JP2023500857A - 新規な化合物およびそれを含むがんの予防または治療用薬学組成物 - Google Patents
新規な化合物およびそれを含むがんの予防または治療用薬学組成物 Download PDFInfo
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- JP2023500857A JP2023500857A JP2022525398A JP2022525398A JP2023500857A JP 2023500857 A JP2023500857 A JP 2023500857A JP 2022525398 A JP2022525398 A JP 2022525398A JP 2022525398 A JP2022525398 A JP 2022525398A JP 2023500857 A JP2023500857 A JP 2023500857A
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- 229940031439 squalene Drugs 0.000 description 1
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- 229940124597 therapeutic agent Drugs 0.000 description 1
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- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
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- 230000001131 transforming effect Effects 0.000 description 1
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Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
Abstract
Description
本出願は、新規な化合物および前記化合物またはその薬学的に許容可能な塩を含むがんの予防または治療用薬学組成物に関する。
また、本出願の他の一態様は、新規な化合物を含むがんの予防または治療用薬学組成物を提供することにある。
また、本出願の他の一態様は、新規な化合物を含む耐性がんの予防または治療用薬学組成物を提供することにある。
また、本出願の他の一態様は、新規な化合物の耐性がんの予防または治療用途を提供することにある。
本出願の解決課題は、以上で言及されたものに限定されず、言及されていない他の解決課題は、下記の記載から当業者が明確に理解できる。
R1は、水素、直鎖または分岐鎖アルキル、アルコキシ、ハロアルキル、ハロアルコキシ、アリール、ヘテロアリール、アルキルアリールまたはアルキルヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C3~C6シクロアルキル、C1~C6ハロアルキル、C1~C6ハロアルコキシ、オキソ、シアノ、非置換もしくは置換のアリール、または非置換もしくは置換のヘテロアリールのうち少なくとも一つで置換されてもよく;
R2とR4は、5員~10員のモノサイクリックまたはビサイクリック環を形成することで連結されてもよく、ここで、R4′は、水素であり;
mは、1または2の整数であり、nは、1~4の整数であり;
本出願の一実施例は、前記化学式1またはその薬学的に許容可能な塩のうち少なくとも一つを含む耐性がんの治療または予防用薬学組成物を提供する。
本出願の一実施例による化合物またはその薬学的に許容可能な塩を含む組成物は、幹細胞性がんを効果的に治療することができる。
本出願による効果は、以上で例示された内容によって限定されず、さらに多様な効果が本明細書内に含まれている。
本明細書において使用される「ハロ」という用語は、クロロ、ブロモ、ヨードおよびフルオロを含む。
本出願の一実施例は、下記化学式1で表される化合物またはその薬学的に許容可能な塩を提供する。
置換もしくは置換のC1~C4直鎖アルキル,
本出願による化合物は、下記表1の化学式からなる群から選ばれた少なくとも一つの化合物でありうるが、これに限定されない。
本明細書において使用される「薬学的に許容可能な塩」は、薬学的に許容可能な本出願の化合物の有機または無機塩をいう。
本出願の一実施例による薬学組成物は、カプセル、錠剤、顆粒、注射剤、軟膏剤、粉末または飲料形態でありうる。
また、本出願は、耐性がんの治療に使用するための化学式1で表される化合物またはその薬学的に許容可能な塩の用途を提供する。
また、本出願は、幹細胞性がんの治療に使用するための化学式1で表される化合物またはその薬学的に許容可能な塩の用途を提供する。
耐性がんと、化学式1で表される化合物またはその薬学的に許容可能な塩は、前述した内容と同一で、具体的な説明は省略する。
用語「投与」は、適切な方法で個体に所定の物質を導入することを意味する。
耐性がん、耐性がんを有する対象、化学式1で表される化合物またはその薬学的に許容可能な塩は、前述した内容と同一で、具体的な説明は省略する。
下記製造例の方法で表1の化合物を製造した。
[化学式7]
1)段階1
2)段階2
3)段階3
4)段階4
5)段階5
6)段階6
7)段階7
8)段階8
9)段階9
10)段階10
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 344.1427, found 344.1423.
MS (ESI) m/z for C19H23N3O2S [M+H]+ : calcd 358.1584, found 358.1579.
MS (ESI) m/z for C22H29N3O2S [M+H]+ :calcd 400.2053, found 400.4056.
MS (ESI) m/z for C24H31N3O2S [M+H]+ :calcd 426.2210, found 426.2210.
MS (ESI) m/z for C21H23N3O2S [M+H]+ :calcd 382.1584, found 382.1594.
MS (ESI) m/z for C21H27N3O2S2 [M+H]+ :calcd 418.1618, found 418.1618.
MS (ESI) m/z for C26H29N3O2S2 [M+H]+ :calcd 480.1774, found 480.1782.
MS (ESI) m/z for C21H25N3O2S [M+H]+ :calcd 384.1740, found 384.1746.
MS (ESI) m/z for C25H27N3O2S [M+H]+ :calcd 434.1897, found 434.1895.
MS (ESI) m/z for C25H26ClN3O2S [M+H]+ :calcd 468.1507, found 468.1507.
MS (ESI) m/z for C25H26BrN3O2S [M+H]+ :calcd 512.1002, found 512.1002.
MS (ESI) m/z for C25H26FN3O2S [M+H]+ :calcd 452.1803, found 452.1798.
MS (ESI) m/z for C25H25F2N3O2S [M+H]+ :calcd 470.1708, found 470.1702.
MS (ESI) m/z for C26H26F3N3O2S [M+H]+ :calcd 502.1771, found 502.1758.
MS (ESI) m/z for C26H26N4O2S [M+H]+ :calcd 459.1849, found 459.1833.
MS (ESI) m/z for C25H26N4O4S [M+H]+ :calcd 479.1748, found 479.1732.
MS (ESI) m/z for C31H31N3O2S [M+H]+ :calcd 510.2210, found 510.2193.
MS (ESI) m/z for C32H33N3O3S [M+H]+ :calcd 540.2315, found 540.2292.
MS (ESI) m/z for C29H29N3O2S [M+H]+ : calcd 484.2053, found 484.2047
MS (ESI) m/z for C29H29N3O2S [M+H]+ : calcd 484.2053, found 484.2044
MS (ESI) m/z for C22H29N3O2S [M+H]+ : calcd 400.2053, found 400.2053.
MS (ESI) m/z for C24H25N3O2S [M+H]+ : calcd 420.1740, found 420.1740.
MS (ESI) m/z for C22H27N3O2S [M+H]+ : calcd 398.1897, found 398.1891.
MS (ESI) m/z for C26H27N3O2S [M+H]+ :calcd 446.1896, found 446.1889.
MS (ESI) m/z for C25H33N3O3S [M+H]+ :calcd 456.2315, found 465.2308.
MS (ESI) m/z for C32H39N3O2S [M+H]+ : calcd 530.2836, found 530.2824.
MS (ESI) m/z for C32H33N3O2S [M+H]+ :calcd 524.2366, found 524.2364.
MS (ESI) m/z for C31H43N3O2S [M+H]+ : calcd 522.3154, found 522.3143.
MS (ESI) m/z for C31H37N3O2S [M+H]+ : calcd 516.2679, found 516.2677.
MS (ESI) m/z for C19H23N3O2S [M+H]+ : calcd 358.1584, found 358.1576.
MS (ESI) m/z for C20H25N3O2S [M+H]+ : calcd 372.1740, found 372.1734.
MS (ESI) m/z for C22H29N3O2S [M+H]+ : calcd 400.2053, found 400.2042.
MS (ESI) m/z for C24H33N3O2S [M+H]+ : calcd 428.2366, found 428.2352.
MS (ESI) m/z for C25H27N3O2S [M+H]+ : calcd 434.1897, found 434.1892.
MS (ESI) m/z for C26H29N3O2S [M+H]+ : calcd 448.2053, found 448.2055.
MS (ESI) m/z for C25H26ClN3O2S [M+H]+ : calcd 468.1507, found 468.1477.
MS (ESI) m/z for C25H26BrN3O2S [M+H]+ : calcd 512.1002, found 512.0997.
MS (ESI) m/z for C25H26FN3O2S [M+H]+ : calcd 452.1803, found 452.1781.
MS (ESI) m/z for C26H26F3N3O2S [M+H]+ : calcd 502.1771, found 502.1766.
MS (ESI) m/z for C26H26N4O2S [M+H]+ : calcd 459.1849, found 459.1828.
MS (ESI) m/z for C25H26N4O4S [M+H]+ : calcd 479.1748, found 479.1727.
MS (ESI) m/z for C31H31N3O2S [M+H]+ : calcd 510.2210, found 510.2210.
MS (ESI) m/z for C26H29N3O2S [M+H]+ : calcd 448.2053, found 448.2026.
MS (ESI) m/z for C26H28FN3O2S [M+H]+ : calcd 466.1959, found 466.1935.
MS (ESI) m/z for C25H33N3O2S [M+H]+ : calcd 440.2366, found 440.2360.
MS (ESI) m/z for C29H29N3O2S [M+H]+ : calcd 484.2053, found 484.2053.
MS (ESI) m/z for C29H29N3O2S [M+H]+ : calcd 484.2053, found 484.2041.
MS (ESI) m/z for C26H29N3O3S [M+H]+ : calcd 464.2002, found 464.1991.
MS (ESI) m/z for C27H31N3O4S [M+H]+ : calcd 494.2108, found 494.2101.
MS (ESI) m/z for C16H17N3O2S [M+H]+ : calcd 316.112, found 316.1115.
MS (ESI) m/z for C17H19N3O2S [M+H]+ : calcd 330.1276, found 330.1273.
MS (ESI) m/z for C20H25N3O2S [M+H]+ : calcd 372.1746, found 372.1748.
MS (ESI) m/z for C22H29N3O2S [M+H]+ : calcd 400.2059, found 400.2070.
MS (ESI) m/z for C23H23N3O2S [M+H]+ : calcd 406.1589, found 406.1605.
MS (ESI) m/z for C24H25N3O2S [M+H]+ : calcd 420.1746, found 420.1740.
MS (ESI) m/z for C23H22ClN3O2S [M+H]+ : calcd 440.12, found 440.1199.
MS (ESI) m/z for C23H22BrN3O2S [M+H]+ : calcd 484.0694, found 484.0660.
MS (ESI) m/z for C23H22FN3O2S [M+H]+ : calcd 424.1495, found 424.1490.
MS (ESI) m/z for C29H27N3O2S [M+H]+ : calcd 482.1902, found 482.1898.
MS (ESI) m/z for C23H29N3O2S [M+H]+ : calcd 412.2059, found 412.2052.
MS (ESI) m/z for C24H26N4O2 [M+Na]+ :calcd 425.1948, found 425.1949.
MS (ESI) m/z for C23H23BrN4O2 [M+H]+ :calcd 467.1077, found 467.1079.
MS (ESI) m/z for C24H26N4O3 [M+H]+ :calcd 419.2078, found 419.2070.
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 529.2598, found 529.2598.
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 529.2598, found 529.2605.
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 479.2442, found 479.2446.
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 555.2755, found 555.2752.
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 530.2551, found 530.2549.
MS (ESI) m/z for C30H30N4O3 [M+H]+ :calcd 495.2390, found 495.2386.
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 465.2285, found 465.2281.
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 451.2129, found 451.2129.
MS (ESI) m/z for C18H21N3O2S [M+H]+ : calcd 431.2078, found 431.2072.
MS (ESI) m/z for C17H17N3O3S [M+H]+ :calcd 344.1063, found 344.1061.
MS (ESI) m/z for C16H16N4O2 [M+H]+ : calcd 299.1502, found 299.1502.
1.SKOV3とSKOV3-TRの準備
上皮性卵巣がん細胞株であるSKOV3とこれに由来してパクリタキセル(Paclitaxel)抗がん剤に抵抗性を有する耐性がん細胞株で製作されたSKOV3-TRを対象に細胞実験を進め、図1(a)は、SKOV3のパクリタキセル抗がん剤IC50値を示す図であり、(b)は、SKOV3-TRのパクリタキセル抗がん剤IC50値を示す図である。図2(a)は、SKOV3のドセタキセル抗がん剤IC50値を示す図であり、(b)は、SKOV3-TRのドセタキセル抗がん剤IC50値を示す図である。
細胞の物質代謝を分析するWST-1分析結果によれば、パクリタキセル処理によってSKOV3-TRおよびSKOV3で物質代謝の減少を誘発した。パクリタキセルのSKOV3-TRの102種に対するWST-1分析結果とSKOV3の102種に対するWST-1分析結果を図3~図10に示した。
細胞生存率および細胞数を分析するCrystal violet染色によれば、パクリタキセル処理によってSKOV3-TRおよびSKOV3で細胞生存率減少を通した細胞数減少を誘発した。代表的にパクリタキセルとドセタキセル抗がん増強効能を示したS101とS105をSKOV3-TRおよびSKOV3細胞株でパクリタキセルとドセタキセルを3日間単独処理したり、パクリタキセルまたはドセタキセルと3日間併用処理した後、イメージをキャプチャーした。パクリタキセルに対するSKOV3-TRのCrystal violet染色結果を図11に示し、SKOV3のCrystal violet染色結果を図12に示した。ドセタキセルに対するSKOV3-TRのCrystal violet染色結果を図25に示し、SKOV3のCrystal violet染色結果を図26に示した。
1)細胞数変化の分析(In vitro)
幹細胞性がん細胞であるselected-MDA-MB231 cellとselected-MCF7に対してER stressがないG(+):glucoseが存在するときとER stressがあるG(-):glucoseが存在しないときのS101化合物100、50、10nMを処理後に細胞数の変化を図31に示し、Crystal violetで染色したイメージをキャプチャーした結果を図32に示した。また、glucose deprivation後、S101のがん細胞死滅効果をTUNEL assayで測定して図33に示した。
Cancer stem cellで証明されたselected-MDA-MB231 cellをin vitroで培養してharvest後、mouse in vivoモデルを構築して抗がん効果を検証した。Control groupとsevere ER stressを誘発し、抗がん剤の代用として2-deoxy-d-glucoseを使用したものを比較例1(2DG)とした。S101 2mgを単独使用したものを実施例2(S101単独)とし、2-deoxy-d-glucose 10mgとS101 2mgを使用したものを実施例3(S101+2DG、2mg:10mg)として検証した。tumor体積の変化結果を図34に示した。Dissected tumorの重さとサイズを各group間に比較した結果をそれぞれ図35の(a)および(b)に示した。selected-MDA-MB231 cell xenograft modelでS101と2DG併用抗がん効果の測定時に各group間のbody wight変化量を測定して図36に示した。
Claims (15)
- 下記化学式1:
R1は、水素、直鎖または分岐鎖アルキル、アルコキシ、ハロアルキル、ハロアルコキシ、アリール、ヘテロアリール、アルキルアリールまたはアルキルヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C3~C6シクロアルキル、C1~C6ハロアルキル、C1~C6ハロアルコキシ、オキソ、シアノ、非置換もしくは置換のアリール、または非置換もしくは置換のヘテロアリールのうち少なくとも一つで置換されてもよく;
R3は、水素、直鎖または分岐鎖アルキル、シクロアルキル、アリール、ヘテロアリール、アルキルアリールまたはアルキルヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~C6ハロアルコキシ、オキソ、シアノ、非置換もしくは置換のアリール、または非置換もしくは置換のヘテロアリールのうち少なくとも一つで置換されてもよく;
L1は、C1~C10アルキレンであり、ここで、前記アルキレンは、C1~C6アルキル、C3~C6シクロアルキル、C1~C6アルコキシ、ヒドロキシル、オキソまたはハロゲンのうち少なくとも一つで置換されてもよく、前記C1~C6アルキル、C3~C6シクロアルキル、C1~C6アルコキシは、非置換もしくは置換のアリールで置換されてもよく;
Qは、S、Se、NR、P、P(O)、P(O)2またはP(O)ORであり、ここで、前記Rは、水素、直鎖または分岐鎖アルキル、シクロアルキル、ビまたはトリシクロアルキル、アルコキシ、ハロアルキル、ハロアルコキシ、アリール、ヘテロアリール、アルキルアリールまたはアルキルヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~C6ハロアルコキシ、オキソ、シアノ、非置換もしくは置換のアリール、または非置換もしくは置換のヘテロアリールのうち少なくとも一つで置換されてもよく;
R2は、水素、直鎖アルキル、シクロアルキル、アルコキシ、ハロアルコキシ、ハロアルキル、アリール、ヘテロアリール、アルキルアリールまたはアルキルヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~C6ハロアルコキシ、非置換もしくは置換のアリール、非置換もしくは置換のヘテロアリール、オキソ、ニトロ、シアノまたはトリフルオロメチルのうち少なくとも一つで置換されてもよく;
R4およびR4′は、それぞれ独立して、水素、直鎖または分岐鎖アルキル、シクロアルキル、アルケニル、アルキニル、アルキルチオ、アリール、ヘテロアリール、アルキルアリールまたはアルキルヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~C6ハロアルコキシ、非置換もしくは置換のアリール、非置換もしくは置換のヘテロアリール、オキソ、ニトロ、シアノまたはトリフルオロメチルのうち少なくとも一つで置換されてもよく;
R2とR4は、5員~10員のモノサイクリックまたはビサイクリック環を形成することで連結されてもよく、ここで、R4′は、水素であり;
mは、1または2の整数であり、nは、1~4の整数であり;
X、Y、Zは、それぞれ独立して、水素、直鎖または分岐鎖アルキル、シクロアルキル、アリール、ヘテロアリール、アルキルアリールまたはアルキルヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~C6ハロアルコキシ、非置換もしくは置換のアリール、非置換もしくは置換のヘテロアリール、オキソ、ニトロ、シアノ、またはトリフルオロメチルのうち少なくとも一つで置換されてもよい。)
で表される
ことを特徴とする化合物またはその薬学的に許容可能な塩: - 前記mとnは、1である
請求項1に記載の化合物またはその薬学的に許容可能な塩。 - 前記R1は、水素、C1~C6直鎖アルキル、C3~C6分岐鎖アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~C6ハロアルコキシ、アリール、ヘテロアリール、アルキル(C1~C6)アリールまたはアルキル(C1~C6)ヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C3~C6シクロアルキル、C1~C6ハロアルキル、C1~C6ハロアルコキシ、オキソ、シアノ、非置換もしくは置換のC6~C10アリール、または非置換もしくは置換のC5~C10ヘテロアリールのうち少なくとも一つで置換されてもよく;
前記R3は、水素、C1~C6直鎖アルキル、C3~C6分岐鎖アルキル、C3~C6シクロアルキル、アリール、ヘテロアリール、アルキル(C1~C6)アリールまたはアルキル(C1~C6)ヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~
C6ハロアルコキシ、オキソ、シアノ、非置換もしくは置換のC6~C10アリール、または非置換もしくは置換のC5~C10ヘテロアリールのうち少なくとも一つで置換されてもよく;
前記R2は、水素、C1~C6直鎖アルキル、C3~C6シクロアルキル、C1~C6アルコキシ、C1~C6ハロアルコキシ、C1~C6ハロアルキル、アリール、ヘテロアリール、アルキル(C1~C6)アリールまたはアルキル(C1~C6)ヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~C6ハロアルコキシ、非置換もしくは置換のC6~C10アリール、非置換もしくは置換のC5~C10ヘテロアリール、オキソ、ニトロ、シアノまたはトリフルオロメチルのうち少なくとも一つで置換されてもよく;
前記R4およびR4′は、それぞれ独立して、水素、C1~C6直鎖アルキル、C3~C6分岐鎖アルキル、C3~C6シクロアルキル、C2~C6アルケニル、C2~C6アルキニル、C1~C6アルキルチオ、アリール、ヘテロアリール、アルキル(C1~C6)アリールまたはアルキル(C1~C6)ヘテロアリールであり、これら各々は、独立して、ヒドロキシル、ハロゲン、C1~C6アルキル、C1~C6アルコキシ、C1~C6ハロアルキル、C1~C6ハロアルコキシ、非置換もしくは置換のC6~C10アリール、非置換もしくは置換のC5~C10ヘテロアリール、オキソ、ニトロ、シアノまたはトリフルオロメチルのうち少なくとも一つで置換されてもよく;
R2とR4は、5員~10員のモノサイクリックまたはビサイクリック環を形成することで連結されてもよく、ここで、R4′は、水素である
請求項2に記載の化合物またはその薬学的に許容可能な塩。 - 前記R1は、水素、非置換もしくは置換のC1~C6直鎖アルキル、非置換もしくは置換のベンジル、または非置換もしくは置換の2-フェニルエチルであり、ここで、前記置換のC1~C6直鎖アルキルは、C3~C6シクロアルキルで置換されたものであり、前記置換のベンジルまたは前記置換の2-フェニルエチルは、オルト、メタおよびパラ位置のうち少なくとも一つがハロで置換されるか、フェニルで置換されたものであり;
前記R3は、水素、非置換もしくは置換のC1~C6直鎖アルキル、非置換もしくは置換のC1~C6アルコキシ、ハロゲン、または非置換もしくは置換の2-フェニルエチルであり、ここで、前記置換の2-フェニルエチルは、オルト、メタおよびパラ位置のうち少なくとも一つがハロで置換されたものであり、前記置換のC1~C6アルコキシは、フェニルまたはベンジルで置換されたものであり;
前記L1は、C1~C4アルキレンであり、ここで、前記アルキレンは、水素、オキソ、ヒドロキシル、C1~C4アルコキシまたはC1~C4アルキルで置換されたものであり、前記C1~C4アルコキシは、ベンジルで置換されたものであり;
前記R2は、水素、非置換もしくは置換のC1~C6直鎖アルキル、非置換もしくは置換のベンジル、または非置換もしくは置換の2-フェニルエチルであり、ここで、前記置換の直鎖アルキルは、ハロで置換されたものであり、前記置換のベンジルは、オルト、メタおよびパラ位置のうち少なくとも一つがハロ、C1~C3直鎖アルキル、トリフルオロメチル、シアノ、ニトロ、C1~C3アルコキシまたはアリールで置換されたものであり、前記2-フェニルエチルは、オルト、メタおよびパラ位置のうち少なくとも一つがハロで置換されたものであり;
前記R4およびR4′は、それぞれ独立して、水素、非置換もしくは置換のC1~C6直鎖アルキル、C3~C6分岐鎖アルキル、C3~C6シクロアルキル、C2~C6アルキニル、C1~C6アルキルチオ、非置換もしくは置換のベンジル、2-ナフチルメチルまたは1-ナフチルメチルであり、ここで、前記置換の直鎖アルキルは、メチルチオ、アルキニルまたはベンジルオキシカルボニルアミノで置換されたものであり、前記置換のベンジルは、オルト、メタおよびパラ位置のうち少なくとも一つがハロ、アリール、ニトロ、シアノ、C1~C3アルコキシ、トリフルオロメチルまたはベンジルオキシで置換されてもよく;
R2とR4は、5員~10員のモノサイクリックまたはビサイクリック環を形成することで連結されてもよく、ここで、R4′は、水素である
請求項2に記載の化合物またはその薬学的に許容可能な塩。 - 請求項1ないし7のいずれかに記載の化合物、その薬学的に許容可能な塩、水和物、溶媒和物、構造異性体、光学異性体、立体異性体、またはこれらの組み合わせを含む
ことを特徴とするがんまたは耐性がんの予防または治療用薬学組成物。 - 前記耐性がんは、
抗がん薬物に対する耐性を有するか、放射能に対する耐性を有する
請求項8に記載のがんまたは耐性がんの予防または治療用薬学組成物。 - 前記耐性がんは、
卵巣がん、大腸がん、すい臓がん、胃がん、肝がん、乳がん、子宮頸がん、甲状腺がん、副甲状腺がん、肺がん、非小細胞性肺がん、前立腺がん、胆のうがん、胆道がん、血液がん、膀胱がん、腎臓がん、黒色腫、結腸がん、骨がん、皮膚がん、頭頸部がん、子宮がん、直腸がん、脳がん、肛門付近がん、ラッパ管がん腫、子宮内膜がん腫、膣がん、陰門がん腫、食道がん、小腸がん、内分泌腺がん、副腎がん、軟組織肉腫、尿道がん、陰茎がん、輸尿管がん、腎臓細胞がん腫、腎臓骨盤がん腫、中枢神経系(central nervous system;CNS)腫瘍、脊髄腫瘍、脳幹神経膠腫および脳下垂体腺腫からなる群から選ばれた少なくとも一つである
請求項8に記載のがんまたは耐性がんの予防または治療用薬学組成物。 - 前記抗がん薬物は、
ナイトロジェンマスタード、イマチニブ、オキサリプラチン、リツキシマブ、エルロチニブ、ネラチニブ、ラパチニブ、ゲフィチニブ 、バンデタニブ、ニロチニブ、セマサニブ、ボスチニブ、アキシチニブ、マシチニブ、セジラニブ、レスタウルチニブ、トラスツズマブ、ゲフィチニブ、ボルテゾミブ、スニチニブ、パゾパニブ、トセラニブ、ニンテダニブ、レゴラフェニブ、セマクサニブ、チボザニブ、ポナチニブ、カボザンチニブカルボプラチン、ソラフェニブ、レンバチニブ、ベバシズマブ、シスプラチン、セツキシマブ、ビスカムアルバム、アスパラギナーゼ、トレチノイン、ヒドロキシカルバミド、ダサチニブ、エストラムスチン、ゲムツズマブオゾガマイシン、イブリツモマブチウキセタン、ヘプタプラチン、メチルアミノレブリン酸、アムサクリン、アレムツズマブ、プロカルバジン、アルプロスタジル、硝酸ホルミウムキトサン、ゲムシタビン、ドキシフルリジン、ペメトレキセド、テガフール、カペシタビン、ギメラシン、オテラシル、アザシチジン、メトトレキサート、ウラシル、シタラビン、5-フルオロウラシル、フルダラビン、エノシタビン、フルタミド、カペシタビン、デシタビン、メルカプトプリン、チオグアニン、クラドリビン、カルモフール、ラルチトレキセド、ドセタキセル、パクリタキセル、カバジタキセル、イリノテカン、ベロテカン、トポテカン、ビノレルビン、エトポシド、ビンクリスチン、ビンブラスチン、テニポシド、ドキソルビシン、イダルビシン、エピルビシン、ミトキサントロン、マイトマイシン、ブレオマイシン、ダウノルビシン、ダクチノマイシン、ピラルビシン、アクラルビシン、ペプロマイシン、テムシロリムス、テモゾロミド、ブスルファン、イホスファミド、シクロホスファミド、メルファラン、アルトレタミン、ダカルバジン、チオテパ、ニムスチン、クロラムブシル、ミトラクトル、ロイコボリン、トレトニン、エキセメスタン、アミノグルテチミド、アナグレリド、オラパリブ、ナベルビン、ファドロゾール、タモキシフェン、トレミフェン、テストトラクトン、アナストロゾール、レトロゾール、ボロゾール、ビカルタミド、ロムスチン、ボリノスタット、エンチノスタットおよびカルムスチンからなる群から選ばれた少なくとも一つである
請求項9に記載のがんまたは耐性がんの予防または治療用薬学組成物。 - 請求項1ないし7のいずれかに記載の化合物、その薬学的に許容可能な塩、水和物、溶媒和物、構造異性体、光学異性体、立体異性体、またはこれらの組み合わせ;の治療学的有効量を耐性がんを有する個体に投与することを含む
ことを特徴とする腫瘍学的療法に対して耐性を示すがんを治療する方法。 - がんまたは増殖性病気の治療に有用な化学療法剤を同時に、個別的に、または順次に投与することを含む
請求項12に記載の腫瘍学的療法に対して耐性を示すがんを治療する方法。 - がんまたは耐性がんの治療のための薬剤を製造するための請求項1から7のいずれか一項に記載の化合物またはその薬学的に許容可能な塩の用途。
- 幹細胞性がんの治療のための薬剤を製造するための請求項1ないし7のいずれかに記載の化合物、またはその薬学的に許容可能な塩の用途。
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CN114630830A (zh) | 2022-06-14 |
AU2020374208A1 (en) | 2022-05-26 |
EP4053127A4 (en) | 2023-11-29 |
JP7471685B2 (ja) | 2024-04-22 |
KR20210052322A (ko) | 2021-05-10 |
BR112022007998A2 (pt) | 2022-07-05 |
IL292631A (en) | 2022-07-01 |
US20230019094A1 (en) | 2023-01-19 |
EP4053127A1 (en) | 2022-09-07 |
AU2020374208B2 (en) | 2024-03-14 |
CA3159791A1 (en) | 2021-05-06 |
KR102622152B1 (ko) | 2024-01-08 |
MX2022004739A (es) | 2022-07-19 |
WO2021086038A1 (ko) | 2021-05-06 |
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