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产品数：86101
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T74735-Bromoindole5 Bromoindole,5Bromoindole
5-bromoindole is a potential inhibitor of glycogen synthase kinase 3 (GSK-3)and an important pharmaceutical chemical intermediate
价 格：￥电议型 号：T7473产 地：中国大陆
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T6473DioscinAutophagy,CCRIS-4123,CCRIS4123,Apoptosis,Dioscin,inhibit,Inhibitor
Dioscin is a saponin with antitumor activities.
价 格：￥电议型 号：T6473产 地：中国大陆
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T8473MLS000532223GTPases,Inhibitor,MLS-000532223,MLS 000532223,MLS000532223,Rab,cytoskeleton,actin,Rho GT
MLS000532223 is a selectiveRho family GTPases inhibitor(EC50 : 16 μM to 120 μM).
价 格：￥电议型 号：T8473产 地：中国大陆
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TP2325LEndotoxin Inhibitor acetate(147396-10-9 free base)Endotoxin Inhibitor acetate(147396 10 9 free base)
Endotoxin Inhibitor acetate has a strong blocking effect on bacterial physiological activity, thus producing antibacterial toxin Inhibitor sequences with disulfide bonds and a large amount of lysine. Endotoxin Inhibitor acetate is more likely to exert physiological activity under acidic conditions
价 格：￥电议型 号：TP2325L产 地：中国大陆
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T6785BI-847325BI 847325,inhibit,Apoptosis,MEK,MAPKK,MAP2K,Inhibitor,Aurora Kinase,Mitogen-activated prote
BI-847325 is a selective dual inhibitor of MEK and aurora kinases (AK) with IC50 values of 4 and 15 nM for human MEK2 and AK-C, respectively.
价 格：￥电议型 号：T6785产 地：中国大陆
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T94734SC-203tumor,antineoplastic,Fms like tyrosine kinase 3,Vascular endothelial growth factor receptor,4
4SC-203 is a multikinase inhibitor with potential antineoplastic activity. 4SC-203 selectively inhibits FMS-related tyrosine kinase 3 (FLT3/STK1), FLT3 mutated forms, and vascular endothelial growth factor receptors (VEGFRs).
价 格：￥电议型 号：T9473产 地：中国大陆
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T11321FR194738 free baseFR194738 free base,FR-194738 free base
FR194738 free base inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.?
价 格：￥电议型 号：T11321产 地：中国大陆
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T6328Desmethyl ErlotinibO-Desmethyl Erlotinib；OSI-420；CP-473420
OSI-420 is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).
价 格：￥电议型 号：T6328产 地：中国大陆
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T6305SNX2112SNX 2112；PF 04928473；SNX-2112
SNX-2112 is an orally active Hsp90 inhibitor, with a Kd of 16 nM.
价 格：￥电议型 号：T6305产 地：中国大陆
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T6274RO4929097RG-4733
RO4929097, a γ secretase inhibitor (IC50: 4 nM), inhibits cellular processing of Aβ40 and Notch (EC50: 14/5 nM).
价 格：￥电议型 号：T6274产 地：中国大陆
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T5473ASP5878ASP-5878
ASP5878 potently inhibited the tyrosine kinase activities of recombinant FGFR1, 2, 3, and 4 with IC50 values of 0.47, 0.60, 0.74, and 3.5 nmol/L.
价 格：￥电议型 号：T5473产 地：中国大陆
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T4739Sodium creatine phosphate dibasic tetrahydrateCreatine phosphate disodium salt tetrahydrate；磷酸肌酸二钠盐
Creatine phosphate disodium salt tetrahydrate is a substrate for the assay of creatine kinase
价 格：￥电议型 号：T4739产 地：中国大陆
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T4738Sodium 2-hydroxybutanoate2-羟基丁酸钠；2-Hydroxybutyric acid sodium salt；DL-2-Hydroxybutyric Acid Sodium S
2-Hydroxybutyric acid is formed as a by-product of the formation of alpha-ketobutyrate via a reaction catalyzed by lactate dehydrogenase (LDH) or alpha-hydroxybutyrate dehydrogenase (alphaHBDH).
价 格：￥电议型 号：T4738产 地：中国大陆
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T4736Cruzain-IN-1ML092
Cruzain-IN-1 is a covalent and reversible Cruzain inhibitor (IC50: 10 nM).
价 格：￥电议型 号：T4736产 地：中国大陆
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T4734Suberic acidOctanedioic acid；1,8-Octanedioic acid；辛二酸
Suberic acid is present in the urine of patients with fatty acid oxidation disorders. A metabolic breakdown product derived from oleic acid. Elevated levels of this unstaruated dicarboxylic acid are found in individuals with medium-chain acyl-CoA dehydrog
价 格：￥电议型 号：T4734产 地：中国大陆
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T4733SucroseD(+)-Sucrose；D-(+)-Saccharose；蔗糖
Sucrose is a nonreducing disaccharide composed of glucose and fructose linked via their anomeric carbons.
价 格：￥电议型 号：T4733产 地：中国大陆
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T4732L-CarnosineL-肌肽；Karnozin；beta-Alanyl-L-histidine
L-Carnosine is is an antioxidant naturally found in skeletal muscle, brain tissue. It has the potential to suppress many of the biochemical changes that accompany aging.
价 格：￥电议型 号：T4732产 地：中国大陆
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T4490PF-01247324PF 01247324；PF01247324
PF-01247324 is a selective and orally bioavailable Nav1.8 channel blocker (IC50: 196 nM).
价 格：￥电议型 号：T4490产 地：中国大陆
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T4473IbiglustatSAR402671；Venglustat；GZ402671
Ibiglustat is a potent and selective Glucosylceramide synthase inhibitor and ceramide glucosyltransferase inhibitor. Ibiglustat blocks the formation of glucosylceramide (GL-1), a key intermediate in the synthesis of GL-3. Ibiglustat is potentially useful
价 格：￥电议型 号：T4473产 地：中国大陆
