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产品数：86095
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T6344Sevelamer hydrochlorideSevelamer HCl
Sevelamer HCl is a phosphate binding drug used to treat hyperphosphatemia via binding to dietary phosphate and prevents its absorption.
价 格：￥电议型 号：T6344产 地：中国大陆
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T6343GeldanamycinNSC 122750；格尔德霉素
Geldanamycin, an HSP90 inhibitor (Kd: 1.2 μM), specifically disrupts glucocorticoid receptor (GR)/HSP association.
价 格：￥电议型 号：T6343产 地：中国大陆
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T6342NSC 23766 trihydrochlorideNSC 23766；Rac1 Inhibitor
NSC 23766 is an inhibitor of Rac GTPase targeting Rac activation by GEFs (IC50: ~50 μM); no inhibitory for the closely related targets, RhoA or Cdc42.
价 格：￥电议型 号：T6342产 地：中国大陆
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T6341PF04929113PF-04929113；SNX-5422；PF 04929113
SNX-5422 is a synthetic, novel, small molecule Hsp90 Inhibitor. As an oral formulation that demonstrates strong efficacy and tolerability, SNX-5422 is positioned as a breakthrough therapy with broad applicability across a wide range of cancers.
价 格：￥电议型 号：T6341产 地：中国大陆
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T6340Enalaprilat Dihydrate依那普利拉二水合物；MK-422 Dihydrate；MK-422
Enalaprilat（IC50=1.94 nM） is a potent angiotensin-converting enzyme (ACE) inhibitor.
价 格：￥电议型 号：T6340产 地：中国大陆
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T6339AG14361AG-14361；AG 14361
AG14361 is an effective inhibitor of PARP1 (Ki<5 nM).
价 格：￥电议型 号：T6339产 地：中国大陆
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T6338PHA-680632PHA 680632；PHA680632
PHA-680632 is potent inhibitor of Aurora A, Aurora B and Aurora C with IC50 of 27 nM, 135 nM and 120 nM, respectively. It has 10- to 200-fold higher IC50 for FGFR1, FLT3, LCK, PLK1, STLK2, and VEGFR2/3.
价 格：￥电议型 号：T6338产 地：中国大陆
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T6337RepSoxALK5 Inhibitor II；SJN 2511；E-616452
RepSox is a potent and selective of the TGFβR-1/ALK5 inhibitor.
价 格：￥电议型 号：T6337产 地：中国大陆
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T6336AmonafideNafidimide；Quinamed；AS1413；NSC308847,AS1413；氨萘非特
Amonafide(AS1413) produces protein-associated DNA-strand breaks through a topoisomerase II-mediated reaction, but does not produce topoisomerase I-mediated DNA cleavage.
价 格：￥电议型 号：T6336产 地：中国大陆
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T6335Tie2 kinase inhibitor 1Tie2 kinase inhibitor
Tie2 kinase inhibitor, an optimized compound of SB-203580, is selective to Tie2 with IC50 of 0.25 μM, which is 200-fold more effective than p38.
价 格：￥电议型 号：T6335产 地：中国大陆
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T6333MM-102MM102；MM 102；HMTase Inhibitor IX
MM-102 is a high-affinity peptidomimetic MLL1 inhibitor with IC50 of 0.4 μM.
价 格：￥电议型 号：T6333产 地：中国大陆
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T6332PevonedistatMLN4924
MLN4924 is an effective and specific small molecule NEDD8-activating enzyme (NAE) inhibitor (IC50: 4.7 nM).
价 格：￥电议型 号：T6332产 地：中国大陆
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T6331Allitinib tosylateAST-1306 TsOH；AST-6；Allitinib；AST-1306 (TsOH)；AST-1306；艾力替尼
AST-1306 is a novel irreversible inhibitor of EGFR and ErbB2 with IC50 of 0.5 nM and 3 nM, respectively.
价 格：￥电议型 号：T6331产 地：中国大陆
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T6330LinperlisibPI3Kδ-IN-2
PI3Kδ-IN-2 is a potent and selective inhibitor of PI3Kδ
价 格：￥电议型 号：T6330产 地：中国大陆
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T63293-Aminobenzamide3-AB；INO 1001；3-ABA；INO1001；INO-1001；PARP-IN-1
INO-1001 is an effective inhibitor of PARP (IC50<50 nM in CHO cells) and a mediator of oxidant-induced myocyte dysfunction during reperfusion.
价 格：￥电议型 号：T6329产 地：中国大陆
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T6328Desmethyl ErlotinibO-Desmethyl Erlotinib；OSI-420；CP-473420
OSI-420 is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).
价 格：￥电议型 号：T6328产 地：中国大陆
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T6327Tubacin
Tubacin is a highly potent and selective, reversible, cell-permeable HDAC6 inhibitor with an IC50 of 4 nM, approximately 350-fold selectivity over HDAC1.
价 格：￥电议型 号：T6327产 地：中国大陆
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T6326BMS-345541BMS345541；IKK Inhibitor III；BMS 345541；BMS-345541 free base
BMS-345541 is a highly selective inhibitor of the catalytic subunits of IKK-2 and IKK-1 with IC50 of 0.3 μM and 4 μM, respectively.
价 格：￥电议型 号：T6326产 地：中国大陆
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T6325PCI-34051N-羟基-1-(4-甲氧基苄基)-1H-吲哚-6-甲酰胺；PCI 34051；PCI34051
PCI-34051 is an effective and selective HDAC8 inhibitor (IC50: 10 nM).
价 格：￥电议型 号：T6325产 地：中国大陆
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T6324BIX02188334949-59-6
BIX02188 is a specific MEK5 inhibitor (IC50: 4.3 nM), also inhibits ERK5 catalytic activity (IC50: 810 nM), and does not inhibit closely related kinases MEK1/2, JNK2, and ERK2.
价 格：￥电议型 号：T6324产 地：中国大陆
