracellular matrix (ECM) communication. RGD motifs are recognized by specific integrins, leading to a cascade of signaling events that influence cellular behavior such as migration, proliferation, and differentiation. Inhibitors of RGD1564058 can interfere with these interactions by binding to the integrin receptors and preventing the adhesion of cells to the ECM. These inhibitors are often characterized by their ability to mimic the RGD sequence, thus competitively inhibiting integrin binding to their natural ligands, but with structural modifications that enhance specificity and affinity for the target integrins.

Chemically, RGD1564058 inhibitors are designed with a core molecular scaffold that typically includes cyclic peptides, small molecules, or peptidomimetics. These structures are engineered to ensure high stability and minimal degradation within experimental environments. Structural modifications, such as the incorporation of non-natural amino acids or rigidifying elements, are used to optimize binding interactions and improve the selectivity of these inhibitors for specific integrin subtypes. The molecular architecture of these compounds is critical for their ability to precisely disrupt integrin-mediated processes, thereby offering valuable tools for investigating the biochemical pathways of cell adhesion, matrix remodeling, and signal transduction in various experimental models. The specificity of RGD1564058 inhibitors makes them essential in probing the fundamental mechanisms underlying cellular interactions with the ECM and the regulation of integrin-mediated signal transduction in biochemical studies.

SEE ALSO...

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
$74.00
$243.00
$731.00
$2572.00
$21848.00
53
(3)

Actinomycin D inhibits gene expression by intercalating into DNA, potentially disrupting the transcription of the WD repeat domain 83 opposite strand gene.

Cycloheximide

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

Cycloheximide inhibits protein synthesis, which could lead to reduced levels of the WD repeat domain 83 opposite strand protein.

Puromycin

53-79-2sc-205821
sc-205821A
10 mg
25 mg
$166.00
$322.00
436
(1)

Puromycin is a protein synthesis inhibitor that can lead to premature chain termination during translation, potentially reducing the levels of the WD repeat domain 83 opposite strand protein.

Fluorouracil

51-21-8sc-29060
sc-29060A
1 g
5 g
$37.00
$152.00
11
(1)

5-Fluorouracil interferes with RNA synthesis and inhibits DNA synthesis, potentially impacting the expression of the WD repeat domain 83 opposite strand gene at the transcriptional level.

Rifampicin

13292-46-1sc-200910
sc-200910A
sc-200910B
sc-200910C
1 g
5 g
100 g
250 g
$97.00
$328.00
$676.00
$1467.00
6
(1)

Rifampicin inhibits bacterial RNA polymerase and can potentially impact the expression of the WD repeat domain 83 opposite strand gene in bacterial cells.

Triptolide

38748-32-2sc-200122
sc-200122A
1 mg
5 mg
$90.00
$204.00
13
(1)

Triptolide has been suggested to inhibit RNA polymerase II-mediated transcription, potentially impacting the expression of the WD repeat domain 83 opposite strand gene.

Mycophenolic acid

24280-93-1sc-200110
sc-200110A
100 mg
500 mg
$69.00
$266.00
8
(1)

Mycophenolic acid inhibits inosine monophosphate dehydrogenase, potentially leading to reduced levels of guanosine nucleotides, which may affect the expression of the WD repeat domain 83 opposite strand gene.