公开(公告)号：US20150274663A1

公开(公告)日：2015-10-01

申请号：US14443912

申请日：2013-11-20

Applicant: BIOGEN IDEC MA INC.

Inventor： Hairuo Peng ,  Edward Yin-Shiang Lin ,  Jianhua Chao ,  Zhili Xin ,  Bin Ma ,  Kevin Guckian ,  Timothy Chan ,  Gnanasambandam Kumaravel ,  Arthur G. Taveras

IPC: C07D211/22 ,  C07D401/12 ,  A61K31/4545 ,  C07D295/15 ,  A61K45/06 ,  C07D403/04 ,  A61K31/501 ,  A61K31/506 ,  C07D401/04 ,  A61K31/451 ,  A61K31/495

CPC classification number: C07D211/22 ,  A61K31/451 ,  A61K31/4545 ,  A61K31/495 ,  A61K31/501 ,  A61K31/506 ,  A61K45/06 ,  C07D207/08 ,  C07D211/56 ,  C07D211/62 ,  C07D211/70 ,  C07D213/74 ,  C07D237/22 ,  C07D239/47 ,  C07D295/15 ,  C07D295/155 ,  C07D401/04 ,  C07D401/12 ,  C07D403/04

Abstract: Compounds of formula (I) wherein: X is —O—, —S(O)r—, —CH2—, or —NR—, wherein r is 0, 1, or 2; X1, X2, and X5 are each independently CR7 or N; one of X3 or X4 is C and is attached by a single bond to -L-, and the other is CR7 or N, provided that no more than three of X1, X2, X3, X or X5 are N; Ring A is monocyclic C5-6scycloalkyl or a 5- to 6-membered monocyclic heterocyclyl comprising from 1 to 5 heteroatoms independently selected from N, S, or O; wherein Ring A is further optionally substituted with from 1 to 3 R4; provided that Ring A is not morpholinyl, thiomorpholinyl or tetrahydro-2H-pyranyl; L is a bond, —O—, —NR—, —S(O)n—, —CH2—, or —C(O)—, wherein n is 0, 1, or 2; 1 2 L1 is an C1-8alkylene, C3-scycloalkylene, —CH2-L2-, or a 3- to 8-membered heterocyclylene comprising 1 to 5; R1 is C6-20alkyl or a monocyclic C3-8cycloalkyl; wherein said C3-8cycloalkyl is substituted with at least one R6 and may be optionally substituted with from 1 to 5 additional R6 substituents, wherein R6 for each occurrence is independently selected; and R2 is —C(O)OR3, —C(O)N(R3)—S(O)2R3, —S(O)2OR3, —C(O)NHC(O)R3, —Si(O)OH, —B(OH)2, —N(R3)S(O)2R3, —S(O)2N(R3)2, —O—P(O)(OR3)2, or —P(O)(OR3)2, —CN, —S(O)2NHC(O)R3, —C(O)NHS(O)2R3, —C(O)NHOH, —C(O)NHCN, —CH(CF3)OH, —C(CF3)2OH, or a selected heteroaryl or heterocyclyl; and pharmaceutically acceptable salts thereof, can modulate the activity of one or more SIP receptors and/or the activity of autotaxin (ATX).

公开(公告)号：US20150232492A1

公开(公告)日：2015-08-20

申请号：US14620700

申请日：2015-02-12

Applicant: BIOGEN IDEC MA INC.

Inventor： Richard D. Caldwell ,  Kevin Guckian ,  Gnanasambandam Kumaravel ,  Wen-Cherng Lee ,  Edward Yin-Shiang Lin ,  Xiaogao Liu ,  Bin Ma ,  Daniel M. Scott ,  Zhan Shi ,  Jermaine Thomas ,  Arthur G. Taveras ,  Guo Zhu Zheng

IPC: C07F9/6512 ,  C07C229/36 ,  C07D239/80 ,  C07D263/24 ,  C07D215/20 ,  C07F9/60 ,  C07C233/47 ,  C07C217/58

CPC classification number: C07F9/6512 ,  C07C217/58 ,  C07C217/74 ,  C07C229/36 ,  C07C233/47 ,  C07C2602/10 ,  C07D215/06 ,  C07D215/20 ,  C07D215/227 ,  C07D233/32 ,  C07D239/74 ,  C07D239/80 ,  C07D263/24 ,  C07D277/64 ,  C07D401/04 ,  C07F9/091 ,  C07F9/60 ,  C07F9/65744

Abstract: Compounds that have agonist activity at one or more of the S1P receptors are provided. The compounds are sphingosine analogs that, after phosphorylation, can behave as agonists at S1P receptors.

Abstract translation: 提供了在一种或多种S1P受体上具有激动剂活性的化合物。 化合物是鞘氨醇类似物，其在磷酸化之后可以作为S1P受体的激动剂。

公开(公告)号：US09181191B2

公开(公告)日：2015-11-10

申请号：US13646143

申请日：2012-10-05

Applicant: BIOGEN IDEC MA INC.

Inventor： Richard D. Caldwell ,  Kevin M. Guckian ,  Gnanasambandam Kumaravel ,  Wen-Cherng Lee ,  Edward Yin-Shiang Lin ,  Xiaogao Liu ,  Bin Ma ,  Daniel M. Scott ,  Zhan Shi ,  Jermaine Thomas ,  Arthur G. Taveras ,  Guo Zhu Zheng

IPC: A61K31/47 ,  C07D215/20 ,  C07C217/74 ,  C07D215/06 ,  C07D215/227 ,  C07D233/32 ,  C07D239/74 ,  C07D277/64 ,  C07D401/04 ,  C07F9/09 ,  C07F9/60 ,  C07F9/6512 ,  C07F9/6574

CPC classification number: C07F9/6512 ,  C07C217/58 ,  C07C217/74 ,  C07C229/36 ,  C07C233/47 ,  C07C2602/10 ,  C07D215/06 ,  C07D215/20 ,  C07D215/227 ,  C07D233/32 ,  C07D239/74 ,  C07D239/80 ,  C07D263/24 ,  C07D277/64 ,  C07D401/04 ,  C07F9/091 ,  C07F9/60 ,  C07F9/65744

Abstract: Compounds that have agonist activity at one or more of the S1P receptors are provided. The compounds are sphingosine analogs that, after phosphorylation, can behave as agonists at S1P receptors.

Abstract translation: 提供了在一种或多种S1P受体上具有激动剂活性的化合物。 化合物是鞘氨醇类似物，其在磷酸化之后可以作为S1P受体的激动剂。