Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2052 |
KY02111
|
Wnt/beta-catenin | Cytoskeletal Signaling; Stem Cells |
KY02111 是典型的 WNT 信号抑制剂,能够促进人多潜能干细胞向心肌细胞分化,可用于研究人类心肌细胞再生。 | |||
T2437 |
O4I2
O-4I2,O4I2 |
OCT | Membrane transporter/Ion channel |
O4I2 是一种 Oct3/4诱导剂,可增强多能干细胞相关基因 Lin28、Sox2和 Nanog 的表达,并抑制 Rex1。 | |||
T8647 |
BCH001
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
BCH001 是喹啉衍生物,是一种选择性PAPD5抑制剂。它可以恢复先天性角化病诱导的多能干细胞中的端粒酶活性和端粒长度。它对聚 (A)-特异性核糖核酸酶或几种其他多核苷酸聚合酶均无抑制作用。它可用于调控衰老。 | |||
T2040 |
OAC1
BAS 00287861 |
OCT | Membrane transporter/Ion channel |
OAC1 (BAS 00287861) 是一种能够激活 Octamer 结合转录因子 4 的化合物。 它提高了 iPSC 重编程效率并加速重编程过程。 | |||
T1725 |
Y-27632 dihydrochloride
反式-4-[(R)-1-氨基乙基]-N-(4-吡啶基)环己烷甲酰胺二盐酸盐,Y-27632 2HCl |
ROCK; Apoptosis | Apoptosis; Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Y-27632 dihydrochloride (Y-27632 2HCl) 是一种 ROCK-I 和 ROCK-II 抑制剂,具有口服有效性、ATP 竞争性。Y-27632 dihydrochloride 还抑制分离诱导的小鼠前列腺干或祖细胞凋亡。 | |||
T16287 |
Neurodazine
|
DNA Methyltransferase | Chromatin/Epigenetic |
Neurodazine 是一种神经性诱导剂,可促进多能细胞分化为神经元细胞。Neurodazine 通过激活 Wnt 和 Shh 信号传导促进分化。 | |||
T22814 |
GSA-10
|
Hedgehog/Smoothened | GPCR/G Protein; Stem Cells |
GSA-10是新型的喹啉甲酰胺衍生物,有效激动平滑受体剂,EC50为 1.2 μM。它作用于Smo,促进多能间充质干细胞分化为成骨细胞。它介导 Hedgehog 信号传导,这可能对癌症疾病的再生医学具有研究意义。 | |||
TP1828 |
N-Acetyl-Ser-Asp-Lys-Pro
|
RAAS | Endocrinology/Hormones |
N-Acetyl-Ser-Asp-Lys-Pro 通过酶促处理胸腺素 β4 在骨髓细胞中形成。 它抑制多能造血干细胞进入细胞周期的 S 期,并防止小鼠中的 Ara-C 致死性。 | |||
T3684 |
CP21R7
CP21 |
GSK-3; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Stem Cells |
CP21R7 (CP21) 是一种 GSK-3β抑制剂,其 IC50=1.8 nM。它也是一种 PKCα抑制剂,其 IC50=1900 nM。 | |||
T2019 |
OAC2
|
OCT | Membrane transporter/Ion channel |
OAC2 是一种 Oct4 激活剂,通过 Oct4 基因启动子激活表达, 通过提高胚胎成纤维细胞诱导多能干细胞的产生速率来提高重编程效率,是 OAC1 的类似物。 | |||
T36301 | PluriSIn #2 | ||
PluriSIn #2 acts as a selective transcriptional inhibitor of topoisomerase II α (TOP2A) and effectively eliminates undifferentiated human pluripotent stem cells (hPSCs)[1]. | |||
T33652 |
Neurodazole
|
||
Neurodazole is a neurogenic inducer for converting pluripotent P19 cells into electrophysiologically active neurons. | |||
T70520 |
TWS-119
|
||
TWS-119 is an inhibitor of glycogen synthase kinase-3β (GSK-3β) that induces neuronal differentiation in pluripotent murine embryonal carcinoma cells and embryonic stem cells (ESCs). | |||
TP2339 |
Goralatide
|
||
Goralatide, isolated from fetal calf bone marrow, exerts a high inhibitory activity on the proliferation of hematopoietic pluripotent stem cells. | |||
T32416 |
KP-1
KP 1,KP1,Kyoto Probe 1 |
||
KP-1 is a selective fluorescent probe for labeling human pluripotent stem cells. | |||
T23271 |
RSC-133
|
Others | Others |
promotes the reprogramming of human somatic cells to pluripotent stem cells | |||
T81698 |
NBD-LLLLpY
|
||
NBD-LLLLpY Y为通过酶催化生成的核内肽,专门用于靶向毁灭人类诱导多能干细胞。 | |||
T13769 |
TA-316
Megakaryocytes/platelets inducing agent |
Others | Others |
Megakaryocytes/platelets inducing agent being useful in treating diseases involving thrombopenia. Megakaryocytes/platelets inducing agent is an inducing agent for megakaryocytes and/or platelets from pluripotent stem cells. | |||
T72388 | CBB1007 hydrochloride | ||
CBB1007 hydrochloride,一种可逆的、选择性的高效组蛋白去甲基化酶LSD1的底物竞争性抑制剂,其对hLSD1的IC50值为5.27 uM。 | |||
T82642 |
Cyclo(RGDfK(Mal))
|
||
Cyclo(RGDfK(Mal))为一种五肽,能促进人多能干细胞的附着与渗透,适用于三维干细胞培养及其扩增。 | |||
T72244 | CBB1007 trihydrochloride | ||
CBB1007三盐酸盐是 LSD1选择性抑制剂,IC50值为5.27uM。 | |||
T78520 |
CYT296
|
Others | Others |
CYT296是一种靶向染色质去凝集的化合物,能增强定义因子(OSKM)介导诱导多能干细胞(iPSC)的生成,并通过诱导小鼠胚胎成纤维细胞(MEFs)染色质的开放状态来促进体细胞的重编程,适用于细胞替代治疗和药物筛选的研究领域。 | |||
T75752 |
N-Acetyl-Ser-Asp-Lys-Pro acetate
|
||
N-Acetyl-Ser-Asp-Lys-Pro (Ac-SDKP) acetate 是血管紧张素转换酶 (ACE) N 端活性位点的特异性底物。N-Acetyl-Ser-Asp-Lys-Pro acetate 是多能干细胞增殖的天然抑制剂。N-Acetyl-Ser-Asp-Lys-Pro acetate 具有抗炎和抗纤维化特性。 | |||
T35567 |
BIX01294 (hydrochloride hydrate)
|
||
The methylation of lysine residues on histones plays a central role in determining euchromatin structure and gene expression. The histone methyltransferase (HMTase) G9a can mono- or dimethylate lysine 9 on histone 3 (H3), contributing to early embryogenesis, genomic imprinting, and lymphocyte development. BIX01294 (hydrochloride hydrate) is a selective inhibitor of G9a HMTase (IC50 = 1.7 μM). It less effectively inhibits the HMTase G9a-like protein (GLP; IC50 = 38 μM) and has no effect on other ... | |||
T35541 |
Lipoxygenin
|
||
Lipoxygenin is an inhibitor of 5-lipoxygenase (5-LO) with an IC50value of 5 μM for inhibition of 5-LO product synthesis in isolated human granulocytes stimulated with the cation ionophore A23187 .1It inhibits hedgehog-dependent signaling in Shh-LIGHT2 cells and TGF-β-, activin A-, bone morphogenic protein (BMP)-, or Wnt-dependent signaling in HEK293T cells (IC50s = 9.3, 3.2, 8.2, 9.6, and 3.7 μM, respectively, in luciferase reporter assays). Lipoxygenin (5 and 10 μM) increases levels of troponin... | |||
T76068 |
Cyclo(Arg-Gly-Asp-D-Phe-Cys) TFA
|
||
Cyclo(Arg-Gly-Asp-D-Phe-Cys) TFA 是一种环状RGD多肽, 对αvβ3有高亲和性,能干扰细胞整合素之间的相互作用。此化合物能抑制胚胎干细胞(ESC)的多潜能性基因表达,并可在体内减少mESC的致瘤潜力,因此适用于肿瘤研究领域。 | |||
T74247 |
TPE-MI
|
||
TPE-MI(Tetraphenylethene maleimide)在与马来酰亚胺与硫醇反应前不具荧光性。在与游离的半胱氨酸硫醇标记时,其荧光被激活,后者多在球形蛋白质的核心,仅在展开时显露。TPE-MI适用于测量细胞中未折叠蛋白质的负荷,并能在亨廷顿病诱导的多能干细胞模型中监测蛋白质平衡失衡,以及在形成可见聚合体之前,监测转染突变亨廷顿外显子1的细胞的状况。此外,TPE-MI用于检测双氢青蒿素处理后疟疾寄生虫的蛋白质损伤。应暗处储存。 |