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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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1989.00/5mg
05mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1548.00/5mg
05mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

850.00/5mg
05mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1050.00/5mg
05mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

7440.00/100mg
0100mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1116.00/10mg
010mg起訂
詢價(jià)

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]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

720.00/100mg
0100mg起訂
詢價(jià)

Capecitabine
Capecitabine is an anti-cancer chemotherapy drug.公司介紹：MedChemExpress(MCE)專注于各種抑制劑、激動(dòng)劑、API及化合物庫，
2016-01-11 11:08 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

670.00/1g
01g起訂
詢價(jià)

Lomustine
Lomustine (CCNU) is an alkylating nitrosourea compound used in chemotherapy.公司介紹：MedChemExpress(MCE)專注于各種抑制
2016-01-11 11:05 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

960.00/200mg
0200mg起訂
詢價(jià)

AZD-7762
AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM; equally potent against Chk2 and less potent again
2016-01-11 11:03 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

884.00/5mg
05mg起訂
詢價(jià)

Taltobulin (trifluoroacetate)
Taltobulin trifluoroacetate (HTI-286; SPA-110) is an analogue of Hemiasterlin; potent tubulin inhibitor; ADCs cytotoxin.
2016-01-11 11:01 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3080.00/5mg
05mg起訂
詢價(jià)

LEE011
LEE011 is an orally available cyclin-dependent kinase (CDK) inhibitor targeting cyclin D1/CDK4 and cyclin D3/CDK6 cell c
2016-01-11 11:00 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

960.00/5mg
05mg起訂
詢價(jià)

SBE13
SBE13 is a potent and selective PLK1 with IC50 of 0.2 nM; no inhibition om Aurora A kinase, Plk2 and Plk3.IC50 value: 0.
2016-01-11 10:58 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

980.00/10mg
010mg起訂
詢價(jià)

SBE13 (Hydrochloride)
SBE13 Hcl is a potent and selective PLK1 with IC50 of 0.2 nM; no inhibition om Aurora A kinase, Plk2 and Plk3.IC50 value
2016-01-11 10:57 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

980.00/10mg
010mg起訂
詢價(jià)

Ro-3306
Ro-3306 is a potent and selective inhibitor of CDK1 with Ki value of 35 nM for CDK1/cyclin B1, 10-fold selectivity relat
2016-01-11 10:55 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1150.00/5mg
05mg起訂
詢價(jià)

CX-4945 (sodium salt)
CX-4945 (Silmitasertib) sodium salt is a potent and selective ATP-competitive small molecule protein kinase CK2 inhibito
2016-01-11 10:53 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1100.00/5mg
05mg起訂
詢價(jià)

VER-155008
VER-155008 is a novel, small molecule inhibitor of Hsc70/Hsp70 with GI50 of 5.3-14.4 uM in human breast and colon cancer
2016-01-11 10:49 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

800.00/5mg
05mg起訂
詢價(jià)

VAL-083
VAL-083 is a bi-functional alkylating agent; inhibit U251 and SF188 cell growth in monolayer better than TMZ and caused
2016-01-11 10:47 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2604.00/5mg
05mg起訂
詢價(jià)

CHIR-124
CHIR-124 is a novel and potent Chk1 inhibitor with IC50 of 0.3 nM; 2,000-fold selectivity against Chk2, 500- to 5,000-fo
2016-01-11 10:45 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

930.00/5mg
05mg起訂
詢價(jià)

SP2509
SP2509 is a novel histone demethylase LSD1 (KDM1A) antagonist with IC50 of 13 nM; no inhibition on MAO-A and MAO-B.IC50
2016-01-11 10:44 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]