27
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TP2292 |
survivin (baculoviral IAP repeat-containing protein 5) (21-28)
|
Others | Others |
Survivin (baculoviral inhibitor of apoptosis IAP repeat-containing protein-5) is a member of the IAP gene family, which has been implicated in both inhibitions of apoptosis and mitosis regulation1. Survivin is one of the most uniformly up-regulated genes | |||
T8469 |
LQZ-7I
|
Survivin | Apoptosis |
LQZ-7I 能口服有效地抑制异种移植肿瘤生长并诱导肿瘤中生存素的损失。它是一种靶向生存素的抑制剂,抑制生存素二聚化。 | |||
T11383 |
GDP366
|
Survivin | Apoptosis |
GDP366 有效且特异性地抑制 survivin 和 Op18 的表达。 GDP366 增加染色体不稳定性,并通过抑制端粒酶活性诱导细胞衰老。 | |||
T2111 |
Sepantronium bromide
YM155 |
Survivin; Autophagy | Apoptosis; Autophagy |
Sepantronium bromide (YM155) 是一种小分子促凋亡剂,具有潜在抗肿瘤活性。它是一种生存素抑制剂,IC50为 0.54 nM。 | |||
T83774 |
Shepherdin TFA
Lys-His-Ser-Ser-Gly-Cys-Ala-Phe-Leu-OH,Survivin (79-87) |
||
Shepherdin是人体survivin的79-87氨基酸对应的合成肽,也是survivin与heat shock protein 90 (Hsp90)之间蛋白质-蛋白质相互作用的抑制剂。它以浓度依赖的方式与Hsp90的N末端结构域结合,并在150 µM的浓度下抑制了在分离的人源网状红细胞提取物中重组人survivin与Hsp90之间的相互作用。结合了穿膜肽penetratin或HIV Tat序列的Shepherdin肽结合物,体内外具有抗癌活性。 | |||
T13410 |
ZLDI-8
|
Apoptosis; Phosphatase; Gamma-secretase; Immunology/Inflammation related | Apoptosis; Immunology/Inflammation; Metabolism; Neuroscience; Proteases/Proteasome; Stem Cells |
ZLDI-8 是 Notch 激活/裂解酶 ADAM-17 的抑制剂,可抑制 Notch 蛋白裂解,并降低促存活/抗凋亡和上皮-间质转化相关蛋白的表达。它还是竞争性不可逆酪氨酸磷酸酶抑制剂,以IC50为 5.32 μM 抑制 MHCC97-H 细胞的生长。 | |||
T22424 |
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
|
Apoptosis; STAT | Apoptosis; JAK/STAT signaling; Stem Cells |
SC-1 是一种 Sorafenib 的衍生物,可抑制 STAT3磷酸化,通过依赖 SHP-1 的 STAT3失活诱导细胞凋亡,具有抗癌作用。 | |||
T9945 |
MNK8
3-methyl-6-(naphthalen-1-yl)pyrimidine-2,4(1H,3H)-dione |
STAT | JAK/STAT signaling; Stem Cells |
MNK8 (3-methyl-6-(naphthalen-1-yl)pyrimidine-2,4(1H,3H)-dione) 是一种有效的STAT3抑制剂,降低STAT3与DNA 结合的能力,对肝癌细胞也有良好的生长抑制作用。 | |||
T61184 |
LQZ-7F
|
Apoptosis; Survivin | Apoptosis |
LQZ-7F 是一种小分子生存素二聚化抑制剂,具有抗癌活性。LQZ-7F 诱导蛋白酶体依赖性存活素降解、有丝分裂停滞和细胞凋亡,并在小鼠异种移植试验中阻断人类肿瘤的生长。 | |||
T12896L |
Shepherdin 79-87 acetate
Shepherdin 79-87 acetate (861224-28-4 free base) |
HSP; Survivin | Apoptosis; Cytoskeletal Signaling; Metabolism |
Shepherdin 79-87 acetate 是 Hsp90 和 survivin 之间复合物的拟肽拮抗剂,survivin 是肿瘤细胞活力的另一个关键调节剂。 | |||
T3708 |
BP-1-102
|
STAT | JAK/STAT signaling; Stem Cells |
BP-1-102 是可口服的转录因子Stat3小分子抑制剂,IC50值为 6.8 μM。 | |||
T77701 |
FL118
FL 118,FL-118,10,11-(Methylenedioxy)-20(S)-camptothecin |
Survivin | Apoptosis |
FL118是一种新型存活素抑制剂,可抑制癌症干细胞样特性。FL118 是一种新型喜树碱类似物,具有抗癌活性,通过 Wnt/β-catenin 信号通路抑制上皮-间充质转化,从而抑制人乳腺癌细胞的迁移和侵袭。 | |||
T15137 |
DK419
|
Wnt/beta-catenin; AMPK | Chromatin/Epigenetic; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling; Stem Cells |
DK419 是一种具有口服活性的 Wnt/β-catenin 信号通路抑制剂,IC50 为 0.19 μM。 DK419 降低 Axin2、β-catenin、c-Myc、Cyclin D1 和 Survivin 的蛋白质水平。它还诱导 pAMPK 的产生。 | |||
T61030 |
STAT3-IN-11
|
Apoptosis; STAT | Apoptosis; JAK/STAT signaling; Stem Cells |
STAT3-IN-11 是一种选择性 STAT3 抑制剂,对 STAT3pTyr705位点的磷酸化和Survivin 的磷酸化有抑制作用。STAT3-IN-11 促使癌细胞凋亡,是治疗癌症的候选化合物。 | |||
T35610 |
2,5-dimethyl Celecoxib
|
Apoptosis; Wnt/beta-catenin; Prostaglandin Receptor | Apoptosis; Cytoskeletal Signaling; GPCR/G Protein; Immunology/Inflammation; Stem Cells |
2,5-dimethyl Celecoxib 是塞来昔布衍生物和微粒体前列腺素 E 合酶 1 (mPGES-1) 的靶向抑制剂,mPGES-1 是炎症介质 PGE2 合成途径中的关键酶。 | |||
T25746 |
LLP6
LLP 6,LLP-6 |
||
LLP6 is used as a survivin modulator. | |||
T70733 | APX2009 | ||
APX2009 is a second-generation APE1/Ref-1 redox-specific inhibitor. APX2009 significantly reduces NFkB transcriptional activity, survivin mRNA, and survivin protein levels. APX2009 decreases prostate cancer cell proliferation and induces cell cycle arrest. | |||
T26832 |
BKM1740
BKM-1740,BKM 1740 |
||
BKM1740 induced apoptosis in prostate cancer (PCa) cells by repressing survivin at both the mRNA and protein levels in vitro. | |||
T69845 |
MX107
|
||
MX107 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation. | |||
T69840 |
MX106
|
||
MX106 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation. | |||
T21834 |
YM-155 hydrochloride
|
||
Sepantronium hydrochloride (YM-155 hydrochloride) 是一种新型survivin 抑制剂,抑制survivin 启动子的IC50为 0.54 nM。 | |||
T12896 |
Shepherdin (79-87)
Shepherdin 79-87 |
Others | Others |
Shepherdin 79-87, comprising amino acids 79 to 87 of Shepherdin, acts as a peptidomimetic antagonist targeting the Hsp90-Survivin complex, exhibiting anticancer properties. | |||
T38414 |
NSC 80467
|
||
NSC 80467, a selective DNA damaging agent, functions by inhibiting survivin. Specifically, it preferentially targets DNA synthesis, leading to the induction of two distinct markers of DNA damage, namely γH2AX and pKAP1. | |||
T35542 |
LLP-3
|
||
Survivin (also known as baculoviral IAP repeat-containing protein 5 (BIRC5)) is a member of the inhibitor of apoptosis (IAP) family that interacts with and inhibits the apoptotic function of several proteins. LLP-3 is a cell-permeable ligand of Survivin that blocks its interaction with Ran, resulting in the induction of apoptosis (IAP) in glioma stem cells (IC50 = 31 μM). It abolishes the growth of glioblastoma multiforme cell in spheres and in tumor slice cultures. | |||
T71925 |
Isonanangenine B
|
||
Isonanangenine B is a drimane sesquiterpene lactone that has been found in Aspergillus. It decreases survivin mRNA expression in a reporter assay when used at concentrations of 13.6, 18.42, and 26.31 µM. Isonanagenine B (18.42 µM) inhibits STAT3 and NF-κB binding to the survivin promoter in chromatin immunoprecipitation (ChIP) assays. It also induces apoptosis in COLO 320DM cells. | |||
T70988 |
Ibulocydine
|
||
Ibulocydine is a potent CDK inhibitor. Ibulocydine has high activity against Cdk7/cyclin H/Mat1 and Cdk9/cyclin T. Ibulocydine inhibited the growth of HCC cells more effectively than other Cdk inhibitors, including olomoucine and roscovitine, whereas ibulocydine as well as the other Cdk inhibitors and BMK-Y101 minimally influenced the growth of normal hepatocyte cells. Ibulocydine induced apoptosis in HCC cells, most likely by inhibiting Cdk7 and Cdk9. In vitro treatment of HCC cells with ibuloc... | |||
T35729 |
Nemadipine-A
|
||
Nemadipine A is an L-type calcium channel blocker that induces morphological and growth defects in wild-type C. elegans and those with hypoexpression of egl-19, which encodes the only L-type calcium channel α1-subunit in the C. elegans genome. It also inhibits L-type calcium channels in chick ciliary neurons. Nemadipine A increases TRAIL-induced cytotoxicity and synergistically enhances caspase-8 and caspase-3 activation in a concentration-dependent manner in H1299 lung adenocarcinoma cells. It ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8213 |
Isolinderalactone
|
NOS; STAT | Immunology/Inflammation; JAK/STAT signaling; Stem Cells |
Isolinderalactone 具有抗炎和抗癌能力,具有中等的 iNOS 抑制活性,IC50 值为 0.30 uM。 | |||
T3S1471 |
Cucurbitacin IIA
葫芦素Iia,Dihydrocucurbitacin Q1,Hemslecin A,Curcurbitacin IIA |
Apoptosis; Survivin | Apoptosis |
Cucurbitacin IIA (Dihydrocucurbitacin Q1) 是从园果雪胆中分离得到的一种三萜烯,可诱导细胞凋亡和增强自噬,有助于葫芦素IIA 对炎症相关疾病的抗炎活性。它可降低癌细胞中生存素的表达,降低磷酸化组蛋白 H3 的水平,增加裂解的 PARP 的水平。 |