CAS 3650-93-9

cytosine-5-carboxylic acid

Description:

Cytosine-5-carboxylic acid, with the CAS number 3650-93-9, is a derivative of the nucleobase cytosine, which is one of the building blocks of nucleic acids. This compound features a carboxylic acid functional group (-COOH) at the 5-position of the cytosine ring, which distinguishes it from its parent compound. It is a white to off-white crystalline solid that is soluble in water due to the presence of the polar carboxylic acid group. The presence of this functional group also contributes to its acidic properties. Cytosine-5-carboxylic acid can participate in various biochemical reactions, including those involving nucleic acid metabolism and modification. Its structural similarity to cytosine allows it to interact with biological systems, potentially influencing nucleic acid synthesis and function. This compound is of interest in biochemical research and may have applications in the study of genetic material and cellular processes. However, specific applications and biological activities may vary and require further investigation.

Formula: C₅H₅N₃O₃

InChI: InChI=1/C5H5N3O3/c6-3-2(4(9)10)1-7-5(11)8-3/h1H,(H,9,10)(H3,6,7,8,11)

InChI key: InChIKey=BLQMCTXZEMGOJM-UHFFFAOYSA-N

SMILES: C(O)(=O)C1=C(N)NC(=O)N=C1

Synonyms:

• 5-Carboxycytosine
• 5-Carboxylcytosine
• 5-Pyrimidinecarboxylic acid, 4-amino-1,2-dihydro-2-oxo-
• 5-Pyrimidinecarboxylic acid, 6-amino-1,2-dihydro-2-oxo-
• 6-Amino-1,2-dihydro-2-oxo-5-pyrimidinecarboxylic acid
• 6-Amino-2-Oxo-1,2-Dihydropyrimidine-5-Carboxylic Acid
• NSC 9309
• Cytosine-5-carboxylic acid
• 6-azanyl-2-oxo-1H-pyrimidine-5-carboxylic acid
• 4-Amino-1,2-dihydro-2-oxo-5-pyrimidinecarboxylic acid
• Uracil Impurity 8
• 4-amino-2-hydroxypyrimidine-5-carboxylic acid hydrobromide
• 4-AMINO-5-CARBOXY-2-HYDROXYPYRIMIDINE 97%
• 4-Amino-2-hydroxypyrimidine-5-carboxylic acid
• 6-amino-2-keto-1H-pyrimidine-5-carboxylic acid
• Imidacloprid Impurity 30
• 4-amino-2-hydroxy-5-pyrimidinecarboxylic acid(SALTDATA: FREE)
• 5-CARBOXYCYTOSINE ISO 9001：2015 REACH
• 4-AMINO-2-OXO-1,2-DIHYDRO-PYRIMIDINE-5-CARBOXYLIC ACID
• 4-AMINO-5-CARBOXY-2-HYDROXYPYRIMIDINE
• 4-Amino-2-hydroxy-5-pyrimidinecarboxylicacid

4-Amino-2-hydroxypyrimidine-5-carboxylic acid hydrobromide

CAS: 3650-93-9

Formula: C₅H₅N₃O₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 155.1115

Ref: IN-DA00C8JM

4-Amino-2-hydroxy-5-pyrimidinecarboxylic acid

CAS: 3650-93-9

4-Amino-2-hydroxy-5-pyrimidinecarboxylic acid

Purity: 98%

Molecular weight: 155.11g/mol

Ref: 54-OR1034039

5-Carboxy-Cytosine

CAS: 3650-93-9

Formula: C₅H₅N₃O₃

Molecular weight: 155.11

Ref: 4Z-C-954

5-Carboxycytosine

Controlled Product

CAS: 3650-93-9

Formula: C₅H₅N₃O₃

Color and Shape: Neat

Molecular weight: 155.11

Ref: TR-C177975

5-Carboxycytosine

CAS: 3650-93-9

5-Carboxycytosine is a glycosylase that catalyses the removal of a sugar molecule from 5-carboxymethylaminomethyluracil (5-CMAM) to form 5-carboxymethylaminomethyluracil (5-CMA), which is not found in mammalian cells. The enzyme is a member of the family of glycosylases, which use hydrogen bonds to cleave the carbon-oxygen bond. It has been shown to be involved in transcriptional regulation and DNA repair. 5-Carboxycytosine has also been used as an analytical reagent for determining the presence of 5-CMAM in DNA samples.
5-Carboxycytosine has been shown to induce cellular transformation, which may be due to its ability to bind dna with high affinity and act as a template for dna synthesis. It is also able to produce 5-C

Formula: C₅H₅N₃O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 155.11 g/mol

Ref: 3D-FA137002

4-Amino-2-hydroxy-5-pyrimidinecarboxylic acid

CAS: 3650-93-9

Formula: C₅H₅N₃O₃

Purity: 98%

Molecular weight: 155.113

Ref: 10-F233365