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SAR407899 (hydrochloride)
SAR407899 Hcl is a potent, ATP-competitive ROCK inhibitor woth Ki value of 36 nM/41 nM for human ROCK/Rat ROCK respectiv
2015-12-21 16:47 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3500.00/5mg
05mg起訂
詢價(jià)

Balaglitazone
Balaglitazone (DRF-2593; NN-2344) is a novel partial agonist of PPAR-.IC50 Value:Target: PPARin vitro: The Rs for the se
2015-12-21 16:45 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

13020.00/100mg
0100mg起訂
詢價(jià)

PCI-34051
PCI-34051 is a specific inhibitor of HDAC8 with IC50 of 10 nM, with 200-fold selectivity over the other HDAC isoforms.IC
2015-12-21 16:44 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1252.00/10mg
010mg起訂
詢價(jià)

Romidepsin
Romidepsin (FK228, depsipeptide) is a potent HDAC1 and HDAC2 inhibitor with IC50 of 36 nM and 47 nM, respectively.IC50 V
2015-12-21 16:41 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2980.00/1mg
01mg起訂
詢價(jià)

AZD1152
AZD1152 (barasertib), pro-drug of barasertib-hQPA(HY-10126), is a selective Aurora B kinase inhibitor, AZD1152 inhibited
2015-12-21 16:39 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1228.00/5mg
05mg起訂
詢價(jià)

AT13387
AT13387 is a selective potent Hsp90 inhibitor with IC50 of 18 nM in A375 cells, displays a long duration of anti-tumor a
2015-12-21 16:38 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1989.00/5mg
05mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1252.00/10mg
010mg起訂
詢價(jià)

sirtuin modulator
6-phenylimidazo[2,1-b]thiazole derivatives; sirtuin modulator.公司介紹：MedChemExpress(MCE)專注于各種抑制劑、激動(dòng)劑、API
2015-12-21 16:34 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2372.00/5mg
05mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2558.00/5mg
05mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1989.00/5mg
05mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2727.00/100mg
0100mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2346.00/10mg
010mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

837.00/10mg
010mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2744.00/100mg
0100mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1989.00/50mg
050mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1300.00/5mg
05mg起訂
詢價(jià)

Ispinesib
Ispinesib (SB-715992) is a potent, specific and reversible inhibitor of KSP (HsEg5) with Ki of 1.7 nM.公司介紹：MedChemE
2015-12-09 11:10 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2358.00/10mg
010mg起訂
詢價(jià)

Fenofibrate
Fenofibrate is PPAR agonist with EC50 of 18 M and 30 M for mouse and human PPAR, respectively. 公司介紹：MedChemExpress(
2015-12-09 11:08 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

350.00/5g
05g起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1400.00/10mg
010mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]