39 Results for "

chitinase inhibitor

" in MedChemExpress (MCE) Product Catalog:
Products (39)

39 Results for "chitinase inhibitor" in MCE Product Catalog:

12
12 Publications Verification
Cat. No.: HY-17596
CAS No.: 57808-65-8
Target:  

Parasite

Research Areas:  

Infection

Closantel is a halogenated salicylanilide with a potent anti-parasitic activity. Closantel is a potent and highly specific Onchocerca volvulus chitinase (OvCHT1) inhibitor with an IC50 of 1.6 μM and a Ki of 468 nM. Closantel inhibits the O. volvulus L3 to L4 molt of developing .
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12
12 Publications Verification
Cat. No.: HY-17596A
CAS No.: 61438-64-0
Target:  

Parasite

Research Areas:  

Infection

Closantel sodium is a halogenated salicylanilide with a potent anti-parasitic activity. Closantel sodium is a potent and highly specific Onchocerca volvulus chitinase (OvCHT1) inhibitor with an IC50 of 1.6 μM and a Ki of 468 nM. Closantel sodium inhibits the O. volvulus L3 to L4 molt of developing .
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2
2 Cited Publications
Cat. No.: HY-15275
CAS No.: 582315-72-8
Purity:  99.59%
BMS-265246 is a potent and selective cyclin-dependent kinase CDK1 and CDK2 inhibitor, with IC50 values of 6 and 9 nM, respectively. BMS-265246 inhibits CHI3L1 (chitinase 3-like-1) stimulation of ACE2 (angiotensin converting enzyme 2) and SPP (viral spike protein priming proteases). BMS-265246 can be used for ovarian cancer and COVID-19 research .
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1
1 Cited Publications
Cat. No.: HY-137464A
CAS No.: 2088453-21-6
Purity:  99.11%
Target:  

Glycosidase

Research Areas:  

Inflammation/Immunology

OATD-01 is a highly potent, first-in-class, orally active and selective chitinase inhibitor with low nanomolar activity toward CHIT1 (hCHIT1,IC50=23 nM). OATD-01 shows excellect PK profile in multiple species and is selectivity against a panel of other off-targets. OATD-01 exhibits significant antifibrotic efficacy in vivo and can be used for pulmonary fibrosis (IPF) research .
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1
1 Cited Publications
Cat. No.: HY-18599A
CAS No.: 2070014-83-2
Target:  

Insecticide

Research Areas:  

Others

Chitinase-IN-2 hydrochloride is an inhibitor of insect chitinase and N-acetylhexosaminidase.
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1
1 Cited Publications
Cat. No.: HY-18599
CAS No.: 1579991-63-1
Target:  

Insecticide

Research Areas:  

Others

Chitinase-IN-2 is an insecticide that can inhibit the activity of chitinase and N-acetylhexosaminidase, with inhibition percentages of 98% and 92% at concentrations of 50 μM and 20 μM, respectively.
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Cat. No.: HY-163387
CAS No.: 2982256-78-8
CHI3L1-IN-1 (Compound 30) is an inhibitor for Chitinase-3-like protein 1 (CHI3L1) (YKL-40) with IC50 of 50 nM. CHI3L1-IN-1 inhibits hERG channel with an IC50 of 2.3 μM .
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Cat. No.: HY-126389B
CAS No.: 1398-61-4
Chitin, from shrimp shells (chitinase substrate) serves as a substrate for chitinase. Chitin, from shrimp shells (chitinase substrate) is a long-chain polymer of N-acetylglucosamine with β-(1-4) linkages. Chitin, from shrimp shells (chitinase substrate) is found in the exoskeleton of crabs. Chitin, from shrimp shells (chitinase substrate) inhibits the activation of NF-κB p65, alters the translocation of NF-κB p65 to the nucleus, and interacts with the cell wall of Candida species. Chitin, from shrimp shells (chitinase substrate) exerts antifungal and anti-inflammatory effects. Chitin, from shrimp shells (chitinase substrate) can be used in the research of gastric ulcer and candidiasis .
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Cat. No.: HY-P2797A
CAS No.: 9001-06-3
Synonyms: AMCase, Streptomyces griseus
Research Areas:  

Others

Chitinase, Streptomyces griseus is a chitinase from Streptomyces griseus. Chitinase is a chitin-targeting enzyme with chitin hydrolysis activity. Chitinase inhibits chitin-induced innate type 2 inflammation in the lung. Chitinase augments chitin-free, allergen-induced Th2 inflammation. Chitinase mediates effector functions of IL-13 .
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Cat. No.: HY-P10304
CAS No.: 74838-83-8
Synonyms: Cyclo(Pro-Arg)
Target:  

Fungal

Research Areas:  

Others

Cyclo(Arg-Pro) (Cyclo(Pro-Arg)) is an inhibitor for chitinase. Cyclo(Arg-Pro) inhibits cell separation of Saccharomyces cerevisiae, without affecting its growth. Cyclo(Arg-Pro) inhibits the morphological change of Candida albicans from yeast form to filamentous form .
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Cat. No.: HY-P2797
CAS No.: 9001-06-3
Synonyms: AMCase, Serratia marcescens
Chitinase, Serratia marcescens is a chitinase from Serratia marcescens. Chitinase is a chitin-targeting enzyme with chitin hydrolysis activity. Chitinase inhibits chitin-induced innate type 2 inflammation in the lung. Chitinase augments chitin-free, allergen-induced Th2 inflammation. Chitinase mediates effector functions of IL-13 .
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Cat. No.: HY-P2797B
CAS No.: 9001-06-3
Research Areas:  

Inflammation/Immunology

Chitinase is a chitin-targeting enzyme with chitin hydrolysis activity. Chitinase inhibits chitin-induced innate type 2 inflammation in the lung. Chitinase augments chitin-free, allergen-induced Th2 inflammation. Chitinase mediates effector functions of IL-13 .
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Cat. No.: HY-P2274
CAS No.: 243975-37-3
Argifin is a sub-nanomolar chitinase inhibitor produced by soil microorganisms, with IC50s of 0.025 μM, 6.4 μM , 1.1 μM and 4.5 μM for SmChiA (Serratia marcescens chitinaese A), SmChiB, Aspergillus fumigatus chitinase B1 and human chitotriosidase, respectively .
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Cat. No.: HY-75828
CAS No.: 538-58-9
Synonyms: Dibenzalacetone
Target:  

Bacterial

Research Areas:  

Infection

Dibenzylideneacetone (Dibenzalacetone) is a potent inhibitor of chitinase with an IC50 value of 13.10 μM. The MIC value of Dibenzylideneacetone against Botrytis cinerea is 32 μg/mL, and the EC50 values for inhibiting mycelium growth and spore germination are 16.29 and 14.64 μg/mL, respectively. Dibenzylideneacetone can be used in research on fruit and vegetable preservatives .
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Cat. No.: HY-120827
CAS No.: 103782-08-7
Synonyms: A82516
Target:  

Parasite

Research Areas:  

Infection

Allosamidin (A82516) is an insect chitinase inhibitor with an IC50 of 0.35 μM against Bombyx mori chitinase .
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Cat. No.: HY-P3461
CAS No.: 289665-92-5
Target:  

Parasite

Research Areas:  

Infection

Argadin is a cyclopentapeptide chitinase inhibitor. Argadin inhibits chitinase B (ChiB) with a Ki value of 20 nM. Argadin can be used for the research of fungicid and insecticid .
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Cat. No.: HY-18598
CAS No.: 1579991-61-9
Target:  

Insecticide

Research Areas:  

Infection

Chitinase-IN-1 is an insecticide that can inhibit the activity of chitinase and N-acetylglucosaminidase. The inhibition percentages for glycosidase and N-acetylglucosaminidase at concentrations of 50 uM and 20 uM are 75% and 67%, respectively.
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Cat. No.: HY-P10304A
Synonyms: Cyclo(Pro-Arg) TFA
Target:  

Fungal

Research Areas:  

Infection

Cyclo (Arg-Pro) TFA is a chitinase inhibitor. Cyclo (Arg-Pro) TFA disrupts cell separation and morphological transition of yeast by inhibiting chitinase activity. Cyclo (Arg-Pro) TFA prevents cell separation of Saccharomyces cerevisiae, leading to the formation of grape-like cell clusters, without inhibiting cell growth. Cyclo (Arg-Pro) TFA blocks the morphological transition of Candida albicans from yeast form to hyphal form, without inhibiting cell growth .
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Cat. No.: HY-163388
CAS No.: 2982257-63-4
Target:  

Glycosidase

Research Areas:  

Others

CHI3L1-IN-2 (Compound 36) is a CHI3L1 (Chitinase-3-Like Protein 1) inhibitor. CHI3L1-IN-2 inhibits the? interaction between CHI3L1 and heparan sulfate (CHI3L1:HSIII), with an IC50 of 26 nM. CHI3L1, also known as YKL-40, is a glycoprotein associated with inflammation, fibrosis, and cancer .
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Cat. No.: HY-116541
CAS No.: 135158-54-2
Purity:  99.77%
Synonyms: ASM
Acibenzolar-S-methyl (ASM) is a synthetic analog of Salicylic acid (HY-B0167) and a plant activator. Acibenzolar‑S‑methyl induces increased activities of defense-related enzymes such as peroxidase and chitinase, activates stomatal defense responses and PR defense gene expression, induces the production of ROS, triggers local and systemic acquired resistance, and inhibits the proliferation of bacterial and fungal pathogens in plants. Acibenzolar‑S‑methyl can be used in studies related to plant infection .
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