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T71392(R)-FTY-720 Vinylphosphonate；化合物 (R)-FTY-720 Vinylphosphonate(R)-FTY-720 Vinylphosphonate
(R)-FTY-720 Vinylphosphonate is a sphingosine 1-phosphate type 1 (S1P1) receptor agonist and lacks anti-apoptotic activity.
价 格：￥电议型 号：T71392产 地：中国大陆
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T71391BRL 37344；化合物 BRL 37344BRL 37344
BRL 37344 is a beta 3-adrenoceptor agonist.
价 格：￥电议型 号：T71391产 地：中国大陆
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T71390AY 29315；化合物 AY 29315AY 29315
AY 29315 is a histamine H2-receptor antagonist with antisecretory and antiulcer activities.
价 格：￥电议型 号：T71390产 地：中国大陆
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T71139EXP3892；化合物 EXP3892EXP3892
EXP3892 is an angiotensin II receptor antagonist.
价 格：￥电议型 号：T71139产 地：中国大陆
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T70909AY 31390；化合物 AY 31390AY 31390
AY 31390 is a phosphodiesterase (PDE) inhibitor with antithrombotic activity.
价 格：￥电议型 号：T70909产 地：中国大陆
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T70782PF-05139962；化合物 PF-05139962PF-05139962
PF-05139962 is a novel potent mTOR inhibitor with excellent mTOR biochemical inhibition, cellular potency, kinase selectivity and in vitro ADME properties. PF-05139962 has pS473 and pS6 cellular IC50 = 48 and 6 nM respectively. PF-05139962 has great selectivity against other receptors and kinases. No genotoxicity was observed on this compound and no more than 25% inhibiton was observed for major CYP enzymes (3A4, 1A2, 2C9, 2D6) at 3 uM. This compound has LE = 0.35 and LipE up to 6.8 which is in
价 格：￥电议型 号：T70782产 地：中国大陆
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T70703DK-139；化合物 DK-139DK-139
DK-139 is an inhibitor of NF-kappaB-mediated GROalpha expression, suppressing the TNFalpha-induced invasive capability of MDA-MB-231 human breast cancer cells.
价 格：￥电议型 号：T70703产 地：中国大陆
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T70356F-1394；化合物 F-1394F-1394
F-1394 is an acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. F-1394 both prevents the formation of atherosclerosis and accelerates its regression without affecting the serum TC level, indicating that F-1394 acts directly on the arterial wall. F-1394 significantly reduced neointimal thickening and the extent of macrophages in lesions without affecting serum cholesterol levels. In vitro, F-1394 attenuated foam cell formation in mouse peritoneal macrophages.
价 格：￥电议型 号：T70356产 地：中国大陆
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T70332JNJ-61393215；化合物 JNJ-61393215JNJ-61393215
JNJ-61393215 is a novel selective orexin-1 receptor (OX1R) antagonist.
价 格：￥电议型 号：T70332产 地：中国大陆
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T70139MSD-D；化合物 MSD-DMSD-D
MSD-D is an inhibitor of voltage-gated K(+) (Kv) channels Kv1.5.
价 格：￥电议型 号：T70139产 地：中国大陆
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T6S0139Neobavaisoflavone；新补骨脂异黄酮Neobavaisoflavone
1. Neobavaisoflavone is isolated as a DNA polymerase inhibitor. 2. Neobavaisoflavone might be a potential anabolic agent to treat bone loss-associated diseases. 3. Neobavaisoflavone has anti-inflammatory activity, can significantly inhibit the production of reactive oxygen species (ROS), reactive nitrogen species (RNS) and cytokines: IL-1β, IL-6, IL-12p4, IL-12p7, TNF-α in LPS+IFN-γ- or PMA- stimulated RAW264.7 macrophages.
价 格：￥电议型 号：T6S0139产 地：中国大陆
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T69452AG-13958 monohydrochloride；化合物 AG-13958 monohydrochlorideAG-13958 monohydrochloride
AG-13958 monohydrochloride is the HCl salt of AG-13958 --- a VEGFA inhibitor potentially for the treatment of age-related macular degeneration. Neovascular AMD, a subtype characterized by the growth of new, pathologic blood vessels, results in most of the cases of severe and rapid vision loss associated with AMD. A critical activator of angiogenesis in neovascular AMD is VEGF.
价 格：￥电议型 号：T69452产 地：中国大陆
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T69139Thalicarpine；化合物 ThalicarpineThalicarpine
Thalicarpine is a natural aporphine benzylisoquinoline vinca alkaloid with antineoplastic activity. Thalicarpine binds to and inhibits p-glycoprotein, the multidrug resistance efflux pump. Thalicarpine also induces single-strand breaks in DNA and arrests cancer cells at the G2/M and G1 phase of the cell cycle. Check for active clinical trials or closed clinical trials using this agent.
价 格：￥电议型 号：T69139产 地：中国大陆
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T68637NSC13987；化合物 NSC13987NSC13987
NSC13987 is an inhibitor of Nef-calnexin interaction.
价 格：￥电议型 号：T68637产 地：中国大陆
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T68610CGS 13928C；化合物 CGS 13928CCGS 13928C
CGS 13928C is a potent converting enzyme inhibitor
价 格：￥电议型 号：T68610产 地：中国大陆
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T6826Emricasan；恩利卡生PF 03491390|||IDN-6556；PF 03491390|||恩利卡生|||IDN-6556
Emricasan (IDN-6556) is a pan-caspase inhibitor with irreversible properties. Emricasan has anti-inflammatory and anti-apoptotic activity and can be used in the treatment of infections and liver failure, etc. Emricasan also inhibits Zika virus infections.
价 格：￥电议型 号：T6826产 地：中国大陆
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T67455-Iodotubercidin；5-碘代杀结核菌素5-ITu|||NSC 113939；5-碘代杀结核菌素|||5-ITu|||NSC 113939
5-Iodotubercidin (NSC-113939) is a potent adenosine kinase inhibitor with IC50 of 26 nM. It inhibits nucleoside transporter, CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2 and PKC.
价 格：￥电议型 号：T6745产 地：中国大陆
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T671393-(Trifluoromethyl)benzamide；化合物 3-(Trifluoromethyl)benzamide3-(Trifluoromethyl)benzamide
3-(Trifluoromethyl)benzamide is a useful organic compound for research related to life sciences. The catalog number is T67139 and the CAS number is 1801-10-1.
价 格：￥电议型 号：T67139产 地：中国大陆
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T661394-Amino-3,5-dichlorobenzaldehyde；化合物 4-Amino-3,5-dichlorobenzaldehyde4-Amino-3,5-dichlorobenzaldehyd
4-Amino-3,5-dichlorobenzaldehyde is a useful organic compound for research related to life sciences. The catalog number is T66139 and the CAS number is 62909-66-4.
价 格：￥电议型 号：T66139产 地：中国大陆
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T651392-Amino-3-methoxypropanoic acid；化合物 2-Amino-3-methoxypropanoic acid2-Amino-3-methoxypropanoic acid
2-Amino-3-methoxypropanoic acid is a useful organic compound for research related to life sciences. The catalog number is T65139 and the CAS number is 19794-53-7.
价 格：￥电议型 号：T65139产 地：中国大陆
