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T7778LGlypromate acetate(32302-76-4 free base)Glypromate acetate(32302 76 4 free base),Glypromate acetate(
Glypromate acetate is a neuroprotective agent, is a weak NMDA receptor agonist.
价 格：￥电议型 号：T7778L产 地：中国大陆
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T5605EZM 2302GSK3359088
EZM2302 is a selective, and orally available arginine methyltransferase CARM1 inhibitor (IC50: 6 nM).
价 格：￥电议型 号：T5605产 地：中国大陆
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T23027MRT-10MRT 10
MRT 10 is a smoothened (Smo) receptor antagonist (an IC50 = 0.5 μM in HEK293 cells transiently expressing mouse Smo). It also inhibits bodipy-cyclopamine binding to the murine Smo receptor (an IC50 = 0.5 μM
价 格：￥电议型 号：T23027产 地：中国大陆
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T2302CNX-774CNX774；CNX 774
CNX-774 is a highly specific, irreversible, and orally active BTK inhibitor (IC50<1 nM).
价 格：￥电议型 号：T2302产 地：中国大陆
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T12302OMDM-1(Z)-N-[(2S)-1-hydroxy-3-(4-hydroxyphenyl)propan-2-yl]octadec-9-enamide
OMDM-1 is a selective and metabolically stable anandamide cellular uptake (ACU)inhibitor with a Ki of 2.4 μM.
价 格：￥电议型 号：T12302产 地：中国大陆
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T2302CNX-774CNX-774,CNX774,CNX 774
CNX-774 is a highly specific, irreversible, and orally active BTK inhibitor (IC50<1 nM).
价 格：￥电议型 号：T2302产 地：美洲
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T5605EZM 2302EZM 2302,GSK3359088,
EZM2302 is a selective, and orally available arginine methyltransferase CARM1 inhibitor (IC50: 6 nM).
价 格：￥电议型 号：T5605产 地：美洲
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T82883BIM-23027；化合物 BIM-23027BIM-23027
BIM-23027 is a selective sst 2 receptor agonist (EC 50 = 0.32 nM) with effects analogous to the cyclic tetradecapeptide somatostatin (SRIF). It promotes dopamine release through a Glu-dependent mechanism [1] [2].
价 格：￥电议型 号：T82883产 地：中国大陆
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T82302Glucodichotomine B；化合物 Glucodichotomine BGlucodichotomine B
Glucodichotomine B (Compound 13), a natural product extracted from the roots of the Chinese medicinal plant Stellaria dichotoma L. var. lanceolata, exhibits antitumor activity [1].
价 格：￥电议型 号：T82302产 地：中国大陆
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T7778LGlypromate acetate(32302-76-4 free base)；化合物Glypromate acetateGlypromate acetate(32302-76-4 free bas
Glypromate acetate is a neuroprotective agent, is a weak NMDA receptor agonist.
价 格：￥电议型 号：T7778L产 地：中国大陆
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T72302Mtb-cyt-bd oxidase-IN-6；化合物 Mtb-cyt-bd oxidase-IN-6Mtb-cyt-bd oxidase-IN-6
Mtb-cyt-bd oxidase-IN-6, a potent inhibitor of Mycobacterium tuberculosis (Mtb) cytochrome bd (cyt-bd) oxidase (MtbCyt-bd Oxidase), exhibits an inhibitory concentration (IC50) of 0.35 μM and effectively suppresses Mtb growth with a minimum inhibitory concentration (MIC) of 4 μM. This compound is utilized in tuberculosis research [1].
价 格：￥电议型 号：T72302产 地：中国大陆
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T70569MD-230254；化合物 MD-230254MD-230254
MD-230254 is an inhibitor of MAO-B.
价 格：￥电议型 号：T70569产 地：中国大陆
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T70344BJ-2302；化合物 BJ-2302BJ-2302
BJ-2302 is a SRC inhibitor. BJ-2302 effectively suppressed MDA-MB-231 cell invasion (Matrigel invasion assay) and metastasis (chorioallantoic membrane assay xenografted with MDA-MB-231-luc2-tdTomato cancer cells). Additionally, BJ-2302 (1 mg/kg) strongly suppressed TNBC cell proliferation in vitro and tumor growth in a xenograft mouse tumor model. The anti-metastatic and anti-tumor effects of BJ-2302 were superior to those of Z-FL-COCHO (1 mg/kg) or batimastat (30 mg/kg), a pan-MMP inhibitor.
价 格：￥电议型 号：T70344产 地：中国大陆
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T62302ALK5-IN-28；化合物 ALK5-IN-28ALK5-IN-28
ALK5-IN-28 is a selective inhibitor of ALK-5 with an IC50 ≤ 10 nM that inhibits TGF-β-induced SMAD signalling.ALK5-IN-28 has the potential to inhibit tumour growth in vivo.ALK5-IN-28 can be used to study proliferative diseases (e.g. cancer, fibrotic diseases, systemic sclerosis).
价 格：￥电议型 号：T62302产 地：中国大陆
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T5605EZM 2302；化合物EZM 2302GSK3359088；GSK3359088
EZM 2302 (GSK3359088) is a selective, and orally available arginine methyltransferase CARM1 inhibitor (IC50: 6 nM).
价 格：￥电议型 号：T5605产 地：中国大陆
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T34881Tilnoprofen arbamel；化合物 T34881Y23023|||Y 23023|||Y-23023；Y23023|||Y 23023|||Y-23023
Tilnoprofen arbamel is a biochemical.
价 格：￥电议型 号：T34881产 地：中国大陆
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T32302JNJ-16567083；化合物 T32302JNJ-16567083
JNJ-16567083 is a bioactive chemical.
价 格：￥电议型 号：T32302产 地：中国大陆
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T23842Butaclamol free base；化合物 T23842Butaclamol|||AY 23028|||AY 23,028|||AY-23028|||AY23,028|||AY-23,028；B
Butaclamol is a typical antipsychotic which was never marketed. It also acts as a dopamine receptor antagonist.
价 格：￥电议型 号：T23842产 地：中国大陆
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T23029MS 245 oxalate化合物 T23029MS 245 oxalate
MS 245 oxalate is a 5-HT6 antagonist.
价 格：￥电议型 号：T23029产 地：中国大陆
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T23028MRT67307 HCl (1190378-57-4 free base)；化合物 T23028MRT67307 HCl；MRT67307 HCl
MRT67307 is an inhibitor for TBK1, IKKε , MARK1-4 and NUAK1 with IC50 value of 19, 160, 27-52 and 230nM , respectively [1]. It is an inhibitor for ULK1and ULK2 with IC50 value of 45 and 38nM, respectively [2]. Also, it is a salt inducible kinase (SIK) inhibitor with IC50 value of 250, 67 and 430nM for SIK1, SIK2 and SIK3, respectively.
SIKs prevent the formation of regulatory macrophages and their inhibition induces increasing in some markers of regulatory macrophages, such as IL-10 and oth价 格：￥电议型 号：T23028产 地：中国大陆
