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产品数：86101
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T11105DS88790512；化合物 T11105DS88790512
DS88790512, IC50 at 11 nM, is an effective, selective, oral bioeffective TRPC6 inhibitor.
价 格：￥电议型 号：T11105产 地：中国大陆
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T11048LDIPQUO hydrochloride；化合物DIPQUO盐酸盐DIPQUO hydrochloride(1269365-82-3 Free base)；DIPQUO hydrochloride(1
DIPQUO hydrochloride is an activator of the bone marker alkaline phosphatase (ALP), with an EC50 of 6.27 μM in C2C12 cells. DIPQUO hydrochloride promotes mouse and human osteoblast differentiation via activation of p38 MAPK-β.
价 格：￥电议型 号：T11048L产 地：中国大陆
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T11021DHODH-IN-12；化合物DHODH-IN-12DHODH-IN-12
DHODH-IN-12 is a leflunomide derivative and a weak dihydrorotate dehydrogenase (DHODH) inhibitor with a pKa of 5.07.
价 格：￥电议型 号：T11021产 地：中国大陆
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T11015Midaglizole hydrochloride；咪格列唑盐酸盐(±)-DG5128|||(±)-DG5128 hydrochloride|||DG5128 hydrochloride|||DG
Midaglizole hydrochloride ((±)-DG5128) (DG5128) is a preferred α2-adrenoceptor antagonist. Midazolazole hydrochloride (DG5128) has an affinity for α2-adrenoceptor (pKi = 6.28) 7.4 times higher than that of α1-adrenoceptor.
价 格：￥电议型 号：T11015产 地：中国大陆
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T11012Dextran；葡聚糖Dextran 40；Dextran 40|||葡聚糖
Dextran has an inhibitory effect on platelet aggregation and coagulation factors, and is used as an agent for increasing plasma volume.
价 格：￥电议型 号：T11012产 地：中国大陆
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T10965DBPR112；化合物DBPR112DBPR112
DBPR112 is an orally active furanopyrimidine-based EGFR inhibitor with IC50s of 15 nM and 48 nM for EGFRWT and EGFRL858R/T790M, respectively. DBPR112 can occupy the ATP-binding site. DBPR112 has significant antitumor efficacy.
价 格：￥电议型 号：T10965产 地：中国大陆
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T10958Dapagliflozin-d5；化合物 T10958BMS-512148 D5；BMS-512148 D5
Dapagliflozin D5 (BMS-512148 D5) is deuterated Dapagliflozin. Dapagliflozin is a competitive SGLT2 inhibitor.
价 格：￥电议型 号：T10958产 地：中国大陆
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T10952LDabuzalgron HCl；化合物 T10952LR1240|||R-450|||R450|||RO-1151240|||R-1240|||RO1151240；R1240|||R-450|||R4
Dabuzalgron, an adrenoceptor agonist, is used potentially for the treatment of urinary incontinence.
价 格：￥电议型 号：T10952L产 地：中国大陆
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T10952Dabuzalgron；达布扎琼Ro 115-1240；达布扎琼|||Ro 115-1240
Dabuzalgron (Ro 115-1240) is an orally active selective alpha-1A adrenergic receptor agonist used to treat urinary incontinence. Dabuzaron prevents cardiotoxicity caused by doxorubicin by maintaining mitochondrial function.
价 格：￥电议型 号：T10952产 地：中国大陆
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T10912S1PR1-MO-1；化合物 T10912S1PR1-MO-1
S1PR-MO-1 is a modulator of sphingosine-1-phosphate receptor and is used to study hyperproliferative inflammatory diseases.
价 格：￥电议型 号：T10912产 地：中国大陆
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T10849CMLD012612；化合物 T10849CMLD012612
CMLD012612 is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor. It inhibits cell translation and is cytotoxic to NIH/3T3 cells (IC50: 2 nM).
价 格：￥电议型 号：T10849产 地：中国大陆
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T10848CMLD012073；化合物 T10848CMLD012073
CMLD012073 is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor. It inhibits NIH/3T3 cells (IC50: 10 nM). CMLD012073 inhibits eukaryotic translation initiation by modifying the behavior of the RNA helicase (eIF4A).
价 格：￥电议型 号：T10848产 地：中国大陆
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T10847CMLD012072；化合物 T10847CMLD012072
CMLD012072 is a potent eukaryotic initiation factor 4A (eIF4A) inhibitor with potent anti-neoplastic activity. It can induce RNA clamping of eIF4A1 and eIF4A2.
价 格：￥电议型 号：T10847产 地：中国大陆
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T10812Cicloprolol hydrochloride；环丙洛尔盐酸盐Cicloprolol hydrochloride
Cicloprolol hydrochloride is a new potent and selective beta 1-adrenoceptor antagonist with partial agonist activity for the study of coronary heart disease.
价 格：￥电议型 号：T10812产 地：中国大陆
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T10792LCHK1-IN-4 hydrochloride；化合物CHK1-IN-4盐酸盐CHK1-IN-4 hydrochloride（2120398-41-4 Free base）；CHK1-IN-4 hyd
CHK1-IN-4 hydrochloride is a potent inhibitor of checkpoint kinase 1 (chk1). CHK1-IN-4 hydrochloride potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 hydrochloride has anti-tumor activity.
价 格：￥电议型 号：T10792L产 地：中国大陆
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T10778CGP 20712 A；化合物 CGP 20712 ACGP 20712 mesylate；CGP 20712 mesylate
CGP 20712 A (CGP 20712 mesylate) is a selective and potent β1-adrenergic receptor antagonist (IC50: 0.7 nM) with antihypertensive activity that reverses RKT-induced gastric relaxation.
价 格：￥电议型 号：T10778产 地：中国大陆
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T10759CEP-28122 mesylate salt (1022958-60-6 free base)；化合物CEP-28122 mesylate saltCEP-28122 mesylate salt；C
CEP-28122 mesylate salt (1022958-60-6 free base) is a highly selective orally active ALK inhibitor (IC50: 1.9 nM in an enzyme-based TRF assay).
价 格：￥电议型 号：T10759产 地：中国大陆
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T10744LSEL120-34A HCl；化合物SEL120-34A HClSEL120-34A HCl
SEL120-34A HCl is a selective, orally available and ATP-competitive inhibitor of CDK8(CDK8/CycC and CDK19/CycC with IC50s of 4.4 nM and 10.4 nM , respectively), with antitumor activity.
价 格：￥电议型 号：T10744L产 地：中国大陆
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T10744SEL120-34A；化合物SEL120-34ASEL120-34A
SEL120-34A is a selective and ATP-competitive inhibitor of CDK8 with IC50s of 4.4 nM, 10.4 nM and 1070 nM for CDK8/CycC, CDK19/CycC and CDK9/cycT. SEL120-34A possesses antitumor activity.
价 格：￥电议型 号：T10744产 地：中国大陆
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T10712CCR2 antagonist 3；化合物CCR2 antagonist 3AZD-2927|||AZD2927；AZD-2927|||AZD2927
CCR2 antagonist 3 (AZD-2927) is an antagonist of CCR2.
价 格：￥电议型 号：T10712产 地：中国大陆
