JP2019514687A5 - - Google Patents

Info

Publication number

JP2019514687A5

JP2019514687A5 JP2019508155A JP2019508155A JP2019514687A5 JP 2019514687 A5 JP2019514687 A5 JP 2019514687A5 JP 2019508155 A JP2019508155 A JP 2019508155A JP 2019508155 A JP2019508155 A JP 2019508155A JP 2019514687 A5 JP2019514687 A5 JP 2019514687A5

Authority

JP

Japan

Prior art keywords

charged

group

charge

block

static charge

Prior art date

2017-04-26

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Granted

Links

• Espacenet
• Global Dossier
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• 239000000463 material Substances 0.000 claims 23
• 230000003068 static effect Effects 0.000 claims 8
• 125000000524 functional group Chemical group 0.000 claims 6
• 238000000034 method Methods 0.000 claims 5
• 125000003342 alkenyl group Chemical group 0.000 claims 3
• 125000000217 alkyl group Chemical group 0.000 claims 3
• 239000002861 polymer material Substances 0.000 claims 3
• 239000002202 Polyethylene glycol Substances 0.000 claims 2
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
• 125000003118 aryl group Chemical group 0.000 claims 2
• 239000003795 chemical substances by application Substances 0.000 claims 2
• 150000001875 compounds Chemical class 0.000 claims 2
• -1 diethylaminoethyl group Chemical group 0.000 claims 2
• 125000005842 heteroatom Chemical group 0.000 claims 2
• 239000000203 mixture Substances 0.000 claims 2
• 229920001223 polyethylene glycol Polymers 0.000 claims 2
• 239000011148 porous material Substances 0.000 claims 2
• 239000000126 substance Substances 0.000 claims 2
• PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 claims 1
• 125000003277 amino group Chemical group 0.000 claims 1
• 125000004122 cyclic group Chemical group 0.000 claims 1
• 238000007306 functionalization reaction Methods 0.000 claims 1
• 102000039446 nucleic acids Human genes 0.000 claims 1
• 108020004707 nucleic acids Proteins 0.000 claims 1
• 150000007523 nucleic acids Chemical class 0.000 claims 1
• 229920000642 polymer Polymers 0.000 claims 1
• 102000004169 proteins and genes Human genes 0.000 claims 1
• 108090000623 proteins and genes Proteins 0.000 claims 1
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
• 238000000926 separation method Methods 0.000 claims 1
• 125000000542 sulfonic acid group Chemical group 0.000 claims 1