MD4393C1 - Ингибитор клеток HL-60 миелоидной лейкемии человека на основе нитрато-[N′-(1-пиридин-2-илметилиден)морфолин-4-карботиогидразидо(1-)]меди - Google Patents
Ингибитор клеток HL-60 миелоидной лейкемии человека на основе нитрато-[N′-(1-пиридин-2-илметилиден)морфолин-4-карботиогидразидо(1-)]меди Download PDFInfo
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- MD4393C1 MD4393C1 MDA20150083A MD20150083A MD4393C1 MD 4393 C1 MD4393 C1 MD 4393C1 MD A20150083 A MDA20150083 A MD A20150083A MD 20150083 A MD20150083 A MD 20150083A MD 4393 C1 MD4393 C1 MD 4393C1
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- MD
- Moldova
- Prior art keywords
- myeloid leukemia
- human myeloid
- copper
- ylmethylidene
- nitrato
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- 208000025113 myeloid leukemia Diseases 0.000 title claims abstract description 16
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 10
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 10
- 239000010949 copper Substances 0.000 title claims abstract description 10
- 239000003112 inhibitor Substances 0.000 title claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 13
- 230000015572 biosynthetic process Effects 0.000 abstract description 4
- 239000003814 drug Substances 0.000 abstract description 4
- 238000003786 synthesis reaction Methods 0.000 abstract description 3
- 229910052723 transition metal Inorganic materials 0.000 abstract description 3
- 150000003624 transition metals Chemical class 0.000 abstract description 3
- 238000011282 treatment Methods 0.000 abstract description 3
- 230000002265 prevention Effects 0.000 abstract 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 5
- CSDSSGBPEUDDEE-UHFFFAOYSA-N 2-formylpyridine Chemical compound O=CC1=CC=CC=N1 CSDSSGBPEUDDEE-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 230000001093 anti-cancer Effects 0.000 description 4
- 239000003446 ligand Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- FGHSTPNOXKDLKU-UHFFFAOYSA-N nitric acid;hydrate Chemical compound O.O[N+]([O-])=O FGHSTPNOXKDLKU-UHFFFAOYSA-N 0.000 description 4
- -1 2-formylpyridine ([N′-(1-pyridin-2-ylmethylidene)morpholine-4- carbothiohydrazide]) Chemical compound 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- KZIPCMQIGBQYAS-UHFFFAOYSA-N (morpholin-4-ylamino)thiourea Chemical compound NC(=S)NNN1CCOCC1 KZIPCMQIGBQYAS-UHFFFAOYSA-N 0.000 description 1
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 1
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 1
- 229930182816 L-glutamine Natural products 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- 239000012980 RPMI-1640 medium Substances 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 230000003327 cancerostatic effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000004699 copper complex Chemical class 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 239000012091 fetal bovine serum Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 208000032839 leukemia Diseases 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 238000011321 prophylaxis Methods 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003573 thiols Chemical group 0.000 description 1
- BRWIZMBXBAOCCF-UHFFFAOYSA-N thiosemicarbazide group Chemical group NNC(=S)N BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Изобретение относится к химии, а именно к синтезу координационных соединений класса тиосемикарбазонатов переходных металлов и может найти применение в медицине для профилактики и лечения миелоидной лейкемии человека.Сущностьизобретения заключается в том, что в качестве ингибитора миелоидной лейкемии человека (клетки HL-60) предлагается нитрато-[N′-(1-пиридин-2-илметилиден)морфолин-4-карботиогидразидо(1-)]медь формулы:Заявляемое соединение ингибирует рост и размножение 72% клеток HL-60 миелоидной лейкемии человека при концентрации 10-7 моль/л.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDA20150083A MD4393C1 (ru) | 2015-09-04 | 2015-09-04 | Ингибитор клеток HL-60 миелоидной лейкемии человека на основе нитрато-[N′-(1-пиридин-2-илметилиден)морфолин-4-карботиогидразидо(1-)]меди |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MDA20150083A MD4393C1 (ru) | 2015-09-04 | 2015-09-04 | Ингибитор клеток HL-60 миелоидной лейкемии человека на основе нитрато-[N′-(1-пиридин-2-илметилиден)морфолин-4-карботиогидразидо(1-)]меди |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MD4393B1 MD4393B1 (ru) | 2016-01-31 |
| MD4393C1 true MD4393C1 (ru) | 2016-08-31 |
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| MDA20150083A MD4393C1 (ru) | 2015-09-04 | 2015-09-04 | Ингибитор клеток HL-60 миелоидной лейкемии человека на основе нитрато-[N′-(1-пиридин-2-илметилиден)морфолин-4-карботиогидразидо(1-)]меди |
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| MD (1) | MD4393C1 (ru) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| MD4434C1 (ru) * | 2015-10-09 | 2017-04-30 | Государственный Университет Молд0 | Использование N'-[1-(2-пиридил)этилиден]морфолин-4-карботиогидразида в качестве ингибитора пролиферации клеток HL-60 миелоидной лейкемии человека |
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| MD4190C1 (ru) * | 2011-06-16 | 2013-07-31 | Государственный Университет Молд0 | Ингибитор миелоидной лейкемии человека на основе {бис[2-(3,5-дибром-2-гидроксифенил)-2-оксоэтил-пиперидин-1-карбодитиоато(1-)-O,O']меди} |
| MD4215C1 (ru) * | 2012-07-09 | 2013-11-30 | Государственный Университет Молд0 | Ингибитор миелоидой лейкемии человека на основе N-(4-(5-( пиридин-2-ил)-4,5-дигидро-1Н-пиразол-3-ил)фенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамида |
-
2015
- 2015-09-04 MD MDA20150083A patent/MD4393C1/ru not_active IP Right Cessation
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| MD4190C1 (ru) * | 2011-06-16 | 2013-07-31 | Государственный Университет Молд0 | Ингибитор миелоидной лейкемии человека на основе {бис[2-(3,5-дибром-2-гидроксифенил)-2-оксоэтил-пиперидин-1-карбодитиоато(1-)-O,O']меди} |
| MD4215C1 (ru) * | 2012-07-09 | 2013-11-30 | Государственный Университет Молд0 | Ингибитор миелоидой лейкемии человека на основе N-(4-(5-( пиридин-2-ил)-4,5-дигидро-1Н-пиразол-3-ил)фенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамида |
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| V. Graur, E. Zariciuc, V. Tsapkov, A. Gulea. SYNTHESIS AND BIOLOGICAL ACTIVITY OF NICKEL AND COPPER COORDINATION COMPOUNDS OF 5-NITROFURAN-2-CARBALDEHYDE N(4)-ALLYL-3-THIOSEMICARBAZONE. STUDIA UNIVERSITATIS MOLDAVIAE, 2014, nr.6(76). Seria "Stiinte reale si ale naturii", p.119--123 ISSN online 1857-498X (publicat on-line 2014.12.23). Regăsit în Internet la 2015.12.08, url: http://studiamsu.eu/wp-content/uploads/19.-p.119-123-Chimie.pdf pag. 122, Table 3 * |
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| Publication number | Publication date |
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| MD4393B1 (ru) | 2016-01-31 |
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