隨著腫瘤對人類健康的威脅逐漸加大,人類對癌癥的細(xì)胞生物學(xué)和生物醫(yī)�(xué)研究有了飛速的�(fā)展,癌基�、抑癌基因、細(xì)胞凋�、腫瘤血管形成等使腫瘤研究由�(xì)胞生物學(xué)水平�(zhuǎn)變到分子生物�(xué)水平[1]。以膜上或細(xì)胞內(nèi)特異性表�(dá)或高表達(dá)的分子為作用靶點,包括靶向酪氨酸激�,血管新生,腫瘤�(xì)胞周期相�(guān)因子,組蛋白去乙酰酶抑制劑,微環(huán)�,腫瘤干�(xì)�,腫瘤代謝異常等因素成為研究靶點特異性抗腫瘤藥物的關(guān)�[2]。百靈威作為專業(yè)試劑供應(yīng)�,可提供120余種腫瘤研究靶點抑制劑和激活劑�(chǎn)��
- 多種熱門靶點抑制�,滿足前沿科研需�
- 作用靶點清晰,易于客戶選�
- �(chǎn)品純度高,質(zhì)量穩(wěn)�,現(xiàn)貨供�(yīng)
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�1:Immunofluorescence and flow cytometric analyses of the translocation of ABCG2 in MCF-7 FLV1000 cells before and after treatment with the PI3K inhibitor LY294002[3].
References
[1] Mbengue A, Bhattacharjee S, Pandharkar T, et al. A molecular mechanism of artemisinin resistance in Plasmodium falciparum malaria[J]. Nature, 2015, 520(7549):683-7.
[2] Sapey E, Greenwood H, Walton G, Mann E, Love A, Aaronson N, Insall RH, Stockley RA, Lord JM: Phosphoinositide 3-kinase inhibition restores neutrophil accuracy in the elderly: toward targeted treatments for immunosenescence[J]. Blood. 2014,123(2):239-248.
[3] To K K W, Tomlinson B. Targeting the ABCG2-overexpressing multidrug resistant (MDR) cancer cells by PPARγ agonists[J]. British Journal of Pharmacology, 2013, 170(5):1137–1151.
� 腫瘤研究化合�
�(chǎn)品編�
|
英文名稱
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中文名稱
|
CAS
|
作用靶點
|
150037
|
5-Azacytidine, 99%
|
5-氮雜胞嘧啶核�, 99%
|
320-67-2
|
DNA Methyltransferase抑制�
|
268355
|
2-Amino-6-purinethiol, 98%
|
2-氨基-6-嘌呤硫醇, 98%
|
154-42-7
|
DNA Methyltransferase抑制�
|
180939
|
5-Fluorouracil, 99%
|
5-氟尿嘧啶, 99%
|
51-21-8
|
DNA/RNA Synthesis抑制�
|
251696
|
Oxaliplatin, 95%
|
奧沙利鉑, 95%
|
61825-94-3
|
DNA/RNA Synthesis抑制�
|
258050
|
2-Chloro-2'-deoxyadenosine, 99%
|
2-�-2'-脫氧腺苷, 99%
|
4291-63-8
|
DNA/RNA Synthesis抑制�
|
271269
|
Gemcitabine hydrochloride, 99%
|
鹽酸吉西他濱, 99%
|
122111-03-9
|
DNA/RNA Synthesis抑制�
|
274584
|
Carboplatin, 98%
|
碳鉑, 98%
|
41575-94-4
|
DNA/RNA Synthesis抑制�
|
275688
|
cis-Diamineplatinum(II) dichloride, 99%
|
順式-二氨二氯化鉑, 99%
|
15663-27-1
|
DNA/RNA Synthesis抑制�
|
381488
|
Ara-G hydrate, 98%
|
阿糖鳥苷, 98%
|
38819-10-2
|
DNA/RNA synthesis抑制�
|
341249
|
Erlotinib, 98%
|
埃羅替尼, 98%
|
183321-74-6
|
EGFR抑制�
|
795123
|
Lapatinib ditosylate, 98%
|
二甲苯磺酸拉帕替�, 98%
|
388082-77-7
|
EGFR抑制�
|
831262
|
Lapatinib, 98%
|
拉帕替尼, 98%
|
231277-92-2
|
EGFR抑制�
|
996037
|
Afatinib, 98%
|
阿法替尼, 98%
|
850140-72-6
|
EGFR抑制�
|
303595
|
Trichostatin A, 98%
|
曲古柳菌�A, 98%
|
58880-19-6
|
HDAC抑制�
|
628151
|
Vorinostat, 99%
|
伏立諾他, 99%
|
149647-78-9
|
HDAC抑制�
|
625238
|
Entinostat, 99%
|
恩替諾特, 99%
|
209783-80-2
|
HDAC抑制�
|
837002
|
Panobinostat, 98%
|
帕比司他, 98%
|
404950-80-7
|
HDAC抑制�
|
1349106
|
Ruxolitinib phosphate salt, 99%
|
魯索利替尼磷酸鹽, 99%
|
1092939-17-7
|
JAK抑制�
|
1430418
|
Tofacitinib citrate, 99%
|
檸檬酸托法替�, 99%
|
540737-29-9
|
JAK抑制�
|
912849
|
Tofacitinib, 99%
|
托法替尼, 99%
|
477600-75-2
|
JAK抑制�
|
951485
|
Ruxolitinib, 99%
|
魯索替尼, 99%
|
941678-49-5
|
JAK抑制�
|
1272662
|
Cabazitaxel, 99%
|
卡巴他賽, 99%
|
183133-96-2
|
Microtubule Associated抑制�
|
181603
|
Docetaxel, 98%
|
多西他賽, 98%
|
114977-28-5
|
Microtubule Associated抑制�
|
266725
|
Combretastatin A-4, 98%
|
康普瑞汀, 98%
|
117048-59-6
|
Microtubule Associated抑制�
|
369172
|
6-Amino-3-methylpurine, 90%
|
6-氨基-3-甲基嘌呤, 90%
|
5142-23-4
|
PI3K抑制�
|
268623
|
Quercetin, 98%
|
槲皮�, 98%
|
117-39-5
|
PI3K抑制�
|
114089
|
7-Ethyl-10-hydroxycamptothecin, 99%
|
7-乙基-10-羥基喜樹�, 99%
|
86639-52-3
|
Topoisomerase抑制�
|
116557
|
Daunorubicin hydrochloride, 97%
|
道諾霉素鹽酸�, 97%
|
23541-50-6
|
Topoisomerase抑制�
|
194237
|
Epirubicin hydrochloride, 98%
|
表柔比星鹽酸�, 98%
|
56390-09-1
|
Topoisomerase抑制�
|
814262
|
Vandetanib, 99%
|
凡德他尼, 99%
|
443913-73-3
|
VEGFR2抑制�
|
1109982
|
Vatalanib dihydrochloride, 99%
|
瓦他拉尼堿二鹽酸�, 99%
|
212141-51-0
|
VEGFR2抑制�
|
1239124
|
Ponatinib, 99%
|
帕納替尼, 99%
|
943319-70-8
|
VEGFR2抑制�
|
812864
|
Axitinib, 98%
|
阿西替尼, 98%
|
319460-85-0
|
VEGFR2抑制�
|
1386067
|
A 769662, 98%
|
A 769662, 98%
|
844499-71-4
|
AMPK激活劑
|
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