“soluble guanylyl cyclase sgc”的搜索结果
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soluble guanylyl cyclase inhibitor
ODQ is a potent and selective soluble guanylyl cyclase (sGC, nitric oxide-activated enzyme) inhibitor. ODQ enhances the pro-apoptotic effects of Cisplatin in human mesothelioma cells.
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GAK 抑制剂
SGC GAK 1是一种高亲和力细胞周期蛋白G相关激酶(GAK)抑制剂。
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DOT1L 抑制剂
SGC 0946是有效的DOT1L甲基转移酶抑制剂,可阻断A431细胞和MCF10A细胞中的H3K79甲基化。
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CBP/p300 bromodomain 抑制剂
SGC-CBP30是一种有效且选择性的CREBBP(CBP)和EP300抑制剂,无细胞试验中IC50分别为21 nM和38 nM。它们是一般的转录共激活因子。
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glutaminyl cyclase inhibitor
Glutaminyl Cyclase Inhibitor 1 is a glutaminyl cyclase inhibitor with an IC50 of 0.5 μM.
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glutaminyl cyclase inhibitor
Glutaminyl Cyclase Inhibitor 2 is a glutaminyl cyclase inhibitor with an IC50 of 1.23 μM.
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MLLT1/3-histone interactions inhibitor
SGC-iMLLT is a first-in-class chemical probe and a potent, selective inhibitor of MLLT1/3-histone interactions with an IC50 of 0.26 μM.
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PRMT3 抑制剂
SGC 707是PRMT3的有效变构抑制剂(IC50 = 50 nM),其选择性是其他甲基转移酶和其他非表观遗传靶标的100倍以上。
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sGC inhibitor
NS-2028 is a highly selective soluble Guanylyl Cyclase (sGC) inhibitor with IC50 values of 30 nM and 200 nM for basal and NO-stimulated enzyme activity.
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GC inhibitor
Glutaminyl Cyclase Inhibitor 3 (compound 212 ), a designed anti-Alzheimer??s compound, is a potent human Glutaminyl Cyclase (GC) inhibitor, with an IC50 of 4.5 nM.
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guanylate cyclase (sGC) stimulator
Olinciguat (IW-1701) is an oral guanylate cyclase (sGC) stimulator with concentration-dependent stimulation of sGC in purified rat and human enzyme assays and a whole cell assay.
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guanylate cyclase stimulator
Praliciguat (IW-1973) is a potent and orally active soluble guanylate cyclase stimulator, enhances NO signaling, acts as a vasodilator. Praliciguat (IW-1973) stimulates sGC in HEK-293 cells with an EC50 of 197 nM.
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sGC activator
Cinaciguat is an activator of guanylate cyclase (sGC), and used for acute decompensated heart failure.
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soluble guanylate cyclase stimulator
Runcaciguat is an orally active stimulator of soluble guanylate cyclase, and is used in the research of cardiovascular and renal diseases combined with selective partial adenosine A1 receptor agonists.
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soluble adenylyl cyclase inhibitor
LRE1 is a specific and allosteric inhibitor of soluble adenylyl cyclase.
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guanylate cyclase stimulator
Nelociguat (BAY60-4552) is a nitric oxide sensitive soluble guanylate cyclase stimulator.
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guanylate cyclase stimulator
Vericiguat (BAY1021189) is a potent, orally available and soluble guanylate cyclase stimulator.
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guanylate cyclase (GC) activator
Cinaciguat hydrochloride is a potent soluble guanylate cyclase (GC) activator with EC50 of 15 nM in platelets.
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sGC activator?
BAY 41-2272是一种直接且不依赖NO的可溶性鸟苷酸环化酶(sGC)刺激物。
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sGC activator
YC-1 (Lificiguat)是可溶性胍基环化酶(sGC)的直接活化剂,独立于一氧化氮。
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sGC stimulator
Riociguat (BAY 63-2521)是可溶性鸟苷酸环化酶(sGC)的刺激物。
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adenylate cyclase inhibitor
CB-7921220 is an adenylate cyclase inhibitor.
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guanylate cyclase activator
(4-Acetamidocyclohexyl) nitrate (BM121307) is a guanylate cyclase activator that was in phase I development for the treatment of ischaemic heart disorders. The research has been discontinued.
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sAC-specific inhibitor
KH7 is a soluble adenylyl cyclase (sAC)-specific inhibitor, with IC50s of 3-10 μM toward both recombinant purified human sACt protein and heterologously expressed sACt in cellular assays.
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Cy3 NHS (Cyanine3 NHS ester) is a water-soluble and yellow emitting fluorescent dye for labeling amino-groups in biomolecules. Used to label soluble proteins, peptides, and oligonucleotides/DNA.
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PDE10A inhibitor
THPP-1, a SGC chemical probe, is a potent and orally bioavailable phosphodiesterase 10A (PDE10A) inhibitor, with Ki values of 1 nM and 1.3 nM for human and rat PDE10A, respectively. THPP-1 has excellent pharmacokinetic properties in preclinical species.
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HNE inhibitor
BAY-678 racemate is a racemate of BAY-678. BAY-678 is an orally bioavailable, highly potent, selective and cell-permeable inhibitor of human neutrophil elastase (HNE), with an IC50 of 20 nM. BAY-678 is also nominated as a chemical probe to the public via the Structural Genomics Consortium (SGC).
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HNE 抑制剂
BAY-678是人嗜中性粒细胞弹性蛋白酶(HNE)的口服生物利用型,高效,选择性和细胞渗透性抑制剂,IC50为20 nM。BAY-678还被结构基因组学联盟(SGC)提名为化学探针。
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PRMT3 抑制剂
XY1是SGC 707的负控制。SGC 707(Adooq目录号A15450)是PRMT3的有效,选择性变构抑制剂(IC50 = 50 nM)。
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AC1 inhibitor
ST034307 is a potent and selective adenylyl cyclase 1 (AC1) inhibitor, with IC50 of 2.3 μM.
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GC-C receptor agonist
Plecanatide acetate is a guanylate cyclase-C (GC-C) receptor agonist, with an EC50 of 190 nM in T84 cells. Plecanatide acetate shows anti-inflammatory activity in models of murine colitis.
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RNA 3'-Terminal Phosphate Cyclase Human Recombinant
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adenylyl cyclase 抑制剂
SQ22536是腺苷酸环化酶的抑制剂,IC50为1.4 uM。它可以抑制完整人血小板中PGE1刺激的cAMP水平升高。
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Guanylate cyclase C 激动剂
Linaclotide是鸟苷酸环化酶2C的肽激动剂。
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Adenylyl Cyclase 抑制剂
NKY 80是腺苷酸环化酶(AC)的抑制剂。 与AC3和AC2相比,对AC5的亲和力更大(IC50值分别为8.3μM,132μM和1.7 mM)。
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sEH inhibitor
AUDA (compound 43) is a potent soluble epoxide hydrolase (sEH) inhibitor with IC50s of 18 and 69 nM for the mouse and human sEH, respectively. AUDA has anti-inflammatory activity.
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GSK620 is Potent, selective, and Highly Soluble Bromo and Extraterminal Domain (BET) Second Bromodomain (BD2) Inhibitor.
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non-NMDA receptor antagonist
DNQX Disodium is a water-soluble form of selective non-NMDA receptor antagonist DNQX.
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sEH inhibitor
1-Cyclohexyl-3-dodecyl urea (CDU; N-Cyclohexyl-N-dodecyl urea; NCND) is a highly selective soluble epoxide hydrolase (sEH) inhibitor.
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eIF4G1 inhibitor
SBI-0640756 (SBI-756) is a water soluble inhibitor of eIF4G1 and disrupts the eIF4F complex.
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recombinant human sEH inhibitor
GSK2256294A is a potent, reversible, tight binding inhibitor of isolated recombinant human sEH (soluble epoxide hydrolase) (IC50 = 27 pM; t1/2 = 121 min) and displays potent inhibition against the rat (IC50 = 61 pM) and murine (IC50 = 189 pM) orthologs of sEH.
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Oxaquin (MCB-3837) is a water-soluble, injectable prodrug that is rapidly converted to the active sub-stance MCB3681 in vivo following intravenous (i.v.) administration, active against Gram-positive bacterial species. Oxaquin (MCB-3837) itself has no antimicrobial effects.
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sEH inhibitor
TTPU is a soluble epoxide hydrolase (sEH) inhibitor with IC50 values of 37 and 3.7 nM for monkey and human sEH, respectively.
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Rilmazafone is a water-soluble benzodiazepine prodrug that acts as a sedative and hypnotic neuropsychiatric agent.
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Moniliformin sodium salt is a potent, water-soluble mycotoxin isolate from Fusarium moniliforme.
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TMB-PS(102062-36-2) is N-(3-sulfopropyl)-3,3',5,5'-tetramenthylbenzidine sodium salt; White - pale yellow crystalline powder, soluble in water, can be used under neutral, acidic and alkaline conditions.
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BCRP inhibitor
YHO-13351 (free base) is the water-soluble prodrug of YHO-13177, which is a potent and specific inhibitor of BCRP.
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NF-κB inhibitor
DMAPT (Dimethylamino Parthenolide), a water soluble analogue of Parthenolide (PTL), is an oral active NF-κB inhibitor, with a LD50 of 1.7 μM for cell population in AML cells. Has potential anti-cancer and anti-metastatic effect.
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Hsp90 inhibitor
Retaspimycin is a potent and water-soluble inhibitor of Hsp90, with EC50s of 119 nM for both Hsp90 and Grp9.
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IRE1α inhibitor
MKC3946 is a potent and soluble IRE1α inhibitor, used for cancer research.
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