IL86686A - History of nitrotriazole containing fluorine and radiation-sensitive preparations containing them - Google Patents

History of nitrotriazole containing fluorine and radiation-sensitive preparations containing them

Info

Publication number: IL86686A
Authority: IL; Israel
Prior art keywords: nitro; group; solution; nmr; added
Prior art date: 1987-06-10

Application number

IL8668688A

Other languages

English (en)

Hebrew (he)

Other versions

IL86686A0 (en

Original Assignee

Nishijima Yasunori

Kyoto And Daikin Ind Ltd

Priority date (The priority date 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 date listed.)

1987-06-10

Filing date

1988-06-09

Publication date

1994-06-24

1988-01-29 Priority claimed from JP63020456A external-priority patent/JP2848602B2/ja

1988-03-31 Priority claimed from JP63079230A external-priority patent/JP2602887B2/ja

1988-06-09 Application filed by Nishijima Yasunori, Kyoto And Daikin Ind Ltd filed Critical Nishijima Yasunori

1988-06-09 Priority to IL8866588A priority Critical patent/IL88665A/en

1988-11-30 Publication of IL86686A0 publication Critical patent/IL86686A0/xx

1994-06-24 Publication of IL86686A publication Critical patent/IL86686A/en

Links

229910052731 fluorine Inorganic materials 0.000 title claims abstract description 24
239000002534 radiation-sensitizing agent Substances 0.000 title claims description 8
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 title abstract description 14
239000011737 fluorine Substances 0.000 title abstract description 14
YXFWFUSVDJIVIV-UHFFFAOYSA-N 4-nitro-2h-triazole Chemical class [O-][N+](=O)C=1C=NNN=1 YXFWFUSVDJIVIV-UHFFFAOYSA-N 0.000 title description 9
239000000203 mixture Substances 0.000 title description 9
125000001153 fluoro group Chemical group F* 0.000 claims abstract description 9
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 31
SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical class N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 claims description 30
125000000217 alkyl group Chemical group 0.000 claims description 9
125000003709 fluoroalkyl group Chemical group 0.000 claims description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
125000003368 amide group Chemical group 0.000 claims description 3
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
125000003545 alkoxy group Chemical group 0.000 claims 2
125000002947 alkylene group Chemical group 0.000 claims 1
229910052801 chlorine Inorganic materials 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 1
125000004430 oxygen atom Chemical group O* 0.000 claims 1
229910052717 sulfur Inorganic materials 0.000 claims 1
125000004434 sulfur atom Chemical group 0.000 claims 1
-1 3-nitro-1,2,4-triazol-1-yl Chemical group 0.000 abstract description 10
125000000962 organic group Chemical group 0.000 abstract description 3
229910052799 carbon Inorganic materials 0.000 abstract 3
125000004432 carbon atom Chemical group C* 0.000 abstract 3
FTBBGQKRYUTLMP-UHFFFAOYSA-N 2-nitro-1h-pyrrole Chemical class [O-][N+](=O)C1=CC=CN1 FTBBGQKRYUTLMP-UHFFFAOYSA-N 0.000 abstract 1
125000002883 imidazolyl group Chemical group 0.000 abstract 1
239000000243 solution Substances 0.000 description 110
IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 72
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 66
238000006243 chemical reaction Methods 0.000 description 56
238000005481 NMR spectroscopy Methods 0.000 description 47
238000002360 preparation method Methods 0.000 description 45
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 42
238000000746 purification Methods 0.000 description 42
238000010898 silica gel chromatography Methods 0.000 description 41
238000004293 19F NMR spectroscopy Methods 0.000 description 35
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 33
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 30
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 28
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 28
150000001875 compounds Chemical class 0.000 description 26
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 24
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 22
239000000706 filtrate Substances 0.000 description 21
101150041968 CDC13 gene Proteins 0.000 description 20
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 20
238000002955 isolation Methods 0.000 description 20
229910052943 magnesium sulfate Inorganic materials 0.000 description 20
235000019341 magnesium sulphate Nutrition 0.000 description 20
CSJLBAMHHLJAAS-UHFFFAOYSA-N diethylaminosulfur trifluoride Chemical compound CCN(CC)S(F)(F)F CSJLBAMHHLJAAS-UHFFFAOYSA-N 0.000 description 18
210000004027 cell Anatomy 0.000 description 17
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
238000001816 cooling Methods 0.000 description 11
238000003756 stirring Methods 0.000 description 10
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
239000002904 solvent Substances 0.000 description 9
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
230000000694 effects Effects 0.000 description 8
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 8
ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 description 7
238000005160 1H NMR spectroscopy Methods 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
206010021143 Hypoxia Diseases 0.000 description 6
206010028980 Neoplasm Diseases 0.000 description 6
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
230000001146 hypoxic effect Effects 0.000 description 6
230000000637 radiosensitizating effect Effects 0.000 description 6
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 5
230000005855 radiation Effects 0.000 description 5
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
239000003638 chemical reducing agent Substances 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 3
KUEFXPHXHHANKS-UHFFFAOYSA-N 5-nitro-1h-1,2,4-triazole Chemical class [O-][N+](=O)C1=NC=NN1 KUEFXPHXHHANKS-UHFFFAOYSA-N 0.000 description 3
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
241000699666 Mus <mouse, genus> Species 0.000 description 3
206010029350 Neurotoxicity Diseases 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
206010044221 Toxic encephalopathy Diseases 0.000 description 3
239000000010 aprotic solvent Substances 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
238000000338 in vitro Methods 0.000 description 3
238000001727 in vivo Methods 0.000 description 3
230000001965 increasing effect Effects 0.000 description 3
OBBCSXFCDPPXOL-UHFFFAOYSA-N misonidazole Chemical compound COCC(O)CN1C=CN=C1[N+]([O-])=O OBBCSXFCDPPXOL-UHFFFAOYSA-N 0.000 description 3
230000007135 neurotoxicity Effects 0.000 description 3
231100000228 neurotoxicity Toxicity 0.000 description 3
239000012299 nitrogen atmosphere Substances 0.000 description 3
239000012279 sodium borohydride Substances 0.000 description 3
229910000033 sodium borohydride Inorganic materials 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
DJFUGDQHPBDGPE-UHFFFAOYSA-N 3-nitro-1-(1,2,3,3,3-pentafluoroprop-1-enyl)-1,2,4-triazole Chemical compound [O-][N+](=O)C=1N=CN(C(F)=C(F)C(F)(F)F)N=1 DJFUGDQHPBDGPE-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical class CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
241000699670 Mus sp. Species 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
102000004142 Trypsin Human genes 0.000 description 2
108090000631 Trypsin Proteins 0.000 description 2
ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 description 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
201000011510 cancer Diseases 0.000 description 2
150000001244 carboxylic acid anhydrides Chemical class 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 2
239000003814 drug Substances 0.000 description 2
229940079593 drug Drugs 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000003682 fluorination reaction Methods 0.000 description 2
VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 description 2
239000002609 medium Substances 0.000 description 2
229950010514 misonidazole Drugs 0.000 description 2
239000003921 oil Substances 0.000 description 2
230000000144 pharmacologic effect Effects 0.000 description 2
239000000047 product Substances 0.000 description 2
239000001294 propane Substances 0.000 description 2
WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
230000035945 sensitivity Effects 0.000 description 2
230000001235 sensitizing effect Effects 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
150000003852 triazoles Chemical group 0.000 description 2
239000012588 trypsin Substances 0.000 description 2
210000004881 tumor cell Anatomy 0.000 description 2
HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
KIPSRYDSZQRPEA-UHFFFAOYSA-N 2,2,2-trifluoroethanamine Chemical compound NCC(F)(F)F KIPSRYDSZQRPEA-UHFFFAOYSA-N 0.000 description 1
NBUKAOOFKZFCGD-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropan-1-ol Chemical compound OCC(F)(F)C(F)F NBUKAOOFKZFCGD-UHFFFAOYSA-N 0.000 description 1
CNDWHJQEGZZDTQ-UHFFFAOYSA-N 2-(2-amino-2-oxoethoxy)acetamide Chemical compound NC(=O)COCC(N)=O CNDWHJQEGZZDTQ-UHFFFAOYSA-N 0.000 description 1
GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
BPGIOCZAQDIBPI-UHFFFAOYSA-N 2-ethoxyethanamine Chemical compound CCOCCN BPGIOCZAQDIBPI-UHFFFAOYSA-N 0.000 description 1
BJNYOCHWLQCDHC-UHFFFAOYSA-N 2-fluorooxetane Chemical compound FC1CCO1 BJNYOCHWLQCDHC-UHFFFAOYSA-N 0.000 description 1
SOYBEXQHNURCGE-UHFFFAOYSA-N 3-ethoxypropan-1-amine Chemical compound CCOCCCN SOYBEXQHNURCGE-UHFFFAOYSA-N 0.000 description 1
FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 description 1
JLLYLQLDYORLBB-UHFFFAOYSA-N 5-bromo-n-methylthiophene-2-sulfonamide Chemical compound CNS(=O)(=O)C1=CC=C(Br)S1 JLLYLQLDYORLBB-UHFFFAOYSA-N 0.000 description 1
NALREUIWICQLPS-UHFFFAOYSA-N 7-imino-n,n-dimethylphenothiazin-3-amine;hydrochloride Chemical compound [Cl-].C1=C(N)C=C2SC3=CC(=[N+](C)C)C=CC3=NC2=C1 NALREUIWICQLPS-UHFFFAOYSA-N 0.000 description 1
KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical group NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 1
KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 1
241000699802 Cricetulus griseus Species 0.000 description 1
HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 description 1
LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
241000282414 Homo sapiens Species 0.000 description 1
WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
101000800755 Naja oxiana Alpha-elapitoxin-Nno2a Proteins 0.000 description 1
WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
239000002253 acid Substances 0.000 description 1
238000007259 addition reaction Methods 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
ZXKINMCYCKHYFR-UHFFFAOYSA-N aminooxidanide Chemical compound [O-]N ZXKINMCYCKHYFR-UHFFFAOYSA-N 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
230000000259 anti-tumor effect Effects 0.000 description 1
229940058965 antiprotozoal agent against amoebiasis and other protozoal diseases nitroimidazole derivative Drugs 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
CBHOOMGKXCMKIR-UHFFFAOYSA-N azane;methanol Chemical compound N.OC CBHOOMGKXCMKIR-UHFFFAOYSA-N 0.000 description 1
150000007980 azole derivatives Chemical class 0.000 description 1
150000003851 azoles Chemical class 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
150000001728 carbonyl compounds Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
238000002512 chemotherapy Methods 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
HWDVTQAXQJQROO-UHFFFAOYSA-N cyclopropylazanide Chemical compound [NH-]C1CC1 HWDVTQAXQJQROO-UHFFFAOYSA-N 0.000 description 1
238000010908 decantation Methods 0.000 description 1
125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
230000002900 effect on cell Effects 0.000 description 1
239000003480 eluent Substances 0.000 description 1
QLZTYFICDNPHAU-HYXAFXHYSA-N ethyl (z)-2-(trifluoromethyl)but-2-enoate Chemical compound CCOC(=O)C(=C\C)\C(F)(F)F QLZTYFICDNPHAU-HYXAFXHYSA-N 0.000 description 1
239000012025 fluorinating agent Substances 0.000 description 1
150000002222 fluorine compounds Chemical class 0.000 description 1
238000005194 fractionation Methods 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
ALBYIUDWACNRRB-UHFFFAOYSA-N hexanamide Chemical compound CCCCCC(N)=O ALBYIUDWACNRRB-UHFFFAOYSA-N 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
QOTKGSVSGMIHGN-UHFFFAOYSA-N hydron;4,4,4-trifluorobutan-1-amine;chloride Chemical compound Cl.NCCCC(F)(F)F QOTKGSVSGMIHGN-UHFFFAOYSA-N 0.000 description 1
CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 1
230000036039 immunity Effects 0.000 description 1
230000002779 inactivation Effects 0.000 description 1
238000011534 incubation Methods 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
229940102253 isopropanolamine Drugs 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
230000003278 mimic effect Effects 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
229940113083 morpholine Drugs 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
150000004957 nitroimidazoles Chemical class 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000008363 phosphate buffer Substances 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
XUWVIABDWDTJRZ-UHFFFAOYSA-N propan-2-ylazanide Chemical compound CC(C)[NH-] XUWVIABDWDTJRZ-UHFFFAOYSA-N 0.000 description 1
229960000380 propiolactone Drugs 0.000 description 1
NJSJBTVAKUBCKG-UHFFFAOYSA-N propylazanide Chemical compound CCC[NH-] NJSJBTVAKUBCKG-UHFFFAOYSA-N 0.000 description 1
GRJJQCWNZGRKAU-UHFFFAOYSA-N pyridin-1-ium;fluoride Chemical compound F.C1=CC=NC=C1 GRJJQCWNZGRKAU-UHFFFAOYSA-N 0.000 description 1
238000001959 radiotherapy Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000012047 saturated solution Substances 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
239000002356 single layer Substances 0.000 description 1
238000010186 staining Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
239000000829 suppository Substances 0.000 description 1
230000004083 survival effect Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
208000024891 symptom Diseases 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
210000000689 upper leg Anatomy 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/91—Nitro radicals

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Catalysts (AREA)
Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

IL8668688A 1987-06-10 1988-06-09 History of nitrotriazole containing fluorine and radiation-sensitive preparations containing them IL86686A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
IL8866588A IL88665A (en)	1987-06-24	1988-06-09	History of nitroamidazole-containing fluoride-sensitive fluorine containing them

Applications Claiming Priority (6)

Application Number	Priority Date	Filing Date	Title
JP14745987		1987-06-10
JP15678787		1987-06-24
JP24157487		1987-09-26
JP31468687		1987-12-10
JP63020456A JP2848602B2 (ja)	1987-06-24	1988-01-29	新規含フッ素２−ニトロイミダゾールおよびそれを含む放射線増感剤
JP63079230A JP2602887B2 (ja)	1987-06-10	1988-03-31	新規含フッ素３−ニトロ−１，２，４−トリアゾールおよびそれを含む放射線増感剤

Publications (2)

Publication Number	Publication Date
IL86686A0 IL86686A0 (en)	1988-11-30
IL86686A true IL86686A (en)	1994-06-24

Family

ID=27548921

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL8668688A IL86686A (en)	1987-06-10	1988-06-09	History of nitrotriazole containing fluorine and radiation-sensitive preparations containing them

Country Status (9)

Country	Link
US (1)	US4927941A (fr)
EP (1)	EP0294847B1 (fr)
KR (1)	KR910000236B1 (fr)
AT (1)	ATE101601T1 (fr)
AU (2)	AU614288B2 (fr)
CA (2)	CA1329206C (fr)
DE (1)	DE3887776T2 (fr)
ES (1)	ES2063000T3 (fr)
IL (1)	IL86686A (fr)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1329206C (fr) *	1987-06-10	1994-05-03	Tsutomu Kagiya	Derives nitroazole fluores et radiosensibilisant en contenant
IL92597A0 (en) *	1988-12-14	1990-08-31	Yasunori Nishijima President K	Novel fluorine-containing 2-nitroimidazole derivatives and radiosensitizer comprising the same
GB9113487D0 (en) *	1991-06-21	1991-08-07	Amersham Int Plc	Agents for hypoxic cells
US6252087B1 (en)	1992-11-19	2001-06-26	The Trustees Of The University Of Pennsylvania	Nitroaromatic compounds for the detection of hypoxia
US6855828B1 (en)	1992-11-19	2005-02-15	The Trustees Of The University Of Pennsylvania	Detection of hypoxia
EP0669913B1 (fr) *	1992-11-19	2003-03-05	The Trustees Of The University Of Pennsylvania	Detection de l'hypoxie
US5721265A (en) *	1994-08-05	1998-02-24	Sri International	Fluorinated 2-nitroimidazole analogs for detecting hypoxic tumor cells
US6060604A (en) *	1995-03-31	2000-05-09	Florida State University	Pharmaceutical compounds comprising polyamines substituted with electron-affinic groups
US20050026974A1 (en) *	1996-02-08	2005-02-03	Trustees Of The University Of Pennsylvania	Detection of hypoxia
US6331286B1 (en)	1998-12-21	2001-12-18	Photogen, Inc.	Methods for high energy phototherapeutics
US8974363B2 (en) *	1997-12-11	2015-03-10	Provectus Pharmatech, Inc.	Topical medicaments and methods for photodynamic treatment of disease
US20090117199A1 (en) *	1998-08-06	2009-05-07	Scott Timothy C	Method of treatment of cancer
US8557298B2 (en) *	1998-08-06	2013-10-15	Provectus Pharmatech, Inc.	Medicaments for chemotherapeutic treatment of disease
US8470296B2 (en) *	1998-12-21	2013-06-25	Provectus Pharmatech, Inc.	Intracorporeal medicaments for high energy phototherapeutic treatment of disease
US20020001567A1 (en) *	1998-12-21	2002-01-03	Photogen, Inc.	Intracorporeal medicaments for high energy phototherapeutic treatment of disease
US7384623B1 (en)	1998-12-21	2008-06-10	Provectus Pharmatech, Inc.	High energy phototherapeutic agents
AU2003300076C1 (en)	2002-12-30	2010-03-04	Angiotech International Ag	Drug delivery from rapid gelling polymer composition
EP1590440A4 (fr) *	2003-02-03	2009-03-18	Palo Alto Inst Of Molecular Me	Molecules d'elimination de cellules et methodes d'utilisation associees
US7875602B2 (en)	2005-10-21	2011-01-25	Sutter West Bay Hospitals	Camptothecin derivatives as chemoradiosensitizing agents
US9056136B2 (en) *	2006-10-06	2015-06-16	Natural Pharmacia International, Inc.	Weakly basic 2-nitroimidazoles for the non-invasive detection of tissue hypoxia
WO2021224186A1 (fr) *	2020-05-04	2021-11-11	Institut Curie	Nouveaux dérivés de pyridine en tant que radiosensibilisateurs
CN115745953B (zh) *	2022-06-29	2024-06-11	上海凌凯医药科技有限公司	一种羟基氟代试剂及羟基氟代方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IE47132B1 (en) *	1977-08-19	1983-12-28	Roche Products Ltd	Novel nitroimidazoles and pharmaceutical preparations containing these as well as their manufacture
ZW8781A1 (en) *	1980-05-23	1981-12-16	Hoffmann La Roche	2-nitroimidazoles and preparation thereof
ATE23041T1 (de) *	1982-05-27	1986-11-15	Nat Res Dev	Verbindungen anwendbar in strahlentherapie und chemotherapie.
CA1227211A (fr) *	1982-05-27	1987-09-22	National Research Development Corporation	Nitro-imidazolylaziridinopropanols
EP0212558B1 (fr) *	1985-08-15	1991-12-04	Asahi Denka Kogyo Kabushiki Kaisha	Sensibilisateur aux radiations
CA1329206C (fr) *	1987-06-10	1994-05-03	Tsutomu Kagiya	Derives nitroazole fluores et radiosensibilisant en contenant

1988
- 1988-06-08 CA CA000568966A patent/CA1329206C/fr not_active Expired - Fee Related
- 1988-06-09 AU AU17551/88A patent/AU614288B2/en not_active Ceased
- 1988-06-09 IL IL8668688A patent/IL86686A/en not_active IP Right Cessation
- 1988-06-09 US US07/204,367 patent/US4927941A/en not_active Expired - Lifetime
- 1988-06-10 KR KR1019880007004A patent/KR910000236B1/ko not_active Expired
- 1988-06-10 DE DE3887776T patent/DE3887776T2/de not_active Expired - Fee Related
- 1988-06-10 ES ES88109316T patent/ES2063000T3/es not_active Expired - Lifetime
- 1988-06-10 EP EP88109316A patent/EP0294847B1/fr not_active Expired - Lifetime
- 1988-06-10 AT AT88109316T patent/ATE101601T1/de not_active IP Right Cessation
- 1988-12-20 AU AU27307/88A patent/AU615700B2/en not_active Ceased
1989
- 1989-01-06 CA CA000587688A patent/CA1329207C/fr not_active Expired - Fee Related

Also Published As

Publication number	Publication date
US4927941A (en)	1990-05-22
EP0294847B1 (fr)	1994-02-16
KR890000442A (ko)	1989-03-14
ATE101601T1 (de)	1994-03-15
AU1755188A (en)	1988-12-15
AU2730788A (en)	1989-05-25
AU615700B2 (en)	1991-10-10
CA1329206C (fr)	1994-05-03
AU614288B2 (en)	1991-08-29
CA1329207C (fr)	1994-05-03
DE3887776D1 (de)	1994-03-24
ES2063000T3 (es)	1995-01-01
DE3887776T2 (de)	1994-07-07
KR910000236B1 (ko)	1991-01-23
IL86686A0 (en)	1988-11-30
EP0294847A1 (fr)	1988-12-14

Legal Events

Date	Code	Title
1998-11-26	KB	Patent renewed
2002-07-25	KB	Patent renewed
2007-03-08	MM9K	Patent not in force due to non-payment of renewal fees

Publication	Publication Date	Title
IL86686A (en)	1994-06-24	History of nitrotriazole containing fluorine and radiation-sensitive preparations containing them
US5304654A (en)	1994-04-19	Fluorine-containing nitroimidazole compounds
US4977273A (en)	1990-12-11	Fluorine-containing 2-nitroimidazole derivatives
RU2131417C1 (ru)	1999-06-10	Производные азола, способы их получения и антигрибковое средство
LV12887B (en)	2003-01-20	N-heterocyclic derivatives as nos inhibitors
US20080058304A1 (en)	2008-03-06	N-hydroxyamide derivatives possessing antibacterial activity
PT98771A (pt)	1992-07-31	Processo para a preparacao de novos derivados do triazol e de composicoes farmaceuticas ou veterinarias que os contem
Baji et al.	1995	Synthesis and antifungal activity of novel (1-aryl-2-heterocyclyl) ethylideneaminooxymethyl-substituted dioxolanes
EP0435081A2 (fr)	1991-07-03	Dérivés de triazole
EA004957B1 (ru)	2004-10-28	Новые разветвленные замещенные аминопроизводные 3-амино-1-фенил-1h[1,2,4]триазола, способы их получения и содержащие их фармацевтические композиции
EP1144406B1 (fr)	2003-07-30	Derives d'azole antifongiques comprenant un groupe vinyle fluore et procede de preparation associe
EP0212558B1 (fr)	1991-12-04	Sensibilisateur aux radiations
EP0316967B1 (fr)	1992-09-09	Dérivés de nitrazoles contenant du fluor et sensibilisateurs aux radiations les comprenant
RU2703997C1 (ru)	2019-10-23	Гибридные амиды на основе триазола и тиазолидина, обладающие антимикробной активностью
EP0432717A2 (fr)	1991-06-19	Dérivés d'azole, leurs préparation et application
JP2602887B2 (ja)	1997-04-23	新規含フッ素３−ニトロ−１，２，４−トリアゾールおよびそれを含む放射線増感剤
CA1292736C (fr)	1991-12-03	Derives d'ergoline et leurs sels additifs acides
JPH05163269A (ja)	1993-06-29	新規なトリアゾール誘導体およびその塩
JPH02275863A (ja)	1990-11-09	新規含フッ素２―ニトロイミダゾールおよびそれを含む放射線増感剤
JPH0723308B2 (ja)	1995-03-15	放射線増感剤
RU1809607C (ru)	1995-02-09	1-метил-3-(морфолинопропин-1-ил)пиразола гидрохлорид, обладающий противогипоксической активностью
JPH01249755A (ja)	1989-10-05	新規な２−アゾリル−１−シクロプロピルエタノール誘導体およびその塩
JPH0720864B2 (ja)	1995-03-08	放射線増感剤
JPH0616647A (ja)	1994-01-25	新規２−ニトロイミダゾール誘導体およびそれを含有するグルタチオン捕捉能を有する放射線増感剤
JPWO1994026734A1 (ja)	1995-08-03	アゾリルアミン誘導体