上海_化學(xué)藥品_產(chǎn)品搜索_第68頁(yè)

S1RA
S1RA(E-52862) is a potent and selective sigma-1 receptor(1R, Ki=17 nM) antagonist, showed good selectivity against 2R (K
2016-01-12 16:29 [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
詢價(jià)

HY-13510
SA4503 2Hcl(AGY-94806 2Hcl; Cutamesine 2Hcl) is a selective sigma 1 receptor(1R) agonist; high affinity for the sigma 1
2016-01-12 16:25 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1190.00/10mg
010mg起訂
詢價(jià)

Purvalanol B
Purvalanol B(NG-95) is a cyclin-dependent kinase inhibitor with IC50 values of 6, 6, 9,10,000, and 6 nM for cdc2/cyclin
2016-01-12 16:23 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1450.00/10mg
010mg起訂
詢價(jià)

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
2016-01-12 16:21 [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)

PF-3758309
PF-3758309 is an inhbitor of PAKs with IC50 of 1.3 nM for PAK4; inhbits tumor growth in HCT116, A549, M24met and other x
2016-01-12 16:20 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

698.00/5mg
05mg起訂
詢價(jià)

EI1
EI1 is a potent and selective small molecule inhibitor of EZH2 with IC50 values of 15 nM and 13 nM for wild type EZH2 an
2016-01-12 16:18 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2195.00/5mg
05mg起訂
詢價(jià)

Altretamine (hydrochloride)
Altretamine is an alkylating agent proposed as an antineoplastic.公司介紹：MedChemExpress(MCE)專注于各種抑制劑、激動(dòng)劑、
2016-01-11 14:30 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1188.00/500mg
0500mg起訂
詢價(jià)

Altretamine
Altretamine is an alkylating agent proposed as an antineoplastic.公司介紹：MedChemExpress(MCE)專注于各種抑制劑、激動(dòng)劑、
2016-01-11 14:28 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1188.00/500mg
0500mg起訂
詢價(jià)

XL228
XL228 is a protein kinase inhibitor targeting IGF1R, the Aurora kinases, FGFR1-3, ABL and SRC family kinases.IC50 Value:
2016-01-11 14:26 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

6975.00/100mg
0100mg起訂
詢價(jià)

Rigosertib
Rigosertib (ON-01910) is a non-ATP-competitive inhibitor of PLK1 with IC50 of 9 nM; shows 30-fold greater selectivity ag
2016-01-11 14:25 [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
詢價(jià)

D-64131
D-64131 is a novel inhibitor of Tubulin polymerization that competitively binds with [(3)H]colchicine to -Tubulin.公司介
2016-01-11 14:24 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

818.00/10mg
010mg起訂
詢價(jià)

IPA-3
IPA-3 is a selective non-ATP competitive PAK1 inhibitor with IC50 of 2.5 M, no inhibition to group II PAKs (PAKs 4-6).IC
2016-01-11 14:22 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

515.00/5mg
05mg起訂
詢價(jià)

GSK-923295
GSK923295 is a first-in-class, specific allosteric inhibitor of CENP-E kinesin motor ATPase with Ki of 3.2 nM, and less
2016-01-11 14:15 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2864.00/10mg
010mg起訂
詢價(jià)

FRAX486
FRAX486 is a selective inhibitor of group I PAKs with IC50s of 8.25/39.5, /55.3 nM for PAK1/PAK2/PAK3 respectivelt; less
2016-01-11 14:13 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1450.00/10mg
010mg起訂
詢價(jià)

NMS-859
NMS-859 is a potent and specific small molecule covalent inhibitor of the ATPase VCP/p97 (IC50 ~0.37 M), identified by h
2016-01-11 14:12 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3500.00/5mg
05mg起訂
詢價(jià)

PYR-41
PYR-41 is a specific and cell permeable inhibitor of ubiquitin-activating enzyme E1 with an IC50 of10 uM, with no or lit
2016-01-11 14:10 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1083.00/10mg
010mg起訂
詢價(jià)

Betulinic acid
Betulinic acid, a pentacyclic triterpene, selectively induces apoptosis in tumor cells, also is a inhibitor of HIV-1 wit
2016-01-11 14:09 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

5079.00/500mg
0500mg起訂
詢價(jià)

Troglitazone
Troglitazone(CS-045), PPAR agonist, is an anti-diabetic thiazolidinedione (TZD) with anti-inflammatory and anti-tumor ac
2016-01-11 14:07 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

790.00/10mg
010mg起訂
詢價(jià)

PYZD-4409
PYZD-4409 is a novel small molecule inhibitor of Ubiquitin-activating enzyme UBA1/E1 enzyme with an IC50 of 20 uM (cell-
2016-01-11 14:06 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2325.00/5mg
05mg起訂
詢價(jià)

Chidamide
Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM for HDAC1/2/3/8; also inhibits HDA
2016-01-11 14:04 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]