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T10333Antifungal agent 1；化合物 T10333Antifungal agent 1
Antifungal agent 1 is an effective antifungal agent.
价 格：￥电议型 号：T10333产 地：中国大陆
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T10331Anticancer agent 3；化合物 T10331Anticancer agent 3
Anticancer agent 3 (Compound 4) is a anti-cancer agent.
价 格：￥电议型 号：T10331产 地：中国大陆
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T10329anti-TB agent 1；化合物anti-TB agent 1anti-TB agent 1
anti-TB agent 1 is a potent and orally active anti-tuberculosis agent (MICs: < 2 nM against the Mtb strains H37Rv, rRMP and rINH).
价 格：￥电议型 号：T10329产 地：中国大陆
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T10328Anti-parasitic agent 3；化合物 T10328Anti-parasitic agent 3
Anti-parasitic agent 3 is an anti-parasitic agent active against drug-resistant parasites.
价 格：￥电议型 号：T10328产 地：中国大陆
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T10320Androgen receptor antagonist 1化合物 T10320Androgen receptor antagonist 1
Androgen receptor antagonist 1 is an orally available full androgen receptor antagonist (IC50: 59 nM). It can be used in the synthesis of PROTAC AR degraders, which results in 24% and 47 % AR protein degradation in LNCaP cells at 1 μM and 10 μM, respectively.
价 格：￥电议型 号：T10320产 地：中国大陆
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T10272AHR antagonist 5；化合物 T10272AHR antagonist 5
AHR antagonist 5 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist(example 39; IC50 < 0.5 μΜ). It significantly inhibits tumor growth combined with checkpoint inhibitor anti-PD-1.
价 格：￥电议型 号：T10272产 地：中国大陆
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T10271AHR antagonist 4；化合物 T10271AHR antagonist 4
AHR antagonist 4 is a potent aryl hydrocarbon receptor (AHR) antagonist(example 293; IC50: 82.2 nM).It has anti-cancer effects.
价 格：￥电议型 号：T10271产 地：中国大陆
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T10269AHR antagonist 2；AHR拮抗剂2AHR antagonist 2
AHR antagonist 2 is an antagonist of the aryl hydrocarbon receptor. The IC50s for human AHR and mouse AHR are 0.885 and 2.03 nM, respectively.
价 格：￥电议型 号：T10269产 地：中国大陆
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T10268AGX51；化合物AGX51AGX51
AGX51 is an antagonist of inhibitor of DNA binding (ID) proteins. AGX51 treatment lead to pan-Id degradation, cell cycle arrest, and cell death.
价 格：￥电议型 号：T10268产 地：中国大陆
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T10267Agomelatine (L(+)-Tartaric acid)；阿戈美拉汀 L(+)-酒石酸S-20098 L(+)-Tartaric acid；阿戈美拉汀 L(+)-酒石酸|||S-20098 L
Agomelatine (S-20098) L(+)-Tartaric acid is a specific agonist of MT1 and MT2 receptors (Kis: 0.1, 0.06, 0.12, and 0.27 nM for CHO-hMT1, HEK-hMT1, CHO-hMT2, and HEK-hMT2). It also is a selective 5-HT2C receptor antagonist (pKis: 6.4 and 6.2 at native (porcine) and cloned (human) 5-HT2C receptors).
价 格：￥电议型 号：T10267产 地：中国大陆
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T10266Agomelatine-d6；化合物 T10266Agomelatine D6|||S-20098 D6；Agomelatine D6|||S-20098 D6
Agomelatine D6 (S-20098 D6) is a deuterium-labeled Agomelatine. Agomelatine is a specific agonist of MT1 and MT2 receptors.
价 格：￥电议型 号：T10266产 地：中国大陆
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T10265AGN 194078；化合物 T10265AGN 194078
AGN 194078 is a selective RARα agonist (Kd: 3 nM; EC50: 112 nM).
价 格：￥电议型 号：T10265产 地：中国大陆
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T10264AGN 192836；化合物 T10264AGN 192836
AGN 192836 is a potent and selective α2 adrenergic agonist (EC50s: 8.7, 41 and 6.6 nM for α2A, α2B and α2C receptor).
价 格：￥电议型 号：T10264产 地：中国大陆
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T10263AGN 205728；化合物 T10263AGN 205728
AGN 205728 is a potent and selective RARγ antagonist (Ki: 3 nM; IC95: 0.6 nM) and has no inhibition on RARα and RARβ.
价 格：￥电议型 号：T10263产 地：中国大陆
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T10262AGN 205327；化合物 T10262AGN 205327
AGN 205327 is a potent synthetic RARs agonist with EC50 of 3766/734/32 nM for RARα/β/γ respectively without inhibition of RXR. IC50 value: 3766/734/32 nM for RARα/β/γ Target: RAR agonist
价 格：￥电议型 号：T10262产 地：中国大陆
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T10261AGN 196996；化合物AGN 196996AGN 196996
AGN 196996 is a potent and selective inhibitor of RARα (Ki: 2 nM).AGN 196996 has very low affinity for RARβ and RARγ, with a Ki of 1087 nM and 8523 nM, respectively.
价 格：￥电议型 号：T10261产 地：中国大陆
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T10260Aglafoline；化合物 T10260Rocaglamide U|||Aglafolin|||(-)-Methyl rocaglate；Rocaglamide U|||Aglafolin|||(-
Aglafoline inhibits in a concentration-dependent manner the aggregation and ATP release reaction induced in washed rabbit platelets by PAF (platelet-activating factor). The IC50 values of Aglafoline on PAF (3.6 nM)-induced platelet aggregation were about 50 μM.
价 格：￥电议型 号：T10260产 地：中国大陆
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T10259AGI-25696；化合物AGI-25696AGI-25696
AGI-25696 is an inhibitor of methionine adenosyltransferase 2A (MATA2). AGI-25696 blocks the growth of MTAP-deleted tumors in vivo and can be used for studies about the treatment of cancer.
价 格：￥电议型 号：T10259产 地：中国大陆
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T10250ADRA1D receptor antagonist 1 HCl；ADRA1D receptor antagonist 1 盐酸盐ADRA1D receptor antagonist 1 HCl（11
ADRA1D receptor antagonist 1 HCl is an orally active, potent and selective α1D adrenergic receptor antagonist (Ki: 1.6 nM) with potential antiproliferative activity.
价 格：￥电议型 号：T10250产 地：中国大陆
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T10248Adenosine antagonist-1；腺苷拮抗剂1Adenosine antagonist-1
Adenosine antagonist-1 acts as an adenosine A3 receptor (AA3R) antagonist.
价 格：￥电议型 号：T10248产 地：中国大陆
