T60032BRM/BRG1 ATP Inhibitor-2Epigenetic Reader Domain,Inhibitor,BRM/BRG1 ATP Inhibitor 2,inhibit,BRM/BRG1

BRM/BRG1 ATP Inhibitor-2 is an inhibitor of BRG1/BRM ATPase and can be used in studies about the treatment of BAF-related disorders.

价 格：￥电议型 号：T60032产 地：中国大陆

T6615Ondansetron5-hydroxytryptamine Receptor,GR38032,SN307,Inhibitor,Ondansetron,Serotonin Receptor,GR-38

Ondansetron is a serotonin 5-HT3 receptor antagonist used mainly as an antiemetic.

价 格：￥电议型 号：T6615产 地：中国大陆

T9573GSK3685032Inhibitor,GSK 3685032,lymphoma,DNMTs,cancer,DNA MTases,GSK-3685032,inhibit,GSK3685032,DNA

GSK3685032 is a non-covalent and selective DNMT1 inhibitor(IC50 = 36 nM). The inhibitory effect is time-independent and reversible. GSK3685032 induces loss of DNA methylation and transcriptional activation and inhibits cancer cell growth.

价 格：￥电议型 号：T9573产 地：中国大陆

TJS0328Nordalberginpromyelocytic,Inhibitor,coumarin,HL-60,cells,leukemia,differentiation,Nordalbergin,inhib

价 格：￥电议型 号：TJS0328产 地：中国大陆

T10329anti-TB agent 1antiTB agent 1,anti TB agent 1

anti-TB agent 1 is a potent and orally active anti-tuberculosis agent (MICs: < 2 nM against the Mtb strains H37Rv, rRMP and rINH).

价 格：￥电议型 号：T10329产 地：中国大陆

T80324-Pentenoic acidEndogenous Metabolite,inhibit,4 Pentenoic acid,4Pentenoic acid,4-Pentenoic acid,Inhi

4-Pentenoic acid, also known as allyl acetic acid or 4-pentenate, belongs to the class of organic compounds known as straight chain fatty acids. These are fatty acids with a straight aliphatic chain. 4-Pentenoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

价 格：￥电议型 号：T8032产 地：中国大陆

TQ0042BAY-1436032Inhibitor,BAY1436032,Isocitrate Dehydrogenase (IDH),BAY-1436032,inhibit,BAY 1436032

BAY-1436032 is a novel, selective and orally available inhibitor of pan-mutant isocitrate dehydrogenase 1 (IDH1).

价 格：￥电议型 号：TQ0042产 地：中国大陆

T7000Tiagabine hydrochlorideNO050328,TGB,NO-050328,γ-Aminobutyric acid Receptor,NO 050328,inhibit,NO-328,

Tiagabine Hydrochloride is the hydrochloride salt form of tiagabine, a nipecotic acid derivative with anticonvulsant property. A selective gamma-aminobutyric acid (GABA) reuptake inhibitor.

价 格：￥电议型 号：T7000产 地：中国大陆

T8654Plx-4032Plx 4032,Plx4032

PLX-4032 is a small-molecule B-Raf inhibitor for the potential treatment of malignant melanoma.

价 格：￥电议型 号：T8654产 地：中国大陆

T41032LysostaphinLysostaphin

Lysostaphin is an antistaphylococcal agent. Lysostaphin has activities of three enzymes namely, glycylglycine endopeptidase, endo-β-N-acetyl glucosamidase and N-acteyl muramyl-L-alanine amidase.

价 格：￥电议型 号：T41032产 地：中国大陆

T29106VH032VH032

VH032 commonly used as a precursor to a PROTAC that hijacks VHL as the E3 ubiquitin ligase component.VH032 is a VHL/HIF-1α interaction inhibitor with a KdPROTACs, which can recruit von Hippel-Lindau (VHL) proteins as a ligand of VHL.

价 格：￥电议型 号：T29106产 地：中国大陆

TN1032Geissoschizine methyl ether5-HT Receptor,Geissoschizine methyl ether,Inhibitor,inhibit,5-hydroxytryp

Geissoschizine methyl ether, a major indole alkaloid found in Uncaria hook, is a major active component of Yokukansan with psychotropic effects. Geissoschizine methyl ether is a potent serotonin A receptor agonist and candidate for amelioration of aggressiveness and sociality by yokukansan

价 格：￥电议型 号：TN1032产 地：中国大陆

T6S0325GlyciteinGlycitein,Inhibitor,Apoptosis,inhibit

1. Gycitein has weak estrogenic activity. 2. Glycitein inhibits glioma cell invasion through down-regulation of MMP-3 and MMP-9 gene expression.

价 格：￥电议型 号：T6S0325产 地：中国大陆

T9032MGH-CP1MGH CP1,Lats1/2 deletion,Myc,MGHCP1,TEAD auto-palmitoylation,Apoptosis,Epithelial,MGH-CP1,inh

MGH-CP1 is a potent and selective inhibitor TEAD palmitoylation. It exhibits dose-dependent and potent inhibition of TEAD2/4 auto-palmitoylation in vitro with IC50 of 710 nM and 672 nM, respectively.

价 格：￥电议型 号：T9032产 地：中国大陆

T23253RS 100329

RS 100329 hydrochloride is an antagonist of α1A-adrenergic receptor.

价 格：￥电议型 号：T23253产 地：中国大陆

T6578ME0328ME 0328,inhibit,poly ADP ribose polymerase,ME-0328,ME0328,PARP,Inhibitor

ME0328 is a potent and selective PARP inhibitor with IC50 of 0.89 μM for PARP3, about 7-fold selectivity over PARP1.

价 格：￥电议型 号：T6578产 地：中国大陆

T7526JNJ-17203212management,inhibit,pain,migrainem,Transient receptor potential channels,TRP Channel,JNJ-

JNJ-17203212 is a potent and selective antagonist of TRPV1 (human TRPV1 and rat TRPV1, IC50 of 65 nM and 102 nM).

价 格：￥电议型 号：T7526产 地：中国大陆

T10325ANI-7ANI 7,ANI7

ANI-7 is an activator of aryl hydrocarbon receptor (AhR) pathway. ANI-7 inhibits the growth of multiple cancer cells and potently and selectively inhibits the growth of MCF-7 breast cancer cells (GI50: 0.56 μM).

价 格：￥电议型 号：T10325产 地：中国大陆

T60322Procainamide

Procainamide is a specific and potent DNA methyltransferase 1 ( DNMT1 ) inhibitor. Procainamide is a Class 1A antiarrhythmic agent. Procainamide has the potential for the research of cancer and arrhythmias [1] [2].

价 格：￥电议型 号：T60322产 地：中国大陆

T7032Eupatorininhibit,Eupatorin,Inhibitor

Eupatorin has antiproliferative and antiangiogenic effects. Eupatorin has antiproliferative and cytostatic effects on MDA-MB-468 human breast cancer cells due to CYP1-mediated metabolism. Eupatorin-induced cell death is mediated by both the extrinsic and the intrinsic apoptotic pathways and through a mechanism dependent on reactive oxygen species generation. Eupatorin also has meaningful anti-inflammatory property.

价 格：￥电议型 号：T7032产 地：中国大陆