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2015-09-16

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[北京]

2015-09-17

藿香正氣丸

中國醫(yī)藥化工網

[北京]

2015-09-16

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[北京]

2015-09-16

人工牛黃甲硝唑膠囊

中國醫(yī)藥化工網

[北京]

2015-09-16

布洛芬緩解膠囊

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2015-09-16

手術器械

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2015-11-23

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2015-09-18

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2015-09-15

和龍市人民醫(yī)院等脈動真空滅菌器等設備采購公告

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2015-09-18

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2015-09-18

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2015-09-16

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ELR510444
ELR510444 is a novel microtubule disruptor; inhibits MDA-MB-231 cell proliferation with IC50 of 30.9 nM; not a substrate
2015-12-24 16:59 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1400.00/5mg
05mg起訂

3-Deazaneplanocin A
3-Deazaneplanocin A (DZNep) is an attractive epigenetic anticancer agent through the inhibition of the cellular enhancer
2015-12-24 16:58 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

4201.00/5mg
05mg起訂

AMG 925
AMG 925 is a potent and selective dual inhibtor of CDK4/FLT3 with IC50s of 1.5 nM and 2.4 nM for CDK4 and FLT3, respecti
2015-12-24 16:54 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

9114.00/5mg
05mg起訂

Teniposide
Teniposide(VM-26) is a semisynthetic derivative of podophyllotoxin and are increasingly used in cancer medicine; causing
2015-12-24 16:52 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1308.00/50mg
050mg起訂

ARRY-520
ARRY-520 is a synthetic, small molecule kinesin spindle protein (KSP) inhibitor with IC50 of 6 nM. 公司介紹：MedChemExpr
2015-12-24 16:50 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

884.00/5mg
05mg起訂

DC_05
DC_05 is a non-nucleoside DNMT1 inhibitor(IC50=10.3 uM) with low micromolar IC50 values and significant selectivity towa
2015-12-24 16:48 [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

360A
360A is a strong affinity and selectivity inhibitor of G-quadruplex structures.IC50 Value:Target: G-quadruplexin vitro:
2015-12-24 16:43 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

2320.00/5mg
05mg起訂

EX-527
EX 527 is a potent and selective SIRT1 inhibitor with IC50 of 38 nM, exhibits 200-fold selectivity against SIRT2 and SIR
2015-12-24 16:39 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

589.00/10mg
010mg起訂

Cycloguanil D6
Cycloguanil D6 is the deuterium labeled Cycloguanil, which is a dihydrofolate reductase inhibitor.公司介紹：MedChemExpre
2015-12-24 16:37 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

900.00/1mg
01mg起訂

GW9662
GW9662 is a selective PPAR antagonist for PPAR with IC50 of 3.3 nM, with ~10 and ~1000-fold functional selectivity in ce
2015-12-24 16:36 [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

Poloxime
The phosphoserine/phosphothreonine recognition site of the polo-box domain of polo-like kinase 1 is the binding pocket f
2015-12-24 16:34 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1265.00/10mg
010mg起訂

M344
M344 is a potent HDAC inhibitor, which can also induced expression of the pro-apoptotic genes, Puma and Bax, together wi
2015-12-24 16:21 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1265.00/10mg
010mg起訂

SCH-1473759
SCH 1473759 is a novel sub-nanomolar Aurora A/B inhibitor with IC50 of 4 nM and 13 nM, respectively.IC50 Value: 4 nM (Au
2015-12-24 16:05 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

2604.00/5mg
05mg起訂

SRT 1720
SRT1720 is a selective activator of human SIRT1 (EC1.5 = 0.16 M) versus the closest sirtuin homologues, SIRT2 and SIRT3(
2015-12-24 16:03 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1252.00/5mg
05mg起訂

KU-57788
KU-57788(NU7441) is a potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor with IC50 value of are 14 nM;
2015-12-24 16:01 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

837.00/10mg
010mg起訂

KU-60019
KU-60019 is an improved analogue of KU-55933, with IC50 of 6.3 nM for ATM.IC50 Value: 6.3 nMTarget: ATMin vitro: KU-6001
2015-12-24 16:00 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1116.00/10mg
010mg起訂

KU-55933
KU-55933 is a potent ATM inhibitor with an IC50 and Ki of 13 and 2.2 nM, respectively; highly selective for ATM as compa
2015-12-24 15:58 [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

CP-466722
CP-466722 is rapidly reversible potential ATM kinase inhibitor.IC50 Value:Target: ATMCP-466722 is non-toxic and does not
2015-12-24 15:56 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

1252.00/5mg
05mg起訂

Flumequine
Flumequine is a synthetic chemotherapeutic antibiotic, inhibiting topoisomerase II with IC50 of 15 M.Target: Topoisomera
2015-12-24 15:54 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]

500.00/10mg
010mg起訂

Resminostat (hydrochloride)
Resminostat Hcl(RAS2410; 4SC-201) is a potent inhibitor of HDAC1/3/6(IC50=43-72 nM); less potent to HDAC8 with IC50 of 8
2015-12-24 15:52 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實]