참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 1-Cyclohexyl-3-(2-morpholinoethyl)carbodiimide | HCID 84998 | — |
| 반응물 | Biotin | HCID 171548 | — |
| 반응물 | Nicotinamide-6(2-aminoethylamino)purine dinucleotide | HCID 191523 | — |
| 촉매 | Sodium Hydroxide | HCID 14798 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Nicotinamide adenine dinucleotide biotin | HCID 131711938 | — |
반응 단계
A 16 mg quantity of biotin was suspended in 1 ml of water containing 22 mg of nicotinamide 6-(2-aminoethylamino)purine dinucleotide prepared as in Example 1. A few drops of 0.1N sodium hydroxide was added to aid dissolution of the biotin. A 240 mg quantity of 1-cyclohexyl-3-(2-morpholinoethyl)-carbodiimide metho-p-tolulene sulfonate was added to the resulting solution and brought into solution by dropwise addition of 0.1N hydrochloric acid. The reaction mixture was allowed to incubate at room temperature for 5 hours and was then poured into 10 ml of acetone at -10° C. The oil which formed was separated, washed twice with from 5 to 10 ml of ether and dissolved in from 1 to 2 ml of water. The resulting material was purified by electrophoresis on paper as in Example 1. Two fluorescent bands appeared after spraying with sodium cyanide, one having migrated toward the cathode and the other toward the anode. The latter band, which contained the NAD-biotin conjugate, was eluted with water and stored at -20° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04791055 |
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| 출처 데이터셋 | uspto-grants-1988_12 |
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| ORD ID | ord-8289a0765432432a886ef8a7ed271183 |
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| 출처 메모 | uspto-grants-1988_12 |
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