3373-53-3
3373-53-3
Chemical Structure
Isoguanine
- CAS 番号: 3373-53-3
- Formula:C5H5N5O
- Molecular Weight:151.13
IUPAC Name: 6-amino-3,7-dihydro-2H-purin-2-one
InChIKey: DRAVOWXCEBXPTN-UHFFFAOYSA-N
SMILES: NC1=NC(NC2=C1NC=N2)=O
Biological Activity: Isoguanine is a purine base that is an isomer of Guanine. A building block in organic synthesis.
| 製品番号 | 製品名 | 純度 | 製品説明 | Pricing | |||||||||||||||||||
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Isoguanine | 99.64% | Isoguanine is a purine base that is an isomer of Guanine. A building block in organic synthesis. | ||||||||||||||||||||
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7H-Purine-2,6-diamine | 99.99% | 7H-Purine-2,6-diamine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2-Chloroadenine | 99.48% | 2-Chloroadenine (6-Amino-2-chloropurine) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Xanthine sodium, 98% | 99.57% | Xanthine sodium, 98%, a plant alkaloid found in tea, coffee, and cocoa, is a mild stimulant of the central nervous system. Xanthine sodium, 98% also acts as an intermediate product on the pathway of purine degradation. | ||||||||||||||||||||
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Guanine-13C2,15N | Guanine-13C2,15N is the 13C- and 15N-labeled Guanine (HY-Y1055). Guanine is one of the fundamental components of nucleic acids (DNA and RNA). Guanine is a purine derivative, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Guanine has the potential to serve as a large-capacity N pool. Guanine has cytotoxic, antinociceptive and neuroprotective effects. | |||||||||||||||||||||
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Guanine-13C2,7-15N | Guanine-13C2,15N is the 13C- and 15N-labeled Guanine (HY-Y1055). Guanine is one of the fundamental components of nucleic acids (DNA and RNA). Guanine is a purine derivative, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Guanine has the potential to serve as a large-capacity N pool. Guanine has cytotoxic, antinociceptive and neuroprotective effects. | |||||||||||||||||||||
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Guanine | 98.0% | Guanine is one of the fundamental components of nucleic acids (DNA and RNA). Guanine is a purine derivative, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Guanine has the potential to serve as a large-capacity N pool. Guanine has cytotoxic, antinociceptive and neuroprotective effects. | ||||||||||||||||||||
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Guanine hydrochloride | 98.78% | Guanine hydrochloride is one of the fundamental components of nucleic acids (DNA and RNA). Guanine hydrochloride is a purine derivative, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Guanine hydrochloride has the potential to serve as a large-capacity N pool. Guanine hydrochloride has cytotoxic, antinociceptive and neuroprotective effects. | ||||||||||||||||||||
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Guanine-13C | 99.5% | Guanine-13C is the 13C labeled Guanine (HY-Y1055). Guanine is one of the fundamental components of nucleic acids (DNA and RNA). Guanine is a purine derivative, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Guanine has the potential to serve as a large-capacity N pool. Guanine has cytotoxic, antinociceptive and neuroprotective effects. | ||||||||||||||||||||
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Guanine-13C,15N2 | 98.6% | Guanine-13C,15N2 is the 13C and 15N labeled Guanine (HY-Y1055). Guanine is one of the fundamental components of nucleic acids (DNA and RNA). Guanine is a purine derivative, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Guanine has the potential to serve as a large-capacity N pool. Guanine has cytotoxic, antinociceptive and neuroprotective effects. | ||||||||||||||||||||
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Guanine-15N5 | 98% | Guanine-15N5 is 15N labeled Guanine (HY-Y1055). Guanine is one of the fundamental components of nucleic acids (DNA and RNA). Guanine is a purine derivative, consisting of a fused pyrimidine-imidazole ring system with conjugated double bonds. Guanine has the potential to serve as a large-capacity N pool. Guanine has cytotoxic, antinociceptive and neuroprotective effects. | ||||||||||||||||||||
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