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Merck
CN

SML1845

Sigma-Aldrich

Thapsigargin Ready Made Solution

≥98% (HPLC), 10 mM in DMSO

别名:

CHEBI:9516, CHEMBL96926, MFCD00083511, UNII-Z96BQ26RZD, Z96BQ26RZD, [(3S,3aR,4S,6S,6aR,7S,8S,9bS)-6-acetyloxy-4-butanoyloxy-3,3a-dihydroxy-3,6,9-trimethyl-8-[(Z)-2-methylbut-2-enoyl]oxy-2-oxo-4,5,6a,7,8,9b-hexahydroazuleno[4,5-b]furan-7-yl] octanoate

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关于此项目

经验公式(希尔记法):
C34H50O12
CAS Number:
分子量:
650.75
UNSPSC代码:
12352200
NACRES:
NA.77
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生物来源

(Thapsia garganica L seeds)

质量水平

方案

≥98% (HPLC)

表单

DMSO solution

浓度

10 mM in DMSO

运输

dry ice

储存温度

−20°C

SMILES字符串

O1[C@@H]2[C@]([C@H](C[C@@]([C@H]3[C@@H]([C@H](C(=C32)C)OC(=O)\C(=C/C)\C)OC(=O)CCCCCCC)(OC(=O)C)C)OC(=O)CCC)([C@@](C1=O)(O)C)O

InChI

1S/C34H50O12/c1-9-12-13-14-15-17-24(37)43-28-26-25(20(5)27(28)44-30(38)19(4)11-3)29-34(41,33(8,40)31(39)45-29)22(42-23(36)16-10-2)18-32(26,7)46-21(6)35/h11,22,26-29,40-41H,9-10,12-18H2,1-8H3/b19-11-/t22-,26+,27-,28-,29-,32-,33+,34+/m0/s1

InChI key

IXFPJGBNCFXKPI-FSIHEZPISA-N

应用

毒胡萝卜素即配型溶液可作为体内生长和体外翻译检测的阴性对照。

生化/生理作用

毒胡萝卜素是一种有效的钙离子泵抑制剂,位于骨骼肌、心肌、肌肉和脑组织的肌质网(SR)和内质网(ER)微粒体上。
毒胡萝卜素是一种有效的钙离子泵抑制剂,位于骨骼肌、心肌、肌肉和脑组织的肌质网(SR)和内质网(ER)微粒体上。钙离子泵的抑制会导致细胞内钙离子水平上升。100nM浓度的毒胡萝卜素可有效抑制心肌和骨骼肌中的SR Ca2+ -三磷酸腺苷酶(ATP酶)。毒胡萝卜素还可通过干扰自噬体-溶酶体融合而有效阻断自噬。

其他说明

在浓度为10 mM的DMSO中提供了毒胡萝卜素即用型溶液。该溶液可用 DMSO 进一步稀释至 2 mM 浓度。建议将预先制好的毒胡萝卜素溶液小等份保存于-20°C下。

储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

188.6 °F - closed cup

闪点(°C)

87 °C - closed cup


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Partial inactivation of cardiac 14-3-3 protein in vivo elicits endoplasmic reticulum stress (ERS) and activates ERS-initiated apoptosis in ERS-induced mice
<BIG>Sari FR, et al.</BIG>
Cellular Physiology and Biochemistry, 167-178 (2010)
M Alsaqati et al.
British journal of pharmacology, 171(3), 701-713 (2013-10-22)
The P2Y₁₄ receptor is the newest member of the P2Y receptor family; it is G(i/o) protein-coupled and is activated by UDP and selectively by UDP-glucose and MRS2690 (2-thiouridine-5'-diphosphoglucose) (7-10-fold more potent than UDP-glucose). This study investigated whether P2Y₁₄ receptors were
Thapsigargin blocks the induction of long-term potentiation in rat hippocampal slices
<BIG>Harvey J and Collingridge GL</BIG>
Neuroscience Letters, 197-200 (1992)
J Lytton et al.
The Journal of biological chemistry, 266(26), 17067-17071 (1991-09-15)
The role of ATP-dependent calcium uptake into intracellular storage compartments is an essential feature of hormonally induced calcium signaling. Thapsigargin, a non-phorboid tumor promoter, increasingly is being used to manipulate calcium stores because it induces a hormone-like elevation of cytosolic
Y Kijima et al.
The Journal of biological chemistry, 266(34), 22912-22918 (1991-12-05)
Thapsigargin is found to be a potent inhibitor of the intracellular Ca2+ pump proteins from skeletal muscle sarcoplasmic reticulum (SR), cardiac SR, and brain microsomes. For skeletal muscle SR, the molar ratio of thapsigargin to Ca2+ pump protein for complete

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