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Cat. No.	Product Name	Target	Signaling Pathways
T8372	VU0134992 VU 0134992	Potassium Channel	Membrane transporter/Ion channel
	VU 0134992 是一个亚型偏好的，口服有效的和选择性的内向整流钾通道 Kir4.1阻滞剂，IC50为 0.97 μM。在 -120 mV 时，VU0134992对同分 Kir4.1 比 Kir4.1/5.1 共分通道 (IC50=9 μM) 高出 9 倍的选择性。
T13316	VU0134992 hydrochloride	Potassium Channel	Membrane transporter/Ion channel
	VU0134992 hydrochloride 是一个亚型偏好的，具有口服活性和选择性的内向整流钾通道Kir4.1阻滞剂，IC50为 0.97 μM。在 -120 mV 时，VU0134992 hydrochloride 对同分 Kir4.1 比 Kir4.1/5.1 共分通道 (IC50=9 μM) 高出 9 倍的选择性。
T6658	SB-408124 N-(6,8-二氟-2-甲基-4-喹啉)- N-[4-(二甲氨基)苯基]尿素	OX Receptor	GPCR/G Protein; Neuroscience
	SB408124 是一种 OX1 受体的非肽拮抗剂，在全细胞和膜中的 Ki 值分别为 57 和 27 nM，其选择性是 OX2 受体的 50 倍。
T4367	Mycro 3 Mycro-3	c-Myc; Autophagy	Autophagy; Cell Cycle/Checkpoint
	Mycro 3 在全细胞分析中对 c-Myc 具有强效选择性，可用于胰腺癌的研究。
T16383	Olinciguat IW-1701	Guanylate cyclase	GPCR/G Protein
	Olinciguat (IW-1701) 是一种口服鸟苷酸环化酶 (sGC) 刺激剂，在纯化的大鼠和人类酶测定以及全细胞测定中对 sGC 具有浓度依赖性刺激作用。
T76870	Narsoplimab OMS 721	SARS-CoV	Microbiology/Virology
	Narsoplimab (OMS 721) 是一种选择性全人免疫球蛋白γ 4 (IgG4) 单克隆抗体，是一种甘露聚糖结合凝集素相关的丝氨酸蛋白酶-2（MASP-2）抑制剂，可结合 MASP-2 并阻止凝集素通路激活，对凝集素通路有抑制作用。Narsoplimab 可用于研究成人造血干细胞移植相关疾病。
T12844	SB-408124 Hydrochloride	Others	Others
	SB-408124 Hydrochloride is a non-peptide OX1 receptor antagonist(Ki of 57 nM and 27 nM in both whole cell and membrane, respectively).
T11243	Ethyl tosylcarbamate	Others	Others
	Gliclazide is a whole-cell beta-cell ATP-sensitive potassium currents blocker with an IC50 of 184 nM. Ethyl tosylcarbamate is an intermediate in the synthesis of Gliclazide (G409877).
T61446	BioA-IN-13
	BioA-IN-13 is a highly effective inhibitor of the Mycobacterium tuberculosis BioA enzyme, displaying potent cell permeability and whole-cell activity [1].
T30990	CMFDA 5-Chloromethylfluorescein diacetate,Cell Tracker Green,CM-FDA,CM FDA
	CMFDA can be used as a fluorescent whole-cell-tracking reagent.
T33407	MitoEbselen-2 chloride MitoPeroxidase-2,MitoPeroxidase 2,MitoEbselen 2,MitoEbselen-2
	MitoEbselen-2 is a radiation mitigator which reduces lipid hydroperoxides and prevents apoptotic cell death. When administered 24 hours postirradiation, MitoEbselen-2 was shown to increase the survival of mice exposed to whole body γ-irradiation.
T40650	Dihydroisopimaric acid
	Dihydroisopimaric acid activates BK channels alphabeta1, which are large conductance Ca 2+ activated K + channels. This compound directly measures the opening of BKalphabeta1 under a whole-cell voltage clamp.
T38266	Nirogacestat dihydrobromide
	Potent γ-secretase inhibitor (IC50 values are 1.2 and 6.2 nM in whole cell and cell-free assays, respectively). Reduces Aβ in brain, CSF and plasma in mice and guinea pigs. Lanz et al (2010) Pharmacodynamics and pharmacokinetics of the gamma-secretase inhibitor PF-3084014. J.Pharmacol.Exp.Ther. 334 269 PMID:20363853
T37763	BTD
	Selective TRPC5 activator (EC50 = 1.4 μM in a calcium influx assay, 1.3 μM in whole cell patch clamp assay). Displays >14.5-fold selectivity for TRPC5 over other TRP channels (EC50 = 20.6 μM for TRPM8). Also activates TRPC1:5 and TRPC4:5 heteromers. Beckmann et al (2017) A benzothiadiazine derivative and methylprednisolone are novel and selective activators of transient receptor potential canonical 5 (TRPC5) channels. Cell Calcium. 66 10 PMID:28807145
T83326	4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic acid disodium
	4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic acid disodium 是荧光染料，用于逆行轴突运输二抗标记显示和全细胞荧光染色。
T41212	FTI 277
	FTI 277 is a prodrug form of FTI 276 that inhibits farnesyltransferase (FTase) (IC50 = 0.5 nM). Inhibits H-Ras and K-Ras processing in whole cells (IC50 values are 0.1 and 10μM respectively) and disrupts constitutive H-Ras-specific activation of MAPK. Causes significant antiproliferative effects in human malignant glioma cells and many other tumor cell lines.
T26447	A 78773 A78773,A-78773
	A 78773 is a potent, selective, direct, and reversible 5-lipoxygenase inhibitor. It has activity in a variety of purified cells and in more complex biological systems such as whole blood, lung fragments, and tracheal tissues. A 78773 acts against inflamma
T26865	BMS-933043 BMS933043
	BMS-933043 is a Selective α7 nAChR partial agonist. BMS-933043 showed potent binding affinity to native rat (Ki = 3.3 nM) and recombinant human alpha7 nicotinic acetylcholine receptors (Ki = 8.1 nM). BMS-933043 shows agonist activity in a calcium fluoresc
T80455	ω-Conotoxin CVIB	Sodium Channel	Membrane transporter/Ion channel
	ω-Conotoxin CVIB为非选择性N型及P/Q型电压门控钙通道(VGCC)拮抗剂，能够抑制背根神经节(DRG)中神经元去极化后激活全细胞VGCC电流，其pIC50值为7.64。
T63405	NAZ2329
	NAZ2329 是受体型蛋白质酪氨酸磷酸酶 (RPTPs) R5 亚家族的一个细胞可渗透抑制剂，与其他 PTPs 相比，其变构且能够优先抑制 PTPRZ (hPTPRZ1 的IC50= 7.5 μM) 和PTPRG (hPTPRGIC50= 4.8 μM)。NAZ2329 能够与PTPRZ 的 D1结构域结合，与PTPRZ 整个 (D1 + D2) 片段相比，其能够更有效地抑制 PTPRZ1-D1片段 (IC50: 1.1 μM)。NAZ2329 能够抑制胶质母细胞瘤细胞的肿瘤生长，并表现出抑制干细胞样特性。
T83701	TRPV1-Tat TFA Transient Receptor Potential Vanilloid 1-Tat,736-745-Tat
	TRPV1-Tat是一种针对瞬时受体电位范烤苷1 (TRPV1) 的肽类拮抗剂。它由来自TRPV1的A-激酶锚蛋白(AKAP)结合域的736-745个氨基酸以及来自HIV Tat的细胞穿透肽序列组成。TRPV1-Tat (200 µM) 能够在使用初级小鼠背根神经节的整细胞膜片钳技术中抑制由热或棕榈酸酯12-肉豆蔻酸13-醋酸酯(PMA014)引起的电流。当以10或30 µM剂量给药时，它能增加大鼠后爪机械痛阈。
T83962	C 101248
	C 101248是一种选择性且强效的小鼠和人类串联孔道卤素抑制K+通道1（THIK-1, IC50= 50 nM）抑制剂，对K2P家族成员TREK-1和TWIK-2以及Kv2.1无活性。C 101248能够阻断小鼠海马微胶质细胞中THIK-1 K+电流的整细胞膜片钳记录中的音调和ATP激发的电流。C 101248通过防止NLRP3依赖性IL-1β的释放，从而减少在分离的微胶质细胞中的神经炎症。
T70538	PD-85639
	PD-85639 is a voltage-gated sodium (Na+) channel blocker (75% in 10 min & >95% in 25 min blockage of Na+ current by 25 μM PD85,639; whole-cell patch clamp using primary rat brain neurons) that is shown to target rat brain Nav1.2 with simultaneous high- and low-affinity modes of binding (EC50 = 56 nM/40% & 20 μM/60% at pH 9.0, 5 nM/28% & 3 μM/72% at pH 7.4, against 2 nM [3H]-PD85,639 for binding rat brain synaptosomes; EC50 = 17 nM/39% & 10 μM/61% using at pH 9.0 using rat brain synaptosome membr...
T35536	Tpl2 Kinase Inhibitor (hydrochloride)
	Tpl2 kinase inhibitor is an inhibitor of tumor progression locus 2 (Tpl2; IC50= 0.05 μM).1It is selective for Tpl2 over MEK, p38 MAPK, Src, MK2, and PKC (IC50s = >40, 180, >400, 110, and >400 μM, respectively). Tpl2 kinase inhibitor inhibits LPS-induced TNF-α production in isolated human monocytes and whole blood (IC50s = 0.7 and 8.5 μM, respectively). It enhances differentiation induced by calcitriol in HL-60 and U937 leukemia cells when used at a concentration of 5 μM.2Tpl2 kinase inhibitor (5...
T37297	Ru360
	Ru360, an oxygen-bridged dinuclear ruthenium amine complex, is a selective mitochondrial calcium uptake inhibitor. Ru360 potently inhibits Ca2+ uptake into mitochondria with an IC50 of 0.184 nM. Ru360 binds to mitochondria with high affinity (Kd of 0.34 nM). Ru360 has antiarrhythmic and cardioprotective effects[1][2]. Ru360 permeates slowly into the cell, and specifically inhibits mitochondrial calcium uptake in intact cardiomyocytes and in isolated heart. 1 μm Ru360 is taken up by myocardial ce...

化合物

Cat.No: T8372

Synonym: VU 0134992

Target: Potassium Channel

VU0134992 hydrochloride

Cat.No: T13316

Target: Potassium Channel

Cat.No: T6658

Synonym: N-(6,8-二氟-2-甲基-4-喹啉)- N-[4-(二甲氨基)苯基]尿素

Target: OX Receptor

Cat.No: T4367

Synonym: Mycro-3

Target: c-Myc, Autophagy

Cat.No: T16383

Synonym: IW-1701

Target: Guanylate cyclase

Cat.No: T76870

Synonym: OMS 721

Target: SARS-CoV

SB-408124 Hydrochloride

Cat.No: T12844

Target: Others

Ethyl tosylcarbamate

Cat.No: T11243

Target: Others

Cat.No: T61446

Cat.No: T30990

Synonym: 5-Chloromethylfluorescein diacetate,Cell Tracker Green,CM-FDA,CM FDA

MitoEbselen-2 chloride

Cat.No: T33407

Synonym: MitoPeroxidase-2,MitoPeroxidase 2,MitoEbselen 2,MitoEbselen-2

Dihydroisopimaric acid

Cat.No: T40650

Nirogacestat dihydrobromide

Cat.No: T38266

Cat.No: T37763

4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic acid disodium

Cat.No: T83326

Cat.No: T41212

Cat.No: T26447

Synonym: A78773,A-78773

Cat.No: T26865

Synonym: BMS933043

ω-Conotoxin CVIB

Cat.No: T80455

Target: Sodium Channel

Cat.No: T63405

Cat.No: T83701

Synonym: Transient Receptor Potential Vanilloid 1-Tat,736-745-Tat

Cat.No: T83962

Cat.No: T70538

Tpl2 Kinase Inhibitor (hydrochloride)

Cat.No: T35536

Cat.No: T37297

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