MAPK Signaling(MAPK信号通路)

Products for MAPK Signaling
- ERK(90)
- MEK1/2(64)
- NKCC(6)
- MNK(10)
- PKA(53)
- p38(100)
- Rac(2)
- Raf(68)
- RasGAP (Ras- P21)(1)
- JNK(60)
- cAMP(35)
- Protein Kinase G(2)
- RSK(32)
- Other(4)
- MAPKAPK(1)
- MKK(2)
- KLF(3)
- MAP3K(20)
- MAP4K(25)
- MAPKAPK2 (MK2)(9)
- Mixed Lineage Kinase(10)
- Cat.No. 产品名称 Information
-
GC44085
L-Sulforaphene
莱菔素
A natural isothiocyanate -
GC44022
L-858,051 (hydrochloride)
A water-soluble activator of adenylate cyclase
-
GC43885
Hypothemycin
寄端霉素
A resorcylic acid lactone polyketide with diverse biological activities -
GC43803
HA-1077 (hydrochloride)
盐酸法舒地尔,HA-1077 dihydrochloride; AT-877 dihydrochloride
A ROCK inhibitor -
GC43798
Guanylyl Imidodiphosphate (lithium salt)
Gpp(NH)p lithium
Guanylyl Imidodiphosphate (lithium salt)是一种稳定的GTP类似物,是腺苷酸环化酶的有效激活剂。 -
GC43734
Ganglioside GQ1b Mixture (sodium salt)
神经节苷脂GQ1B四钠盐
A mixture of ganglioside GQ1b
-
GC43624
ERK Inhibitor
Extracellular Regulated Kinase Inhibitor
An ERK inhibitor -
GC43611
Enniatin B1
恩镰孢菌素 B1
An antibiotic ionophore -
GC43610
Enniatin A1
恩镰孢菌素 A1
An ionophore antibiotic -
GC43341
Cyclic GMP
鸟苷-3ˊ,5ˊ-环磷酸一钠盐
A second messenger
-
GC43332
Cuspin-1
Chemical Upregulator of SMN Protein-1
An upregulator of SMN protein -
GC43198
CAY10717
A multi-targeted kinase inhibitor
-
GC43167
CAY10561
Pyrazolylpyrrole ERK Inhibitor
A selective inhibitor of ERK -
GC43065
C2 Phytoceramide (t18:0/2:0)
N-Acetyl Phytosphingosine, C2:0 Phytoceramide, Cer(t18:0/2:0), Ceramide (t18:0/2:0), NAPS
A bioactive sphingolipid -
GC42968
BPIQ-II (hydrochloride)
PD 158294
A potent, selective EGFR inhibitor -
GC42622
8-bromo-Cyclic AMP
8-溴腺苷-3',5'-环单磷酸
A PKA activator -
GC42616
7-oxo Staurosporine
BMY 41950, RK-1409
An antibiotic with diverse biological activities -
GC41740
(S)-p38 MAPK Inhibitor III
(S)-p38 MAP Kinase Inhibitor III, (S)-p38 Mitogen-activated Protein Kinase Inhibitor III
A cell-permeable p38 MAP kinase inhibitor -
GC41656
(±)2-(14,15-Epoxyeicosatrienoyl) Glycerol
(±)214,15EG
A cytochrome P450 metabolite of 2-AG -
GC41635
Phosphodiesterase 4 Inhibitor
PDE4 Inhibitor
An inhibitor of PDE4 -
GC41573
Theaflavin 3,3'-digallate
茶黄素-3,3'-双没食子酸; TF-3; ZP10
Theaflavin 3,3'-digallate(茶黄素-3,3'-双没食子酸; TF-3; ZP10)是一种有效的寨卡病毒(ZIKV)蛋白酶抑制剂,IC50值为2.3μM。 -
GC41423
5-trans Prostaglandin E2
transDinoprostone, 5,6trans PGE2
An impurity in commercial lots of PGE1 -
GC40650
CAY10706
A TrxR inhibitor
-
GC40484
Ferulic Acid methyl ester
阿魏酸甲酯; Methyl ferulate
A lipophilic antioxidant -
GC40352
Cafestol
咖啡醇
A natural diterpene which increases serum cholesterol -
GC34918
MW-150 dihydrochloride dihydrate
MW01-18-150SRM dihydrochloride dihydrate
An inhibitor of p38α MAPK -
GC34831
Tauroursodeoxycholate dihydrate
牛磺熊去氧胆酸二水合物; Tauroursodeoxycholic acid dihydrate; TUDCA dihydrate; UR 906 dihydrate
Tauroursodeoxycholatedihydrate(TUDCAdihydrate;UR906dihydrate;Taurolitedihydrate)是一种内质网应激抑制剂。Tauroursodeoxycholate显著降低凋亡分子如caspase-3和caspase-12表达。Tauroursodeoxycholate也抑制ERK。 -
GC34650
Longdaysin
Longdaysin is a Casein Kinase inhibitor with IC50 values of 8.8 μM, 5.6 μM, 52 μM and 29 μM for CKIδ, CKIα, ERK2 and CDK7.
-
GC19507
LUT-014
LUT-014 是一种 B-Raf 抑制剂,IC50 为 11.7 nM,用于减少与 EGFR 抑制剂治疗相关的剂量限制性痤疮样病变。
-
GC40231
Milrinone-d3
An internal standard for the quantification of milrinone
-
GC40213
Regorafenib-13C-d3
瑞戈非尼-13C-D3,BAY 73-4506-13C,d3
An internal standard for the quantification of regorafenib -
GC40054
CCT241161
A multi-kinase inhibitor
-
GC34342
BAY885
An ERK5 inhibitor
-
GC34275
L-JNKI-1
L-JNKI-1是一种针对JNK的细胞渗透性多肽抑制剂。
-
GC34208
GNE 220 Hydrochloride
GNE220(Hydrochloride)是一种有效的选择性MAP4K4抑制剂,其IC50值为7nM。
-
GC34197
FMK-MEA
FMK-MEA 是一种有效的选择性 p90 核糖体 S6 激酶 (RSK) 抑制剂。
-
GC34181
Tauroursodeoxycholate (TUDCA)
牛磺熊去氧胆酸; Tauroursodeoxycholic acid; TUDCA; UR 906
牛磺酸脱氧胆酸盐(TUDCA)是包括肝细胞在内的多种细胞的细胞保护剂,也是癌症细胞凋亡的诱导剂。 -
GC34140
TC13172
TC13172是MLKL的抑制剂,作用于HT-29细胞,其EC50值为2nM。
-
GC34072
Talmapimod (SCIO-469)
他匹莫德; SCIO-469
A p38 MAPK inhibitor -
GC34057
TBHQ (tert-Butylhydroquinone)
特丁基对苯二酚; tert-Butylhydroquinone
TBHQ(tert-Butylhydroquinone)是一种强效的酚类抗氧化剂,能够减轻氧化应激和炎症反应。 -
GC33857
Omtriptolide
昂曲托来
Omtriptolide(PG490-88)是从中草药纯化的雷公藤内酯的水溶性衍生物前药。 -
GC33844
Isovitexin (Saponaretin)
异牡荆黄素; Saponaretin; Homovitexin
Isovitexin 是从西番莲、大麻和棕榈得到的黄酮类物质,具有抗氧化、抗炎的活性;Isovitexin 作用与 JNK1/2 的抑制剂类似,能够抑制 NF-κB 的活化。
-
GC33831
Lidocaine hydrochloride (Lignocaine hydrochloride)
盐酸利多卡因; Lignocaine hydrochloride
An Analytical Reference Standard -
GC33771
Metadoxine
美他多辛
Metadoxine (Metadoxil, Metasin, pyridoxine-pyrrolidone carboxylat), also known as pyridoxine-pyrrolidone carboxylate, is a drug used to treat chronic and acute alcohol intoxication. Metadoxine is a novel 5-HT2B receptor antagonist with a possible therapeutic role in treating ADHD. -
GC33388
MEK-IN-1
MEK-IN-1是来自专利WO2008076415A1的MEK抑制剂。
-
GC33305
Balamapimod (MKI 833)
MKI 833
Balamapimod (MKI 833) (MKI 833) 是一种可逆的 Ras/Raf/MEK 抑制剂,具有潜在的抗肿瘤活性。 -
GC33238
SJFδ
SJFδ是一种含10个原子连接桥的PROTAC。SJFδ降解p38α,DC50为46.17nM,但不降解其他p38亚型(p38α,p38β和p38γ)。
-
GC33229
SJFα
SJFα是一种含13个原子连接桥的PROTAC。SJFα降解p38α,DC50为7.16nM,但降解p38δ效果较差(DC50=299nM),且在浓度高达2.5μM时也不会降解其他p38亚型(β和γ)。
-
GC33206
ERK-IN-1
ERK-IN-1(化合物 B)是一种可口服的 ERK1 和 ERK2 抑制剂,用于治疗以激活 MAPK 通路突变为特征的增殖性疾病。该活性尤其与 KRAS 突变 NSCLC、BRAF 突变 NSCLC、KRAS 突变胰腺癌、KRAS 突变结直肠癌 (CRC) 和 KRAS 突变卵巢癌的治疗有关。 ERK-IN-1 hydrochloride 也可以抑制 RAF。
-
GC33142
MK2-IN-1 (MK2 Inhibitor)
MK2-IN-1 (MK2 Inhibitor) 是一种有效的、选择性的 MAPKAPK2(MK2) 抑制剂 (IC50=0.11 uM),具有非 ATP 竞争性结合模式。