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         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) 

�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]. Blood2014,123(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

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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