Date published: 2026-1-11

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Ym2 Inhibitors

Ym2 inhibitors are chemical compounds designed to specifically target and inhibit the activity of Ym2, a member of the chitinase-like protein family. While Ym2 lacks the enzymatic activity typically associated with true chitinases, it still binds chitin-like molecules and is implicated in processes related to tissue remodeling and cellular signaling. The Ym2 protein, along with its family members, is expressed in certain tissues and under specific physiological conditions, often in response to environmental cues. This protein is part of a broader class of lectin-like proteins that contribute to cellular interactions with extracellular matrix components, thus playing a role in maintaining structural and functional integrity at the cellular and tissue levels.

Inhibitors of Ym2 function by binding to the protein and blocking its ability to interact with chitin-like substrates or other molecular partners, thereby disrupting its role in extracellular matrix remodeling or cellular signaling pathways. These inhibitors can modulate how cells respond to external signals related to tissue structure or damage, impacting cellular adhesion, migration, and overall homeostasis. Since Ym2 is involved in protein-protein and protein-carbohydrate interactions, inhibition of its activity could have significant effects on cellular communication and structural maintenance, particularly in tissues that are actively undergoing remodeling or repair. The precise structural characteristics of Ym2 inhibitors and their interaction with the protein are essential for understanding how these compounds can alter Ym2's role in cellular processes, including its contribution to extracellular matrix dynamics and other associated pathways.

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Items 1 to 10 of 11 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
$74.00
$243.00
$731.00
$2572.00
$21848.00
53
(3)

Actinomycin D inhibits RNA synthesis, potentially reducing the transcription of chitinase-like 4 and hence its expression.

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 may lead to reduced translation of chitinase-like 4, resulting in decreased expression.

Puromycin dihydrochloride

58-58-2sc-108071
sc-108071B
sc-108071C
sc-108071A
25 mg
250 mg
1 g
50 mg
$42.00
$214.00
$832.00
$66.00
394
(15)

Puromycin is an inhibitor of protein synthesis, potentially reducing the translation of chitinase-like 4 and leading to decreased expression.

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, which may indirectly affect chitinase-like 4 expression by reducing its transcription.

Sorafenib

284461-73-0sc-220125
sc-220125A
sc-220125B
5 mg
50 mg
500 mg
$57.00
$100.00
$250.00
129
(3)

Sorafenib inhibits several kinases involved in cell signaling pathways, potentially affecting the expression of chitinase-like 4 at a post-translational level.

Wortmannin

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

Wortmannin inhibits phosphatidylinositol 3-kinase (PI3K), a protein involved in various cellular functions, potentially affecting the expression of chitinase-like 4.

Tunicamycin

11089-65-9sc-3506A
sc-3506
5 mg
10 mg
$172.00
$305.00
66
(3)

Tunicamycin inhibits protein glycosylation, which may disrupt the folding and trafficking of chitinase-like 4, leading to reduced expression.

Brefeldin A

20350-15-6sc-200861C
sc-200861
sc-200861A
sc-200861B
1 mg
5 mg
25 mg
100 mg
$31.00
$53.00
$124.00
$374.00
25
(3)

Brefeldin A disrupts protein transport from the endoplasmic reticulum to the Golgi apparatus, potentially causing retention of chitinase-like 4 within the ER and reducing its expression.

Geldanamycin

30562-34-6sc-200617B
sc-200617C
sc-200617
sc-200617A
100 µg
500 µg
1 mg
5 mg
$39.00
$59.00
$104.00
$206.00
8
(1)

Geldanamycin inhibits Hsp90, a chaperone protein involved in folding and stabilization of chitinase-like 4, potentially leading to reduced expression.

Monensin A

17090-79-8sc-362032
sc-362032A
5 mg
25 mg
$155.00
$525.00
(1)

Monensin disrupts ion gradients across cell membranes, potentially affecting the membrane localization of chitinase-like 4 and reducing its expression.