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T14939LCGP-42112 acetate；CGP-42112醋酸CGP-42112 acetate(127060-75-7 Free base）；CGP-42112 acetate(127060-75-7
CGP-42112 acetate is a potent angiotensin receptor AT2 agonist that inhibits the increase in protein kinase A activity produced by LPS.
价 格：￥电议型 号：T14939L产 地：中国大陆
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T14939CGP-42112化合物 T14939CGP42112A
CGP-42112 is an agonist of the Angiotensin-II subtype 2 receptor (AT2 R).
价 格：￥电议型 号：T14939产 地：中国大陆
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T14937CG-806；化合物 T14937CG-806
CG-806 is an inhibitor that can inhibit a variety of kinases such as FLT3/BTK.
价 格：￥电议型 号：T14937产 地：中国大陆
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T14936Ivaltinostat；化合物 T14936CG-200745；CG-200745
CG-200745 is a potent inhibitor of HDAC. CG200745 induces apoptosis and also inhibits the deacetylation of histone H3 and tubulin.
价 格：￥电议型 号：T14936产 地：中国大陆
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T14935Elexacaftor；化合物ElexacaftorVX-445；VX-445
Elexacaftor (VX-445) is a modulator of cystic fibrosis transmembrane conductance regulator (CFTR) and it also facilitates the processing and trafficking of CFTR to increase the amount of CFTR at the cell surface.
价 格：￥电议型 号：T14935产 地：中国大陆
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T14934Cethromycin；化合物 T14934Abbott-195773|||ABT-773|||A-195773；Abbott-195773|||ABT-773|||A-195773
Cethromycin (ABT-773) is an antibiotic of ketolide.
价 格：￥电议型 号：T14934产 地：中国大陆
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T14933Cetaben；西他苯Cetaben
Cetaben is a PPARα-independent peroxisome proliferator. Cetaben is a non-fibrotic lipid-lowering drug that effectively reduces cholesterol and triglyceride concentrations.
价 格：￥电议型 号：T14933产 地：中国大陆
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T14932L1Ceruletide Ammonium Salt；化合物Ceruletide Ammonium SaltCaerulein Ammonium Salt|||Ceruletide Ammonium Sa
Ceruletide Ammonium Salt is a decapeptide, originating from the skin of tropical frogs, which is a potent cholecystokinin receptor agonist and a safe and effective cholecystokinin receptor agonist with direct spasmodic effects on the gallbladder muscle and bile ducts. Ceruletide Ammonium Salt has sedative activity and has been used in the study of chronic schizophrenia.Ceruletide Ammonium Salt is a decapeptide, originating from the skin of tropical frogs.
价 格：￥电议型 号：T14932L1产 地：中国大陆
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T14932LCeruletide Ammonium acetate；化合物Ceruletide Ammonium acetateFI-6934 Ammonium acetate|||Caerulein Ammon
Ceruletide Ammonium acetate (FI-6934 Ammonium acetate) is a cholecystokinin (CCK) receptor agonist. Ceruletide Ammonium acetate is a safe and effective cholecystokinetic agent and small bowel and exocrine pancreatic stimulant.
价 格：￥电议型 号：T14932L产 地：中国大陆
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T14932Ceruletide；雨蛙素Cerulein|||Caerulein|||FI-6934；Cerulein|||Caerulein|||雨蛙素|||FI-6934
Ceruletide (Caerulein) is a potent agonist of cholecystokinin receptor and it also is a safe and effective cholecystokinetic agent. It has a direct spasmogenic effect on the gallbladder muscle and bile ducts.
价 格：￥电议型 号：T14932产 地：中国大陆
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T14931Cerivastatin；西立伐他汀Cerivastatin
Cerivastatin is a highly potent, well-tolerated, and orally active HMG-CoA reductase inhibitor (Ki: 1.3 nM/L). Cerivastatin also inhibits proliferation and invasiveness of MDA-MB-231 cells, mainly by RhoA inhibition with anti-cancer effect. Cerivastatin reduces low-density lipoprotein cholesterol levels.
价 格：￥电议型 号：T14931产 地：中国大陆
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T14930Ceralifimod化合物 T14930ONO-4641
Ceralifimod (ONO-4641) is a potent agonist for sphingosine 1-phosphate receptors 1 and 5 (EC50s: 27.3, 334 pM for human S1P receptor 1 and 5).
价 格：￥电议型 号：T14930产 地：中国大陆
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T14895Tanzisertib；化合物TanzisertibCC-930；CC-930
Tanzisertib (CC-930) (CC-930) is a potent inhibitor of JNK1/2/3 with IC50s of 61/7/6 nM, respectively, with potential antifibrotic activity.
价 格：￥电议型 号：T14895产 地：中国大陆
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T14893CC-885；化合物CC-885CC-885
CC-885 is a modulator of cereblon (CRBN). It has potent anti-tumour activity.
价 格：￥电议型 号：T14893产 地：中国大陆
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T14835BTRX-335140；化合物BTRX-335140CYM-53093；CYM-53093
BTRX-335140 (CYM-53093) is a potent and selective, orally active κ opioid receptor (KOR) antagonist, has antagonist activity for κOR, μOR and δOR with IC50 values of 0.8 nM, 110 nM, and 6500 nM, respectively. BTRX-335140 can distribute well into the CNS. ADMET (absorption, distribution, metabolism, excretion, and toxicity) . BTRX-335140 endows with favorable in vitro ADMET and in vivo pharmacokinetic profiles and medication-like duration of action in rats.
价 格：￥电议型 号：T14835产 地：中国大陆
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T14693BN201；化合物 T14693BN201
BN201, a chemical compound, actively crosses the blood-brain barrier and activates the IGF-1 pathway, which is associated with stress response and neuron survival. It facilitates neuronal differentiation and the maturation of precursor cells into oligodendrocytes with an EC50 of 6.3 μM, in addition to promoting the myelination of new axons with an EC50 of 16.6 μM in vitro. BN201 exhibits potent neuroprotective effects[1].
价 格：￥电议型 号：T14693产 地：中国大陆
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T14689BMS493；化合物 BMS493BMS-493；BMS-493
BMS493 is an inverse agonist of the pan-retinoic acid receptor (RAR) that inhibits retinoic acid-induced differentiation, enhances the interaction of nuclear co-inhibitors with RARs, attenuates RA signaling, potentiates TPP-induced toxicity, and inhibits the increase in phospholipase A2 activity.
价 格：￥电议型 号：T14689产 地：中国大陆
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T14681BMS-935177；化合物BMS-935177BMS-935177
BMS-935177 is a reversible BTK inhibitor with IC50 value of 3 nM.
价 格：￥电议型 号：T14681产 地：中国大陆
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T14671BMS-193885；化合物BMS-193885BMS-193885
BMS-193885 is a selective, brain-penetrant, and competitive antagonist of the neuropeptide Y1 receptor with a Ki of 3.3 nM, and an IC50 of 5.9 nM for hY1.
价 格：￥电议型 号：T14671产 地：中国大陆
