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Sarcophine

更新时间:2025-09-19 09:24:11

Sarcophine结构式
Sarcophine结构式
品牌特惠专场
常用名 Sarcophine 英文名 Sarcophine
CAS号 55038-27-2 分子量 316.43500
密度 1.08g/cm3 沸点 472.8ºC at 760 mmHg
分子式 C20H28O3 熔点 N/A
MSDS N/A 闪点 203.5ºC

 Sarcophine用途


肌黄嘌呤((+)-肌黄嘌呤)是一种有效的甘氨酸受体(GlyR)抑制剂,IC50值为3.9μM。石灰质是一种天然产物,可以从红海软珊瑚石灰质中分离出来[1]。

 Sarcophine名称

英文名 Sarcophine
英文别名 更多

 Sarcophine生物活性

描述 肌黄嘌呤((+)-肌黄嘌呤)是一种有效的甘氨酸受体(GlyR)抑制剂,IC50值为3.9μM。石灰质是一种天然产物,可以从红海软珊瑚石灰质中分离出来[1]。
相关类别
体外研究 肌松((+)-肌松)是一种重组甘氨酸受体抑制剂,Ki公司值为 2.1μM[1]石竹碱(1-100 mM;24小时)对 HEK293型细胞具有细胞毒性,LD50型值为 29.3毫摩尔[1]
参考文献

[1]. Saleh HA, et, al. Sarcophine and (7S, 8R)-dihydroxydeepoxysarcophine from the Red Sea soft coral Sarcophyton glaucum as in vitro and in vivo modulators of glycine receptors. Neurotoxicology. 2020 Sep;80:105-111.  

 Sarcophine物理化学性质

密度 1.08g/cm3
沸点 472.8ºC at 760 mmHg
分子式 C20H28O3
分子量 316.43500
闪点 203.5ºC
精确质量 316.20400
PSA 38.83000
LogP 4.63260
InChIKey CGAKBBMRMLAYMY-QLOJAFMTSA-N
SMILES CC1=CCCC2(C)OC2CCC(C)=CC2OC(=O)C(C)=C2CC1
折射率 1.536

 Sarcophine毒性和生态

 Sarcophine合成线路

~82%

Sarcophine结构式

Sarcophine

55038-27-2

文献:Frincke, James M.; McIntyre, Douglas E.; Faulkner, John D. Tetrahedron Letters, 1980 , vol. 21, p. 735 - 738

~%

Sarcophine结构式

Sarcophine

55038-27-2

详细
文献:Kobayashi, Masaru Journal of Chemical Research, Miniprint, 1991 , # 11 p. 2840 - 2852

 Sarcophine靶点实验

查看更多实验

实验名称:Antiproliferative activity against human MDA-MB-231 cells at 5 to 50 uM after 24 hrs ...
来源:ChEMBL
靶标:MDA-MB-231
External Id:CHEMBL1816444
实验名称:Antiproliferative activity against human PC3 cells at 5 to 50 uM after 24 hrs by MTT ...
来源:ChEMBL
靶标:PC-3
External Id:CHEMBL1816446
实验名称:Inhibition of TPA-induced EBV-early antigen activation in human Raji cells assessed a...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL949831
实验名称:Inhibition of TPA-induced EBV-early antigen activation in human Raji cells assessed a...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL949830
实验名称:Reduction in human pancreatic recombinant 1B PLA2 activity expressed in Escherichia c...
来源:ChEMBL
靶标:Phospholipase A2
External Id:CHEMBL1026212
实验名称:Cytotoxicity against human Raji cells assessed as cell viability at 500 molar ratio
来源:ChEMBL
靶标:Raji
External Id:CHEMBL949833
实验名称:Cytotoxicity against human Raji cells assessed as cell viability at 1000 molar ratio
来源:ChEMBL
靶标:Raji
External Id:CHEMBL949832
实验名称:Inhibition of TPA-induced EBV-early antigen activation in human Raji cells assessed a...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL949829
实验名称:Inhibition of TPA-induced EBV-early antigen activation in human Raji cells assessed a...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL949828
实验名称:Inhibition of residual DNA repair ability in Homo sapiens (human) MCF7 cells assessed...
来源:ChEMBL
靶标:MCF7
External Id:CHEMBL3056897
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 Sarcophine英文别名

Oxireno(9,10)cyclotetradeca(1,2-B)furan-9(1ah)-one,2,3,6,7,10A,13,14,14A-octahydro-1A,5,8,12-tetramethyl-(van) (9ci)
(1aS,4E,10aS,11E,14aS)-2,3,6,7,10a,13,14,14a-Octahydro-1a,5,8,12-tetramethyloxireno[9,10]cyclotetradeca[1,2-b]furan-9(1aH)-one
Sarcophyne
Sarcophin
Oxireno(9,10)cyclotetradeca(1,2-B)furan-9(1ah)-one,2,3,6,7,10A,13,14,14A-octahydro-1A,5,8,12-tetramethyl-,(1as-(1ar*,4E,10ar*,11E,14ar*))
Sarcophin a
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