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T1175Bromopride；溴灭吐灵Bromoprida|||Valopride|||Artomey；Bromoprida|||溴灭吐灵|||Valopride|||Artomey
Bromopride (Valopride) is a dopamine antagonist with prokinetic properties closely related to metoclopramide, and is widely used as an antiemetic. It is not available in the United States or the United Kingdom.
价 格：￥电议型 号：T1175产 地：中国大陆
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T11732JTV-519 hemifumarate；化合物 T11732K201 hemifumarate；K201 hemifumarate
JTV-519 hemifumarate,Antiarrhythmic and cardioprotective properties. is a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA) and a partial agonist of ryanodine receptors in striated muscle.
价 格：￥电议型 号：T11732产 地：中国大陆
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T11731LJTV-519 Formate；化合物JTV-519 FormateJTV-519 Formate (145903-06-6 Free base)；JTV-519 Formate (145903-06
JTV-519 Formate is a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA). JTV-519 Formate is also a partial agonist of ryanodine receptors in striated muscle. JTV-519 Formate exhibits antiarrhythmic and cardioprotective properties.
价 格：￥电议型 号：T11731L产 地：中国大陆
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T11731JTV-519 free base；化合物 T11731K201 free base；K201 free base
JTV-519 free base (K201 free base), recognized for its antiarrhythmic and cardioprotective properties, functions as a Ca2+-dependent blocker of sarcoplasmic reticulum Ca2+-stimulated ATPase (SERCA) and serves as a partial agonist of ryanodine receptors in striated muscle.
价 格：￥电议型 号：T11731产 地：中国大陆
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T1171LMethylprednisolone Aceponate；醋丙甲泼尼龙MPA|||SH 440|||SH-440|||SH440|||Advantan；MPA|||SH 440|||SH-440|||
Methylprednisolone Aceponate (SH 440), a non-halogenated corticosteroid, is a potent anti-inflammatory agent.
价 格：￥电议型 号：T1171L产 地：中国大陆
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T11719LJMV 2959；化合物 T11719LJMV 2959
JMV 2959 is an antagonist of growth hormone secretagogue receptor type 1a (GHS-R1a) (IC50: 32 nM).
价 格：￥电议型 号：T11719L产 地：中国大陆
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T11719JMV 2959 hydrochloride (925238-89-7 free base)；化合物JMV 2959 hydrochlorideJMV 2959 hydrochloride；JMV 2
JMV 2959 hydrochloride (925238-89-7 free base) is a growth hormone secretagogue receptor type 1a (GHS-R1a) antagonist with an IC50 of 32±3 nM in LLC-PK1 cells.
价 格：￥电议型 号：T11719产 地：中国大陆
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T11709JAK3 covalent inhibitor-1；化合物 T11709JAK3 covalent inhibitor-1
JAK3 Covalent Inhibitor-1 is a compound characterized by its potent and selective inhibition of Janus kinase 3 (JAK3), possessing an IC50 of 11 nM and demonstrating a 246-fold selectivity compared to other JAKs.
价 格：￥电议型 号：T11709产 地：中国大陆
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T11696Ivachtin；化合物IVACHTINCaspase-3 Inhibitor VII；Caspase-3 Inhibitor VII
Ivachtin (Caspase-3 Inhibitor VII) is a nonpeptide, noncompetitive and reversibl caspase-3 inhibitor(IC50 = 23 nM) and is a modest inhibitor of the remaining caspases.
价 格：￥电议型 号：T11696产 地：中国大陆
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T11695N-Demethyl ivabradine hydrochloride；化合物 T11695Ivabradine metabolite N-Demethyl Ivabradine hydrochlor
N-Demethyl Ivabradine Hcl is a specific inhibitor of the funny channel.N-Demethyl Ivabradine Hcl is a metabolite of Ivabradine.
价 格：￥电议型 号：T11695产 地：中国大陆
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T11694Ivabradine-d6 hydrochloride；盐酸伊伐布雷定 D6Ivabradine D6 hydrochloride；盐酸伊伐布雷定 D6|||Ivabradine D6 hydroch
Ivabradine hydrochloride is a new If inhibitor with IC50 of 2.9 μM, and used as a pure heart rate lowering agent. Ivabradine D6 hydrochloride is the deuterium labeled Ivabradine hydrochloride.
价 格：￥电议型 号：T11694产 地：中国大陆
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T11692Ivabradine-d3 hydrochloride；盐酸伊伐布雷定 D3Ivabradine D3 Hydrochloride；盐酸伊伐布雷定 D3|||Ivabradine D3 Hydroch
Ivabradine hydrochloride is a new If inhibitor with IC50 of 2.9 μM, and used as a pure heart rate lowering agent. Ivabradine D3 Hydrochloride is the deuterium labeled Ivabradine hydrochloride.
价 格：￥电议型 号：T11692产 地：中国大陆
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T11691IV-23；化合物 T11691IV-23
IV-23, a potent inhibitor of cell growth both in vitro and in vivo, effectively reduces colony formation, arrests the cell cycle at the M phase, and induces apoptosis in esophageal squamous cell carcinoma through Noxa-mediated pathways. This compound emerges as a promising anticancer agent with significant potential.
价 格：￥电议型 号：T11691产 地：中国大陆
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T11684Isoguvacine hydrochloride；异四氢烟酸1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride；1,2,3,6-te
Isoguvacine hydrochloride (1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride) is a GABA receptor agonist. Isoguvacine hydrochloride binds to rat synaptic cortical membranes and activates α1β2γ2S, α2β2γ2S, α3β2γ2S, α5β2γ2S, and ρ1 subunit GABAA receptors.
价 格：￥电议型 号：T11684产 地：中国大陆
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T11660Insulin levels modulator；化合物 T11660Insulin levels modulator
Insulin level regulators can be used to treat diabetes.
价 格：￥电议型 号：T11660产 地：中国大陆
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T11654Indirubin Derivative E804；化合物 T11654Indirubin Derivative E804
Indirubin Derivative E804 is an effective inhibitor of IGF1R, which has an IC50 value of 0.65.
价 格：￥电议型 号：T11654产 地：中国大陆
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T11643Impurity B of Calcitriol；化合物 T116431β,25-Dihydroxyvitamin-D3|||1-Epicalcitriol；1β,25-Dihydroxyvitami
Impurity B of Calcitriol is an impurity of Calcitriol. Calcitriol is the hormonally active form of vitamin D, Calcitriol is the active metabolite of vitamin D3 that activates the vitamin D receptor (VDR).
价 格：￥电议型 号：T11643产 地：中国大陆
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T1163Betamethasone valerate；倍他米松戊酸酯Betnovate|||Betaderm|||Betamethasone 17-valerate|||Luxiq；Betnovate|||倍
Betamethasone valerate (Luxiq) is a synthetic glucocorticoid with metabolic, immunosuppressive and anti-inflammatory actions.
价 格：￥电议型 号：T1163产 地：中国大陆
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T11608Epanolol；化合物 T11608Visacor|||ICI141292；Visacor|||ICI141292
Epanolol is a potent β-adrenoceptor partial agonist with a greater affinity for β1- than β2-adrenoceptors.
价 格：￥电议型 号：T11608产 地：中国大陆
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T11599Ibiglustat (L-Malic acid)；化合物Ibiglustat (L马来酸)Ibiglustat L-Malic acid|||GZ402671 (L-Malic acid)|||Ve
Ibiglustat (L-Malic acid) (Ibiglustat L-Malic acid) is a selective, brain-penetrant, and allosteric inhibitor of glucosylceramide synthase. Ibiglustat (L-Malic acid) can be used in studies about PD Parkinson’s disease, SRT in Fabry’s and Gaucher’s.
价 格：￥电议型 号：T11599产 地：中国大陆
