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T25529IMM-01IMM01；IMM 01
IMM-01 is a novel class of small-molecule agonists of the mammalian Diaphanous (mDia)-related formins, which act downstream of Rho GTPases to assemble actin filaments, and their organization with microfilaments to establish and maintain cell polarity duri
价 格：￥电议型 号：T25529产 地：中国大陆
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T2552SuccimerDimercaptosuccinic acid；meso-2,3-dimercaptosuccinic acid；DMSA；二巯基丁二酸；内消旋-2,3-二巯基丁二酸
Succimer is a Lead Chelator. The mechanism of action of succimer is as a Lead Chelating Activity.
价 格：￥电议型 号：T2552产 地：中国大陆
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T25455LGlutaurine aceate
Glutaurine aceate containing glutamine and taurine residues is an orally active hormone of the parathyroid. Glutaurine aceate, as a hormone, is isolated from parathyroid gland oxyphil cells. Glutaurine aceate can be used for the research of antiepileptic
价 格：￥电议型 号：T25455L产 地：中国大陆
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T2530LevosimendanOR1855；OR1259；左西孟旦
Levosimendan is a calcium sensitizer used in the management of acutely decompensated congestive heart failure. It increases the sensitivity of the heart to calcium, thus increasing cardiac contractility without a rise in intracellular calcium. Levosimenda
价 格：￥电议型 号：T2530产 地：中国大陆
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T24855TASIN-1 Hydrochloride塔辛-1盐酸盐；TASIN 1 Hydrochloride；TASIN 1 HCl；TASIN1 HCl；TASIN-1 HCl；TASIN1 Hydroch
TASIN-1 Hydrochloride is a selective inhibitor of truncated APC that acts by selectively killing colorectal cancer cells that express truncated APC by reducing cellular cholesterol levels and inducing apoptotic cell death through the ER stress/ROS/JNK sig
价 格：￥电议型 号：T24855产 地：中国大陆
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T2458CID755673
CID755673 is an effective and specific cell-active inhibitor for PKD (IC50: 182 nM); exhibits selective PKD1 inhibition when compared with PLK1, AKT, CAMKIIα, CAK, and PKC isoforms.
价 格：￥电议型 号：T2458产 地：中国大陆
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T24557NSC756093NSC 756093；NSC-756093
NSC756093 potentially inhibits GBP1:PIM1 interaction. NSC756093 can be used in ovarian cancer studies.
价 格：￥电议型 号：T24557产 地：中国大陆
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T2455PFK-015PFK15；PFK 015；PFK015
PFK-015 is an effective inhibitor of PFKFB3 (IC50: 110 nM) and inhibits PFKFB3 activity in Y cells (IC50: 20 nM).
价 格：￥电议型 号：T2455产 地：中国大陆
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T24055FAUC 213FAUC213；FAUC-213
FAUC-213 is a selective full antagonist of the dopamine D4 receptor.
价 格：￥电议型 号：T24055产 地：中国大陆
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T2398Tofacitinib Citrate柠檬酸托法替尼；枸橼酸托法替尼；Tasocitinib citrate；Tofacitinib (CP-690550) Citrate；CP-690550 cit
Tofacitinib citrate is a a potent, cell-permeable inhibitor of JAK1/2/3 (IC50s: 1/20/112 nM).
价 格：￥电议型 号：T2398产 地：中国大陆
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T2370AC-55541AOB2796
AOB2796 is a novel PAR2 agonist; activated PAR2 signaling in cellular proliferation assays, phosphatidylinositol hydrolysis assays, and Ca(2+) mobilization assays, with potencies ranging from 200 to 1000 nM.
价 格：￥电议型 号：T2370产 地：中国大陆
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T2361LY2874455LY-2874455；LY 2874455
LY2874455 has been used in trials studying the treatment of Advanced Cancer.
价 格：￥电议型 号：T2361产 地：中国大陆
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T23552YZ9
Y29 is a potent PFKFB3 inhibitor with an IC50 of 0.183 ?M, and acts as a competitive inhibitor against Fru-6-P with a Ki of 0.094 ?M[1].
价 格：￥电议型 号：T23552产 地：中国大陆
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T23550YM-750YM 750
YM-750 is a potent acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor (IC50=0.18 μM). ACAT catalyzes the formation of cholesteryl esters from cholesterol and long-chain fatty-acyl-coenzyme A.
价 格：￥电议型 号：T23550产 地：中国大陆
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T2355CFTR(inh)-172CFTR Inhibitor-172；CFTRinh172；CFTRinh-172；CFTRinh 172
CFTRinh-172 is a voltage-independent, selective CFTR inhibitor.
价 格：￥电议型 号：T2355产 地：中国大陆
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T23508VU 0255035
VU 0255035 is a highly selective, competitive and brain penetrant muscarinic M1 receptor antagonist with an IC50 of 130 nM. It reduces pilocarpine-induced seizures in mice. It is used to examine the role of the M1 receptor in diverse situations.
价 格：￥电议型 号：T23508产 地：中国大陆
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T2328RadotinibIY-5511；Supect；雷度替尼
Radotinib, and sometimes referred to by its investigational name IY5511, is a drug for the treatment of different types of Y, most notably Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) with resistance or intolerance of other tyrosi
价 格：￥电议型 号：T2328产 地：中国大陆
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T22946LY255283LY 255283
LY 255283 is a specific antagonit of leukotriene B4 (LTB4) receptor. It inhibits the production of LTB(4) in human peripheral blood polymorphonuclear leukocytes (PMNL) and in monocytes activated by calcium ionophore A23187.
价 格：￥电议型 号：T22946产 地：中国大陆
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T2277Losmapimod6-[5-(环丙基氨基甲酰基)-3-氟-2-甲基苯基]-N-(2,2-二甲基丙基)吡啶-3-甲酰胺；洛批莫德；SB856553；GSK-AHAB；GW856553；GW856553
Losmapimod (GW856553X; SB856553; GSK-AHAB) is a specific, potent, and orally active p38 MAPK inhibitor (pKi: 8.1/7.6 for p38α/β).
价 格：￥电议型 号：T2277产 地：中国大陆
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