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Merck
CN

M6502

6-Methylpurine

≥99%

别名:

MeP

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关于此项目

经验公式(希尔记法):
C6H6N4
化学文摘社编号:
分子量:
134.14
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
217-903-2
MDL number:
Assay:
≥99%
Biological source:
synthetic (organic)
Form:
powder
Solubility:
water: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow
Storage temp.:
−20°C
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InChI key

SYMHUEFSSMBHJA-UHFFFAOYSA-N

InChI

1S/C6H6N4/c1-4-5-6(9-2-7-4)10-3-8-5/h2-3H,1H3,(H,7,8,9,10)

SMILES string

Cc1ncnc2[nH]cnc12

biological source

synthetic (organic)

assay

≥99%

form

powder

mp

237-238 °C (lit.)

solubility

water: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow

storage temp.

−20°C

Quality Level

Application

6-Methylpurine (MeP) is a toxic adenine analog used as a bisubstrate inhibitor of enzymes that bind adenosyl moieties and which may become phosphorylated to levels that inhibit RNA and protein synthesis.

存储类别

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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H Ohgaki et al.
Journal of cancer research and clinical oncology, 117(1), 13-18 (1991-01-01)
The formation of O6-methyldeoxyguanosine (O6-MedGuo) was determined by an immuno-slot-blot assay in DNA of various tissues of F344 rats exposed to N-methyl-N-nitrosourea (MNU) in the drinking water at 400 ppm for 2 weeks. Although the pyloric region of the glandular
Norma Susana Pano-Farias et al.
Journal of food and drug analysis, 25(3), 501-509 (2017-09-16)
In this paper a method of using the "quick, easy, cheap, effective, rugged, and safe" (QuEChERS) extraction and gas chromatography coupled to mass spectrometry detection (GC-MS) was developed for the analysis of five frequently applied pesticides in papaya and avocado.
G Klobus et al.
Plant physiology, 87, 878-882 (1988-01-01)
The nature of the injury and recovery of nitrate uptake (net uptake) from NaCl stress in young barley (Hordeum vulgare L, var CM 72) seedlings was investigated. Nitrate uptake was inhibited rapidly by NaCl, within 1 minute after exposure to
Juan Li et al.
Water research, 135, 75-84 (2018-02-20)
This work investigated impacts of iodide (I-) on the transformation of the widely used phenolic preservative methylparaben (MeP) as well as 11 other phenolic compounds by potassium permanganate (KMnO4). It was found that KMnO4 showed a low reactivity towards MeP
Yingxin Yu et al.
Ecotoxicology and environmental safety, 182, 109419-109419 (2019-07-14)
Parabens are a kind of preservatives widely used in cosmetic and personal care products and ubiquitously detected in the environment. However, little is known on human exposure to these chemicals. Our study mainly investigated the urinary parabens in adults from

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