TN7110Ginsenoside Rs2Ginsenoside Rs2,Ginsenoside Rs-2

Ginsenoside Rs2 is a natural product isolated from the leaves of Panax japonicus var..

价 格：￥电议型 号：TN7110产 地：中国大陆

TQ0289LY450108Inhibitor,inhibit,AMPA,Parkinson’s,LY 450108,depression,iGluR,LY-450108,LY450108,Ionotropic

LY450108 is a potentiator of the AMPA receptor that can be used in Parkinson´s disease studies.

价 格：￥电议型 号：TQ0289产 地：中国大陆

T9154Sodium taurodeoxycholate hydrateSodium taurodeoxycholate hydrate,Sodium taurodeoxycholate,inhibit,In

Sodium taurodeoxycholate hydrate has been used in a study to assess the effect of submicellar concentrations of bile salts on the lipid bilayer membrane.

价 格：￥电议型 号：T9154产 地：中国大陆

T7575L[Sar1, Ile8]-Angiotensin II 3TFA[Sar1, Ile8] Angiotensin II 3TFA,[Sar1, Ile8]Angiotensin II 3TFA,[Sa

[Sar1, Ile8]-Angiotensin II(3TFA) is a peptide that has multiple effects on vascular smooth muscle.

价 格：￥电议型 号：T7575L产 地：中国大陆

T39965NF-κΒ activator 1NFκΒ activator 1,NF κΒ activator 1

NF-κΒ activator 1 is a potent NF-κΒ activator with an EC 50 of 0.9 μM. NF-κΒ activator 1 induces superoxide dismutase (SOD)2 mRNA expression.

价 格：￥电议型 号：T39965产 地：中国大陆

T8596Ceefourin 1P-glycoprotein,chemosensitizers,inhibit,efflux,protein,resistance,Ceefourin 1,Ceefourin1,

Ceefourin 1 is a highly selective multidrug resistance protein 4 (MRP4) inhibitor.

价 格：￥电议型 号：T8596产 地：中国大陆

T64347ALDH1A3-IN-3ALDH1A3IN3

ALDH1A3-IN-3 (compound 16) is a potent inhibitor of ALDH1A3, with an IC50 of 0.26 μM. ALDH1A3-IN-3 is also a good ALDH3A1 substrate. ALDH1A3-IN-3 can be used for the research of prostate cancer.

价 格：￥电议型 号：T64347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

T7015Vps34-IN-1inhibit,Autophagy,Vps34IN1,PI3K,Vps-34-IN-1,Inhibitor,Phosphoinositide 3-kinase,Vps34 IN 1

Vps34-IN1 is a potent and highly selective Vps34 inhibitor with IC50 of 25 nM invitro, which does not significantly inhibit the isoforms of class I as well as class II PI3Ks.

价 格：￥电议型 号：T7015产 地：中国大陆

TN71802-Pyrimidinamine, 4-(5-bromo-1H-indol-3-yl)-

2-Pyrimidinamine, 4-(5-bromo-1H-indol-3-yl)- is a marine derived natural products found in Aplidium meridianum.

价 格：￥电议型 号：TN7180产 地：中国大陆

T27691JNJ-DGAT2-AJNJ DGAT2 A,JNJ-DGAT-2-A

JNJ-DGAT2-A, a specific inhibitor of DGAT2(IC50 = 0.14 μM), can be used in studies about the synthesis of triglycerides.

价 格：￥电议型 号：T27691产 地：中国大陆

T10775c-Fms-IN-2c Fms IN 2,cFmsIN2

c-Fms-IN-2 is an inhibitor of c-FMS kinase (IC50 = 24 nM).

价 格：￥电议型 号：T10775产 地：中国大陆

T7310PaquinimodABR-25757,Inhibitor,ABR25757,inhibit,Paquinimod

Paquinimod is a S100A9 inhibitor preventing S100A9 binding to TLR-4.

价 格：￥电议型 号：T7310产 地：中国大陆

T10623BSH-IN-1BSH IN 1,BSHIN1

BSH-IN-1 is a potent and covalent inhibitor of gut bacterial recombinant bile salt hydrolases (BSHs; IC50s: 108 nM and 427 nM for B. longum BSH and B. theta BSH).

价 格：￥电议型 号：T10623产 地：中国大陆

T6815HS-1371HS-1371,Inhibitor,Receptor-interacting protein kinases,RIPK,inhibit,HS 1371,RIP kinase,HS1371

HS-1371 is a novel kinase inhibitor of receptor-interacting protein kinase 3 (RIP3) with an IC50 of 20.8 nM.

价 格：￥电议型 号：T6815产 地：中国大陆

T8722iKIX1antifungal,Inhibitor,drug-resistant,Fungal,CgGal11A,CgPdr1,infection,C. glabrata,iKIX1,inhibit,

iKIX1 is an Pdr1-dependent gene activation. It re-sensitizes drug-resistant C. glabrata to azole antifungals in vitro and in animal models for disseminated and urinary tract C. glabrata infection.

价 格：￥电议型 号：T8722产 地：中国大陆

TN1656Ganoderenic acid AInhibitor,inhibit,Ganoderenic acid A

Ganoderenic acid A has a potent hepatoprotective, and cytotoxic effects, it shows inhibitory activity on human aldose reductase in vitro.

价 格：￥电议型 号：TN1656产 地：中国大陆

TN6710Methyl acetylsalicylateMethyl acetylsalicylate

Methyl acetylsalicylate is a natural product isolated from Pisum sativum. Inhibition of collagen-induced human platelet rich plasma aggregation

价 格：￥电议型 号：TN6710产 地：中国大陆

T9100BP 897inhibit,BP-897,BP897,cocaine drug-seeking,BP 897,Dopamine Receptor,Inhibitor,addiction,behavio

2-Naphthalenecarboxamide, N-[4-[4-(2-methoxyphenyl)-1-piperazinyl]butyl]- is a potent and selective dopamine D3 receptor agonist, and a weak dopamine D2 receptor antagonist, with Kis of 0.92 nM and 61 nM for D3 and D2 receptors, and shows low affinities at D1 and D4 receptors (Kis, 3 and 0.3 μM, respectively).

价 格：￥电议型 号：T9100产 地：中国大陆

Fr13619Compound Fr13619Compound Fr13619

价 格：￥电议型 号：Fr13619产 地：中国大陆