Date published: 2026-4-1

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GARNL3 Inhibitors

GARNL3 inhibitors are chemical compounds designed to specifically inhibit the activity of the GTPase-activating Rap/Ran-GEF domain-like protein 3 (GARNL3). GARNL3 is a member of the Ras superfamily of small GTPases, which are involved in various cellular processes, including cell signaling, cytoskeletal dynamics, and vesicular trafficking. Structurally, GARNL3 inhibitors often contain motifs that facilitate binding to the active site of the GARNL3 protein, blocking its ability to interact with its physiological partners and downstream signaling pathways. These inhibitors typically function by interfering with the guanine nucleotide exchange factor (GEF) activity of GARNL3, preventing the activation of its associated GTPase targets. By modulating the nucleotide exchange process, these compounds effectively inhibit the normal cellular processes regulated by GARNL3, making them important tools for studying the biochemical and cellular functions of this protein.

The chemical design of GARNL3 inhibitors usually features high selectivity for the GARNL3 protein, ensuring minimal cross-reactivity with other GTPase-activating proteins. This selectivity is achieved through molecular structures that precisely match the binding pockets or active sites of GARNL3, allowing for specific inhibition. Various structural scaffolds can be used to develop these inhibitors, ranging from small molecules to larger macrocyclic compounds, each optimized to balance potency, stability, and bioavailability. Due to their ability to precisely target GARNL3, these inhibitors are often utilized in research to dissect the role of GARNL3 in cell biology. They allow researchers to explore how GARNL3 influences processes such as cytoskeletal reorganization, cell migration, and intracellular transport. As research tools, GARNL3 inhibitors are valuable in mapping the functional contributions of this protein within signaling pathways and in understanding the broader regulatory networks in which GARNL3 is involved.

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$67.00
$223.00
$425.00
97
(3)

Inhibits PI3K, which can alter the phosphorylation state and activity of proteins downstream.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

Also targets PI3K, potentially affecting protein interactions and functions in related pathways.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

Binds mTOR, possibly affecting signaling pathways that regulate protein synthesis and degradation.

Triciribine

35943-35-2sc-200661
sc-200661A
1 mg
5 mg
$104.00
$141.00
14
(1)

Specifically inhibits AKT, which can modulate multiple downstream proteins.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

Inhibits JNK, thereby potentially altering transcription factor activity and protein expression.

U-0126

109511-58-2sc-222395
sc-222395A
1 mg
5 mg
$64.00
$246.00
136
(2)

Inhibits MEK, which could affect MAPK/ERK pathway proteins and their functions.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$90.00
$349.00
284
(5)

P38 MAPK inhibitor, could change the phosphorylation state of dependent proteins.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

Inhibits MEK1, potentially affecting proteins downstream in the MAPK/ERK pathway.

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$135.00
$1085.00
115
(2)

Proteasome inhibitor, can affect the degradation of a wide range of proteins.

MG-132 [Z-Leu- Leu-Leu-CHO]

133407-82-6sc-201270
sc-201270A
sc-201270B
5 mg
25 mg
100 mg
$60.00
$265.00
$1000.00
163
(3)

Proteasome inhibitor, may stabilize proteins that regulate the ubiquitin-proteasome pathway.