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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(shí)]

1252.00/5mg
05mg起訂
詢價(jià)

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(shí)]

500.00/10mg
010mg起訂
詢價(jià)

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(shí)]

10230.00/100mg
0100mg起訂
詢價(jià)

Purvalanol A
Purvalanol A(NG-60) is a potent, cell-permeable, and selective inhibitor of cyclin-dependent kinases (CDKs) with IC50 va
2015-12-24 15:50 [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)

RGFP966
RGFP966 is specific inhibitor of HDAC3, with an IC50 of 0.08 M and no effective inhibition of any other HDAC at concentr
2015-12-24 15:48 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1004.00/5mg
05mg起訂
詢價(jià)

CUDC-907
CUDC-907 potently inhibits class I PI3Ks as well as classes I and II HDAC enzymes.IC50 Value: 1.7/5.0/1.8/2.8 nM (HDAC1/
2015-12-21 17:30 [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)

HY-13911A
Hydroxyfasudil Hcl(HA1100 Hcl), metabolite of Fasudil, is a potent Rho-kinase inhibitor and vasodilator.IC50 Value: 0.12
2015-12-21 17:29 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

4604.00/50mg
050mg起訂
詢價(jià)

Hydroxyfasudil
Hydroxyfasudil(HA1100), metabolite of Fasudil, is a potent Rho-kinase inhibitor and vasodilator.IC50 Value: 0.12 uM (ROC
2015-12-21 17:26 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1051.00/10mg
010mg起訂
詢價(jià)

SN-38
SN-38(NK-012) is an active metabolite of CPT-11, inhibits DNA topoisomerase I, DNA synthesis and causes frequent DNA sin
2015-12-21 17:24 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

990.00/100mg
0100mg起訂
詢價(jià)

360A (iodide)
360A is a strong affinity and selectivity inhibitor of G-quadruplex structures.IC50 Value:Target: G-quadruplexin vitro:
2015-12-21 17:22 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2320.00/5mg
05mg起訂
詢價(jià)

H-1152 (dihydrochloride)
H-1152 2Hcl, an isoquinolinesulfonamide derivative, is a more specific, stronger and membrane-permeable inhibitor of Rho
2015-12-21 17:20 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3255.00/10mg
010mg起訂
詢價(jià)

H-1152
H-1152, an isoquinolinesulfonamide derivative, is a more specific, stronger and membrane-permeable inhibitor of Rho-kina
2015-12-21 17:19 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1860.00/5mg
05mg起訂
詢價(jià)

NU 7026
NU 7026 is a novel and potential inhibitor of the DNA repair enzyme DNA-dependent protein kinase (DNA-PK) with IC50 of 0
2015-12-21 17:17 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

560.00/5mg
05mg起訂
詢價(jià)

RG2833
RG2833 (RGFP109) is a brain-penetrant HDAC inhibitor with IC50 of 60 nM and 50 nM for HDAC1 and HDAC3, respectively.IC50
2015-12-21 17:14 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

714.00/10mg
010mg起訂
詢價(jià)

GSK2606414
GSK2606414 is an orally available, potent, and selective PERK inhibitor with an IC50 of 0.4 nM.IC50 Value: 0.4 nM [1]Tar
2015-12-21 17:12 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1451.00/5mg
05mg起訂
詢價(jià)

Reversine
Reversine, a small synthetic purine analogue (2,6-disubstituted purine), is a potent inhibitior of Aurora A/B/C with IC5
2015-12-21 17:11 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

651.00/5mg
05mg起訂
詢價(jià)

Pyridostatin
Pyridostatin(RR-82) is a G-quadruplex-interacting drug which can promote growth arrest in human cancer cells by inducing
2015-12-21 17:09 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

9380.00/100mg
0100mg起訂
詢價(jià)

Resminostat
Resminostat(RAS2410; 4SC-201) is a potent inhibitor of HDAC1/3/6(IC50=43-72 nM); less potent to HDAC8 with IC50 of 877 n
2015-12-21 17:07 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1989.00/10mg
010mg起訂
詢價(jià)

PR-619
PR-619 is a broad-range DUB inhibitor with potential for further development as a chemotherapeutic agent in cancer thera
2015-12-21 16:59 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

800.00/10mg
010mg起訂
詢價(jià)

Tenovin-1
Tenovin-1 is a inhibitor of SIRT1 and SIRT2; activator of p21 and p53.IC50 Value:Target: SirtuinTenovin-1 is a compound
2015-12-21 16:57 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]