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Cat. No. | Product Name | Target | Signaling Pathways |
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T12365 |
PARP/PI3K-IN-1
|
PARP; PI3K | Chromatin/Epigenetic; DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
PARP/PI3K-IN-1 是一种 新型双重聚(ADP-核糖)聚合酶(PARP)和磷酸肌醇 3-激酶(PI3K)双重抑制剂,具有抗癌、抗肿瘤和抗癌细胞增殖活性,可用于研究乳腺癌、胰腺癌和肺癌。 | |||
T12459 |
PI3K/mTOR Inhibitor-2
|
PI3K; mTOR | PI3K/Akt/mTOR signaling |
PI3K/mTOR Inhibitor-2 是一种有效的 PI3K 和 mTOR 泛抑制剂,对 PI3Kα、PI3Kβ、PI3Kδ、PI3Kγ 和 mTOR 的 IC50 分别为 3.4、34、16,1 和 4.7 nM。 PI3K/mTOR Inhibitor-2 具有抗肿瘤活性。 | |||
T12455 | PI3K/HDAC-IN-1 | PI3K | PI3K/Akt/mTOR signaling |
PI3K/HDAC-IN-1 is a potent PI3K and HDAC dual inhibitor(IC50s of 8.1 nM and 1.4 nM, respectively). | |||
T12460 |
PI3K/mTOR Inhibitor-1
|
PI3K | PI3K/Akt/mTOR signaling |
PI3K/mTOR Inhibitor-1 is a potent, orally bioavailable dual inhibitor of PI3K/mTOR (PI3Kα/PI3Kβ/PI3Kδ/PI3Kγ/mTOR with IC50s of 20/376/204/46/186 nM) | |||
T12457 |
PI3K-IN-6
|
PI3K | PI3K/Akt/mTOR signaling |
PI3K-IN-6 is an oral active and highly selective inhibitor of phosphoinositide 3-kinase (PI3K) β/δ(IC50 values of 7.8 nM/5.3 nM , respectively). | |||
T12458 |
PI3K-IN-9
|
PI3K | PI3K/Akt/mTOR signaling |
PI3K-IN-9 is a potent and selective inhibitor of PI3Kδ(IC50 of 8.9 nM). | |||
T12456 |
PI3K-IN-10
|
PI3K | PI3K/Akt/mTOR signaling |
PI3K-IN-10 is a potent inhibitor of pan-PI3K . | |||
T36087 |
PI3K-IN-22
CAY10626 |
||
PI3K-IN-22 是 PI3Kα 和 mTOR 双重激酶抑制剂,IC50s 分别为 0.9、0.6 nM。PI3K-IN-22 可用于癌症研究。 | |||
T1826 |
PI3K-IN-1
Voxtalisib Analogue,Voxtalisib (SAR245409, XL765) Analogue,XL765,SAR245409 |
DNA-PK; PI3K | DNA Damage/DNA Repair; PI3K/Akt/mTOR signaling |
PI3K-IN-1 (Voxtalisib Analogue) 是 PI3K 抑制剂,PI3K-IN-1(25 μM) 能够阻断 PI3K/Akt 信号通路。 | |||
T39581 |
PI3K-IN-19 hydrochloride
PI3K-IN-19 hydrochloride |
||
PI3K-IN-19 hydrochloride (WO2017153220, step 5) acts as a phosphatidylinositol-3-kinase (PI3K) inhibitor. | |||
T24637 |
PI3K inhibitor C 96
PI3K IN C96,PI3K-IN-C96 |
||
PI3K inhibitor C 96 is an inhibitor of phosphatidylinositol 3-kinase. It shows effective activity against multiple myeloma in vitro and in vivo. | |||
T6784 |
BI-78D3
|
JNK | MAPK |
BI-78D3 是底物竞争性的 JNK 抑制剂(IC50:280 nM),对 JNK 激酶活性具有抑制作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1205 |
Chloramphenicol
Chlornitromycin,Levomycetin,Chloromycetin,氯霉素 |
ribosome; HIF/HIF Prolyl-Hydroxylase; Antibacterial; Antibiotic | Chromatin/Epigenetic; Metabolism; Microbiology/Virology |
Chloramphenicol (Chloromycetin) 是一种广谱抗生素,有效抑制细菌蛋白质生物合成。它主要作用于细菌 70S 核糖体的 50S 亚基,对肽基转移酶有活性,抑制肽键的形成。 |