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T24656PQ-10A-844337；A 844337；A844337；PQ 10；PQ10
PQ-10 is a PDE-10 inhibitor. PQ-10 induces brain glucose metabolism patterns, which may be a potential translational biomarker.
价 格：￥电议型 号：T24656产 地：中国大陆
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T2465PF-562271PF562271；PF 562271
PF-562271 is an effective ATP-competitive, reversible inhibitor of FAK(IC50=1.5 nM) and Pyk2 kinase(IC50=13 nM).
价 格：￥电议型 号：T2465产 地：中国大陆
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T2464NSC319726ZMC1
NSC319726, a mutant p53R175 reactivator, suppresses growth of fibroblasts that expresses the p53R175 mutation (IC50 = 8 nM).
价 格：￥电议型 号：T2464产 地：中国大陆
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T2463ML141CID-2950007
ML141 is an effective, specific and reversible non-competitive inhibitor of Rho family GTPase cdc42 (IC50: 200 nM).
价 格：￥电议型 号：T2463产 地：中国大陆
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T2462SB-505124SB 505124；SB505124
SB505124 is a selective inhibitor of TGFβR for ALK4, ALK5.
价 格：￥电议型 号：T2462产 地：中国大陆
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T2461PIK-90PIK 90；PIK90
PIK-90, a DNA-PK and PI3K inhibitor, suppresses p110α( IC50=11 nM), p110γ(IC50=18 nM) and DNA-PK(IC50=13 nM) .
价 格：￥电议型 号：T2461产 地：中国大陆
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T2452C646
C646, a histone acetyltransferase inhibitor, inhibits p300 (Ki: 400 nM, in a cell-free assay).
价 格：￥电议型 号：T2452产 地：中国大陆
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T2446KI8751
KI8751 is a potent and selective inhibitor of VEGFR2 with IC50 of 0.9 nM.
价 格：￥电议型 号：T2446产 地：中国大陆
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T24446LMEN 10207 acetate
MEN 10207 acetate is a selective antagonist for NK-2 tachykinin receptor.
价 格：￥电议型 号：T24446L产 地：中国大陆
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T2433NU 7026DNA-PK Inhibitor II；LY293646；NU7026
NU7026 is an effective DNA-PK inhibitor (IC50: 0.23 μM, in cell-free assays), 60-fold selective for DNA-PK than PI3K and no inhibition against both ATM and ATR.
价 格：￥电议型 号：T2433产 地：中国大陆
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T23646AF 399AF-399；AF399
AF 399 is a CCR4 antagonist. It reverses the tumor-promoting environment.
价 格：￥电议型 号：T23646产 地：中国大陆
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T2362QNZ46
QNZ46 is a NR2C/NR2D-selective NMDA receptor non-competitive antagonist.
价 格：￥电议型 号：T2362产 地：中国大陆
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T23469TQS4-Naphthalen-1-yl-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline-8-sulfonamide
TQS is a positive allosteric modulator of α7 nACh receptors.
价 格：￥电议型 号：T23469产 地：中国大陆
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T2346Enasidenib恩西地平；AG-221
Enasidenib is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity.
价 格：￥电议型 号：T2346产 地：中国大陆
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T23449TCS 46b
TCS 46b is a NR1A/NR2B NMDA receptor antagonist with oral activity.
价 格：￥电议型 号：T23449产 地：中国大陆
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T23146PHA 568487 free basePHA 568487
The quinuclidine PHA 568487 is an agonist of the alpha 7 nicotinic acetylcholine receptor that was designed to mitigate the bioactivation associated with the core scaffold and subsequently remove associated liabilities with in vivo tolerability.
价 格：￥电议型 号：T23146产 地：中国大陆
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T23046N-tert-butyl-α-Phenylnitrone(Z)-N-benzylidene-2-Methylpropan-2-aMine oxide；N-叔丁基-α-苯基硝酮
N-tert-butyl-α-Phenylnitrone inhibits COX2 catalytic activity. N-tert-butyl-α-Phenylnitrone possesses potent reactive oxygen species scavenging, anti-inflammatory, neuroprotective, anti-aging, and anti-diabetic activities, and can penetrate the blood-brai
价 格：￥电议型 号：T23046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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T2269Pirinixic Acid匹立尼酸；Wy-14643；NSC 310038
Pirinixic Acid is a synthetic thiacetic acid derivative used in biomedical research, carcinogenic Pirinixic acid is a peroxisome proliferator that activates specific peroxisome proliferator-activated receptors (PPAR).
价 格：￥电议型 号：T2269产 地：中国大陆
