「Pyrimidine」の共起表現一覧(1語右で並び替え)
該当件数 : 64件
HCFU (1-hexylcarbamoyl-5-fluorouracil) is a | pyrimidine analogue used as an antineoplastic agent. |
pyrimidine analogues | |
Pyrimidine analogues are antimetabolites which mimic th | |
ine is a chemical compound composed of fused | pyrimidine and pyrazine rings. |
ts as a coenzyme in the synthesis of purine, | pyrimidine and other amino acids. |
ssential coenzyme synthesised by coupling of | pyrimidine and thiazole moieties in bacteria. |
Because of the asymmetry in | pyrimidine and purine use in coding sequences, the stra |
is position should contain the complementary | pyrimidine, and not also be a purine. |
Isocytosine or 2-aminouracil is a | pyrimidine base that is an isomer of cytosine. |
dine is ribose (a pentose sugar) joined to a | pyrimidine base and is similar to cytidine, uridine, 2- |
ation in DNA that has neither a purine nor a | pyrimidine base, usually due to DNA damage. |
nce of hydrogen bonds between the purine and | pyrimidine bases of DNA were crucial to Watson and Cric |
The various purine and | pyrimidine bases are linked to the backbone by methylen |
Loss of | pyrimidine bases (Cytosine and Thymine) occurs by a sim |
Pyrimidine biosynthesis occurs both in the body and thr | |
(or CTP synthetase) is an enzyme involved in | pyrimidine biosynthesis that interconverts UTP and CTP. |
d upstream of a variety of genes involved in | pyrimidine biosynthesis and transport. |
oribosyltransferase is an enzyme involved in | pyrimidine biosynthesis. |
otic acid which serves as an intermediate in | pyrimidine biosynthesis. |
novo purine biosynthesis pathway and some in | pyrimidine biosynthesis. |
de) is a chemical compound, more precisely a | pyrimidine deoxynucleoside. |
yase (photosensitive), and deoxyribonucleate | pyrimidine dimer lyase (photosensitive). |
cur, which results in the elimination of the | pyrimidine dimer, returning it to its original state. |
Right: Cyclobutane | pyrimidine dimer. |
phosphate fragment while the β-subunit binds | pyrimidine fragment of TPP, forming together a catalyti |
ydropyrimidine hydrase, hydantoin peptidase, | pyrimidine hydrase, and D-hydantoinase. |
This enzyme participates in | pyrimidine metabolism and one carbon pool by folate. |
in 3 metabolic pathways: purine metabolism, | pyrimidine metabolism, and bladder cancer. |
enzyme participates in 3 metabolic pathways: | pyrimidine metabolism, beta-alanine metabolism, and pan |
enzyme participates in 3 metabolic pathways: | pyrimidine metabolism, beta-alanine metabolism, and pan |
This enzyme participates in | pyrimidine metabolism. |
enzyme participates in purine metabolism and | pyrimidine metabolism. |
ic sequences rich with repetitive purine and | pyrimidine motifs. |
se include N-ribosylpyrimidine nucleosidase, | pyrimidine nucleosidase, N-ribosylpyrimidine ribohydrol |
Thus, the two substrates of this enzyme are | pyrimidine nucleoside and H2O, whereas its two products |
Thus, the two substrates of this enzyme are | pyrimidine nucleoside and phosphate, whereas its two pr |
er of 2',3'‐dideoxy‐3'‐thiacytidine and is a | pyrimidine nucleoside analogue. |
kinase, ATP:UMP-CMP phosphotransferase, and | pyrimidine nucleoside monophosphate kinase. |
The chemical compound 5-methyluridine is a | pyrimidine nucleoside. |
"Synthesis of C-5 substituted | pyrimidine nucleosides via organopalladium intermediate |
it also catalyzes the preceding reaction in | pyrimidine nucleotide biosynthesis, the transfer of rib |
Other names in common use include | pyrimidine nucleotide N-ribosidase, and Pyr5N. |
Pyrimidine nucleotide synthesis starts with the formati | |
e (OMP), also known as orotidylic acid, is a | pyrimidine nucleotide which is the last intermediate in |
Uridine triphosphate, which is a | pyrimidine nucleotide, has the ability to act as an ene |
lly at phosphodiester linkages adjacent to a | pyrimidine nucleotide, yielding 5'-phosphate-terminated |
Cytidine triphosphate is a | pyrimidine nucleotide. |
It is from UMP that other | pyrimidine nucleotides are derived. |
related classes of molecules resembling the | pyrimidine nucleotides found in DNA. |
By inhibiting the formation of precursor | pyrimidine nucleotides, raltitrexed prevents the format |
Other names in common use include | pyrimidine phosphorylase, UrdPase, UPH, and UPase. |
Other names in common use include | pyrimidine phosphorylase, thymidine-orthophosphate deox |
of the azine series have (such as pyridine, | pyrimidine, pyridazine, pyrazine, 1,3,5-triazine and te |
dehydrogenase, dihydrothymine dehydrogenase, | pyrimidine reductase, thymine reductase, uracil reducta |
obutadipyrimidine (in DNA), and one product, | pyrimidine residues (in DNA). |
Other names in common use include | pyrimidine ribonucleoside kinase, uridine-cytidine kina |
group is usually attached to carbon 5 of the | pyrimidine ring of uracil and cytosine. |
higher score to transitions (changes from a | pyrimidine such as C or T to another pyrimidine, or fro |
Pyrimidine synthesis inhibitors are used in active mode | |
occurs with carbamoyl phosphate entering the | pyrimidine synthesis pathway. |
uridine (abbreviated as D, DHU, or UH2) is a | pyrimidine which is the result of adding two hydrogen a |
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