JP2014129317A5 - - Google Patents

Info

Publication number

JP2014129317A5

JP2014129317A5 JP2013032363A JP2013032363A JP2014129317A5 JP 2014129317 A5 JP2014129317 A5 JP 2014129317A5 JP 2013032363 A JP2013032363 A JP 2013032363A JP 2013032363 A JP2013032363 A JP 2013032363A JP 2014129317 A5 JP2014129317 A5 JP 2014129317A5

Authority

JP

Japan

Prior art keywords

group

naphthalocyanine

silicon

nanoparticle according

nanoparticle

Prior art date

2013-02-21

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.)

Withdrawn

Links

• Espacenet
• Global Dossier
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• 239000002105 nanoparticle Substances 0.000 claims 18
• XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 8
• 229910052710 silicon Inorganic materials 0.000 claims 8
• 239000010703 silicon Substances 0.000 claims 8
• 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims 5
• 125000000217 alkyl group Chemical group 0.000 claims 5
• 125000003277 amino group Chemical group 0.000 claims 5
• 125000004432 carbon atom Chemical group C* 0.000 claims 5
• 125000004093 cyano group Chemical group *C#N 0.000 claims 5
• 125000005843 halogen group Chemical group 0.000 claims 5
• LKKPNUDVOYAOBB-UHFFFAOYSA-N naphthalocyanine Chemical compound N1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)N3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 LKKPNUDVOYAOBB-UHFFFAOYSA-N 0.000 claims 5
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 5
• 239000000126 substance Substances 0.000 claims 4
• 239000004094 surface-active agent Substances 0.000 claims 4
• 125000000524 functional group Chemical group 0.000 claims 3
• XIINLOVCJKUOQC-UHFFFAOYSA-N 389927_sial Chemical compound N1=C(C2=CC3=CC=CC=C3C=C2C2=NC=3C4=CC5=CC=CC=C5C=C4C(=N4)N=3)N2[Si](Cl)(Cl)N2C4=C(C=C3C(C=CC=C3)=C3)C3=C2N=C2C3=CC4=CC=CC=C4C=C3C1=N2 XIINLOVCJKUOQC-UHFFFAOYSA-N 0.000 claims 2
• 125000003118 aryl group Chemical group 0.000 claims 2
• 239000002872 contrast media Substances 0.000 claims 2
• 239000002245 particle Substances 0.000 claims 2
• 125000001424 substituent group Chemical group 0.000 claims 2
• FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims 1
• 125000003275 alpha amino acid group Chemical group 0.000 claims 1
• UHZAFCVNWQGRLM-UHFFFAOYSA-N bis(trihexylsiloxy)silicon 2,3-naphthalocyanine Chemical compound N1=C(C2=CC3=CC=CC=C3C=C2C2=NC=3C4=CC5=CC=CC=C5C=C4C(=N4)N=3)N2[Si](O[Si](CCCCCC)(CCCCCC)CCCCCC)(O[Si](CCCCCC)(CCCCCC)CCCCCC)N2C4=C(C=C3C(C=CC=C3)=C3)C3=C2N=C2C3=CC4=CC=CC=C4C=C3C1=N2 UHZAFCVNWQGRLM-UHFFFAOYSA-N 0.000 claims 1
• 229910052799 carbon Inorganic materials 0.000 claims 1
• 239000000470 constituent Substances 0.000 claims 1
• -1 diisobutyloctadecylsiloxane Chemical class 0.000 claims 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
• 238000003384 imaging method Methods 0.000 claims 1
• CTZCIINFSBLHAS-UHFFFAOYSA-N iso-bosinc Chemical compound [Si+4].CCCCCCCCCCCCCCCCCC[Si]([O-])(CC(C)C)CC(C)C.CCCCCCCCCCCCCCCCCC[Si]([O-])(CC(C)C)CC(C)C.C12=CC3=CC=CC=C3C=C2C(N=C2[N-]C(C3=CC4=CC=CC=C4C=C32)=N2)=NC1=NC([C]1C=C3C=CC=CC3=CC1=1)=NC=1N=C1[C]3C=C4C=CC=CC4=CC3=C2[N-]1 CTZCIINFSBLHAS-UHFFFAOYSA-N 0.000 claims 1
• 229920006395 saturated elastomer Polymers 0.000 claims 1
• 125000004417 unsaturated alkyl group Chemical group 0.000 claims 1