LU101206B1 - PDEdelta Inhibitors - Google Patents
PDEdelta Inhibitors Download PDFInfo
- Publication number
- LU101206B1 LU101206B1 LU101206A LU101206A LU101206B1 LU 101206 B1 LU101206 B1 LU 101206B1 LU 101206 A LU101206 A LU 101206A LU 101206 A LU101206 A LU 101206A LU 101206 B1 LU101206 B1 LU 101206B1
- Authority
- LU
- Luxembourg
- Prior art keywords
- alkyl
- cancer
- substituted
- compound according
- phenyl
- Prior art date
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- 101100082610 Plasmodium falciparum (isolate 3D7) PDEdelta gene Proteins 0.000 title abstract description 20
- 239000003112 inhibitor Substances 0.000 title abstract description 12
- 150000001875 compounds Chemical class 0.000 claims abstract description 75
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- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 14
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- 101710113436 GTPase KRas Proteins 0.000 claims description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 9
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- 229910052792 caesium Inorganic materials 0.000 claims description 5
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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Claims (13)
- N .\ \X \ x Ansprüche 3 LU101206 \NNNS xN ; i a © ‘ N 4, Verbindung gemäß Formel () \ \N xNNNNN 8 . N Raw, Ro 2 * x À S JOH 3 or Sn \ 7 \ QO=P-DR4 \ 3 N - x 0 N i CT 55 Ra ” SQ S | x ; x wobel, \ \ ; an ; Ce x n ist eine ganze Zahl zwischen 1 und 10, vorzugsweise 4 Dis 10, mehr bevorzugt 5 bis 10, \ an meisten bevorzugt 8, hesondears bevorzugt 8 to 9, nach mehr besonders bevorzugt §; \S ; - x Ryisi H, ~Q0OR,, SCORa, oder -OHRe, vorzugsweise ~CORy; \ x x . er mee ge ~ x Re ist H, -COR, -SCHR,, oder CHR; vorzugsweise MH; \ x x . ; a sn aa > ; x Rs ist substituipries oder unsubatituiertes -(Cy- Ay: Ar, VOTZUGSWEISE subatluieries oder \ unsubstituiertes (O-ColAn \ \ ; AUS : — N Rz ist {64 -CalAkıd, vorzugsweise Methyl or Ethyl; \ 3 ; ; ; . x Ra ist COG JAK oder ACC AR, VOTEUGEWE(SS -CO.Et oder Methyl \ x \ Rs ist AD, -DalAlkyt vorzugsweise Methyl, Fhenyt, Bu, Î und ein Solval, ein Hydral, ein Salz, sin Komplex, eine racermiache Mischung, sin \ Diasteraomer, ein Enantiomer, ein Tautomer und isclogisch angereicharte Forma davon,N \S x x x x x . . 3 N2. Die Verbindung gemäß Anspruch 1, wwohei \N y Ra BE AOC. plAr, vorzugsweise Phenyl, subsiituiert mit mindestens einem Dubatituent, Î ausgewshit aus OOOH, COO{T-Taalkyd, NO, Hal, OCCA, CHals, ACC; Alt, \ {Os Cu Oyaloalkyl, und -NHz oder Î x Un . x 11 Re ist {000047 vorzugsweise Phenyl, substitulert mit mindestens zwei Substituenten, unabhängig ausgewählt aus COOH, ZOO Ca Alkyl, NO, Mal, OXC,-Cs Alt Hat, - Î (Ce Alt, Ca D dveloalky{, und NH; oder \ HD Ry ist -{(Cs-CyabAr, vorzugsweise Phenyl, subatituiert mit mindestens zwei Substituentan, \ unabhängig ausgewählt! aus COOH, -COU(G,-CpAlkyi und NH, oder ©XS ®SX ©X ©NX 3N ed\ \XXXXXXSXS . 45 4 Le - \ Ca . . N RY Ry ist Phenyl, substituent mit mindestens zwei Bubstituenten, wobei ein Substituent in LU101206 \ para-Posifion ist, ausgewählt! aus der Gruppe bestehend aus —CQOH und ~-COWC- CA \ und ein zweiter Subefiluent in mata-Position ist, zusgewähl! aus der Gruppe bestehend aus \ 3 Sa. \XXSXSXXX . ; en oo N3. Die Verbindung gemäß Anspruch 1, wobel \S Ra ist Phenyl subsfituert mit mindestens einem Subsiituant weicher in para-Pogition \ lokalisiert ist. \XXXXXXXS . at zer - x sue > Là me 2 + 5 N À. Die Verbindung gemäß einem der Ansprüche 1 is 3, wobal Ry Ist DOC Gaal, \ vorzugsweise -CO.Me oder -CO:Et, mehr bevorzugt COLE \N \NN 38. Dis Verbindung gemäß einem der Ansprüche 1 his 3, wobel \NN { aa SN x N X à + X i : N Ra ist {0G laiky, vorzugsweise Methyl oder Ethyl, mehr bevorzugt Matty,SNNNXNX5. Die Verbindung gemäß einem der Ansprüche 1 bis 8, wobel \NX gy TN COUNT x 3 All : \ fi ep COM fn DEG eg AR \ * eld i AR _ H N x Ned, * N ; Net Na \ Rgist "2 oder Ps . \NNN © ÿX7. Die Verbindung gemäß einem der Ansprüche 1 bis 6, wobs! \SS RE 3 ist GORE, \ \ Le £a X Ry lat HE \N - aig I CoN en N und Ra ist substituiertes oder unsubsfituieries {Cs-Czatèr. \XXXSX ©S8. Verbindung ausgewähl! aus \S \ \ 3 ès» \ SS Nr cs ° x 8 COMER BG LOOM ° DL À a gual ay +5 5 N md 3 RE: D des $, Pa NH, Ned A Me & AN N ie SU ra A Neen, Nerd? 3 FN rem a vom Ne £ SAS N FTN X 3 , 2 G ; \ÀXX ÿX ÿX ÿX ÿX ÿX ÿXX ÿX ÿX ÿX ÿXXSNAA N N N N N N NN NSSN \ ® 3N $X ©SS =S Ne oe = FEF LU101206 , 2 wl _ N >, x NS ÉOOME 2-0 SOON À } TPG Fd I 3 N eed x : x £ A . 3 A 7 \ / \ . 3 LA TTY QA PR? es, vu. \ 3 E a ’ EW / \ HN — HN \ Q und © a ; \S \XXXXS à 8, Dis Verbindung gemäß ainem der Ansprüche 1 oder &, zur Verwendung in der Medizin, \S 3 © 3 \19. Die Verbindung gemäß einem der Anspriiche 1 bis 8, zur Verwendung in der Behandlung \ À ue 7 von Krebs. \ \X x xN \ Ce ; .. ae N . N N S11. Die Verbindung zur Verwendung gemäß Anspruch 10, wobei der Krebs ausgewählt ist \ . Go ; : ; Ste ns NT N S aus K-Ras abhängigen Krebsarten, vorzugswetes aus Krebsarten, wobel das K-Ras Gen \ 24 3 TE $ mutiert ist, 7 \ àA 3 $ © 12, Dip Verbindung zur Verwendung gemäß Anspruch 10 oder 11, wobei der Krebs ; RTE x : : a. sn s ran CR EN a Fey RENE = 3 gusgewihi ist aus einem Gliom, Brustkrebs, Darmkrebs, Pacresskrabs, Magenkrebs, : 3 3 A ; a Eiaraïinntkl x on Sy RSE IY Bk ÿ Lungenkrebs, Gebärmulterhalskrebs, Gebärmufterkrebs, Kiersigckkreiis, VOTEUGSWEISE ;N À Brustkrebs, ;N à $ $ $ $ “ay en ~~ fon ca es tie nites x 3 x ÿ 13, Fharmareufische Zusammensetzung, umfassend die Verbindung gemäß einem der \ “os : ÿ Ansprüche 1 bis 5, \ \ \ \ \ \ \ \ \ \ \ \ \A \ \ \ \NA 3 3 3 3 3 3 3 ÿ } 3 3 ÿ 3 3 3 3 3 3NN 3NNNNNNNNNNNN $ $ $ $ $ $ $ $ $ $ 3 ; $ $ 3N 3 $N Ae
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LU101206A LU101206B1 (en) | 2019-05-06 | 2019-05-06 | PDEdelta Inhibitors |
PCT/EP2020/062530 WO2020225285A1 (en) | 2019-05-06 | 2020-05-06 | Pdedelta inhibitors |
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LU101206A LU101206B1 (en) | 2019-05-06 | 2019-05-06 | PDEdelta Inhibitors |
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LU101206A LU101206B1 (en) | 2019-05-06 | 2019-05-06 | PDEdelta Inhibitors |
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LU (1) | LU101206B1 (de) |
WO (1) | WO2020225285A1 (de) |
Citations (2)
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EP0050327A1 (de) * | 1980-10-21 | 1982-04-28 | Roche Diagnostics GmbH | Neue schwefelhaltige Phospholipide, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
WO2015189433A1 (en) | 2014-06-13 | 2015-12-17 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Pyridazinones for the treatment of cancer |
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2019
- 2019-05-06 LU LU101206A patent/LU101206B1/en active IP Right Grant
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0050327A1 (de) * | 1980-10-21 | 1982-04-28 | Roche Diagnostics GmbH | Neue schwefelhaltige Phospholipide, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Arzneimittel |
WO2015189433A1 (en) | 2014-06-13 | 2015-12-17 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Pyridazinones for the treatment of cancer |
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