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Description | SP600125isabroad-spectrumJNKinhibitorforJNK1,JNK2andJNK3withIC50of40nM,40nMand90nM,respectively. |
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IC50&Target | IC50:40/40/90nM(JNK1/2/3)[1] |
InVitro | SP600125isanATP-competitiveinhibitorofJNK2withaKivalueof0.19±0.06μM.SP600125inhibitsthephosphorylationofc-JunwithIC50of5μMto10μMinJurkatTcells.InCD4+cells,suchasTh0cellsisolatedfromeitherhumancordorperipheralblood,SP600125blockscellactivationanddifferentiationandinhibitstheexpressionofinflammatorygenesCOX-2,IL-2,IL-10,IFN-γ,andTNF-α,withIC50of5μMto12μM[1].InamousebetacellsMIN6,SP600125(20μM)inducesthephosphorylationofp38MAPKanditsdownstreamCREB-dependentpromoteractivation[2].InHCT116cells,SP600125(20μM)blockstheG2phasetomitosistransitionandinducesendoreplication.ThisABIlityofSP600125isindependentofJNKinhibition,butduetoitsinhibitionofCDK1-cyclinBactivationupstreamofAuroraAandPolo-likekinase1[3]. |
InVivo | AdmiNISTrationofSP600125at15or30mg/kgi.v.significantlyinhibitsTNF-αserumlevels,whereasoraladministrationdose-dependentlyblocksTNF-αexpressionwithsignificantinhibitionobservedat30mg/kgperos[1].SP600125attenuatesLPS-inducedALIinratsinvivo.TheexpressionlevelsofTNF-αandIL-6intheBALFinratsintheSP600125grouparesignificantlydecreased[4]. |
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Pleaserefertothesolubilityinformationtoselecttheappropriatesolvent. | ||||||||||||||||
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CellAssay [1] | SP600125isdissolvedinDMSO(20mM)andstored,andthendilutedwithappropriatemedia(DMSO0.1%)beforuse[1]. DeterminationofmRNAhalf-lifeisperformedessentially,exceptthatCD14+cellsarestimulatedwith(bacterial)lipopolysaccharide(LPS;50ng/mL)for2hbeforeadditionofactinomycinD(5μg/mL).SP600125(25μM)orvehicle(0.5%DMSOvol/vol)isaddedimmediatelyfollowingtheactinomycinD.Analysisisperformedbyusingreal-timereversetranscription(RT)-PCR.TotalRNAisextractedwithanRNeasyMinikit.TNFmRNAismeasuredbyrealtimeRT-PCR,usingaTNFTaqmanprobe.Alldataarenormalizedbyusingglyceraldehyde-3-phosphatedehydrogenase(GAPDH)expression.TheTNF-αforwardprimeris5′-CTGGCCCAGGCAGTCAGAT-3′andthereverseprimeris5′-TATCTCTCAGCTCCACGCCATT-3′.TheTaqmanprobesequenceis5′-FAM-CCTGTAGCCCATGTTGTAGCAAACCCTCA-TAMRA-3′[1].MCEhasnotindependentlyconfirmedtheaccuracyofthesemethods.Theyareforreferenceonly. | ||||||||||||||||
AnimalAdministration [1][4] | SP600125isdissolvedin30%PEG-400/20%polypropyleneglycol/15%CremophorEL/5%ethanol/30%saline(Mice)[1]. Mice[1] | ||||||||||||||||
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MolecularWeight | 220.23 | ||||||||||||
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Formula | C₁₄H₈N₂O | ||||||||||||
CASNo. | 129-56-6 | ||||||||||||
Storage |
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Shipping | RoomtemperatureincontinentalUS;mayvaryelsewhere | ||||||||||||
Solvent&Solubility | DMSO:≥45mg/mL *"<1 mg/ml"="" means="" slightly="" soluble="" or="" insoluble.="" "≥"="" means="" soluble,="" but="" saturation="">1> Purity:98.69% 品牌介绍
托烷司琼临床评价药物相关作用适应症托烷司琼CAS号:89565-68-4英文名称:Tropisetron英文同义词:icf205-930;TROPICACID;TROPISETRON;SS-TROPISETRON;BETA-TROPISETRON;Tropisetron(ICS205930);TROPISHTRONHYDROCHLORIDE;Indole-3-carbonylchloride;3-Tropanylindole-3-carboxylate;lαH,5Αh-Tropan-3α-ylindole-3-carboxylate中文名称:托烷司琼中文同义词:托普西隆;托普西龙;曲匹西龙;托烷司琼;Β-托烷司琼;CS-348;Β-内托烷司琼;吲哚-3-甲酰氯;Β-托烷司琼(光学异构体);Β-托烷司琼,托烷司琼异构体CBNumber:CB3236404分子式:C17H20N2O2分子量:284.35MOLFile:89565-68-4.mol化学性质安全信息用途供应商112化学性质安全信息用途供应商112托烷司琼化学性质熔点:201-202°C沸点:448.5±35.0°C(Predicted)密度:1.26储存条件:2-8°C溶解度:H2O:soluble形态:solid酸度系数(pKa):15.38±0.30(Predicted)颜色:whiteCAS数据库:Chemicalbook89565-68-4(CASDataBaseReference)安全信息WGKGermany:3托烷司琼化学药品说明书托烷司琼|药物应用信息托烷司琼性质、用途与生产工艺临床评价Sorbe等报道本品对含顺铂(剂量50~89mg/m2)化疗方案引起的急性呕吐完全控制率为63%。58例恶性肿瘤化疗所致恶心、呕吐者,应用托烷司琼或昂丹司琼8mg分别在同一病人前后2个化疗周期的第1d给药前30min静脉注射,并用地塞米松10mg静脉滴注。结果两药控制急性及迟发性恶心、呕吐的疗效基本相似,均可达81%~100%。本品对强致吐化疗药物顺铂的止吐疗效突出。药物相关作用饮食可略为延长本品的吸收。本品与利福平、苯巴比妥等肝酶诱导药同时使用,可加快代谢,故快代谢型者需增加剂量,慢者则不必。西咪替丁等肝酶抑制药对本品血药浓度无明显影响。适应症托烷司琼临床用于预防和治疗癌症化疗引起的恶心和呕吐。化学性质结晶,熔点201-202℃(二氯甲烷-乙酸乙酯)。单盐酸托烷司琼(TropisetronMonohydroehloride):C17H20N2O2?HCI。[105826-92-4]。熔点283-285℃(分解)。用途有高效性和选择性的5-HT3受体拮抗剂。用于化疗所致的呕吐。用途为5-羟色胺拮抗药生产方法托品醇(I)和酰氯(Ⅱ)反应,可得托烷司琼。托烷司琼上下游产品信息上游原料托品醇下游产品
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