1-Methylcytosine
CAS No. 1122-47-0
1-Methylcytosine( 4-amino-1-methylpyrimidin-2(1H)-one | 1-methylcytosin | N-Methylcytosine )
Catalog No. M26011 CAS No. 1122-47-0
1-Methylcytosine is a methylated form of the cytosine and can be used as the nucleobase of hachimoji DNA paired with isoguanine.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
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| 10MG | 28 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name1-Methylcytosine
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NoteResearch use only, not for human use.
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Brief Description1-Methylcytosine is a methylated form of the cytosine and can be used as the nucleobase of hachimoji DNA paired with isoguanine.
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Description1-Methylcytosine is a methylated form of the cytosine and can be used as the nucleobase of hachimoji DNA paired with isoguanine.
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In Vitro——
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In Vivo——
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Synonyms4-amino-1-methylpyrimidin-2(1H)-one | 1-methylcytosin | N-Methylcytosine
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PathwayCell Cycle/DNA Damage
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TargetNucleoside Antimetabolite/Analog
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RecptorEndogenous Metabolite| T-type calcium channel
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Research Area——
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Indication——
Chemical Information
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CAS Number1122-47-0
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Formula Weight125.131
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Molecular FormulaC5H7N3O
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Purity>98% (HPLC)
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Solubility——
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SMILESCn1ccc(N)nc1=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Enocitabine
Enocitabine is a nucleoside analog. Enocitabine inhibits the replication of human cytomegalovirus(HCMV) and it also has antileukemic and antiviral activities.
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2′-Deoxy-2′-fluorogu...
2′-Deoxy-2′-fluoroguanosine is a nucleoside analog that potently inhibits influenza virus A and B strains(EC90 <0.35 μM). 2'-Deoxy-2'-fluoroguanosine is an inhibitor of influenza virus replication in the upper respiratory tract, improving fever and nasal inflammation.
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Ara-G
Ara-G is a deoxyguanosine (GdR) analog and a nucleoside analogue that is rapidly converted by cells of the T lymphoid lineage to its corresponding arabinosylguanine nucleotide triphosphate (araGTP), resulting in inhibition of DNA synthesis and selective in vitro toxicity to T lymphoblastoid cell lines as well as to freshly isolated leukemia cells from patients with T cell acute lymphoblastic leukemia (ALL).
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