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T6S0655CorynoxeineExtracellular signal regulated kinases,ERK,Corynoxeine,Inhibitor,inhibit
1. Corynoxeine is a potent ERK1/2 inhibitor of key PDGF-BB-induced VSMC proliferation and may be useful in the prevention and treatment of vascular diseases and restenosis after angioplasty.
价 格：￥电议型 号：T6S0655产 地：中国大陆
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T60109Protein kinase inhibitor H-7
Protein kinase inhibitor H-7 is a potent inhibitor of protein kinase C (PKC) with a Ki of 6 μM. Protein kinase inhibitor H-7 is also a cyclic nucleotide dependent protein kinase inhibitor.
价 格：￥电议型 号：T60109产 地：中国大陆
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T7014VoxtalisibSAR-245409,SAR 245409,inhibit,Phosphoinositide 3-kinase,Mammalian target of Rapamycin,XL 7
Voxtalisib (SAR245409, XL765) is a dual inhibitor of mTOR/PI3K, mostly for p110γ with IC50 of 9 nM; also inhibits DNA-PK and mTOR. Phase 1/2.
价 格：￥电议型 号：T7014产 地：中国大陆
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T7955EB-3Dlipid,inhibit,lymphoblastic,AMP-activated protein kinase,EB3D,acute,tumorigenesis,Apoptosis,hom
EB-3D is a potent and selective choline kinase alpha 1 (ChoKα1) inhibitor(IC50 : 1 μM).with anti-cancer activity.
价 格：￥电议型 号：T7955产 地：中国大陆
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T6546IPA-3inhibit,Inhibitor,IPA-3,p21 activated kinases,PAK
IPA-3 is a selective non-ATP competitive Pak1 inhibitor with IC50 of 2.5 μM, no inhibition to group II PAKs (PAKs 4-6).
价 格：￥电议型 号：T6546产 地：中国大陆
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T7155JH-II-127HEK293,JHII127,3T3 cells,Inhibitor,LRRK2-G2019S,Ser935,Leucine-rich repeat kinase 2,LRRK2,p
JH-II-127 is an orally inhibitor of leucine-rich repeat kinase 2 (LRRK2). It inhibits WT LRRK2, G2019S LRRK2 and A2016T LRRK2 (IC50s = 6.6, 2.2, and 47.7 nM, respectively),
价 格：￥电议型 号：T7155产 地：中国大陆
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T6854GSK621Apoptosis,CHOP,GSK 621,inhibit,AMP-activated protein kinase,Inhibitor,UPR,PERK,GSK621,Autophag
GSK621 is a specific and potent AMPK activator.
价 格：￥电议型 号：T6854产 地：中国大陆
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T6993Tauroursodeoxycholate sodiummolecules,UR-906,Caspase,UR 906,Extracellular signal regulated kinases,r
Tauroursodeoxycholate Sodium is an endoplasmic reticulum (ER) stress inhibitor, used for the treatment of gallstones and liver cirrhosis.
价 格：￥电议型 号：T6993产 地：中国大陆
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T6840FRAX486PAK,p21 activated kinases,FRAX 486,Inhibitor,FRAX-486,inhibit,FRAX486
FRAX486 is a potent p21-activated kinase (PAK) inhibitor with IC50 values of 14, 33, 39 and 575 nM for PAK1, PAK2, PAK3 and PAK4 respectively.
价 格：￥电议型 号：T6840产 地：中国大陆
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T8719SC99orally,ERK,c-Src,SC 99,ATP-binding,phosphorylation,platelet,AKT,Janus kinase,activation,anti-mye
SC99 is a selective inhibitor of JAK2-STAT3 activation. SC99 downregulates the expression of STAT3-modulated genes.SC99 inhibits platelet activation, aggregation and displays potent anti-myeloma, anti-thrombotic activities
价 格：￥电议型 号：T8719产 地：中国大陆
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TQ0242Fenebrutinibinhibit,Inhibitor,GDC0853,GDC 0853,Fenebrutinib,Btk,Bruton tyrosine kinase
Fenebrutinib is a selective and noncovalent Btk inhibitor (Ki: 0.91 nM).
价 格：￥电议型 号：TQ0242产 地：中国大陆
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T9615CK7Inhibitor,Nek1,CDK,CK-7,Cdk9,CK 7,kidney development,CK7,inhibit,Cyclin dependent kinase,Cdk2
CK7, a?Cdk2/9?inhibitor, can be used for the synthesis of Nek1 inhibitor BSc5231 and BSc5367.
价 格：￥电议型 号：T9615产 地：中国大陆
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T6773AZD8186Phosphoinositide 3-kinase,inhibit,AZD-8186,AZD8186,PI3K,Inhibitor,AZD 8186
AZD8186 is an effective and specific PI3Kβ/δ inhibitor (IC50: 4/12 nM).
价 格：￥电议型 号：T6773产 地：中国大陆
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T6605NH125NH 125,Calmodulin-dependent protein kinases,NH-125,Calmodulin-dependent kinases,NH125,Inhibitor
NH125 is a selective eEF-2 kinase inhibitor with IC50 of 60 nM, >125-fold selectivity over PKC, PKA, and CaMKII, and also a potent histidine kinase inhibitor.
价 格：￥电议型 号：T6605产 地：中国大陆
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T8801SRI-29329Cyclin dependent kinase,inhibit,SRI29329,SRI-29329,Inhibitor,SRI 29329,CDK
SRI-29329 is a potent, specific inhibitor of CDC-like kinase (with IC50 of 78 nM, 16 nM and 86 nM for CLK1, CLK2 and CLK4, respectively).
价 格：￥电议型 号：T8801产 地：中国大陆
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T9460iMDKinhibit,iMDK,midkine,factor,PI3K,NSCLC,growth,Inhibitor,Phosphoinositide 3-kinase,MDK
iMDK quarterhydrate is a potent PI3K inhibitor that inhibits the growth factor MDK (also known as midkine or MK). iMDK quarterhydrate synergistically inhibits non-small cell lung cancer (NSCLC) with MEK inhibitors without harming normal cells and mice.
价 格：￥电议型 号：T9460产 地：中国大陆
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TP2310Autocamtide-2-related inhibitory peptideCalmodulin-dependent protein kinases,Autocamtide2related inh
Autocamtide-2-related inhibitory peptide is a highly specific and potent inhibitor of CaMKII with an IC50 of 40 nM.
价 格：￥电议型 号：TP2310产 地：中国大陆
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T64338AKI603AKI603,Aurora Kinase,chronic,CML,leukemia,myeloid,inhibit,imatinib-resistant,Inhibitor
AKI603 is a novel small molecule inhibitor of Aurora kinase A (AurA)(IC50 = 12.3 nM). AKI603 is developed to overcome resistance mediated by BCR-ABL-T315I mutation. AKI603 exhibits strong anti-proliferative activity in leukemic cells[1][2].
价 格：￥电议型 号：T64338产 地：中国大陆
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T7764CCG-222740Rho-associated kinase,CCG222740,Rho-kinase,Rho,CCG-222740,CCG 222740,Inhibitor,inhibit,mus
CCG-222740 is an inhibitor of Rho/MRTF pathway
价 格：￥电议型 号：T7764产 地：中国大陆
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T6659SB 415286inhibit,GSK-3,Inhibitor,Glycogen synthase kinase 3,Glycogen synthase kinase-3,Apoptosis,SB-
SB415286 is a potent GSK3α inhibitor with IC50/Ki of 78 nM/31 nM with equally effective inhibition of GSK-3β.
价 格：￥电议型 号：T6659产 地：中国大陆
