医药化工网_第103页_产品

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Ifosfamide
Ifosfamide is a nitrogen mustard alkylating agent used in the treatment of cancer.IC50 Value: 1mM (in MCF-7 and MDA-MB23
2016-01-05 15:04 [上海]
上海皓元生物医药科技有限公司 [已核实]

600.00/200mg
0200mg起订

Mocetinostat
MGCD0103 (Mocetinostat) is a potent HDAC inhibitor with IC50 of 0.15, 0.29 and 1.66 M for HDAC 1, HDAC 2 and HDAC 3, res
2016-01-05 15:02 [上海]
上海皓元生物医药科技有限公司 [已核实]

800.00/5mg
05mg起订

Belinostat
Belinostat (PXD101) is a novel pan-HDAC inhibitor with IC50 of 27 nM, with activity demonstrated in cisplatin-resistant
2016-01-05 15:00 [上海]
上海皓元生物医药科技有限公司 [已核实]

780.00/10mg
010mg起订

Geldanamycin
Geldanamycin is a natural existing HSP90 inhibitor with Kd of 1.2 M.IC50 Value: 1.2 M(Kd)Target: HSP90in vitro: Geldanam
2016-01-05 14:55 [上海]
上海皓元生物医药科技有限公司 [已核实]

1989.00/10mg
010mg起订

Vorinostat
Vorinostat (SAHA) is an HDAC1/3 inhibitor with IC50 of ~10 nM.IC50 Value: ~10 nMTarget: HDACsin vitro: Vorinostat inhibi
2016-01-05 14:49 [上海]
上海皓元生物医药科技有限公司 [已核实]

1083.00/250mg
0250mg起订

PHA-848125
PHA-848125(Milciclib) is a potent, ATP-competitive CDK inhibitor for CDK2 with IC50 of 45 nM; 3-fold more selective for
2016-01-05 14:48 [上海]
上海皓元生物医药科技有限公司 [已核实]

1860.00/5mg
05mg起订

RI-2
RI-2 is an optimized RAD51 inhibitor with an IC50 of 44.17 M in the standard DNA binding assay; specifically inhibits HR
2016-01-05 14:46 [上海]
上海皓元生物医药科技有限公司 [已核实]

3500.00/5mg
05mg起订

Pracinostat
Pracinostat(SB939) is a potent pan-HDAC inhibitor with IC50 of 40-140 nM with exception for HDAC6; has no activity again
2016-01-05 14:43 [上海]
上海皓元生物医药科技有限公司 [已核实]

1548.00/5mg
05mg起订

Fludarabine (phosphate)
Fludarabine Phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporati
2016-01-05 14:41 [上海]
上海皓元生物医药科技有限公司 [已核实]

2697.00/100mg
0100mg起订

Fludarabine
Fludarabine(NSC 118218), a DNA synthesis inhibitor, is a chemotherapy drug used in the treatment of hematological malign
2016-01-05 14:39 [上海]
上海皓元生物医药科技有限公司 [已核实]

428.00/5mg
05mg起订

Kif15-IN-2
Kif15-IN-2 is a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in tumor cell lines.IC50 value:Target: K
2016-01-05 14:37 [上海]
上海皓元生物医药科技有限公司 [已核实]

4650.00/10mg
010mg起订

Kif15-IN-1
Kif15-IN-1 is a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in tumor cell lines.IC50 value:Target: K
2016-01-05 14:36 [上海]
上海皓元生物医药科技有限公司 [已核实]

19530.00/100mg
0100mg起订

HY-10210
Retaspimycin Hcl(IPI504 Hcl) is the hydrochloride salt of a small-molecule inhibitor of heat shock protein 90 (HSP90) wi
2016-01-05 14:34 [上海]
上海皓元生物医药科技有限公司 [已核实]

2558.00/10mg
010mg起订

HY-15145
SRT1720 hydrochloride is a selective activator of human SIRT1 (EC1.5 = 0.16 M) versus the closest sirtuin homologues, SI
2016-01-05 14:32 [上海]
上海皓元生物医药科技有限公司 [已核实]

1252.00/5mg
05mg起订

HY-13502A
Mitoxantrone Dihydrochloride, a type II topoisomerase inhibitor, is an anthracenedione-derived antineoplastic agent.Targ
2016-01-05 14:30 [上海]
上海皓元生物医药科技有限公司 [已核实]

883.00/100mg
0100mg起订

Trichostatin A
Trichostatin A (TSA) is a selective and potent HDAC inhibitor with IC50 of ~1.8 nM; HDAC8 is the only known member of th
2016-01-05 14:28 [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

Tubastatin A (Hydrochloride)
Tubastatin A Hcl is a potent and selective HDAC6 inhibitor with IC50 of 15 nM; is selective (1000-fold more) against all
2016-01-05 14:25 [上海]
上海皓元生物医药科技有限公司 [已核实]

512.00/5mg
05mg起订

Amonafide
Droxinostat(NS41080) is a selective inhibitor of HDAC3, HDAC6, and HDAC8 with IC50 of 16.9, 2.47 and 1.46 M, respectivel
2016-01-05 14:23 [上海]
上海皓元生物医药科技有限公司 [已核实]

670.00/5mg
05mg起订

Droxinostat
Droxinostat(NS41080) is a selective inhibitor of HDAC3, HDAC6, and HDAC8 with IC50 of 16.9, 2.47 and 1.46 M, respectivel
2016-01-05 14:16 [上海]
上海皓元生物医药科技有限公司 [已核实]

502.00/5mg
05mg起订

BS-181
BS-181 is a highly selective CDK7 inhibitor with IC50 of 21 nM.公司介绍：MedChemExpress(MCE)专注于各种抑制剂、激动剂、AP
2016-01-05 14:12 [上海]
上海皓元生物医药科技有限公司 [已核实]

1786.00/5mg
05mg起订

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