MAPK Signaling(MAPK信号通路)
Products for MAPK Signaling
- ERK(78)
- MEK1/2(60)
- NKCC(6)
- MNK(8)
- PKA(53)
- p38(98)
- Rac(2)
- Raf(64)
- RasGAP (Ras- P21)(1)
- JNK(58)
- cAMP(37)
- Protein Kinase G(2)
- RSK(30)
- Other(4)
- MAPKAPK(1)
- MKK(2)
- KLF(3)
- MAP3K(20)
- MAP4K(20)
- MAPKAPK2 (MK2)(9)
- Mixed Lineage Kinase(8)
- Cat.No. 产品名称 Information
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GC15814
Pamapimod (R-1503, Ro4402257)
Ro4402257; R1503
An orally bioavailable inhibitor of p38α MAP kinase - GC16997 BMS-582949 A p38α MAP kinase inhibitor
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GC10324
PLX7904
PB04
A RAF inhibitor -
GC16039
LJH685
2,6-二氟-4-[4-[4-(4-甲基-1-哌嗪基)苯基]-3-吡啶基]苯酚
An inhibitor of RSKs -
GC17818
Vacquinol-1
NSC13316
An activator of cell death in glioblastoma cells - GC16601 LJI308 An inhibitor of RSKs
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GC16214
DEL-22379
N-[2,3-二氢-3-[(5-甲氧基-1H-吲哚-3-基)亚甲基]-2-氧代-1H-吲哚-5-基]-1-哌啶丙酰胺
An inhibitor of ERK dimerization -
GC17425
Sodium Tauroursodeoxycholate (TUDC)
牛磺熊去氧胆酸钠; Tauroursodeoxycholic acid sodium; TUDCA sodium; UR 906 sodium
Tauroursodeoxycholate (Tauroursodeoxycholic acid; TUDCA) sodium 是一种内质网 (ER) 应激抑制剂。 Tauroursodeoxycholate 显着降低凋亡分子的表达,例如 caspase-3 和 caspase-12。 Tauroursodeoxycholate 也抑制 ERK。 - GC17828 BI-847325 A selective dual MEK/Aurora kinase inhibitor
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GC11857
Pexmetinib (ARRY-614)
ARRY-614
A dual inhibitor of Tie2 and p38 MAPK - GC17702 K-Ras(G12C) inhibitor 9 An allosteric inhibitor of oncogenic K-Ras(G12C)
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GC14938
PF-03394197(Oclacitinib)
奥拉替尼
A JAK family kinase inhibitor -
GC10010
AS601245
AS-601245, c-Jun N-terminal Kinase Inhibitor V
A potent JNK inhibitor used in cells and animals - GC10005 SEP-0372814 A PDE10A inhibitor
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GC14647
SCH772984 HCl
A selective inhibitor of ERK1/2
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GC15044
SCH772984 TFA
A selective inhibitor of ERK1/2
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GC13980
LY3009120
DP-4978
LY3009120 是一种泛 RAF 和 RAF 二聚体抑制剂,可抑制所有 RAF 亚型并占据 RAF 二聚体中的两个原聚体。 -
GC12406
RO5126766(CH5126766)
Ro 5126766; CH5126766
A dual inhibitor of MEK1 and Raf kinases -
GC12006
GDC-0994
Ravoxertinib
A selective ERK1/2 inhibitor - GC12089 LY2584702 A p70S6K inhibitor
- GC11922 SB 706504 p38 MAPK inhibitor
- GC11635 TA 02 An inducer of cardiomyocyte differentiation
- GC13825 TA 01 An inducer of cardiomyocyte differentiation
- GC13244 DTP3 DTP3 TFA 是一种有效的选择性 GADD45β/MKK7 抑制剂。 DTP3 TFA 靶向 NF-κB 通路下游的一个重要的癌症选择性细胞存活模块。
- GC15004 URMC-099 URMC-099作为一种基于7-氮杂吲哚的MLK3抑制剂,其IC50为14 nM,可特异性影响参与疾病病理生物学的特定aβ物种。
- GC16511 OTS964 A TOPK inhibitor
- GC12304 OTS514 A TOPK inhibitor
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GC12834
6-Bnz-cAMP sodium salt
6-Bnz-cAMP
A PKA-selective activator - GC12646 AL 8697 AL 8697 是一种具有口服活性的特异性 p38α MAPK 抑制剂,IC50 为 6 nM。
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GC10666
CGP 57380
N3-(4-氟苯基)-1H-吡唑并[3,4-D]嘧啶-3,4-二胺
Inhibitor of MAPK-interacting kinase1 - GC14853 TC ASK 10 A inhibitor of ASK1
- GC17485 PD 334581 A MEK inhibitor
- GC15477 DBM 1285 dihydrochloride p38 MAPK inhibitor
- GC16652 SR 3576 A JNK3 inhibitor
- GC17963 CHPG Sodium salt CHPG 钠盐是一种选择性 mGluR5 激动剂,可通过 BV2 小胶质细胞中的 TSG-6/NF-κB 通路减弱 SO2 诱导的氧化应激和炎症。
- GC17957 SX 011 p38α inhibitor
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GC11542
SU 3327
2-氨基-5-[(5-硝基-2-噻唑基)硫代]-1,3,4-噻二唑
A JNK1 inhibitor with antidiabetic and antibiotic activity -
GC17282
TCS JNK 6o
JNK Inhibitor VIII
A JNK inhibitor -
GC15924
L-779,450
4-(4-氯-3-羟基苯基)-2-苯基-5-(吡啶-4-基)-1H-咪唑
A B-Raf inhibitor -
GC16169
XRP44X
[4-(3-氯苯基)哌嗪-1-基](5-甲基-2-苯基-2H-吡唑-3-基)甲酮
XRP44X 抑制 Ras 诱导的转录激活,IC50 为 10 nM。 -
GC10403
EO 1428
EO 1428, p38 MAP Kinase Inhibitor VIII, p38 Mitogen-activated Protein Kinase Inhibitor VIII
An inhibitor of p38α and p38β MAP kinases -
GC13116
JX 401
p38 MAPK Inhibitor VI, p38 Mitogen-activated Protein Kinase Inhibitor VI
A potent, reversible inhibitor of p38α MAPK -
GC11180
CMPD-1
CMPD 1
A substrate-selective p38α MAPK inhibitor -
GC17658
Guggulsterone
香胶甾酮; Z/E-Guggulsterone
Guggulsterone 是一种植物甾醇,来自于 Commiphora wightii 的树胶树脂。 Guggulsterone 通过下调抗凋亡基因产物(IAP1、xIAP、Bfl-1/A1、Bcl-2、cFLIP 和 survivin),调节细胞周期蛋白(cyclin D1 和c-Myc),激活半胱天冬酶和 JNK,抑制 Akt。 Guggulsterone 是一种法尼醇 X 受体 (FXR) 拮抗剂,可降低 CDCA 诱导的 FXR 活化,对 Z- 和 E-Guggulsterone 的 IC50 分别为 17 和 15 μM。 - GC17725 SKF 86002 dihydrochloride An anti-inflammatory agent
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GC11559
Anisomycin
茴香霉素; Flagecidin; Wuningmeisu C
Anisomycin是一种从灰链霉菌中分离出来的抗生素,也是一种JNK激活剂。 -
GC12532
CHPG
Chlorohydroxyphenylglycine, CHPG
A potent and selective mGluR5 agonist -
GC11605
C-1
1-(5-异喹啉磺酰基)哌嗪盐酸盐
C-1 是一种有效的蛋白激酶抑制剂,IC50 为 4 μM, 8 μM, 12 μM 和 240 μM 用于 cGMP 依赖性蛋白激酶 (PKG)、cAMP 依赖性蛋白激酶 (PKA) ,分别为蛋白激酶 C (PKC) 和 MLC 激酶。 C-1 也用作 ROCK 抑制剂。 -
GC12201
HI TOPK 032
TOPK抑制剂(HI-TOPK-032)
An inhibitor of TOPK, Chk1, and MEK1 kinases -
GC17407
Pluripotin
SC1
A synthetic compound that promotes self-renewal of murine embryonic stem cells