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mitogen-activated protein kinase 11

Target Id 1500
缩写名 p38β
家族 p38 subfamily

基因和蛋白信息

Species Transmembrane Domains Amino Acids Chromosomal Location Gene Symbol Gene Name
Human 2 364 22q13.33 MAPK11 mitogen-activated protein kinase 11
Mouse 2 364 15 E3 Mapk11 mitogen-activated protein kinase 11
Rat 2 364 7q34 Mapk11 mitogen-activated protein kinase 11

作用于该靶标的配体

Ligand Id Ligand Ligand Type Action on Target 对应产品货号 产品名称
5269 SB203580 Synthetic organic Inhibition S131899 SB-203580,p38 MAPK抑制剂
6059 VX-702 Synthetic organic Inhibition V125198 VX-702,p38 MAP激酶抑制剂
7817 talmapimod Synthetic organic Inhibition S339037 SCIO 469盐酸盐
7818 PH-797804 Synthetic organic Inhibition P127738 PH-797804,ATP竞争性p38α抑制剂
5719 neflamapimod Synthetic organic Inhibition V126681 VX-745,p38 alpha MAPK抑制剂
5668 doramapimod Synthetic organic Inhibition D125100 达马莫德
9328 TAK-715 Synthetic organic Inhibition T125460 TAK-715
9915 pamapimod Synthetic organic Inhibition P413914 帕马皮莫德
9917 pexmetinib Synthetic organic Inhibition P413835 Pexmetinib (ARRY-614)
12122 compound 4e [PMID: 35546685] Synthetic organic Inhibition T609257 1-[5-tert-butyl-2-[1-[2-(dimethylamino)ethyl]pyrazol-4-yl]pyrazol-3-yl]-3-[(1S,4R)-4-[[3-[(2S)-2-methylpiperidin-1-yl]-[1,2,4]triazolo[4,3-a]pyridin-6-yl]oxy]-1,2,3,4-tetrahydronaphthalen-1-yl]urea

参考文献

1. Bech-Hansen NT, Naylor MJ, Maybaum TA, Pearce WG, Koop B, Fishman GA, Mets M, Musarella MA, Boycott KM.  (1998)  Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness..  Nat Genet,  19  (3):  (264-7).  [PMID:9662400]
2. Singh A, Hamedinger D, Hoda JC, Gebhart M, Koschak A, Romanin C, Striessnig J.  (2006)  C-terminal modulator controls Ca2+-dependent gating of Ca(v)1.4 L-type Ca2+ channels..  Nat Neurosci,  (9):  (1108-16).  [PMID:16921373]
3. Strom TM, Nyakatura G, Apfelstedt-Sylla E, Hellebrand H, Lorenz B, Weber BH, Wutz K, Gutwillinger N, Rüther K, Drescher B et al..  (1998)  An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness..  Nat Genet,  19  (3):  (260-3).  [PMID:9662399]

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品牌简介

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