“soluble guanylyl cyclase sgc”的搜索结果
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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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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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soluble adenylyl cyclase inhibitor
LRE1 is a specific and allosteric inhibitor of soluble adenylyl cyclase.
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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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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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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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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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s-EH inhibitor
AR9281 is a potent and selective inhibitor of soluble epoxide hydrolase (s-EH), with potential for the treatment of hypertension and type 2 diabetes.
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GARFT inhibitor
Pelitrexol is a GARFT inhibitor, and is also a water soluble antifolate with anti-proliferative activity.
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AC1 inhibitor
NB001 (HTS 09836) is an adenylcyclase 1 (AC1) inhibitor which has effect on neural and non-neural pain by modulating AC1 activity.
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CARM1 inhibitor
SGC2085 is a potent and selective coactivator associated arginine methyltransferase 1 (CARM1) inhibitor with an IC50 of 50 nM.
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