Nucleosides
Nucleosides are glycosylamines that can be thought of as nucleotides without a phosphate group. A nucleoside consists simply of a nucleobase (also termed a nitrogenous base) and a five-carbon sugar (either ribose or deoxyribose), whereas a nucleotide is composed of a nucleobase, a five-carbon sugar, and one or more phosphate groups. In a nucleoside, the anomeric carbon is linked through a glycosidic bond to the N9 of a purine or the N1 of a pyrimidine. Examples of nucleosides include cytidine, uridine, adenosine, guanosine, thymidine and inosine.
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223 product(s) in total
2′,3′-ddA
C10H13N5O2
2′,3′-ddC
C9H13N3O3
2′,3′-ddG
C10H13N5O3
2′,3′-ddT
C10H14N2O4
2′,3′-ddU
C9H12N2O4
2′,3′-ddI
C10H12N4O3
2-NH2-ddA
C10H14N6O2
D4A
C10H13N5O2
D4I
C10H12N4O3
5-ethynyl-U
C11H12N2O6
dW
5-I-2′-FANA-dU
2′-F-5-(Tips-ethynyl)-dU
2′-F-5-ethynyl-dU
2′-OMe-5-ethynyl-U
2′-OMe-5-(Tips-ethynyl)-U
iso-dU
4′-Thio-U
5-MOM-pU
5-MOM-U
5-carboxymethylester-U
5-hydroxymethyl-C
N2-DM-G
N-(L)-lactoyl-G
N3-BOM-3′-O-Bz-2′-O-Me-U
C25H26N2O8
3′,5′-TIPDS-15N3-Ur
C21H38N2O7Si2
3′,5′-TIPDS-15N1-Gr
C22H39N5O6Si2
2′-dT
5-I-2′-dU
2′-dA·H2O
2′-dG·H2O
2′-dC
2′-dC·HCl
Cr
Gr
Ur
Biotin-14-N6-(6-Aminohexyl)-dA
Biotin-14-N4-(6-Aminohexyl)-dC
3′-N3-ddU xiaoxu
3′-N3-ddT
Ar
5′-ethyl dimethyl phosphonate-2′-OMe-U
C13H21N2O8P
N1-Me-Pseudo-iso-Cytidine
7-I-7-deaza-dG
N6-(6-Aminohexyl-TFA)-dA
N4-(6-Aminohexyl-TFA)-dC
3′-N3-dG
3′-NH2-dG
N1-Me-A
N6-Me-A
7-deaza-7-I-Ar
7-deaza-7-I-dA
7-deaza-dG
5′-O-DMTr-2′-O-Me-A(iBu)
5′-O-DMTr-2′-O-MOE-5-Me-C(Ac)
5′-O-Ts-3′-O-TBDMS-2′-O-4′-C-Locked-Ur
5′-N3-3′-O-TBDMS-2′-O-4′-C-Locked-Ur
5′-NH2-3′-O-TBDMS-2′-O-4′-C-Locked-Ur
7-deaza-dA
5-[N-(naphthalen-2-ylmethyl)formamide]-dU
5-formyl-2′-dU
6-methylmercapto-9-(β-D-ribofuranosyl)purine
5′-O-TBDMS-3′-NH2-ddT
C16H29N3O4Si
3′,5′-di-O-TBDMS-2′-O-4′-C-Locked-Gr
5-amineallyl-2′-dU
5-hydroxy methyl-2′-dC
5-Hydroxymethyl-Ur
5-hydroxymethyl-2′-dU
6-SH-dG
TFA-AA-dU
N7-Me-Gr
5′-F-Ur
5-amineallyl-Ur
N2-iBu-3′,5′-TIPDS-15N1-Gr
iso-dG
2-Thio-Ur
13C8-Gr
13C8-Ar
13C6-Ur
13C6-Cr
2,3′-Anhydro-5-Me-Ur
2′,4-Anhydro-pU
3′,2-cyclo-Anhydro-dU
15N1-Gr
C10H13N5O5
15N3-Ur
2′-FANA-Ur
2′-FANA-Tr
3′-O-Me-Cr
3′-O-Me-Ur
7-Me-3′-O-Me-Gr
2-I-purine-ribose
2′-FANA-Ar
2′-FANA-Gr
2′-FANA-Cr
2′-O-propargyl-Ur
2′-OMe-Ar
2′-OMe-Gr
7-Me-2′-O-Me-Gr
2-Cl-dA
3′-O-propargyl-2-amino-Ar
2′-O-propargyl-Gr
3′-O-propargyl-Gr
2′-O-propargyl-Ar
2′-O-propargyl-Cr
Ara-Ur
5-methyl-Ara-Ur; Ara-Tr
Ara-Ir
2′-O-propargyl-2-amino-Ar
2-F-Ara-Ar
2-NH2-Ara-Ar
Ara-Gr
Ara-Cr
5-I-2′-F-dU
5-I-2′-F-dC
Ara-Ar
2′-F-dC
2′-F-dU
2′-F-dI
2-NH2-2′-F-dA
3′-NH2-ddT
C10H15N3O4
N4-NH2-Cr
2′-F-dA
2′-F-dG
3′-NH2-ddA
C10H14N6O2
3′-NH2-ddC
3′-NH2-ddG
C10H14N6O3
3′-NH2-ddI
C10H13N5O3
2′-NH2-dA
2′-NH2-dG
2′-NH2-dI
2′-NH2-dU
2-NH2-purine-riboside
2-F-3′-NH2-ddA
C10H13FN6O2
2-NH2-2′-NH2-dA
3′-NH2-2-NH2-ddA
C10H15N7O2
2-NH2-Ar
3′-N3-5′-O-Bz-ddT
C17H17N5O5
3′-N3-ddA
C10H12N8O2
3′-N3-ddC
3′-N3-ddU
7-deaza-7-I-ddG
6-Chloro-7-deazapurine-β-D-riboside
2′-N3-2′-dC
2′-N3-2′-dU
8-Br-2′-dA
8-Br-2′-dG
8-Br-Gr
7-deaza-7-I-ddA
6-Chloropurine riboside
6-Cl-purine-2′-deoxyriboside
2-NH2-6-Cl-purine-riboside
8-Br-Ar
5-I-ddC
5-I-ddU
5-I-2′-dU
5-I-Ur
5-F-2′-dU
3′,5′-Di-O-Ac-5-I-2′-dU
5-I-Cr
5-I-2′-dC
5-Br-2′-dC
5-Br-2′-dU
5-Br-Ur
5-F-2′-dC
5-Me-2′-O-(2-fluoroethyl)-Ur
2,6-Dichloropurine riboside
2′-Br-dU
2-NH2-6-Cl-purine-2′-deoxyriboside
SAM-I
5-Ethynyl-dU
2′-methylene-dU
8-Hydroxy-Gr
pU
2-Thio-Ar
4-Thiouridine
SAM-Cl
Cyclo-Cr·HCl
2, 2′-Anhydro-Ur
5-methyl-2, 2′-Anhydro-Ur
N1-Me-pU
5-OMe-Ur
3′-O-Me-Ar
3′-O-Me-Gr
Cyclo-Cr
2-NH2-2′-O-Me-Ar
5-Me-2′-O-Me-Cr
5-Me-2′-O-Me-Ur
5-I-2′-O-Me-Ur
5-I-2′-O-Me-Cr
5-Me-2′-O-MOE-Cr
2′-O-MOE-Tr
2′-OMe-Ur
2′-OMe-Ir
iso-Gr
iso-Cr
2′-O-MOE-Ar
2′-O-MOE-Gr
PMO Adesnosine Precursor
C36H32N6O3
PMO-C Precursor
C35H32N4O4
PMO Thymidine Precursor
C29H29N3O4