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Ampicillin → (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal

HRID 10126
Notes
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Reaction equation

HRID 10126 reaction equation
C[C@]1(O)[C@@H]2C(=[C:12]([OH:30])[C@:13]3([OH:29])[C:20](=[O:21])[C:19](C(N)=O)=[C:18]([OH:25])[C@@H:17](N(C)C)[C@@H]3C2)C(=O)C2C(O)=CC=CC1=2.CC1(C)S[C@@H]2[C@H](NC([C@H](N)C3C=CC=CC=3)=O)C(=[O:41])N2[C@H]1C(O)=O>>[O:30]=[CH:12][C@@H:13]([C@@H:20]([C@H:19]([C@H:18]([CH3:17])[OH:25])[OH:41])[OH:21])[OH:29]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6249AmpicillinHCID 178418840HCID 178418840, compound

Product 1

HCID 19233(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal

Procedure

The plasmid pBRsacH3 (Example 1) was used for cloning the rMET1 antibody (Example 9). In this case, the kappa and heavy chains were engineered with human ceruloplasmin and human neutrophil defensin signal sequences, respectively (Example 9). This plasmid was electroporated into E. coli strain DH10B rha+ to generate clone rMET1.LS.1, which was cultured under 10 μg/mL tetracycline selection. The plasmid was also electroporated into E. coli strain ECL339 rha− to generate clone rMET1.ECL.1 which was cultured under 100 μg/mL ampicillin selection.

Sources & evidence

ORD record
ord-fbe48744c0294939ba6d1cf3cf9c9148
Source dataset
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07094579B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes