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Reversine
Reversine, a small synthetic purine analogue (2,6-disubstituted purine), is a potent inhibitior of Aurora A/B/C with IC5
2015-12-21 17:11 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

651.00/5mg
05mg起訂
詢價(jià)

Pyridostatin
Pyridostatin(RR-82) is a G-quadruplex-interacting drug which can promote growth arrest in human cancer cells by inducing
2015-12-21 17:09 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

9380.00/100mg
0100mg起訂
詢價(jià)

Resminostat
Resminostat(RAS2410; 4SC-201) is a potent inhibitor of HDAC1/3/6(IC50=43-72 nM); less potent to HDAC8 with IC50 of 877 n
2015-12-21 17:07 [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
詢價(jià)

PR-619
PR-619 is a broad-range DUB inhibitor with potential for further development as a chemotherapeutic agent in cancer thera
2015-12-21 16:59 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

800.00/10mg
010mg起訂
詢價(jià)

Tenovin-1
Tenovin-1 is a inhibitor of SIRT1 and SIRT2; activator of p21 and p53.IC50 Value:Target: SirtuinTenovin-1 is a compound
2015-12-21 16:57 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

558.00/10mg
010mg起訂
詢價(jià)

Ciprofibrate D6
Ciprofibrate D6 is deuterium labeled Ciprofibrate, which is a peroxisome proliferator-activated receptor agonist. 公司介
2015-12-21 16:56 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1100.00/1mg
01mg起訂
詢價(jià)

HY-17557
Calcium N5-methyltetrahydrofolate(NSC173328) is the calcium salt of levomefolic acid, which has been proposed for treatm
2015-12-21 16:54 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3255.00/5mg
05mg起訂
詢價(jià)

Levoleucovorin (Calcium)
Levoleucovorin calcium is the calcium salt of Levoleucovorin, which is the enantiomerically active form of folinic acid.
2015-12-21 16:52 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

650.00/5mg
05mg起訂
詢價(jià)

Topotecan (Hydrochloride)
Topotecan Hcl (SKF 104864A; NSC 609669) is the first topoisomerase I-directed cytotoxic agent to enter clinical trials i
2015-12-21 16:51 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

500.00/10mg
010mg起訂
詢價(jià)

AZ20
AZ20 is a potent and selective inhibitor of ATR with an IC50 of 5 nM; 8-fold selectivity over mTOR(IC50=38 nM).IC50 Valu
2015-12-21 16:49 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1972.00/10mg
010mg起訂
詢價(jià)

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)]