Hydrochloric Acid → Amphetamine

HRID 260225

反応式

HRID 260225 の反応式
[NH2:1][CH:2]([CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[CH3:3].P(OC[C@H]1O[C@@H](N2C3N=CN=C(N)C=3N=C2)[C@H](O)[C@@H]1O)(OP(OP(O)(O)=O)(O)=O)(=O)O.N(S)C(CC1C=CC=CC=1)C.C1C(CN2C(=O)C=CC2=O)CCC(C(ON2C(=O)CCC2=O)=O)C1.Cl>C(=O)([O-])[O-].[K+].[K+].CO>[NH2:1][CH:2]([CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[CH3:3]

参加物

7

実験手順

Amphetamine-ATP (0.095 g, 3×10-4 mol, Example 12) was dissolved in 50 ml of 0.12M potassium carbonate in 80% methanol/20% water. After 5 min at room temperature the thiol concentration was determined by reaction with DTNB to be 25 mM. The amphetamine thiol (7.6 ml, 1.9×10-4 mol) was added with stirring to 20.3 ml (0.4 g, 5.9×10-6 mol) of SMCC-BSA, 10/1. The pH of the solution was adjusted to 7 with 1N hydrochloric acid. The container was purged with argon and the solution was stirred at room temperature for 2 hr. The conjugate solution was then dialyzed with a PYROSTART ultrafiltration module against 10 mM morpholineethanesulfonic acid, pH 5.77 and 110 ml of 3.57 mg/ml BSA-amphetamine was collected. The protein solution was frozen at -70° C.

後処理

  1. concentrationAfter 5 min at room temperature the thiol concentration
  2. customwas determined by reaction with DTNB
  3. customThe container was purged with argon
  4. filtrationThe conjugate solution was then dialyzed with a PYROSTART ultrafiltration module against 10 mM morpholineethanesulfonic acid, pH 5.77 and 110 ml of 3.57 mg/ml BSA-amphetamine
  5. customwas collected
  6. temperatureThe protein solution was frozen at -70° C.

出典と根拠

ORDレコード
ord-763baf9c6aec4270b6b858c31a580c6a
出典データセット
uspto-grants-1996_06
特許番号
US05525524

関連ノート

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