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HDAC-IN-1
HDAC-IN-1 is a chemical analog of MC 1568, which is a potent and selective class IIa HDACs inhibitor.公司介紹：MedChemEx
2015-12-09 10:42 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

884.00/10mg
010mg起訂

RG108
RG108 is a non-nucleoside inhibitor of DNA methyltransferase with IC50 of 115 nM.IC50 Value: 115 nMTarget: DNMTin vitro:
2015-12-09 10:40 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

847.00/10mg
010mg起訂

LY2835219 (free base)
LY2835219 is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM and 10 nM, respectively.IC50 Value: 2 n
2015-12-09 10:38 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1023.00/5mg
05mg起訂

LY2835219
LY2835219 is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM and 10 nM, respectively.IC50 Value: 2 n
2015-12-09 10:36 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

8835.00/100mg
0100mg起訂

CDK9-IN-2
CDK9-IN-2 is a novel cyclin-dependent kinase 9(CDK9) inhibitor.IC50 value:Target: CDK9公司介紹：MedChemExpress(MCE)專注
2015-12-09 10:34 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

2660.00/5mg
05mg起訂

Aleglitazar
Aleglitazar(R1439; RO-0728804) is a new dual PPAR-/ agonist with IC50 of 2.8 nM/4.6 nM.IC50 Value: 2.8 nM(PPAR-); 4.6 nM
2015-12-09 10:32 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

2660.00/5mg
05mg起訂

INNO-206
INNO-206 (Aldoxorubicin) is the 6-maleimidocaproyl hydrazone derivative prodrug of the anthracycline antibiotic doxorubi
2015-12-09 10:30 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1740.00/10mg
010mg起訂

ARRY-520 (R enantiomer)
ARRY-520 R enantiomer is the R form of ARRY-520, which is a synthetic, small molecule kinesin spindle protein (KSP) inhi
2015-12-09 10:28 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

884.00/5mg
05mg起訂

MI-3
MI-3 is a Menin-MLL interaction inhibitor with IC50 value of 64825 nM.IC50 value: 64825 nM [1]Target: Menin-MLLin vitro:
2015-12-09 10:26 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

10044.00/100mg
0100mg起訂

MI-3
MI-3 is a Menin-MLL interaction inhibitor with IC50 value of 64825 nM.IC50 value: 64825 nM [1]Target: Menin-MLLin vitro:
2015-12-09 10:26 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

10044.00/100mg
0100mg起訂

Scriptaid
Scriptaid(Scriptide; GCK-1026) is an inhibitor of HDAC; shows a greater effect on acetylated H4 than H3.IC50 Value:Targe
2015-12-09 10:24 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1650.00/10mg
010mg起訂

HY-16568
Irinotecan Hcl-trihydrate prevents DNA from unwinding by inhibition of topoisomerase 1.IC50 Value: 15.8 M(LoVo cells); 5
2015-12-09 10:22 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1950.00/200mg
0200mg起訂

Irinotecan
Irinotecan(CPT-11) prevents DNA from unwinding by inhibition of topoisomerase 1.IC50 Value: 15.8 M(LoVo cells); 5.17 M(H
2015-12-09 10:20 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

515.00/100mg
0100mg起訂

AT7519 (trifluoroacetate)
AT7519 trifluoroacetate is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210 nM; less potent to CDK3 and
2015-12-09 10:18 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

810.00/5mg
05mg起訂

HY-13627
Estramustine phosphate sodium is an antimicrotubule chemotherapy agent; arrests prostate cancer cells in the G2/M phase
2015-12-09 10:16 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

600.00/10mg
010mg起訂

Mc-MMAE
Monomethyl auristatin E (MMAE), a potent tubulin inhibitor, is a toxin payload in antibody drug conjugate; Mc-MMAE is a
2015-12-09 10:14 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

13950.00/10mg
010mg起訂

SGI-1027
SGI-1027 is a potent and selective inhibitor of DNA methyltransferase (DNMT) with IC50 of 6, 8, 7.5 M for DNMT1, DNMT3A,
2015-12-09 10:10 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1083.00/10mg
010mg起訂

Rosiglitazone
Rosiglitazone(BRL-49653) is a high-affinity selective agonist of the peroxisome proliferator-activated receptor-(PPAR).I
2015-12-09 10:08 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1800.00/200mg
0200mg起訂

面議

Amberlyst?16離子交換樹脂
Amberlyst16離子交換樹脂Amberlyst 16 wet strongly acidic, H+-formCAS Number: 125004-35-5MDL number: MFCD03791386Propertie
2015-12-07 09:42 [北京]
北京中西科儀科技有限責任公司 [已核實]