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T2448CH-223191CH 223191
CH-223191 is a potent and specific antagonist for aryl hydrocarbon receptor (AhR).
价 格：￥电议型 号：T2448产 地：中国大陆
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T2310CHIR-99021CHIR 99021；CHIR99021；CT99021；CHIR-99021
CHIR-99021 is a GSK-3α/β inhibitor (IC50: 10/6.7 nM).
价 格：￥电议型 号：T2310产 地：中国大陆
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T22698TLR3-IN-1CU CPT 4a
CU CPT 4a is a selective TLR3 inhibitor (IC50: 3.44 μM in RAW 264.7 cells). It can inhibit TLR3/dsRNA complex-mediated downstream signaling pathways and inhibit the production of TNF-α and IL-1β in whole cells.
价 格：￥电议型 号：T22698产 地：中国大陆
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T22661CHM-1CHM 1
CHM-1 is an inducer of apoptosis, and displays potent antitumor ability in human hepatocellular carcinoma by activation of Cdc2 kinase activity. CHM-1 inhibits tubulin polymerization in vitro and in vivo.
价 格：￥电议型 号：T22661产 地：中国大陆
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T22349JNJ-38158471CS-2660
CS-2660, a highly selective, orally available, well tolerated VEGFR2 inhibitor with IC50 of 40 nM, inhibits closely related tyrosine kinases such as Ret and Kit with IC50 of 180 nM and 500 nM.
价 格：￥电议型 号：T22349产 地：中国大陆
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T22142RO8191CDM-3008；RO4948191
RO8191 (CDM-3008), an imidazonaphthyridine compound, is an agonist of interferon (IFN) receptor.
价 格：￥电议型 号：T22142产 地：中国大陆
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T2194Direct Blue 1Chicago Sky Blue 6B；Pontamine sky blue；滂胺天蓝
Chicago sky blue 6B, a vesicular glutamate transporters inhibitor, attenuates methamphetamine-induced hyperactivity and behavioral sensitization in mice.
价 格：￥电议型 号：T2194产 地：中国大陆
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T2100CX-5461CX5461
CX-5461, a selective inhibitor of rRNA synthesis, suppresses Pol I-driven transcription of rRNA.
价 格：￥电议型 号：T2100产 地：中国大陆
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T15609JC-1CBIC2
JC-1 is a fluorescent lipophilic carbocyanine dye. It has been used to measure mitochondrial membrane potential. JC 1 can be used in a probe for measuring mitochondrial membrane potential by flow cytometry.
价 格：￥电议型 号：T15609产 地：中国大陆
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T15418GS-6201CVT-6883
GS-6201 is a selective antagonist of adenosine A2B receptor. GS-6201 shows high affinity and selectivity for the human adenosine A2B receptors with a Ki of 22 nM.
价 格：￥电议型 号：T15418产 地：中国大陆
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T14991CMS-121CMS121
CMS-121, a quinolone derivative, is an orally active acetyl-CoA carboxylase 1 (ACC1) inhibitor. CMS-121 protects HT22 cells against ischemia and oxidative damage (EC50: 7 nM and 200 nM). CMS-121 shows strong neuroprotective, antioxidative, anti-inflammato
价 格：￥电议型 号：T14991产 地：中国大陆
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T14151AKR1C1-IN-1
AKR1C1-IN-1 is a human 20α-hydroxysteroid dehydrogenase (AKR1C1) inhibitor (Ki: 4 nM for AKR1C1).
价 格：￥电议型 号：T14151产 地：中国大陆
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T1092Zolmitriptan311C90；BW-311C90；佐米曲普坦
Zolmitriptan selectively binds to and activates serotonin (5-HT) 1B receptors expressed in intracranial arteries and 5-HT 1D receptors located on peripheral trigeminal sensory nerve terminals in the meninges and central terminals in brainstem sensory nucl
价 格：￥电议型 号：T1092产 地：中国大陆
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T10643c-Fms-IN-1c-Fms-IN-1
c-Fms-IN-1 is an inhibitor of FMS kinase (IC50: 0.0008 μM).
价 格：￥电议型 号：T10643产 地：美洲
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T10655c-Met inhibitor 1c-Met inhibitor 1
c-Met inhibitor 1 is a c-Met receptor signaling pathway inhibitor, used for the treatment of cancer including glioblastoma, gastric, and pancreatic cancer.
价 格：￥电议型 号：T10655产 地：美洲
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T10659Ca2+ 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：美洲
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T10682LCARM1-IN-1CARM1-IN-1
CARM1-IN-1 is a potent and specific CARM1(Coactivator-associated arginine methyltransferase 1) inhibitor (IC50: 8.6 uM). It shows very low activity against PRMT1 and SET7(IC50 > 600 uM).
价 格：￥电议型 号：T10682L产 地：美洲
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T10690Cav 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：美洲
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T10695CB1151CB1151
CB1151 is a 20-epi analogue of 1,25 dihydroxyvitamin D3 with anti-tumor effects. It inhibits MCF-7 cell growth (IC50: 0.82 nM).
价 格：￥电议型 号：T10695产 地：美洲
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T10716CCR7 Ligand 1CCR7 Ligand 1,CCR7-Cmp2105,
CCR7 Ligand 1 (CCR7-Cmp2105) is an allosteric Ligand and antagonist for human CC chemokine receptor 7 (CCR7) with a Kd of 3 nM. CCR7 Ligand 1, thiadiazole-dioxide ligan, suppresses arrestin binding in response to activation by CCL19 with an IC50 of 7.3 μM
价 格：￥电议型 号：T10716产 地：美洲
