Antimetabolito / análogo nucleósido
Los antimetabolitos y análogos de nucleósidos son compuestos que imitan a los nucleósidos naturales y se incorporan al ADN durante la replicación, lo que provoca la terminación de la cadena o la inhibición de la síntesis de ADN. Estos compuestos se utilizan ampliamente como agentes quimioterapéuticos en el tratamiento del cáncer y las infecciones virales. Al interrumpir la síntesis de ADN, los análogos de nucleósidos inducen el arresto del ciclo celular y la apoptosis. En CymitQuimica, ofrecemos una amplia gama de antimetabolitos y análogos de nucleósidos de alta calidad para apoyar su investigación en el tratamiento del cáncer, la terapia antiviral y la replicación del ADN.
Se han encontrado 1388 productos de "Antimetabolito / análogo nucleósido"
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5'-O-Benzoyl-3'-O-(4-methoxybenzyl)-2'-O,4'-C-methyleneuridine
<p>5’-O-Benzoyl-3’-O-(4-methoxybenzyl)-2’-O,4’-C-methyleneuridine is a purine nucleoside analog with broad antitumor activity, primarily targeting indolent</p>Fórmula:C25H24N2O8Forma y color:SolidPeso molecular:480.47N4-(3,3,3-Trifluoropropanoyl)cytidine
<p>N4-(3,3,3-Trifluoropropanoyl)cytidine, a cytidine analog, inhibits DNA methyltransferases, possibly anti-metabolic and anti-cancer.</p>Fórmula:C12H14F3N3O6Forma y color:SolidPeso molecular:353.256-Amino-3-(furan-2-yl)-4-methoxy-1-(β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine
<p>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 by</p>Fórmula:C15H17N5O6Forma y color:SolidPeso molecular:363.336-Amino-4-hydrozino-1-(2-deoxy-β-D-ribofuranosyl)-1H-pyrazolo[3,4-d]pyrimidine
<p>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 and</p>Fórmula:C10H17N7O3Forma y color:SolidPeso molecular:283.292'-O-Methyladenosine 5'-monophosphate triethyl ammonium
<p>2’-O-Methyladenosine 5’-monophosphate triethyl ammonium is an adenosine analog.</p>Fórmula:C11H14N5O7P2Forma y color:SolidPeso molecular:359.231-(β-D-Xylofuranosyl)-N6-(m-trifluoromethylbenzyl)adenine
<p>1-(β-D-Xylofuranosyl)-N6-(m-trifluoromethylbenzyl)adenine is an adenosine analog.</p>Fórmula:C18H18F3N5O4Forma y color:SolidPeso molecular:425.36m7GpppUmpG
CAS:<p>m7GpppUmpG, a trinucleotide cap analogue, enables RNA synthesis with cap 0 or 1 structures.</p>Fórmula:C31H42N12O26P4Forma y color:SolidPeso molecular:1122.63N1-Methyl-2'-O-(2-methoxyethyl) adenosine
<p>N1-Methyl-2’-O-(2-methoxyethyl) adenosine, a purine nucleoside analog, exhibits broad antitumor effects, particularly against indolent lymphoid malignancies.</p>Fórmula:C14H21N5O5Forma y color:SolidPeso molecular:339.35N1-Methyl-2'-O-(2-methoxyethyl) guanosine
<p>N1-Methyl-2’-O-(2-methoxyethyl) guanosine, a purine nucleoside analog, exhibits broad antitumor activity against indolent lymphoid malignancies.</p>Fórmula:C14H21N5O6Forma y color:SolidPeso molecular:355.352-(3-Methyln-propylidene hydrazino) adenosine
<p>2-(3-Methyln-propylidene hydrazino) adenosine: a purine analog with antitumor properties, inhibits DNA synthesis, induces apoptosis.</p>Fórmula:C15H23N7O4Forma y color:SolidPeso molecular:365.39(R)-N-(2,3-Dihydro-1H-indenyl)-2-amino adenosine
<p>(R)-N-(2,3-Dihydro-1H-indenyl)-2-amino adenosine, a purine analog, targets lymphoid cancer via DNA synthesis inhibition and apoptosis.</p>Fórmula:C19H22N6O4Forma y color:SolidPeso molecular:398.423'-Deoxy-N1-Methyl inosine
<p>3’-Deoxy-N1-Methyl inosine, a purine nucleoside analog, exhibits broad antitumor activity against indolent lymphoid malignancies.</p>Fórmula:C11H14N4O4Forma y color:SolidPeso molecular:266.252'-O-Methyl-5-methyluridine 5'-triphosphate triethylammonium
<p>2’-O-Methyl-5-methyluridine 5’-triphosphate (triethylammonium), a thymidine analog, exhibits insertional activity in replicated DNA.</p>Fórmula:C29H64N5O15P3Forma y color:SolidPeso molecular:815.766-O-Methyl-2'-O-methylinosine
<p>6-O-Methyl-2’-O-methylinosine is a purine nucleoside analog known for its broad antitumor activity, particularly against indolent lymphoid malignancies.</p>Fórmula:C12H16N4O5Forma y color:SolidPeso molecular:296.283'-O-DMT-N2-isobutyryl-2'-O-(2-methoxyethyl)guanosine
<p>3’-O-DMT-N2-isobutyryl-2’-O-(2-methoxyethyl)guanosine, a purine nucleoside analog, exhibits broad antitumor activity particularly against indolent lymphoid</p>Fórmula:C38H43N5O9Forma y color:SolidPeso molecular:713.78N6-Methyl-2'-β-C-ethynyl adenosine
<p>N6-Methyl-2’-beta-C-ethynyl adenosine is a purine nucleoside analog.</p>Fórmula:C13H15N5O4Forma y color:SolidPeso molecular:305.292'-Deoxy-2'-fluoroadenosine 5'-monophosphate triethylammonium
<p>2’-Deoxy-2’-fluoroadenosine 5’-monophosphate (triethylammonium) is a purine nucleoside analog with extensive antitumor properties, particularly effective</p>Fórmula:C22H43FN7O6PForma y color:SolidPeso molecular:551.592-Amino-6-O-methyl-2'-O-methyl purine riboside
<p>2-Amino-6-O-methyl-2’-O-methyl purine riboside, a purine nucleoside analog, exhibits broad antitumor activity, particularly against indolent lymphoid</p>Fórmula:C12H17N5O5Forma y color:SolidPeso molecular:311.293'-β-C-Ethynyl-4-deoxyuridine
<p>3’-Beta-C-Ethynyl-4-deoxyuridine is a purine nucleoside analog.</p>Fórmula:C11H12N2O5Forma y color:SolidPeso molecular:252.223'-β-C-Methyl-2-thiouridine
<p>3’-β-C-Methyl-2-thiouridine, a purine nucleoside analog, exhibits extensive antitumor activity, particularly against indolent lymphoid malignancies.</p>Fórmula:C10H14N2O5SForma y color:SolidPeso molecular:274.29
