Search Result
Results for "
CBZ
" in MedChemExpress (MCE) Product Catalog:
5
Biochemical Assay Reagents
7
Isotope-Labeled Compounds
Cat. No. |
Product Name |
Target |
Research Areas |
Chemical Structure |
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- HY-B0246
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- HY-136626
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CBZ-Ala-Ala-Asn-AMC
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Fluorescent Dye
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Cancer
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Z-Ala-Ala-Asn-AMC (Cbz-Ala-Ala-Asn-AMC) is the legumain substrate. Overexpressed legumain in 293 HEK-Leg cells potently cleaved CBZ-Ala-Ala-Asn-AMC .
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- HY-W103577
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CBZ-cycloleucine
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Biochemical Assay Reagents
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Others
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1-(Cbz-amino)cyclopentanecarboxylic acid (Cbz-cycloleucine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-W013905
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- HY-P10198
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- HY-160255
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CBZ-cysteine
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Beta-lactamase
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Infection
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N-Cbz-L-Cysteine (Cbz-cysteine) (compound 5) is a potent β-lactamase II inhibitor with a Ki value of 97 µM .
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- HY-160255A
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CBZ-D-Cys
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Beta-lactamase
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Infection
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N-Cbz-D-Cysteine (Cbz-D-Cys) (compound 5) is a potent β-lactamase II inhibitor with a Ki value of 20.1 µM .
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- HY-78897
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- HY-I1061
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- HY-126375R
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Benzyloxycarbonyl valacyclovir (Standard)
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Drug Intermediate
Reference Standards
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Infection
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Cbz-Valaciclovir (Standard) is the analytical standard of Cbz-Valaciclovir. This product is intended for research and analytical applications. Cbz-Valaciclovir (Benzyloxycarbonyl valacyclovir) can be used to prepare Valaciclovir (HY-17425) and for antiviral research .
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- HY-P5027
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- HY-W009503
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- HY-150242A
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Liposome
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Others
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Cbz-Ala-Ala-Asn TFA is a peptide that designed based on the sequence of the substrate of legumain. Legumain is a cysteine protease. Cbz-Ala-Ala-Asn TFA can be applied as a scaffold for drug delivery .
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- HY-400312
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- HY-114267
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mTOR
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Others
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Cbz-B3A is a potent and selective inhibitor of mTORC1 signaling that appear to bind to ubiquilins 1, 2, and 4, and Cbz-B3A inhibits the phosphorylation of eIF4E-binding protein 1 (4EBP1).
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- HY-172292
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Biochemical Assay Reagents
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Others
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Cbz-GGFG-Bn is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-W009121
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- HY-126375
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Benzyloxycarbonyl valacyclovir
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Drug Intermediate
HSV
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Infection
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Cbz-Valaciclovir (Benzyloxycarbonyl valacyclovir) can be used to prepare Valaciclovir (HY-17425) and for antiviral research .
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- HY-W011197
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- HY-44312
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Biochemical Assay Reagents
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Others
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Cbz-TRIS tri-acid is a small molecule compound containing several functional groups, including a carbamate group, a tris group, and three carboxylic acid groups.
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- HY-140490
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PROTAC Linkers
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Cancer
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Cbz-N-PEG10-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-143832
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PROTAC Linkers
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Cancer
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Cbz-PEG5-Br is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-W190968
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PROTAC Linkers
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Cancer
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Cbz-PEG2-bromide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140443
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PROTAC Linkers
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Cancer
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Cbz-aminooxy-PEG8-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-W095029
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Biochemical Assay Reagents
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Others
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Cbz-Gly-Pro-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-W011750
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- HY-159617
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PROTAC Linkers
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Cancer
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Cbz-Pip-2C-Pip-C-Pip is a PROTAC linker. Cbz-Pip-2C-Pip-C-Pip can be used for synthesis PROTAC Cbl-b-IN-1 (HY-159608) .
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- HY-163382
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Beta-lactamase
Cholinesterase (ChE)
Amyloid-β
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Neurological Disease
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Cbz-Gly-Pro-Ala-O-cinnamyl (compound 25) is a small peptide targeting BACE-1 and AChE with the IC50 values of 0.02 μM and 1 μM, respectively. Cbz-Gly-Pro-Ala-O-cinnamyl shows neuroprotective effect and can be used for study of Alzheimer’s disease .
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- HY-140491
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PROTAC Linkers
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Cancer
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Cbz-N-amido-PEG20-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140238
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PROTAC Linkers
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Cancer
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Cbz-N-PEG15-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140444
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PROTAC Linkers
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Cancer
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Cbz-aminooxy-PEG8-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-129352
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ADC Linker
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Cancer
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Cbz-Phe-(Alloc)Lys-PAB-PNP is an cleavable linker for antibody-drug conjugates (ADC) design.
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- HY-W009033
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- HY-172790
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COX
Lipoxygenase
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Inflammation/Immunology
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Cbz-(S,S)-Pro-Pro-allyl (compound 1a) is a dual inhibitor of cyclooxygenase-2 and 5-lipoxygenase with IC50 values of 0.146 nM, 0.003 nM, 0.64 nM for COX-1, COX-2, 5-LOX, respectively. Cbz-(S,S)-Pro-Pro-allyl has anti-inflammatory activity .
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- HY-47812
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- HY-133358
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG12-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140489
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG5-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-W019796
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG4-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-133359
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG24-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140488
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG3-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-133360
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG36-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-130192
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG8-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-130443
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG6-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-140487
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG2-C2-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135923
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG2-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135942
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG8-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135925
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG1-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135919
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG5-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-133357
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG10-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135913
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG3-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-135926
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PROTAC Linkers
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Cancer
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Cbz-NH-PEG1-CH2CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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- HY-B0246S
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- HY-129126
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CBZ-Lys(Acr)-PEG2-dansyl
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Glutaminase
Microtubule/Tubulin
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Others
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NC9 (Cbz-Lys(Acr)-PEG2-dansyl) is an irreversible transglutaminase (TG) inhibitor. NC9 inhibits osteoblast differentiation and mineralization. NC9 destabilizes microtubules. NC9 can be used for the research of osteoblast differentiation .
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- HY-B0246S3
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- HY-B0246S4
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- HY-B0246R
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CBZ (Standard); NSC 169864 (Standard)
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Reference Standards
Sodium Channel
Autophagy
Mitophagy
Potassium Channel
Calcium Channel
HDAC
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Neurological Disease
Cancer
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Carbamazepine (Standard) is the analytical standard of Carbamazepine. This product is intended for research and analytical applications. Carbamazepine is an orally active pressure-sensitive sodium ion channel blocker with an IC50 of 131 μM. Carbamazepine blocks voltage gated Na +, Ca 2+, and K + channels, and is also a HDAC inhibitor (IC50: 2 μM). Carbamazepine is an anticonvulsant and can be used for research of epilepsy and neuropathic pain .
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- HY-B0246S2
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- HY-B0246S1
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- HY-W348348
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Biochemical Assay Reagents
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Others
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CbzNH-PEG3-CH2CH2NH2 is a PEG linker containing an amine group and a benzyl (Cbz) protecting group. The hydrophilic PEG spacer increases the water solubility of a compound in aqueous media. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde), etc. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
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- HY-W403327
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Biochemical Assay Reagents
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Others
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CbzNH-PEG4-CH2COOH is a PEG linker containing an carboxylic acid (CO2H) group and a benzyl (Cbz) protecting group. The hydrophilic PEG spacer increases the water solubility of a compound in aqueous media. The terminal carboxylic acid is reactive with primary amine groups in the presence of activators (e.g. HATU) forming a stable amide bond. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
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- HY-W653882
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- HY-P1759
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Z-FR-AMC
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Cathepsin
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Others
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N-CBZ-Phe-Arg-AMC (Z-FR-AMC) is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
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- HY-P1759A
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Z-FR-AMC hydrochloride
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Biochemical Assay Reagents
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Others
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N-CBZ-Phe-Arg-AMC (Z-FR-AMC) hydrochloride is a tissue protease substrate that can be used to assess the activity of lysosomal tissue proteases .
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- HY-77475
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ADC Linker
PROTAC Linkers
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Cancer
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1-Cbz-3-Hydroxyazetidine is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). 1-Cbz-3-Hydroxyazetidine is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs.
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- HY-147354
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LYTACs
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Cardiovascular Disease
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TriGalNAc CBz is a GalNAc derivative and tri-GalNAc is an asialoglycoprotein receptor (ASGPR) ligand. TriGalNAc CBz can be used for mRNA drug delivery as well as lysosomal targeted chimerism (LYTAC) studies .
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- HY-173261
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Biochemical Assay Reagents
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Others
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Tri-GalNAc(OAc)3-Cbz is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-46346
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PROTAC Linkers
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Cancer
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Fmoc-Gly-NH-CH2-O-CH2-Cbz is a PROTAC linker and a maleimide-GGFG peptide linker. Fmoc-Gly-NH-CH2-O-CH2-Cbz can be used in the synthesis of the Deruxtecan .
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- HY-W016042
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N-CBZ-Hydroxy-L-Proline
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Biochemical Assay Reagents
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Others
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N-Cbz-hydroxy-L-proline is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-W402032
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Biochemical Assay Reagents
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Others
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Bis-Cbz-cyclen is a bifunctional chelator. Bifunctional chelating agents are used to stably link the radiometal to the carrier moiety of the radiopharmaceutical .
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- HY-Y0588
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L-CBZ-Proline
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MMP
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Others
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Carbobenzoxyproline (L-Cbz-Proline) is an inhibitor of prolidase. Carbobenzoxyproline can be used for prolidase deficiency (PD) research .
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- HY-45669
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PROTAC Linkers
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Cancer
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Fmoc-Gly-Gly-Phe-Gly-CH2-O-CH2-Cbz is a PROTAC linker and a maleimide-GGFG peptide linker. Fmoc-Gly-Gly-Phe-Gly-CH2-O-CH2-Cbz can be used in the synthesis of the Deruxtecan .
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- HY-48321
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ADC Linker
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Cancer
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N-Cbz-glycyl-glycyl-D-phenylalanine is a cleavable ADC linker.
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- HY-76317
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N-CBZ-DL-proline; DL-CBZ-Proline
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Amino Acid Derivatives
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Others
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Z-DL-Pro-OH (N-Cbz-DL-proline) is a proline derivative, can be used for the synthesis of agents or other compounds .
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- HY-W904851
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PROTAC Linkers
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Cancer
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Boc-Piperidine-piperazine-Cbz is a PROTAC linker that can be used in the synthesis of ZLC491 (HY-168162) .
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- HY-W160298
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Biochemical Assay Reagents
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Others
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N-Cbz-7-Aminoheptanoic acid is a six carbon linker containing an carboxylic acid (CO2H) group and a benzyl (Cbz) protecting group. The terminal carboxylic acid is reactive with primary amine groups in the presence of activators (e.g. EDC, or HATU) forming a stable amide bond. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
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- HY-W004868
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ADC Linker
PROTAC Linkers
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Cancer
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1-Cbz-azetidine-3-carboxylic acid is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). 1-Cbz-azetidine-3-carboxylic acid is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1]
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- HY-116011
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Drug Intermediate
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Cancer
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N,N'-bis-Cbz-β-Alethine is an active ester used in the synthesis of β-alethine, which induces cell differentiation and has potential anti-tumor applications. β-Alethine is synthesized by removing the carbobenzoxy (CBZ) groups with hydrogen bromide in glacial acetic acid.
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- HY-49453
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PROTAC Linkers
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Cancer
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Fmoc-Gly-Gly-(D-Phe)-Gly-CH2-O-CH2-Cbz is a PROTAC linker and a maleimide-GGFG peptide linker. Fmoc-Gly-Gly-(D-Phe)-Gly-CH2-O-CH2-Cbz can be used in the synthesis of the Deruxtecan .
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- HY-W019226
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ADC Linker
PROTAC Linkers
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Cancer
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Methyl 1-Cbz-azetidine-3-carboxylate is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Methyl 1-Cbz-azetidine-3-carboxylate is also a alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs[1
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- HY-W097167
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- HY-168197
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PROTACs
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Cancer
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Thalidomide-F-piperidine-piperazine-Cbz Conjugate 110 is a conjugate of E3 ligase and linker for the synthesis of CDK12/13 PROTAC degrader (HY-168162) .
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- HY-156810
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ADC Linker
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Cancer
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Fmoc-PEG4-GGFG-CH2-O-CH2-Cbz is a cleavable ADC linker containing 4 units of PEG, which can be used to synthesize active antibody conjugation molecules (ADC) .
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- HY-400676
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ADC Linker
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Cancer
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NH2-PEG4-GGFG-CH2-O-CH2-Cbz is a reactant for the synthesis of ADC linker and is used to synthesize Antibody-Drug Conjugates (ADCs) .
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- HY-75332
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D-CBZ phenylglycine
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Amino Acid Derivatives
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Others
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Z-D-Phg-OH (D-Cbz phenylglycine) is a N-blocked amino acids with Kd values of 390 μM and 323 μM for tBuCQN and tBuCQD, respectively .
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- HY-W097106
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Drug Isomer
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Neurological Disease
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(S)-3-N-Cbz-Amino-succinimide (Compound 1d) is an antiepileptic agent that can inhibit pentylenetetrazole (PTZ) and maximal electroshock (MES)-induced tonic convulsions in mice .
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- HY-141148
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Drug-Linker Conjugates for ADC
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Cancer
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7-O-(Cbz-N-amido-PEG4)-paclitaxel is a PEG-class Drug-linker conjugates for ADC, containing a paclitaxel moiety and a amino group. The amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. 7-O-(Cbz-N-amido-PEG4)-paclitaxel can be used in the synthesis of Antibody-Drug Conjugates (ADCs) .
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- HY-32685
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- HY-156896
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Drug-Linker Conjugates for ADC
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Cancer
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Val-Cit-amide-Cbz-N(Me)-Maytansine is an antibody and bispecific antigen-binding mol. that bind hepatocyte growth factor receptor c-Met (MET) or antibody-drug conjugates (ADCs) .
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- HY-P1759B
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Z-FR-AMC TFA
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Cathepsin
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Others
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N-CBZ-Phe-Arg-AMC (Z-FR-AMC) TFA is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
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- HY-W777099
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- HY-49463
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ADC Linker
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Neurological Disease
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Fmoc-Gly-Gly-Phe-Gly-CH2-O-CH2-Gly-CH2-O-CH2-Cbz is an ADC linker that can be used in the synthesis of ADCs (such as Trastuzumab deruxtecan and U3-1402).
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- HY-W011092
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Nα-Boc-Nδ-CBZ-L-ornithine
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Biochemical Assay Reagents
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Others
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Boc-Orn(Z)-OH (Nα-Boc-Nδ-Cbz-L-ornithine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research .
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- HY-W011024
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Biochemical Assay Reagents
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Others
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(2R,3S)-N-Cbz-6-oxo-2,3-diphenylmorpholine is a chiral building block, which can be used in the stereoselective synthesis of fluorescent and non-fluorescent amino acids .
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- HY-P1010
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Caspase
Apoptosis
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Neurological Disease
Cancer
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Z-LEHD-FMK is a selective and irreversible inhibitor of caspase-9, protects against lethal reperfusion injury and attenuates apoptosis. Z-LEHD-FMK exhibits the neuroprotective effect in a rat model of spinal cord trauma .
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- HY-P2269
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Drug Derivative
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Cancer
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MAIT-203, a cyclopentyalanin-derived peptidomimetic, potently inhibits the interaction of adenomatous polyposis coli (APC) and Asef (RhoGEF4), but not APC-Sam68 or APC-striatin interactions. MAIT-203 binds APC-ARM with a Ki of 0.015 μM and a Kd of 0.036 μM. MAIT-203 significantly represses the migration and invasion of colorectal cancer cells.
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- HY-P2269A
-
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Drug Derivative
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Cancer
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MAIT-203 acetate is a cyclopentyalanin-derived peptidomimetic, potently inhibits the interaction of adenomatous polyposis coli (APC) and Asef (RhoGEF4), but not APC-Sam68 or APC-striatin interactions. MAIT-203 acetate binds APC-ARM with a Ki value of 0.015 μM and aKd value of 0.036 μM. MAIT-203 acetate significantly represses the migration and invasion of colorectal cancer cells .
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- HY-151468
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Fluorescent Dye
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Others
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AIECbz-LD-C7 is an aggregation-induced emission (AIE) probe based on the conjugation of quinoline-malononitrile (QM) and carbazole. AIECbz-LD-C7 has excellent LD-specificity. AIECbz-LD-C7 can be used for tracking the dynamic changes of LDs and studying the association between LDs and lysosome/endoplasmic reticulum (ER) .
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- HY-W003991
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- HY-W800833
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Biochemical Assay Reagents
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Others
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Benzyl N-[2-(prop-2-enamido)ethyl]carbamate is a short aliphatic linker featuring a Cbz-protected amine and an acrylamide. Acrylamide is a Michael acceptor which is a good Michael acceptor which can be used in thiol-based bioconjugation or polymerization. Meanwhile, the Cbz protecting group can be removed using Pd-C hydrogenation to reveal a free amine that can participate in a wide variety of reactions such as couplings or reductive amination.
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-
- HY-W008753
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N-CBZ-L-valine
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Biochemical Assay Reagents
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Others
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Z-L-Val-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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-
- HY-W060779
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-
- HY-W591969
-
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Biochemical Assay Reagents
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Others
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Benzyl (6-oxohexyl)carbamate is a linker containing an aldehyde group and a benzyl (Cbz) protecting group. The aldehyde can react with hydrazine or hydrazide to form a hydrolytic acyl hydrozone linkage. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
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- HY-W451433
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Biochemical Assay Reagents
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Others
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OTs-PEG1-NHCbz is a PEG linker containing a tosyl group and benzyl (Cbz) protecting group. The hydrophilic PEG spacer increases the water solubility of the compound in aqueous media. The tosyl group is a very good leaving group for nucleophilic substitution reactions. The benzyl protecting group can be removed via hydrogenolysis to form a free amine.
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-
- HY-159608
-
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PROTACs
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Cancer
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PROTAC Cbl-b-IN-1 (compound 64) is a PROTAC targeting Cbl-b. PROTAC Cbl-b-IN-1 is composed of PROTAC target protein ligand Cbl-b-IN-21 (HY-159615), PROTAC Linker Cbz-Pip-2C-Pip-C-Pip (HY-159617) and E3 ubiquitin ligase ligand (3S) Lenalidomide-5-Br (HY-W797329), where the E3 ubiquitin ligase ligand + Linker conjugate is (3S) Lenalidomide-5-Pip-C-Pip-2C-Pip (HY-159618) [1] .
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- HY-P3106
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(Z-Ala-Ala-Ala-Ala)2Rhodamine110; bis-CBZ-L-alanyl-L-arginine amide Rhodamine 110
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Fluorescent Dye
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Others
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(Z-Ala-Ala-Ala-Ala)2Rh110 is a sensitive fluorogenic elastase substrate. The colorless and nonfluorescent (Z-Ala-Ala-Ala-Ala)2Rh110 is selectively cleaved by elastase to yield the highly fluorescent compound rhodamine 110, which can be analyzed with an excitation wavelength of 485 nm and emission wavelength of 525 nm.
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Cat. No. |
Product Name |
Type |
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- HY-W016042
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N-CBZ-Hydroxy-L-Proline
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Biochemical Assay Reagents
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N-Cbz-hydroxy-L-proline is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-32685
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Cell Assay Reagents
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N-Cbz-1,2,3,6-tetrahydropyridine-4-boronic acid pinacol ester is a biochemical reagent.
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-
- HY-W008753
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N-CBZ-L-valine
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Biochemical Assay Reagents
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Z-L-Val-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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- HY-P1759A
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Z-FR-AMC hydrochloride
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Cell Assay Reagents
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N-CBZ-Phe-Arg-AMC (Z-FR-AMC) hydrochloride is a tissue protease substrate that can be used to assess the activity of lysosomal tissue proteases .
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- HY-W402032
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Chelators
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Bis-Cbz-cyclen is a bifunctional chelator. Bifunctional chelating agents are used to stably link the radiometal to the carrier moiety of the radiopharmaceutical .
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Cat. No. |
Product Name |
Target |
Research Area |
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- HY-136626
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CBZ-Ala-Ala-Asn-AMC
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Fluorescent Dye
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Cancer
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Z-Ala-Ala-Asn-AMC (Cbz-Ala-Ala-Asn-AMC) is the legumain substrate. Overexpressed legumain in 293 HEK-Leg cells potently cleaved CBZ-Ala-Ala-Asn-AMC .
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- HY-W013905
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- HY-P10213
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- HY-P10198
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- HY-78897
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-
- HY-I1061
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-
- HY-P5027
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-
- HY-W009503
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-
- HY-400312
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-
- HY-P5040
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-
- HY-W011750
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-
- HY-P5008
-
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Peptides
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Others
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Cbz-Asn-Gly-OH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
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- HY-P5042
-
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Peptides
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Others
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Cbz-Tyr-Ala-OH is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
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- HY-P5024
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NSC 333754
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Peptides
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Others
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Cbz-Ile-Pro-OH (NSC 333754) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
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- HY-P5012
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NSC 186902
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Peptides
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Others
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Cbz-Glu-Gly-OH (NSC 186902) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
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- HY-134113
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CBZ-Chromozym TH
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Peptides
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Others
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Z-Gly-Pro-Arg-pNA (z-GPR-pNA) is a photometric substrate in Prostate-Specific Antigen (PSA) activation protease assays. Z-Gly-Pro-Arg-pNA (z-GPR-pNA) can be used for the test of trypsin activity .
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-
- HY-P1759
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Z-FR-AMC
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Cathepsin
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Others
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N-CBZ-Phe-Arg-AMC (Z-FR-AMC) is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
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-
- HY-76317
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N-CBZ-DL-proline; DL-CBZ-Proline
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Amino Acid Derivatives
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Others
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Z-DL-Pro-OH (N-Cbz-DL-proline) is a proline derivative, can be used for the synthesis of agents or other compounds .
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-
- HY-75332
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D-CBZ phenylglycine
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Amino Acid Derivatives
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Others
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Z-D-Phg-OH (D-Cbz phenylglycine) is a N-blocked amino acids with Kd values of 390 μM and 323 μM for tBuCQN and tBuCQD, respectively .
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-
- HY-P1759B
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Z-FR-AMC TFA
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Cathepsin
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Others
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N-CBZ-Phe-Arg-AMC (Z-FR-AMC) TFA is a cathepsin substrate used in assessment activity of lysosomal cathepsin enzymes .
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-
- HY-P1010
-
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Caspase
Apoptosis
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Neurological Disease
Cancer
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Z-LEHD-FMK is a selective and irreversible inhibitor of caspase-9, protects against lethal reperfusion injury and attenuates apoptosis. Z-LEHD-FMK exhibits the neuroprotective effect in a rat model of spinal cord trauma .
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-
- HY-P2269
-
|
Drug Derivative
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Cancer
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MAIT-203, a cyclopentyalanin-derived peptidomimetic, potently inhibits the interaction of adenomatous polyposis coli (APC) and Asef (RhoGEF4), but not APC-Sam68 or APC-striatin interactions. MAIT-203 binds APC-ARM with a Ki of 0.015 μM and a Kd of 0.036 μM. MAIT-203 significantly represses the migration and invasion of colorectal cancer cells.
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-
- HY-P2269A
-
|
Drug Derivative
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Cancer
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MAIT-203 acetate is a cyclopentyalanin-derived peptidomimetic, potently inhibits the interaction of adenomatous polyposis coli (APC) and Asef (RhoGEF4), but not APC-Sam68 or APC-striatin interactions. MAIT-203 acetate binds APC-ARM with a Ki value of 0.015 μM and aKd value of 0.036 μM. MAIT-203 acetate significantly represses the migration and invasion of colorectal cancer cells .
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-
- HY-W003991
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-
- HY-W060779
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-
- HY-P3106
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(Z-Ala-Ala-Ala-Ala)2Rhodamine110; bis-CBZ-L-alanyl-L-arginine amide Rhodamine 110
|
Fluorescent Dye
|
Others
|
(Z-Ala-Ala-Ala-Ala)2Rh110 is a sensitive fluorogenic elastase substrate. The colorless and nonfluorescent (Z-Ala-Ala-Ala-Ala)2Rh110 is selectively cleaved by elastase to yield the highly fluorescent compound rhodamine 110, which can be analyzed with an excitation wavelength of 485 nm and emission wavelength of 525 nm.
|
Cat. No. |
Product Name |
Chemical Structure |
-
- HY-B0246S
-
|
Carbamazepine-d10 is the deuterium labeled Carbamazepine. Carbamazepine (CBZ), a sodium channel blocker, is an anticonvulsant agent .
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-
-
- HY-B0246S2
-
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Carbamazepine-d8 is the deuterium labeled Carbamazepine. Carbamazepine, a sodium channel blocker, is an anticonvulsant agent, with an IC50 of 131 μM .
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-
-
- HY-W653882
-
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Carbamazepine-d2,15N is a deuterated labeled Carbamazepine-d2,15N .
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-
-
- HY-B0246S3
-
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Carbamazepine-(Ph)d8 (CBZ-(Ph)d8; NSC 169864-(Ph)d8) is the deuterium labeled Carbamazepine-(Ph) (HY-B0246) .
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-
-
- HY-B0246S4
-
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Carbamazepine-d4 (CBZ-d4; NSC 169864-d4) is the deuterium labeled Carbamazepine-d4 (HY-B0246S4) .
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-
-
- HY-B0246S1
-
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Carbamazepine-d2 is the deuterium labeled Carbamazepine. Carbamazepine, a sodium channel blocker, is an anticonvulsant agent.
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-
-
- HY-W777099
-
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N-Cbz-O-Bzl-L-Glu-S-Bzl-L-Cys-Gly[ 13C2, 15N]-OBzl is the 13C- and 15N-labeled N-Cbz-O-Bzl-L-Glu-S-Bzl-L-Cys-Gly-OBzl.
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-
Cat. No. |
Product Name |
|
Classification |
-
- HY-173261
-
|
|
Azide
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Tri-GalNAc(OAc)3-Cbz is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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-
- HY-159608
-
|
|
Azide
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PROTAC Cbl-b-IN-1 (compound 64) is a PROTAC targeting Cbl-b. PROTAC Cbl-b-IN-1 is composed of PROTAC target protein ligand Cbl-b-IN-21 (HY-159615), PROTAC Linker Cbz-Pip-2C-Pip-C-Pip (HY-159617) and E3 ubiquitin ligase ligand (3S) Lenalidomide-5-Br (HY-W797329), where the E3 ubiquitin ligase ligand + Linker conjugate is (3S) Lenalidomide-5-Pip-C-Pip-2C-Pip (HY-159618) [1] .
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