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InChi: InChI=1S/C11H12N2O3S/c1-13-7-9(12-17(2
indicating its involvement in carcinogenesis and its potential as a therapeutic target
C[N+](C)(C)CCOP([O-])([O-])=O
InChi: InChI=1S/C90H130N28O29/c1-44(2)28-65(89(146)147)116-78(135)54(14-9-10-26-91)107-79(136)56(20-23-67(93)121)109-84(141)61(31-49-36-96-41-101-49)113-86(143)63(33-51-38-98-43-103-51)115-88(145)73(45(3)4)118-81(138)58(22-25-70(125)126)110-82(139)59(30-48-16-18-52(120)19-17-48)105-68(122)39-100-76(133)66(40-119)117-87(144)64(35-72(129)130)114-85(142)62(32-50-37-97-42-102-50)112-77(134)55(15-11-27-99-90(94)95)108-83(140)60(29-47-12-7-6-8-13-47)111-80(137)57(21-24-69(123)124)106-74(131)46(5)104-75(132)53(92)34-71(127)128/h6-8
Recent Progress in JAK Inhibitors for the Treatment of Rheumatoid Arthritis
Arimoclomol 0396 InChi: InChI=1S/C11H12N2O3S/c1-13-7-9(12-17(2Arimoclomol (BRX 220 free base) is a co inducer of heat shock proteins (HSP). Arimoclomol protects motor neurons by enhancing Hsp expression, thus directly affecting protein aggregation and clearance of misfolded assemblies via the proteasome ubiquitin system. Product information CAS Number: 289893 25 0 Molecular Weight: 313. 78 Formula: C14H20ClN3O3 Chemical Name: 3 [(1Z) chloro({[(2R) 2 hydroxy 3 (piperidin 1 yl)propoxy]imino})methyl]pyridin 1 ium 1
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