R136
Ro 31-8220 甲磺酸盐
solid
别名:
2-{1-[3-（脒基）丙基]-1H-吲哚-3-基}-3-（1-甲基吲哚-3-基）马来酰亚胺 甲磺酸盐, 双吲哚基马来酰亚胺IX
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关于此项目
线性分子式:
C25H23N5O2S · CH3SO3H
CAS Number:
分子量:
553.65
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
生物来源
synthetic (organic)
方案
≥98% (HPLC)
表单
solid
颜色
orange to red
溶解性
H2O: 7.3 mg/mL
储存温度
2-8°C
SMILES字符串
CS(O)(=O)=O.Cn1cc(C2=C(C(=O)NC2=O)c3cn(CCCSC(N)=N)c4ccccc34)c5ccccc15
InChI
1S/C25H23N5O2S.CH4O3S/c1-29-13-17(15-7-2-4-9-19(15)29)21-22(24(32)28-23(21)31)18-14-30(11-6-12-33-25(26)27)20-10-5-3-8-16(18)20;1-5(2,3)4/h2-5,7-10,13-14H,6,11-12H2,1H3,(H3,26,27)(H,28,31,32);1H3,(H,2,3,4)
InChI key
SAWVGDJBSPLRRB-UHFFFAOYSA-N
一般描述
Ro 31-8220是星形孢菌素的一种双吲哚基马来酰亚胺衍生物。Ro 31-8220可阻断MAP激酶磷酸酶-1（MKP-1）的表达、诱导c-Jun表达并刺激Jun N末端激酶（JNK1）。它具有免疫抑制特性。
生化/生理作用
抑制GRK-5（G蛋白偶联受体激酶）；PKC（蛋白激酶C）；MAPKAP激酶1β及p70 S6激酶。
特点和优势
这种化合物是激酶磷酸酶生物学研究的特色产品。点击此处发现更多特色激酶磷酸酶生物产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。
免责声明
光敏性
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
Ro 31-8220, A Novel Protein Kinase C Inhibitor, Inhibits Early And Late T Cell Activation Events1
Geiselhart L, et al.
Transplantation, 61(11), 1637-1642 (1996)
The selective protein kinase C inhibitor, Ro-31-8220, inhibits mitogen-activated protein kinase phosphatase-1 (MKP-1) expression, induces c-Jun expression, and activates Jun N-terminal kinase
Beltman J, et al.
The Journal of Biological Chemistry, 271(43), 27018-27024 (1996)
J Beltman et al.
The Journal of biological chemistry, 271(43), 27018-27024 (1996-10-25)
The role of protein kinase C (PKC) in inflammation, mitogenesis, and differentiation has been deduced in part through the use of a variety of PKC inhibitors. Two widely used inhibitors are the structurally related compounds GF109203X and Ro-31-8220, both of
D R Alessi
FEBS letters, 402(2-3), 121-123 (1997-02-03)
The protein kinase C (PKC) inhibitors Ro 318220 and GF 109203X have been used in over 350 published studies to investigate the physiological roles of PKC. Here we demonstrate that these inhibitors are not selective for PKC isoforms as was
The protein kinase C inhibitors bisindolylmaleimide I (GF 109203x) and IX (Ro 31-8220) are potent inhibitors of glycogen synthase kinase-3 activity
Hers I, et al.
Febs Letters, 460(3), 433-436 (1999)
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