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T2421SKLB1002；化合物SKLB1002SKLB1002
SKLB1002 is a potent and ATP-competitive VEGFR2 inhibitor with IC50 of 32 nM.
价 格：￥电议型 号：T2421产 地：中国大陆
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T24100GR 122222X；化合物 T24100GR122222X|||GR-122222X；GR122222X|||GR-122222X
GR 122222X is an inhibitor of topoisomerase II.
价 格：￥电议型 号：T24100产 地：中国大陆
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T23973DDD100097；化合物DDD100097DDD 100097|||DDD-100097；DDD 100097|||DDD-100097
DDD100097 is a potent N-myristoyltransferase inhibitor with potential inhibitory effects on Trypanosoma brucei, which can be used to study neurological disorders.
价 格：￥电议型 号：T23973产 地：中国大陆
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T2395LVortioxetine hydrobromide；盐酸沃替西汀Vortioxetine (Lu AA21004) HBr|||Vortioxetine HBr|||Lu AA21004 hydrob
Vortioxetine hydrobromide (Lu AA21004 hydrobromide) is a serotonin (5-HT) modulator and stimulator (SMS), inhibits 5-HT1A/1B/3A/7 receptor and SERT (IC50: 15/33/3.7/19/1.6 nM).
价 格：￥电议型 号：T2395L产 地：中国大陆
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T2395Vortioxetine；沃替西汀Lu AA 21004；沃替西汀|||Lu AA 21004
Vortioxetine (Lu AA 21004) is a serotonergic antidepressant used for major depression disorders. Vortioxetine has been associated with a low rate of minor serum aminotransferase elevations during treatment.
价 格：￥电议型 号：T2395产 地：中国大陆
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T23945DA-11004；化合物 T23945DA11004|||UNII-48M66E9ER2；DA11004|||UNII-48M66E9ER2
DA-11004 is a potent NADP-dependent isocitrate dehydrogenase inhibitor (IC50: 1.49 μM for IDPc). DA-11004 inhibited fatty acid synthesis in adipose tissues via IDPc inhibition. It also decreased the plasma glucose levels and FFA in HF diet-induced obesity of C57BL/6J mice.
价 格：￥电议型 号：T23945产 地：中国大陆
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T23788BI1002494；化合物 T23788BI 1002494|||BI-1002494；BI 1002494|||BI-1002494
BI1002494 is an effective and selective Syk inhibitor.
价 格：￥电议型 号：T23788产 地：中国大陆
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T23768Azothoate；化合物 T23768Caswell No. 206A|||L 1058|||L-1058|||EPA Pesticide Chemical Code 206100|||L1058；
Azothoate is an insecticide agent.
价 格：￥电议型 号：T23768产 地：中国大陆
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T23676AHR-10037；化合物 T23676AHR-10037
AHR-10037 is a nonsteroidal anti-inflammatory drug with analgesic and antipyretic properties as well as a high therapeutic index and low gastric toxicity. AHR-10037 was comparable to indomethacin in suppressing acute (Evans blue-carrageenan pleural effusion) and chronic (adjuvant-induced arthritis) inflammation. Studies have shown that it is converted in vivo to a prodrug of cyclooxygenase inhibitors.
价 格：￥电议型 号：T23676产 地：中国大陆
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T23513VU10010；化合物VU 10010VU 10010；VU 10010
VU10010 (VU 10010) is allosteric potentiator of M4 acetylcholine receptors.
价 格：￥电议型 号：T23513产 地：中国大陆
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T23434GPR35 agonist 2；GPR35拮抗剂2TC-G 1001；TC-G 1001
GPR35 agonist 2 (TC-G 1001) is a potent GPR35 agonist.The EC50 values of GPR35 agonist 2 in the β-arrestin and Ca2+ release assays were 26 and 3.2 nM, respectively.
价 格：￥电议型 号：T23434产 地：中国大陆
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T23343SDZ 21009；化合物 T23343SDZ 21009
β-adrenoceptor and 5-HT1A/1B receptor antagonist
价 格：￥电议型 号：T23343产 地：中国大陆
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T23340SD 1008化合物 T23340SD 1008
SD 1008 is a JAK2/STAT3 signaling pathway inhibitor. SD 1008 inhibits activation of STAT3, JAK2, and Src.
价 格：￥电议型 号：T23340产 地：中国大陆
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T232832-Methoxyidazoxan monohydrochloride；化合物RX 821002 hydrochlorideRX 821002 hydrochloride；RX 821002 hydr
L-Albizziin (2-Methoxyidazoxan monohydrochloride) is a highly potent selective antagonist of the alpha 2r adrenergic receptor, with little or no antagonistic effect on imidazoline. It has a significantly higher affinity for the alpha 2D adrenergic receptor (pKd9.7) in guinea pigs than for the alpha 2A adrenergic receptor (pKd8.2) in rabbits.
价 格：￥电议型 号：T23283产 地：中国大陆
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T23253RS 100329 hydrochloride；化合物 RS 100329 hydrochlorideRS-100329；RS-100329
RS 100329 hydrochloride is an antagonist of α1A-adrenergic receptor.
价 格：￥电议型 号：T23253产 地：中国大陆
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T23073NNC 26-9100化合物 T23073NNC 269100|||NNC 26 9100
Somatostatin sst4 receptor agonist
价 格：￥电议型 号：T23073产 地：中国大陆
