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thymine

Catalog No.
M1406
Pyrimidine bases that are components of DNA and can be used in biochemical research.
Grouped product items
SizePriceStock Qty
1g
$54.00
In stock
For scientific research use only and should not be used for diagnostic or medical purposes.

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Background

Thymine is one of the four important bases in DNA and belongs to the pyrimidine class of bases. It pairs with adenine (A) through two hydrogen bonds to form the double helix structure of DNA. In organisms, the metabolism of Thymine is mainly catalyzed by dihydropyrimidine dehydrogenase (DPD). Studies have shown that DPD in the liver of rats has a high affinity for Thymine, with a Km value of approximately 2.2 μM, indicating that DPD has a strong affinity for Thymine and a high catalytic efficiency. Abnormal DPD activity may lead to metabolic disorders of Thymine, thereby affecting the DNA synthesis and repair processes. The structural stability and metabolic pathways of Thymine are crucial for maintaining genomic stability, and related studies are of great significance for understanding genetic diseases and drug metabolism.

Chemical Properties

Physical AppearanceSolid
StorageStore at -20°C
M.Wt126.11
Cas No.65-71-4
Formula C5H6N2O2
SynonymsThymine
Solubility≥0.83 mg/mL in EtOH with ultrasonic; ≥1.21 mg/mL in H2O with ultrasonic; ≥23.4 mg/mL in DMSO
Chemical Name5-methylpyrimidine-2,4-diol
SDFDownload SDF
Canonical SMILES CC1=CN=C(O)N=C1O
Shipping ConditionSmall Molecules with Blue Ice, Modified Nucleotides with Dry Ice.
General tips We do not recommend long-term storage for the solution, please use it up soon.

Quality Control

Chemical structure

thymine