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T32613LCB 03-0110 dihydrochlorideLCB 030110 dihydrochloride,LCB 03 0110 dihydrochloride
LCB 03-0110 Dihydrochloride is a potent inhibitor of the c-Src kinase (IC50 = 1.3 nM) and tyrosine kinases in the BTK and SYK family, as well as in the DDR2 family. It inhibits LPS-induced activation of macrophages and TGF-β1-induced activation of fibroblasts in vitro, inhibits activation of macrophages and fibroblasts, and inhibits scarring in wound healing models.
价 格：￥电议型 号：T32613产 地：中国大陆
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T6668SGC-CBP30inhibit,IL-17A,HAT,HATs,BRD,Histone Acetyltransferase,ankylosing,SGCCBP30,cells,epigenetic,
SGC-CBP30 is an effective CREBBP/EP300 inhibitor (IC50: 21/38 nM).
价 格：￥电议型 号：T6668产 地：中国大陆
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T39340Sulfo-NHS-LC-Biotin sodiumSulfo NHS LC Biotin sodium,SulfoNHSLCBiotin sodium
Sulfo-NHS-LC-Biotin sodium is an amine-reactive biotinylation reagent for antibody labeling.
价 格：￥电议型 号：T39340产 地：中国大陆
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T60193CB-53391HIndole4carboxamide,2methyl1[5,6,7,8tetrahydro4[(phenylmethyl)amino]pyrido[2,3d]pyrimidin2yl
p97-IN-1 is a potent inhibitor of p97 with an IC 50 <30 nM [1].
价 格：￥电议型 号：T60193产 地：中国大陆
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T9264ECBN HCLInhibitor,inhibit,ECBN HCL,A-30912A nucleus
A-30912A nucleus hydrochloride is the reaction product catalyzed by Echinocandin B (ECB) deacylase.
价 格：￥电议型 号：T9264产 地：中国大陆
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T9343N-Cbz-DL-tryptophanNCbzDLtryptophan,N Cbz DL tryptophan
N-Cbz-DL-tryptophan is a cholecystokinin receptor antagonist, abolished the response of the isolated heart to CCK-8.
价 格：￥电议型 号：T9343产 地：中国大陆
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TQ0009UCB9608Phosphatidylinositol 4 kinases,UCB-9608,Inhibitor,UCB 9608,UCB9608,PI4 kinases,PI4K,inhibit
UCB9608 is a selective and orally active PI4KIIIβ inhibitor (IC50: 11 nM), selective over PI3KC2 α, β, and γ lipid kinases.
价 格：￥电议型 号：TQ0009产 地：中国大陆
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T13378Z-Asp-CH2-DCBZAspCH2DCB,Z Asp CH2 DCB,Z-Asp-CH-2-DCB
Z-Asp-CH2-DCB is an irreversible inhibitor of broad spectrum caspase.
价 格：￥电议型 号：T13378产 地：中国大陆
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T8389TrifluoperazineInhibitor,morphogenesis,Calmodulin-dependent protein kinases,antipsychotic,ABCB1,P-gl
Trifluoperazine is a Dopamine D2 receptor inhibitor(IC50 : 1.2 nM), and Treatment of schizophrenia.
价 格：￥电议型 号：T8389产 地：中国大陆
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TQ0044SeletalisibInhibitor,Phosphoinositide 3-kinase,Seletalisib,UCB-5857,UCB 5857,inhibit,PI3K
Seletalisib (UCB5857) is a potent and specific PI3Kδ inhibitor (IC50: 12 nM).
价 格：￥电议型 号：TQ0044产 地：中国大陆
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T9659LCB 03-0110LCB 030110,LCB 03 0110
LCB 03-0110 is a potent inhibitor of discoidin domain receptor family tyrosine kinases and strongly inhibits several tyrosine kinases, including the c-Src family, spleen tyrosine kinase, Bruton´s tyrosine kinase, and vascular endothelial growth factor receptor 2, which are important for immune cell signaling and inflammatory reactions.
价 格：￥电议型 号：T9659产 地：中国大陆
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T6886MCB-613inhibit,Inhibitor,MCB613,MCB-613
MCB-613 is an effective steroid receptor coactivator (SRC) stimulator.
价 格：￥电议型 号：T6886产 地：中国大陆
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T8658NEO2734PER-403,SPOP,NEO-2734,CBP,NEO 2734,MYC,HAT,NEO2734,Epigenetic Reader Domain,TC-797,Histone Ac
NEO2734 is an orally active and selective inhibitor of p300/CBP and BET bromodomain(IC50 of <30 nM for both p300/CBP and BET bromodomains).
价 格：￥电议型 号：T8658产 地：中国大陆
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T9370dCBP-1Inhibitor,p300,multiple,CRBN,myeloma,cell,degrader,PROTACs,MYC,CBP,inhibit,dCBP 1,dCBP1,hetero
dCBP-1 is a chemical degrader of p300/CBP. dCBP-1 hijacks the E3 ubiquitin ligase CRBN for selective degradation of p300/CBP. Degradation of p300/CBP by dCBP-1 leads to effective multiple myeloma cell killing.
价 格：￥电议型 号：T9370产 地：中国大陆
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TJS1159ChrysosplenetinP-glycoprotein,Cluster of differentiation 243,CYPs,Ferroptosis,Inhibitor,ABCB1,Chryso
1. Chrysosplenetin is a metabolic inhibitor of artemisinin.
价 格：￥电议型 号：TJS1159产 地：中国大陆
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T9687MAGL-IN-4Monoacylglycerol lipase,CB1,lipase,monoacylglycerol,CB2,Inhibitor,inhibit,BBB,barrier,MAGLI
MAGL-IN-4 is one of the monoacylglycerol lipase (MAGL) inhibitors in central nervous system-related diseases.
价 格：￥电议型 号：T9687产 地：中国大陆
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T14551BevenopranInhibitor,CB 5945,Bevenopran,CB5945,inhibit,Opioid Receptor,ADL 5945,ADL5945
Bevenopran is a peripheral antagonist of μ-opioid receptor and can be used in studies about the treatment of opioid-induced bowel dysfunction.
价 格：￥电议型 号：T14551产 地：中国大陆
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T6797TelaglenastatGlutaminase,antiproliferative,HCC-1806,TNBC,Telaglenastat,breast,Inhibitor,Autophagy,sp
CB-839(IC50 of 24 nM), an effective, specific, and oral inhibitor, which is bioavailable glutaminase, for recombinant human GAC.
价 格：￥电议型 号：T6797产 地：中国大陆
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T61111UCB-5307
UCB-5307 is a TNF signaling inhibitor with a K D of 9 nM. UCB-5307 can penetrate the preformed hTNF/hTNFR1 complex [1].
价 格：￥电议型 号：T61111产 地：中国大陆
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T6796CB-5083Inhibitor,inhibit,multiple,p97,VCP,solid,tumors,myeloma,AAA,ATPase,Cdc48,CB-5083
CB-5083 is a potent, selective, and orally bioavailable p97 AAA ATPase inhibitor ( IC50=11 nM).
价 格：￥电议型 号：T6796产 地：中国大陆
