T5480BI-4464

BI-4464 is a highly selective ATP competitive inhibitor of PTK2/FAK, with an IC50 of 17 nM. A PTK2 ligand for PROTAC

价 格：￥电议型 号：T5480产 地：中国大陆

T5410PD158780

PD 158780 reversibly inhibits auto and transphosphorylation of all four members of the ErbB receptor superfamily: EGFR, ErbB2, ErbB3, and ErbB4 (IC50s: 8μM, 49 nM, 52 nM, and 52 nM in cell assay).

价 格：￥电议型 号：T5410产 地：中国大陆

T5408BI-3802

BI-3802 is a highly potent BCL6 degrader and inhibits the Bric-à-brac (BTB) domain of BCL6 with an IC50 value of ≤3 nM. BI-3802 induces the polymerization of BCL6 and promotes BCL6 degration depended on E3 ligase SIAH1. BI-3802 has antitumor activity[1][2

价 格：￥电议型 号：T5408产 地：中国大陆

T5398BMS 599626 2HCl (873837-23-1(HCl))AC480 dihydrochloride

BMS-599626 (AC480) is a selective inhibitor of HER1 and HER2 (IC50s: 20 nM and 30 nM), ~8-fold less potent to HER4, >100-fold to Lck, VEGFR2, c-Kit, MET, etc.

价 格：￥电议型 号：T5398产 地：中国大陆

T5380Ansofaxine hydrochlorideAnsofaxine盐酸盐；LPM570065；LY03005

Ansofaxine (LY03005; LPM570065) is a serotonin-norepinephrine-dopamine reuptake inhibitor (IC50s: 723, 763 and 491 nM, respectively).

价 格：￥电议型 号：T5380产 地：中国大陆

T5333Rimeporide hydrochlorideEMD-87580 hydrochloride；盐酸Rimeporide

Rimeporide (EMD-87580) is a potent and selective Sodium hydrogen exchange 1 (NHE-1) inhibitor.

价 格：￥电议型 号：T5333产 地：中国大陆

T5319RimeporideEMD-87580

Rimeporide (EMD-87580) is a potent and selective Sodium hydrogen exchange 1 (NHE-1) inhibitor.

价 格：￥电议型 号：T5319产 地：中国大陆

T5265PhenylacetylglutamineN-苯乙酰基-L-谷氨酰胺；Phenylacetyl-L-glutamine；Phenyl-Ac-Gln-OH；NSC 203800

Phenylacetylglutamine is a normal constituent of human urine, but other mammals such as the dog, cat, rat, monkey, sheep, and horse do not excrete this compound. Phenylacetylglutamine is a major nitrogenous metabolite that accumulates in uremia. Phenylace

价 格：￥电议型 号：T5265产 地：中国大陆

T5208BAY-8002BAY8002；BAY 8002

BAY-8002 is a potent dual MCT1/2 inhibitor (IC50 values are 3, 8, and 12 nM at rat (C6), human (DLD-1) and mouse (4T1) MCT1 respectively).

价 格：￥电议型 号：T5208产 地：中国大陆

T5186Oseltamivir acid奥斯他伟酸；GS 4071；Ro 64-0802；oseltamivir carboxylate

Oseltamivir acid (GS4071) is a potent influenza virus neuraminidase inhibitor and the prodrug of GS4071.

价 格：￥电议型 号：T5186产 地：中国大陆

T5180SKA-31SKA 31；Naphtho[1,2-d]thiazol-2-ylamine；SKA31

SKA 31 is an activator of KCa3.1 and KCa2 channels (EC50s: 260, 2900, 2900 nM for KCa3.1, KCa2.1 and KCa2.2 respectively).

价 格：￥电议型 号：T5180产 地：中国大陆

T5146Eptifibatide acetate (148031-34-9 free base)依菲巴特醋酸盐；Eptifibatide acetate

Eptifibatide, an antiplatelet drug of the glycoprotein IIb/IIIa inhibitor class, is a cyclic heptapeptide constructed from 6 amino acids and a mercaptopropionyl residue.

价 格：￥电议型 号：T5146产 地：中国大陆

T5080Spermidine trihydrochloride三盐酸亚精胺；亚精胺盐酸盐；4-Azaoctamethylenediamine trihydrochloride；Spermidine hydro

Spermidine, a natural polyamine, is a novel autophagy inducer and negatively modulates N-methyl-d-aspartate (NMDA).

价 格：￥电议型 号：T5080产 地：中国大陆

T5056PF-4800567PF4800567；PF 4800567

PF-4800567 is a selective inhibitor of casein kinase 1ε (CK1ε; IC50 = 32 nM) with greater than 20-fold selectivity over CK1δ.

价 格：￥电议型 号：T5056产 地：中国大陆

T5047PD-168077 maleate

PD-168077 maleate is a selective agonist of dopamine D4 receptor(Ki : 9 nM)

价 格：￥电议型 号：T5047产 地：中国大陆

T50080MC2184

MC2184 is the inhibitor of human recombinant SIRT1.

价 格：￥电议型 号：T50080产 地：中国大陆

T4S1980Maoecrystal A

价 格：￥电议型 号：T4S1980产 地：中国大陆

T4S0800Demethyleneberberine

Demethyleneberberine, which is composed of a potential antioxidant structure, could penetrate the membrane of mitochondria and accumulate in mitochondria either in vitro or in vivo.Demethyleneberberine suppresses CYP2E1, hypoxia inducible factor α, and in

价 格：￥电议型 号：T4S0800产 地：中国大陆

T4986Imidafenacin咪达那新；ONO-8025；KRP-197

Imidafenacin(KRP-197; ONO-8025) is a potent and selective inhibitor of M3 receptors with Kb of 0.317 nM.

价 格：￥电议型 号：T4986产 地：中国大陆

T4980Betrixaban maleate

Betrixaban is a non-vitamin K oral anticoagulant whose action is driven by the competitive and reversible inhibition of the factor Xa [1]. It was selected among all lead compounds due to its low hERG channel affinity while sustaining its factor Xa inhibit

价 格：￥电议型 号：T4980产 地：中国大陆