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T13568LBCX 1470 hydrochloride；BCX 1470 盐酸盐BCX 1470 hydrochloride(217099-43-9 Free base)|||BCX1470 HCl；BCX 1
BCX 1470 hydrochloride is a potent serine protease inhibitor with anti-inflammatory activity that inhibits the ester hydrolysis and haemolytic activity of factor D and C1s, and can be used to study oedema.
价 格：￥电议型 号：T13568L产 地：中国大陆
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T13568BCX 1470；化合物 T13568BCX 1470
BCX 1470 inhibits the esterolytic activity of factor D and C1s (IC50: 96 nM and 1.6 nM), 3.4- and 200-fold better than that of trypsin, respectively.
价 格：￥电议型 号：T13568产 地：中国大陆
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T13567BCX 1470 methanesulfonate化合物 T13567BCX 1470 methanesulfonate
BCX 1470 methanesulfonate inhibits the esterolytic activity of factor D and C1s (IC50: 96 nM and 1.6 nM), 3.4- and 200-fold better than that of trypsin, respectively.
价 格：￥电议型 号：T13567产 地：中国大陆
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T13566Bamirastine；巴麦斯汀TAK-427；TAK-427
Bamirastine inhibits ligand binding to recombinant human histamine H1 receptor (rhH1R) with an IC50 value of 17.3 nM.Bamirastine has an inhibitory effect on allergic skin inflammation.
价 格：￥电议型 号：T13566产 地：中国大陆
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T13564L2AZ7550 trimesylate salt；AZ7550甲磺酸盐AZ7550 Mesylate|||AZ7550 trimesylate salt (1421373-99-0 free base)
AZ7550 trimesylate salt (AZ7550 Mesylate) is the active metabolite of ositinib, AZ7550 trimesylate salt inhibits IGF1R activity and can be used in the study of non-small cell lung cancer.
价 格：￥电议型 号：T13564L2产 地：中国大陆
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T13564LAZ7550 hydrochloride；化合物AZ7550 hydrochlorideAZ7550 hydrochloride (1421373-99-0 free base)；AZ7550 hyd
AZ7550 hydrochloride (AZ7550 hydrochloride ), an active metabolite of AZD9291, inhibits the activity of IGF1R (IC50: 1.6 μM).
价 格：￥电议型 号：T13564L产 地：中国大陆
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T13564AZ7550；化合物AZ7550AZ7550
AZ7550, an active metabolite of AZD9291, inhibits the activity of IGF1R (IC50: 1.6 μM).
价 格：￥电议型 号：T13564产 地：中国大陆
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T13563AZ-1355；化合物AZ-1355AZ-1355
AZ-1355 is a novel dibenzoxepine derivative with lipid-lowering properties.
价 格：￥电议型 号：T13563产 地：中国大陆
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T13562Atorvastatin methyl ester；化合物 T13562Atorvastatin methyl ester
Atorvastatin methyl ester is a derivative of Atorvastatin. It inhibits the 9-cis-RA-induced Gal4 reporter activity more strongly than Atorvastatin.
价 格：￥电议型 号：T13562产 地：中国大陆
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T13561AT6；化合物 T13561AT6
AT6 is a PROTAC AT1 analog which is a highly selective bromodomain (Brd4) degrader.
价 格：￥电议型 号：T13561产 地：中国大陆
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T13560LAT-1002 TFA (835872-35-0 free base)；化合物 T13560LAT-1002 TFA；AT-1002 TFA
AT-1002 TFA is a tight junction regulator and absorption enhancer. It is a 6-mer synthetic peptide.
价 格：￥电议型 号：T13560L产 地：中国大陆
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T13560AT-1002；化合物 T13560AT-1002
AT-1002 is a tight junction regulator and absorption enhancer. It is a 6-mer synthetic peptide.
价 格：￥电议型 号：T13560产 地：中国大陆
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T13564-Hydroxy-3-methoxybenzylamine hydrochloride；香兰素胺盐酸盐N-Vanillylamine hydrochloride；香兰素胺盐酸盐|||N-Vanill
4-Hydroxy-3-methoxybenzylamine hydrochloride (N-Vanillylamine hydrochloride) is an alkaloid that is an intermediate in the biosynthesis of capsaicin. 4-Hydroxy-3-methoxybenzylamine hydrochloride is produced from vanillin by the enzyme vanillin aminotransferase.
价 格：￥电议型 号：T1356产 地：中国大陆
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T13556Ascr#3；化合物 T13556Ascr#3
Ascr#3, an ascaroside isolated from Caenorhabditis elegans, acts as a potent male attractant, and also promotes dauer formation combined with ascr#2 at low concentration.
价 格：￥电议型 号：T13556产 地：中国大陆
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T13471(±)-WS75624B；化合物 T13471(±)-WS75624B
(±)-WS75624B is a potent ECE inhibitor (IC50:0.03 μg/mL), a serotonin receptor agonist.
价 格：￥电议型 号：T13471产 地：中国大陆
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T13456(S)-Willardiine；尿嘧啶基丙氨酸(-)-Willardiine|||L-willardiine|||Willardiine；(-)-Willardiine|||L-willardiine
(S)-Willardiine (L-willardiine) is present in the seeds of Acacia and Mimosa. (S)-Willardiine is an AMPA/kainate receptor agonist (EC50 = 44.8 μM).
价 格：￥电议型 号：T13456产 地：中国大陆
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T13423L(1S,2R)-2-PCCA；化合物(1S,2R)-2-PCCA(1S,2R)-2-PCCA（Iso-1609563-71-4）；(1S,2R)-2-PCCA（Iso-1609563-71-4）
(1S,2R)-2-PCCA is a novel and potent small molecule GPR88 receptor agonist with an EC50 value of 3 nM in the non-cellular system and 603 nM in the cellular system.
价 格：￥电议型 号：T13423L产 地：中国大陆
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T13414ZT 52656A hydrochloride；化合物ZT 52656A hydrochlorideZT 52656A hydrochloride
ZT 52656A is a selective agonist of kappa opioid, and used for the prevention or alleviation of pain in the eye.
价 格：￥电议型 号：T13414产 地：中国大陆
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T13356XEN723；化合物XEN723XEN723
XEN723 is a potent thiazolylimidazolidinone Stearoyl-CoA Desaturase (SCD1) inhibitor(IC50s of 45 and 524 nM in mouse and HepG2 cell, respectively).
价 格：￥电议型 号：T13356产 地：中国大陆
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T13321VU6005649；化合物VU6005649VU6005649
VU6005649 is an agonist of CNS penetrant mGlu7/8 receptor (EC50s: 0.65 μM and 2.6 μM for mGlu7 receptor and mGlu8 receptor, respectively).
价 格：￥电议型 号：T13321产 地：中国大陆
