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Merck
CN

SML1845

Sigma-Aldrich

Thapsigargin

From (Thapsia garganica L seeds), ≥98% (HPLC), calcium ion pumps inhibitor, DMSO solution

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
化学文摘社编号:
分子量:
650.75
UNSPSC代码:
12352200
NACRES:
NA.77
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产品名称

Thapsigargin Ready Made Solution, ≥98% (HPLC), 10 mM in DMSO

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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Zhouteng Tao et al.
Human molecular genetics, 24(9), 2426-2441 (2015-01-13)
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are the two common neurodegenerative diseases that have been associated with the GGGGCC·GGCCCC repeat RNA expansion in a noncoding region of C9orf72. It has been previously reported that unconventional repeat-associated non-ATG (RAN)
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
The Plasmodium falciparum cytoplasmic translation apparatus: a promising therapeutic target not yet exploited by clinically approved anti-malarials
<BIG>Sheridan CM, et al.</BIG>
Malaria Journal, 465-465 (2018)
Yuniesky Andrade-Talavera et al.
Cerebral cortex (New York, N.Y. : 1991), 26(8), 3637-3654 (2016-06-11)
Spike timing-dependent plasticity (STDP) is a Hebbian learning rule important for synaptic refinement during development and for learning and memory in the adult. Given the importance of the hippocampus in memory, surprisingly little is known about the mechanisms and functions
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

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