33312-93-5
33312-93-5
Chemical Structure
6-(Methylthio)purine-d3-1
Synonym(s): 6-Methylmercaptopurine-d3-d3-1
- CAS No.: 33312-93-5
- Formula:C6H3D3N4S
- Molecular Weight:169.22
IUPAC Name: 4,4'-(propane-2,2-diyl)bis(phen-2,3,5,6-d4-ol)
InChIKey: UIJIQXGRFSPYQW-FIBGUPNXSA-N
SMILES: [2H]C([2H])([2H])SC1=C2C(N=CN2)=NC=N1
Biological Activity: 6-(Methylthio)purine-d3-1 (6-Methylmercaptopurine-d3-1) is the deuterated-labeled 6-(Methylthio)purine (HY-W097453). 6-(Methylthio)purine (6-Methylmercaptopurine) is a thiopurine compound[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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6-(Methylthio)purine-d3-1 | 99.56% | 6-(Methylthio)purine-d3-1 (6-Methylmercaptopurine-d3-1) is the deuterated-labeled 6-(Methylthio)purine (HY-W097453). 6-(Methylthio)purine (6-Methylmercaptopurine) is a thiopurine compound. | ||||||||||||||||||||
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6-(Methylthio)purine (Standard) | ≥98% | 6-(Methylthio)purine (Standard) (6-Methylmercaptopurine (Standard)) is the analytical standard of 6-(Methylthio)purine (HY-W097453). This product is intended for research and analytical applications. 6-(Methylthio) purine (6-Methylmercaptopurine) is a thiopurine compound. | ||||||||||||||||||||
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6-(Methylthio)purine | 99.90% | 6-(Methylthio)purine (6-Methylmercaptopurine) is a thiopurine compound. | ||||||||||||||||||||
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N6-Methyladenine | 98.79% | N6-Methyladenine is a DNA epigenetic modification that involves the addition of a methyl group to the sixth position of adenine. N6-Methyladenine plays an important role in distinguishing host DNA from exogenous DNA and controls many biological functions, such as DNA replication, transcription, mismatch repair, and chromosome replication. N6-Methyladenine can be used for the kidney diseases. | ||||||||||||||||||||
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6-Mercaptopurine-13C2,15N | 96.0% | 6-Mercaptopurine-13C2,15N is the 13C- and 15N-labeled 6-Mercaptopurine. 6-Mercaptopurine is a purine analogue which acts as an antagonist of the endogenous purines and has been widely used as antileukemic agent and immunosuppressive agent. | ||||||||||||||||||||
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Purine | 99.83% | Purine is an endogenous metabolite. Purine bases are the building blocks of the nucleic acids. Purine inhibits the activation of PARP. Purine protects against oxidant-induced cell injury. Purine can be used in the research of cancer and nervous system diseases. | ||||||||||||||||||||
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Adenine hydrochloride (Standard) | ≥98% | Adenine (hydrochloride) (Standard) is the analytical standard of Adenine (hydrochloride). This product is intended for research and analytical applications. Adenine hydrochloride (6-Aminopurine hydrochloride), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine hydrochloride acts as a chemical component of DNA and RNA. Adenine hydrochloride also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis. | ||||||||||||||||||||
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Adenine (Standard) | 99.91% | Adenine (Standard) is the analytical standard of Adenine. This product is intended for research and analytical applications. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis. | ||||||||||||||||||||
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Adenine-13C | 99.06% | Adenine-13C is the 13C labeled Adenine. Adenine (6-Aminopurine), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine acts as a chemical component of DNA and RNA. Adenine also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis. | ||||||||||||||||||||
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6-(Dimethylamino)purine | 99.90% | 6-(Dimethylamino) purine (6-Dimethylaminopurine) is a serine threonine protein kinase inhibitor. 6-(Dimethylamino) purine can inhibit prolactin induced expression of lactoprotein genes in rabbit mammary gland cells. 6-(Dimethylamino) purine can affect the maturation of mammalian oocytes. 6-(Dimethylamino) purine can lead to downregulation of genes related to cell proliferation and cell cycle progression, such as proliferating cell nuclear antigen, insulin-like gene 1, and serine protease inhibitor 2 genes, and induce apoptosis in lymphoma cells (apoptosis). | ||||||||||||||||||||
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Adenine-15N5 hydrochloride | Adenine-15N5 (6-Aminopurine-15N5) hydrochloride is the 15N-labeled Adenine hydrochloride (HY-B0152A). Adenine hydrochloride (6-Aminopurine hydrochloride), a purine, is one of the four nucleobases in the nucleic acid of DNA. Adenine hydrochloride acts as a chemical component of DNA and RNA. Adenine hydrochloride also plays an important role in biochemistry involved in cellular respiration, the form of both ATP and the cofactors (NAD and FAD), and protein synthesis. | |||||||||||||||||||||
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6-Chloropurine | 99.47% | 6-Chloropurine is a building block in chemical synthesis. Intermediate in the preparation of 9-alkylpurines and 6-rnercaptopurine. Antitumor activities. | ||||||||||||||||||||
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