Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Succinimidyl 4-(N-maleimidomethyl)cyclohexanecarboxylate | HCID 125175 | — |
| Edukt | Amphetamine thiol | HCID 23498394 | — |
| Edukt | Amphetamine ATP | HCID 86749546 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Potassium Carbonate | HCID 11430 | — |
| Produkt | Amphetamine | HCID 3007 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05525524 |
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| Quelldatensatz | uspto-grants-1996_06 |
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| ORD ID | ord-763baf9c6aec4270b6b858c31a580c6a |
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| Quellennotiz | uspto-grants-1996_06 |
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