3
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12598 |
Pz-1
|
VEGFR; c-RET | Angiogenesis; Apoptosis; Tyrosine Kinase/Adaptors |
Pz-1 是 VEGFR2 和 RET 酪氨酸激酶的抑制剂,可阻断 RET 刺激生长所需的血液供应。 | |||
T81336 |
PZ-1190
|
Dopamine Receptor | GPCR/G Protein; Neuroscience |
PZ-1190是一种多靶点配体,针对啮齿动物的serotonin和dopamine受体,展现出潜在的抗精神病活性。 | |||
T81335 | PZ-1922 | 5-HT Receptor | GPCR/G Protein; Neuroscience |
PZ-1922(Compound 16),是能穿透大脑屏障的5-HT6R/5-HT3R拮抗剂,其Ki值分别为17 nM和0.45 nM。该化合物还能可逆地抑制MAO-B(pIC50:8.93)。在大鼠的新物体识别(NOR)测试中,PZ-1922逆转了Scopolamine (SCOP)诱导的记忆缺陷;同样,在T迷宫测试中,它防止了Aβ诱发的记忆衰退。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T37442 |
Aspergillin PZ
|
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Aspergillin PZ is a fungal metabolite originally isolated from A. awamori. It induces morphological deformation of P. oryzae conidia when used at a concentration of 89 nM. Aspergillin PZ is active against S. epidermidis (MIC = 20 μM) but not S. aureus, E. coli, or B. cereus (MICs = >20 μM). It is cytotoxic to HL-60 promyelocytic leukemia cells (IC50 = 56.61 μM) but not THP-1 acute monocytic leukemia or PC3 prostate cancer cells (IC50s = >80 μM). |