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产品数：86101
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T15382GI 181771GI 181771
GI 181771 is an agonist of the cholecystokinin 1 receptor. GI 181771 can be used in studies about obesity.
价 格：￥电议型 号：T15382产 地：中国大陆
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T8153glycohyodeoxycholic acidBile,metabolite,7α-hydroxylase,Inhibitor,hyodeoxycholic,preventative,gallsto
glycohyodeoxycholic acid is a major metabolite of the secondary bile acid hyodeoxycholic acid in humans.
价 格：￥电议型 号：T8153产 地：中国大陆
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T9239RS-25344RS25344,RS 25344
RS-25344 is a potent and selective phosphodiesterase (PDE) 4 inhibitor. It inhibits eosinophil chemotaxis and increases progressive motility of spermatozoa in vitro.
价 格：￥电议型 号：T9239产 地：中国大陆
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T6853GSK591GSK 591,EPZ-015866,GSK591,Inhibitor,GSK 3203591,EPZ 015866,inhibit,GSK-3203591,GSK-591,Histone
GSK591, Alternative Names are EPZ015866, GSK3203591, is a potent selective inhibitor of the arginine methyltransferase PRMT5 (IC50=11 nM).
价 格：￥电议型 号：T6853产 地：中国大陆
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TP2308TB500 acetate(885340-08-9 free base)TB500 acetate(885340089 free base),TB500 acetate(885340 08 9 fre
TB500 Acetate is a synthetic version of an active region of thymosin β4. It promote endothelial cell differentiation, angiogenesis in dermal tissues, keratinocyte migration, collagen deposition and decrease inflammation.
价 格：￥电议型 号：TP2308产 地：中国大陆
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TN1053Aloe-emodin-8-O-β-D-glucopyranosideinhibit,Aloe emodin 8 O β D glucopyranoside,Phosphatase,Aloeemodi
Aloe-emodin-8-O-beta-D-glucopyranoside shows moderate bioactivity against human Protein Tyrosine Phosphatase 1B (hPTP1B) in vitro.
价 格：￥电议型 号：TN1053产 地：中国大陆
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T6893MK-886leukotriene,FLAP,5-LOX,5-LO activating protein,non-competitive,L-663536,L663536,keratin-1,Leuk
MK-886 is an inhibitor of leukotriene biosynthesis, inhibiting 5-lipoxygenase-activating protein (FLAP). It is also a moderately potent PPARα antagonist.
价 格：￥电议型 号：T6893产 地：中国大陆
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TN12533-hydroxymorindoneinhibit,3-Hydroxymorindone,anthraquinone,Inhibitor,dye,3 hydroxymorindone,3hydroxy
3-hydroxymorindone is a natural product from Morinda citrifolia. 3-hydroxymorindone is a pigment.
价 格：￥电议型 号：TN1253产 地：中国大陆
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T6S1537Cryptochlorogenic acidCryptochlorogenic acid,Inhibitor,inhibit,Endogenous Metabolite
1. Cryptochlorogenic acid has antioxidant activity.
价 格：￥电议型 号：T6S1537产 地：中国大陆
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T6536HJC0350inhibit,HJC-0350,Inhibitor,HJC 0350,HJC0350
HJC0350 is an effective and specific EPAC2 inhibitor (IC50: 0.3 μM), and no inhibition of Epac1.
价 格：￥电议型 号：T6536产 地：中国大陆
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T9165AZD5305repair,AZD5305,Inhibitor,poly ADP ribose polymerase,DNA,AZD-5305,PARP,inhibit,pathway,synthet
AZD5305 is a potent, selective and oral active PARP inhibitor.
价 格：￥电议型 号：T9165产 地：中国大陆
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T9530W 36017W-36017,W 36017,pain,inhibit,Inhibitor,W36017,nerve blocking
W 36017 is a chemical compound.
价 格：￥电议型 号：T9530产 地：中国大陆
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TP2135LcAC 253 acetate
cAC 253 acetate is an amylin antagonist. cAC 253 acetate inhibits 125I-adrenomedullin binding, with an IC50 of 25 nM.
价 格：￥电议型 号：TP2135L产 地：中国大陆
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T15363FzM1.8FzM-1.8,FzM1.8
FzM1.8 is an allosteric FZD4 agonist with a pEC50 of 6.4. FzM1.8 binds to FZD4, promotes TCF/LEF transcriptional activity in the absence of any WNT ligand, and activates the WNT/β-catenin pathway.
价 格：￥电议型 号：T15363产 地：中国大陆
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T37806JNJ-55308942JNJ 55308942,JNJ55308942
JNJ-55308942 is a selective and brain-penetrant antagonist of P2X7 functional with IC50s of 10 and 15 nM and Kis of 7.1 and 2.9 nM for hP2X7 and rP2X7, respectively.
价 格：￥电议型 号：T37806产 地：中国大陆
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T22049BMS 753BMS 753
BMS 753 is an agonist of isotype-selective retinoic acid receptor α (RARα, Ki= 2 nM).
价 格：￥电议型 号：T22049产 地：中国大陆
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TQ0266MSC2530818Cyclin dependent kinase,Inhibitor,CDK,MSC2530818,inhibit,MSC 2530818,MSC-2530818
MSC2530818 is an effective, selective and orally available CDK8 inhibitor (IC50: 2.6 nM).
价 格：￥电议型 号：TQ0266产 地：中国大陆
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T8773MID-1MID-1,inhibit,Inhibitor,MG53,ubiquitination,Insulin Receptor,insulin,association,glucose,MID1,I
MID-1 is an inhibitor of MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) interaction. It disrupts molecular association of MG53 with IRS-1 and abolishes MG53-induced IRS-1 ubiquitination and degradation in skeletal muscle, leading to elevated IRS-1 expression level and increased insulin signaling and glucose uptake
价 格：￥电议型 号：T8773产 地：中国大陆
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T8774MS7972inhibit,Inhibitor,MDM-2/p53,MS-7972,MS7972,MS 7972
MS7972 is CREBBP inhibitor that blocks human p53 and CREB binding protein association. MS7972 can almost completely block this BRD interaction at 50 μM
价 格：￥电议型 号：T8774产 地：中国大陆
