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T7083GLPG1837GLPG-1837,ABBV 974,Cystic fibrosis transmembrane conductance regulator,Inhibitor,CFTR,Autoph
GLPG1837 is an effective CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively.
价 格：￥电议型 号：T7083产 地：中国大陆
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T38163ML-148ML-148,ML 148,selective,Inhibitor,prostaglandin-signaling,15-PGDH,15-Hydroxyprostaglandin dehy
ML-148 is a selective inhibitor of 15-hydroxy prostaglandin dehydrogenase (15-PGDH, IC50 = 56 nM). ML-148 can be used to profile across a panel of related dehydrogenase or reductase enzymes and in studies about prostaglandin-signaling pathways.
价 格：￥电议型 号：T38163产 地：中国大陆
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T9098DMG-PEG 2000Inhibitor,therapy,T2D,lPEI/DNA nanoparticle,type II diabete,A549,HepG2,inhibit,HeLa,DMG-
DMG-PEG2000 is a lipid excipient that has been used in combination with other lipids in the formation of lipid nanoparticles. Formulations containing DMG-PEG2000 have been used in the development of lipid nanoparticles for the delivery of mRNA-based vaccines.
价 格：￥电议型 号：T9098产 地：中国大陆
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T7295MiridesapGSK 2315698,GSK-2315698,Miridesap,Inhibitor,inhibit
Miridesap is a divalent crosslinker of SAP that causes rapid depletion of circulating SAP via hepatic clearance. It also produces significant reduction of SAP from cerebrospinal fluid and visceral amyloid deposits
价 格：￥电议型 号：T7295产 地：中国大陆
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T9753LEI110HepG2 cells,inhibit,thiol hydrolases,LEI110,Inhibitor,LEI-110,lipolysis,Phospholipase,LEI 110
LEI110 is a potent Phospholipase A2, group XVI (PLA2G16) inhibitor with an Ki value of 20 nM. LEI110 is a selective pan-inhibitor of the HRASLS family of thiol hydrolases (i.e., PLA2G16, HRASLS2, RARRES3 and iNAT).
价 格：￥电议型 号：T9753产 地：中国大陆
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T7948HPGDS inhibitor 2HPGDS inhibitor2,PGE synthase,Inhibitor,inhibit,HPGDS inhibitor-2,HPGDS inhibitor 2
HPGDS inhibitor 2 is a potent, selective hematopoietic prostaglandin D synthase (h-pgds) inhibitor, IC50 = 9.9 nm.
价 格：￥电议型 号：T7948产 地：中国大陆
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T9720T3Inh-1T3Inh1,T3Inh 1,inhibit,O-glycosylation,Inhibitor,T-3Inh-1,ppGalNAc-T3,breast cancer cells,FGF
T3Inh-1 is an effective and selective inhibitor of ppGalNAc-T3 with an IC50 of 7 ?M. T3Inh-1 prevents breast cancer cells. T3Inh-1 reduces FGF23 hormone levels in both tissue cells and mice, without causing any toxic side effects.
价 格：￥电议型 号：T9720产 地：中国大陆
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T9945MNK8?MNK-8,HepG2,Bcl-2 Family,STAT3 inhibitor,inhibit,MNK8,MNK8?,Antimigratory agent,Inhibitor,STAT,
3-methyl-6- (naphthalen-1-yl)pyrimidine-2,4(1H, 3H)-dione is a potent STAT3 inhibitor that reduces the ability of STAT3 to bind to DNA and also has a good growth inhibition effect on liver cancer cells [1].
价 格：￥电议型 号：T9945产 地：中国大陆
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TP1952LPG 106 acetatePG 106 acetate
PG 106 acetate is an effective and selective antagonist of the human melanocortin 3 (hMC3) receptor with an IC50 of 210 nM. PG 106 acetate has no activity with the hMC5 receptor and hMC4 receptors with an EC50 of 9900 nM.
价 格：￥电议型 号：TP1952L产 地：中国大陆
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T10808CHPG sodium saltCHPG sodium salt
CHPG sodium salt is a selective agonist of mGluR5 and activates the ERK and Akt signaling pathways. CHPG sodium salt can be used in studies about traumatic brain injury.
价 格：￥电议型 号：T10808产 地：中国大陆
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TP1773LPGLa acetatePGLa acetate
PGLa acetate is a 21-residue member of the magainin family of antibiotic peptides.
价 格：￥电议型 号：TP1773L产 地：中国大陆
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T9044SORT-PGRN interaction inhibitor 1inhibit,PPI,Inhibitor,sortilin,SORTPGRN interaction inhibitor 1,pro
SORT-PGRN interaction inhibitor 1 is a potent sortilin-progranulin interaction inhibitor(IC50 of 2 μM).
价 格：￥电议型 号：T9044产 地：中国大陆
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T7149S29434cell-permeable,inhibit,selective,S 29434,HepG2,mice,NMDPEF,S-29434,ROS,Autophagy,S29434,Inhibi
S29434 (NMDPEF) is a potent, competitiveinhibitor of quinone reductase 2 (QR2;IC50:5-16nM).
价 格：￥电议型 号：T7149产 地：中国大陆
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T11410LGLPG0492GLPG0492,GLPG-0492
GLPG0492 is a novel selective androgen receptor modulator. After oral dosing, it showed anabolic activity on muscle, strongly dissociated from the androgenic activity on the prostate.
价 格：￥电议型 号：T11410L产 地：中国大陆
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T9984Antimalarial agent 13Antimalarial agent13,P. falciparum,Inhibitor,Antimalarial agent 13,inhibit,HepG
N2-(3-chlorophenyl)-N4-(furan-2-ylmethyl)quinazoline-2,4-diamine (antimalarial agent 13 ) is a potent antimalarial agent.
价 格：￥电议型 号：T9984产 地：中国大陆
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T8949UDP-g acidUDPg acid,UDP g acid
UDP-g acid is a sugar used in the production of polysaccharides and is an intermediate in the biosynthesis of ascorbic acid
价 格：￥电议型 号：T8949产 地：中国大陆
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T8198VisnaginCYP1A1,inhibit,HepG2,vascular,acute,vasodilator,Visnagin,muscles,Inhibitor,pancreatitis,smoo
Visnagin has acute hypotensive, anti-inflammatory, and neuroprotective effects, it protects against doxorubicin-induced cardiomyopathy through modulation of mitochondrial malate dehydrogenase.
价 格：￥电议型 号：T8198产 地：中国大陆
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T17232VidupiprantProstaglandin Receptor,AMG-853,Inhibitor,orally,acid,cAMP,phenylacetic,asthma,PGD2,AMG 00
Vidupiprant is an effective dual antagonist of CRTH2 and prostanoid D receptor with IC50s of 8 nM and 35 nM in human plasma. Vidupiprant can be used in studies about the treatment of asthma.
价 格：￥电议型 号：T17232产 地：中国大陆
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T6583MG-101RKO,MG-101,colon cancer,Bax,HepG2,Proteasome,MG 101,Inhibitor,mitochondria,HCT116,inhibit,Apop
MG-101 (ALLN) is a cell-permeable and potent inhibitor of cysteine proteases including calpains and lysosomal cathepsins.
价 格：￥电议型 号：T6583产 地：中国大陆
