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T8086Decyl aldehydeInhibitor,Decyl aldehyde,Endogenous Metabolite,inhibit
Decyl aldehyde is a natural organic compound
价 格：￥电议型 号：T8086产 地：中国大陆
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T10804CHMFL-PI3KD-317CHMFL-PI-3KD-317,CHMFLPI3KD317,CHMFL PI3KD 317
CHMFL-PI3KD-317 is a highly potent, selective and orally active PI3Kδ inhibitor, with an IC50 of 6 nM, and exhibits over 10-1500 fold selectivity over other class I, II and III PIKK family isoforms, such as PI3Kα (IC50, 62.6 nM), PI3Kβ (IC50, 284 nM), PI3Kγ (IC50, 202.7 nM), PIK3C2A (IC50, >10000 nM), PIK3C2B (IC50, 882.3 nM), VPS34 (IC50, 1801.7 nM), PI4KIIIA (IC50, 574.1 nM) and PI4KIIIB (IC50, 300.2 nM). CHMFL-PI3KD-317 inhibits PI3Kδ-mediated Akt T308 phosphorylation in Raji cells, with an E
价 格：￥电议型 号：T10804产 地：中国大陆
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T9805BAY 2666605anticancer effect,inhibit,BAY 2666605,orally active,PDE3A-SLFN12 Complex,Phosphodiesteras
BAY 2666605 is an orally active inhibitor of PDE3A and PDE3B with IC50s of 87 nM and 50 nM, respectively. BAY 2666605 has anticancer effects.
价 格：￥电议型 号：T9805产 地：中国大陆
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T9680IrloxacinInhibitor,acid pH,antibacterial agent,Bacterial,gram-positive,oral,Irloxacin,Pirfloxacin,gr
Irloxacin is a new quinolone derivative, and shows greater activity with an acid pH. Irloxacin has a good in vitro antimicrobial spectrum against both gram-positive and gram-negative bacteria.
价 格：￥电议型 号：T9680产 地：中国大陆
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T9692PaltusotinePaltusotine,Somatostatin Receptor,CRN-00808,CRN 00808,Inhibitor,IGF-1,orally,CRN00808,SST
Paltusotine is a nonpeptide, small molecule somatostatin type 2 (SST2) receptor agonist with high oral bioavailability. Paltusotine maintains GH and IGF-1 levels in acromegaly patients
价 格：￥电议型 号：T9692产 地：中国大陆
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T6352(-)-Dizocilpine maleate(-)-MK 801 (Maleate)；C13737；(-)-MK 801 Maleate；(-)-MK 801马来酸
MK-801 is a potent, selective and non-competitive NMDA receptor antagonist with Kd of 37.2 nM in rat brain membranes.
价 格：￥电议型 号：T6352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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T6322CopanlisibBAY 80-6946；可泮利塞；库潘尼西
Copanlisib is a phosphoinositide 3-kinase (PI3K) inhibitor with potential antineoplastic activity. Copanlisib inhibits the activation of the PI3K signaling pathway, which may result in inhibition of tumor cell growth and survival in susceptible tumor cell
价 格：￥电议型 号：T6322产 地：中国大陆
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T6315MLN8054
MLN8054 is a potent and selective Aurora A kinase inhibitor with an IC50 of 4 nM.
价 格：￥电议型 号：T6315产 地：中国大陆
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T6294NVP-BSK805 2HCl (1092499-93-8(free base))BSK 805
NVP-BSK805 2HCl(IC50=0.5 nM), a specific and effective ATP-competitive JAK2 inhibitor, is more than 20-fold specificity over JAK1, JAK3 and TYK2.
价 格：￥电议型 号：T6294产 地：中国大陆
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T6280EnzastaurinLY317615；恩扎妥林
Enzastaurin (LY317615) is an effective PKCβ selective inhibitor (IC50: 6 nM), 6- to 20-fold selectivity against PKCα/γ/ε.
价 格：￥电议型 号：T6280产 地：中国大陆
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T6259DizocilpineMK-801；地佐环平
MK-801 (Dizocilpine) is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30.5 nM.
价 格：￥电议型 号：T6259产 地：中国大陆
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T6210Pifithrin-μPFTμ；2-Phenylethynesulfonamide；NSC 303580
Pifithrin-μ is an inhibitor of p53 and HSP70, with neuroprotective and antitumor activity.
价 格：￥电议型 号：T6210产 地：中国大陆
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T6194Fidaxomicin非达米星；PAR-101；Tiacumicin B；OPT-80；Clostomicin B1
Fidaxomicin is a semisynthetic macrolide antibiotic used to treat Clostridium difficile-associated diarrhea in adults. Fidaxomicin has minimal systemic absorption and has not been linked to serum enzyme elevations during therapy or to instances of clinica
价 格：￥电议型 号：T6194产 地：中国大陆
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T6180INH6
INH6, an effective Hec1 inhibitor, selectively disrupts the Hec1/Nek2 interaction and induces chromosome mis-alignment.
价 格：￥电议型 号：T6180产 地：中国大陆
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T6152PD318088
PD318088 is a non-ATP competitive allosteric MEK1/2 inhibitor, binding simultaneously with ATP in a region of the MEK1 active site that is adjacent to the ATP-binding site.
价 格：￥电议型 号：T6152产 地：中国大陆
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T6136CanertinibPD-183805；CI-1033；卡纽替尼
Canertinib is a pan-erbB tyrosine kinase inhibitor which work against esophageal squamous cell carcinoma in vitro and in vivo. Canertinib treatment significantly affects tumour metabolism, proliferation and hypoxia as determined by PET.
价 格：￥电议型 号：T6136产 地：中国大陆
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T6109Darapladib达拉地；SB-480848
Darapladib(IC50=0.25 nM) is a substituted pyrimidone with inhibitory activity towards lipoprotein-associated phospholipase-A2 (Lp-PLA2).
价 格：￥电议型 号：T6109产 地：中国大陆
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T6080NVP-AEW541AEW541
NVP-AEW541, a potent inhibitor of IGF-1R(IC50=150 nM) and InsR(IC50=140 nM), exhibits excellent efficiency and specificity for IGF-1R in a cell-based assay.
价 格：￥电议型 号：T6080产 地：中国大陆
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T6069Gemcitabine hydrochlorideLY 188011 hydrochloride；LY188011；Gemzar；Gemcitabine HCl；吉西他滨盐酸盐；盐酸吉西他滨
Gemcitabine is a DNA synthesis inhibitor (IC50s: 12, 18, 40, 92.7, 89.3 in Capan2, BxPC-3, Mia Paca-2, PANC-1, and PL-45 cells, respectively).
价 格：￥电议型 号：T6069产 地：中国大陆
