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Merck
CN

A9546

Sigma-Aldrich

2-氨基-6-甲基巯基嘌呤

≥95%

别名:

2-氨基-6-甲基硫嘌呤

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About This Item

经验公式(希尔记法):
C6H7N5S
CAS号:
分子量:
181.22
EC 号:
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.51

质量水平

方案

≥95%

表单

solid

SMILES字符串

[H]n1cnc2c(SC)nc(N)nc12

InChI

1S/C6H7N5S/c1-12-5-3-4(9-2-8-3)10-6(7)11-5/h2H,1H3,(H3,7,8,9,10,11)

InChI key

YEGKYFQLKYGHAR-UHFFFAOYSA-N

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应用

2-氨基-6-甲基巯基嘌呤是一种2-氨基-6-烷基二硫代嘌呤,已与其他6位碳类似物一起用于研究大脑特异性地西泮的结合。
2-氨基-6-甲基巯基嘌呤(6-MTG)已用作Dulbecco′s改良的Eagles培养基(DMEM)培养基的补充剂,用于选择表达GPT的重组病毒mCMVhMIEPE-gpt.lacZ(巨细胞病毒主要立即早期启动子-增强子复合物-gpt.lacz)。它也已用作高效液相色谱(HPLC)中的标准品,以评估巯嘌呤甲基转移酶(TPMT)酶的活性。

生化/生理作用

2-氨基-6-甲基巯基嘌呤是由6-巯基嘌呤通过硫嘌呤甲基转移酶(TMPT)酶的S甲基化活性合成的。

象形图

CorrosionExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

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Effect of 9-alkyl derivatives of 6-methylthioguanine on brain specific binding of [3H]diazepam.
S C Sung et al.
Biochemical pharmacology, 35(20), 3645-3646 (1986-10-15)
A Practical Non-Extraction Direct Liquid Chromatography Method for Determination of Thiopurine S-Methyltransferase Activity in Inflammatory Bowel Disease
Bahrehmand F, et al.
Acta Medica Iranica, 55(6), 360-367 (2017)
S C Sung et al.
Biochemical pharmacology, 33(11), 1737-1739 (1984-06-01)
Various derivatives of 2-amino-6- methylthiopurine with substituents at the 6-position of purine were tested for their abilities to displace [3H]diazepam binding to rat brain membranes. The potency was dependent on the carbon chain-length in the 6-position of purine. Among the
In vivo replication of recombinant murine cytomegalovirus driven by the paralogous major immediate-early promoter-enhancer of human cytomegalovirus
Grzimek NKA, et al.
Journal of Virology, 73(6), 5043-5055 (1999)
G R Erdmann et al.
Biomedical chromatography : BMC, 4(2), 47-51 (1990-03-01)
A reversed phase high performance liquid chromatographic procedure was developed to quantify 6-thioguanine, 6-mercaptopurine, methylthioguanine, and methylmercaptopurine in red blood cells. The free base of each thiopurine was liberated from the respective nucleoside and nucleotide moiety by acid hydrolysis, which

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