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XL413
XL413 is a potent and selective Cdc7 inhibitor with an IC50 of 3.7 nM, 60-fold selectivity against CK2, 10-fold selectiv
2015-11-19 14:40 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1330.00/5mg
05mg起訂

6-Thioguanine
6-Thioguanine(6-TG) belongs to the thiopurine family of drugs that also include mercaptopurine and azathioprine, which a
2015-11-19 14:38 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1252.00/500mg
0500mg起訂

HY-15777C
LEE011 succinate hydrate is an orally available cyclin-dependent kinase (CDK) inhibitor targeting cyclin D1/CDK4 and cyc
2015-11-19 14:36 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3534.00/10mg
010mg起訂

Fasudil
Fasudil Hcl(HA-1077; AT-877) is a potent inhibitor of ROCK-II, PKA, PKG, PKC, and MLCK with Ki of 0.33 M, 1.6 M, 1.6 M,
2015-11-19 14:34 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1252.00/500mg
0500mg起訂

Pralatrexate
Pralatrexate(Folotyn) is an antifolate, and structurally a folate analog.公司介紹：MedChemExpress(MCE)專注于各種抑制劑、
2015-11-19 14:32 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1534.00/5mg
05mg起訂

Eribulin
Eribulin (E7389; ER-086526), a synthetic analogue of halichondrin B in phase III clinical trials for breast cancer, bind
2015-11-19 14:30 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

35000.00/1mg
01mg起訂

Bezafibrate
Bezafibrate(BM15075) is the first clinically tested dual and pan-PPAR co-agonism.Target: PPARBezafibrate is a lipid-lowe
2015-11-19 14:28 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

450.00/100mg
0100mg起訂

Eribulin (mesylate)
Eribulin Mesylate (E7389 Mesylate), a synthetic analogue of halichondrin B in phase III clinical trials for breast cance
2015-11-19 14:26 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

35000.00/1mg
01mg起訂

GSK-J1
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 14:24 [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

Zebularine
Zebularine(NSC309132; 4-Deoxyuridine) is a DNA methylation inhibitor that forms a covalent complex with DNA methyltransf
2015-11-19 14:22 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

715.00/10mg
010mg起訂

FRAX597
FRAX597, a small-molecule pyridopyrimidinone, is a potent and ATP competitive inhibitor of the group I PAKs (PAK1 IC50=
2015-11-19 14:20 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

13950.00/50mg
050mg起訂

SJB2-043
SJB2-043 is one of analogs/derivatives of C527, which is a novel and potent USP1 (ubiquitin-specific protease 1) inhibit
2015-11-19 14:17 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

7821.00/50mg
050mg起訂

EPZ004777
EPZ004777 is a potent, selective DOT1L inhibitor with IC50 of 0.4 nM.IC50 value: 0.4 nM [1]Target: DOT1Lin vitro: EPZ004
2015-11-19 14:16 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1674.00/5mg
05mg起訂

SJB3-019A
SJB3-019A is a potent and novel usp1 inhibitor.公司介紹：MedChemExpress(MCE)專注于各種抑制劑、激動劑、API及化合物庫，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

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

DMAT
DMAT is a potent and specific CK2 inhibitor with an IC50 of 0.13 uM.公司介紹：MedChemExpress(MCE)專注于各種抑制劑、激動
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

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

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

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

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)]