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VE-822
VE-822 is a selective ATR inhibitor with an Ki value of 0.2 nM, 150 fold selectivity over ATM (Ki=34 nM), DNA-PK (Ki 4 u
2016-01-11 13:40 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

5626.00/100mg
0100mg起訂

CARM1-IN-1
CARM1-IN-1 is a potent and specific CARM1(Coactivator-associated arginine methyltransferase 1) inhibitor with IC50 of 8.
2016-01-11 13:39 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

3500.00/5mg
05mg起訂

ML324
ML324 is a potent JMJD2 demethylase inhibitor with demonstrated antiviral activity.IC50 value: 920 nM(JMJD2E) [1]Target:
2016-01-11 13:36 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

780.00/10mg
010mg起訂

NMS-873
NMS-873 is a potent, selective allosteric VCP/p97 inhibitor with IC50 value of 20 nM (Wild Type, 1 mM ATP).IC50 value: 2
2016-01-11 13:33 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

714.00/5mg
05mg起訂

EPZ015666
EPZ015666 is a potent, selective and orally bioavailable PRMT5 inhibitor with Ki of 5 nM, 20,000-fold selectivity over o
2016-01-11 13:31 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1550.00/5mg
05mg起訂

LSD1-IN-1
LSD1-IN-1 is a potent LSD1 inhibitor extracted from patent WO2013057322A1.公司介紹：MedChemExpress(MCE)專注于各種抑制劑
2016-01-11 13:30 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

3500.00/5mg
05mg起訂

Ro3280
RO3280 is a potent, highly selective inhibitor of Polo-like kinase 1 (PLK1) with IC50 of 3 nM.IC50 Value: 3 nM (PLK1) [1
2016-01-11 13:26 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

13020.00/50mg
050mg起訂

Cytarabine
Cytarabine (AraC) is an antimetabolic agent and DNA synthesis inhibitor.Target: DNA/RNA SynthesisCytarabine (AraC) is ph
2016-01-11 13:24 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

920.00/500mg
0500mg起訂

Cytarabine
Cytarabine (AraC) is an antimetabolic agent and DNA synthesis inhibitor.Target: DNA/RNA SynthesisCytarabine (AraC) is ph
2016-01-11 13:22 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

920.00/500mg
0500mg起訂

Cytarabine (hydrochloride)
Cytarabine (AraC) is an antimetabolic agent and DNA synthesis inhibitor.Target: DNA/RNA SynthesisCytarabine (AraC) is ph
2016-01-11 13:21 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

920.00/500mg
0500mg起訂

4'-Demethylepipodophyllotoxin
4'-Demethylepipodophyllotoxin(4'-DMEP) is a key intermediate compound for the preparation of podophyllotoxin-type anti-c
2016-01-11 13:19 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

450.00/50mg
050mg起訂

ABT-751
ABT-751(E 7010) is a novel bioavailable tubulin-binding and antimitotic sulfonamide agent with IC50 of about 1.5 and 3.4
2016-01-11 13:17 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

884.00/10mg
010mg起訂

P 22077
P22077 is a potent inhibitor of ubiquitin-specific protease (USP) 7 (EC50=8.6 uM), P22077 also inhibits the closely rela
2016-01-11 13:16 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1083.00/10mg
010mg起訂

Teprenone
Teprenone(Geranylgeranylacetone; GGA)is commonly utilized to protect the gastric mucosa in peptic ulcer disease; has bee
2016-01-11 13:14 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

940.00/1g
01g起訂

GSK-J4
GSK J4 is a cell permeable prodrug rapidly hydrolyzed by macrophage esterases to GSK-J1, a potent selective jumonji H3K2
2016-01-11 13:07 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1200.00/10mg
010mg起訂

EX-527 (R-enantiomer)
EX-527 R-enantiomer is a negative control of the active form EX-527 S-enantiomer(Speculated for reference); IC50100 uM,
2016-01-11 13:05 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

3500.00/5mg
05mg起訂

EX-527 (S-enantiomer)
EX-527 S-enantiomer is a potent and selective SIRT1 inhibitor with IC50 of 123 nM; no inhibition on SIRT3 and SIRT3.IC50
2016-01-11 13:04 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

3500.00/5mg
05mg起訂

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
2016-01-11 13:02 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

2195.00/5mg
05mg起訂

Fosbretabulin (disodium)
Fosbretabulin disodium(CA 4DP; CA 4P) is a microtubule destabilizing drug, a type of vascular-targeting agent, a drug de
2016-01-11 13:00 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

893.00/5mg
05mg起訂

HY-15687
SAR407899 Hcl is a potent, ATP-competitive ROCK inhibitor woth Ki value of 36 nM/41 nM for human ROCK/Rat ROCK respectiv
2016-01-11 12:59 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]