Description
Thymidine (T) is a pyrimidine nucleoside base that pairs with adenosine (A) in double-stranded DNA. Thymidine is sometimes used to synchronize cells in the S phase of mitosis.
Thymidine (T) is a pyrimidine nucleoside base that pairs with adenosine (A) in double-stranded DNA. Thymidine is sometimes used to synchronize cells in the S phase of mitosis.
Cas No. | 50-89-5 |
---|---|
Purity | ≥98% |
Formula | C10H14N2O5 |
Formula Wt. | 242.23 |
IUPAC Name | 1-[(2R,4R, 5S)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione |
Synonym | Deoxythymidine, deoxyribosylthymine, thymine deoxyriboside |
Appearance | White to off white powder |
Store Temp | Ambient |
---|---|
Ship Temp | Ambient |
MSDS | |
---|---|
Info Sheet |
Wang X, Pan L, Mao N, et al. Cell-cycle synchronization reverses Taxol resistance of human ovarian cancer cell lines. Cancer Cell Int. 2013 Jul 30;13(1):77. PMID: 23899403.
Banfalvi G. Synchronization of mammalian cells and nuclei by centrifugal elutriation. Methods Mol Biol. 2011;761:25-45. PMID: 21755439.
Langridge R, Marvin DA, Seeds WE, et al. The molecular configuration of deoxyribonucleic acid *: II. Molecular models and their fourier transforms. J Mol Bio. Apr 1960;2(1):38-62.
Doty, P. The physical chemistry of deoxyribonucleic acids. J Cell and Comp Phys. May 1957;49(S1);27-57.
Nrf2-Keap1-ARE complex activator.
Caffeic acid derivative.
Vinca alkaloid found in Catharanthus; microtubu...
Laminin-derived peptapeptide.
GLP-1/GIP receptor co-agonist
RET inhibitor.
Dihydropyrazine found in Ligusticum walliichi. ...
Nav1.7 and Nav1.8 N1+ channel blocker.
Prolyl hydroxylase inhibitor.
L-type and T-type Ca2+ and TRP antagonist.
Peptide, alters hormone secretion and feeding b...
VEGF-C/Nrp2 inhibitor. Leukotriene receptor ant...
Semi-synthetic avermectin; GABA potentiator.
VEGFR inhibitor.
Cannabinoid receptor 2 selective agonist.
MET, FGFR, PDGFR inhibitor.
Inhibitor of ALK2, ALK3, ALK6, and AMPK.
Serotonin/melatonin analog found in various pla...
Dihydropyridine; L-type and N-type Ca2+ channel...
NMDA NR1/NR2B antagonist.