Thapsigargin
CAS No. 67526-95-8
Thapsigargin ( G-202 | G 202 | G202 )
产品货号. M15579 CAS No. 67526-95-8
一种有效的、选择性的、非竞争性的肌浆/内质网 Ca2+ ATP 酶 (SERCA) 抑制剂,可引起内质网应激并诱导哺乳动物细胞自噬。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 100MG | 获取报价 | 有现货 |
|
| 200MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Thapsigargin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述一种有效的、选择性的、非竞争性的肌浆/内质网 Ca2+ ATP 酶 (SERCA) 抑制剂,可引起内质网应激并诱导哺乳动物细胞自噬。
-
产品描述A potent, selective, non-competitive inhibitor of the sarco/endoplasmic reticulum Ca2+ ATPase (SERCA), causes ER stress and induces autophagy in mammalian cells; inhibits the Ca2+ ATPase of rat liver ER about 100% at 170 nM, but no inhibition for skeletal muscle SR; increases the concentration of cytosolic free Ca2+ in sensitive cells by an acute and highly specific arrest of the endoplasmic reticulum Ca2+ pump.
-
体外实验Cell Proliferation Assay Cell Line:MH7A human rheumatoid arthritis synovial cells Concentration:0.001, 0.1, and 1?μM Incubation Time:For 2 and 4 days Result:Arrested cell proliferations in a time- and dose-dependent manner.Apoptosis Analysis Cell Line:MH7A human rheumatoid arthritis synovial cells Concentration:0.001, 0.1, and 1?μM Incubation Time:For 2 and 4 days Result:Induces cell apoptosis in a time- and dose-dependent manner.Western Blot Analysis Cell Line:MH7A human rheumatoid arthritis synovial cells Concentration:0.001, 0.1, and 1?μM Incubation Time:For 2 and 4 days Result:Impairs mTOR activity and leads to cyclin D1 expressions
-
体内实验Animal Model:Male Balb/c mice (20-25 g) Dosage:0.25 ug/g, 0.5 ug/g and 1 ug/g Administration:Injection; 24 hours Result:Increased of 2 to 5-fold in chemokine and pro-inflammatory expression.
-
同义词G-202 | G 202 | G202
-
通路Autophagy
-
靶点Autophagy
-
受体Autophagy
-
研究领域Cancer
-
适应症——
化学信息
-
CAS Number67526-95-8
-
分子量650.76
-
分子式C34H50O12
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 50 mg/mL (76.83 mM)
-
SMILESCCCCCCCC(O[C@@H]1[C@@H](OC(/C(C)=C\C)=O)C(C)=C2[C@@]1([H])[C@@](C)(OC(C)=O)C[C@H](OC(CCC)=O)[C@@]([C@@]3(O)C)(O)[C@@]2([H])OC3=O)=O
-
化学全称(3S,3aR,4S,6S,6AR,7S,8S,9bS)-6- (Acetyloxy)-2,3,3a,4,5,6,6a,7,8,9b-decahydro-3,3a-dihydroxy-3,6,9-trimethyl-8-[[(2Z)-2-methyl-1-oxo-2-butenyl]oxy]-2-oxo-4-(1-oxobutoxy)azuleno[4,5-b]furan-7-yl octanoate
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Davidson GA, et al. J Biol Chem. 1995 May 19;270(20):11731-4.
2. Thastrup O, et al. Proc Natl Acad Sci U S A. 1990 Apr;87(7):2466-70.
3. Yu M, et al. J Biol Chem. 1998 Feb 6;273(6):3542-6.
4. Panagaki T, et al. Sci Rep. 2017 Nov 23;7(1):16158.
产品手册
关联产品
-
Indophagolin
Indophagolin 是一种有效的含二氢吲哚自噬抑制剂,IC50 为 140 nM。
-
Nilotinib hydrochlor...
Nilotinib (AMN107) hydrochloride 是一种口服可用的具有抗肿瘤活性的 Bcr-Abl 酪氨酸激酶抑制,可用于慢性骨髓性白血病的研究。
-
Mefloquine hydrochlo...
Mefloquine hydrochloride (Mefloquin hydrochloride) 是一种喹啉抗疟药,是一种抗 SARS-CoV-2 进入抑制剂。Mefloquine hydrochloride 也是一种 K+ 通道 (KvQT1/minK) 拮抗剂,IC50 为 ~1 μM。Mefloquine hydrochloride 可用于疟疾、系统性红斑狼疮和癌症的研究。
021-51111890
购物车()
sales@molnova.cn

