医药化工网_第98页_产品

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医药中间体 (1369)

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Busulfan
Busulfan is a bifunctional alkylating agent.Target: DNA alkylatorBusulfan, a cytotoxic alkylating agent used for treatme
2016-01-11 12:35 [上海]
上海皓元生物医药科技有限公司 [已核实]

500.00/1g
01g起订

Pioglitazone
Pioglitazone (U 72107) is a selective peroxisome proliferator-activated receptor gamma(PPAR) stimulator.IC50 Value:Targe
2016-01-11 12:33 [上海]
上海皓元生物医药科技有限公司 [已核实]

1252.00/50mg
050mg起订

GSK126
GSK126 is a potent, highly selective, S-adenosyl-methionine-competitive, small-molecule inhibitor of EZH2 methyltransfer
2016-01-11 12:32 [上海]
上海皓元生物医药科技有限公司 [已核实]

781.00/5mg
05mg起订

CDK4-IN-1
CDK4 inhibitor is a novel and specific CDK4/Cyclin D1 inhibitor with an IC50 of 10 nM; 1500 and 500 fold than CDK1/Cycli
2016-01-11 12:30 [上海]
上海皓元生物医药科技有限公司 [已核实]

2325.00/5mg
05mg起订

UNC0379 (trifluoroacetate)
UNC0379 trifluoroacetate is a selective, substrate-competitive inhibitor of the lysine methyltransferase SETD8 with IC50
2016-01-11 12:28 [上海]
上海皓元生物医药科技有限公司 [已核实]

1000.00/5mg
05mg起订

Rosiglitazone (maleate)
Rosiglitazone maleate(BRL-49653C) is a high-affinity selective agonist of the peroxisome proliferator-activated receptor
2016-01-11 12:27 [上海]
上海皓元生物医药科技有限公司 [已核实]

4350.00/500mg
0500mg起订

Rosiglitazone (maleate)
Rosiglitazone maleate(BRL-49653C) is a high-affinity selective agonist of the peroxisome proliferator-activated receptor
2016-01-11 12:25 [上海]
上海皓元生物医药科技有限公司 [已核实]

面议

GSK343
GSK343 is a potent and selective EZH2 inhibitor with IC50 of 4 nM, showing 60 fold selectivity against EZH1, and 1000 fo
2016-01-11 11:30 [上海]
上海皓元生物医药科技有限公司 [已核实]

714.00/5mg
05mg起订

ETP-46464
ETP-46464 is a cell-permeable quinoline-containing heterotricyclic compound that acts as a potent inhibitor against mTOR
2016-01-11 11:28 [上海]
上海皓元生物医药科技有限公司 [已核实]

10462.00/100mg
0100mg起订

3-Deazaneplanocin A
3-Deazaneplanocin A (DZNep) is an attractive epigenetic anticancer agent through the inhibition of the cellular enhancer
2016-01-11 11:26 [上海]
上海皓元生物医药科技有限公司 [已核实]

4201.00/5mg
05mg起订

Cyclophosphamide
Cyclophosphamide is a synthetic alkylating agent chemically related to the nitrogen mustards with antineoplastic and imm
2016-01-11 11:25 [上海]
上海皓元生物医药科技有限公司 [已核实]

884.00/100mg
0100mg起订

Streptozocin
Streptozotocin is a DNA alkylating agent that enters cells exclusively via the GLUT2 glucose transport protein.公司介绍
2016-01-11 11:23 [上海]
上海皓元生物医药科技有限公司 [已核实]

744.00/500mg
0500mg起订

Olaparib
Olaparib (AZD2281, KU0059436) is a potent PARP inhibitor with IC50 of 5 and 1 nM for PARP-1and PARP-2, respectively.IC50
2016-01-11 11:22 [上海]
上海皓元生物医药科技有限公司 [已核实]

515.00/10mg
010mg起订

EPZ005687
EPZ-005687 is a potent and selective inhibitor of EZH2 with Ki of 24 nM, 50-fold selectivity against EZH1 and 500-fold s
2016-01-11 11:20 [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

SCH900776
SCH900776 is a potent, selective and orally bioavailable inhibitor of checkpoint kinase Chk1 (IC50 = 3 nM), highly selec
2016-01-11 11:18 [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

Mps1-IN-1
Mps1-IN-1 is a highly potent and selectibe Mpsl inhibitor with IC50 of 367 nM; 1000-fold selectivity relative to the 352
2016-01-11 11:17 [上海]
上海皓元生物医药科技有限公司 [已核实]

850.00/5mg
05mg起订

Gemcitabine (elaidate)
Gemcitabine elaidate(CP-4126; CO-101) is a lipophilic, unsaturated fatty acid ester derivative of gemcitabine (dFdC), an
2016-01-11 11:15 [上海]
上海皓元生物医药科技有限公司 [已核实]

1050.00/5mg
05mg起订

SCH900776 (S-isomer)
SCH900776 (S-isomer) is the S-isomer form of SCH900776(HY-15532), which is a potent, selective and orally bioavailable i
2016-01-11 11:13 [上海]
上海皓元生物医药科技有限公司 [已核实]

7440.00/100mg
0100mg起订

RKI-1447
RKI-1447 is a potent small molecule inhibitor of ROCK1 and ROCK2.IC50 Value: 15.4 nM (ROCK1); 6.2 nM (ROCK2) [1]Target:
2016-01-11 11:11 [上海]
上海皓元生物医药科技有限公司 [已核实]

1116.00/10mg
010mg起订

Gemcitabine (Hydrochloride)
GemcitabineHcl (LY 188011 Hcl) is a DNA synthesis inhibitor with IC50 of 50 nM, 40 nM, 18 nM and 12 nM in PANC1, MIAPaCa
2016-01-11 11:09 [上海]
上海皓元生物医药科技有限公司 [已核实]

720.00/100mg
0100mg起订

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