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T13715GSK9311 hydrochloride；化合物 T13715GSK9311 hydrochloride
GSK9311 hydrochloride, a less active analog of GSK6853, can be used as a negative control. GSK9311 hydrochloride inhibits BRPF bromodomain (pIC50s: 6.0 and 4.3 for BRPF1 and BRPF2).
价 格：￥电议型 号：T13715产 地：中国大陆
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T13705GLPG2451；化合物 T13705GLPG2451
GLPG2451 is a cystic fibrosis transmembrane conductance regulator (CFTR) potentiator. It effectively potentiates low temperature rescued F508del CFTR (EC50: 11.1 nM).
价 格：￥电议型 号：T13705产 地：中国大陆
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T125608Gypenoside GD5；化合物 Gypenoside GD5Gypenoside GD5
Gypenoside GD5 is a useful organic compound for research related to life sciences. The catalog number is T125608 and the CAS number is 1704440-94-7.
价 格：￥电议型 号：T125608产 地：中国大陆
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T11525GW311616；化合物 T11525GW311616
GW-311616 is a long duration, orally bioavailable, and selective human neutrophil elastase (HNE) inhibitor (IC50: 22 nM; Ki: 0.31 nM).
价 格：￥电议型 号：T11525产 地：中国大陆
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T11495GSK4028；化合物 T11495GSK4028
GSK4028 is the enantiomeric negative control of GSK4027, which is a PCAF/GCN5 bromodomain chemical probe. The pIC50 of GSK4028 is 4.9 in a TR-FRET assay.
价 格：￥电议型 号：T11495产 地：中国大陆
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T11475GSK-J1 lithium salt化合物 T11475GSKJ1 lithium salt|||GSK J1 lithium salt|||GSK-J-1 lithium salt
GSK-J1 lithium salt is an effective inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A, with an IC 50 of 60 nM for KDM6B.
价 格：￥电议型 号：T11475产 地：中国大陆
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T11455GPR35 agonist 1；化合物 T11455GPR35 agonist 1
GPR35 agonist 1 is a highly effective and specific GPR35/CXCR8 agonist (EC50: 5.8 nM).
价 格：￥电议型 号：T11455产 地：中国大陆
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T11445GNF179 (Metabolite)；化合物 T11445GNF179 Metabolite；GNF179 Metabolite
GNF179 Metabolite, the derivative of GNF179—an optimized 8,8-dimethyl IP analog—demonstrates significant potency (4.8 nM against the multidrug-resistant W2 strain) alongside in vitro metabolic stability and in vivo oral bioavailability.
价 格：￥电议型 号：T11445产 地：中国大陆
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T11435GlyT1 Inhibitor 1；化合物 T11435GlyT1 Inhibitor 1
GlyT1 Inhibitor 1 is a potent and selective GlyT1 inhibitor (IC50: 38 nM for rGlyT1) with antipsychotic activity.
价 格：￥电议型 号：T11435产 地：中国大陆
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T11425Glutaminyl Cyclase Inhibitor 2；化合物 T11425Glutaminyl Cyclase Inhibitor 2
Glutaminyl Cyclase Inhibitor 2 is a glutaminyl cyclase inhibitor (IC50: 1.23 μM).
价 格：￥电议型 号：T11425产 地：中国大陆
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T11415Glucagon receptor antagonists-3；化合物 T11415Glucagon receptor antagonists-3
Glucagon receptor antagonist -3 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11415产 地：中国大陆
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T11411GLPG1205；化合物GLPG1205GLPG1205
GLPG1205 is a potent, orally active GPR84 (G protein-coupled receptor) antagonist with anti-inflammatory activity. GLPG1205 shows good PK/PD characteristics and can be used to study pulmonary fibrosis.
价 格：￥电议型 号：T11411产 地：中国大陆
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T11405GLP-1 receptor agonist 4；化合物 T11405GLP-1 receptor agonist 4
GLP-1 receptor agonist 4 is a glucagon-like peptide-1 receptor (GLP-1R) agonist , has an EC50 of 64.5 nM. GLP-1 receptor agonist 4 can be used in the research for treatment of diabetes.
价 格：￥电议型 号：T11405产 地：中国大陆
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T11395GF 15；化合物 T11395GF 15
GF 15 is a potent inhibitor of centrosomal clustering in tumor cells.
价 格：￥电议型 号：T11395产 地：中国大陆
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T11385Gefitinib N-oxide；化合物 T11385Gefitinib N-oxide
Gefitinib is an EGFR tyrosine kinase inhibitor, with IC50 of 2-37 nM in NR6wtEGFR cells. Gefitinib N-oxide is the N-oxide derivative of Gefitinib.
价 格：￥电议型 号：T11385产 地：中国大陆
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T11345Lerociclib；化合物 T11345G1T38；G1T38
Lerociclib (G1T38) is a potent and selective inhibitor of CDK4/6, with IC50s of 2nM, 1 nM for CDK6/CyclinD3 and CDK4/CyclinD1, respectively.
价 格：￥电议型 号：T11345产 地：中国大陆
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T11342LG-5555；化合物G-5555G-5555
G-5555 is a potent inhibitor of p21-activated kinase 1 (PAK1) (Kis: 3.7 nM and 11 nM for PAK1 and PAK2, respectively).
价 格：￥电议型 号：T11342L产 地：中国大陆
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T10909Cyclic-di-GMP；化合物 T10909c-di-GMP|||cyclic diguanylate|||5GP-5GP；c-di-GMP|||cyclic diguanylate|||5GP-
Cyclic-di-GMP is a STING agonist and ubiquitous second messenger, which regulates the formation, motility and virulence of biofilms in various bacterial species.
价 格：￥电议型 号：T10909产 地：中国大陆
