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T15430GSK2256294AGSK 2256294
GSK2256294A is potent, selective inhibitor of recombinant human, rat and mouse sEH with IC50 of 27 pM, 61 pM and 189 pM, respectively.
价 格：￥电议型 号：T15430产 地：中国大陆
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T1543Naftifine hydrochloride盐酸萘替芬；Exoderil；Naftifungin；Naftin；Naftifine HCl
Naftifine Hydrochloride is the hydrochloride salt form of naftifine, an allylamine derivate with synthetic broad-spectrum antifungal activity. Although the exact mechanism through which naftifine hydrochloride exerts its effect is unknown, it appears to s
价 格：￥电议型 号：T1543产 地：中国大陆
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T15286FlindokalnerBMS-204352
Flindokalner is a potassium channel modulator and a positive modulator of all neuronal Kv7 channel subtypes expressed in HEK293 cells. Flindokalner is a large conductance calcium-activated K channel (BKca) positive modulator. Flindokalner displays a negat
价 格：￥电议型 号：T15286产 地：中国大陆
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T14968Cinanserin hydrochlorideSQ 10643
Cinanserin hydrochloride is a high affinity antagonist of the 5-HT2 receptor (Ki: 41 nM) and a 3C-like protease inhibitor of severe acute respiratory syndrome coronavirus.
价 格：￥电议型 号：T14968产 地：中国大陆
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T14944CGS 15943
CGS 15943 is an orally bioavailable non-xanthine antagonist of Adenosine Receptor. In transfected CHO cells, its Ki for human A1, A2A, A2B, and A3 Adenosine Receptors are 3.5, 4.2, 16, and 50 nM , respectively.
价 格：￥电议型 号：T14944产 地：中国大陆
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T14943CGP60474
CGP60474 is an inhibitor of VEGFR-2 (IC50 = 84 nM) and an inhibitor of ATP-competitive PKC. CGP60474 is also a highly potent anti-endotoxemic agent and inhibits cyclin-dependent kinase (CDK) potently.
价 格：￥电议型 号：T14943产 地：中国大陆
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T1485Methotrexate甲氨蝶呤；Amethopterin；CL14377；WR19039；NCI-C04671
Methotrexate is a folate analog metabolic inhibitor with immunosuppressant and antineoplastic properties.
价 格：￥电议型 号：T1485产 地：中国大陆
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T14844BX430
BX430 is used for chronic pain and cardiovascular disease and it is a potent and selective noncompetitive allosteric human P2X4 receptor channels antagonist with an IC50 of 0.54 μM. BX430 has species specificity.
价 格：￥电议型 号：T14844产 地：中国大陆
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T14665LMotixafortide TFA(664334-36-5,Free)TF 14016 TFA；BKT140 TFA；T140 TFA；BL-8040 TFA
Motixafortide is an antagonist of CXCR4 with IC50 of ～1 nM. It induces the apoptosis of AML blasts by down-regulating ERK, BCL-2, MCL-1 and cyclin-D1 via altered miR-15a/16-1 expression.
价 格：￥电议型 号：T14665L产 地：中国大陆
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T14511BAY1082439N-[8-[[(2R)-2-羟基-3-(吗啉-4-基)丙基]氧基]-7-甲氧基-2,3-二氢咪唑并[1,2-C]喹唑啉-5-基]-2-甲基吡啶-3-甲酰胺
BAY1082439 is highly effective in inhibiting Pten-null prostate cancer growth[1][2] and it is an orally bioavailable, selective PI3Kα/β/δ inhibitor. BAY1082439 also inhibits mutated forms of PIK3CA.
价 格：￥电议型 号：T14511产 地：中国大陆
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T1443Memantine hydrochloride3,5-二甲基金刚胺盐酸盐；盐酸美金刚；Memantine HCl；Namenda；D-145 (hydrochloride)
Memantine hydrochloride is an AMANTADINE derivative that has some dopaminergic effects. Memantine hydrochloride has been proposed as an antiparkinson agent.
价 格：￥电议型 号：T1443产 地：中国大陆
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T14391Azidamfenicol
Azidamfenicol inhibits ribosomal peptidyltransferase (Ki=22 μM)[1]. Azidamfenicol is a broad-spectrum chloramphenicol-like antibiotic.
价 格：￥电议型 号：T14391产 地：中国大陆
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T1439Lacidipine拉西地平；SN-305；GR-43659X；GX-1048
Lacidipine is a lipophilic dihydropyridine calcium antagonist with an intrinsically slow onset of activity. Due to its long duration of action, lacidipine does not lead to reflex tachycardia. It displays specificity in the vascular smooth muscle, where it
价 格：￥电议型 号：T1439产 地：中国大陆
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T14388AZD 4017
AZD 4017 is an inhibitor of 11β-Hydroxysteroid Dehydrogenase Type 1(11β-HSD1) (IC50: 7 nM).
价 格：￥电议型 号：T14388产 地：中国大陆
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T14385AZD9056 hydrochloride
AZD9056 hydrochloride is a P2X7 inhibitor，Which plays a significant role in pain-causing diseases and inflammation.
价 格：￥电议型 号：T14385产 地：中国大陆
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T14381AZD7624AZD-7624
AZD7624 is an p38 inhibitor. It has potent anti-inflammatory activity.
价 格：￥电议型 号：T14381产 地：中国大陆
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T14380AZD7507
AZD7507 is a CSF-1R inhibitor with an IC50 of 32 nM. AZD7507 has antitumor activity.
价 格：￥电议型 号：T14380产 地：中国大陆
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T1438Butoconazole nitrate硝酸布康唑；RS 35887
Butoconazole Nitrate is the nitrate salt form of butoconazole, a synthetic imidazole derivative with fungistatic properties. Butoconazole nitrate interferes with steroid biosynthesis by inhibiting the conversion of lanosterol to ergosterol, thereby changi
价 格：￥电议型 号：T1438产 地：中国大陆
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T14379AZD5904
AZD5904 is a potent and irreversible inhibitor of human Myeloperoxidase (MPO, IC50: 140 nM) which has similar potency in mouse and rat.
价 格：￥电议型 号：T14379产 地：中国大陆
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T14378LAZD5582 acetate (1258392-53-8 free base)
AZD5582 acetate is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis.
价 格：￥电议型 号：T14378L产 地：中国大陆
