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T10858COH34 analog 1；COH34类似物1COH34 analog 1
COH34 analog 1 is a COH34 oxidation analogue that can be used to synthesize active compounds.
价 格：￥电议型 号：T10858产 地：中国大陆
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T10853CNT2 inhibitor-1；化合物CNT2 抑制剂-1CNT2 inhibitor-1
CNT2 inhibitor-1 is a potent inhibitor of concentrative nucleoside transporter 2 (CNT2; IC50: 640 nM for hCNT2).
价 格：￥电议型 号：T10853产 地：中国大陆
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T10831Cl-amidine；化合物 T10831Cl-amidine
Cl-amidine is an orally active inhibitor of peptidyl arginine deminase (PAD) (IC50s: 0.8 μM, 6.2 μM, and 5.9 μM for PAD1, PAD3, and PAD4). Cl-amidine induces apoptosis in cancer cells.
价 格：￥电议型 号：T10831产 地：中国大陆
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T10821Cirsiliol；化合物 T10821Cirsiliol
Cirsiliol is a selective inhibitor of 5-lipoxygenase and a competitive low-affinity ligand of benzodiazepine receptors.
价 格：￥电议型 号：T10821产 地：中国大陆
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T10801CHMFL-ABL/KIT-155；化合物 T10801CHMFL-ABL-KIT-155；CHMFL-ABL-KIT-155
CHMFL-ABL/KIT-155 is a highly potent and orally active type II ABL/c-KIT dual kinase inhibitor (IC50s: 46 nM/75 nM). It arrests cell cycle progression and induces apoptosis.
价 格：￥电议型 号：T10801产 地：中国大陆
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T10771CETP-IN-3；化合物 T10771CETP-IN-3
CETP-IN-3 is an inhibitor of the plasma glycoprotein cholesterol ester transfer protein (CETP), elevating HDL-C through inhibition of CETP.
价 格：￥电议型 号：T10771产 地：中国大陆
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T10762Ceranib1；化合物Ceranib1Ceranib1
Ceranib1 is an inhibitor of ceramidase. It inhibits the proliferation of ovarian cancer cells. Ceranib1 inhibits ceramidase activity toward an exogenous ceramide analog, induces the accumulation of multiple ceramide species, decreases levels of S1P and sphingosine.
价 格：￥电议型 号：T10762产 地：中国大陆
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T10741CDK9-IN-1；化合物 T10741CDK9-IN-1
CDK9-IN-1 is a novel, selective CDK9 inhibitor for the treatment of HIV infection (IC50: 39 nM for CDK9/CycT1).
价 格：￥电议型 号：T10741产 地：中国大陆
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T10740CDK8-IN-1；化合物CDK8-IN-1CDK8-IN-1
CDK8-IN-1 is a selective CDK8 inhibitor (IC50: 3 nM).
价 格：￥电议型 号：T10740产 地：中国大陆
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T10731CDD0102；化合物 T10731CDD0102A；CDD0102A
CDD0102 is a potent agonist of M1 Muscarinic receptor.
价 格：￥电议型 号：T10731产 地：中国大陆
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T10730CDC801；化合物CDC801CDC-801；CDC-801
CDC801 is an inhibitor of PDE4 and TNF-α with IC50s of 1.1 μM and 2.5 μM, respectively.
价 格：￥电议型 号：T10730产 地：中国大陆
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T10721CD73-IN-1；CD73 抑制剂1CD73-IN-1
CD73-IN-1 is a CD73 inhibitor with anticancer activity.
价 格：￥电议型 号：T10721产 地：中国大陆
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T10717Inobrodib；化合物CBP-IN-1CBP-IN-1；CBP-IN-1
Inobrodib (CBP-IN-1) is a potent inhibitor of p300/CBP bromodomain.
价 格：￥电议型 号：T10717产 地：中国大陆
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T10715CCR6 inhibitor 1；化合物CCR6 inhibitor 1CCR6 inhibitor 1
CCR6 inhibitor 1 is an effective and selective inhibitor of CCR6 (IC50 of monkey and human CCR6 was 0.45 nM and 6 nM, respectively). CCR6 is associated with both autoimmune and non-autoimmune diseases, so CCR6 inhibitor 1 is useful for in vitro and in vivo pathophysiology studies as a small molecule inhibitor of CCR6.
价 格：￥电议型 号：T10715产 地：中国大陆
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T10711CCR2 antagonist 1；化合物 T10711CCR2 antagonist 1
CCR2 antagonist 1 is a high-affinity and long-residence-time antagonist of CCR2 (Ki: 2.4 nM).
价 格：￥电议型 号：T10711产 地：中国大陆
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T10696CB2 modulator 1；化合物CB2 modulator 1CB2 modulator 1
CB2 modulator 1 is a potent CB2 modulator. It can be used for the research for immune disorders, osteoporosis, inflammation, renal ischemia.
价 格：￥电议型 号：T10696产 地：中国大陆
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T10690Cav 2.2 blocker 1；化合物Cav 2.2 blocker 1Cav 2.2 blocker 1
Cav 2.2 blocker 1 is an N-type calcium channel (Cav 2.2; IC50: 1 nM) blocker for the treatment of pain.
价 格：￥电议型 号：T10690产 地：中国大陆
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T10682LCARM1-IN-1；化合物CARM1-IN-1CARM1-IN-7G；CARM1-IN-7G
CARM1-IN-1 (CARM1-IN-7G) is a selective inhibitor of CARM1 with IC50 of 8.6 μM. CARM1-IN-1 shows weak activity against PRMT1 and SET7 with IC50 > 600 μM.
价 格：￥电议型 号：T10682L产 地：中国大陆
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T10659Ca2+ channel agonist 1；化合物Ca2+ channel agonist 1Ca2+ channel agonist 1
Ca2+ channel agonist 1 is an agonist of N-type Ca2+ channel and an inhibitor of Cdk2 (EC50s: 14.23 μM and 3.34 μM) and is used as a potential treatment for motor nerve terminal dysfunction.
价 格：￥电议型 号：T10659产 地：中国大陆
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T10643c-Fms-IN-1；化合物c-Fms-IN-1c-Fms-IN-1
c-Fms-IN-1 is an inhibitor of c-FMS kinase (IC50 = 0.8 nM).
价 格：￥电议型 号：T10643产 地：中国大陆
