
Nucleoside Antimetabolita/Analoga
Gli antimicotici e analoghi dei nucleosidi sono composti che imitano i nucleosidi naturali e vengono incorporati nel DNA durante la replicazione, portando alla terminazione della catena o all'inibizione della sintesi del DNA. Questi composti sono ampiamente utilizzati come agenti chemioterapici nel trattamento del cancro e delle infezioni virali. Interrompendo la sintesi del DNA, gli analoghi dei nucleosidi inducono l'arresto del ciclo cellulare e l'apoptosi. Presso CymitQuimica, offriamo una vasta gamma di antimicotici e analoghi dei nucleosidi di alta qualità per supportare la tua ricerca sul trattamento del cancro, la terapia antivirale e la replicazione del DNA.
Trovati 1421 prodotti di "Nucleoside Antimetabolita/Analoga"
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
5'-O-Benzoyl-3'-O-(4-methoxybenzyl)-2'-O,4'-C-methyleneuridine
5’-O-Benzoyl-3’-O-(4-methoxybenzyl)-2’-O,4’-C-methyleneuridine is a purine nucleoside analog with broad antitumor activity, primarily targeting indolentFormula:C25H24N2O8Colore e forma:SolidPeso molecolare:480.47N4-(3,3,3-Trifluoropropanoyl)cytidine
N4-(3,3,3-Trifluoropropanoyl)cytidine, a cytidine analog, inhibits DNA methyltransferases, possibly anti-metabolic and anti-cancer.Formula:C12H14F3N3O6Colore e forma:SolidPeso molecolare:353.256-Amino-3-(furan-2-yl)-4-methoxy-1-(β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine
6-Amino-3-(furan-2-yl)-4-methoxy-1-(β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine, a purine nucleoside analogue, exhibits broad antitumor activity byFormula:C15H17N5O6Colore e forma:SolidPeso molecolare:363.336-Amino-4-hydrozino-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine
6-Amino-4-hydrozino-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine, a pyrimidine nucleoside analog, boasts a broad spectrum of biochemical andFormula:C10H17N7O3Colore e forma:SolidPeso molecolare:283.292'-O-Methyladenosine 5'-monophosphate triethyl ammonium
2’-O-Methyladenosine 5’-monophosphate triethyl ammonium is an adenosine analog.Formula:C11H14N5O7P2Colore e forma:SolidPeso molecolare:359.23m7GpppUmpG
CAS:m7GpppUmpG, a trinucleotide cap analogue, enables RNA synthesis with cap 0 or 1 structures.Formula:C31H42N12O26P4Colore e forma:SolidPeso molecolare:1122.63N4-Benzoyl-2'-deoxy-2'-fluoro-β-D-arabinocytidine
N4-Benzoyl-2’-deoxy-2’-fluoro-β-D-arabinocytidine, a purine nucleoside analog, exhibits widespread antitumor activity, particularly against indolent lymphoidFormula:C16H16FN3O5Colore e forma:SolidPeso molecolare:349.31N1-Methyl-2'-O-(2-methoxyethyl) adenosine
N1-Methyl-2’-O-(2-methoxyethyl) adenosine, a purine nucleoside analog, exhibits broad antitumor effects, particularly against indolent lymphoid malignancies.Formula:C14H21N5O5Colore e forma:SolidPeso molecolare:339.35N1-Methyl-2'-O-(2-methoxyethyl) guanosine
N1-Methyl-2’-O-(2-methoxyethyl) guanosine, a purine nucleoside analog, exhibits broad antitumor activity against indolent lymphoid malignancies.Formula:C14H21N5O6Colore e forma:SolidPeso molecolare:355.352-(3-Methyln-propylidene hydrazino) adenosine
2-(3-Methyln-propylidene hydrazino) adenosine: a purine analog with antitumor properties, inhibits DNA synthesis, induces apoptosis.Formula:C15H23N7O4Colore e forma:SolidPeso molecolare:365.39(R)-N-(2,3-Dihydro-1H-indenyl)-2-amino adenosine
(R)-N-(2,3-Dihydro-1H-indenyl)-2-amino adenosine, a purine analog, targets lymphoid cancer via DNA synthesis inhibition and apoptosis.Formula:C19H22N6O4Colore e forma:SolidPeso molecolare:398.423'-Deoxy-N1-Methyl inosine
3’-Deoxy-N1-Methyl inosine, a purine nucleoside analog, exhibits broad antitumor activity against indolent lymphoid malignancies.Formula:C11H14N4O4Colore e forma:SolidPeso molecolare:266.252'-O-Methyl-5-methyluridine 5'-triphosphate triethylammonium
2’-O-Methyl-5-methyluridine 5’-triphosphate (triethylammonium), a thymidine analog, exhibits insertional activity in replicated DNA.Formula:C29H64N5O15P3Colore e forma:SolidPeso molecolare:815.766-O-Methyl-2'-O-methylinosine
6-O-Methyl-2’-O-methylinosine is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies.Formula:C12H16N4O5Colore e forma:SolidPeso molecolare:296.283'-O-DMT-N2-isobutyryl-2'-O-(2-methoxyethyl)guanosine
3’-O-DMT-N2-isobutyryl-2’-O-(2-methoxyethyl)guanosine, a purine nucleoside analog, exhibits broad antitumor activity particularly against indolent lymphoidFormula:C38H43N5O9Colore e forma:SolidPeso molecolare:713.78N6-Methyl-2'-β-C-ethynyl adenosine
N6-Methyl-2’-beta-C-ethynyl adenosine is a purine nucleoside analog.Formula:C13H15N5O4Colore e forma:SolidPeso molecolare:305.292'-Deoxy-2'-fluoroadenosine 5'-monophosphate triethylammonium
2’-Deoxy-2’-fluoroadenosine 5’-monophosphate (triethylammonium) is a purine nucleoside analog with extensive antitumor properties, particularly effectiveFormula:C22H43FN7O6PColore e forma:SolidPeso molecolare:551.592-Amino-6-O-methyl-2'-O-methyl purine riboside
2-Amino-6-O-methyl-2’-O-methyl purine riboside, a purine nucleoside analog, exhibits broad antitumor activity, particularly against indolent lymphoidFormula:C12H17N5O5Colore e forma:SolidPeso molecolare:311.293'-β-C-Ethynyl-4-deoxyuridine
3’-Beta-C-Ethynyl-4-deoxyuridine is a purine nucleoside analog.Formula:C11H12N2O5Colore e forma:SolidPeso molecolare:252.223'-β-C-Methyl-2-thiouridine
3’-β-C-Methyl-2-thiouridine, a purine nucleoside analog, exhibits extensive antitumor activity, particularly against indolent lymphoid malignancies.Formula:C10H14N2O5SColore e forma:SolidPeso molecolare:274.29

