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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
175 Results for "
chitinase digestion
" in MedChemExpress (MCE) Product Catalog:
Products (175)
175 Results for "chitinase digestion" in MCE Product Catalog:
28
Target:
Research Areas:
Proteinase K (Protease K) is a nonspecific serine protease that is useful for general digestion of proteins. Proteinase K is active in the presence of SDS or urea and over a wide range of pH (4-12), salt concentrations, and temperatures. Proteinase K can be use for promoting methods of viral nucleic acid extraction, and detection .
12
12 Cited Publications
Cat. No.: HY-17596
CAS No.: 57808-65-8
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 .
12
12 Cited Publications
Cat. No.: HY-17596A
CAS No.: 61438-64-0
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 .
5
5 Cited Publications
4
4 Cited Publications
Cat. No.: HY-P70030
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CHI3L1; HCGP-39; chitinase 3 Like 1; CGP-39; chitinase-3-Like Protein 1; YKL-40; YKL40; GP-39; YK-40; CHI3L1 Protein; GP39; HC-Gp39; chitinase 3-Like 1 (Cartilage Glycoprotein-39); HCGP-3P; Cartilage Glycoprotein-39; YYL-40; Cartilage Glycoprotein 39; ASR
Species:
Human
Source:
HEK293
3
3 Cited Publications
Cat. No.: HY-P7845
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Ym1; Chi3l3; Chil3; Secreted protein Ym1; Eosinophil chemotactic cytokine; ECF-L; chitinase-3-like protein 3; Beta-N-acetylhexosaminidase Ym1; EC:3.2.1.52; chitinase-like protein 3; rMuchitinase-like protein 3/YM1, His
Species:
Mouse
Source:
HEK293
3
3 Cited Publications
Cat. No.: HY-N1425
CAS No.: 20316-62-5
Category:
Flavonols Flavonoids Platanus occidentalis L. Metabolic Disease Phenols Polyphenols Plants Platanaceae Extract Disease Research Fields
Target:
2
2 Cited Publications
Synonyms: Cholecystokinin-33(human); CCK-33(human)
Target:
Research Areas:
2
Target:
Research Areas:
Collagenases are enzymes that break the peptide bonds in collagen. Collagenases are derived from the Clostridium histolyticum. Collagenases (Type I) are proteolytic enzymes that break peptide bonds in collagen and can be used for tissue digestion and dissociation.
2
2 Cited Publications
Research Areas:
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 .
2
2 Cited Publications
Cat. No.: HY-108717A
CAS No.: 39450-01-6
Synonyms: Recombinant Protease K (DNase & RNase free, animal free)
Target:
Research Areas:
Recombinant Proteinase K (Protease K) (DNase & RNase free, animal free) is a nonspecific serine protease that is useful for general digestion of proteins. Proteinase K (DNase & RNase free, animal free) is active in the presence of SDS or urea and over a wide range of pH (4-12), salt concentrations, and temperatures. Proteinase K (DNase & RNase free, animal free) can be use for promoting methods of viral nucleic acid extraction, and detection. This product is of molecular biology grade, free of animal-derived ingredients, and is recombinantly purified from yeast .
1
1 Cited Publications
Cat. No.: HY-18599A
CAS No.: 2070014-83-2
Target:
Research Areas:
Chitinase-IN-2 hydrochloride is an inhibitor of insect chitinase and N-acetylhexosaminidase.
1
1 Cited Publications
Cat. No.: HY-18599
CAS No.: 1579991-63-1
Target:
Research Areas:
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.
1
1 Cited Publications
Cat. No.: HY-P76702
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CHI3L1; HCGP-39; chitinase 3 Like 1; CGP-39; chitinase-3-Like Protein 1; YKL-40; YKL40; GP-39; YK-40; CHI3L1 Protein; GP39; HC-Gp39; chitinase 3-Like 1 (Cartilage Glycoprotein-39); HCGP-3P; Cartilage Glycoprotein-39; YYL-40; Cartilage Glycoprotein 39; ASR
Species:
Mouse
Source:
HEK293
1
1
1 Cited Publications
Cat. No.: HY-163727
CAS No.: 2065197-82-0
MMV1557817 is an orally active and potent antimalarial compound. MMV1557817 is a selective, nanomolar inhibitor of both Plasmodium falciparum and Plasmodium vivax aminopeptidases M1 and M17, leading to inhibition of end-stage hemoglobin digestion in asexual parasites .
1
1 Cited Publications
Target:
Research Areas:
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 .
1
1 Cited Publications
Cat. No.: HY-E70365A
Target:
Research Areas:
IdeS (Immobilized, Microspin) is a resin that covalently couples IdeS protease to agarose beads and cleaves IgG at specific sites to generate F(ab')2 and Fc fragments. After IdeS (Immobilized, Microspin) digestion, F(ab')2 and Fc fragments are obtained in the solution without IdeS enzyme.
1
1 Cited Publications
Cat. No.: HY-W105970
CAS No.: 7758-16-9
Synonyms: Disodium pyrophosphate; Sodium acid pyrophosphate; SAPP
Cat. No.: HY-163387
CAS No.: 2982256-78-8
Target:
Research Areas:
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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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
