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Betulinic acid
Betulinic acid, a pentacyclic triterpene, selectively induces apoptosis in tumor cells, also is a inhibitor of HIV-1 wit
2016-01-11 14:09 [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)

Troglitazone
Troglitazone(CS-045), PPAR agonist, is an anti-diabetic thiazolidinedione (TZD) with anti-inflammatory and anti-tumor ac
2016-01-11 14:07 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

790.00/10mg
010mg起訂
詢價(jià)

PYZD-4409
PYZD-4409 is a novel small molecule inhibitor of Ubiquitin-activating enzyme UBA1/E1 enzyme with an IC50 of 20 uM (cell-
2016-01-11 14:06 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

2325.00/5mg
05mg起訂
詢價(jià)

Chidamide
Chidamide(CS055; HBI-8000) is a class I HDAC inhibitor with IC50s of 95/160/67/733 nM for HDAC1/2/3/8; also inhibits HDA
2016-01-11 14:04 [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)

PHA-767491
PHA-767491 (CAY10572) is a potent, ATP-competitive dual Cdc7/Cdk9 inhibitor with IC50 values of 10/34 nM.公司介紹：MedCh
2016-01-11 14:03 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

663.00/10mg
010mg起訂
詢價(jià)

Cabazitaxel
3-Deazaneplanocin A (hydrochloride)/aCabazitaxel(XRP6258; RPR-116258A) is a semi-synthetic derivative of the natural tax
2016-01-11 14:01 [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)

HY-12186
3-Deazaneplanocin A hydrochloride(DZNep hydrochloride) is an attractive epigenetic anticancer agent through the inhibiti
2016-01-11 14:00 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

4427.00/5mg
05mg起訂
詢價(jià)

Procarbazine (Hydrochloride)
Procarbazine Hcl, an antineoplastic chemotherapy drug, is an alkylating agent for the treatment of Hodgkin's lymphoma an
2016-01-11 13:58 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

630.00/100mg
0100mg起訂
詢價(jià)

ISRIB (trans-isomer)
ISRIB (trans-isomer) is a potent inhibitor of PERK signaling; inhibition of the ATF4 luciferase reporter in HEK293T cell
2016-01-11 13:57 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1080.00/10mg
010mg起訂
詢價(jià)

CC0651
CC0651 is an allosteric inhibitor of the human cdc34 ubiquitin-conjugating enzyme that potently (IC50 = 1.72 uM) inhibit
2016-01-11 13:55 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

13950.00/10mg
010mg起訂
詢價(jià)

UNC1999
UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM, respectiv
2016-01-11 13:53 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

714.00/5mg
05mg起訂
詢價(jià)

Ansamitocin P-3
Ansamitocin P-3 is a maytansine analog which displays potent cytotoxicity against the human solid tumor cell lines A-549
2016-01-11 13:51 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

1300.00/5mg
05mg起訂
詢價(jià)

Ixabepilone
Ixabepilone (Azaepothilone B; BMS 247550) is an epothilone B analog and nontaxane microtubule-stabilizing compound with
2016-01-11 13:49 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3580.00/5mg
05mg起訂
詢價(jià)

7-xylosyltaxol
7-xylosyltaxol(Taxol-7-xyloside) is a taxol (Paclitaxel) derivative; Paclitaxel binds to tubulin and inhibits the disass
2016-01-11 13:42 [上海]
上海皓元生物醫(yī)藥科技有限公司 [已核實(shí)]

3329.00/10mg
010mg起訂
詢價(jià)

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(shí)]

5626.00/100mg
0100mg起訂
詢價(jià)

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(shí)]

3500.00/5mg
05mg起訂
詢價(jià)

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(shí)]

780.00/10mg
010mg起訂
詢價(jià)

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(shí)]

714.00/5mg
05mg起訂
詢價(jià)

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(shí)]

1550.00/5mg
05mg起訂
詢價(jià)

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(shí)]