Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6948 |
Pluripotin
SC1 |
ERK; Raf; S6 Kinase | MAPK; PI3K/Akt/mTOR signaling |
Pluripotin (SC1) 是ERK1和RasGAP 的双重抑制剂,KD 分别为 98 和 212 nM。它还抑制RSK1、RSK2、RSK3和RSK4,IC50分别为 0.5、2.5、3.3 和 10.0 μM。 | |||
T9743 |
FEN1-IN-SC13
|
Others | Others |
FEN1-IN-SC13 是有效的DNA 片段化核酸内切酶 1 抑制剂。 | |||
T6207 |
SC144
|
Apoptosis; Interleukin | Apoptosis; Immunology/Inflammation |
SC144 是一种口服活性 gp130 抑制剂。它结合 gp130,诱导 gp130 磷酸化(S782) 和去糖基化,消除 Stat3 磷酸化和核易位,进一步抑制下游靶基因的表达。它对 gp130 配体触发的信号转导有明显的抑制作用,可诱导人卵巢癌细胞凋亡。 | |||
T25885 |
NSC12404
CID 224134,CID224134,CID-224134,NSC 12404,NSC-12404 |
||
NSC-12404 is a selective non-lipid LPA2/3 agonist. | |||
T16351 | NSC16168 | Estrogen/progestogen Receptor | Endocrinology/Hormones |
NSC16168 inhibits DNA repair and potentiates CDDP efficacy in cancer. NSC16168 is a specific ERCC1-XPF inhibitor (IC50: 0.42 μM). | |||
T33752 |
NSC190488
|
||
NSC190488 is a bioactive chemical. | |||
T41260 |
SC144 hydrochloride
|
||
SC144 hydrochloride 是首创的口服活性gp130 (IL6-beta)抑制剂。SC144 hydrochloride 结合 gp130,诱导 gp130 磷酸化(S782) 和去糖基化,消除 Stat3 磷酸化和核易位,进而抑制下游靶基因的表达。SC144 hydrochloride 对 gp130 配体触发的信号转导显示有效的抑制作用。SC144 hydrochloride 诱导人卵巢癌细胞凋亡。 | |||
T61177 |
NSC114126
|
||
NSC114126 is a highly effective and orally bioavailable inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR-TK). This compound exhibits robust antiproliferative properties, making it a promising candidate for further investigation in the field of cancer research [1]. | |||
T28203 |
NSC156529
NSC-156529,NSC 156529 |
||
NSC156529 downregulates AKT1 signaling. NSC156529 efficiently decreases the proliferation of human cancer cells in vitro, and substantially inhibits the growth of prostate tumor xenografts in vivo. | |||
T33749 |
NSC107392
NSC 107392,NSC-107392 |
||
NSC107392 is a substrate of ABCG2. | |||
T71527 | NSC145366 | ||
NSC145366 is an inhibitor of Hsp90 activities which targets the Hsp90 C-terminal domain to induce allosteric inhibition and selective client downregulation. NSC145366 increases Hsp90 oligomerization resulting in allosteric inhibition of NTD ATPase activity (IC50=119μM) but does not compete with NTD or CTD-ATP binding. | |||
T78203 |
NSC194598
|
||
NSC194598是一种p53 DNA结合抑制剂,其体外和体内抑制p53序列特异性DNA结合的IC50值分别约为180 nM和2-40 μM。在人甲状腺髓样癌TT细胞中,NSC194598能够干扰突变RET基因的转录激活。该化合物可应用于研究放射及化学疗法对正常组织造成的急性毒性。 | |||
T62722 |
SC13
|
||
SC13 是一种新型的 mitragynine 类似物,具有低效Muopioid receptor 激动作用,具有麻醉作用和较轻的不良反应。 | |||
T69141 |
NSC1008
|
||
NSC1008 is an inhibitor of the Ras Converting Enzyme 1 (Rce1) protease that disrupts Ras membrane localization in human cells. | |||
T33751 |
NSC145021
NSC-145021,NSC 145021 |
||
NSC145021 is a bioactive chemical. | |||
T33750 |
NSC127916
NSC 127916,NSC-127916 |
||
NSC127916 is a bioactive chemical. | |||
T81640 |
NSC15520
|
||
NSC15520是一种小分子RPA抑制剂,特异性结合RPA的N端DNA结合域(DBD),阻断其与p53或RAD9的相互作用。它还能够抑制双链DNA(dsDNA)寡核苷酸的螺旋不稳定性,影响DNA复制、修复、重组及损伤反应信号。 | |||
T28201 |
NSC1011
NSC 1011,NSC-1011 |
||
NSC1011 is an inhibitor of ras converting enzyme 1 (Rce1). | |||
T68637 |
NSC13987
|
||
NSC13987 is an inhibitor of Nef-calnexin interaction. | |||
T12114 |
MSC1094308
|
p97 | Ubiquitination |
MSC1094308 is a reversible and allosteric inhibitor of the type II AAA ATPase. | |||
T69893 |
NSC109131
|
||
NSC109131 is an inhibitor of human tyrosyl-DNA phosphodiesterase 1 (TDP1). | |||
T24549 |
NSC114792
NSC-114792,NSC 114792 |
||
NSC114792 is a selective JAK3 inhibitor. | |||
T12260 | NSC117079 | Others | Others |
NSC117079 is an inhibitor of PHLPP. | |||
T25884 |
NSC103054
NSC-103054,NSC 103054 |
||
NSC103054 is an ABCG2 transporter function inhibitor. | |||
T24548 |
NSC10010 hydrochloride
NSC#10010,NSC 10010,NSC# 10010,NSC#-10010,NSC-10010 |
||
NSC10010 hydrochloride is an effective growth inhibitor for gammaherpesvirus-associated B-lymphomas. It acts through activation of both the NF-κB and c-Myc-mediated signaling pathways. | |||
T60095 |
CCF0058981
|
SARS-CoV | Microbiology/Virology |
CCF0058981 (CCF981) 是3-氯苯基类似物,是一种非共价 SARS-CoV-2 3CLpro(SC2)抑制剂,IC50为 68 nM。CCF0058981 抑制 SC1 (SARS-CoV-1 3CLpro),IC50为 19 nM。CCF0058981 具有抗病毒功效,具有用于 COVID-19 研究的潜力。 |