Isoquinolinesulfonamides, novel and potent inhibitors of cyclic nucleotide dependent protein kinase and protein kinase C.
about
DSIF, a novel transcription elongation factor that regulates RNA polymerase II processivity, is composed of human Spt4 and Spt5 homologsAngiogenin stimulates endothelial cell prostacyclin secretion by activation of phospholipase A2Use of D-erythro-sphingosine as a pharmacological inhibitor of protein kinase C in human plateletsTrans-activation of HIV-1 LTR-directed gene expression by tat requires protein kinase CBoundary conditions for the maintenance of memory by PKMzeta in neocortexThe selectivity of protein kinase inhibitors: a further updateMechanisms intrinsic to 5-HT2B receptor-induced potentiation of NMDA receptor responses in frog motoneuronesRho-stimulated contractility drives the formation of stress fibers and focal adhesionsDynamic properties of ankyrin in T lymphocytes: colocalization with spectrin and protein kinase C betaInhibition of Plasmodium falciparum choline kinase by hexadecyltrimethylammonium bromide: a possible antimalarial mechanismCombining RNA interference and kinase inhibitors against cell signalling components involved in cancer.Ten things you should know about protein kinases: IUPHAR Review 14Targeting cancer with kinase inhibitorsCrystal Structures of Two Aminoglycoside Kinases Bound with a Eukaryotic Protein Kinase InhibitorAnomalous dispersion analysis of inhibitor flexibility: a case study of the kinase inhibitor H-89Structural basis for selectivity of the isoquinoline sulfonamide family of protein kinase inhibitorsNuclear import and export of influenza virus nucleoprotein.Specific binding of CAP-50 to calcyclinPhosphorylation-dependent human immunodeficiency virus type 1 infection and nuclear targeting of viral DNAThe regulatory region of calcium/calmodulin-dependent protein kinase I contains closely associated autoinhibitory and calmodulin-binding domainsIonizing radiation stimulates a Grb2-mediated association of the stress-activated protein kinase with phosphatidylinositol 3-kinaseDual effect of cAMP agonist on ameliorative function of PKA inhibitor in morphine-dependent miceDioxin-dependent activation of murine Cyp1a-1 gene transcription requires protein kinase C-dependent phosphorylationA nuclear casein kinase 2 activity is involved in early events of transcriptional activation induced by salicylic acid in tobaccoProstaglandin E(2) increases cyclic AMP and inhibits endothelin-1 production/secretion by guinea-pig tracheal epithelial cells through EP(4) receptorsThrombin and C-kinase activators potentiate calcium-stimulated arachidonic acid release in human plateletsInhibition of carbachol stimulated acid secretion by interleukin 1beta in rabbit parietal cells requires protein kinase CNaphthalenesulphonamides block neutrophil superoxide production by intact cells and in a cell-free system: is myosin light chain kinase responsible for these effects?Isoquinolinesulphonamide derivatives inhibit transcriptional elongation of human immunodeficiency virus type 1 RNA in a promyelocytic model of latencyPentoxifylline and other protein kinase C inhibitors down-regulate HIV-LTR NF-kappa B induced gene expressionDiscovery of diverse small molecule chemotypes with cell-based PKD1 inhibitory activity.High-throughput assay for the identification of compounds regulating osteogenic differentiation of human mesenchymal stromal cellsNaringin-sensitive phosphorylation of plectin, a cytoskeletal cross-linking protein, in isolated rat hepatocytesAnisoosmotic regulation of the Nopp140 mRNA in H4IIE rat hepatoma cells and primary hepatocytesThe murine haemopexin receptor. Evidence that the haemopexin-binding site resides on a 20 kDa subunit and that receptor recycling is regulated by protein kinase CProtein kinases--the major drug targets of the twenty-first century?Enteric bacterial toxins: mechanisms of action and linkage to intestinal secretion.Adenosine analogue-oligo-arginine conjugates (ARCs) serve as high-affinity inhibitors and fluorescence probes of type I cGMP-dependent protein kinase (PKGIalpha)Pseudomonas aeruginosa exotoxin Y is a promiscuous cyclase that increases endothelial tau phosphorylation and permeabilityElectrical activity regulates AChR gene expression via JNK, PKCzeta and Sp1 in skeletal chick muscle.
P2860
Q24328838-277A792E-DFF0-4E05-A528-BFFCA00C056FQ24338956-A00BDAFA-AD16-49A9-9AE8-39C90E4BC670Q24529582-F09469D5-27C5-40BD-BA9D-BC208BD98B89Q24556556-C43B6B14-FA49-476F-9C83-2B262DA862FAQ24652516-24C871A4-4AFC-4B0E-B1F6-D895167E12A9Q24654622-5ADEF529-7FF1-4070-A38B-367C01C33361Q24671497-E0C52F34-AA4B-44DF-B5C5-F6E415F0A5E9Q24671788-7E5E1040-3307-40D3-A42B-AF03A984A61DQ24673372-F96DF60D-9ABC-4ACB-9E41-D22E9762015DQ24675578-837584C6-CA60-4123-967F-44DD33ED9DC9Q24814879-F2F2E3A3-6547-4891-895F-55F310C9A4DCQ26849417-84CFABEA-1568-4416-8B4B-C4E151AD1F2DQ26865765-4988C42B-2C62-415C-A6E4-D09CD1853210Q27667856-B895820C-258F-4104-8CD7-A10A97C9768CQ27671230-C2814CB2-5D2A-4B81-AEC3-22AE9CE8DDD3Q27733158-56CFB0E2-CD15-4BDD-B12A-6DAF6E9611FEQ27867703-C16262C9-83CB-475B-AECA-B360717ACCCCQ28207404-76A56436-F7DA-49B5-8A75-B28D64EEFACFQ28272788-B1955E9E-5D44-4074-9317-B24565AB57DEQ28289472-BE4B38C9-E334-4D3C-A416-1F89D678E0CEQ28295568-2D4256CF-B961-4C1C-ACE0-525CA79A9ADEQ28298439-4CEBEF37-D948-4305-8F43-7A2F3F5DFDD5Q28343069-230034E5-8676-42F6-838F-C5C72BD57FC4Q28345748-823F76E8-3C28-439B-B092-D03A08E7A9F9Q28354162-626C9E46-A6D7-4221-B694-364C7C909D76Q28360984-B8D96D54-0CF4-4362-A629-9017621322E4Q28365352-82E47C32-EA40-419E-8014-8CA229BA0148Q28367777-3FCBA4FB-0E05-4BCB-8264-2E69727F84BFQ28376959-0B68A3E6-FE8A-4F71-9428-16CB28AF567CQ28379107-F5A9DE7E-D6F4-4902-9409-D211145C65D7Q28477356-019F2C7B-E8B5-410B-8B73-BDB26F1B2884Q28477636-3C41075F-9B08-4982-B7DF-1967BAC7028FQ28567931-9C235F65-2114-4553-96E7-744C21838858Q28569820-864071BF-BB8E-4D92-8565-629AFE56D8F0Q28677937-564D3BFE-68B5-4B7D-B8D1-988F498DB20FQ29615339-6A335E9A-E6B1-414E-AACA-0E2E2E6A404CQ30449794-07C9C6B7-6C59-4FFB-808A-79621BBB3465Q30499343-CEB8278C-F318-4AC3-923F-B22C935EC371Q30523756-3DD6DB62-F817-420D-B8B6-6A8C81F57C57Q31860680-0E89A847-5EAE-4CF0-8F3C-B887A430E7DA
P2860
Isoquinolinesulfonamides, novel and potent inhibitors of cyclic nucleotide dependent protein kinase and protein kinase C.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
1984年论文
@zh
1984年论文
@zh-cn
name
Isoquinolinesulfonamides, nove ...... n kinase and protein kinase C.
@en
Isoquinolinesulfonamides, nove ...... n kinase and protein kinase C.
@nl
type
label
Isoquinolinesulfonamides, nove ...... n kinase and protein kinase C.
@en
Isoquinolinesulfonamides, nove ...... n kinase and protein kinase C.
@nl
prefLabel
Isoquinolinesulfonamides, nove ...... n kinase and protein kinase C.
@en
Isoquinolinesulfonamides, nove ...... n kinase and protein kinase C.
@nl
P2093
P356
P1433
P1476
Isoquinolinesulfonamides, nove ...... n kinase and protein kinase C.
@en
P2093
P304
P356
10.1021/BI00316A032
P407
P577
1984-10-01T00:00:00Z