国产精品vr无码专区,久久精品国产亚洲一区二区三区

SJB3-019A
SJB3-019A is a potent and novel usp1 inhibitor.公司介紹：MedChemExpress(MCE)專(zhuān)注于各種抑制劑、激動(dòng)劑、API及化合物庫(kù)，總
2015-11-19 14:14 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

7952.00/50mg
050mg起訂
詢價(jià)

TG-101348
TG-101348 (SAR302503) is a selective inhibitor of JAK2 with IC50 of 3 nM, 35- and 334-fold more selective for JAK2 versu
2015-11-19 14:10 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1252.00/10mg
010mg起訂
詢價(jià)

DMAT
DMAT is a potent and specific CK2 inhibitor with an IC50 of 0.13 uM.公司介紹：MedChemExpress(MCE)專(zhuān)注于各種抑制劑、激動(dòng)
2015-11-19 14:08 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

744.00/10mg
010mg起訂
詢價(jià)

TBB
TBB(NSC 231634) is a highly selective, ATP/GTP-competitive inhibitor of casein kinase-2 (CK2)with IC50s of 0.9 and 1.6 M
2015-11-19 14:06 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

530.00/10mg
010mg起訂
詢價(jià)

TTP 22
TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/Ki of 0.1 uM/40 nM; shows selectivi
2015-11-19 14:04 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1023.00/10mg
010mg起訂
詢價(jià)

HY-B0080
Folinic Acid is a reduced folic acid, which is used in combination with other chemotherapy drugs.Target: Folate analogAp
2015-11-19 14:03 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

560.00/100mg
0100mg起訂
詢價(jià)

GSK-J1 (lithium salt)
GSK-J1 is a potent and selective inhibitor of the H3K27 histone demethylases JMJD3 and UTX (IC50 = 60 nM for human JMJD3
2015-11-19 14:01 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1240.00/10mg
010mg起訂
詢價(jià)

Pirarubicin
Pirarubicin is an analogue of the anthracycline anti-neoplastic doxorubicin, which is an inhibitor of Topo IITarget: Top
2015-11-19 13:59 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

781.00/10mg
010mg起訂
詢價(jià)

CAY10603
CAY10603 is a potent and selective inhibitor of HDAC6 with IC50 of 2 pM, as compared with 271, 252, 0.42, 6851, and 90.7
2015-11-19 13:57 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

750.00/1mg
01mg起訂
詢價(jià)

Epirubicin
Epirubicin, a semisynthetic L-arabino derivative of doxorubicin, is an antineoplastic agent by inhibiting Topoisomerase.
2015-11-19 13:53 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2009.00/10mg
010mg起訂
詢價(jià)

Epirubicin
Epirubicin, a semisynthetic L-arabino derivative of doxorubicin, is an antineoplastic agent by inhibiting Topoisomerase.
2015-11-19 13:53 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2009.00/10mg
010mg起訂
詢價(jià)

GSK2656157
GSK2656157 is an ATP-competitive inhibitor of PERK enzyme activity with an IC(50) of 0.9 nM; is highly selective for PER
2015-11-19 13:51 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1350.00/10mg
010mg起訂
詢價(jià)

Leucovorin (Calcium)
Leucovorin Calcium is a reduced folic acid.IC50 Value: 30 M for zcSHMT and70 M for zmSHMT [2]Target: Antifolatein vitro:
2015-11-19 13:49 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1800.00/500mg
0500mg起訂
詢價(jià)

FH535
FH535 is a compound that suppresses both Wnt/beta-catenin and peroxisome proliferator-activated receptor (PPAR) signalin
2015-11-19 13:47 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

558.00/10mg
010mg起訂
詢價(jià)

LY2606368 (dihydrochloride)
LY2606368 2Hcl is a potent and selective ATP competitive inhibitor(IC50=1.5 nM in SW1990 cell) of the Chk1 protein kinas
2015-11-19 13:45 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

21000.00/100mg
0100mg起訂
詢價(jià)

Floxuridine
Floxuridine (5-fluorodeoxyuridine) is an oncology drug that belongs to the class known as antimetabolites with an GI50 o
2015-11-19 13:44 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3000.00/500mg
0500mg起訂
詢價(jià)

GSK-J2
GSK-J2 is a pyridine regio-isomer of GSK-J1 which poorly inhibits JMJD3 (IC50100 M), making it an appropriate negative c
2015-11-19 13:42 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

5200.00/50mg
050mg起訂
詢價(jià)

GSK269962A
GSK269962A(GSK269962) is a potent ROCK inhibitor (IC50 values are 1.6 and 4 nM for recombinant human ROCK1 and ROCK2 res
2015-11-19 13:40 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

744.00/5mg
05mg起訂
詢價(jià)

UNC 0631
UNC 0631 is a potent G9a inhibitor with IC50 value of 4 nM.IC50 value: 4 nM [1]Target: G9aUNC 0631, which had high in vi
2015-11-19 13:37 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1070.00/5mg
05mg起訂
詢價(jià)

C646
C646 is a selective competitive histone acetyltransferase p300 inhibitor with Ki of 400 nM; less potent for other acetyl
2015-11-19 13:35 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]