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3’-O-tert-butyldimethylsilyl-5’-deoxy-5’-mercaptothymidine | 144944-96-7

中文名称
——
中文别名
——
英文名称
3’-O-tert-butyldimethylsilyl-5’-deoxy-5’-mercaptothymidine
英文别名
3'-O-tert-butyldimethylsilyl-5'-deoxy-5'-thiothymidine;3'-0-tert-butyldimethylsilyl-5'-deoxy-5'-thiothymidine;TBDMS(-3)2-deoxy-D-eryPenf5SH(b)-thymin-1-yl;1-[(2R,4S,5S)-4-[tert-butyl(dimethyl)silyl]oxy-5-(sulfanylmethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione
3’-O-tert-butyldimethylsilyl-5’-deoxy-5’-mercaptothymidine化学式
CAS
144944-96-7
化学式
C16H28N2O4SSi
mdl
——
分子量
372.561
InChiKey
REQNQGIOFHGMNA-YNEHKIRRSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    2.45
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    68.9
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis, Dynamic Combinatorial Chemistry, and PCR Amplification of 3′-5′ and 3′-6′ Disulfide-linked Oligonucleotides
    作者:Dennis Jul Hansen、Ilenia Manuguerra、Michael Brøndum Kjelstrup、Kurt Vesterager Gothelf
    DOI:10.1002/anie.201405761
    日期:2014.12.22
    Disulfide dithymidines linked 3′–5′ or 3′–6′ were synthesized and incorporated into oligonucleotides through a combined phosphotriester and phosphoramidite solid‐phase oligonucleotide synthesis approach. The disulfide links are cleaved and formed reversibly in the presence of thiols and oligonucleotides. This link was shown to be sequence‐adaptive in response to given templates in the presence of mercaptoethanol
    合成了通过3'-5'或3'-6'连接的二胸苷,并通过磷酸三酯和亚酰胺固相寡核苷酸合成方法将其掺入寡核苷酸。在醇和寡核苷酸的存在下,二键被裂解并可逆地形成。在存在巯基乙醇的情况下,该链接显示出对指定模板的序列适应性。在聚合酶链反应(PCR)中,聚合酶可以耐受人工的3'-5'和3'-6'二键。通过使用测序分析,我们显示了单个突变经常在PCR的扩增产物中随机发生。
  • A versatile approach to the synthesis of dinucleotide analogs containing neutral 5′-thioformacetal internucleoside linkages
    作者:Yves Ducharme、Kimberly A. Harrison
    DOI:10.1016/00404-0399(50)1393-v
    日期:1995.9
    Activation of nucleoside donors 5 by sulfuryl chloride followed by the addition of 5′-thionucleoside acceptors 3 yields 5′-thioformacetal dinucleotide analogs 6 with in situ trapping of liberated methanesulfenyl chloride with cyclohexene. Purine as well as pyrimidine derivatives can be part of a coupling reaction as nucleoside donors or acceptors. The dimethoxytrityl protecting group is compatible
    通过硫酰氯活化核苷供体5,然后添加5'-代核苷受体3,得到5'-甲醛缩醛二核苷酸类似物6,其用环己烯原位捕获释放的甲磺酰氯嘌呤以及嘧啶生物可以作为核苷供体或受体参与偶联反应。二甲氧基三苯甲基保护基与本偶联方法相容,从而允许差动的3',5'-末端保护以及随之而来的正交碱基保护。
  • Nucleoside H-Phosphonates, XXII: Synthesis and Properties of New Nucleotide Analogues - H-Phosphonothiolate Diesters
    作者:Jacek Stawinski、Renata Hiresova
    DOI:10.1055/s-2007-991072
    日期:——
    Nucleoside H-phosphonates, XXII: Synthesis and properties of new nucleotide analogues - H-phosphonothiolate diesters
    核苷 H-膦酸酯,XXII:新核苷酸类似物的合成和性质 - H-膦酸二酯
  • Dinucleoside Monophosphate Analogues Containing Disulfide Linkages
    作者:Emma M. Witch、Richard Cosstick
    DOI:10.1080/07328319708006228
    日期:1997.7
    Two dinucleoside monophosphate analogues containing disulfide linkages (1 and 2) have been prepared for incorporation into oligonucleotides. The modified oligomers will be tested for their potential as antisense agents.
  • Kawai, Stephen H.; Wang, Daguang; Just, George, Canadian Journal of Chemistry, 1992, vol. 70, # 5, p. 1573 - 1580
    作者:Kawai, Stephen H.、Wang, Daguang、Just, George
    DOI:——
    日期:——
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同类化合物

鲁西他滨 化合物 T14195 [1,1'-联苯基]-2,3,3',4,4',5'-六醇 [(2R,3R,5S)-3-(氨基甲基)-5-(5-甲基-2,4-二氧代嘧啶-1-基)四氢呋喃-2-基]N-[[(2R,3S,5R)-3-羟基-5-(5-甲基-2,4-二氧代嘧啶-1-基)四氢呋喃-2-基]甲基]氨基甲酸酯 9-(2-S-苯甲基-5-脱氧-2-硫代五呋喃糖基)-9H-嘌呤-6-胺 5-脱氧胸苷 5-脱氧-5-[(碘乙酰基)氨基]-胸腺嘧啶脱氧核苷 5-碘-5-脱氧胸腺嘧啶脱氧核苷 5-氨基-5-脱氧胸腺嘧啶脱氧核苷 5-氨基-2,5-二脱氧腺苷酸 5-叠氮基-5-脱氧胸腺嘧啶脱氧核苷 5-三氟乙酰氨基-5-脱氧胸腺嘧啶脱氧核苷 5'-脱氧-5'氟胸苷 5'-脱氧-5'-氯胸苷-3'-(4-硝基苯基)硫代磷酸酯 5'-脱氧-5'-{[4-(甲硫基)苯胺基羰基]氨基}胸苷 5'-脱氧-5'-{[3-(甲硫基)苯胺基羰基]氨基}胸苷 5'-脱氧-5'-[4-苯基-(1,2,3)三唑-1-基]胸苷 5'-脱氧-5'-[4-(甲硫基)苯甲酰氨基]胸苷 5'-脱氧-5'-[4-(吡啶-3-基)-(1,2,3)三唑-1-基]胸苷 5'-脱氧-5'-[4-(4-氟苯基)-(1,2,3)三唑-1-基]胸苷 5'-脱氧-5'-<(苯氧基羰基)氨基>胸苷 5'-硫代-胸苷3',5'-二乙酸酯 5'-溴乙酰氨基-5'-脱氧胸苷 5'-氨基-5-碘-2',5'-二脱氧尿苷 4-氨基-1-((2R,3R,4R,5R)-4-((叔丁基二甲基硅烷基)氧基)-5-(( 2-氯-N-[[3-羟基-5-(5-甲基-2,4-二氧代嘧啶-1-基)四氢呋喃-2-基]甲基]乙酰胺 2-{[(2Z)-3,7-二甲基辛-2,6-二烯-1-基](亚硝基)氨基}乙醇 2,5-二脱氧腺苷 2',5'-二脱氧尿苷 1-[(2R,4S,5R)-4-羟基-5-(异氰基甲基)四氢呋喃-2-基]嘧啶-2,4-二酮 1-[(2R,4S,5R)-4-羟基-5-(异氰基甲基)四氢呋喃-2-基]-5-甲基嘧啶-2,4-二酮 1-(2,5-二脱氧-2-氟-β-D-呋喃阿拉伯糖基)嘧啶-2,4(1H,3H)-二酮 1-(2,5-二脱氧-2-氟-β-D-呋喃阿拉伯糖基)-5-碘嘧啶-2,4(1H,3H)-二酮 N-{9-[(2R,4S,5R)-5-Azidomethyl-4-(tert-butyl-diphenyl-silanyloxy)-tetrahydro-furan-2-yl]-9H-purin-6-yl}-benzamide (Z)-4-(1-(((2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3-((1-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-1H-1,2,3-triazol-4-yl)methyl)-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-2-yl)methyl)-1H-1,2,3-triazol-4-ylamino)-4-oxobutane-1,2-diyl dioleate 5'-[4-((1,2-distearoyl-sn-glycer-1-yl)methyl)-1H-1,2,3-triazol-1-yl]-N-3-propargylthymidine 5'-deoxy-5'-hydrazinothymidine hydrochloride N-<5'-Desoxy-thymidinyl-(5')>-phosphorsaeure-<β,β,β-trichlorethylester>-amid Acetic acid (2S,3S,5R)-2-fluoromethyl-5-(5-methyl-2-oxo-4-thioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester N-<5'-Desoxy-thymidinyl-(5')>-phosphorsaeure--amid N-<5'-Desoxy-thymidinyl-(5')>-phosphorsaeure-bis--amid N4-Benzoyl-5'-chlor-2',5'-dideoxycytidin 5'-(bromoacetamido)-2',5'-dideoxy-5-iodouridine 5'-[3-(3-methoxy-2-methyl-acryloyl)-ureido]-5'-deoxy-thymidine 3'-deoxy-5'- O-methyl-3'-(N-(L-p-methoxyphenylalanyl)amino)adenosine 1-(2-deoxy-2-fluoro-4-C-methyl-β-D-arabinofuranosyl)cytosine hydrochloride 5'-N-Isobutyloxycarbonyl-5'-amino-5'-deoxythymidin 4'-chloromethyl-2'-deoxy-2'-fluoro-3'-O-dodecanoylcytidine 3'-O-methylene-5'-deoxy-5'-thiothymidylyl-(3'->5')-N6-benzoyl-3'-O-tert-butyldimethylsilyl-2',5'-dideoxy-5'-thioadenosine