JP2021512150A - 免疫調節剤として有用な2,8−ジアシル−2,8−ジアザスピロ[5.5]ウンデカン化合物 - Google Patents
免疫調節剤として有用な2,8−ジアシル−2,8−ジアザスピロ[5.5]ウンデカン化合物 Download PDFInfo
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- JP2021512150A JP2021512150A JP2020561587A JP2020561587A JP2021512150A JP 2021512150 A JP2021512150 A JP 2021512150A JP 2020561587 A JP2020561587 A JP 2020561587A JP 2020561587 A JP2020561587 A JP 2020561587A JP 2021512150 A JP2021512150 A JP 2021512150A
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- diazaspiro
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- SOWBGXRSXRTENO-MIJJZIGMSA-N tert-butyl 8-[4-[(3R)-3-phenylmethoxypyrrolidin-1-yl]butanoyl]-2,8-diazaspiro[5.5]undecane-2-carboxylate Chemical compound C(C1=CC=CC=C1)O[C@H]1CN(CC1)CCCC(=O)N1CC2(CCCN(C2)C(=O)OC(C)(C)C)CCC1 SOWBGXRSXRTENO-MIJJZIGMSA-N 0.000 description 1
- 201000003120 testicular cancer Diseases 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontyl alcohol Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- ZRKFYGHZFMAOKI-QMGMOQQFSA-N tgfbeta Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@H](CC(C)C)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CCSC)C(C)C)[C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CC=1C=CC=CC=1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(C)C)C(=O)N1[C@@H](CCC1)C(=O)N1[C@@H](CCC1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O)C1=CC=C(O)C=C1 ZRKFYGHZFMAOKI-QMGMOQQFSA-N 0.000 description 1
- 231100001274 therapeutic index Toxicity 0.000 description 1
- 229940021747 therapeutic vaccine Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 201000002510 thyroid cancer Diseases 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- PBIMIGNDTBRRPI-UHFFFAOYSA-N trifluoro borate Chemical compound FOB(OF)OF PBIMIGNDTBRRPI-UHFFFAOYSA-N 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 230000005747 tumor angiogenesis Effects 0.000 description 1
- 229940030325 tumor cell vaccine Drugs 0.000 description 1
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
- 241000701161 unidentified adenovirus Species 0.000 description 1
- 241000712461 unidentified influenza virus Species 0.000 description 1
- 201000005112 urinary bladder cancer Diseases 0.000 description 1
- 206010046885 vaginal cancer Diseases 0.000 description 1
- 208000013139 vaginal neoplasm Diseases 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
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- 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
- C07D471/02—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 two hetero rings
- C07D471/10—Spiro-condensed systems
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/70503—Immunoglobulin superfamily
- C07K14/70532—B7 molecules, e.g. CD80, CD86
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Abstract
Description
nは、1または2であり;
n'は、0または1であり;
R1は、水素およびベンジルから選択され;
R2は、
mは、0、1、または2であり;
Zは、-O(CH2)Arであり;
Arは、フェニルおよびピリジニルから選択されるが;但し、各環は、C1-C4アルコキシカルボニル、C1-C4アルキル、アミド、カルボキシ、シアノ、およびホルミルから選択される1つの置換基で適宜置換されてもよく;
R3はハロゲンであり;
R4は、-(CH2)NR5R6であるが;但し、
R5は、水素およびC1-C4アルキルから選択され;
R6は、水素、C1-C4アルキル、および
R9は、水素およびC1アルキルから選択され;および
各R9'は独立して、水素およびC1-C3アルキルから選択される]
の化合物、またはその医薬的に許容される塩を提供する。
a) The Practice of Medicinal Chemistry, Camille G. Wermuth et al., Ch 31, (Academic Press, 1996);
b) Design of Prodrugs, edited by H. Bundgaard, (Elsevier, 1985);
c) A Textbook of Drug Design and Development, P. Krogsgaard-Larson and H. Bundgaard, eds. Ch 5, pgs 113 - 191 (Harwood Academic Publishers, 1991);および
d) Hydrolysis in Drug and Prodrug Metabolism, Bernard Testa and Joachim M. Mayer, (Wiley-VCH, 2003)
に記載されている。
インジェクション1条件: カラム: Waters BEH C18, 2.0 x 50mm; 粒子径: 1.7μm; 移動相 A: 5:95 アセトニトリル:水(10mM酢酸アンモニウム含有); 移動相 B: 95:5 アセトニトリル:水(10mM酢酸アンモニウム含有); 温度: 50℃; グラジエント: 0%B、0-100%Bで3分かけて溶出後、次いで100%Bで0.75分間溶出; 流速: 1mL/分; 検出: UV(220nm)
インジェクション2条件: カラム: Waters BEH C18, 2.0 x 50mm; 粒子径: 1.7μm; 移動相 A: 5:95 アセトニトリル:水(0.1%トリフルオロ酢酸含有); 移動相 B: 95:5 アセトニトリル:水(0.1%トリフルオロ酢酸含有); 温度: 50℃; グラジエント: 0%B、0-100%Bで3分かけて溶出後、次いで100%Bで0.75分間溶出; 流速: 1.0mL/分; 検出: UV(220nm)
LCMS (インジェクション1条件) Rt(保持時間)=0.527分、ESI m/z 465 (M+1)
LCMS (インジェクション2条件) Rt=0.689分、ESI m/z 465 (M+1)
1H NMR (500MHz、DMSO-d6) δ 4.18 (br. s., 2H), 3.11 - 3.04 (m, 1H), 2.99 - 2.90 (m, 1H), 2.70 (m, 2H), 2.57 (m, 2H), 2.48-2.15 (m, 16H), 1.97 (dd, J=13.0, 7.5 Hz, 2H), 1.70 - 1.58 (m, 4H), 1.58-1.32 (m, 12H), 1.24 (br. s., 2H)
水酸化リチウム溶液(1M、0.569mL、0.569mmol)を、tert-ブチル3-(2-クロロ-5-((5-シアノピリジン-3-イル)メトキシ)-4-ホルミルフェニル)プロパノエート(57mg、0.142mmol)/MeOH(1mL)およびTHF(1mL)溶液に加えた。得られた溶液を室温で一夜撹拌した。溶媒を除去し、残渣をさらに精製せず次のステップにそのまま用いた。LCMSでは、生成物の3-(2-クロロ-5-((5-シアノピリジン-3-イル)メトキシ)-4-ホルミルフェニル)プロパン酸および3-(2-クロロ-4-ホルミル-5-((5-(イミノ(メトキシ)メチル)ピリジン-3-イル)メトキシ)フェニル)プロパン酸が存在することを示した。
インジェクション1条件: カラム: Waters Acquity UPLC BEH C18、2.1 x 50mm; 粒子径: 1.7μm; 移動相 A: 5:95 アセトニトリル:水(10mM酢酸アンモニウム含有); 移動相 B: 95:5 アセトニトリル:水(10mM酢酸アンモニウム含有); 温度: 50℃; グラジエント: 0-100%Bで3分かけて溶出後、次いで100%Bで0.75分間溶出; 流速: 1.0mL/分; 検出: UV(220nm)
インジェクション2条件: カラム: Waters Acquity UPLC BEH C18、2.1 x 50mm; 粒子径: 1.7μm; 移動相 A: 5:95 アセトニトリル:水(0.1%トリフルオロ酢酸含有); 移動相 B: 95:5 アセトニトリル:水(0.1%トリフルオロ酢酸含有); 温度: 50℃; グラジエント: 0-100%Bで3分かけて溶出後、次いで100%Bで0.75分間溶出; 流速: 1.0mL/分; 検出: UV(220nm)
LCMS (インジェクション1条件) Rt=1.215分、ESI m/z 847 (M+1)、m/z 845 (M-1)
LCMS (インジェクション2条件) Rt=1.308分、ESI m/z 847 (M+1)、m/z 845 (M-1)
1H NMR (500MHz、DMSO-d6) δ 9.26 (br. s., 1H), 8.97 (s, 1H), 8.78 (s, 1H), 8.64 (br. s., 1H), 7.56 - 7.45 (m, 1H), 7.41 - 7.17 (m, 7H), 5.26 (br. s., 2H), 4.40 (d, J=12.1 Hz, 2H), 4.20 - 3.96 (m, 3H), 3.62 - 3.50 (m, 4H), 3.48 - 3.11 (m, 4H), 2.93 (br. s., 3H), 2.65 (br. s., 5H), 2.44 - 2.20 (m, 6H), 2.09 - 1.93 (m, 1H), 1.77 - 1.31 (m, 10H), 1.29 - 1.19 (m, 1H), 1.26 (s, 3H)
インジェクション1条件: カラム: Waters Acquity UPLC BEH C18、2.1 x 50mm; 粒子径: 1.7μm; 移動相 A: 5:95 アセトニトリル:水(10mM酢酸アンモニウム含有); 移動相 B: 95:5 アセトニトリル:水(10mM酢酸アンモニウム含有); 温度: 50℃; グラジエント: 0-100%Bで3分かけて溶出後、次いで100%Bで0.75分間溶出; 流速: 1.0mL/分; 検出: UV(220nm)
インジェクション2条件: カラム: Waters Acquity UPLC BEH C18、2.1 x 50mm; 粒子径: 1.7μm; 移動相 A: 5:95 アセトニトリル:水(0.1%トリフルオロ酢酸含有); 移動相 B: 95:5 アセトニトリル:水(0.1%トリフルオロ酢酸含有); 温度: 50℃; グラジエント: 0-100%Bで3分かけて溶出後、次いで100%Bで0.75分間溶出; 流速: 1.0mL/分; 検出: UV(220nm)
LCMS (インジェクション1条件) Rt=1.326分、m/z 829 (M+1)、m/z 827 (M-1)
LCMS (インジェクション2条件) Rt=1.332分、m/z 829 (M+1)
1H NMR (500MHz、DMSO-d6) δ 9.00 (s, 2H), 8.46 (br. s., 1H), 7.54 - 7.46 (m, 1H), 7.41 - 7.22 (m, 5H), 7.14 (d, J=16.5 Hz, 1H), 5.26 (br. s., 2H), 4.41 (d, J=10.6 Hz, 2H), 4.15 - 4.02 (m, 1H), 3.91 (br. s., 2H), 3.63 - 3.47 (m, 1H), 3.4-3.1(m, 5H), 2.90 (br. s., 3H), 2.61 (br. s., 5H), 2.45 - 2.16 (m, 6H), 2.09 - 1.94 (m, 1H), 1.81 - 1.29 (m, 12H), 1.29 - 1.17 (m, 1H), 1.22 (s, 3H)
インジェクション1条件: カラム: Waters Acquity UPLC BEH C18、2.1 x 50mm; 粒子径: 1.7μm; 移動相 A: 5:95 アセトニトリル:水(10mM酢酸アンモニウム含有); 移動相 B: 95:5 アセトニトリル:水(10mM酢酸アンモニウム含有); 温度: 50℃; グラジエント: 0-100%Bで3分かけて溶出後、次いで100%Bで0.75分間溶出; 流速: 1.0mL/分; 検出: UV(220nm)
インジェクション2条件: カラム: Waters Acquity UPLC BEH C18、2.1 x 50mm; 粒子径: 1.7μm; 移動相 A: 5:95 アセトニトリル:水(0.1%トリフルオロ酢酸含有); 移動相 B: 95:5 アセトニトリル:水(0.1%トリフルオロ酢酸含有); 温度: 50℃; グラジエント: 0-100%Bで3分かけて溶出後、次いで100%Bで0.75分間溶出; 流速: 1.0mL/分; 検出: UV(220nm)
LCMS (インジェクション1条件) Rt=1.344分、ESI m/z 862 (M+1)、m/z 860 (M-1)
LCMS (インジェクション2条件) Rt=1.314分、ESI m/z 862 (M+1)
1H NMR (500MHz、DMSO-d6) δ 9.05 (s, 1H), 8.96 (s, 1H), 8.41 (br. s., 1H), 7.54 - 7.47 (m, 1H), 7.38 - 7.23 (m, 5H), 7.20 - 7.12 (m, 1H), 5.29 (br. s., 2H), 4.41 (d, J=12.1 Hz, 2H), 4.13 - 4.00 (m, 1H), 3.94 - 3.84 (m, 2H), 3.90 (s, 3H), 3.53 (d, J=18.7 Hz,1H), 3.4-3.1 (m, 5H), 2.90 (m, 3H), 2.75-2.48 (br. s., 5H), 2.46 - 2.15 (m, 6H), 2.09 - 1.93 (m, 1H), 1.79 - 1.29 (m, 12H), 1.28 - 1.17 (m, 1H), 1.20 (s, 3H)
式(I)の化合物のPD-L1に対する結合能を、PD-1/PD-L1ホモジニアス時間分解蛍光(HTRF)バインディングアッセイを用いて調査した。
PD-1およびPD-L1の相互作用は、可溶性かつ精製された、その2つのタンパク質の細胞外ドメインの標品を用いることで評価され得る。PD-1およびPD-L1のタンパク質細胞外ドメインは、検出タグにより融合タンパク質として発現され、PD-1におけるタグは、免疫グロブリン(PD-1-Ig)のFc部分であり、PD-L1におけるタグは、6ヒスチジンモチーフ(PD-L1-His)であった。全てのバインディングの研究は、0.1%ウシ血清アルブミンおよび0.05%(v/v)Tween-20が添加されたdPBSを含む、HTRFアッセイ緩衝液中で行われた。h/PD-L1-Hisバインディングアッセイには、阻害剤をPD-L1-His(最終濃度10nM)と共に15分間アッセイ緩衝液(4μL)中、予めインキュベートし、次いでPD-1-Ig(最終濃度20nM)/アッセイ緩衝液(1μL)を加え、さらに15分間インキュベートした。HTRFの検出は、ユウロピウムクリプテート標識抗Ig(最終濃度1nM)およびアロフィコシアニン(APC)標識抗His(最終濃度20nM)を用いて行った。抗体をHTRF検出緩衝液に希釈し、その5μLを結合反応液の上部に分注した。反応混合物を30分間平衡化し、生じたシグナル(665nm/620nmの比)を、蛍光光度計(EnVision)を用いて得た。別のバインディングアッセイを、ヒトタンパク質のPD-1-Ig/PD-L2-His(それぞれ20nM/5nM)間およびCD80-His/PD-L1-Ig(それぞれ100nM/10nM)間で行った。
Claims (13)
- 式(I):
nは、1または2であり;
n'は、0または1であり;
R1は、水素およびベンジルから選択され;
R2は、
mは、0、1、または2であり;
Zは、-O(CH2)Arであり;
Arは、フェニルおよびピリジニルから選択されるが;但し、各環は、C1-C4アルコキシカルボニル、C1-C4アルキル、アミド、カルボキシ、シアノ、およびホルミルから選択される1つの置換基で適宜置換されてもよく;
R3は、ハロゲンであり;
R4は、-(CH2)NR5R6であるが;但し、
R5は、水素およびC1-C4アルキルから選択され;
R6は、水素、C1-C4アルキル、および
R9は、水素およびC1アルキルから選択され;および
各R9'は独立して、水素およびC1-C3アルキルから選択される]
の化合物、またはその医薬的に許容される塩。 - mは1であり、およびR3はハロゲンである、請求項1の化合物、またはその医薬的に許容される塩。
- Zが、-O(CH2)Arであり;
ここでArは、ピリジニルであり、C1-C4アルコキシカルボニル、C1-C4アルキル、アミド、カルボキシ、シアノ、およびホルミルから選択される1つの置換基で適宜置換されてもよい、請求項4の化合物、またはその医薬的に許容される塩。 - 1,1'-(2,8-ジアザスピロ[5.5]ウンデカン-2,8-ジイル)ビス(4-((R)-3-(ベンジルオキシ)ピロリジン-1-イル)ブタン-1-オン);
1,1'-(2,8-ジアザスピロ[5.5]ウンデカン-2,8-ジイル)ビス(4-((R)-3-ヒドロキシピロリジン-1-イル)ブタン-1-オン);
(2S)-2-((4-(3-(8-(4-((R)-3-(ベンジルオキシ)ピロリジン-1-イル)ブタノイル)-2,8-ジアザスピロ[5.5]ウンデカン-2-イル)-3-オキソプロピル)-2-((5-カルバモイルピリジン-3-イル)メトキシ)-5-クロロベンジル)アミノ)-3-ヒドロキシ-2-メチルプロパン酸;
(2S)-2-((4-(3-(8-(4-((R)-3-(ベンジルオキシ)ピロリジン-1-イル)ブタノイル)-2,8-ジアザスピロ[5.5]ウンデカン-2-イル)-3-オキソプロピル)-5-クロロ-2-((5-シアノピリジン-3-イル)メトキシ)ベンジル)アミノ)-3-ヒドロキシ-2-メチルプロパン酸;および
(2S)-2-((4-(3-(8-(4-((R)-3-(ベンジルオキシ)ピロリジン-1-イル)ブタノイル)-2,8-ジアザスピロ[5.5]ウンデカン-2-イル)-3-オキソプロピル)-5-クロロ-2-((5-(メトキシカルボニル)ピリジン-3-イル)メトキシ)ベンジル)アミノ)-3-ヒドロキシ-2-メチルプロパン酸
から選択される化合物、またはその医薬的に許容される塩。 - 請求項1の化合物、またはその医薬的に許容される塩、および医薬的に許容される担体を含む医薬組成物。
- 免疫応答を強化、刺激、および/または増大するための、それが必要な患者に対する方法であり、治療上の有効量の請求項1の化合物またはその治療的に許容される塩を患者に投与することを特徴とする、方法。
- がん細胞の成長、増殖、または転移を阻害するための、それが必要な患者に対する方法であり、治療上の有効量の請求項1の化合物またはその治療的に許容される塩を患者に投与することを特徴とする、方法。
- 感染性疾患を治療するための、それが必要な患者に対する方法であり、治療上の有効量の請求項1の化合物またはその治療的に許容される塩を患者に投与することを特徴とする、方法。
- 前記感染性疾患がウイルスによって引き起こされる、請求項10の方法。
- 敗血症性ショックを治療するための、それが必要な患者に対する方法であり、治療上の有効量の請求項1の化合物またはその治療的に許容される塩を患者に投与することを特徴とする、方法。
- 患者におけるPD-L1とPD-1および/またはCD80の相互作用を抑制する方法であり、治療上の有効量の請求項1の化合物またはその治療的に許容される塩を患者に投与することを特徴とする、方法。
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