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YM-155 (hydrochloride)
YM155 is a potent survivin suppressant by inhibiting Survivin promoter activity with IC50 of 0.54 nM.IC50 Value: 0.54 nM
2015-11-17 13:07 [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)

AMG 232
AMG 232 is a highly potent, selective and orally bioavailable piperidinone inhibitor of the MDM2-p53 interaction((SPR KD
2015-11-17 13:04 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2020.00/5mg
05mg起訂
詢價(jià)

BOC-D-FMK
BOC-D-FMK is a pan-caspase inhibitor.IC50 value:Target: Capase inhibitorin vitro: BOC-d-fmk prevented TUNEL staining.BOC
2015-11-17 13:02 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1395.00/5mg
05mg起訂
詢價(jià)

SMIP004
SMIP004 is a novel inducer of cancer-cell selective apoptosis of human prostate cancer cells, it was found to downregula
2015-11-17 13:00 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1730.00/5mg
05mg起訂
詢價(jià)

NVP-CGM097
NVP-CGM097(CGM-097) is a potent and selective MDM2 inhibitor; an orally bioavailable HDM2 antagonist with potential anti
2015-11-17 12:58 [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)

AT-101 (acetic acid)
AT101 acetic acid, the R-(-) enantiomer of Gossypol acetic acid, binds with Bcl-2, Bcl-xL and Mcl-1 with Ki of 0.32 M, 0
2015-11-17 12:56 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1100.00/10mg
010mg起訂
詢價(jià)

Gossypol (acetic acid)
Gossypol-acetic acid, a polyphenolic compound isolated from cottonseeds, inhibits Bcl-2 by acting as a BH3 mimetic.IC50
2015-11-17 12:54 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

950.00/200mg
0200mg起訂
詢價(jià)

Apoptosis Activator 2
Apoptosis Activator 2 is a potent apoptosis activator; increases procaspase-9 processing and subsequent caspase-3 activa
2015-11-17 12:51 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

900.00/10mg
010mg起訂
詢價(jià)

NSC319726
NSC319726 is a mutant p53R175 reactivator; inhibits growth of fibroblasts expressing the p53R175 mutation (IC50 = 8 nM);
2015-11-17 12:50 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

800.00/5mg
05mg起訂
詢價(jià)

Roquinimex
Roquinimex (Linomide; PNU212616; ABR212616) is a quinoline derivative immunostimulant which increases NK cell activity a
2015-11-17 12:48 [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
詢價(jià)

Meisoindigo
Meisoindigo(Natura-; N-Methylisoindigotin; Dian III), a derivative of Indigo naturalis, might induce apoptosis and myelo
2015-11-17 12:46 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

4650.00/10mg
010mg起訂
詢價(jià)

RITA
RITA(NSC 652287) induced both DNA-protein and DNA-DNA cross-links with no detectable DNA single-strand breaks. 公司介紹
2015-11-17 12:44 [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)

Marinopyrrole A
Marinopyrrole (Maritoclax) is a novel and specific Mcl-1 inhibitor with an IC50 value of 10.1 uM, 8 fold selectivity tha
2015-11-17 12:43 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3255.00/5mg
05mg起訂
詢價(jià)

Narciclasine
Narciclasine is a Rho/Rho kinase/LIM kinase/cofilin signaling pathway activator. 公司介紹：MedChemExpress(MCE)專注于各種
2015-11-17 12:40 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

837.00/1mg
01mg起訂
詢價(jià)

MI-773
MI-773 is an orally available spiro-oxindole HDM2 (human double minute 2) antagonist with potential antineoplastic activ
2015-11-17 12:38 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

19530.00/100mg
0100mg起訂
詢價(jià)

Lenalidomide
Lenalidomide (Revlimid, CC-5013) is a TNF- secretion inhibitor with IC50 of 13 nM.IC50 Value: 13 nM [1]Target: TNF-alpha
2015-11-17 12:37 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2464.00/1g
01g起訂
詢價(jià)

(20S)-Protopanaxadiol
(20S)-Protopanaxadiol (20-Epiprotopanaxadiol) is an aglycon metabolic derivative of the protopanaxadiol-type ginseng sap
2015-11-17 12:34 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2278.00/50mg
050mg起訂
詢價(jià)

Epibrassinolide
Epibrassinolide (EBR; B1105; 24-Epibrassinolide) is a biologically active compound of the brassinosteroids, steroid-deri
2015-11-17 12:16 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1440.00/5mg
05mg起訂
詢價(jià)

Bioymifi
Bioymifi(DR5 Activator) is the first novel and potent small-molecule activatior of the TRAIL receptor DR5 in human cance
2015-11-17 11:11 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

880.00/5mg
05mg起訂
詢價(jià)

Z-VAD-FMK
Z-VAD-FMK is a cell-permeable, irreversible broad-spectrum caspase inhibitor, blocks all features of apoptosis.IC50 valu
2015-11-17 11:07 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]