z phe tyr(tbu) diazomethylketone

Irreversible cathepsin L inhibitor which is ca 10'000 times more effective in inactivating cathepsin L than cathepsin S.

N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH (TFA)) (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH TFA) is a formyl peptide receptor (FPR) agonist and a potent chemoattractant for human neutrophils, with its radioiodinated form retaining full biological activity.

Tyr-Gly-Gly-Phe-Met-OH (Met-Enkephalin) is a naturally occurring endogenous opioid peptide that inhibits tumor growth by binding to the opioid receptor.

Fmoc-Tyr(tBu)-Thr(psi(Me,Me)pro)-OH is an essential organic compound for life sciences research, identified by catalog number T66619 and CAS number 920519-31-9.

Z-Leu-Leu-Tyr-COCHO is a potent inhibitor of chymotrypsin-like activity, with a Ki value of 3.0 nM [1].

Z-Tyr(tBu)-OH.DCHA, an amino acid derivative, has a wide range of applications in life science-related research.

Cyclo-(Phe-Tyr) shows anticoagulant activities.

Fmoc-Tyr(tBu)-OH, with catalog number T67575 and CAS number 71989-38-3, is a valuable organic compound utilized in life sciences research.

Z-Tyr(Bzl)-OH, catalog number T65607 and CAS number 16677-29-5, is a valuable organic compound for life sciences research.

Z-Leu-Tyr-Chloromethylketone is a calpain inhibitor [1].

Fmoc-Tyr(tBu)-Ser(psi(Me,Me)pro)-OH is a dipeptide comprised of Fmoc-protected tyrosine and serine residues, with tBu (tert-butyl) protecting the tyrosine and a psi(Me,Me)pro modification on the serine.

Fmoc-Tyr(3-F, tBu)-OH is a cyclic peptide compound possessing high membrane permeability and exhibiting specific binding affinity towards a target molecule.

H-D-Tyr(tBu)-OH, catalog number T66723 and CAS number 186698-58-8, is a valuable organic compound for life sciences research.

H-Tyr-Phe-OH (L-Tyrosyl-L-phenylalanine) can be used as a biomarker to distinguish benign thyroid nodules (BTN) from thyroid cancer (TC). It is an orally active Angiotensin-converting enzyme inhibitor with a 48% inhibition rate at 50 μM. Additionally, H-Tyr-Phe-OH exhibits xanthine oxidase inhibitory activity (uric acid lowering) and regulates IL-8 production in neutrophil-like cells [1] [2] [3] [4].

Z-D-Tyr(tBu)-OH.DCHA, an amino acid derivative, has extensive applications in life science research.

Fmoc-D-Tyr(tBu)-OH, with catalog number T65705 and CAS number 118488-18-9, is a valuable organic compound for life sciences research.

Boc-Tyr(tBu)-OH (catalog number T64784, CAS number 47375-34-8) is a valuable organic compound for life sciences research.

Z-Phe-Ala-diazomethylketone directly binds to Aβ42 monomers and small oligomers, inhibiting Aβ42 dodecamer formation and preventing Aβ42 fibrillogenesis in solution. This compound holds potential for research into neurodegenerative disorders [1].

(Rac)-Z-Phe-Phe-FMK (Cathepsin L-IN-2) is a cathepsin L inhibitor that inhibits the tendency of β-amyloid to induce apoptotic changes .

Z-Phe-Leu-OH is a useful organic compound for research related to life sciences. The catalog number is T65512 and the CAS number is 4313-73-9.

Boc-D-Tyr(2-Br-Z)-OH, with catalog number T66218 and CAS number 81189-61-9, is a valuable organic compound for life sciences research.

Boc-Tyr(2-Br-Z)-OH is a useful organic compound for research related to life sciences. The catalog number is T67623 and the CAS number is 47689-67-8.

H-Tyr(tBu)-OH is a useful organic compound for research related to life sciences. The catalog number is T65411 and the CAS number is 18822-59-8.

Z-Tyr-OH is a useful organic compound for research related to life sciences. The catalog number is T67546 and the CAS number is 1164-16-5.

Z-D-Ser(TBu)-OH is an amino acid derivative with diverse applications in life science research.

Z-Phe-Phe-Diazomethylketone is a selective inhibitor of cathepsin L [1].

Z-Gly-Pro-Phe-Leu-CHO (Z-GPFL-CHO) is a tetrapeptide aldehyde that acts as a selective and potent proteasome inhibitor, with inhibition constants (Ki) of 1.5 µM for branched-chain amino acid-preferred, 2.3 µM for small neutral amino acid-preferred, and 40.5 µM for chymotrypsin-like activities, and an inhibitory concentration (IC50) of 3.1 µM for peptidyl-glutamyl peptide hydrolyzing activity [1].

N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA is a formyl peptide receptor (FPR) agonist.