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T63581-Azakenpaullone；1-氮杂坎帕罗酮azakenpaullone；1-氮杂坎帕罗酮|||azakenpaullone
1-Azakenpaullone (azakenpaullone) is a potent and selective GSK-3β inhibitor with IC50 of 18 nM, >100-fold selectivity over CDK1/cyclin B and CDK5/p25.
价 格：￥电议型 号：T6358产 地：中国大陆
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T63579Kallikrein-IN-1；化合物 Kallikrein-IN-1Kallikrein-IN-1
Kallikrein-IN-1 (Formula A) is an inhibitor of the kinin-releasing enzyme Kallikrein.
价 格：￥电议型 号：T63579产 地：中国大陆
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T63578Mrgx2 antagonist-1；化合物 Mrgx2 antagonist-1Mrgx2 antagonist-1
Mrgx2 antagonist-1 is a potent antagonist of Mrgx2 (Mas-related Gene X2) and can be used to study Mrgx2-mediated diseases and disorders.
价 格：￥电议型 号：T63578产 地：中国大陆
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T63577KRAS G12D inhibitor 11；化合物 KRAS G12D inhibitor 11KRAS G12D inhibitor 11
KRAS G12D inhibitor 11 is a potent inhibitor of KRAS G12D. The Ras family of proteins are important intracellular signaling molecules that play an important role in growth and development, and KRAS G12D inhibitor 11 has shown potential for the investigation of KRAS G12D-mediated cancers.
价 格：￥电议型 号：T63577产 地：中国大陆
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T63575PF-8380 hydrochloride；化合物 PF-8380 hydrochloridePF-8380 hydrochloride
PF-8380 hydrochloride is a powerful inhibitor of autotaxin, exhibiting an IC(50) of 2.8 nM in isolated enzyme assays and 101 nM in human whole blood.
价 格：￥电议型 号：T63575产 地：中国大陆
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T63574α-Glucosidase-IN-12；化合物 α-Glucosidase-IN-12α-Glucosidase-IN-12
α-Glucosidase-IN-12 is a potent inhibitor of α-glucosidase (IC50: 10.20 μM).
价 格：￥电议型 号：T63574产 地：中国大陆
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T63573WF-47-JS03；化合物 WF-47-JS03WF-47-JS03
WF-47-JS03 is a selective and potent inhibitor of RET kinase that crosses the blood-brain barrier and is more than 500-fold more selective for the kinase insertion domain receptor (KDR).WF-47-JS03 acts on Ba/F3 cells transfected with KIF5B-RET (IC50: 1.7 nM) and LC-2/ad lung cancer cells transfected with CCDC6-RET (IC50: 5.3 nM). cells (IC50: 5.3 nM).
价 格：￥电议型 号：T63573产 地：中国大陆
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T63572Org 43553；化合物 Org 43553Org 43553
Org 43553 is an orally active low molecular weight (LMW) luteinizing hormone receptor (LH-R) agonist capable of agonizing human LH (EC50: 3.7 nM) and FSH receptors (EC50: 110 nM).Org 43553 can be used for endocrine studies.
价 格：￥电议型 号：T63572产 地：中国大陆
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T63571EGFR-IN-26；化合物 EGFR-IN-26EGFR-IN-26
EGFR-IN-26 is an EGFR inhibitor that can be used in cancer research.
价 格：￥电议型 号：T63571产 地：中国大陆
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T63570Heterophdoid A；化合物 Heterophdoid AHeterophdoid A
Heterophdoid A is an anti-inflammatory agent that inhibits NO production in BV-2 cells (IC50: 5.93 μM).
价 格：￥电议型 号：T63570产 地：中国大陆
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T6357(S)-crizotinib；化合物(S)-crizotinibent-crizotinib；ent-crizotinib
(S)-crizotinib (ent-crizotinib) （IC50 of 72 nM）, an effective MTH1 (NUDT1) inhibitor, is the (S)-enantiomer of crizotinib.
价 格：￥电议型 号：T6357产 地：中国大陆
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T63569HSD-016；化合物 HSD-016HSD-016
HSD-016 is an orally active, selective and potent type 1 11β-hydroxysteroid dehydrogenase (11β-HSD1) inhibitor with strong inhibitory effects on human, mouse and rat 11β-HSD1.HSD-016 can be used in the study of diabetes and metabolic syndrome.
价 格：￥电议型 号：T63569产 地：中国大陆
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T63568PLAP-IN-1；化合物 PLAP-IN-1PLAP-IN-1
PLAP-IN-1 is a potent and selective PLAP inhibitor with an IC50 value of 32 nM and no significant inhibitory effect on tissue non-specific alkaline phosphatase (TNAP) activity.
价 格：￥电议型 号：T63568产 地：中国大陆
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T63567HCV-IN-34；化合物 HCV-IN-34HCV-IN-34
HCV-IN-34 is an orally active HCV entry inhibitor. HCV-IN-35 exhibits good antiviral efficacy (EC50: 0.010 μM, CC50 (half of the maximum cytotoxic concentration): 7.50 μM).
价 格：￥电议型 号：T63567产 地：中国大陆
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T63566HCV-IN-33；化合物 HCV-IN-33HCV-IN-33
HCV-IN-33 (Compound (S)-3i) is an inhibitor of HCV entry.
价 格：￥电议型 号：T63566产 地：中国大陆
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T63565CBP/p300-IN-19 hydrochloride；化合物 CBP/p300-IN-19 hydrochlorideCBP/p300-IN-19 hydrochloride
CBP/p300-IN-19 hydrochloride is a selective and potent inhibitor of p300/CBP HAT, capable of acting on p300-HAT (IC50: 1.4 μM), CBP-HAT (IC50: 2.2 μM), PCAF (IC50>100 μM), Myst3 (IC50>100 μM). CBP/p300-IN-19 hydrochloride has antitumor effects.
价 格：￥电议型 号：T63565产 地：中国大陆
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T63564ATX inhibitor 22；化合物 ATX inhibitor 22ATX inhibitor 22
ATX inhibitor 22 is a novel inhibitor of ATX (autotaxin) (IC50: 218.9 μM) that lacks inhibitory activity against LPAR1.
价 格：￥电议型 号：T63564产 地：中国大陆
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T63563AN-12-H5；化合物 AN-12-H5AN-12-H5
AN-12-H5 is an anti-enteroviral compound that targets the replication process of PV and EV71 viruses.
价 格：￥电议型 号：T63563产 地：中国大陆
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T63562α-Glucosidase-IN-14；化合物 α-Glucosidase-IN-14α-Glucosidase-IN-14
α-Glucosidase-IN-14 is a potent inhibitor of α-glucosidase (IC50: 5.22 μM).
价 格：￥电议型 号：T63562产 地：中国大陆
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T63561PPARγ agonist 5；化合物 PPARγ agonist 5PPARγ agonist 5
PPARγ agonist 5 is a selective and potent PPARγ agonist that has shown research potential for cancer disease.
价 格：￥电议型 号：T63561产 地：中国大陆
