CN108348523A - 包含pi3k抑制剂和hdac抑制剂的组合物 - Google Patents
包含pi3k抑制剂和hdac抑制剂的组合物 Download PDFInfo
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- CN108348523A CN108348523A CN201680058695.6A CN201680058695A CN108348523A CN 108348523 A CN108348523 A CN 108348523A CN 201680058695 A CN201680058695 A CN 201680058695A CN 108348523 A CN108348523 A CN 108348523A
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- alkyl
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- 0 CC(C)CC1=CCCN(C)*=C1 Chemical compound CC(C)CC1=CCCN(C)*=C1 0.000 description 4
- IMRWILPUOVGIMU-UHFFFAOYSA-N Brc1ncccc1 Chemical compound Brc1ncccc1 IMRWILPUOVGIMU-UHFFFAOYSA-N 0.000 description 1
- POOPWPIOIMBTOH-UHFFFAOYSA-N C(C1)C2OC1CNC2 Chemical compound C(C1)C2OC1CNC2 POOPWPIOIMBTOH-UHFFFAOYSA-N 0.000 description 1
- QJIFFAMGOQBKPK-GDVGLLTNSA-N C1[C@@H]2OCC1CNC2 Chemical compound C1[C@@H]2OCC1CNC2 QJIFFAMGOQBKPK-GDVGLLTNSA-N 0.000 description 1
- BMCPUEAFQUTTRV-RQPIMZLSSA-N C=C/C(/CN(c1nccnc1)C1=NCCN=C1)=C\C=C\C(NO)=O Chemical compound C=C/C(/CN(c1nccnc1)C1=NCCN=C1)=C\C=C\C(NO)=O BMCPUEAFQUTTRV-RQPIMZLSSA-N 0.000 description 1
- CDRLDQZAUSVLHW-UHFFFAOYSA-N CC(CC=C1)(c2c1[nH]cc2)c(nc1N2CCOCC2)nc2c1[o]c1ncc(CN3CC(C4)OCC4C3)cc21 Chemical compound CC(CC=C1)(c2c1[nH]cc2)c(nc1N2CCOCC2)nc2c1[o]c1ncc(CN3CC(C4)OCC4C3)cc21 CDRLDQZAUSVLHW-UHFFFAOYSA-N 0.000 description 1
- IMSKCQSWQHRTGF-AATRIKPKSA-N CC/C=C(\CC)/F Chemical compound CC/C=C(\CC)/F IMSKCQSWQHRTGF-AATRIKPKSA-N 0.000 description 1
- CKMSZFGOIMTDBM-HTQZYQBOSA-N CCC[IH]N1[C@H](C2)CO[C@H]2C1 Chemical compound CCC[IH]N1[C@H](C2)CO[C@H]2C1 CKMSZFGOIMTDBM-HTQZYQBOSA-N 0.000 description 1
- BTADFWJICGCHEJ-UHFFFAOYSA-N CN(CC1)CC1(CC1)CCN1I Chemical compound CN(CC1)CC1(CC1)CCN1I BTADFWJICGCHEJ-UHFFFAOYSA-N 0.000 description 1
- FIAOXPWVBZEARE-UHFFFAOYSA-N CN(CC1)CC1(CC1)CN1I Chemical compound CN(CC1)CC1(CC1)CN1I FIAOXPWVBZEARE-UHFFFAOYSA-N 0.000 description 1
- OJRXAGPLRKXVSF-UHFFFAOYSA-N COC(c1ccc(CN(c2nc3ccccc3[o]2)c2ncccc2)cc1)=O Chemical compound COC(c1ccc(CN(c2nc3ccccc3[o]2)c2ncccc2)cc1)=O OJRXAGPLRKXVSF-UHFFFAOYSA-N 0.000 description 1
- UVQLDCUYKWWFKI-UHFFFAOYSA-N COC(c1ccc(CN(c2nccnc2)C2=NC#CCN=C2)cc1)=O Chemical compound COC(c1ccc(CN(c2nccnc2)C2=NC#CCN=C2)cc1)=O UVQLDCUYKWWFKI-UHFFFAOYSA-N 0.000 description 1
- POLWGSSYYZOBPA-UHFFFAOYSA-N COc1cccnc1Nc(cc1)ncc1N1CCOCC1 Chemical compound COc1cccnc1Nc(cc1)ncc1N1CCOCC1 POLWGSSYYZOBPA-UHFFFAOYSA-N 0.000 description 1
- ODOKOLBDMAQALP-UHFFFAOYSA-N Cc1cccc(Nc(cc2)ncc2N2CCOCC2)n1 Chemical compound Cc1cccc(Nc(cc2)ncc2N2CCOCC2)n1 ODOKOLBDMAQALP-UHFFFAOYSA-N 0.000 description 1
- ODKIKYREQOEZER-UHFFFAOYSA-N IN1CCC2(COC2)CC1 Chemical compound IN1CCC2(COC2)CC1 ODKIKYREQOEZER-UHFFFAOYSA-N 0.000 description 1
- OYWPFIUVDKHHGQ-UHFFFAOYSA-N Ic1nccnc1 Chemical compound Ic1nccnc1 OYWPFIUVDKHHGQ-UHFFFAOYSA-N 0.000 description 1
- HZAXXQRCTLQBFN-UHFFFAOYSA-N Nc1cnc(CC2CC2)cn1 Chemical compound Nc1cnc(CC2CC2)cn1 HZAXXQRCTLQBFN-UHFFFAOYSA-N 0.000 description 1
- JPBLHOJFMBOCAF-UHFFFAOYSA-N Nc1nc(cccc2)c2[o]1 Chemical compound Nc1nc(cccc2)c2[o]1 JPBLHOJFMBOCAF-UHFFFAOYSA-N 0.000 description 1
- AKUBFRFGXUVGAO-UHFFFAOYSA-N [U]=Cc(cn1)cc2c1[o]c1c2nc(-c2c(cc[nH]3)c3ccc2)nc1N1CCOCC1 Chemical compound [U]=Cc(cn1)cc2c1[o]c1c2nc(-c2c(cc[nH]3)c3ccc2)nc1N1CCOCC1 AKUBFRFGXUVGAO-UHFFFAOYSA-N 0.000 description 1
- NEFSIDNQUCABGN-UHFFFAOYSA-N c1cc(Nc2cnccn2)nnc1 Chemical compound c1cc(Nc2cnccn2)nnc1 NEFSIDNQUCABGN-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
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- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/4965—Non-condensed pyrazines
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
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- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1514756.4A GB201514756D0 (en) | 2015-08-19 | 2015-08-19 | Compound and method of use |
| GB1514756.4 | 2015-08-19 | ||
| PCT/GB2016/052571 WO2017029514A1 (en) | 2015-08-19 | 2016-08-19 | Compositions comprising a pi3k inhibitor and an hdac inhibitor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN108348523A true CN108348523A (zh) | 2018-07-31 |
Family
ID=54258855
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201680058695.6A Pending CN108348523A (zh) | 2015-08-19 | 2016-08-19 | 包含pi3k抑制剂和hdac抑制剂的组合物 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20180243317A1 (enExample) |
| EP (2) | EP3456355A1 (enExample) |
| JP (1) | JP2018528192A (enExample) |
| KR (1) | KR20180069788A (enExample) |
| CN (1) | CN108348523A (enExample) |
| AU (1) | AU2016307882A1 (enExample) |
| BR (1) | BR112018003026A2 (enExample) |
| CA (1) | CA2995991A1 (enExample) |
| GB (1) | GB201514756D0 (enExample) |
| HK (1) | HK1251466A1 (enExample) |
| IL (1) | IL257521A (enExample) |
| MX (1) | MX2018001990A (enExample) |
| SG (1) | SG10201913619XA (enExample) |
| WO (1) | WO2017029514A1 (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111686097A (zh) * | 2020-07-31 | 2020-09-22 | 上海交通大学医学院附属第九人民医院 | Lmk235在抑制瘢痕形成的药物中的应用 |
| CN114890989A (zh) * | 2022-05-25 | 2022-08-12 | 佛山市晨康生物科技有限公司 | 一种含氮衍生物为Linker的HDAC8降解剂其制备方法和应用 |
| CN116987073A (zh) * | 2023-08-03 | 2023-11-03 | 嘉兴学院 | 一种PI3Kα/HDAC6亚型选择性双重抑制剂及其应用 |
| WO2024184266A1 (en) * | 2023-03-03 | 2024-09-12 | Ionctura Sa | Combination of roginolisib and hdac inhibitor in the treatment of haematological malignancy |
| CN118750492A (zh) * | 2024-07-15 | 2024-10-11 | 中日友好医院(中日友好临床医学研究所) | 一种hdac6高选择抑制剂cay10603的应用 |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5746172B2 (ja) | 2009-08-20 | 2015-07-08 | カルス セラピューティクス リミテッド | ホスホイノシチド3−キナーゼ阻害剤としての三環式複素環化合物 |
| GB201204125D0 (en) | 2012-03-08 | 2012-04-25 | Karus Therapeutics Ltd | Compounds |
| EP2994465B1 (en) | 2013-05-10 | 2018-08-15 | Karus Therapeutics Limited | Novel histone deacetylase inhibitors |
| GB201402431D0 (en) | 2014-02-12 | 2014-03-26 | Karus Therapeutics Ltd | Compounds |
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- 2016-08-19 SG SG10201913619XA patent/SG10201913619XA/en unknown
- 2016-08-19 BR BR112018003026A patent/BR112018003026A2/pt not_active IP Right Cessation
- 2016-08-19 CA CA2995991A patent/CA2995991A1/en not_active Abandoned
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| CN114890989B (zh) * | 2022-05-25 | 2024-03-22 | 广东晨康生物科技有限公司 | 一种含氮衍生物为Linker的HDAC8降解剂其制备方法和应用 |
| WO2024184266A1 (en) * | 2023-03-03 | 2024-09-12 | Ionctura Sa | Combination of roginolisib and hdac inhibitor in the treatment of haematological malignancy |
| CN116987073A (zh) * | 2023-08-03 | 2023-11-03 | 嘉兴学院 | 一种PI3Kα/HDAC6亚型选择性双重抑制剂及其应用 |
| CN118750492A (zh) * | 2024-07-15 | 2024-10-11 | 中日友好医院(中日友好临床医学研究所) | 一种hdac6高选择抑制剂cay10603的应用 |
Also Published As
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|---|---|
| EP3337484A1 (en) | 2018-06-27 |
| WO2017029514A1 (en) | 2017-02-23 |
| MX2018001990A (es) | 2018-06-19 |
| AU2016307882A1 (en) | 2018-03-08 |
| US20180243317A1 (en) | 2018-08-30 |
| SG10201913619XA (en) | 2020-03-30 |
| KR20180069788A (ko) | 2018-06-25 |
| HK1251466A1 (zh) | 2019-02-01 |
| CA2995991A1 (en) | 2017-02-23 |
| GB201514756D0 (en) | 2015-09-30 |
| BR112018003026A2 (pt) | 2018-09-18 |
| IL257521A (en) | 2018-04-30 |
| JP2018528192A (ja) | 2018-09-27 |
| EP3456355A1 (en) | 2019-03-20 |
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