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T27063CP-293019；化合物 T27063CP293019；CP293019
CP-293019 is a potent, selective antagonist of dopamine D4 receptor.
价 格：￥电议型 号：T27063产 地：中国大陆
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T27062CP-281384；化合物 T27062CP-281384
CP-281384 is a potent, p38alpha-selective inhibitor.
价 格：￥电议型 号：T27062产 地：中国大陆
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T27061CP-24879 hydrochloride；化合物CP-24879 hydrochlorideCP-24879 HCl；CP-24879 HCl
CP-24879 hydrochloride (CP-24879 HCl), a Δ5D/Δ6D dual-inhibitor, can significantly reduce intracellular lipid accumulation and inflammatory injury in hepatocytes. CP-24879 hydrochloride exhibits superior antisteatotic and anti-inflammatory actions in fat-1 and ω-3-treated hepatocytes.
价 格：￥电议型 号：T27061产 地：中国大陆
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T27060CP-226269；化合物CP-226269CP 226269|||CP226269；CP 226269|||CP226269
CP-226269 is a potent dopamine D4 receptor agonist that regulates calcium flux and has an EC50 value of 32.0 nM. CP 226269 can be used to study neurological disorders such as schizophrenia.
价 格：￥电议型 号：T27060产 地：中国大陆
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T27059CP-122288；化合物 T27059CP-122288
CP-122288 is a potent and selective agonist for the 5-HT1B, 5-HT1D and 5-HT1F serotonin receptor subtypes. CP-122288 is potent as an inhibitor of plasma protein extravasation and neurogenic inflammation.
价 格：￥电议型 号：T27059产 地：中国大陆
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T27058cp028；化合物 T27058cp 028|||Compound-028|||cp-028|||Compound028|||Compound 028；cp 028|||Compound-028|||
cp028 inhibits pre-mRNA splicing in vitro.
价 格：￥电议型 号：T27058产 地：中国大陆
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T27057CP 154,526；化合物 T27057CP-154,526|||CP154,526；CP-154,526|||CP154,526
CP 154,526 is a selective CRF1 receptor antagonist (Ki = 2.7 nM). CP 154,526 blocks CRF-induced activation of adenylate cyclase and the HPA axis.
价 格：￥电议型 号：T27057产 地：中国大陆
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T26936C188；化合物 T26936Cpd188|||STAT3-IN-C188|||Cpd-188|||C 188|||C-188；Cpd188|||STAT3-IN-C188|||Cpd-188|||C
C188 is a cell-permeable naphthol compound and a STAT3 inhibitor. C188 inhibits IL-6-stimulated STAT3 Tyr705 phosphorylation and nuclear translocation in HepG2 cells by targeting STAT3 SH2 domain peptide-binding pocket, while exhibiting little effect against IFN-γ-stimulated HepG2 cellular STAT1 phosphorylation.
价 格：￥电议型 号：T26936产 地：中国大陆
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T2677Crenolanib；化合物CrenolanibARO 002|||CP-868596；ARO 002|||CP-868596
Crenolanib (ARO 002) is an orally bioavailable type III tyrosine kinases inhibitor of PDGFRα/β and FLT3 (IC50s: 11, 3.2, and 4 nM).
价 格：￥电议型 号：T2677产 地：中国大陆
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T26521ABP-700；化合物 T26521CPMM；CPMM
ABP-700 is a positive allosteric modulator of the GABAA receptor.
价 格：￥电议型 号：T26521产 地：中国大陆
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T263884-CPI；化合物 T263884 CPI；4 CPI
4-CPI inhibits non-active site mutants of cytochrome P450 2B4.
价 格：￥电议型 号：T26388产 地：中国大陆
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T25808MI 1544；化合物 T25808Attcpl-LHRH|||AttcplLHRH|||MI-1544|||MI1544|||Attcpl LHRH；Attcpl-LHRH|||AttcplLHRH
MI 1544 is a LHRH antagonist.
价 格：￥电议型 号：T25808产 地：中国大陆
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T25549JCP174；化合物JCP174JCP 174|||JCP-174；JCP 174|||JCP-174
JCP174 is a depalmitoylase inhibitor that enhances Toxoplasma host-cell invasion by targeting TgPPT1.
价 格：￥电议型 号：T25549产 地：中国大陆
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T25296DDCPPB-Glu；化合物 T25296DDCPPB-Glu
DDCPPB-Glu is a 6-5 fused ring heterocycle antifolate that shows antitumor activity.
价 格：￥电议型 号：T25296产 地：中国大陆
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T25240Chloramphenicol succinate；化合物 T25240Paraxin succinate|||Kemicetine succinate|||CPSA；Paraxin succinat
Chloramphenicol succinate is an inactive precursor of chloramphenicol. It is used for parenteral administration of chloramphenicol.
价 格：￥电议型 号：T25240产 地：中国大陆
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T25154Bim 21009；化合物 T25154LHRH-Ncpapa|||Bim-21009|||Bim21009|||LHRHNcpapa|||LHRH Ncpapa；LHRH-Ncpapa|||Bim-
Bim 21009 is an inhibitor of gonadorelin.
价 格：￥电议型 号：T25154产 地：中国大陆
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T2499Torcetrapib；托彻普CP-529414；CP-529414|||托彻普
Torcetrapib (CP-529414) is a cholesteryl ester transfer protein (CETP) inhibitor that reduces the heterotypic transfer of cholesteryl ester from HDL to LDL and/or VLDL. Torcetrapib failed in phase III trials due to excess deaths.
价 格：￥电议型 号：T2499产 地：中国大陆
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T24610Pegamotecan；化合物PegamotecanProthecan|||PEG-camptothecin|||PEG-beta-CPT；Prothecan|||PEG-camptothecin||
Pegamotecan (PEG-camptothecin) is a topoisomerase I (TOP1) inhibitor with anticancer activity, and it is used in the treatment of esophageal, non-small cell lung and pancreatic cancers.
价 格：￥电议型 号：T24610产 地：中国大陆
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T24598BrBzGCp2化合物 T24598p BrBzGSH(Cp)2|||BBGC|||pBrBzGSH(Cp)2|||p-BrBzGSH(Cp)2|||BBGD
p-BrBzGSH(Cp)2 is a glyoxylase 1 inhibitor. In orthotopic mouse models, it acts by increasing DNA-AGEs, stimulating RAGE expression, and inhibiting brain tumor growth.
价 格：￥电议型 号：T24598产 地：中国大陆
