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T61068AMPA receptor antagonist-2；AMPA受体拮抗剂2AMPA receptor antagonist-2
AMPA receptor antagonist-2 is an AMPA receptor antagonist.
价 格：￥电议型 号：T61068产 地：中国大陆
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T61064nAChR antagonist 1；化合物 nAChR antagonist 1nAChR antagonist 1
nAChR antagonist 1 (compound B15) is a highly effective antagonist of α7 nAChR, demonstrating an IC50 value of 3.3 μM. Its versatility makes it an ideal candidate for investigating the pathogenesis of schizophrenia, Alzheimer´s disease, and inflammatory disorders [1].
价 格：￥电议型 号：T61064产 地：中国大陆
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T61026CaV1.3 antagonist-1；化合物 CaV1.3 antagonist-1CaV1.3 antagonist-1
CaV1.3 antagonist-1 is a cyclopentyl derivative with the potential for the research of Parkinson´s disease. CaV1.3 antagonist-1 inhibits Ca V 1.3 LTCC over 600-fold more effectively than Ca V 1.2 LTCC. CaV1.3 antagonist-1 is a potent and highly selective antagonist of Ca V 1.3 L-type calcium channel (LTCC) with an IC50 value of 1.7 μM [1].
价 格：￥电议型 号：T61026产 地：中国大陆
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T60988Androgen receptor antagonist 4；化合物 Androgen receptor antagonist 4Androgen receptor antagonist 4
Androgen receptor antagonist 4 (Compound AT2) has anticancer activities. Androgen receptor antagonist 4 potently antagonizes the activity of AR transcriptional, inhibits downstream target gene of AR, and blocks the DHT-induced nuclear translocation of AR. Androgen receptor antagonist 4 is an antagonist of androgen receptor (AR) (IC 50 = 0.15 μM) [1].
价 格：￥电议型 号：T60988产 地：中国大陆
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T60987Androgen receptor antagonist 3；化合物 Androgen receptor antagonist 3Androgen receptor antagonist 3
Androgen receptor antagonist 3 (Compound C18) has anticancer activities that is an antagonist of androgen receptor (AR) (IC 50 = 2.4 μM) [1].
价 格：￥电议型 号：T60987产 地：中国大陆
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T60917Dopamine D4 receptor antagonist-1；化合物 Dopamine D4 receptor antagonist-1Dopamine D4 receptor antagoni
Dopamine D4 receptor antagonist-1 can be used in schizophrenia study. Dopamine D4 receptor antagonist-1 is a selective antagonist of Dopamine D4 receptor (DRD4). The Ki value of Dopamine D4 receptor antagonist-1 for Hd4.2 is 9.0 nM [1].
价 格：￥电议型 号：T60917产 地：中国大陆
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T60915A1AR antagonist 5；化合物 A1AR antagonist 5A1AR antagonist 5
A1AR antagonist 5 (compound 20) is a potent and selective antagonist of A1 adenosine receptor (A1AR) with a pKi of 6.11 and a pIC 50 of 5.83 [1].
价 格：￥电议型 号：T60915产 地：中国大陆
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T60872Adenosine receptor antagonist 3；化合物 Adenosine receptor antagonist 3Adenosine receptor antagonist 3
Adenosine receptor antagonist 3 has the potential for cancer disease research which is a potent adenosine receptor antagonist [1].
价 格：￥电议型 号：T60872产 地：中国大陆
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T60840EP4 receptor antagonist 4；化合物 EP4 receptor antagonist 4EP4 receptor antagonist 4
EP4 receptor antagonist 4 is an agonist of EP4 receptor (human pEC 50 = 6.3) [1].
价 格：￥电议型 号：T60840产 地：中国大陆
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T60811CXCR4 antagonist 7；化合物 CXCR4 antagonist 7CXCR4 antagonist 7
CXCR4 antagonist 7 (Compound PARA-B) is able to be used in the HIV infection, inflammatory diseases, cancer, and WHIM syndrome research which is a antagonist of CXCR4 (IC 50 = 9.3 nM) [1].
价 格：￥电议型 号：T60811产 地：中国大陆
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T60792NMDA receptor antagonist-3；化合物 NMDA receptor antagonist-3NMDA receptor antagonist-3
NMDA receptor antagonist-3 is a NMDA receptor antagonist with a significan recovery rate (40.0%, at 100 μM) and safe toxicological characteristics in SH-SY5Y and human adipose mesenchymal stem cells.
价 格：￥电议型 号：T60792产 地：中国大陆
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T607905-HT7R antagonist 1；化合物 5-HT7R antagonist 15-HT7R antagonist 1
5-HT7R antagonist 1 is a G protein-biased antagonist with Ki of 6.5 nM for 5-HT 7R.
价 格：￥电议型 号：T60790产 地：中国大陆
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T60756NLRP3 antagonist 1；化合物 NLRP3 antagonist 1NLRP3 antagonist 1
NLRP3 antagonist 1 shows potential for the cancer research that is a potent NLRP3 antagonist. NLRP3 is involved in the body´s intrinsic immunity against stress injury and pathogenic infections that is mainly expressed in macrophages and neutrophils [1].
价 格：￥电议型 号：T60756产 地：中国大陆
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T60732A2A/A1 AR antagonist-1；化合物 A2A/A1?AR antagonist-1A2A/A1 AR antagonist-1
A2A/A1 AR antagonist-1 (compound 1a) has the potential for ischemic stroke research which is potent A 2A /A 1 AR dual antagonist with Ki s of 5.58 and 24.2 nM, respectively [1].
价 格：￥电议型 号：T60732产 地：中国大陆
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T60719AR antagonist 3；化合物 AR antagonist 3AR antagonist 3
When administered intratumorally, AR antagonist 3 shows effective inhibition on the growth of tumor. AR antagonist 3 is a potent and selective antagonist of androgen receptor (AR) with an IC 50 of 0.47 μM. AR antagonist 3 dose-dependently decrease the FRET signal with an IC50 of 18.05 μM [1].
价 格：￥电议型 号：T60719产 地：中国大陆
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T60696CXCR2 antagonist 8；化合物 CXCR2 antagonist 8CXCR2 antagonist 8
CXCR2 antagonist 8 is a potent and selective antagonist of CXCR2 that can be used for the researching of insulin resistance [1].
价 格：￥电议型 号：T60696产 地：中国大陆
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T60687A1AR antagonist 1；化合物 A1AR?antagonist 1A1AR antagonist 1
A1AR antagonist 1 (compound 18g) is a potent antagonist of A1 adenosine receptor (AR). A1AR antagonist 1 has Ki values of 2.08, 6.91, and 31.2 nM for hA1, hA2A and hA2B, respectively [1].
价 格：￥电议型 号：T60687产 地：中国大陆
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T60615A1AR antagonist 6；化合物 A1AR antagonist 6A1AR antagonist 6
A1AR antagonist 6 (compound 15) is a potent and selective antagonist of A1 adenosine receptor(A1AR) with a pKi of 7.13 and a pIC 50 of 6.38[1].
价 格：￥电议型 号：T60615产 地：中国大陆
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T60591A2AAR antagonist 1；化合物 A2AAR antagonist 1A2AAR antagonist 1
A2AAR antagonist 1 (compound 21a) is an antagonist of A2AAR (adenosine A2A receptor) that shows high ligand efficiency with a Ki value of 20 nM. A2AAR antagonist 1 can be used in neurodegenerative disease research [1].
价 格：￥电议型 号：T60591产 地：中国大陆
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T60580A1AR antagonist 2；化合物 A1AR antagonist 2A1AR antagonist 2
A1AR antagonist 2 (compound 18h) is a potent antagonist of the A1 adenosine receptor (AR). A1AR antagonist 2 has Ki values of 1.49, 10.2, and 50.1 nM for hA 1, hA 2A, and hA 2B, respectively [1].
价 格：￥电议型 号：T60580产 地：中国大陆
