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T10782CGP52411；化合物CGP52411DAPH；DAPH
CGP52411 is an orally active, and ATP-competitive inhibitor of EGFR (IC50: 0.3 μM). CGP52411 blocks the toxic influx of Ca2+ ions into neuronal cells and dramatically inhibits and reverses the formation of β-amyloid Aβ42 fibril aggregates. CGP52411 can be used in studies about Alzheimer´s diseases.
价 格：￥电议型 号：T10782产 地：中国大陆
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T10779CGP 25454A；化合物 T10779CGP 25454A
CGP 25454A is a novel and selective antagonist of the presynaptic dopamine autoreceptor.
价 格：￥电议型 号：T10779产 地：中国大陆
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T10776CFTR corrector 4；CFTR 校正剂 4CFTR corrector 4
CFTR corrector 4 is a potent and orally available transmembrane conductance regulator (CFTR) for cystic fibrosis and is a potent (R,R) type active enantiomer. CFTR corrector 4 increases CFTR levels on the cell surface and is a potential compound for the study of cystic fibrosis.
价 格：￥电议型 号：T10776产 地：中国大陆
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T10774CFM-2；化合物CFM-2CFM-2
CFM-2, a potent and selective non-competitive antagonist of AMPAR (AMPAR), exhibits anticonvulsant activity across various seizure models.
价 格：￥电议型 号：T10774产 地：中国大陆
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T1077Fluvoxamine maleate；氟伏沙明马来酸盐MK-264|||DU-23000 (maleate)；氟伏沙明马来酸盐|||马来酸氟伏沙明|||MK-264|||DU-23000 (male
Fluvoxamine maleate (DU-23000 (maleate)) is a selective serotonin reuptake inhibitor that is used in the treatment of depression and a variety of anxiety disorders.
价 格：￥电议型 号：T1077产 地：中国大陆
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T10769Cetirizine D4；化合物 T10769Cetirizine D4
Cetirizine D4 is a deuterium-labeled Cetirizine. Cetirizine is a second-generation antihistamine and a long-acting histamine H1-receptor antagonist.
价 格：￥电议型 号：T10769产 地：中国大陆
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T10764Cercosporamide；化合物 T10764(-)-Cercosporamide；(-)-Cercosporamide
Cercosporamide is a ATP-competitive Pkc1 kinase inhibitor (IC50 <50 nM; Ki <7 nM). It also is a unique Mnk inhibitor.
价 格：￥电议型 号：T10764产 地：中国大陆
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T10761Ceranib-2；化合物Ceranib-23-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]-4-phenyl-1H-quinolin-2-one；3-[(E)-3-(4
Ceranib-2 (3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]-4-phenyl-1H-quinolin-2-one) is an inhibitor of ceramidase with an IC50 of 28 μM in SKOV3 cells. Ceranib-2 decreases levels of sphingosine and S1P, induces cell apoptosis and exhibits anticancer activity.
价 格：￥电议型 号：T10761产 地：中国大陆
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T10755LCelgosivir；西戈斯韦MX3253|||MBI 3253|||6 O-butanoyl castanospermine|||MDL 28574；MX3253|||MBI 3253|||6 O-
Celgosivir (6 O-butanoyl castanospermine) is an inhibitor of α-glucosidase I. In vitro assay, it inhibits bovine viral diarrhoea virus (BVDV) ( IC50: 1.27 μM ).
价 格：￥电议型 号：T10755L产 地：中国大陆
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T10755Celgosivir hydrochloride；化合物 T10755MX3253 hydrochloride|||MBI 3253 hydrochloride|||MDL 28574 hydroch
Celgosivir hydrochloride (MBI 3253 hydrochloride) is an α-glucosidase I inhibitor and inhibits bovine viral diarrhoea virus (BVDV) (IC50: 1.27 μM).
价 格：￥电议型 号：T10755产 地：中国大陆
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T10754Ceftriaxone sodium salt；头孢曲松钠盐Disodium ceftriaxone；Disodium ceftriaxone|||头孢曲松钠盐
Ceftriaxone sodium salt is an antibiotic useful for the treatment of a number of bacterial infections.
价 格：￥电议型 号：T10754产 地：中国大陆
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T10750Cecropin A TFA (80451-04-3 free base)；化合物 T10750Cecropin A TFA；Cecropin A TFA
Cecropin A TFA is an antimicrobial polypeptide isolated from Hyalaphora cecropia pupae with anti-inflammatory, anti-bacterial, and anti-cancer activity.
价 格：￥电议型 号：T10750产 地：中国大陆
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T10749Cebranopadol ((1α,4α)stereoisomer)；化合物 T10749GRT6005 (1α,4α)stereoisomer；GRT6005 (1α,4α)stereoisomer
Cebranopadol ((1α,4α)stereoisomer) is a stereoisomer of cebranopadol which is a potent ORL-1 agonist.
价 格：￥电议型 号：T10749产 地：中国大陆
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T10748CE(20:5(5Z,8Z,11Z,14Z,17Z)；化合物 T10748CE(20:5(5Z,8Z,11Z,14Z,17Z)
CE(20:5(5Z,8Z,11Z,14Z,17Z) is an endogenous metabolite.
价 格：￥电议型 号：T10748产 地：中国大陆
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T10747CDK9-IN-9；化合物 T10747CDK9-IN-9
CDK9-IN-9 is a potent and selective CDK9 inhibitor (IC50: 1.8 nM) with anti-cancer activity. It inhibits CDK2 (IC50: 155 nM).
价 格：￥电议型 号：T10747产 地：中国大陆
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T10746CDK9-IN-8；化合物 T10746CDK9-IN-8
CDK9-IN-8 is a highly potent and selective CDK9 inhibitor (IC50: 12 nM).
价 格：￥电议型 号：T10746产 地：中国大陆
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T10745CDK9-IN-7；化合物CDK9-IN-7CDK9-IN-7
CDK9-IN-7 is a highly selective and orally active CDK9/cyclin T inhibitor (IC50: 11 nM), which exhibits more potent over other CDKs (CDK4/cyclinD: 148 nM; CDK6/cyclinD: 145 nM).
价 格：￥电议型 号：T10745产 地：中国大陆
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T10744LSEL120-34A HCl；化合物SEL120-34A HClSEL120-34A HCl
SEL120-34A HCl is a selective, orally available and ATP-competitive inhibitor of CDK8(CDK8/CycC and CDK19/CycC with IC50s of 4.4 nM and 10.4 nM , respectively), with antitumor activity.
价 格：￥电议型 号：T10744L产 地：中国大陆
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T10744SEL120-34A；化合物SEL120-34ASEL120-34A
SEL120-34A is a selective and ATP-competitive inhibitor of CDK8 with IC50s of 4.4 nM, 10.4 nM and 1070 nM for CDK8/CycC, CDK19/CycC and CDK9/cycT. SEL120-34A possesses antitumor activity.
价 格：￥电议型 号：T10744产 地：中国大陆
