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T4249AZD3759 hydrochloride
AZD3759 (hydrochloride) is an effective, orally active and central nervous system-penetrant EGFR inhibitor. At Km ATP concentrations, the IC50s are 0.2/0.3/0.2 nM for EGFR (L858R)/EGFR (wt)/EGFR (exon 19Del).
价 格：￥电议型 号：T4249产 地：中国大陆
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T4225Dextrorphan tartrateNIH 4591；Dextrorphan D-tartrate；Dextrophan tartrate；去甲右美沙芬酒石酸盐
Dextrorphan D-tartrate is a noncompetitive NMDA glutamate receptor antagonist.
价 格：￥电议型 号：T4225产 地：中国大陆
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T4209TAK-659 hydrochlorideTAK-659
TAK-659 is a potent and selective inhibitor of spleen tyrosine kinase (SYK) with an IC50 value of 3.2 nM. It is selective against most other kinases, but potent toward both SYK and FLT3.
价 格：￥电议型 号：T4209产 地：中国大陆
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T4114Diffractaic Acid地弗地衣酸；NSC 5901；NSC 685595
Diffractaic Acid can inhibit LTB4 biosynthesis in A-23187-stimulated bovine PMNL cells with activity value of 8 μM.
价 格：￥电议型 号：T4114产 地：中国大陆
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T4059Selamectin司拉克丁；塞拉菌素；UK-124114
Selamectin is a macrocyclic lactone derivative of ivermectin, an anthelmintic that potentiates glutamate- and GABA-gated chloride channel opening in nematodes. In an H. contortus larval development assay, selamectin (0.1 μg/ml) shows the effect of growth
价 格：￥电议型 号：T4059产 地：中国大陆
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T4043ETC-159ETC159；ETC-1922159；ETC 159
ETC-159 is a potent, orally available PORCN inhibitor. It inhibits β-catenin reporter activity with an IC50 of 2.9 nM.
价 格：￥电议型 号：T4043产 地：中国大陆
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T3S2259Methyl eugenol4-allylveratrole；eugenyl methyl ether；O-methyleugenol；Eugenol Methyl ether；甲基丁香酚；丁香酚甲醚
1. Methyleugenol (ME) is a natural constituent of the essential oils of a number of plants widely used in foodstuffs as flavouring agents, in view of the carcinogenic potential of ME, the need to check its presence in food products with effective analytic
价 格：￥电议型 号：T3S2259产 地：中国大陆
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T3S1591Notoginsenoside Fc三七皂苷 FC；三七皂苷Fc
1. Notoginsenoside Fc has perfect anti-platelet aggregatory effect.
价 格：￥电议型 号：T3S1591产 地：中国大陆
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T395984-Chlorocatechol
4-Chlorocatechol is a major degradation product of 4-chloro-2-aminophenol (4C2AP). 4-Chlorocatechol is also a substrate for catechol 1,2-dioxygenases and chlorocatechol dioxygenase [1] [2] .
价 格：￥电议型 号：T39598产 地：中国大陆
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T3959ICA-069673ICA069673
ICA-069673 is an activator of KCNQ2/Q3 potassium channel (IC50: 0.69 μM).
价 格：￥电议型 号：T3959产 地：中国大陆
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T39359Lγ-Glu-Gly acetate
γ-Glu-Gly aceate is a human lipid metabolite that is acetate for γ-glutamine dipeptide.
价 格：￥电议型 号：T39359L产 地：中国大陆
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T38359Dup-721
DuP-721 is a broad spectrum and orally active antibacterial agent against a variety of clinically susceptible and resistant bacteria, especially M. tuberculosis[1].
价 格：￥电议型 号：T38359产 地：中国大陆
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T37859SY-640
SY-640 is a derivative of Acetamide showing potent hepatoprotective effects.
价 格：￥电议型 号：T37859产 地：中国大陆
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T37596Terevalefim
Terevalefim (ANG-3777), an hepatocyte growth factor (HGF) mimetic, selectively activates the c-Met receptor[1][2].
价 格：￥电议型 号：T37596产 地：中国大陆
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T37593,4-Dimethoxycinnamic acid3,4-二甲氧基肉桂酸；O-Methylferulic acid；Dimethylcaffeic acid；Caffeic acid dimethy
3,4-Dimethoxycinnamic acid (O-Methylferulic acid) is a monomer extracted and purified from Securidaca inappendiculata Hassk. 3,4-Dimethoxycinnamic acid exerts anti-apoptotic effects on L-02 cells via the ROS-mediated signaling pathway. Anti-apoptotic effe
价 格：￥电议型 号：T3759产 地：中国大陆
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T3720Tebanicline hydrochloride替巴克兰盐酸盐；Ebanicline hydrochloride；ABT-594 hydrochloride
Tebanicline (ABT-594, Ebanicline), is an effective synthetic nicotinic (non-opioid) analgesic drug.
价 格：￥电议型 号：T3720产 地：中国大陆
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T3699Bay 59-3074
Bay 59-3074 is a CB1/CB2 receptor partial agonist (Ki: 48.3/45.5 nM). In rat models of chronic neuropathic and inflammatory pain, it displays anti-hyperalgesic and antiallodynic properties.
价 格：￥电议型 号：T3699产 地：中国大陆
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T3659ZorifertinibAZD3759
AZD3759 is an orally active, effective and central nervous system-penetrant EGFR inhibitor. The IC50 values were 0.2, 0.3 and 0.2 nM for EGFR L858R mutant, TK wild-type, and Exon 19Del enzymes, respectively.
价 格：￥电议型 号：T3659产 地：中国大陆
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T36520COR659
COR659 is a 2-acylaminothiophene derivative able to suppress alcohol and chocolate self-administration in rats, likely via positive allosteric modulation of the GABAB receptor and antagonism/inverse agonism at the cannabinoid CB1 receptor.
价 格：￥电议型 号：T36520产 地：中国大陆
