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商品详细MedKoo/AZD-1480/1/204510
MedKoo/AZD-1480/1/204510
MedKoo/AZD-1480/1/204510
商品编号: 204510
品牌: MedKoo
市场价: ¥0.00
美元价: 0.00
产地: 美国(厂家直采)
公司:
产品分类: 多肽合成
公司分类: peptide
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

AZD-1480

WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#:204510

CAS#:935666-88-9

Description:AZD1480 is an orally bioavailable inhibitor of Janus-associated kinase 2 (JAK2) with potential antineoplastic activity. JAK2 inhibitor AZD1480 inhibits JAK2 activation, leading to the inhibition of the JAK/STAT (signal transducer and activator of transcription) signaling including activation of STAT3. This may lead to induction of tumor cell apoptosis and a decrease in cellular proliferation. JAK2, often upregulated or mutated in a variety of cancer cells, mediates STAT3 activation and plays a key role in tumor cell proliferation and survival.

Price and Availability

SizePriceShipping out timeQuantity
Inquire bulk and customized quantity

Pricing updated 2021-01-23.Prices are subject to change without notice.

AZD-1480 , purity > 98%, isout of stock

Chemical Structure

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Theoretical Analysis

MedKoo Cat#: 204510Name: AZD-1480CAS#: 935666-88-9Chemical Formula: C14H14ClFN8Exact Mass: 348.1014Molecular Weight: 348.76596Elemental Analysis:C, 48.21; H, 4.05; Cl, 10.17; F, 5.45; N, 32.13

Synonym:AZD1480; AZD-1480; AZD 1480

IUPAC/Chemical Name:(S)-5-chloro-N2-(1-(5-fluoropyrimidin-2-yl)ethyl)-N4-(5-methyl-1H-pyrazol-3-yl)pyrimidine-2,4-diamine

InChi Key:PDOQBOJDRPLBQU-QMMMGPOBSA-N

InChi Code:InChI=1S/C14H14ClFN8/c1-7-3-11(24-23-7)21-13-10(15)6-19-14(22-13)20-8(2)12-17-4-9(16)5-18-12/h3-6,8H,1-2H3,(H3,19,20,21,22,23,24)/t8-/m0/s1

SMILES Code:CC1=CC(NC2=NC(N[C@H](C3=NC=C(F)C=N3)C)=NC=C2Cl)=NN1

Technical Data

Appearance:
white solid powder

Purity:
>98% (or refer to the Certificate of Analysis)

Certificate of Analysis:
View current batch of CoA

Safety Data Sheet (SDS):
View Safety Data Sheet (SDS)

Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition:
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility:
Soluble in DMSO, not in water

Shelf Life:
>2 years if stored properly

Drug Formulation:
This drug may be formulated in DMSO

Stock Solution Storage:
0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code:
2934.99.9001

Additional Information

AZD1480 inhibits STAT3 in tumor-associated myeloid cells, reducing their number and inhibiting tumor metastasis. Myeloid cell-mediated angiogenesis was also diminished by AZD1480, with additional direct inhibition of endothelial cell function in vitro and in vivo. AZD1480 blocked lung infiltration of myeloid cells and formation of pulmonary metastases in both mouse syngeneic experimental and spontaneous metastatic models. Furthermore, AZD1480 reduced angiogenesis and metastasis in a human xenograft tumor model. Although the effects of AZD1480 on the tumor microenvironment were important for the observed antiangiogenic activity, constitutive activation of STAT3 in tumor cells themselves could block these antiangiogenic effects, showing the complexity of the JAK/STAT signaling network in tumor progression. Together, AZD1480 can effectively inhibit tumor angiogenesis and metastasis mediated by STAT3 in stromal cells as well as tumor cells. (source: Cancer Res. 2011 Nov 1;71(21):6601-10.)  

References

1: Liu Y, Holdbrooks AT, De Sarno P, Rowse AL,Yanagisawa LL, McFarland BC, Harrington LE, Raman C, Sabbaj S,Benveniste EN, Qin H. Therapeutic efficacy of suppressing the Jak/STATpathway in multiple models of experimental autoimmune encephalomyelitis.J Immunol. 2014 Jan 1;192(1):59-72. doi: 10.4049/jimmunol.1301513. Epub2013 Dec 9. PubMed PMID: 24323580; PubMed Central PMCID: PMC3934829.

2: Sun ZL, Tang YJ, Wu WG, Xing J, He YF, Xin DM, Yu YL, Yang Y, Han P.AZD1480 can inhibit the biological behavior of ovarian cancer SKOV3cells in vitro. Asian Pac J Cancer Prev. 2013;14(8):4823-7. PubMed PMID:24083752.

3: Gu L, Liao Z, Hoang DT, Dagvadorj A, Gupta S, Blackmon S, EllsworthE, Talati P, Leiby B, Zinda M, Lallas CD, Trabulsi EJ, McCue P, GomellaL, Huszar D, Nevalainen MT. Pharmacologic inhibition of Jak2-Stat5signaling By Jak2 inhibitor AZD1480 potently suppresses growth of bothprimary and castrate-resistant prostate cancer. Clin Cancer Res. 2013Oct 15;19(20):5658-74. doi: 10.1158/1078-0432.CCR-13-0422. Epub 2013 Aug13. PubMed PMID: 23942095.

4: Plimack ER, Lorusso PM, McCoon P, Tang W, Krebs AD, Curt G, EckhardtSG. AZD1480: a phase I study of a novel JAK2 inhibitor in solid tumors.Oncologist. 2013;18(7):819-20. doi: 10.1634/theoncologist.2013-0198.Epub 2013 Jul 11. PubMed PMID: 23847256; PubMed Central PMCID:PMC3720635.

5: Chang Q, Bournazou E, Sansone P, Berishaj M, Gao SP, Daly L, Wels J,Theilen T, Granitto S, Zhang X, Cotari J, Alpaugh ML, de Stanchina E,Manova K, Li M, Bonafe M, Ceccarelli C, Taffurelli M, Santini D, Altan-BonnetG, Kaplan R, Norton L, Nishimoto N, Huszar D, Lyden D, Bromberg J. TheIL-6/JAK/Stat3 feed-forward loop drives tumorigenesis and metastasis.Neoplasia. 2013 Jul;15(7):848-62. PubMed PMID: 23814496; PubMed CentralPMCID: PMC3689247.

6: Yan S, Li Z, Thiele CJ. Inhibition of STAT3 with orally active JAKinhibitor, AZD1480, decreases tumor growth in Neuroblastoma andPediatric Sarcomas In vitro and In vivo. Oncotarget. 2013Mar;4(3):433-45. PubMed PMID: 23531921; PubMed Central PMCID:PMC3717306.

7: Bogani C, Bartalucci N, Martinelli S, Tozzi L, Guglielmelli P, BosiA, Vannucchi AM; Associazione Italiana per la Ricerca sul Cancro AGIMMGruppo Italiano Malattie Mieloproliferative. mTOR inhibitors alone andin combination with JAK2 inhibitors effectively inhibit cells ofmyeloproliferative neoplasms. PLoS One. 2013;8(1):e54826. doi:10.1371/journal.pone.0054826. Epub 2013 Jan 31. PubMed PMID: 23382981;PubMed Central PMCID: PMC3561413.

8: Couto JP, Almeida A, Daly L, Sobrinho-Simões M, Bromberg JF, SoaresP. AZD1480 blocks growth and tumorigenesis of RET- activated thyroidcancer cell lines. PLoS One. 2012;7(10):e46869. doi:10.1371/journal.pone.0046869. Epub 2012 Oct 2. PubMed PMID: 23056499;PubMed Central PMCID: PMC3462763.

9: de Groot J, Liang J, Kong LY, Wei J, Piao Y, Fuller G, Qiao W,Heimberger AB. Modulating antiangiogenic resistance by inhibiting thesignal transducer and activator of transcription 3 pathway inglioblastoma. Oncotarget. 2012 Sep;3(9):1036-48. PubMed PMID: 23013619;PubMed Central PMCID: PMC3660053.

10: Loveless ME, Lawson D, Collins M, Nadella MV, Reimer C, Huszar D,Halliday J, Waterton JC, Gore JC, Yankeelov TE. Comparisons of theefficacy of a Jak1/2 inhibitor (AZD1480) with a VEGF signaling inhibitor(cediranib) and sham treatments in mouse tumors using DCE-MRI, DW-MRI,and histology. Neoplasia. 2012 Jan;14(1):54-64. PubMed PMID: 22355274;PubMed Central PMCID: PMC3281942.

品牌介绍
MedKoo 美帝药库公司以药物化学合成技术为核心,密切结合全球抗癌新药研发领域中的新技术、新理论、新趋势和新的发展方向,不断推出抗癌化合物新品种。 。 美帝药库MedKoo将在中国建立药物化学合成生产基地和多个现代化药物化合物存储仓库。 美帝药库的药物化合物来源于以下几个渠道:自主合成、委托化学合成、合作伙伴、和从国内外市场上选购。 MedKoo美帝药库的抗癌分子库 MedKoo的目标是打造全球规模最大、品种最多、类别最全和质量最好的小分子抗癌化合物库。MedKoo的抗癌药库将由下列5个分子库组成: (1)上市抗癌药库:该库将含有大约100个全球已批准上市的小分子抗癌化合物; (2)抗癌候选药物库:该分子库含有大约400个世界各国正在临床研究中抗癌小分子候选药物; (3)同系抗癌分子库:该分子库将含有多个化学结构类似或抗癌机制类似的分子包; (4)抗癌分子预制模块库:该库主要含有用于组建抗癌目标分子的分子模块包; (5)同位素标记抗癌分子库。