JP2011513298A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2011513298A5 JP2011513298A5 JP2010548248A JP2010548248A JP2011513298A5 JP 2011513298 A5 JP2011513298 A5 JP 2011513298A5 JP 2010548248 A JP2010548248 A JP 2010548248A JP 2010548248 A JP2010548248 A JP 2010548248A JP 2011513298 A5 JP2011513298 A5 JP 2011513298A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- tumor
- peptide
- rgd
- conjugate
- Prior art date
- 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
- 206010028980 Neoplasm Diseases 0.000 claims 19
- 230000001338 necrotic effect Effects 0.000 claims 14
- 239000008196 pharmacological composition Substances 0.000 claims 12
- IYMAXBFPHPZYIK-BQBZGAKWSA-N Arg-Gly-Asp Chemical group NC(N)=NCCC[C@H](N)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(O)=O IYMAXBFPHPZYIK-BQBZGAKWSA-N 0.000 claims 10
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 10
- DSJXIQQMORJERS-AGGZHOMASA-M bacteriochlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC([C@H](CC)[C@H]3C)=[N+]4C3=CC3=C(C(C)=O)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 DSJXIQQMORJERS-AGGZHOMASA-M 0.000 claims 9
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 9
- 108010003118 Bacteriochlorophylls Proteins 0.000 claims 8
- 108010072041 arginyl-glycyl-aspartic acid Proteins 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 229930002875 chlorophyll Natural products 0.000 claims 7
- 235000019804 chlorophyll Nutrition 0.000 claims 7
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- 239000003504 photosensitizing agent Substances 0.000 claims 7
- 108090000765 processed proteins & peptides Proteins 0.000 claims 6
- 229920006395 saturated elastomer Polymers 0.000 claims 6
- 208000026310 Breast neoplasm Diseases 0.000 claims 5
- 101000781681 Protobothrops flavoviridis Disintegrin triflavin Proteins 0.000 claims 5
- 238000003384 imaging method Methods 0.000 claims 5
- 229910052751 metal Inorganic materials 0.000 claims 5
- 239000002184 metal Substances 0.000 claims 5
- 206010006187 Breast cancer Diseases 0.000 claims 4
- 150000001768 cations Chemical class 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 3
- 230000002378 acidificating effect Effects 0.000 claims 3
- 150000001413 amino acids Chemical group 0.000 claims 3
- 210000000481 breast Anatomy 0.000 claims 3
- 125000000524 functional group Chemical group 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- 238000002595 magnetic resonance imaging Methods 0.000 claims 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- 230000004962 physiological condition Effects 0.000 claims 3
- 230000005855 radiation Effects 0.000 claims 3
- NTEDOEBWPRVVSG-FQUUOJAGSA-N (2s)-1-[(2r)-2-[[(2s)-2-[[2-[[(2s)-2-[(2-aminoacetyl)amino]-5-(diaminomethylideneamino)pentanoyl]amino]acetyl]amino]-3-carboxypropanoyl]amino]-3-hydroxypropanoyl]pyrrolidine-2-carboxylic acid Chemical compound NC(N)=NCCC[C@H](NC(=O)CN)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@H](CO)C(=O)N1CCC[C@H]1C(O)=O NTEDOEBWPRVVSG-FQUUOJAGSA-N 0.000 claims 2
- 102000001189 Cyclic Peptides Human genes 0.000 claims 2
- 108010069514 Cyclic Peptides Proteins 0.000 claims 2
- 208000037396 Intraductal Noninfiltrating Carcinoma Diseases 0.000 claims 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical group C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical group C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 150000001447 alkali salts Chemical class 0.000 claims 2
- XRWSZZJLZRKHHD-WVWIJVSJSA-N asunaprevir Chemical compound O=C([C@@H]1C[C@H](CN1C(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)OC1=NC=C(C2=CC=C(Cl)C=C21)OC)N[C@]1(C(=O)NS(=O)(=O)C2CC2)C[C@H]1C=C XRWSZZJLZRKHHD-WVWIJVSJSA-N 0.000 claims 2
- 125000002837 carbocyclic group Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 229940125961 compound 24 Drugs 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- ALEXXDVDDISNDU-JZYPGELDSA-N cortisol 21-acetate Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(=O)COC(=O)C)(O)[C@@]1(C)C[C@@H]2O ALEXXDVDDISNDU-JZYPGELDSA-N 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 2
- 238000012631 diagnostic technique Methods 0.000 claims 2
- 208000028715 ductal breast carcinoma in situ Diseases 0.000 claims 2
- 238000000799 fluorescence microscopy Methods 0.000 claims 2
- 150000004676 glycans Polymers 0.000 claims 2
- 108010053299 glycyl-arginyl-glycyl-aspartyl-seryl-proline Proteins 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000003446 ligand Substances 0.000 claims 2
- 206010061289 metastatic neoplasm Diseases 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 150000002772 monosaccharides Chemical class 0.000 claims 2
- 229920001542 oligosaccharide Polymers 0.000 claims 2
- 150000002482 oligosaccharides Chemical class 0.000 claims 2
- 210000001672 ovary Anatomy 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 150000004804 polysaccharides Polymers 0.000 claims 2
- 238000002600 positron emission tomography Methods 0.000 claims 2
- 238000004393 prognosis Methods 0.000 claims 2
- 108090000623 proteins and genes Proteins 0.000 claims 2
- 102000004169 proteins and genes Human genes 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 238000002603 single-photon emission computed tomography Methods 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- 229910052713 technetium Inorganic materials 0.000 claims 2
- 238000011282 treatment Methods 0.000 claims 2
- 229910052725 zinc Inorganic materials 0.000 claims 2
- ZRVZOBGMZWVJOS-VMXHOPILSA-N (2s)-6-amino-2-[[(2s)-1-[(2s)-2-[[(2s)-2-[[2-[[(2s)-2-[(2-aminoacetyl)amino]-5-(diaminomethylideneamino)pentanoyl]amino]acetyl]amino]-3-carboxypropanoyl]amino]-3-hydroxypropanoyl]pyrrolidine-2-carbonyl]amino]hexanoic acid Chemical compound NCCCC[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCN=C(N)N)NC(=O)CN ZRVZOBGMZWVJOS-VMXHOPILSA-N 0.000 claims 1
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 1
- FYADHXFMURLYQI-UHFFFAOYSA-N 1,2,4-triazine Chemical compound C1=CN=NC=N1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 claims 1
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims 1
- UNILWMWFPHPYOR-KXEYIPSPSA-M 1-[6-[2-[3-[3-[3-[2-[2-[3-[[2-[2-[[(2r)-1-[[2-[[(2r)-1-[3-[2-[2-[3-[[2-(2-amino-2-oxoethoxy)acetyl]amino]propoxy]ethoxy]ethoxy]propylamino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-[(2r)-2,3-di(hexadecanoyloxy)propyl]sulfanyl-1-oxopropan-2-yl Chemical compound O=C1C(SCCC(=O)NCCCOCCOCCOCCCNC(=O)COCC(=O)N[C@@H](CSC[C@@H](COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC)C(=O)NCC(=O)N[C@H](CO)C(=O)NCCCOCCOCCOCCCNC(=O)COCC(N)=O)CC(=O)N1CCNC(=O)CCCCCN\1C2=CC=C(S([O-])(=O)=O)C=C2CC/1=C/C=C/C=C/C1=[N+](CC)C2=CC=C(S([O-])(=O)=O)C=C2C1 UNILWMWFPHPYOR-KXEYIPSPSA-M 0.000 claims 1
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 claims 1
- 206010005003 Bladder cancer Diseases 0.000 claims 1
- 206010072960 Chest wall tumour Diseases 0.000 claims 1
- COLNVLDHVKWLRT-MRVPVSSYSA-N D-phenylalanine Chemical compound OC(=O)[C@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-MRVPVSSYSA-N 0.000 claims 1
- 125000002849 D-tyrosine group Chemical group [H]N([H])[C@@]([H])(C(=O)[*])C([H])([H])C1=C([H])C([H])=C(O[H])C([H])=C1[H] 0.000 claims 1
- 229910052692 Dysprosium Inorganic materials 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- 229910052691 Erbium Inorganic materials 0.000 claims 1
- 208000000461 Esophageal Neoplasms Diseases 0.000 claims 1
- 229910052688 Gadolinium Inorganic materials 0.000 claims 1
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims 1
- 206010073094 Intraductal proliferative breast lesion Diseases 0.000 claims 1
- 206010058467 Lung neoplasm malignant Diseases 0.000 claims 1
- 206010033128 Ovarian cancer Diseases 0.000 claims 1
- 206010061535 Ovarian neoplasm Diseases 0.000 claims 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 claims 1
- 208000000453 Skin Neoplasms Diseases 0.000 claims 1
- 206010054094 Tumour necrosis Diseases 0.000 claims 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 1
- 229910052769 Ytterbium Inorganic materials 0.000 claims 1
- 125000002015 acyclic group Chemical group 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical group N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 claims 1
- RLFFLEZFARXFQF-UHFFFAOYSA-N aziridin-1-amine Chemical group NN1CC1 RLFFLEZFARXFQF-UHFFFAOYSA-N 0.000 claims 1
- 210000004556 brain Anatomy 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 239000013522 chelant Substances 0.000 claims 1
- 150000004697 chelate complex Chemical class 0.000 claims 1
- 210000001072 colon Anatomy 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- 238000001514 detection method Methods 0.000 claims 1
- 238000003745 diagnosis Methods 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 201000004101 esophageal cancer Diseases 0.000 claims 1
- 210000003238 esophagus Anatomy 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 108010064365 glycyl- arginyl-glycyl-aspartyl-seryl-prolyl-lysine Proteins 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-O hydron;1,3-oxazole Chemical compound C1=COC=[NH+]1 ZCQWOFVYLHDMMC-UHFFFAOYSA-O 0.000 claims 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-O hydron;pyrimidine Chemical compound C1=CN=C[NH+]=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-O 0.000 claims 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-O hydron;quinoline Chemical compound [NH+]1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-O 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- AWJUIBRHMBBTKR-UHFFFAOYSA-O isoquinolin-2-ium Chemical compound C1=[NH+]C=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-O 0.000 claims 1
- 210000004072 lung Anatomy 0.000 claims 1
- 201000005202 lung cancer Diseases 0.000 claims 1
- 208000020816 lung neoplasm Diseases 0.000 claims 1
- 229910052748 manganese Inorganic materials 0.000 claims 1
- 238000013507 mapping Methods 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 208000018223 neoplasm of chest wall Diseases 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 150000002892 organic cations Chemical class 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 229910052763 palladium Inorganic materials 0.000 claims 1
- 230000005298 paramagnetic effect Effects 0.000 claims 1
- 239000000816 peptidomimetic Substances 0.000 claims 1
- 238000002428 photodynamic therapy Methods 0.000 claims 1
- 229910052697 platinum Inorganic materials 0.000 claims 1
- 238000004321 preservation Methods 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 102000004196 processed proteins & peptides Human genes 0.000 claims 1
- 210000002307 prostate Anatomy 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims 1
- 229910052702 rhenium Inorganic materials 0.000 claims 1
- 229910052703 rhodium Inorganic materials 0.000 claims 1
- 210000003491 skin Anatomy 0.000 claims 1
- 201000000849 skin cancer Diseases 0.000 claims 1
- 238000001356 surgical procedure Methods 0.000 claims 1
- 229910052716 thallium Inorganic materials 0.000 claims 1
- -1 thiazolium Chemical compound 0.000 claims 1
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical group C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims 1
- 229910052718 tin Inorganic materials 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 1
- 229910052727 yttrium Inorganic materials 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6429808P | 2008-02-27 | 2008-02-27 | |
| US61/064,298 | 2008-02-27 | ||
| PCT/IL2009/000228 WO2009107139A1 (en) | 2008-02-27 | 2009-03-01 | Rgd-(bacterio)chlorophyll conjugates for photodynamic therapy and imaging of necrotic tumors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011513298A JP2011513298A (ja) | 2011-04-28 |
| JP2011513298A5 true JP2011513298A5 (enExample) | 2012-04-12 |
| JP5620279B2 JP5620279B2 (ja) | 2014-11-05 |
Family
ID=40677556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010548248A Expired - Fee Related JP5620279B2 (ja) | 2008-02-27 | 2009-03-01 | 壊死性腫瘍の光線力学的治療及び画像化のためのrgd−(バクテリオ)クロロフィルコンジュゲート |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US8815213B2 (enExample) |
| EP (2) | EP2257309B1 (enExample) |
| JP (1) | JP5620279B2 (enExample) |
| KR (1) | KR101595138B1 (enExample) |
| CN (1) | CN102036684B (enExample) |
| AU (1) | AU2009219682B2 (enExample) |
| BR (1) | BRPI0907791A2 (enExample) |
| CA (1) | CA2717060C (enExample) |
| DK (1) | DK2257309T3 (enExample) |
| ES (1) | ES2764781T3 (enExample) |
| MX (1) | MX2010009530A (enExample) |
| PT (1) | PT2257309T (enExample) |
| RU (1) | RU2518296C2 (enExample) |
| WO (1) | WO2009107139A1 (enExample) |
| ZA (1) | ZA201006789B (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1968648B1 (en) | 2005-12-16 | 2015-05-06 | Catherine M Shachaf | Diagnostic system for the detection and diagnosis of skin cancer |
| US9957293B2 (en) * | 2006-08-23 | 2018-05-01 | Yeda Research And Development Company Ltd. | Conjugates of RGD peptides and porphyrin or (bacterio)chlorophyll photosynthesizers and their uses |
| WO2011020107A2 (en) * | 2009-08-14 | 2011-02-17 | Georgetown University | Compositions and methods for detection and treatment of breast cancer |
| PL219569B1 (pl) | 2010-02-19 | 2015-05-29 | Peptaderm Spółka Z Ograniczoną Odpowiedzialnością | Cykliczne tetrapeptydy i ich zastosowanie |
| US8524239B2 (en) | 2010-07-09 | 2013-09-03 | The United States of America as represented by the Secrectary, Department of Health and Human Services | Photosensitizing antibody-fluorophore conjugates |
| KR101253709B1 (ko) * | 2011-06-02 | 2013-04-12 | 경북대학교 산학협력단 | 분비형 표적 추적 융합 단백질 |
| AU2012305327B2 (en) | 2011-09-05 | 2016-07-14 | Hiroshi Maeda | Polymer-type fluorescent molecule probe |
| CN104303184B (zh) * | 2012-03-21 | 2018-05-15 | 皇家飞利浦有限公司 | 整合医疗成像和活检数据的临床工作站以及使用其的方法 |
| CN103705532B (zh) * | 2012-10-08 | 2016-09-14 | 浙江海正药业股份有限公司 | 靶向胸苷激酶光敏剂及其药物组合物与治疗癌症的用途 |
| US20150343060A1 (en) | 2014-06-02 | 2015-12-03 | Li-Cor, Inc. | Treatment of circulating tumor cells using an extracorporeal device |
| CN111388672A (zh) | 2014-08-08 | 2020-07-10 | 美国政府(由卫生和人类服务部的部长所代表) | 在体内和在体外的靶标的光控移除 |
| SI3215518T1 (sl) | 2014-10-29 | 2021-08-31 | Bicyclerd Limited | Biciklični peptidni ligandi, značilni za MT1-MMP |
| WO2016090471A1 (en) * | 2014-12-08 | 2016-06-16 | University Health Network | System and method for enhanced mass spectrometry imaging |
| JP6793122B2 (ja) * | 2014-12-19 | 2020-12-02 | ブラッコ・イメージング・ソシエタ・ペル・アチオニBracco Imaging S.P.A. | 術中イメージング |
| TR201810532T4 (tr) * | 2015-06-03 | 2018-08-27 | Surgimab S A S | Floresan konjügatlar. |
| AU2016308286B2 (en) | 2015-08-18 | 2022-04-07 | Rakuten Medical, Inc. | Phthalocyanine dye conjugates and their storage |
| US11266383B2 (en) | 2015-09-22 | 2022-03-08 | University Health Network | System and method for optimized mass spectrometry analysis |
| EP3559019A1 (en) * | 2016-12-23 | 2019-10-30 | BicycleTX Limited | Peptide ligands for binding to mt1-mmp |
| JP2020502238A (ja) * | 2016-12-23 | 2020-01-23 | バイスクルアールディー・リミテッド | 新規連結構造を有するペプチド誘導体 |
| US10933134B2 (en) | 2017-03-16 | 2021-03-02 | Memorial Sloan Kettering Cancer Center | Combination therapies for treatment of cancer |
| CN111183147B (zh) | 2017-08-04 | 2024-07-05 | 拜斯科技术开发有限公司 | Cd137特异性的双环肽配体 |
| WO2019032683A2 (en) * | 2017-08-08 | 2019-02-14 | Board Of Trustees Of Michigan State University | LIGHT-EMITTING ORGANIC SALTS FOR ENHANCED PHOTODYNAMIC THERAPY AND IMAGING |
| JP6920931B2 (ja) * | 2017-09-01 | 2021-08-18 | 富士フイルム株式会社 | 医療画像処理装置、内視鏡装置、診断支援装置、及び、医療業務支援装置 |
| WO2019162682A1 (en) | 2018-02-23 | 2019-08-29 | Bicycletx Limited | Multimeric bicyclic peptide ligands |
| US11180531B2 (en) | 2018-06-22 | 2021-11-23 | Bicycletx Limited | Bicyclic peptide ligands specific for Nectin-4 |
| RU2700407C1 (ru) * | 2018-07-23 | 2019-09-16 | Михаил Тимофеевич Александров | Способ лечения опухолевых и воспалительных заболеваний с применением фотодинамической терапии |
| CN111171030B (zh) * | 2018-11-12 | 2022-11-22 | 浙江海正药业股份有限公司 | 细菌叶绿素衍生物及其制备方法 |
| GB201820325D0 (en) | 2018-12-13 | 2019-01-30 | Bicyclerd Ltd | Bicyclic peptide ligands specific for psma |
| GB201820295D0 (en) | 2018-12-13 | 2019-01-30 | Bicyclerd Ltd | Bicyclic peptide ligands specific for MT1-MMP |
| GB201820288D0 (en) | 2018-12-13 | 2019-01-30 | Bicycle Tx Ltd | Bicycle peptide ligaands specific for MT1-MMP |
| WO2020128526A1 (en) | 2018-12-21 | 2020-06-25 | Bicycletx Limited | Bicyclic peptide ligands specific for pd-l1 |
| TWI862640B (zh) | 2019-07-30 | 2024-11-21 | 英商拜西可泰克斯有限公司 | 異質雙環肽複合物 |
| EP4070098B1 (en) * | 2019-12-05 | 2025-12-24 | Tempus AI, Inc. | Large scale organoid analysis |
| CN112933252A (zh) * | 2021-01-28 | 2021-06-11 | 厦门大学附属翔安医院 | 一种乳腺癌特异靶向分子探针及其制备方法和应用 |
| CN115466311A (zh) * | 2021-06-10 | 2022-12-13 | 首都医科大学 | 抗粘附迁移和侵袭的18β-甘草次酸-RGDK,其合成,抗癌转移活性和应用 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4121876A1 (de) | 1991-07-02 | 1993-01-14 | Scheer Hugo | Modifizierte bakteriochlorophylle, verfahren zu ihrer herstellung und ihre verwendung |
| EP0617705B1 (en) | 1991-11-22 | 1997-09-24 | Yeda Research And Development Company, Ltd. | Non-peptidic surrogates of the arg-gly-asp sequence and pharmaceutical compositions comprising them |
| IL102645A (en) * | 1992-07-26 | 1998-02-22 | Yeda Res & Dev | Chlorophyll and bacteriochlorophyll derivatives, their preparation and pharmaceutical compositions comprising them |
| US6147195A (en) | 1993-07-26 | 2000-11-14 | Yeda Research And Development Co., Ltd. | Chlorophyll and bacteriochlorophyll derivatives, their preparation and pharmaceutical compositions comprising them |
| US5789433A (en) * | 1995-01-17 | 1998-08-04 | Quadra Logic Technologies, Inc. | Green porphyrins as immunomodulators |
| IL116126A0 (en) | 1995-11-24 | 1996-01-31 | Yeda Res & Dev | Process for the preparation of bacteriochlorophyllis some novel compounds of this type and pharmaceutical compositions comprising them |
| US6576239B1 (en) | 1996-09-10 | 2003-06-10 | The Burnham Institute | Angiogenic homing molecules and conjugates derived therefrom |
| JP2001501600A (ja) * | 1996-09-10 | 2001-02-06 | ザ バーナム インスティテュート | 腫瘍ホーミング分子、それに由来する結合体、およびその使用方法 |
| DE19756773A1 (de) * | 1997-12-19 | 1999-06-24 | Dade Behring Marburg Gmbh | Neues Verfahren und Diagnosemittel zur Hämostase-Diagnostik |
| CA2353554C (en) | 1998-12-09 | 2011-04-26 | Yeda Research And Development Co. Ltd. | Palladium-substituted bacteriochlorophyll derivatives and use thereof |
| IL133253A0 (en) | 1999-12-01 | 2001-04-30 | Yeda Res & Dev | Chlorophyll and bacteriochlorophyll esters, their preparation and pharmaceutical compositions comprising them |
| US7045117B2 (en) | 1999-12-01 | 2006-05-16 | Yeda Research And Development Co. Ltd. | Method for tumor diagnosis comprising administering of palladium-substituted bacteriochlorophyll derivatives |
| IL152900A0 (en) | 2002-11-17 | 2003-06-24 | Yeda Res & Dev | Water-soluble bacteriochlorophyll derivatives and their pharmaceutical uses |
| EP2322173B1 (en) | 2004-06-07 | 2016-08-10 | Yeda Research And Development Co., Ltd. | Cationic bacteriochlorophyll derivatives and uses thereof |
| EP2019667A4 (en) * | 2006-04-27 | 2012-08-22 | Barnes Jewish Hospital | DETECTION AND IMAGING OF TARGET TISSUE |
| JP2010502574A (ja) * | 2006-08-23 | 2010-01-28 | イエダ リサーチ アンド デベロップメント カンパニー リミテッド | Rgdペプチドとポルフィリン又は(バクテリオ)クロロフィル光合成剤とのコンジュゲート及びその使用 |
| JP2010539163A (ja) * | 2007-09-14 | 2010-12-16 | ヘルス リサーチ インコーポレイテッド | 腫瘍イメージング及び治療用のマルチモーダル剤 |
-
2009
- 2009-03-01 KR KR1020107021381A patent/KR101595138B1/ko not_active Expired - Fee Related
- 2009-03-01 US US12/920,088 patent/US8815213B2/en active Active
- 2009-03-01 RU RU2010139461/15A patent/RU2518296C2/ru active
- 2009-03-01 MX MX2010009530A patent/MX2010009530A/es active IP Right Grant
- 2009-03-01 CA CA2717060A patent/CA2717060C/en not_active Expired - Fee Related
- 2009-03-01 PT PT97141915T patent/PT2257309T/pt unknown
- 2009-03-01 JP JP2010548248A patent/JP5620279B2/ja not_active Expired - Fee Related
- 2009-03-01 CN CN200980115901.2A patent/CN102036684B/zh not_active Expired - Fee Related
- 2009-03-01 BR BRPI0907791-0A patent/BRPI0907791A2/pt not_active Application Discontinuation
- 2009-03-01 EP EP09714191.5A patent/EP2257309B1/en active Active
- 2009-03-01 ES ES09714191T patent/ES2764781T3/es active Active
- 2009-03-01 AU AU2009219682A patent/AU2009219682B2/en not_active Ceased
- 2009-03-01 EP EP13186941.4A patent/EP2712627A3/en not_active Withdrawn
- 2009-03-01 DK DK09714191.5T patent/DK2257309T3/da active
- 2009-03-01 WO PCT/IL2009/000228 patent/WO2009107139A1/en not_active Ceased
-
2010
- 2010-09-22 ZA ZA2010/06789A patent/ZA201006789B/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2011513298A5 (enExample) | ||
| RU2010139461A (ru) | Конъюгаты rgd-(бактерио)хлорофилл для фотодинамической терапии и визуализации некротических опухолей | |
| US11020493B2 (en) | Double-labeled probe for molecular imaging and use thereof | |
| RU2009110226A (ru) | Конъюгаты rgd-пептидов и фотосенсибилизаторов порфирина или (бактериоххлорофилла и их применение | |
| JP2010502574A5 (enExample) | ||
| CN112351974B (zh) | 直接抑制asm活性的新型化合物2-氨基-2-(1,2,3-三唑-4-基)-1,3-丙二醇衍生物及其应用 | |
| CN108026144B (zh) | 18f-标记的前列腺特异性膜抗原(psma)的抑制剂以及它们作为前列腺癌的成像剂的应用 | |
| JP2012520856A (ja) | 光学イメージング剤 | |
| JP2018531243A6 (ja) | 前立腺特異的膜抗原(psma)の18f−タグ付加インヒビターおよび前立腺癌についての画像化剤としてのその使用 | |
| WO2016118188A1 (en) | Compositions for targeting macrophages and other mannose-binding c-type lectin receptor high expressing cells | |
| EP3169792A2 (en) | Compounds and compositions for targeting macrophages and other mannose-binding c-type lectin receptor high expressing cells and methods of treating and diagnosis using same | |
| EP3978033A1 (en) | Rk polypeptide radiopharmaceutical targeting her2, and preparation method therefor | |
| WO2019101729A1 (en) | A double-labeled probe for molecular imaging and use thereof | |
| Murase et al. | Double sentinel lymph node mapping with indocyanine green and 99m-technetium–tin colloid in oral squamous cell carcinoma | |
| JP2019527225A5 (enExample) | ||
| JP7692839B2 (ja) | コンジュゲート及びそのイメージング剤としての使用 | |
| JP2023536358A (ja) | Pet-ct撮像方法、その撮像方法における使用のための造影剤および医薬組成物 | |
| US12115232B2 (en) | Preparation for magnetic resonance diagnostics for oncological diseases, comprising deuterated 3-O-methylglucose, and diagnostic method using said preparation | |
| US12082918B2 (en) | Preparation for magnetic resonance diagnostics for oncological diseases, comprising deuterated 2-amino-2-methylpropionic acid and/or 2-(N-methylamino)-2-methylpropionic acid, and diagnostic method using said preparation | |
| US20190336621A1 (en) | Radioactive compound for diagnosis of malignant melanoma and use thereof | |
| JP2021508335A (ja) | 癌診断における放射性標識プロガストリン | |
| Beiki et al. | Evaluation of a new 99mTc-Bombesin analog in differentiation of malignant from benign breast tumors | |
| US20190071429A1 (en) | Multiple-functional probe and uses thereof | |
| JP2012042215A (ja) | 早期膵がんの検出方法 | |
| SS | Zirconium-89 tetraazamacrocycle complexes may provide a new strategy in 89Zr radiopharmaceutical development PRESENTER: Thaddeus Wadas CURRENT EMPHASIS: Basic Biology and Bioengineering CURRENT CATEGORY: New Probe Concepts |