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SB1317
SB1317(TG-02) is a novel small molecule potent CDK2/JAK2/FLT3 inhibitor with IC50s of 13/73/56 nM respectively.IC50 Valu
2015-12-09 11:03 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1348.00/5mg
05mg起訂

AZ3146
AZ3146 is a potent and selective monopolar spindle 1 (Mps1) kinase inhibitor (IC50 = 35 nM); less potent to FAK, JNK1, J
2015-12-09 11:01 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1105.00/10mg
010mg起訂

Y-27632 (dihydrochloride)
Y-27632 2Hcl is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM, exhibits 200-fold selectivity over other kinas
2015-12-09 10:59 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

874.00/5mg
05mg起訂

EHop-016
EHop-016 is a novel potent and selective inhibitor of Rac GTPase; inhibits Rac1 activity in MDA-MB-435 cells with an IC5
2015-12-09 10:57 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

700.00/10mg
010mg起訂

Cevipabulin
Cevipabulin(TTI-237) is a novel, potent, synthetic small molecule, inhibits binding of vinblastine at the Vinca alkaloid
2015-12-09 10:55 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1500.00/5mg
05mg起訂

Triciribine
Triciribine(API-2; NSC 154020) is a DNA synthesis inhibitor, also inhibits Akt and HIV-1 with IC50 of 130 nM and 20 nM,
2015-12-09 10:54 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

837.00/5mg
05mg起訂

Tasquinimod
Tasquinimod(ABR-215050) is a quinoline-3-carboxamide linomide analogue with antiangiogenic and potential antineoplastic
2015-12-09 10:51 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2864.00/5mg
05mg起訂

RITA
RITA(NSC 652287) induced both DNA-protein and DNA-DNA cross-links with no detectable DNA single-strand breaks.公司介紹：
2015-12-09 10:49 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1989.00/10mg
010mg起訂

GSK343
GSK343 is a potent and selective EZH2 inhibitor with IC50 of 4 nM, showing 60 fold selectivity against EZH1, and 1000 fo
2015-12-09 10:47 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

714.00/5mg
05mg起訂

GSK3787
GSK3787 is as a selective and irreversible antagonist of PPAR with pIC50 of 6.6, with no measurable affinity for hPPAR o
2015-12-09 10:44 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

810.00/10mg
010mg起訂

HDAC-IN-1
HDAC-IN-1 is a chemical analog of MC 1568, which is a potent and selective class IIa HDACs inhibitor.公司介紹：MedChemEx
2015-12-09 10:42 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

884.00/10mg
010mg起訂

RG108
RG108 is a non-nucleoside inhibitor of DNA methyltransferase with IC50 of 115 nM.IC50 Value: 115 nMTarget: DNMTin vitro:
2015-12-09 10:40 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

847.00/10mg
010mg起訂

LY2835219 (free base)
LY2835219 is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM and 10 nM, respectively.IC50 Value: 2 n
2015-12-09 10:38 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1023.00/5mg
05mg起訂

LY2835219
LY2835219 is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM and 10 nM, respectively.IC50 Value: 2 n
2015-12-09 10:36 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

8835.00/100mg
0100mg起訂

CDK9-IN-2
CDK9-IN-2 is a novel cyclin-dependent kinase 9(CDK9) inhibitor.IC50 value:Target: CDK9公司介紹：MedChemExpress(MCE)專注
2015-12-09 10:34 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2660.00/5mg
05mg起訂

Aleglitazar
Aleglitazar(R1439; RO-0728804) is a new dual PPAR-/ agonist with IC50 of 2.8 nM/4.6 nM.IC50 Value: 2.8 nM(PPAR-); 4.6 nM
2015-12-09 10:32 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2660.00/5mg
05mg起訂

INNO-206
INNO-206 (Aldoxorubicin) is the 6-maleimidocaproyl hydrazone derivative prodrug of the anthracycline antibiotic doxorubi
2015-12-09 10:30 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1740.00/10mg
010mg起訂

ARRY-520 (R enantiomer)
ARRY-520 R enantiomer is the R form of ARRY-520, which is a synthetic, small molecule kinesin spindle protein (KSP) inhi
2015-12-09 10:28 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

884.00/5mg
05mg起訂

MI-3
MI-3 is a Menin-MLL interaction inhibitor with IC50 value of 64825 nM.IC50 value: 64825 nM [1]Target: Menin-MLLin vitro:
2015-12-09 10:26 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

10044.00/100mg
0100mg起訂

MI-3
MI-3 is a Menin-MLL interaction inhibitor with IC50 value of 64825 nM.IC50 value: 64825 nM [1]Target: Menin-MLLin vitro:
2015-12-09 10:26 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]