T21014Thonzylamine hydrochloride

Thonzylamine hydrochloride is an anticholinergic and antihistamine used as an antipruritic.

价 格：￥电议型 号：T21014产 地：中国大陆

T8386Esomeprazole Magnesium trihydrateinhibit,K+-ATPase,Esomeprazole magnesium,antioxidant,Proton Pump,(S

Esomeprazole Magnesium trihydrate is a proton pump inhibitor indicated for the short-term treatment of gastroesophageal reflux disease in patients with a history of erosive esophagitis.Esomeprazole magnesium trihydrate acts as an exosome inhibitor by blocking the exosome release via the inhibition of V-H+-ATPases

价 格：￥电议型 号：T8386产 地：中国大陆

T9985Methyl methanesulfonateMethyl methanesulfonate

Methyl methanesulfonate is a DNA alkylator that modifies adenine (3-methyladenine) and guanine (7-methyladenine) respectively, resulting in base mismatch and replication disorders.

价 格：￥电议型 号：T9985产 地：中国大陆

T74373-(3-Hydroxyphenyl)propionic Acidaortic,Inhibitor,rings,Endogenous Metabolite,3(3Hydroxyphenyl)propi

3-(3-Hydroxyphenyl)propionic Acid is one of the major metabolites of ingested caffeic acid.it inhibited osteoclastogenesis and bone osteoclastic resorptive activity.

价 格：￥电议型 号：T7437产 地：中国大陆

T74727-Hydroxyflavone7 Hydroxyflavone,7Hydroxyflavone,Inhibitor,7-Hydroxyflavone,inhibit

7-Hydroxyflavone is a potent inhibitor of CYP1A1 with a Ki value of 0.015 μM and exhibits 6-fold greater selectivity for CYP1A1 over CYP1A2.with anti-inflammatory activity

价 格：￥电议型 号：T7472产 地：中国大陆

T7378BRD9539Histone Methyltransferase,chromatin,PRC2,BRD9539,G9a,senescent,BRD-9539,BRD 9539,inhibit,H3K9

BRD9539 is an inhibitor of euchromatin histone methyltransferase 2 (EHMT2), also known as G9a, with an IC50 value of 6.3 μM

价 格：￥电议型 号：T7378产 地：中国大陆

T6832Fatostatin hydrobromideGolgi,ob/ob,inhibit,Fatostatin hydrobromide,prostate,SREBP-mediated,cancer,mi

Fatostatin ia an inhibitor of sterol regulatory element binding protein (SREBP). It impairs the activation of SREBP-1 and SREBP-2.

价 格：￥电议型 号：T6832产 地：中国大陆

T64344N-Methyl-DL-aspartic acidNMethylDLasparticacid

N-Methyl-DL-aspartic acid is a glutamate analogue and a NMDA receptor agonist and can be used for neurological diseases research.

价 格：￥电议型 号：T64344产 地：中国大陆

T6847GSK-J1GSK-J1,inhibit,Inhibitor,Histone Demethylase,GSKJ1,GSK-J-1

GSK-J1 is a highly potent H3K27 histone demethylase inhibitor with IC50 of 28 nM and 53 nM in cell-free assays for JMJD3 (KDM6B) and UTX (KDM6A), respectively, >10-fold selectivity over other tested demethylases.

价 格：￥电议型 号：T6847产 地：中国大陆

T9417Lgamma-preprotachykinin amide (72-92) acetategammapreprotachykinin amide (7292) acetate,gamma preprot

gamma-preprotachykinin amide (72-92) acetate is a 21 amino acid peptide belonging to the tachykinin (TK) family and including neurokinin A (NKA) in its C-terminal sequence. gamma-preprotachykinin amide (72-92) acetate possesses higher affinity than NKA for central NK-2 receptors; it shows lower affinity for NK-1 receptors, however, it potently stimulates salivary secretion, which is mediated by NK-1 receptor activation.

价 格：￥电议型 号：T9417L产 地：中国大陆

T35528LTD52 dihydrochloride

TD52 dihydrochloride, an Erlotinib derivative, is an orally active, potent cancerous inhibitor of protein phosphatase 2A (CIP2A) inhibitor. TD52 dihydrochloride mediates the apoptotic effect in triple-negative breast cancer (TNBC) cells via regulating the CIP2A/PP2A/p-Akt signalling pathway. TD52 dihydrochloride indirectly reduced CIP2A by disturbing Elk1 binding to the CIP2A promoter. TD52 dihydrochloride has less p-EGFR inhibition and has potent anti-cancer activity.

价 格：￥电议型 号：T35528L产 地：中国大陆

TD0092Naphthoresorcinolbackground,electrolyte,Inhibitor,carbohydrates,Naphthoresorcinol,HCl,red,color,trac

Naphthoresorcinol is a fluorescent dye (λex=330 nm, λem=380 nm).

价 格：￥电议型 号：TD0092产 地：中国大陆

T6429Caffeic Acid Phenethyl EsterApoptosis,Caffeic Acid Phenethyl Ester,Nuclear factor-kappaB,Inhibitor,N

Caffeic Acid Phenethyl Ester (CAPE) inhibits the activation of nuclear transcription factor NF-kappa B and may suppress p70S6K and Akt-driven signaling pathways, with antineoplastic, cytoprotective and immunomodulating activities. CAPE is the phenethyl alcohol ester of caffeic acid and a bioactive component of honeybee hive propolis. In addition, CAPE inhibits PDGF-induced proliferation of vascular smooth muscle cells through the activation of p38 mitogen-activated protein kinase (MAPK) and hypo

价 格：￥电议型 号：T6429产 地：中国大陆

T6554JZL 184MAGL,neurons,JZL-184,inhibit,JZL 184,2-Arachidonoylglycerol,Inhibitor,hydrolysis,Monoacylglyc

JZL 184 is a potent and selective inhibitor of MAGL with IC50 of 8 nM and 4 μM for inhibition of MAGL and FAAH in mouse brain membranes respectively.

价 格：￥电议型 号：T6554产 地：中国大陆

TN1586DihydrorotenoneApoptosis,inhibit,Dihydrorotenone,Inhibitor,Mitochondrial Metabolism

Dihydrorotenone is a potent mitochondrial inhibitor and probably induces Parkinsonian syndrome.

价 格：￥电议型 号：TN1586产 地：中国大陆

TN13287-Amino-4-methylcoumarin-3-acetic acidcoumarin dye,fluorophore,immunofluorescence,7 Amino 4 methylco

7-Amino-4-methylcoumarin is more suitable as a substrate for enteropeptidase than GD(4)K-NA.

价 格：￥电议型 号：TN1328产 地：中国大陆

T643631-Pentalenol, 5-hexyl-1,2,3,3a,6,6a-hexahydro-4-phenyl-3a-(1-phenylethenyl)-, (1R,3aS,6aS)-rel-1Pent

1-Pentalenol, 5-hexyl-1,2,3,3a,6,6a-hexahydro-4-phenyl-3a-(1-phenylethenyl)-, (1R,3aS,6aS)-rel- is a potent liver receptor homolog 1 (LRH-1, NR5A2) and steroidogenic factor-1 (SF-1, NR5A1) agonist with pEC 50 s of 6.4 and 7.2, respectively.

价 格：￥电议型 号：T64363产 地：中国大陆

TN7024Hyocholic acidHyocholic acid

价 格：￥电议型 号：TN7024产 地：中国大陆

TN12663-O-Methylquercetin3OMethylquercetin,Phosphodiesterase (PDE),inhibit,3 O Methylquercetin,Inhibitor

3-O-Methylquercetin is a selective and competitive PDE3/PDE4 inhibitor, and inhibits PDE3 than PDE4 with a low Km value. 3-O-Methylquercetin inhibits total cAMP- and cGMP-phosphodiesterase (PDE) of guinea pig trachealis at low concentrations.

价 格：￥电议型 号：TN1266产 地：中国大陆

TN1451Brevifolincarboxylic acidGlucosidase,AhR,Brevifolincarboxylic acid,Inhibitor,Aryl Hydrocarbon Recept

Brevifolincarboxylic acid is a natural product isolated from Polygonum capitatum, it has inhibitory effect on the aryl hydrocarbon receptor (AhR). Brevifolincarboxylic acid is an α-glucosidase inhibitor with an IC50 of 323.46 μM.

价 格：￥电议型 号：TN1451产 地：中国大陆