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T63708Calpain-2-IN-1；化合物 Calpain-2-IN-1Calpain-2-IN-1
Calpain-2-IN-1 is a selective calpain-2 inhibitor that prolongs ERK activation and thus enhances learning and memory.
价 格：￥电议型 号：T63708产 地：中国大陆
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T63702Cap-dependent endonuclease-IN-21；化合物 Cap-dependent endonuclease-IN-21Cap-dependent endonuclease-IN-2
Cap-dependent endonuclease-IN-21 is a potent inhibitor of cap-dependent nucleic acid endonucleases (CEN) and has inhibitory effects on influenza virus replication. cap-dependent endonuclease-IN-21 has shown research potential against influenza virus infection (influenza A).
价 格：￥电议型 号：T63702产 地：中国大陆
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T63680Cap-dependent endonuclease-IN-11；化合物 Cap-dependent endonuclease-IN-11Cap-dependent endonuclease-IN-1
Cap-dependent endonuclease-IN-11 is a potent inhibitor of cap-dependent nucleic acid endonucleases (CEN). cap-dependent endonuclease-IN-11 has shown research potential for viral infections.
价 格：￥电议型 号：T63680产 地：中国大陆
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T63656c-Met-IN-11；化合物 c-Met-IN-11c-Met-IN-11
c-Met-IN-11 is a potent inhibitor of c-MET (IC50: 41.4 nM) and VEGFR-2 (IC50: 71.1 nM).
价 格：￥电议型 号：T63656产 地：中国大陆
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T63642CQ211；化合物CQ211CQ211
CQ211 is a potent and selective RIOK2 inhibitor with a Kd of 6.1 nM.CQ211 has shown potent proliferation inhibitory activity against various cancer cell lines in vitro.
价 格：￥电议型 号：T63642产 地：中国大陆
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T63496CYP2C9/CYP2C19-IN-1；化合物 CYP2C9/CYP2C19-IN-1CYP2C9/CYP2C19-IN-1
CYP2C9/CYP2C19-IN-1 is a potent inhibitor of CYP2C9/CYP2C19 without liver toxicity or genotoxicity and can be used to study Zika virus (ZIKV) infection.
价 格：￥电议型 号：T63496产 地：中国大陆
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T63479Caspase-3-IN-1；化合物 Caspase-3-IN-1Caspase-3-IN-1
Caspase-3-IN-1 is a potent inhibitor of Caspase-3 (IC50: 14.5 nM).
价 格：￥电议型 号：T63479产 地：中国大陆
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T63398COX-2/sEH-IN-1；化合物 COX-2/sEH-IN-1COX-2/sEH-IN-1
COX-2/sEH-IN-1 is an orally active dual inhibitor of COX-2 (IC50: 1.24 μM) and sEH (IC50: 0.40 μM), a soluble epoxide hydrolase. COX-2/sEH-IN-1 increases anti-inflammatory effects and significantly reduces cardiovascular risk.
价 格：￥电议型 号：T63398产 地：中国大陆
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T63353Chitin synthase inhibitor 11；化合物 Chitin synthase inhibitor 11Chitin synthase inhibitor 11
Chitin synthase inhibitor 11 is a potent chitin synthase (CHS) inhibitor that significantly inhibits CHS activity (IC50: 0.10 mM) and has broad-spectrum in vitro fungal inhibition.
价 格：￥电议型 号：T63353产 地：中国大陆
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T63347ChemR23-IN-1；化合物 ChemR23-IN-1ChemR23-IN-1
ChemR23-IN-1 is a ChemR23 inhibitor that acts on human and mouse ChemR23 with IC50 values of 38 nM and 100 nM, respectively. chemR23-IN-1 is able to block Chemerin-triggered CAL-1 chemotaxis in vitro.
价 格：￥电议型 号：T63347产 地：中国大陆
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T63337CYP2C19-IN-1；化合物 CYP2C19-IN-1CYP2C19-IN-1
CYP2C19-IN-1 is a potent, non-genotoxic, non-hepatotoxic inhibitor of CYP2C19. CYP2C19-IN-1 inhibits RNA-dependent RNA polymerase (RdRP) (Ki: 6.16 μM) and can be used to study Zika virus (ZIKV) infection.
价 格：￥电议型 号：T63337产 地：中国大陆
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T63186Cav 3.2 inhibitor 1；化合物 Cav 3.2 inhibitor 1Cav 3.2 inhibitor 1
Cav 3.2 inhibitor 1 is a T-type calcium channel inhibitor with low binding affinity for the dopamine receptor (D2 receptor.) Cav 3.2 inhibitor 1 can be used in studies of physical and visceral pain.
价 格：￥电议型 号：T63186产 地：中国大陆
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T63071CDK6/PIM1-IN-1；化合物 CDK6/PIM1-IN-1CDK6/PIM1-IN-1
CDK6/PIM1-IN-1 is a balanced, potent, dual CDK6 (IC50: 39 nM) and PIM1 (IC50: 88 nM) inhibitor. CDK6/PIM1-IN-1 showed inhibitory effect on CDK4 with IC50 value of 3.6 nM. CDK6/PIM1-IN-1 can significantly inhibit the proliferation of acute myeloid leukemia (AML) cells, arrest the cell cycle in G1 phase and induce cell apoptosis. CDK6/PIM1-IN-1 showed anti-AML activity.
价 格：￥电议型 号：T63071产 地：中国大陆
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T63059CRK12-IN-1；化合物CRK12-IN-1CRK12-IN-1
CRK12-IN-1 is a potent CRK12 inhibitor.CRK12-IN-1 has insecticidal activity, with inhibitory effects on Trypanosoma brucei (T.b. brucei) and Trypanosoma congolense (T. congolense) with EC50s of 1.3 and 18 nM, respectively.CRK12-IN-1 kills the pathogenic cells rapidly.
价 格：￥电议型 号：T63059产 地：中国大陆
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T63049CHD1Li 6.11；化合物CHD1Li 6.11CHD1Li 6.11
CHD1Li 6.11 is a potent inhibitor of oncogenic CHD1L, acting on the cat-CHD1L recombinant protein (IC50: 3.3 μM). CHD1Li 6.11 is an orally active antitumour agent that significantly reduces the tumour volume of CRC xenografts generated from isolated quasi-mesenchymal cells (M phenotype) with enhanced tumourigenic properties. These cells have enhanced tumourigenic properties.
价 格：￥电议型 号：T63049产 地：中国大陆
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T63005Carbonic anhydrase inhibitor 11；化合物 Carbonic anhydrase inhibitor 11Carbonic anhydrase inhibitor 11
Carbonic anhydrase inhibitor 11 (compound VI) is a potent, selective carbonic anhydrase inhibitor that acts on CA II (Ki: 40 nM), CA IX (Ki: 39 nM) and CA XII (Ki: 900 nM).
价 格：￥电议型 号：T63005产 地：中国大陆
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T62998COX-2/15-LOX-IN-1；化合物 COX-2/15-LOX-IN-1COX-2/15-LOX-IN-1
COX-2/15-LOX-IN-1 (Compound 14) is a COX-2 and 15-lipoxygenase (15-LOX) inhibitor that acts on COX-1 (IC50: 10.65 μM), COX-2 (IC50: 0.075 μM) and 15-LOX (IC50: 2.98 μM). 25 has an anti-inflammatory effect.
价 格：￥电议型 号：T62998产 地：中国大陆
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T62970CDK1-IN-1；化合物 CDK1-IN-1CDK1-IN-1
CDK1-IN-7 is a potent inhibitor of CDK1 with an IC50 value of 161.2 nM for CDK1/CycB. CDK1-IN-7 induces apoptosis in a p53-dependent manner via the apoptosis-intrinsic pathway. CDK1-IN-7 selectively acts on tumour tissue and has potential anti-proliferative effects. CDK1-IN-7 is a potential CDK1-IN-7 is a potential targeted anti-tumour agent.
价 格：￥电议型 号：T62970产 地：中国大陆
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T62926CDK7/12-IN-1；化合物 CDK7/12-IN-1CDK7/12-IN-1
CDK7/12-IN-1 is a selective inhibitor of CDK7/12, acting on CDK7 (IC50: 3 nM) and CDK 12 (IC50: 277 nM). Inhibition of CDK7 and CDK12 is an effective inhibitor of tumour growth.
价 格：￥电议型 号：T62926产 地：中国大陆
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T62761CB1 agonist 1；CB1激动剂1CB1 agonist 1
CB1 agonist 1 is a potent CB1 agonist with a pIC50 value of 5.7 for CB1 receptors.CB1 agonist 1 can be used to study brain disorders, pain, and inflammation.
价 格：￥电议型 号：T62761产 地：中国大陆
