Glycine → HCID 178418600, compound
Reaction equation
[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[CH2:3][C:4](=O)O.[NH2:10][C@H:11](C(O)=O)CCC(=O)O.[NH2:20][CH2:21]C(O)=O.[NH2:25][C@H](C(O)=O)C.N[C@H](C(O)=O)CS.N[C@H](C(O)=O)[C@H](CC)C.N[C@H](C(O)=O)CC(C)C.N[C@H](C(O)=O)CCCC.N[C@H](C(O)=O)CC1C=CC(O)=CC=1.N[C@H](C(O)=O)CC1C=CC=CC=1>>[NH2:1][C@H:2]([C:7]([OH:9])=[O:8])[CH2:3][CH2:4][CH2:21][NH:20][C:11](=[NH:10])[NH2:25]Participants
11
Procedure
1.02 ×2, Asp: 1.00 ×2, Ser: 0.89 ×5, Glu: 0.98, Gly: 0.99 ×5, Ala: 1.00, Cys: 0.76 ×2, Ile: 0.90, Leu: 1.00 ×2, Nle: 0.90, Tyr: 0.86, Phe: 0.98 ×2
Sources & evidence
- ORD record
- ord-c4b498dbc7b346d48e7dec0e5ae3e743
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04670540
Reaction notes
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