FB2024_03 , released June 25, 2024
Chemical: N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal
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General Information
Name
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal
FlyBase ID
FBch0000905
ChEBI Name
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal
ChEBI ID
PubChem Name
Z-Leu-leu-leu-al
PubChem ID
462382 (PubChem link: Z-Leu-leu-leu-al)
Chemical Structure
Chemical structure of N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal
N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal
InChIKey

TZYWCYJVHRLUCT-VABKMULXSA-N

Definition (ChEBI)

ChEBI: N-benzyloxycarbonyl-L-leucyl-L-leucyl-L-leucinal is a tripeptide that is L-leucyl-L-leucyl-L-leucine in which the C-terminal carboxy group has been reduced to the corresponding aldehyde and the N-terminal amino group is protected as its benzyloxycarbonyl derivative. It has a role as a proteasome inhibitor. It is a tripeptide, an amino aldehyde and a carbamate ester.

Roles Classification (ChEBI)
Comment
Synonyms and Secondary IDs (41)
Synonyms
(S)-N-((phenylmethoxy)carbonyl)-L-leucyl-N-(1-formyl-3-methylbutyl)-L-leucinamide
133407-82-6
Cbz-L-Leu-L-Leu-L-Leu-CHO
Cbz-L-Leu-L-Leu-L-Leu-H
Cbz-Leu-Leu-Leu-CHO
Cbz-Leu-Leu-Leu-H
Cbz-Leu-Leu-Leucinal
PubChem:462382
Z-LLL-H
Z-LLLal
Z-Leu-Leu-Leu-CHO
Z-Leu-Leu-Leu-H
Z-Leu-Leu-Leu-al
Z-Leu-Leu-Leucinal
Z-Leu-leu-leu-al
Z-Leu-leu-leucinal
ZLLL-CHO
ZLLLal
Zlll-cho
benzyloxycarbonyl-leu-leu-leu-aldehyde
benzyloxycarbonyl-leucyl-leucyl-leucinal
benzyloxycarbonylleucyl-leucyl-leucine aldehyde
carbobenzoxy-Leu-Leu-leucinal
carbobenzoxy-leucyl-leucyl-leucinal
carbobenzoxyl-leucinyl-leucinyl-leucinal-H
pubchem:462382
z-leu-leu-leu-al
z-leu-leu-leu-h
z-leu-leu-leucinal
z-lll-cho
zlll-cho
Secondary FlyBase IDs
    References (22)