15
1
Cat. No. | Product Name | Target | Signaling Pathways |
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T2168 |
2-(1,8-naphthyridin-2-yl)phenol
|
STAT | JAK/STAT signaling; Stem Cells |
2-NP 是选择性的STAT1转录增强剂。它能够增强 IFN-γ 的功能,提高对人乳腺癌和纤维肉瘤细胞增殖的抑制能力。 | |||
T9107 |
NP-G2-044
|
Others | Others |
NP-G2-044 是fascin 蛋白抑制剂,具有口服活性,IC50值约为 2 μM。它可阻断肿瘤转移并增强抗肿瘤免疫应答。 | |||
T39396 |
2-NP-AOZ
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2-NP-AOZ is a chemical compound that is a 2-nitrophenyl derivative of AOZ, which is a tissue-bound metabolite of Furazolidone. 2-NP-AOZ is specifically used for the determination of AOZ residues. | |||
T39270 | 2-NP-AMOZ | ||
2-NP-AMOZ is a 2-nitrophenyl derivative of AMOZ, which is a metabolite of the antibiotic Furaltadone. This chemical compound specifically serves as a reliable tool for protein bound AMOZ detection. | |||
T40710 |
2-NP-AHD
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2-NP-AHD is a 2-nitrophenyl derivative of AHD, which is a metabolite of nitrofurans, a class of antibiotics. It serves as an indicator for the detection of illicit use of nitrofuran drugs. | |||
T24542 |
NP-313
NP 313,NSC 4264,NSC-4264,NSC4264 |
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NP-313 (NSC-4264) 是一种有效的抗血栓剂,对血栓素 A 2 合成和选择性抑制由 SOCC 介导的 Ca 2+ 内流有抑制作用,可以抑制血小板的聚集和活化。 | |||
T6187 |
TDZD-8
GSK-3β Inhibitor I,NP 01139 |
GSK-3 | PI3K/Akt/mTOR signaling; Stem Cells |
TDZD-8 (NP 01139) 是抑制GSK-3β的抑制剂,其 IC50=2 μM。它对 Cdk-1/cyclin B,CK-II,PKA 和 PKC 的作用较弱,IC50值均 >100 μM。 | |||
T76503 |
Defensin NP-3A
|
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Defensin NP-3A (NP-3A; Corticostatin 1) 是一种人粒细胞肽,具有抗 ACTH 活性。防御素是一种具有杀伤活性的抗菌肽。 | |||
T71155 | NP-1815-PX | P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
NP-1815-PX是一种选择性P2X4R拮抗剂,显示出抗炎活性并可缓解慢性疼痛模型的疼痛症状。此外,NP-1815-PX能够抑制豚鼠气管/支气管平滑肌(TSM和BSM)的收缩。 | |||
T17296 |
Zotatifin
eFT226 |
Others | Others |
Zotatifin is a potent and well-tolerated eIF4A inhibitor. Zotatifin promotes eIF4A binding to specific mRNA sequences with recognition motifs in the 5’-UTRs (IC50=2 nM). Zotatifin effectively reduces viral infectivity by inhibiting SARS-CoV-2 NP protein b | |||
T75784 |
Apelin-36(rat, mouse) TFA
|
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Apelin-36(rat, mouse) TFA 是一种内源性孤儿 G 蛋白偶联受体 APJ 激动剂。Apelin-36(rat, mouse) TFA 与 APJ 受体结合,IC50为 5.4 nM,显著抑制 cAMP 的产生,EC50为 0.52 nM。Apelin-36(rat, mouse) TFA 阻断 HIV-1和 HIV-2毒株进入表达 APJ 的 NP-2/CD4 细胞。 | |||
TP2093 |
Apelin-36(human)
Apelin-36 (human) |
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Endogenous APJ receptor agonist (EC50 = 20 nM) that is secreted by adipocytes. Binds with high affinity to human APJ receptors expressed in HEK 293 cells (pIC50= 8.61). Involved in regulation of cardiovascular function, fluid homeostasis and feeding. Bloc | |||
TP2094 |
Apelin-36(rat, mouse)
Apelin-36 (rat, mouse) |
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Endogenous APJ receptor agonist that is secreted by adipocytes. Binds with high affinity to APJ receptors (IC50 = 5.4 nM) and potently inhibits cAMP production in vitro (EC50 = 0.52 nM). Involved in regulation of cardiovascular function, fluid homeostasis | |||
T76334 |
Cenderitide
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Cenderitide 是一种有效的颗粒鸟酰基环化酶受体 (pGC) 激动剂。Cenderitide 是一种由 C 型利钠肽 (CNP) 与石斛利钠肽 (DNP) 的 C 端融合而成的利钠肽 (NP) 。Cenderitide 可激活 pGC-A 和 pGC-B,激活第二信使 cGMP,抑制醛固酮 (aldosterone),在不降低血压的情况下保持 GFR 。Cenderitide 可用于心力衰竭的研究。 | |||
T75785 |
Apelin-17(human, bovine) TFA
|
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Apelin-17(human, bovine) TFA 是一种内源性孤儿 G 蛋白偶联受体 APJ 激动剂。Apelin-17(human, bovine) TFA 与在 HEK 293 细胞中表达的人 APJ 受体结合 (pIC50)。Apelin-17(human, bovine) TFA 阻断 HIV-1和 HIV-2毒株进入表达 APJ 的 NP-2/CD4 细胞。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T4S0867 |
Pogostone
DHELWANGIN,广藿香酮 |
Apoptosis; Antibacterial; Autophagy | Apoptosis; Autophagy; Microbiology/Virology |
Pogostone (DHELWANGIN) 是从薄荷中分离出,对革兰氏阴性菌、革兰氏阳性菌、大肠埃希菌等具有强效抗菌、抗真菌活性。它诱导细胞凋亡和自噬。 |