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L-Phenylalanine → Phe-Gly

HRID 2296601
Notes
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Reaction equation

HRID 2296601 reaction equation
N[C@H](C(NCCC(O)=O)=O)CC1C=CC=CC=1.C1C=CC(C[C@H](N)C(N[C@H](C(N)=O)CC2C=CC=CC=2)=O)=CC=1.[NH2:41][C@H:42]([C:50]([NH:52][C@H:53]([C:58]([OH:60])=[O:59])CC(C)C)=[O:51])[CH2:43][C:44]1[CH:49]=[CH:48][CH:47]=[CH:46][CH:45]=1.C[C@H](NC([C@@H](N)CC1C=CC=CC=1)=O)C(O)=O.N[C@H](C(N[C@H](C(O)=O)CC(=O)O)=O)CC1C=CC=CC=1.N[C@H](C(O)=O)CC1C=CC=CC=1>>[CH:47]1[CH:46]=[CH:45][C:44]([CH2:43][C@H:42]([NH2:41])[C:50]([NH:52][CH2:53][C:58]([OH:60])=[O:59])=[O:51])=[CH:49][CH:48]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 6140L-PhenylalanineHCID 76808L-Phenylalanyl-L-leucine2×HCID 85169Phenylalanylphenylalanylamide2×HCID 5488196L-Phenylalanyl-L-alanine2×HCID 6992643Phe-Asp2×HCID 7009621PHE-beta-ALA2×

Product 1

HCID 6992304Phe-Gly

Procedure

Phe-β-Ala (compound 12); Phe-Phe (compound 13); Phe-Leu (compound 14); Phe-Ala (compound 15); and Phe-Asp (compound 16): Phe-Tau (compound 17).

Sources & evidence

ORD record
ord-455fc334c073407e8e592d815e597866
Source dataset
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06489291B1

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes