「IMIDAZOLE」の共起表現一覧(1語左で並び替え)
該当件数 : 47件
This compound (3) is produced by alkylating | imidazole (1) with o-chlorotrityl chloride (2) in acet |
e, and the purine nucleobases all contain an | imidazole ring. |
Antimicrobial Action Fenticonazole is an | imidazole antifungal active against a range of organis |
Fenobam is an | imidazole derivative developed by McNeil Laboratories |
Flutrimazole is an | imidazole derivative. |
Iprodione is an | imidazole fungicide. |
Bifonazole is an | imidazole antifungal drug. |
Propenidazole is an | imidazole derivative used in gynecology. |
Butoconazole is an | imidazole antifungal used in gynecology. |
Both contain an | imidazole ring and a 2,6-dichlorinated phenyl ring. |
Xylometazoline is an | imidazole derivative which is designed to mimic the mo |
In enzymology, an | imidazole N-acetyltransferase (EC 2.3.1.2) is an enzym |
mpound consists of the fusion of benzene and | imidazole. |
increased levels of histidine, histamine and | imidazole in blood, urine and cerebrospinal fluid. |
substrates of this enzyme are acetyl-CoA and | imidazole, whereas its two products are CoA and N-acet |
orbitals is part of an heterocycle, such as | imidazole or triazole. |
le may be synthesized by first deprotonating | imidazole to form a sodium salt followed by methylatio |
c as well as non-basic nitrogen atoms, e.g., | imidazole and purine. |
onitrile, followed by the addition of excess | imidazole. |
ate acid has a pKa of 0.8, compared to 7 for | imidazole. |
glyoxal and formaldehyde in ammonia to form | imidazole (or glyoxaline, as it was originally named). |
eterocycle with formula C3H6N2, derived from | imidazole. |
Other names in common use include | imidazole acetylase, and imidazole acetyltransferase. |
residue is considered to be basic due to its | imidazole ring." |
Like | imidazole, imidazoline-based compounds have been used |
Like | imidazole- and triazole-class antifungals, abafungin in |
between the two) is approximately 7, making | imidazole approximately sixty times more basic than py |
ized on a laboratory scale by methylation of | imidazole at the pyridine-like nitrogen and subsequent |
As an acid, the pKa of | imidazole is 14.5, making it less acidic than carboxyl |
d, rather than doubly bonded for the case of | imidazole. |
Chemical relationship of | imidazole to its reduced derivatives. |
These are ionic liquids based on | imidazole chemistry. |
DNA cyclase, which recloses | imidazole rings of guanine and adenine damaged by x-ir |
As a result, | imidazole engineering has been suggested as a means to |
cleavage of guanine in DNA by rupturing the | imidazole rings present in guanine. |
imidazole with one electron removed from the | imidazole arene group. |
oconazole is an antifungal medication of the | imidazole class used to treat infections caused by a f |
The | imidazole portion of imiloxan is prepared by the react |
The | imidazole sidechain of histidine is a common coordinat |
ratio that forms an insoluble salt with the | imidazole, such as trifluoro- or trichloroacetic acid |
c pathway is not clear, it is known that the | imidazole ring is supplied by histidine, which is then |
e nitrate is an antifungal medication of the | imidazole class. |
The | imidazole backbone is an essential functional unit in |
N-Alkylation of the | imidazole with ethyl iodide gives imiloxan. |
he above example would be constituted by the | imidazole ring or "the imidazole moiety". |
The | imidazole ring of histidine is aromatic at all pH valu |
ed by the addition of four hydrogen atoms to | imidazole. |
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