T5535ERK5-IN-2

ERK5-IN-2 is an orally active, sub-micromolar, selective ERK5 inhibitor with IC50s of 0.82 μM, 3 μM for ERK5 and ERK5 MEF2D, respectively.

价 格：￥电议型 号：T5535产 地：中国大陆

T5534LOC14

LOC14 to be the most potent PDI inhibitor reported to date( EC50 : 500 nM)

价 格：￥电议型 号：T5534产 地：中国大陆

T5533MC180295(rel)-MC180295

MC180295 is a novel potent, highly selective CDK9 inhibitor (IC50: 5 nM), displays >22-fold selectivity over other CDKs.

价 格：￥电议型 号：T5533产 地：中国大陆

T5532BMS-687453

BMS-687453 is a potent and selective PPAR alpha agonist, with an EC(50) of 10 nM for human PPARalpha and approximately 410-fold selectivity vs human PPARgamma in PPAR-GAL4 transactivation assays.

价 格：￥电议型 号：T5532产 地：中国大陆

T5531GSK-4716

GSK4716 is an ERRβ/γ agonist (IC50 = 2 μM) that can activate the receptor with similar potency as the protein ligand

价 格：￥电议型 号：T5531产 地：中国大陆

T5528Cyanidin Chloride

Cyanidin Chloride, the main phenolic antioxidant in the grape (Vitis vinifera), in particular in the liposomal forms, could be used for treatment of diabetes mellitus complications.

价 格：￥电议型 号：T5528产 地：中国大陆

T5524Aurora kinase inhibitor-3Aurora Kinase Inhibitor III

Aurora kinase inhibitor III is a potent inhibitor of Aurora A kinase (IC50 = 42 nM).1 It is selective for Aurora A over BMX, BTK, IGF-1R, c-Src, TRKB, SYK, and EGFR.

价 格：￥电议型 号：T5524产 地：中国大陆

T5523Imidazole ketone erastinIKE

Imidazole ketone erastin (IKE) is an inducer of ferroptosis. It has inhibition of the system Xc- cystine/glutamate transporter.

价 格：￥电议型 号：T5523产 地：中国大陆

T5522NMDAR antagonist 1

价 格：￥电议型 号：T5522产 地：中国大陆

T5521BropirimineU-54461；溴匹立明

Bropirimine (U-54461) is a biological response modifier that is thought to act through the induction of lymphokines.

价 格：￥电议型 号：T5521产 地：中国大陆

T5520LCetrorelix diacetate醋酸西曲瑞克；Cetrorelix acetate；SB-075 diacetate；SB-075 acetate；NS-75A；NS-75A diacetat

Cetrorelix diacetate is is a gonadotropin-releasing hormone antagonist. It works by blocking the action of GnRH upon the pituitary, thus rapidly suppressing the production and action of luteinizing hormone (LH) and follicle-stimulating hormone (FSH).

价 格：￥电议型 号：T5520L产 地：中国大陆

T5520Cetrorelix Acetate醋酸西曲瑞克；Cetrorelix

Cetrorelix Acetate is gonadotropin-releasing hormone (GnRH) receptor antagonist with an IC50 of 1.21 nM.

价 格：￥电议型 号：T5520产 地：中国大陆

T5519Bivalirudin比伐卢定；BG-8967；Hirulog-1

Bivalirudin is a reversible inhibitor of α- and ζ-thrombin (Kis = 2.56 and 1.84 nM, respectively), enzymes that exhibit high fibrinogen-clotting activities.

价 格：￥电议型 号：T5519产 地：中国大陆

T5518N-acetylcysteine amide

N-Acetylcysteine amide is a cell membranes and blood brain barrier permeant thiol antioxidant and neuroprotective agent

价 格：￥电议型 号：T5518产 地：中国大陆

T5517(R)-Carisbamate

(R)-Carisbamate is the R-isomer of Carisbamate . Carisbamate is an experimental anticonvulsant drug.

价 格：￥电议型 号：T5517产 地：中国大陆

T5515HeminHemin chloride；氯化血红素

Hemin is an iron-containing porphyrin and Heme oxygenase (HO)-1 inducer.

价 格：￥电议型 号：T5515产 地：中国大陆

T5514Epibrassinolide24-Epibrassinolide；BP55；B1105；表油菜素内酯

Epibrassinolide (EBR) is a biologically active compound of the brassinosteroids, is a natural brassinosteroid (BR) derivative, is a plant regulator with a similar structure to mammalian steroids.

价 格：￥电议型 号：T5514产 地：中国大陆

T5513RO-3RO3

RO3 is a selective antagonist of homomeric P2X3 and heteromeric P2X2/3 receptor

价 格：￥电议型 号：T5513产 地：中国大陆

T5512JNJ16259685.TN.T 16259685

JNJ16259685 is a selective mGluR1 antagonist, and inhibits the synaptic activation of mGluR1 in a concentration-dependent manner with IC50 of 19 nM.

价 格：￥电议型 号：T5512产 地：中国大陆

T5511L-765314

L-765314 is a drug which acts as a potent and selective antagonist for the Alpha-1 adrenergic receptor subtype α1B. It has mainly been used to investigate the role of α1B receptors in the regulation of blood pressure.

价 格：￥电议型 号：T5511产 地：中国大陆