医药化工网_第111页_产品

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ACY-1215
Rocilinostat (ACY-1215) is a selective HDAC6 inhibitor with IC50 of 5 nM; 10-fold more selective for HDAC6 than HDAC1/2/
2015-12-21 16:36 [上海]
上海皓元生物医药科技有限公司 [已核实]

1252.00/10mg
010mg起订

sirtuin modulator
6-phenylimidazo[2,1-b]thiazole derivatives; sirtuin modulator.公司介绍：MedChemExpress(MCE)专注于各种抑制剂、激动剂、API
2015-12-21 16:34 [上海]
上海皓元生物医药科技有限公司 [已核实]

2372.00/5mg
05mg起订

Voreloxin (Hydrochloride)
Voreloxin Hcl(SNS-595; AG 7352) is a small molecule and a naphthyridine analogue with antineoplastic activity; inhibitor
2015-12-21 16:32 [上海]
上海皓元生物医药科技有限公司 [已核实]

2558.00/5mg
05mg起订

BMS-265246
BMS-265246 is a potent and selective CDK1/2 inhibitor for CDK1/cyclin B and CDK2/cyclin E with IC50 of 6 nM and 9 nM, re
2015-12-21 16:30 [上海]
上海皓元生物医药科技有限公司 [已核实]

1989.00/5mg
05mg起订

Alvespimycin
Alvespimycin (17-DMAG; KOS-1022; NSC 707545) is a potent, water-soluble HSP90 inhibitor with IC50 of 62 nM.IC50 Value: 6
2015-12-21 16:28 [上海]
上海皓元生物医药科技有限公司 [已核实]

2727.00/100mg
0100mg起订

MLN0905
MLN0905 is a small-molecule and potent inhibitor of PLK1 with IC50 of 2 nM.IC50 Value: 2 nMTarget: PLK1in vitro: MLN0905
2015-12-21 16:26 [上海]
上海皓元生物医药科技有限公司 [已核实]

2346.00/10mg
010mg起订

BIBR 1532
BIBR 1532 is a potent, selective, non-competitive telomerase inhibitor with IC50 of 100 nM.IC50 Value: 100 nMTarget: Tel
2015-12-21 16:22 [上海]
上海皓元生物医药科技有限公司 [已核实]

837.00/10mg
010mg起订

17-AAG (Hydrochloride)
17-AAG Hcl is a potent HSP90 inhibitor with IC50 of 5 nM, having a 100-fold higher binding affinity for HSP90 derived fr
2015-12-21 16:20 [上海]
上海皓元生物医药科技有限公司 [已核实]

2744.00/100mg
0100mg起订

CI-994
CI-994 (Tacedinaline) is an anti-cancer drug which inhibits HDAC1 with IC50 of 0.57 M and causes G1 cell cycle arrest.
2015-12-21 16:17 [上海]
上海皓元生物医药科技有限公司 [已核实]

1989.00/50mg
050mg起订

GSK-503
GSK-503 is a potent EZH2 inhibitor with potential anticancer activity.IC50 value:Target: EZH2 inhibitorIn a melanoma mou
2015-12-21 16:15 [上海]
上海皓元生物医药科技有限公司 [已核实]

1300.00/5mg
05mg起订

Ispinesib
Ispinesib (SB-715992) is a potent, specific and reversible inhibitor of KSP (HsEg5) with Ki of 1.7 nM.公司介绍：MedChemE
2015-12-09 11:10 [上海]
上海皓元生物医药科技有限公司 [已核实]

2358.00/10mg
010mg起订

Fenofibrate
Fenofibrate is PPAR agonist with EC50 of 18 M and 30 M for mouse and human PPAR, respectively. 公司介绍：MedChemExpress(
2015-12-09 11:08 [上海]
上海皓元生物医药科技有限公司 [已核实]

350.00/5g
05g起订

PFI-2
PFI-2 is a a first-in-class, potent, highly selective, and cell-active inhibitor of the methyltransferase activity of SE
2015-12-09 11:06 [上海]
上海皓元生物医药科技有限公司 [已核实]

1400.00/10mg
010mg起订

PFI-2 (hydrochloride)
PFI-2 hydrochloride is a a first-in-class, potent, highly selective, and cell-active inhibitor of the methyltransferase
2015-12-09 11:05 [上海]
上海皓元生物医药科技有限公司 [已核实]

1400.00/10mg
010mg起订

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]
上海皓元生物医药科技有限公司 [已核实]

1348.00/5mg
05mg起订

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]
上海皓元生物医药科技有限公司 [已核实]

1105.00/10mg
010mg起订

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]
上海皓元生物医药科技有限公司 [已核实]

874.00/5mg
05mg起订

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]
上海皓元生物医药科技有限公司 [已核实]

700.00/10mg
010mg起订

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]
上海皓元生物医药科技有限公司 [已核实]

1500.00/5mg
05mg起订

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]
上海皓元生物医药科技有限公司 [已核实]

837.00/5mg
05mg起订

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