CCRIS 9483 → HCID 178418840, compound

HRID 1358174Notes

Reaction equation

HRID 1358174 reaction equation
[CH3:1][C@@:2]1([OH:32])[C:17]2[CH:18]=[CH:19][CH:20]=[C:21]([OH:22])[C:16]=2[C:15]([OH:23])=[C:14]2[C@@H:3]1[CH2:4][C@@H:5]1[C@:11]([OH:24])([C:12]2=[O:13])[C:10]([OH:25])=[C:9]([C:26]([NH2:28])=[O:27])[C:7](=[O:8])[C@H:6]1[N:29]([CH3:31])[CH3:30]>O>[CH3:1][C@:2]1([OH:32])[C@@H:3]2[C:14](=[C:12]([OH:13])[C@:11]3([OH:24])[C:10](=[O:25])[C:9]([C:26]([NH2:28])=[O:27])=[C:7]([OH:8])[C@@H:6]([N:29]([CH3:31])[CH3:30])[C@@H:5]3[CH2:4]2)[C:15](=[O:23])[C:16]2[C:21]([OH:22])=[CH:20][CH:19]=[CH:18][C:17]1=2

Participants

3

Reactant 1

HCID 54675776CCRIS 9483

Product 1

HCID 178418840HCID 178418840, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

The second tetracycline labelling solution was prepared by dissolving 288 mg of tetracycline base (Sigma) in 40 ml of deionized water to yield a concentration of 7.2 mg of tetracycline per ml.

Workup

  1. customThe second tetracycline labelling solution was prepared

Sources & evidence

ORD record
ord-1ce952afe12a48dea29229afacae97e8
Source dataset
uspto-grants-2003_07
Patent number
US06596498B1

Reaction notes

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