Aminocyclopyrachlor | CAS:858956-08-8
            
            Aminocyclopyrachlor
            - 名称:环丙嘧啶酸 | Aminocyclopyrachlor
 - CAS号:858956-08-8
 - 别名:6-Amino-5-chloro-2-cyclopropyl-4-pyrimidinecarboxylic acid; DPX-MAT 28
 - 分子式:C8H8ClN3O2
 - 分子量:213.62
 - EINESC号:
 
产品描述
物理化学性质
| 密度 | 1.635±0.06 g/cm3 (20 º | 
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安全数据
| 没有数据 | 没有数据 | 
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SDS
| 来源 | SDS样本 | 
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| 没有数据 | 没有数据 | 
产品合成路线
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                                        Synthesis and antiviral activity of N9-[3-fluoro-2-(phosphonomethoxy)propyl] analogues derived from N6-substituted adenines and 2,6-diaminopurines.Ondřej Baszczyňski et al.Bioorganic & medicinal chemistry, 19(7), 2114-2124 (2011-03-25)
                                        An ab initio study of substituent effects on the excited states of purine derivatives.Elizabeth Mburu et al.The journal of physical chemistry. A, 112(48), 12485-12491 (2008-11-07)
                                        Long-range charge transfer through DNA by replacing adenine with diaminopurine.Kiyohiko Kawai et al.Journal of the American Chemical Society, 132(2), 627-630 (2009-12-18)
                                        Density functional and experimental studies on the FT-IR and FT-Raman spectra and structure of 2,6-diamino purine and 6-methoxy purine.V Krishnakumar et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 69(1), 8-17 (2007-05-01)
                                        Synthesis and oligomerization of Fmoc/Boc-protected PNA monomers of 2,6-diaminopurine, 2-aminopurine and thymine.André H St Amant et al.Organic & biomolecular chemistry, 10(4), 876-881 (2011-12-14)
                                        Simulations of A-RNA duplexes. The effect of sequence, solute force field, water model, and salt concentration.Ivana Beššeová et al.The journal of physical chemistry. B, 116(33), 9899-9916 (2012-07-20)
                                        Monitoring RNA-ligand interactions using isothermal titration calorimetry.Sunny D Gilbert et al.Methods in molecular biology (Clifton, N.J.), 540, 97-114 (2009-04-22)
                                        Formation and helicity control of ssDNA templated porphyrin nanoassemblies.Gevorg Sargsyan et al.Chemical communications (Cambridge, England), 49(10), 1020-1022 (2012-12-22)
                                        Reactions of Pd(II) with chelate-tethered 2,6-diaminopurine derivatives: N3-coordination and reaction of the purine system.Miguel A Galindo et al.Inorganic chemistry, 48(23), 11085-11091 (2009-10-28)
                                        Exposure of mice to arsenic and/or benzo[a]pyrene does not increase the frequency of Aprt-deficient cells recovered from explanted skin of Aprt heterozygous mice.Jared M Fischer et al.Environmental and molecular mutagenesis, 47(5), 334-344 (2006-05-02)
                                        Preparation of the 2'-deoxynucleosides of 2,6-diaminopurine and isoguanine by direct glycosylation.Joseph W Arico et al.The Journal of organic chemistry, 75(5), 1360-1365 (2010-02-12)
                                        Inhibition of the replication of hepatitis B virus in vitro by a novel 2,6-diaminopurine analog, beta-LPA.Xing-Xing He et al.Biochemical and biophysical research communications, 369(2), 513-518 (2008-02-21)
                                        Dissecting direct and indirect readout of cAMP receptor protein DNA binding using an inosine and 2,6-diaminopurine in vitro selection system.Søren Lindemose et al.Nucleic acids research, 36(14), 4797-4807 (2008-07-26)
                                        Chiral introduction of positive charges to PNA for double-duplex invasion to versatile sequences.Takumi Ishizuka et al.Nucleic acids research, 36(5), 1464-1471 (2008-01-22)
                                        Inversing the natural hydrogen bonding rule to selectively amplify GC-rich ADAR-edited RNAs.Rodolphe Suspène et al.Nucleic acids research, 36(12), e72-e72 (2008-06-03)
                                        Highly efficient strand invasion by peptide nucleic acid bearing optically pure lysine residues in its backbone.Yoji Yamamoto et al.Nucleic acids symposium series (2004), (50)(50), 109-110 (2006-12-08)
                                        Conjugated Electron Donor⁻Acceptor Hybrid Polymeric Carbon Nitride as a Photocatalyst for CO2 Reduction.Asif Hayat et al.Molecules (Basel, Switzerland), 24(9) (2019-05-11)
                                        Two isomorphous transition metal complexes containing a protonated diaminopurine ligand: diaquabis(2,6-diamino-7H-purin-1-ium-κN9)bis(homophthalato-κO)nickel(II) tetrahydrate and the cobalt(II) analogue.Ana María Atria et al.Acta crystallographica. Section C, Crystal structure communications, 67(Pt 5), m169-m172 (2011-05-05)
                                        2,6-Diaminopurine as a highly potent corrector of UGA nonsense mutations.Carole Trzaska et al.Nature communications, 11(1), 1509-1509 (2020-03-22)
                                        Long lifetime of hydrogen-bonded DNA basepairs by force spectroscopy.Alexander Fuhrmann et al.Biophysical journal, 102(10), 2381-2390 (2012-06-09)
                                        Nucleobases and corresponding nucleosides display potent antiviral activities against dengue virus possibly through viral lethal mutagenesis.Li Qiu et al.PLoS neglected tropical diseases, 12(4), e0006421-e0006421 (2018-04-20)
                                        Comparisons between chemical mapping and binding to isoenergetic oligonucleotide microarrays reveal unexpected patterns of binding to the Bacillus subtilis RNase P RNA specificity domain.Ruiting Liang et al.Biochemistry, 49(37), 8155-8168 (2010-06-19)
                                        The Formation of Nucleobases from the Ultraviolet Photoirradiation of Purine in Simple Astrophysical Ice Analogues.Christopher K Materese et al.Astrobiology, 17(8), 761-770 (2017-07-21)
                                        Biotransformation of 2,6-diaminopurine nucleosides by immobilized Geobacillus stearothermophilus.Eliana C De Benedetti et al.Biotechnology progress, 28(5), 1251-1256 (2012-07-28)
                                        Recombination R-triplex: H-bonds contribution to stability as revealed with minor base substitutions for adenine.Anna K Shchyolkina et al.Nucleic acids research, 34(11), 3239-3245 (2006-06-27)
                                        Solid-phase synthesis of pseudo-complementary peptide nucleic acids.Makoto Komiyama et al.Nature protocols, 3(4), 646-654 (2008-04-05)
                                        Stability and mismatch discrimination of DNA duplexes containing 2,6-diaminopurine and 2-thiothymidine locked nucleic acid bases.Curtis B Hughesman et al.Nucleic acids symposium series (2004), (52)(52), 245-246 (2008-09-09)
                                        RecA-mediated strand invasion of DNA by oligonucleotides substituted with 2-aminoadenine and 2-thiothymine.Georges Lahoud et al.Nucleic acids research, 36(21), 6806-6815 (2008-10-28)
                                        Effect of substituents on the excited-state dynamics of the modified DNA bases 2,4-diaminopyrimidine and 2,6-diaminopurine.Zsolt Gengeliczki et al.Physical chemistry chemical physics : PCCP, 12(20), 5375-5388 (2010-04-10)
                                        Genome-wide association of functional traits linked with Campylobacter jejuni survival from farm to fork.Koji Yahara et al.Environmental microbiology, 19(1), 361-380 (2016-11-25)
                                    
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            Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1).
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