T8331NUN82647NUN82647,Inhibitor,NUN 82647,inhibit,Apoptosis,QBS,NUN-82647

NUN82647 is an Inhibitor of cell cycle at G2 phase, and apoptosis inducer.

价 格：￥电议型 号：T8331产 地：中国大陆

TQ0283RS102895CC chemokine receptor,CCR,Inhibitor,RS102895,inhibit,RS-102895,RS 102895

RS102895 is a potent CCR2 antagonist (IC50: 360 nM) and shows no effect on CCR1.

价 格：￥电议型 号：TQ0283产 地：中国大陆

T7083GLPG1837GLPG-1837,ABBV 974,Cystic fibrosis transmembrane conductance regulator,Inhibitor,CFTR,Autoph

GLPG1837 is an effective CFTR potentiator, with EC50s of 3 nM and 339 nM for F508del and G551D CFTR, respectively.

价 格：￥电议型 号：T7083产 地：中国大陆

T6683STF-62247renal,STF-62247,VHL,carcinoma,inhibit,cytotoxic,cell,RCC,Inhibitor,STF62247,intracytoplasmi

STF-62247 is TGN inhibitor with IC50 of 0.625 μM and 16 μM in RCC4 and RCC4/VHL cells, respectively.

价 格：￥电议型 号：T6683产 地：中国大陆

T9374AA38-3serine,ABHD6,Fatty acid amide hydrolase,AA38 3,Monoacylglycerol lipase,AA383,ABHD11,FAAH,MAGL,

AA38-3 inhibites three SHs (ABHD6, ABHD11, and FAAH)

价 格：￥电议型 号：T9374产 地：中国大陆

T8383Cyclopentolate Hydrochloridepesticide,inhibit,cycloplegic,mAChR,antimuscarinic,practice,Cyclopentola

Cyclopentolate Hydrochloride is a muscarinic acetylcholine receptors antagonist with Kis of 1.62, 27.5, and 2.63 nM for M1, M2, and M3 receptors, respectively.

价 格：￥电议型 号：T8383产 地：中国大陆

T38344Lalistat 1

Lalistat 1 is an inhibitor of lysosomal acid lipase (LAL, IC50 = 68 nM) and IgA1 protease for H. influenzae. Lalistat 1 can be used in studies about niemann-pick type C diseases.

价 格：￥电议型 号：T38344产 地：中国大陆

T6S1683DemethoxycurcuminBacterial,Inhibitor,Autophagy,Demethoxycurcumin,inhibit,Apoptosis

1. Demethoxycurcumin has antioxidant activity. 2. Demethoxycurcumin has anti-inflammatory activity. 3. Demethoxycurcumin has anti-proliferative activity. 4. Demethoxycurcumin has anti-acanthamoebic effect. 5. Demethoxycurcumin is a potential additive natural product in combination with chemotherapeutic agents in drug-resistant cancers. 6. Demethoxycurcumin inhibits energy metabolic and oncogenic signaling pathways through AMPK activation in triple-negative breast cancer cells.

价 格：￥电议型 号：T6S1683产 地：中国大陆

T9975GPR183GPR183 antagonist-1,SAE-14,inhibit,SAE 14,SAE14,HL-60,GPR183,Inhibitor,GPR183 antagonist SAE-1

GPR183 is a chemotactic receptor known for its role in the maturation of B cells, and the endogenous ligand is the oxysterol 7α,25-dihydroxycholesterol (7α,25-OHC). GPR183 can be used in research on inflammatory bowel disease (IBD).

价 格：￥电议型 号：T9975产 地：中国大陆

T8836CY5-SE triethylamine saltoligonucleotides,reactive,dye,amino-groups,inhibit,CY-5-SE triethylamine sa

Fluorolink Cy5 triethanolamine salt is a hydrophilic amine-reactive fluorescent probe. It displays excitation/emission maxima of 646/662 nm, respectively. Cy5-SE-conjugated ligands have been used in the characterization of hematopoietic tumor microenvironments.

价 格：￥电议型 号：T8836产 地：中国大陆

Fr16683Compound Fr16683Compound Fr16683

价 格：￥电议型 号：Fr16683产 地：中国大陆

T21980PD 198306MAPK,inhibit,neuropathic,Inhibitor,MAP2K,rabies,mitogen-activated protein,drug,MAPKK,PD-198

PD 198306 is a selective inhibitor of MAPK/ERK-kinase (MEK) with antihyperalgesic effects. PD 198306 reduces the Streptozocin-induced increase in the level of active ERK1.

价 格：￥电议型 号：T21980产 地：中国大陆

T8320J14cancer,inhibit,damage,Sulfiredoxin,J14,cytotoxicity,Reactive Oxygen Species,J 14,death,adenocarci

J-14 is an inhibitor of reversible sulfiredoxin(IC50 : 8.1 μM). J14 induces oxidative stress (intracellular ROS accumulation) by inhibiting sulfiredoxin, leading to cytotoxicity and cancer cell death

价 格：￥电议型 号：T8320产 地：中国大陆

T6635EMD638683inhibit,EMD-638683,EMD638683,Serum and glucocorticoid-regulated kinase,EMD 638683,Inhibitor

EMD638683,a novel SGK inhibitor with antihypertensive potency(with an IC50 of 3 μM).

价 格：￥电议型 号：T6635产 地：中国大陆

T8234ML401ML401,Inhibitor,ML 401,EBI2/GPR183,inhibit,ML-401

ML401 is a selectively EBI2(GPR183) receptor antagonist(IC50 of 1.03 nM) .

价 格：￥电议型 号：T8234产 地：中国大陆

T9834(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one(3Z) 1 methyl 3 [2 (4 methylphen

(3Z)-1-methyl-3-[2-(4-methylphenyl)-2-oxo-ethylidene]piperazin-2-one is a chemical agent.

价 格：￥电议型 号：T9834产 地：中国大陆

T7838Losartan CarboxaldehydeDuP 167,EXP-3179,DuP-167,Inhibitor,COX,AT1-R–blocking,intermediate aldehyde m

Losartan Carboxaldehyde is an endothelial cyclooxygenase (COX)-2 inhibitor.

价 格：￥电议型 号：T7838产 地：中国大陆

T8323LolCDE-IN-1antibacterial,inhibit,Bacterial,LolCDEIN1,Inhibitor,LolCDE IN 1,LolCDE

LolCDE-IN-1 is an inhibitor of the Lol proteins (LolCDE) complex. LolCDE-IN-1 shows antibacterial activity.

价 格：￥电议型 号：T8323产 地：中国大陆

T6834FCCPFCCP,inhibit,Mitochondrial Metabolism,Inhibitor

FCCP, a potent uncoupler of oxidative phosphorylation in mitochondria, transport protons across cell membranes leading to disrupts ATP synthesis.

价 格：￥电议型 号：T6834产 地：中国大陆

T6788Bitopertininhibit,Bitopertin,RG 1678,RO-4917838,RG-1678,GlyT,Inhibitor,RO 4917838,Glycine transporte

Bitopertin (RG1678, RO-4917838) is a potent inhibitor of glycine transporter 1 (GlyT1), with Ki of 8.1 nM for human hGlyT1b and IC50 of 22-25 nM in Chinese hamster ovary cells.

价 格：￥电议型 号：T6788产 地：中国大陆