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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
17 Results for "
tripeptidyl
" in MedChemExpress (MCE) Product Catalog:
Products (17)
17 Results for "tripeptidyl" in MCE Product Catalog:
2
2 Cited Publications
Synonyms: UCL-1397 oxalate
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Butabindide (UCL-1397) oxalate is a potent, selective tripeptidvl peptidase II (TPP II) inhibitor with Ki values of 7 nM and 10 μM for TPP II and TPP I, respectively. Butabindide oxalate inhibits TPP II to protect CCK-8 against inactivation .
Cat. No.: HY-P4344
CAS No.: 1926163-52-1
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Cat. No.: HY-P4460
CAS No.: 60354-61-2
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Cat. No.: HY-150070
CAS No.: 175553-48-7
Synonyms: UCL-1397
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Butabindide (UCL-1397) is a potent, selective tripeptidvl peptidase II (TPP II) inhibitor with Ki values of 7 nM and 10 μM for TPP II and TPP I, respectively. Butabindide inhibits TPP II to protect CCK-8 against inactivation .
Cat. No.: HY-P2648
CAS No.: 70968-04-6
Synonyms: N-Succinyl-AAPL-p-nitroanilide
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Cat. No.: HY-P4464
CAS No.: 201732-35-6
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Cat. No.: HY-P4464A
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Cat. No.: HY-P4470
CAS No.: 201738-99-0
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Cat. No.: HY-P2623
CAS No.: 72007-47-7
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Cat. No.: HY-137164A
CAS No.: 62037-42-7
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Cat. No.: HY-P4461
CAS No.: 99524-09-1
Cat. No.: HY-P4528
CAS No.: 749831-27-4
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Cat. No.: HY-129407
CAS No.: 184901-82-4
Synonyms: Ala-ala-phe-chloromethylketone tfa; N-Ala-Ala-Phe-CMK; tripeptidyl Peptidase inhibitor II
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AAF-CMK TFA (Ala-ala-phe-chloromethylketone tfa; N-Ala-Ala-Phe-CMK) is a subtilisin-type serine peptidase that removes tripeptides from the free NH2 termini of oligopeptides. AAF-CMK TFA is an irreversible inhibitor of TPPII and is typically used at concentrations of 10-100 μM. It does not significantly interfere with the chymotrypsin-like activity of the proteasome. AAF-CMK also inhibits bleomycin hydrolase and puromycin-sensitive aminopeptidase when used at a concentration of 50 μM.
Cat. No.: HY-150590
CAS No.: 2028300-31-2
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20S Proteasome-IN-2 is a human 20S proteasome inhibitor. 20S Proteasome-IN-2 shows high selectivity to its β5 subunit with the IC50 of 0.18 μM. 20S Proteasome-IN-2 displays anti-proliferative effect in vitro and in vivo, and arrests cell cycle at G2/M .
Cat. No.: HY-P70980
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: TPP1; tripeptidyl Peptidase I; Prev. CLN2; Ceroid-Lipofuscinosis, Neuronal 2, Late Infantile (Jansky-Bielschowsky Disease); Prev. SCAR7; Spinocerebellar Ataxia, Autosomal Recessive 7; TPP-1; Lysosomal Pepstatin Insensitive Protease; LPIC; Lysosomal Pepsta
Cat. No.: HY-P76112
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: TPP1; tripeptidyl Peptidase I; Prev. CLN2; Ceroid-Lipofuscinosis, Neuronal 2, Late Infantile (Jansky-Bielschowsky Disease); Prev. SCAR7; Spinocerebellar Ataxia, Autosomal Recessive 7; TPP-1; Lysosomal Pepstatin Insensitive Protease; LPIC; Lysosomal Pepsta
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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
