35
4
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19777 |
ODQ
|
Apoptosis; Others; Guanylate cyclase | Apoptosis; GPCR/G Protein; Others |
ODQ 是一种选择性可溶性的鸟苷酰环化酶抑制剂,可增强顺铂促人间皮瘤细胞凋亡的作用。 | |||
T12783 |
RWJ 50271
|
Integrin | Cytoskeletal Signaling |
RWJ 50271 是具有口服活性的选择性LFA-1/ICAM-1相互作用抑制剂,抑制 LFA-1/ICAM-1 介导的细胞粘附,在细胞HL60中的IC50值为 5.0 μM。 | |||
T20812 |
Azamethiphos
甲基吡啶磷,唑啶磷 |
AChE | Neuroscience |
Azamethiphos 是有机磷杀虫剂和神经毒性物质,能够抑制乙酰胆碱酯酶的活性。 | |||
T76173 | Inorganic pyrophosphatase | ||
Inorganic pyrophosphatase (PPase) 无机焦磷酸酶可将焦磷酸盐 (PPi) 转化为磷酸盐。Inorganic pyrophosphatase 是 RNA 体外转录反应的重要组成部分,常用于生化研究。Inorganic pyrophosphatase 是驱动细胞过程,如核酸和蛋白质合成的关键。 | |||
T10009 |
JAK3-IN-7
|
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
JAK3-IN-7 是一种有效的选择性 JAK3 抑制剂(IC50<0.01 μM),可用于治疗器官移植中的排斥反应、器官移植后的移植物抗宿主反应、自身免疫性疾病、过敏性疾病和慢性骨髓增生性疾病。 | |||
T11318 |
Dopexamine hydrochloride
盐酸多培沙明,FPL60278AR |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Dopexamine hydrochloride (FPL60278AR) 是β2肾上腺素能受体激动剂。 | |||
T17105 |
TM6089
|
HIF/HIF Prolyl-Hydroxylase | Chromatin/Epigenetic; Metabolism |
TM6089 是一种脯氨酰羟化酶抑制剂,可在没有铁螯合的情况下刺激 HIF 活性,诱导血管生成,并保护器官免受缺血。 | |||
T13187 |
Topterone
Win 17665 |
Androgen Receptor | Endocrinology/Hormones |
Topterone(Win 17,665) 是一种有效的局部抗雄激素,抑制睾酮和二氢睾酮对阉割未成熟雄性仓鼠腰部器官发育的刺激。 | |||
T6459 |
Cyclosporine
|
Phosphatase | Metabolism |
Cyclosporine 是一种钙调神经磷酸酶通路抑制剂,用作免疫抑制剂以防止器官移植中的排斥反应。 | |||
T60144 |
TDI-011536
|
Others | Others |
TDI-011536 是一种有效的 Lats 激酶抑制剂,能中断 Hippo-Yap 的信号传导,并可启动受损心肌细胞的增殖。TDI-011536 可用于研究器官的保护和再生。 | |||
T21334 |
Bucillamine
DE-019,Thiobutarit,Tiobutarit,布西拉明,SA96,DE 019,DE019 |
VEGFR; Antioxidant | Angiogenesis; oxidation-reduction; Tyrosine Kinase/Adaptors |
Bucillamine (DE019) 可防止高危器官移植中的缺血/再灌注损伤,抑制 VEGF 的产生。 Bucillamine 是一种具有抗风湿和抗血管生成特性的口服活性巯基供体和抗氧化剂。 Bucillamine 可用于脉络膜新生血管和类风湿性关节炎的研究。 | |||
T31615 |
Elsibucol
AGI-1096,UNII-O7T92N1Y8T,AGI 1096 |
Antioxidant | oxidation-reduction |
Elsibucol (AGI 1096) 是一种VCAM1抑制剂,可用于研究器官移植排斥。Elsibucol 是一种代谢稳定的丙醇衍生物,具有抗氧化、抗炎和抗增殖的特性。它能降低血液中的胆固醇水平,减少受伤动脉中的氧化应激和炎症反应,从而抑制动脉粥样硬化,保护动脉损伤后的内皮愈合。 | |||
T76830 |
Teneliximab
Chi220,Anti-Human CD40 Recombinant Antibody,BMS 224819 |
TNF | Apoptosis |
Teneliximab (Chi220) 是一种嵌合的单克隆抗体,也是一种肿瘤坏死因子受体超家族成员5(CD40)抑制剂,可阻断CD40-CD40L 的相互作用。Teneliximab 通过CD40 和外周B细胞损耗发挥部分激动剂活性,可用于研究器官移植排斥和类风湿关节炎。 | |||
T19722 |
Benazeprilat
CGS14831,CGS-14831,CGS 14831 |
RAAS; Endogenous Metabolite | Endocrinology/Hormones; Metabolism |
Benazeprilat(CGS 14831) 是一种具有口服活性的贝那普利活性代谢物。Benazeprilat 具有高效的抗血压活性,可与其他其他类别的化合物(包括噻嗪类利尿剂和钙通道阻滞剂)联合使用来减少与心血管风险和继发性终末器官损伤相关的疾病的发生。Benazeprilat 可能用于研究急性左心室衰竭。 | |||
T74485 |
STC314
|
Others | Others |
STC314 具有抗感染作用,通过中和胞外组蛋白和中性粒细胞诱捕网来逆转机体过度免疫反应造成的器官损伤,可用于研究脓毒症和急性呼吸窘迫综合征(ARDS)。STC314 可保护脂质双层的稳定性,抑制血小板活化和红细胞损伤。 | |||
T9543 |
Syk Inhibitor II hydrochloride
|
Others | Others |
Syk Inhibitor II hydrochloride 信号传导的影响在狼疮中可能很突出。 | |||
T27743 |
KRH-594 free acid
WK14922K,WK-1492,WK-14922K,WK1492 |
||
KRH-594 is a potent, specific and insurmountable AT1 receptor antagonist. KRH-594 ameliorates hyperlipidaemia and nephropathy in diabetic spontaneously hypertensive rats. KRH-594 prevents end-organ damage in stroke-prone spontaneously hypertensive/Izm ra | |||
T34173 |
p-SCN-Bn-HOPO
|
||
p-SCN-Bn-HOPO is an excellent bifunctional chelating agent for (89)Zr ImmunoPET, with low background, good tumor-organ contrast, and importantly, very low bone uptake for BT474 breast cancer imaging. | |||
T69431 |
A-420983
|
||
A-420983 is a novel potent Lck inhibitor, exhibiting oral efficacy in animal models of delayed-type hypersensitivity and organ transplant rejection. | |||
T38672 |
VTP-27999 Hydrochloride
|
||
VTP-27999 Hcl is an alkyl amine Renin inhibitor; VTP-27999 is useful for Hypertension and End-Organ Diseases. IC50 value: Target: Renin | |||
T19848 |
Cyclosporin B
7-L-Alanine-cyclosporin A,Antibiotic S 7481F2 |
||
Cyclosporin B is an immunosuppressant that has revolutionized organ transplantation through its use in the prevention of graft rejection. Cyclosporin B displays antiviral properties, inhibiting the entry of hepatitis B into hepatocytes. Cyclosporin B also | |||
T60483 |
Fasedienol
|
||
Fasedienol 是一种犁鼻器 (VON) 的神经化学刺激剂,可缓解焦虑和经前综合症。 | |||
T82858 |
Bleselumab
ASKP 1240,Anti-Human CD40 Recombinant Antibody |
||
Bleselumab (ASKP 1240)为人源化抗-CD40单克隆抗体,通过高亲和力(Kd: 0.24 nM)与CD40结合,阻断CD40与CD40L配体的相互作用,从而抑制免疫反应,用于预防器官移植排斥。 | |||
T70838 | RO27-3225 TFA | ||
RO27-3225, also known as RO273225 is a melanocortin type 4 receptor agonist with EC50 = 1 nM. It may alleviate intestinal dysfuntion and brain damage. It has been investigated for an anti-obesity medication. Ro 27-3225 shows some activity at the MC1 receptor. Ro 27-3225 reverses hemorrhagic shock, reduces multiple organ damage, and improves survival. | |||
T64239 | Belatacept | ||
Belatacept (BMS 224818) 是一种选择性的 T 细胞共刺激 (T-cell costimulation) 阻滞剂。Belatacept 能够结合 CD 80/86 配体,从而对 CD-28 介导的 T 细胞共刺激表现出抑制作用。Belatacept 能够用于研究器官移植免疫抑制。 | |||
T76719 | Muromonab | ||
Muromonab 是一种靶向 CD3受体的单克隆抗体。Muromonab 可以阻断所有细胞毒性 T 细胞功能。Muromonab 也作为一种免疫抑制剂用于减少急性实体器官移植排斥反应。 | |||
T60238 |
Acloproxalap
|
||
Acloproxalap 是一种基于喹啉的醛清除剂,可用于研究有毒醛积累的疾病,如眼部、皮肤等炎症性疾病,肺炎等呼吸系统疾病,器官疾病以及病毒感染相关性综合症等。 | |||
T37953 |
Sphingomyelins (buttermilk)
|
||
Sphingomyelins (SMs) are bioactive sphingolipids found in mammalian cell membranes.1SMs make up 2-15% of the total organ phospholipid population but are found at higher concentrations in the brain and myelin sheaths surrounding peripheral nerves. They interact with cholesterol to control its distribution within cellular membranes and maintain cholesterol homeostasis in cells. SMs undergo hydrolysis by sphingomyelinase to form ceramides, which are sphingolipid mediators of intracellular signaling... | |||
T75847 |
PG-931 TFA
|
||
PG-931 TFA 是 SHU 9119 的类似物。PG-931 TFA 是一种强效的黑素皮质素 4 (MC4) 受体(IC50=0.58 nM) 激动剂,比 hMC3R (IC50=55 nM) 或 hMC5R (IC50=2.4 nM)更具选择性。PG-931 TFA 在动物实验模型中,可逆转出血休克,防止体内多器官损伤。 | |||
T76958 | Vilobelimab | ||
Vilobelimab (CaCP-29, IFX-1) 是一种单克隆抗 C5a 抗体,过敏毒素 C5a 是一种促炎补体分裂产物,在介导器官功能障碍中起核心作用。Vilobelimab 可作为一种 C5a 抑制剂,抑制中性粒细胞活化、趋化性,减少炎症信号等,可用于败血症,COVID-19 等相关研究。 | |||
T37679 |
3-hydroxy Palmitic Acid
|
||
3-hydroxy Palmitic acid is a form of the 16:0 lipid palmitic acid . The lipid A part of lipopolysaccharides contain various 3-hydroxy fatty acids, making oxylipins such as 3-hydroxy palmitic acid useful as chemical markers of endotoxins. In R. solanacearum, 3-hydroxy palmitic acid is converted by an S-adenosyl methionine-dependent methyltransferase to 3-hydroxy palmitic acid methyl ester, which acts as a quorum sensing signal molecule for post-transcriptional modulation of genes involved in viru... | |||
T67921 |
Retinoic acid-d5
all-trans-Retinoic acid-d5,Isotretinoin-d5,Vitamin A acid-d5,Accutane-d5,ATRA-d5 |
Retinoid Receptor | Metabolism |
Retinoic acid-d5 (Vitamin A acid-d5)是视黄酸的氘标记形式。视黄酸是一种天然的RAR 核受体激动剂, 对 RARα/β/γ 的 IC50 为 14 nM,与 PPARβ/δ 结合的Kd 为 17 nM。视黄酸是维生素a 的代谢物,在细胞生长、分化和器官发育中起着重要作用。视黄酸通过激活视黄酸受体α作为转录因子Nrf2的抑制剂来发挥作用。 | |||
T82474 |
Empasiprubart
ARGX-117 |
||
Empasiprubart (ARGX-117) 是一种针对补体 C2 的人源化抑制性单克隆抗体。该抗体通过结合 C2 的 Sushi-2 结构域来阻止 C3 原转化酶的形成,进而抑制 C3 的激活,并阻断经典途径与凝集素途径的上游激活。Empasiprubart 展现出 pH 和钙依赖性的靶标结合能力,并在自身免疫性溶血性贫血以及抗体介导的器官移植排斥模型中,预防了补体介导的细胞毒性作用。 | |||
T81182 |
Secretin (swine)
|
||
Secretin (swine)为源自猪的神经内分泌激素,由十二指肠黏膜S细胞产生,具有27个氨基酸的多肽结构,并针对分泌素受体起作用。此激素在各类成熟肠内分泌细胞亚群中表达,受脂肪酸的促进。它主要激发胰腺释放水和碳酸氢盐,同时在消化系统、中枢神经系统和能量代谢方面具有广泛应用。 | |||
T37383 |
1,2,3-Trilinoelaidoyl-rac-glycerol
|
||
1,2,3-Trilinoelaidoyl-rac-glycerol is a triacylglycerol that contains linoelaidic acid at the sn-1, sn-2, and sn-3 positions. Dietary administration of 1,2,3-trilinoelaidoyl-rac-glycerol (0.6-6.3% w/w) lowers serum levels of thromboxane B2 , prostaglandin F2 (PGF2), and PGE in rats.1 |1. Bruckner, G., Goswami, S., and Kinsella, J.E. Dietary trilinoelaidate: Effects on organ fatty acid composition, prostanoid biosynthesis and platelet function in rats. J. Nutr. 114(1), 58-67 (1984). |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T4723 |
D-Tagatose
塔格糖,D-(-)-Tagatose,D-塔格糖,d-tagatos |
Others; Endogenous Metabolite | Metabolism; Others |
D-Tagatose (D-(-)-Tagatose) 是自然界中发现的一种罕见的单糖,具有益生元特性。它是研究II 型糖尿病的潜在抗糖尿病药物,也是帮助提升结肠有益细菌、预防结肠癌和抑制胆固醇的益生元。它是蔗糖的替代品,也是口香糖、果汁和饮料等食品中的低热量甜味剂。 | |||
T82636 | Cyclosporin U | ||
Cyclosporin U (SMP0V32C6L)为一种细胞免疫抑制剂,关键用于防止移植器官的排斥反应。 | |||
TN4604 | Myricanone | BCL; HSP; NF-κB; ROS; Caspase; STAT | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; JAK/STAT signaling; Metabolism; NF-κB; Proteases/Proteasome; Stem Cells |
Myricanone has antioxidant, and anticancer activities, it has apoptosis-promoting ability by triggering caspase activation, and suppression of cell proliferation by down-regulation of NF-κB and STAT3 signalling cascades. Myricanone shows in vitro testost | |||
T4752 |
1-Aminocyclopropane-1-carboxylic acid
1-Aminocyclopropanecarboxylic acid,1-氨基环丙烷羧酸,1-Amino-1-carboxycyclopropane,ACC |
Endogenous Metabolite; NMDAR | Metabolism; Neuroscience |
1-Aminocyclopropane-1-carboxylic acid (ACC) 是内源性代谢产物的一种。 |