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产品数：86101
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T7643Fmoc-Ser(O-α-D-GalNAc(OAc)3)-OHFmocSer(OαDGalNAc(OAc)3)OH,Fmoc Ser(O α D GalNAc(OAc)3) OH,inhibit,In
Fmoc-Ser(O-α-D-GalNAc(OAc)3)-OH is an anti-tumor drug
价 格：￥电议型 号：T7643产 地：中国大陆
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T64348WAY-313137
WAY-313137 is an indolyl hydrazide-hydrazone compound with anticancer activity. Antiproliferative agent-16 exhibits specificity toward breast cancer cells (IC50 of 6.94 μM for MCF-7 cells).
价 格：￥电议型 号：T64348产 地：中国大陆
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T7343PF-04979064Inhibitor,Phosphoinositide 3-kinase,Mammalian target of Rapamycin,PF 04979064,PF04979064,
PF-04979064 is a potent and selective PI3K and mTOR dual kinase inhibitor(Ki of 0.13 nM and 1.42 nM,respectively).
价 格：￥电议型 号：T7343产 地：中国大陆
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T10213A-437203
A-437203 is a selective D3 receptor antagonist (Kis: 71, 1.6, and 6220 nM for D2, D3, and D4 receptors).
价 格：￥电议型 号：T10213产 地：中国大陆
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T64318Capecitabine-2’,3’-cyclic Carbonate
Capecitabine-2´,3´-cyclic Carbonate is a antiproliferative agent.
价 格：￥电议型 号：T64318产 地：中国大陆
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T64320ML251cruzi,inhibit,brucei,MRC-5,Inhibitor,nanomolar,Parasite,ML-251,ML 251,ML251
ML251 is a potent novel nanomolar inhibitor of T. brucei and T. cruzi phosphofructokinase[1]. ML251 inhibits T. brucei PFK (IC50=0.37 μM) and T. cruzi PFK (IC50=0.13 μM). ML251 can be used for the research of parasite[1].
价 格：￥电议型 号：T64320产 地：中国大陆
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T64336Izilendustatinmmune response,HIF-PH,colitis,prolyl hydroxylase,Inhibitor,HIF-2,HIFs,Hypoxia-inducibl
Tert-butyl 4-[[1-[(4-chlorophenyl)methyl]-3-hydroxy-2-oxopyridin-4-yl]methyl]piperazine-1-carboxylate inhibit of human recombinant EGLN-1 as substrate after 20 mins by mass spectrophotometric analysis.
价 格：￥电议型 号：T64336产 地：中国大陆
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TN6431Cyclo(Pro-Ala)Cyclo(ProAla),Cyclo(Pro Ala)
Cyclo(Pro-Ala) is a natural product.
价 格：￥电议型 号：TN6431产 地：中国大陆
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T60043DPTIPextracellular,Inhibitor,exosome,DPTIP,Phospholipase,vesicles,inhibit,N-SMase
DPTIP is an effective inhibitor of neutral sphingomyelinase 2 with an IC50 value of 30 nM.
价 格：￥电议型 号：T60043产 地：中国大陆
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T8866GW779439XApoptosis,pazolopyridazine,threonine,cancer,Inhibitor,inhibit,lactam,GW-779439X,derivatives
GW779439X is an inhibitor of CDK.
价 格：￥电议型 号：T8866产 地：中国大陆
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T8843APS6-45APS6-45,calibrated,signaling,TCI,Inhibitor,APS-6-45,APS645,Carcinoma,Thyroid,Ras,antitumor,Me
APS6-45 inhibits RAS/MAPK signaling and exhibits anti-tumor activity.
价 格：￥电议型 号：T8843产 地：中国大陆
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T7610GW284543Inhibitor,inhibit,GW 284543,GW284543,UNC 10225170,MIA PaCa-2,GW-284543,Mitogen-activated pro
GW284543 is a selective inhibitor of MEK5 .
价 格：￥电议型 号：T7610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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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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T6293Mycophenolate MofetilTM-MMF；RS 61443；吗替麦考酚酯
Mycophenolate mofetil, an immunosuppressive agent, is the 2-morpholinoethyl ester of mycophenolic acid (MPA), and an inhibitor of inosine monophosphate dehydrogenase (IMPDH).
价 格：￥电议型 号：T6293产 地：中国大陆
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T6243U-73122U73122
U73122, an effective PLC inhibitor, reduces agonist-induced Ca2+ increases in platelets and PMN.
价 格：￥电议型 号：T6243产 地：中国大陆
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T6232Vilazodone Hydrochloride盐酸维拉佐酮；EMD 68843；Vilazodone HCl；SB659746A
Vilazodone HCl, a partial agonist of 5-HT1A receptors and specific serotonin reuptake inhibitor (SSRI), is utilized in treating of the major depressive disorder.
价 格：￥电议型 号：T6232产 地：中国大陆
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T6160VU 0364439
VU 0364439 is a mGlu4 positive allosteric modulator (C50: 19.8 nM).
价 格：￥电议型 号：T6160产 地：中国大陆
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T6144KB-R7943 mesylateKB-R7943
KB-R7943 mesylate is a widely used inhibitor of the reverse Na+/Ca2+ exchanger (NCXrev) with IC50 of 5.7±2.1 μM.
价 格：￥电议型 号：T6144产 地：中国大陆
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T6143PI-103PI103；PI 103
PI-103 is a potent, cell-permeable, ATP-competitive inhibitor of PI3K family members (IC50s: 2/3/3/15/30/23 nM for p110α/β/δ/γ, mTOR, and DNA-PK).
价 格：￥电议型 号：T6143产 地：中国大陆
