JPWO2019152911A5 - - Google Patents
Download PDFInfo
- Publication number
- JPWO2019152911A5 JPWO2019152911A5 JP2020564033A JP2020564033A JPWO2019152911A5 JP WO2019152911 A5 JPWO2019152911 A5 JP WO2019152911A5 JP 2020564033 A JP2020564033 A JP 2020564033A JP 2020564033 A JP2020564033 A JP 2020564033A JP WO2019152911 A5 JPWO2019152911 A5 JP WO2019152911A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- substituted
- alkoxy
- pharmaceutically acceptable
- amide
- 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.)
- Pending
Links
- 125000000217 alkyl group Chemical group 0.000 claims description 62
- 125000003545 alkoxy group Chemical group 0.000 claims description 50
- 125000005843 halogen group Chemical group 0.000 claims description 50
- 150000001875 compounds Chemical class 0.000 claims description 46
- 150000003839 salts Chemical class 0.000 claims description 44
- 150000001408 amides Chemical class 0.000 claims description 42
- 150000002148 esters Chemical class 0.000 claims description 40
- 239000011780 sodium chloride Substances 0.000 claims description 38
- 239000012453 solvate Substances 0.000 claims description 38
- 125000003118 aryl group Chemical group 0.000 claims description 26
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 20
- -1 amino, hydroxy, thio Chemical group 0.000 claims description 19
- 229960005277 gemcitabine Drugs 0.000 claims description 16
- 125000000304 alkynyl group Chemical group 0.000 claims description 14
- 125000001072 heteroaryl group Chemical group 0.000 claims description 14
- 229910052757 nitrogen Inorganic materials 0.000 claims description 14
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 12
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 150000008298 phosphoramidates Chemical class 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 6
- 230000002062 proliferating Effects 0.000 claims description 6
- FDDDEECHVMSUSB-UHFFFAOYSA-N Sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 claims description 4
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000004171 alkoxy aryl group Chemical group 0.000 claims description 4
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 4
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 4
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 201000011510 cancer Diseases 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 4
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N oxygen atom Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 4
- 150000008299 phosphorodiamidates Chemical class 0.000 claims description 4
- 229960001663 sulfanilamide Drugs 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 125000004434 sulfur atoms Chemical group 0.000 claims description 4
- 210000004881 tumor cells Anatomy 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 3
- 210000004556 Brain Anatomy 0.000 claims description 2
- 210000000481 Breast Anatomy 0.000 claims description 2
- 102100004047 CYP1B1 Human genes 0.000 claims description 2
- 101710036800 CYP1B1 Proteins 0.000 claims description 2
- 210000001072 Colon Anatomy 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 claims description 2
- 108090000790 Enzymes Proteins 0.000 claims description 2
- 210000003128 Head Anatomy 0.000 claims description 2
- 210000003734 Kidney Anatomy 0.000 claims description 2
- 210000004185 Liver Anatomy 0.000 claims description 2
- 210000004072 Lung Anatomy 0.000 claims description 2
- 210000003739 Neck Anatomy 0.000 claims description 2
- 206010028980 Neoplasm Diseases 0.000 claims description 2
- 210000001672 Ovary Anatomy 0.000 claims description 2
- 210000000496 Pancreas Anatomy 0.000 claims description 2
- 210000002307 Prostate Anatomy 0.000 claims description 2
- 210000003491 Skin Anatomy 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L Sulphite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 2
- 210000003932 Urinary Bladder Anatomy 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 125000005041 acyloxyalkyl group Chemical group 0.000 claims description 2
- 125000004946 alkenylalkyl group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000005038 alkynylalkyl group Chemical group 0.000 claims description 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 2
- 125000005418 aryl aryl group Chemical group 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 230000000875 corresponding Effects 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 125000004367 cycloalkylaryl group Chemical group 0.000 claims description 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 2
- 229910052805 deuterium Inorganic materials 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 125000002883 imidazolyl group Chemical group 0.000 claims description 2
- 125000005647 linker group Chemical group 0.000 claims description 2
- 239000002207 metabolite Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims description 2
- 150000002829 nitrogen Chemical class 0.000 claims description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- LURSQGOJGVDZFI-UHFFFAOYSA-M sulfo sulfite Chemical compound OS(=O)(=O)OS([O-])=O LURSQGOJGVDZFI-UHFFFAOYSA-M 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- 150000003536 tetrazoles Chemical class 0.000 claims description 2
- 150000003568 thioethers Chemical class 0.000 claims description 2
- 150000003573 thiols Chemical class 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 4
- 239000000969 carrier Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2024019158A JP2024073414A (ja) | 2018-02-02 | 2024-02-13 | ゲムシタビン誘導体の新規小分子薬物コンジュゲート |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862625779P | 2018-02-02 | 2018-02-02 | |
US62/625,779 | 2018-02-02 | ||
PCT/US2019/016477 WO2019152911A1 (fr) | 2018-02-02 | 2019-02-04 | Nouveaux conjugués de médicaments à petites molécules de dérivés de gemcitabine |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2024019158A Division JP2024073414A (ja) | 2018-02-02 | 2024-02-13 | ゲムシタビン誘導体の新規小分子薬物コンジュゲート |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2021512951A JP2021512951A (ja) | 2021-05-20 |
JPWO2019152911A5 true JPWO2019152911A5 (fr) | 2022-02-14 |
Family
ID=65494546
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2020564033A Pending JP2021512951A (ja) | 2018-02-02 | 2019-02-04 | ゲムシタビン誘導体の新規小分子薬物コンジュゲート |
JP2024019158A Pending JP2024073414A (ja) | 2018-02-02 | 2024-02-13 | ゲムシタビン誘導体の新規小分子薬物コンジュゲート |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2024019158A Pending JP2024073414A (ja) | 2018-02-02 | 2024-02-13 | ゲムシタビン誘導体の新規小分子薬物コンジュゲート |
Country Status (13)
Country | Link |
---|---|
US (1) | US20210380626A1 (fr) |
EP (1) | EP3746133A1 (fr) |
JP (2) | JP2021512951A (fr) |
KR (1) | KR20200118828A (fr) |
CN (1) | CN112135635A (fr) |
AU (1) | AU2019216514A1 (fr) |
BR (1) | BR112020015747A2 (fr) |
CA (1) | CA3090272A1 (fr) |
EA (1) | EA202091857A1 (fr) |
IL (1) | IL276442A (fr) |
PH (1) | PH12020551178A1 (fr) |
SG (1) | SG11202007381YA (fr) |
WO (1) | WO2019152911A1 (fr) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019152955A1 (fr) * | 2018-02-02 | 2019-08-08 | Steven Albert Everett | Conjugués de médicaments à petites molécules de monophosphate de gemcitabine |
CN114349816A (zh) * | 2021-11-30 | 2022-04-15 | 青岛博创生物科学研究院 | 一种基于氨肽酶n/cd13的小分子偶联分子及其制备方法和应用 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69909073T2 (de) | 1998-02-12 | 2004-05-19 | De Montfort University | Durch hydroxylierung aktivierte wirkstofffreigabe |
US7148226B2 (en) | 2003-02-21 | 2006-12-12 | Agouron Pharmaceuticals, Inc. | Inhibitors of hepatitis C virus RNA-dependent RNA polymerase, and compositions and treatments using the same |
GB0317009D0 (en) * | 2003-07-21 | 2003-08-27 | Univ Cardiff | Chemical compounds |
GB0907551D0 (en) | 2009-05-01 | 2009-06-10 | Univ Dundee | Treatment or prophylaxis of proliferative conditions |
EP3078671A4 (fr) * | 2013-12-04 | 2017-05-31 | Hangzhou Minsheng Institutes for Pharma Research Co., Ltd. | Dérivé de gemcitabine, composition contenant le dérivé et utilisation pharmaceutique du dérivé |
WO2015134334A1 (fr) * | 2014-03-03 | 2015-09-11 | Suo Zucai | Analogues de gemcitabine |
CN105001291B (zh) * | 2014-04-15 | 2018-12-04 | 上海知萌生物医药科技有限公司 | 吉西他滨化学传递前药及其制备方法和应用 |
CN107295800A (zh) * | 2015-02-25 | 2017-10-24 | 配体药物公司 | 吉西他滨衍生物 |
-
2019
- 2019-02-04 JP JP2020564033A patent/JP2021512951A/ja active Pending
- 2019-02-04 BR BR112020015747-3A patent/BR112020015747A2/pt not_active IP Right Cessation
- 2019-02-04 AU AU2019216514A patent/AU2019216514A1/en not_active Abandoned
- 2019-02-04 SG SG11202007381YA patent/SG11202007381YA/en unknown
- 2019-02-04 EA EA202091857A patent/EA202091857A1/ru unknown
- 2019-02-04 US US16/967,086 patent/US20210380626A1/en not_active Abandoned
- 2019-02-04 EP EP19706106.2A patent/EP3746133A1/fr not_active Withdrawn
- 2019-02-04 WO PCT/US2019/016477 patent/WO2019152911A1/fr unknown
- 2019-02-04 CA CA3090272A patent/CA3090272A1/fr active Pending
- 2019-02-04 CN CN201980024089.6A patent/CN112135635A/zh active Pending
- 2019-02-04 KR KR1020207025177A patent/KR20200118828A/ko not_active Application Discontinuation
-
2020
- 2020-08-02 IL IL276442A patent/IL276442A/en unknown
- 2020-08-03 PH PH12020551178A patent/PH12020551178A1/en unknown
-
2024
- 2024-02-13 JP JP2024019158A patent/JP2024073414A/ja active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2461683B1 (fr) | Analogues d'arylsphingosine-1-phosphate bicycliques | |
JP2023113615A (ja) | Tead転写因子の新規小分子阻害剤 | |
BR112021005606A2 (pt) | processo de produção de um composto para inibir a atividade de shp2 | |
US8901106B2 (en) | Imidazole prodrug LXR modulators | |
JP2022529166A (ja) | 低酸素誘導因子2(アルファ)阻害剤としてのテトラヒドロ-1H-シクロペンタ[cd]インデン誘導体 | |
EA019309B1 (ru) | Модуляторы ampk (амф-активируемой протеинкиназы) | |
TW201808958A (zh) | 趨化介素受體調節劑及其用途 | |
JP2016531937A (ja) | キナゾリン誘導体及びその製造方法 | |
DK3044211T3 (en) | ANTIBACTERIAL 2H INDEZOL DERIVATIVES | |
CN107848952B (zh) | 稠合三环γ-氨基酸衍生物及其制备方法和在医药上的应用 | |
JP2018513832A5 (fr) | ||
JP2003528146A (ja) | 脳血管疾患の治療 | |
JP2006525227A (ja) | アミノシクロヘキシルエーテル化合物およびそれらの用途 | |
US10633399B2 (en) | Functionalized aminobenzoboroxoles | |
EA032094B1 (ru) | Дейтерированный палбоциклиб | |
WO2019204442A1 (fr) | Modulateurs de k-ras possédant une fraction cyanoacrylamide | |
CA3116129A1 (fr) | Radioligands pour l'imagerie du recepteur lpa1 | |
TWI834127B (zh) | 噻吩類化合物及其應用 | |
KR20200035720A (ko) | 3-아자바이사이클로[3,1,1]헵탄 유도체 및 이를 포함하는 약제학적 조성물 | |
TWI765640B (zh) | 作為dna-pk抑制劑的氨基嘧啶化合物及其衍生物 | |
KR950005823A (ko) | 5-아미노-8-메틸-7-피롤리디닐퀴놀린-3-카르본산유도체 | |
JPWO2020190774A5 (fr) | ||
MX2011006974A (es) | Metodo para preparar acido (+)-1,4-dihidro-7-[(3s,4s)-3-metoxi-4-( metilamino)-1-pirrolidinil]-4-oxo-1-) (2-tiazolil)-1, 8-naftiridin-3-carboxilico. | |
JP2010513533A (ja) | プロスタサイクリン誘導体 | |
JPWO2019152911A5 (fr) |