Cat. No. | Product Name | Target | Signaling Pathways |
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T35922 |
NAADP (sodium salt)
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Nicotinic acid adenine dinucleotide phosphate (NAADP) is a secondary messenger that induces calcium mobilization. It induces calcium release from endosomes and lysosomes via two-pore channel 2 (TPC2) and TPC1, which then stimulates large-scale calcium release from granules and the endoplasmic reticulum mediated by type 1 ryanodine receptors (RyR2s), RyR3s, and inositol-(1,4,5)-triphosphate receptors (IP3Rs). NAADP induces calcium mobilization in sea urchin and starfish eggs post fertilization to... | |||
T83801 |
ε-NAADP+ sodium
Etheno-NAADP,β-Nicotinic Acid-1,N6-Ethenoadenine dinucleotide phosphate,Nicotinic Acid adenine dinucleotide phosphate |
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ε-NAADP+是钙动员诱导剂NAADP的荧光衍生物。在海胆卵细胞匀浆中诱导钙释放(EC50 = 5 µM)。ε-NAADP+在275 nm和410 nm分别显示激发/发射峰值,且在DMSO中的相对发射增加了三倍。 | |||
T23049 |
NAADP tetrasodium salt
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Others | Others |
Ca2+ mobilizing agent | |||
T12205 |
Ned 19
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Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Ned 19 is a selective membrane-permeant non competitive antagonist of NAADP and strongly inhibits tumor growth and vascularization as well as lung metastases in mice. | |||
T22670 |
cis-Ned 19
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Others | Others |
nicotinic acid adenine dinucleotide phosphate (NAADP) antagonist | |||
T12205L |
trans-Ned 19
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Calcium Channel | Membrane transporter/Ion channel; Metabolism |
trans-Ned 19 is a NAADP antagonist and TPC blocker and inhibits the calcium signal in human umbilical vein endothelial cells and the rat aorta relaxation in response to low histamine concentrations. | |||
T63649 |
Ned-K
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Ned-K 是一种烟酸腺嘌呤二核苷酸磷酸 (NAADP) 拮抗剂,对心肌缺血和再灌注 (sIR) 诱导的钙振荡表现出抑制作用。 | |||
T36805 |
TPC2-A1-N
TPC2-A1-N |
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TPC2-A1-N is a novel, lipophilic, membrane permeable isoform-selective small molecule agonist of two-pore channel 2 (TPC2). TPC2-A1-N plays its role by mimicking the physiological actions of NAADP and PI(3,5)P2 through independent binding sites. TPC2-A1-N has inverse effects on key lysosomal activities and increases the pH in the lysosomal lumen in a TPC2-dependent manner[1]. |