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TG003
TG003 is a potent inhibitor of Clk1/Sty and Clk4 with IC50 of 15-20 nM, less potency on Clk2(IC50= 200 nM).IC50 value: 2
2015-11-23 10:02 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1395.00/10mg
010mg起訂

LY2606368
LY2606368 is a potent and selective ATP competitive inhibitor(IC50=1.5 nM in SW1990 cell) of the Chk1 protein kinase.IC5
2015-11-23 10:01 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

13950.00/50mg
050mg起訂

Auristatin E
Auristatin E is a cytotoxic tubulin modifier with potent and selective antitumor activity; MMAE analog and cytotoxin in
2015-11-23 09:59 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

5500.00/1mg
01mg起訂

LEE011 (hydrochloride)
LEE011 Hcl is an orally available cyclin-dependent kinase (CDK) inhibitor targeting cyclin D1/CDK4 and cyclin D3/CDK6 ce
2015-11-23 09:57 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

2325.00/5mg
05mg起訂

Adenosine
Adenosine is a nucleoside composed of a molecule of adenine attached to a ribose sugar molecule (ribofuranose) moiety vi
2015-11-23 09:55 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

650.00/5g
05g起訂

I-BET151
I-BET151(GSK1210151A) is a BET bromodomain inhibitor(pIC50=6.1,BRD4); I-BET151 blocks recruitment of BET to chromatin .
2015-11-23 09:54 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1252.00/5mg
05mg起訂

Fotemustine
Fotemustine (S 10036) is a nitrosourea alkylating agent approved for use in the treatment of metastasising melanoma.Targ
2015-11-23 09:52 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

418.00/10mg
010mg起訂

Methotrexate
Methotrexate(WR19039; CL14377) can interfere with the growth of certain cells of the body, especially cells that reprodu
2015-11-23 09:50 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1083.00/100mg
0100mg起訂

Vinflunine
Vinflunine is a new vinca alkaloid uniquely fluorinated with the properties of mitotic-arresting and tubulin-interacting
2015-11-23 09:48 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1252.00/5mg
05mg起訂

Vidarabine
Vidarabine is an antiviral drug which is active against herpes simplex and varicella zoster viruses.Target: DNA/RNA Synt
2015-11-23 09:47 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1200.00/500mg
0500mg起訂

(+)-JQ-1
(+)-JQ1 is a BET bromodomain inhibitor, with IC50 of 77 nM/33 nM for BRD4(1/2).IC50 Value: 77 nM(for BRD4(1)); 33 nM( fo
2015-11-23 09:44 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1289.00/5mg
05mg起訂

K-115 (free base)
K-115, an isoquinolinesulfonamide compound, is a highly selective and potent (IC50 = 31 nM) Rho-kinase inhibitor; is in
2015-11-23 09:42 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

21000.00/100mg
0100mg起訂

Irinotecan (hydrochloride)
Irinotecan Hcl(CPT-11 Hcl) prevents DNA from unwinding by inhibition of topoisomerase 1.Target: Topoisomerase IIrinoteca
2015-11-23 09:40 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

884.00/500mg
0500mg起訂

PNU-159682
PNU-159682 is a major bioactive metabolite of Nemorubicin in human liver microsomes;3,000-fold cytotoxic than its parent
2015-11-23 09:39 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

21000.00/100mg
0100mg起訂

面議

OTX-015
OTX-015 is a new potent BRD2/3/4 inhibitor with evident anti-proliferative activity in several cell lines representative
2015-11-23 09:37 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

2046.00/5mg
05mg起訂

面議

XL413 (hydrochloride)
XL413 is a potent and selective Cdc7 inhibitor with an IC50 of 3.7 nM, 60-fold selectivity against CK2, 10-fold selectiv
2015-11-23 09:35 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

8370.00/100mg
0100mg起訂

5,5-二甲基海因97%
5,5-二甲基海因97%5,5-Dimethylhydantoin, 97%5,5-二甲基海因, 97%CAS 77-71-4 MDL MFCD00005266 EINECS: 201-051-3分子式: C5H8
2015-11-23 09:35 [北京]
北京中西科儀科技有限責(zé)任公司 [已核實]

面議

2,3,4,5,6-五氟苯甲基溴98+%
2,3,4,5,6-五氟苯甲基溴98+%2,3,4,5,6-Pentafluorobenzyl bromide, 98+%2,3,4,5,6-五氟苯甲基溴, 98+%CAS 1765-40-8 MDL MFCD000
2015-11-23 09:34 [北京]
北京中西科儀科技有限責(zé)任公司 [已核實]