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￥ 0.00 “sb269970 hcl”的搜索结果
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AZD1208 HCl
Catalog No. A16927 -
RS 17053 HCl
Catalog No. A16885 α1A 拮抗剂RS 17053 HCl是α1A受体拮抗剂，对α1A受体具有很高的亲和力（pKi和pA2估计为9.1-9.9），选择性比α1B和α1D亚型高30-100倍（pKi和pA2估计为7.7- 7.8）。 了解更多 -
Desformylflustrabromine HCl
Catalog No. A17103 Desformylflustrabromine HCl是α4β2的正变构调节剂，也是肌肉型nAChR抑制剂。 了解更多 -
Anavex2-73 HCl
Catalog No. A17145 -
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TCS-OX2-29 HCl
Catalog No. A17136 -
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Procyclidine HCl
Catalog No. A17371 Muscarinic antagonistProcyclidine hydrochloride is a muscarinic antagonist that crosses the blood-brain barrier and is used in the treatment of drug-induced extrapyramidal disorders and in Parkinsonism. 了解更多 -
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SAR-7334 HCl
Catalog No. A17237 TRPC6 inhibitorSAR7334 is a novel, highly potent and bioavailable inhibitor of TRPC6 channels that opens new opportunities for the investigation of TRPC channel function in vivo. SAR7334 inhibited TRPC6, TRPC3 and TRPC7-mediated Ca(2+) influx into cells with IC50 s of 9.5, 282 and 226 nM, whereas TRPC4 and TRPC5-mediated Ca(2+) entry was not affected. 了解更多 -
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Ractopamine HCl
Catalog No. A17372 beta-Adrenergic agonistRactopamine HCl is a beta-Adrenergic agonist. It acts by being a full agonist at the TAAR1. 了解更多 -
Acecainide HCl
Catalog No. A22660 Class III antiarrhythmic agentAcecainide, also known as N-acetylprocainamide and ASL 601, is the N-acetylated metabolite of procainamide. Acecainide is a Class III antiarrhythmic agent. It can be given either intravenously or orally, and is eliminated primarily by renal excretion. 了解更多 -
MK-212 HCl
Catalog No. A22531 MK 212 hydrochloride is a 5-HT receptor agonist; displays selectivity for 5-HT2C over 5-HT2A (IC50 values are 0.028 and 0.42 μM for human 5-HT2C and 5-HT2A receptors expressed in HEK293 cells respectively). 了解更多 -
AVN-101 HCl
Catalog No. A22498 5-HT7 receptor antagonistAVN-101 is a very potent 5-HT7 receptor antagonist, with slightly lesser potency toward 5-HT6, 5-HT2A, and 5HT-2C receptors. It is a milti-target drug candidate for the treatment of CNS disorders. 了解更多 -
UK-371804 HCl
Catalog No. A22379 uPA inhibitorUK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibitor with excellent enzyme potency (Ki=10 nM) and selectivity profile (4000-fold versus tPA and 2700-fold versus plasmin). 了解更多 -
SEL24-B489 HCl
Catalog No. A22203 -
Prexasertib HCl
Catalog No. A22156 ATP-competitive CHK1 inhibitorPrexasertib (LY2606368) is an ATP-competitive CHK1 inhibitor with a Ki value of 0.9 nmol/L. For CHK2 and RSK, its IC50 values are 8 nM and 9 nM respectively in cell-free assay. 了解更多 -
17-DMAG HCl (Alvespimycin)
Catalog No. A10011 Hsp90 抑制剂17-DMAG HCl (Alvespimycin)是17-AAG和格尔德霉素的水溶性类似物，与Hsp90的ATP结合位点结合并抑制其伴侣活性。显示出比17-AAG更有效的抗肿瘤活性。 了解更多 -
MLN4924 (HCL Salt)
Catalog No. A11499 -
SB203186 HCl
Catalog No. A22523 -
TP0427736 HCl
Catalog No. A22382 ALK5 kinase activity inhibitorTP0427736 is a potent inhibitor of ALK5 kinase activity with an IC50 of 2.72 nM and this effect is 300-fold higher than the inhibitory effect on ALK3 (IC50 = 836 nM for ALK3). It also inhibits Smad2/3 phosphorylation in A549 cells induced by TGF-β1 with an IC50 value of 8.68 nM. 了解更多 -
AMG-073 HCl (Cinacalcet HCl)
Catalog No. A10219 CaSR activatorAMG-073 HCl（Cinacalcet HCl）是一种用于治疗甲状旁腺功能亢进的化合物，称为拟钙剂，通过增加甲状旁腺钙敏感受体（CaR）对细胞外钙的敏感性来减少甲状旁腺激素（PTH）的合成和分泌 。 了解更多 -
P005672 HCl (Sarecycline HCl)
Catalog No. A11283 P005672 HCl (Sarecycline HCl)是用于抗菌/消炎痤疮治疗的II期药物。 了解更多 -
SB-269970 hydrochloride
Catalog No. A21889 5-HT7 receptor antagonistSB269970 hydrochloride (SB-269970A) is a hydrochloride salt form of SB-269970, which is a 5-HT7 receptor antagonist with the pKi of 8.3, exhibits >50-fold selectivity against other receptors. 了解更多 -
SB269970 HCl
Catalog No. A11925
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