Date published: 2025-11-1

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ZFYVE28 Inhibitors

ZFYVE28 inhibitors belong to a class of chemical compounds that specifically target the zinc finger FYVE domain-containing protein 28 (ZFYVE28). The FYVE domain is a conserved motif found in various proteins involved in membrane trafficking and signaling processes within cells. ZFYVE28, also known as endofin, is one such protein that contains the FYVE domain, playing a crucial role in intracellular membrane dynamics. The inhibition of ZFYVE28 by these specialized compounds disrupts its normal cellular functions, leading to alterations in membrane-related processes.

The primary mechanism of action of ZFYVE28 inhibitors involves interference with the protein's ability to interact with membranes. ZFYVE28 is known to bind to phosphatidylinositol 3-phosphate (PI3P), a phospholipid present in cellular membranes. This interaction is vital for the proper localization and functioning of ZFYVE28 in membrane-associated events. By inhibiting this interaction, ZFYVE28 inhibitors disrupt the normal membrane-related functions mediated by ZFYVE28. This interference may have implications for various cellular processes, including endosomal trafficking, autophagy, and signaling cascades. As research in this field advances, a deeper understanding of the specific effects and potential applications of ZFYVE28 inhibitors in various cellular contexts is likely to emerge.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$66.00
$219.00
$417.00
97
(3)

A potent phosphatidylinositol 3-kinase (PI3K) inhibitor. ZFYVE28 is believed to interact with PI3K products. Inhibition of PI3K activity by Wortmannin could prevent the recruitment of ZFYVE28 to the membrane, thus inhibiting its function.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

A selective inhibitor of PI3Ks. Similar to Wortmannin, LY294002 would likely interfere with ZFYVE28's association with PI3K signaling products, which is essential for its activity.

Autophagy Inhibitor, 3-MA

5142-23-4sc-205596
sc-205596A
50 mg
500 mg
$56.00
$256.00
113
(3)

Inhibitor of autophagy through inhibition of class III PI3K. It can indirectly affect ZFYVE28 function by disrupting the autophagic processes that ZFYVE28 may be involved in.

Spautin-1

1262888-28-7sc-507306
10 mg
$165.00
(0)

A specific inhibitor of autophagy that promotes the degradation of class III PI3K Vps34 complex components. This may indirectly reduce ZFYVE28 function by impairing the autophagic machinery it may interact with.

U-0126

109511-58-2sc-222395
sc-222395A
1 mg
5 mg
$63.00
$241.00
136
(2)

A selective inhibitor of MEK1/2, which are upstream of the ERK pathway. ZFYVE28, if linked to ERK signaling, could have its activity modulated indirectly by U0126 through this pathway.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$39.00
$90.00
212
(2)

An inhibitor of MEK activation, thereby preventing the activation of MAPK/ERK. This could indirectly influence ZFYVE28 if it is involved in ERK signaling.

Bafilomycin A1

88899-55-2sc-201550
sc-201550A
sc-201550B
sc-201550C
100 µg
1 mg
5 mg
10 mg
$96.00
$250.00
$750.00
$1428.00
280
(6)

A specific inhibitor of the vacuolar type H+-ATPase (V-ATPase). By inhibiting V-ATPase, Bafilomycin A1 can disrupt endosomal acidification, potentially affecting ZFYVE28's endosomal localization and function.

Dynamin Inhibitor I, Dynasore

304448-55-3sc-202592
10 mg
$87.00
44
(2)

A non-competitive inhibitor of dynamin, affecting endocytosis. ZFYVE28, being associated with membrane trafficking, could be indirectly inhibited if endocytosis is disrupted.

ML 141

71203-35-5sc-362768
sc-362768A
5 mg
25 mg
$134.00
$502.00
7
(1)

A selective inhibitor of Cdc42 GTPase. If ZFYVE28 is involved in signaling pathways regulated by Cdc42, its function could be indirectly inhibited by ML141.

SecinH3

853625-60-2sc-203260
5 mg
$273.00
6
(1)

An inhibitor of cytohesin, affecting ARF6 activation. As ZFYVE28 may be part of pathways involving ARF6, SecinH3 could indirectly reduce its functional activity.