CAS: 5142-23-4; 3-Methyl-3H-Purin-6-Amine

该化合物是因其作为自发抑制剂的作用而得到广泛承认的纯衍生物,它通过阻塞三类磷酸丁醇3-kinase(PI3K)发挥作用,从而抑制自发性形成,该化合物广泛用于生物化学和细胞生物学研究,研究与自发相关的途径及其在癌症和...

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号76227-27-5 N'-benzyloxy-5-... | CAS号125661-70-3 9-Benzyl-N6-eth... | CAS号3506-01-2 Adenosine, 2'-d... | CAS号76227-20-8 (2R,3S,5R)-5-(1... | CAS号72055-63-1 3-甲基腺苷对甲苯磺酸盐 | CAS号21149-25-7 腺嘌呤-7-氧化物 | CAS号66224-66-6 6H-Purin-6-imin... | CAS号1006-11-7 3-甲基-3H- 嘌呤-6(9H)-酮

合成工艺路线路线简述

  • 合成目标产物 3-Methyladenine 主要起始原料 Adenine-7-Oxide
  • (文献来源)合成步骤主要原料 Adenine-7-Oxide
3-Benzyladenine置于镍 Sodium Hydroxide,硫酸,氢气,Magnesium Monoperoxyphthalate Hexahydrate体系中,用 甲醇,水,甲苯 作为反应溶剂,25.0~40.0 °C,101.33 Kpa 条件下,反应 30.0H,反应生成 6-氨基-3-甲基嘌呤
参考文献:Fujii,Tozo; Ogawa,Kazuo; Saito,Tohru,Heterocycles,1994,Vol. 38,# 3,P. 477-480
标题:Fujii,Tozo; Ogawa,Kazuo; Saito,Tohru,Heterocycles,1994,Vol. 38,# 3,P. 477-480

专利信息


专利号:US-12421628-B2
优先权日:2018-07-23
标题:Massively parallel enzymatic synthesis of nucleic acid strands
发明人:HORGAN ADRIAN; GODRON XAVIER; YBERT THOMAS; NICOL ROBERT
权利人:DNA SCRIPT
摘要:The invention is directed to methods for massively parallel template-free enzymatic synthesis of a plurality of different polynucleotides of predetermined sequences. In one aspect, methods of the invention employ large scale arrays of reaction sites each associated with at least one working electrode for controlling deprotection and deblocking steps at predetermined user selected sites. In another aspect, the invention provides template-free enzymatic synthesis with proofreading, wherein completed polynucleotides at predetermined reaction sites are sequenced using a sequencing by synthesis technique, particularly employing electrochemically labile blocking groups.

专利号:US-2024052391-A1
优先权日:2020-10-29
标 题 :Enzymatic Synthesis of Polynucleotide Probes
发明人:GODRON XAVIER; NIYOMCHON SUPAPORN; CHAMPION ELISE
权利人:DNA SCRIPT
摘要:The present invention is directed to methods and kits for enzymatic synthesis of labeled polynucleotide probes using template-free DNA polymerases.

专利号:US-12391691-B2
优先权日:2018-11-16
标题:Synthesis of key intermediate of KRAS G12C inhibitor compound
发明人:PARSONS ANDREW THOMAS; COCHRAN BRIAN MCNEIL; POWAZINIK IV WILLIAM; CAPORINI MARC ANTHONY
权利人:AMGEN INC
摘要:The present invention relates to an improved, efficient, scalable process to prepare intermediate compounds, such as compound 5M, having the structure n nuseful for the synthesis of compounds that target KRAS G12C mutations, such as

专利号:US-2025206736-A1
优先权日:2019-11-14
标题 :Synthesis of kras g12c inhibitor compound
发明人:CORBETT MICHAEL THOMAS; CAILLE SEBASTIEN
权利人:AMGEN INC
摘要:The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2-isopropyl-4-methylpyridin-3-amine, useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

专利号:US-2024384319-A1
优先权日:2021-09-17
标题 :Synthesis of Oligonucleotides
发明人:LOVELOCK SARAH
权利人:UNIV MANCHESTER
摘要:The present invention relates to a novel method for oligonucleotide synthesis, using a catalytic primer-template, e.g. a hairpin primer, to achieve multiple rounds of oligonucleotide synthesis and dissociation from the template in the same reaction, such that at the end of the reaction the amount of oligonucleotide generated is greater than the amount of template provided in the reaction. The primer contains a cleavable site and the reaction is carried out in a single mixture with a cleavage agent. The cleavable site may be an inosine and the agent an endonuclease V.

专利号:US-2006194214-A1
优先权日:2005-02-28
标题 :Methods for assembly of high fidelity synthetic polynucleotides
发明人:CHURCH GEORGE; JACOBSON JOSEPH; BAYNES BRIAN M
权利人:CHURCH GEORGE; JACOBSON JOSEPH; BAYNES BRIAN M
摘要:Disclosed are methods of manufacturing synthetic DNAs, that is, DNAs made at least in significant part by chemical synthesis of polynucleotide polymers. Also provided are methods for assembling plural DNAs in the same pool by multiplexed assembly of synthetic oligonucleotides. In exemplary embodiments, the methods involve pre-amplification of one or more oligonucleotides using “universalâ€? primers, reduction of the error rate in oligonucleotide and/or polynucleotide products, and sequence optimization and oligonucleotides design.
洛阳德胜生物科技股份有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.adeninechem.com
电话: 0379-63339336👤
📞洛阳德胜生物科技股份有限公司 ⚠️参考联系方式

销售电话:0379-63339336
邮箱:huangxiaofeng99@hotmail.com
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别 ✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
第 1 / 1 页
现货

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献


1: Zheng XY, Li LJ, Li W, Jiang PF, Shen HQ, Chen YH, Chen X. Low concentrations of chloroquine and 3-methyladenine suppress the viability of retinoblastoma cells synergistically with vincristine independent of autophagy inhibition. Graefes Arch Clin Exp Ophthalmol. 2015 Dec;253(12):2309-15. doi: 10.1007/s00417-015-3157-1. doi: 10.11817/j.issn.1672-7347.2016.01.002. Chinese. doi: 10.1111/1440-1681.12323. doi: 10.3109/1061186X.2014.936870. doi: 10.3892/mmr.2015.3588.
6: Horwacik I, Gaik M, Durbas M, Boratyn E, Zając G, Szychowska K, Szczodrak M, Kołoczek H, Rokita H. Inhibition of autophagy by 3-methyladenine potentiates sulforaphane-induced cell death of BE(2)-C human neuroblastoma cells. Mol Med Rep. 2015 Jul;12(1):535-42. doi: 10.3892/mmr.2015.3377. doi: 10.1007/s00210-015-1104-7. doi: 10.1016/j.saa.2014.02.170. Chinese. doi: 10.1007/s00394-014-0707-y.
11: Zhu B, Yang C, Ding LC, Liu N. 3-methyladenine, an autophagic inhibitor, attenuates therapeutic effects of sirolimus on scopolamine-induced cognitive dysfunction in a rat model. Int J Clin Exp Med. 2014 Oct 15;7(10):3327-32.

合成参考文献


参考文献:10.1016/j.canlet.2010.01.006
摘要:Pan J, Cheng C, Verstovsek S, Chen Q, Jin Y, Cao Q. The BH3-mimetic GX15-070 induces autophagy, potentiates the cytotoxicity of carboplatin and 5-fluorouracil in esophageal carcinoma cells. Cancer Lett. 2010 Jul 28;293(2):167–74. doi: 10.1016/j.canlet.2010.01.006.
参考文献:10.1074/jbc.m111.229518
摘要:Karunakaran S, Ramachandran S, Coothankandaswamy V, Elangovan S, Babu E, Periyasamy-Thandavan S, Gurav A, Gnanaprakasam JP, Singh N, Schoenlein PV, Prasad PD, Thangaraju M, Ganapathy V. SLC6A14 (ATB0,+) Protein, a Highly Concentrative and Broad Specific Amino Acid Transporter, Is a Novel and Effective Drug Target for Treatment of Estrogen Receptor-positive Breast Cancer. Journal of Biological Chemistry. 2011 Sep;286(36):31830–8. doi: 10.1074/jbc.m111.229518.
参考文献:10.1186/1749-8546-6-27
摘要:Tan W, Lu J, Huang M, Li Y, Chen M, Wu G, Gong J, Zhong Z, Xu Z, Dang Y, Guo J, Chen X, Wang Y. Anti-cancer natural products isolated from chinese medicinal herbs. Chinese Medicine. 2011 Jul 22;6(1):27. doi: 10.1186/1749-8546-6-27.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知