T9700EZH2-IN-2EZH2IN2,EZH-2-IN-2,EZH2 IN 2

EZH2-IN-2 is a EZH2 inhibitor with an IC50 of 64 nM (Patent WO2018133795A1, Compound Example 69).

价 格：￥电议型 号：T9700产 地：中国大陆

T8374LJ570inhibit,Peroxisome proliferator-activated receptors,LJ-570,LJ 570,LJ570,Inhibitor,PPAR

LJ570 is the first PPARα/γ dual agonist (PPARα,PPARγ with EC50s of 1.05 and 0.12 μM, respectively[)

价 格：￥电议型 号：T8374产 地：中国大陆

T97041-Ethynylpyrene1A1,P450,1 Ethynylpyrene,2B1,1-Ethynylpyrene,Inhibitor,CYPs,Cytochrome P450,1Ethynylp

1-Ethynylpyrene is an aryl acetylenic inhibitor of CYTP450 1A1(IC50=0.18 μM), 1A2(IC50 = 0.32 μM), and 2B1(IC50 = 0.04 μM).

价 格：￥电议型 号：T9704产 地：中国大陆

T7018WZB117GLUT,Inhibitor,WZB-117,WZB 117,WZB117,inhibit,Glucose transporter

WZB117 is a Glucose Transporter 1 (GLUT1) inhibitor. when IC50 of WZB117 approximate 10 μM, it inhibits lung cancer A549 cells and breast cancer MCF7 cells proliferation.

价 格：￥电议型 号：T7018产 地：中国大陆

T7097Cytochalasin BCytochalasin B

Cytochalasin B is a mycotoxin binding to the barbed end of actin filaments. It can disrupt the formation of actin polymers (Kd: 1.4-2.2 nM for F-actin).

价 格：￥电议型 号：T7097产 地：中国大陆

T74706-ChloropurineInhibitor,inhibit,6-Chloropurine,6Chloropurine,6 Chloropurine

6-Chloropurine is a building block in chemical synthesis,with Antitumor activities.

价 格：￥电议型 号：T7470产 地：中国大陆

T99701-ethyl-3-morpholin-4-yl-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile

1-ethyl-3-morpholin-4-yl-5,6,7,8-tetrahydroisoquinoline-4-carbonitrile is a positive allosteric modulator of mGluR3 and can be used in studies about the treatment of Parkinson´s disease.

价 格：￥电议型 号：T9970产 地：中国大陆

T26704AZ13705339

AZ13705339 is an effective inhibitor of PAK1 with an IC50 of 0.33 nM and a Kd of 0.28 nM. AZ13705339 binds PAK2 with a Kd of 0.32 nM. AZ13705339 can be used in studies about cancers.

价 格：￥电议型 号：T26704产 地：中国大陆

T7770Ethylhexyl Triazoneinhibit,Inhibitor,Ethylhexyl Triazone

Ethylhexyl triazone is an ultraviolet-B (UV-B) chemical filter for commercial sunscreens.

价 格：￥电议型 号：T7770产 地：中国大陆

TN7070ErgostenolErgostenol

Ergostenol is a biological precursor and a provitamin of vitamin D2.

价 格：￥电议型 号：TN7070产 地：中国大陆

T70384-Methylayapin4Methylayapin,4 Methylayapin

价 格：￥电议型 号：T7038产 地：中国大陆

TP1215LAbaloparatide acetate(247062-33-5 free base)Abaloparatide acetate(247062335 free base),Abaloparati

Abaloparatide acetate is a parathyroid hormone receptor 1 PTHR1 analogue and an effective and selective activator of the PTHR1 signaling pathway.

价 格：￥电议型 号：TP1215L产 地：中国大陆

T9470HPK1-IN-7HPK1 IN 7,MC38,Inhibitor,PD1,HPK1IN7,tumor,model,oral,selectivity,HPK-1-IN-7,MAP4K,inhibit,

HPK1-IN-7 is an orally active HPK1 inhibitor. It shows selectivity against IRAK4 (59 nM) and GLK (140 nM).

价 格：￥电议型 号：T9470产 地：中国大陆

T8978DD1DD 1,P70S6K degradation,Bax activation,mitochondrial membrane depolarization,S6K,proteasome inhib

DD1 is a proteasome inhibitor that induces human myeloid tumor-selective apoptosis.

价 格：￥电议型 号：T8978产 地：中国大陆

T7010VER-155008Autophagy,Heat shock proteins,inhibit,VER-155008,HSP,VER 155008,Inhibitor

VER-155008 is a potent Hsp70 family inhibitor with IC50 of 0.5 μM, 2.6 μM, and 2.6 μM in cell-free assays for HSP70, HSC70, and GRP78, respectively, >100-fold selectivity over HSP90.

价 格：￥电议型 号：T7010产 地：中国大陆

T1730NPS-2143SB-262470A,Inhibitor,NPS-2143,NPS2143,inhibit,Calcium-sensing receptor,CaSR

NPS-2143 is a novel potent and selective antagonist of Ca(2+) receptor.

价 格：￥电议型 号：T1730产 地：中国大陆

TQ0170Desacetylcinobufagininhibit,Desacetylcinobufagin,Inhibitor

Deacetylcinobufagin, a natural product, shows potent activities against Hela and A375 cells in vitro.

价 格：￥电议型 号：TQ0170产 地：中国大陆

TN1702Glycycoumarininhibit,Glycycoumarin,Autophagy,Inhibitor

Glycycoumarin is an estrogen agonist, it shows moderate inhibitory effects against CYP1A2 and CYP2B6.

价 格：￥电议型 号：TN1702产 地：中国大陆

T37072Nitroxynil

Nitroxynil, anthelmintic agent, is active against parasites in both adult and immature stages. Nitroxynil is widely used for the research of infection of Fasciola hepatica.

价 格：￥电议型 号：T37072产 地：中国大陆

T8720PRX-07034 hydrochlorideflexibility,5-HT6,PRX 07034,working,Serotonin Receptor,cognitive,Inhibitor,in

PRX-07034 is a selective antagonist of 5-HT6 receptor. It has cognition and memory-enhancing properties and potently decreases food intake and body weight in rodents. PRX-07034 is both a potent (Ki = 4-8 nM) and highly selective 5-HT(6) receptor antagonist (≥100-fold selectivity for the 5-HT(6) receptor compared to 68 other GPCRs, ion channels, and transporters, except D(3) (Ki = 71 nM) and 5-HT(1B) (Ki = 260 nM) receptors.

价 格：￥电议型 号：T8720产 地：中国大陆