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T28178NLRP3-IN-9；化合物NLRP3-IN-9INF-4E|||INF 4E|||INF4E；INF-4E|||INF 4E|||INF4E
NLRP3-IN-9 (INF-4E) is an inhibitor of NLRP3 ATPase and caspase-1. NLRP3-IN-9 acts by irreversibly trapping thiol nucleophiles, which prevents both ATP- and nigericin-triggered pyroptosis of human THP-1 cells in a time- and concentration-dependent manner.
价 格：￥电议型 号：T28178产 地：中国大陆
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T27538Hexasodium phytate；化合物 T27538SNF 472|||SNF472|||SNF-472；SNF 472|||SNF472|||SNF-472
Hexasodium phytate is used potentially to treat vascular calcification and calciphylaxis.
价 格：￥电议型 号：T27538产 地：中国大陆
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T27178Dimiracetam地来西坦NT-11624|||NT11624|||BND11624|||ISF4185|||BND-11624|||ISF-4185
Dimiracetam (NT-11624) is an orally active anti-neuropathy compound that inhibits hypersensitivity and neurological alterations and may be used in the study of cognitive disorders, depression and neuropathic pain.
价 格：￥电议型 号：T27178产 地：中国大陆
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T26566ADL-5747 (HCl)；化合物 T26566PF-04856881|||PF 04856881|||PF4856881|||PF-4856881|||PF 4856881|||PF0485688
ADL-5747, an opioid delta receptor agonist, is used potentially for the treatment of pain.
价 格：￥电议型 号：T26566产 地：中国大陆
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T24954YF479；化合物 T24954YF-479|||YF 479；YF-479|||YF 479
YF479 is an inhibitor of histone deacetylase that acts by inhibiting breast tumor growth, metastasis, and recurrence.
价 格：￥电议型 号：T24954产 地：中国大陆
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T23737Anordiol；化合物 T23737H 241|||H241|||AF-45|||AF 45|||AF45；H 241|||H241|||AF-45|||AF 45|||AF45
Anordiol is an antiestrogen with estrogenic activity. It also is known to inhibit fertility.
价 格：￥电议型 号：T23737产 地：中国大陆
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T22397PF-4618433化合物PF-4618433PF4618433|||PF 4618433
PF-4618433 is a dual inhibitor of focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (PYK2).
价 格：￥电议型 号：T22397产 地：中国大陆
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T21420Diphenidol；化合物 T21420SKF-478|||SKF478|||SKF 478|||Difenidolo|||Difenidol；SKF-478|||SKF478|||SKF 478|
Diphenidol, a muscarinic antagonist, is employed as an antivertigo and antiemetic agent.
价 格：￥电议型 号：T21420产 地：中国大陆
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T20100Fluroxypyr；化合物 T20100FF4014；FF4014
Fluroxypyr is an herbicide in the class of synthetic auxins that is used to control broadleaf weeds and woody brush.
价 格：￥电议型 号：T20100产 地：中国大陆
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T2002PF-4708671；化合物PF-4708671PF4708671；PF4708671
PF-4708671 is a cell-permeable inhibitor of p70 ribosomal S6 kinase (S6K1 isoform) .In cell-free assays, PF-4708671(PF4708671) is potent for S6K1(Ki50=20 nM, IC50=160 nM).
价 格：￥电议型 号：T2002产 地：中国大陆
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T19031NBD-F；化合物NBD-F4-Fluoro-7-nitrobenzofurazan；4-Fluoro-7-nitrobenzofurazan
NBD-F (4-Fluoro-7-nitrobenzofurazan) is a fluorescent derivatization compound for amino acid analysis.
价 格：￥电议型 号：T19031产 地：中国大陆
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T16069MF498化合物 T16069MF498|||MF-498
MF498 is a novel and selective E prostanoid receptor 4 (EP4 receptor) antagonist, displayed a strong binding affinity for the EP4 receptor (Ki: 0.7 nM).
价 格：￥电议型 号：T16069产 地：中国大陆
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T13530AF40431化合物 T13530AF-40431|||AF40431
AF40431 is the first reported small-molecule ligand of sortilin (IC50: 4.4 μM; Kd: 0.7 μM). AF40431 is bound in the neurotensin-binding site of sortilin.
价 格：￥电议型 号：T13530产 地：中国大陆
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T12616LCE3F4；化合物CE3F4CE3F4
CE3F4 is a selective antagonist of exchange protein directly activated by cAMP (Epac1; IC50s of 10.7 μM and 66 μM for Epac1 and Epac2(B), respectively).
价 格：￥电议型 号：T12616L产 地：中国大陆
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T12616(R)-CE3F4；化合物 T12616(R)-CE3F4
(R)-CE3F4 is a selective inhibitor of exchange protein directly activated by cAMP isoform 1 (Epac1)(IC50 of 4.2 μM),
价 格：￥电议型 号：T12616产 地：中国大陆
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T12437PF429242 dihydrochloride；化合物PF429242 dihydrochloridePF429242 dihydrochloride
PF429242 dihydrochloride can reversibly inhibit S1P (IC50 of 175 nM).
价 格：￥电议型 号：T12437产 地：中国大陆
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T11447GNF4877；化合物GNF4877GNF4877
GNF4877 is a potent DYRK1A and GSK3β inhibitor (IC50s: 6 nM and 16 nM). It leads to blockade of nuclear factor of activated T-cells (NFATc) nuclear export and increased β-cell proliferation cells.
价 格：￥电议型 号：T11447产 地：中国大陆
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T11171eIF4A3-IN-2；化合物 T11171eIF4A3-IN-2
eIF4A3-IN-2 is a highly selective and noncompetitive eukaryotic initiation factor 4A-3 inhibitor with an IC50 of 110 nM.
价 格：￥电议型 号：T11171产 地：中国大陆
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T11170eIF4A3-IN-1；化合物 T11170eIF4A3-IN-1
eIF4A3-IN-1 is a selective eukaryotic initiation factor 4A3 (eIF4A3) inhibitor (IC50=0.26 μM; Kd=0.043 μM), which binds to a non-ATP binding site of eIF4A3 and shows significant cellular nonsense-mediated RNA decay (NMD) inhibition at 10 and 3 μM and can be as a probe for further study of eIF4A3, the exon junction complex (EJC), and NMD.
价 格：￥电议型 号：T11170产 地：中国大陆
