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Adarotene
Adarotene (ST1926) is an effective apoptosis inducer and surprisingly produced DNA damage.ST1926 exhibites a potent anti
2015-11-18 09:18 [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)

CUDC-427
CUDC-427(GDC-0917) is a small-molecule peptide mimetic of SMAC/DIABLO; directly antagonize inhibitors of apoptosis prote
2015-11-18 09:16 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1750.00/5mg
05mg起訂
詢價(jià)

CID 2011756
CID-2011756 is a cell-active ATP competitive and specific PKD1 inhibitor that inhibits phorbol ester-induced endogenous
2015-11-18 09:15 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

884.00/10mg
010mg起訂
詢價(jià)

kb NB 142-70
kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28.3, 58.7 and 53.2 nM for PKD1, 2 and 3 r
2015-11-18 09:13 [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)

Necrostatin 2
Necrostatin 2 is a potent necroptosis inhibitor with EC50 of 50 nM.IC50 Value: 50 nM (EC50) [1]Target: TNF-alphaNecrosta
2015-11-18 09:11 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

6250.00/50mg
050mg起訂
詢價(jià)

PM00104
Zalypsis(PM00104) is an alkaloid analog to certain natural marine compound. 公司介紹：MedChemExpress(MCE)專注于各種抑制
2015-11-18 09:08 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

27900.00/1mg
01mg起訂
詢價(jià)

SJ-172550
SJ-172550 is the first MDMX inhibitor with EC50 of 0.84 uM; binds reversibly to MDMX and effectively kills retinoblastom
2015-11-18 09:06 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1160.00/10mg
010mg起訂
詢價(jià)

BAM7
BAM 7 is a direct and selective activator of proapoptotic Bax with EC50 of 3.3 M.IC50 Value: 3.3 uM(EC50) [1]Target: Bcl
2015-11-18 09:04 [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)

ABT-737
ABT-737 is a BH3 mimetic inhibitor of Bcl-xL, Bcl-2 and Bcl-w with EC50 of 78.7 nM, 30.3 nM and 197.8 nM, respectively;
2015-11-18 09:02 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

884.00/5mg
05mg起訂
詢價(jià)

Necrostatin-1
Necrostatin-1 is a specific RIP1 inhibitor and inhibits TNF--induced necroptosis with EC50 of 490 nM.IC50 Value: 490 nM
2015-11-18 09:01 [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)

WEHI-539
WEHI-539, has high affinity (subnanomolar) and selectivity for BCL-XL and potently kills cells by selectively antagonizi
2015-11-18 08:59 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2492.00/10mg
010mg起訂
詢價(jià)

Navitoclax
ABT-263 (Navitoclax) is a potent inhibitor of Bcl-xL, Bcl-2 and Bcl-w with Ki of0.5 nM, 1 nM and 1 nM.IC50 Value:0.5 nM(
2015-11-18 08:57 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

884.00/5mg
05mg起訂
詢價(jià)

WEHI-539 (hydrochloride)
WEHI-539, has high affinity (subnanomolar) and selectivity for BCL-XL and potently kills cells by selectively antagonizi
2015-11-18 08:55 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1944.00/5mg
05mg起訂
詢價(jià)

TW-37
TW-37 is a novel nonpeptide inhibitor to recombinant Bcl-2, Bcl-xL and Mcl-1 with Ki of 0.29 M, 1.11 M and 0.26 M, respe
2015-11-18 08:53 [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)

Necrostatin 2 (S enantiomer)
Necrostatin 2 is a potent necroptosis inhibitor with EC50 of 50 nM.IC50 Value: 50 nM (EC50) [1]Target: TNF-alphaNecrosta
2015-11-18 08:51 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

7952.00/50mg
050mg起訂
詢價(jià)

10058-F4
10058-F4 is a cell-permeable thiazolidinone that specificallly inhibits the c-Myc-Max interaction and prevents transacti
2015-11-18 08:48 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

480.00/5mg
05mg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
2015-11-17 13:11 [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)

Nutlin-3
Nutlin-3 is MDM2 antagonist.公司介紹：MedChemExpress(MCE)專注于各種抑制劑、激動(dòng)劑、API及化合物庫(kù)，總部位于美國(guó)新澤西，分
2015-11-17 13:09 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1600.00/10mg
010mg起訂
詢價(jià)

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)]