369656-75-7
Chemical Structure
Uridine-13C,15N2
Synonym(s): β-Uridine-13C,15N2
- CAS. Nr.: 369656-75-7
- Formula:C813CH1215N2O6
- Molecular Weight:247.18
IUPAC Name: 1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione-2-13C-1,3-15N2
InChIKey: DRTQHJPVMGBUCF-CNANCEAGSA-N
SMILES: O[C@H]1[C@@H](O[C@H](CO)[C@H]1O)[15N]2[13C]([15NH]C(C=C2)=O)=O
Biological Activity: Uridine-13C,15N2 (β-Uridine-13C,15N2) is a 13C- and 15N-labeled Uridine (HY-B1449).
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
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Uridine-13C,15N2 | Uridine-13C,15N2 (β-Uridine-13C,15N2) is a 13C- and 15N-labeled Uridine (HY-B1449). | |||||||||||||||||||||
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Uridine (Standard) | 99.98% | Uridine (Standard) is the analytical standard of Uridine. This product is intended for research and analytical applications. | ||||||||||||||||||||
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Uridine-13C9 | 96.8% | Uridine-13C9 (β-Uridine-13C9) is a 13C9-labeled form of Uridine (HY-B1449). Uridine (β-Uridine) is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. | ||||||||||||||||||||
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Uridine-13C | 99.82% | Uridine-13C is the 13C labeled Uridine. | ||||||||||||||||||||
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Uridine-d2-1 | 98.47% | Uridine-d2-1 is the deuterium labeled Uridine. | ||||||||||||||||||||
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Uridine-13C-3 | Uridine-13C-3 is the 13C labeled Uridine. | |||||||||||||||||||||
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Uridine-13C9, 15N2 | 99.80% | Uridine-13C9,15N2 (β-Uridine-13C9,15N2) is 13C and 15N labeled Uridine (HY-B1449). Uridine is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. | ||||||||||||||||||||
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Uridine-d12 | Uridine-d12 (β-Uridine-d12) is the deuterium labeled Uridine (HY-B1449). Uridine is a glycosylated pyrimidine-analog containing uracil attached to a ribose ring (or more specifically, aribofuranose) via a β-N1-glycosidic bond. | |||||||||||||||||||||
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Uridine 13C-4 | 99% | Uridine 13C-4 is the 13C labeled Uridine. | ||||||||||||||||||||
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Uridine-13C-2 | 99.9% | Uridine-13C-2 is the 13C labeled Uridine. | ||||||||||||||||||||
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Uridine-d2 | 99.0% | Uridine-d2 is the deuterium labeled Uridine. | ||||||||||||||||||||
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Uridine-d | Uridine-d is the deuterium labeled Uridine.. | |||||||||||||||||||||
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Uridine-13C5 | 99.90% | Uridine-13C5 (β-Uridine-13C5) is a 13C labeled Uridine (HY-B1449). Uridine (β-Uridine) is a nucleoside compound consisting of uracil and a ribose ring, which are linked by a β-N1- glycosyl bond. | ||||||||||||||||||||
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Uridine-13C-1 | Uridine-13C-1 is the 13C labeled Uridine. | |||||||||||||||||||||
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Uridine-15N2 | 98% | Uridine-15N2 is the 15N labeled Uridine. | ||||||||||||||||||||
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Uridine | 99.97% | Uridine (β-Uridine) is a nucleoside compound composed of uracil and a ribose ring, which are connected by a β-N1-glycosidic bond. | ||||||||||||||||||||
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5-Aminouridine | 99.31% | 5-Aminouridine can modify nucleobases and can be incorporated into the target DNA. 5-Aminouridine exhibits a wide range of biological activity and it inhibits the growth of tumors, fungi and viruses. | ||||||||||||||||||||
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5-Chlorouridine | 5-Chlorouridine, a ribonucleoside, is an inhibitor of RNase A (Ki = 44.5 μM) and eosinophil derived neurotoxin (EDN) (Ki = 1080.1 μM; IC50 = 1462.8 μM). 5-Chlorouridine can be used for the researches of inflammatory disorders and hypereosinophilic syndromes. | |||||||||||||||||||||
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Cytarabine-d2 | 98.0% | Cytarabine-d2 is the deuterium labeled Cytarabine. Cytarabine, a nucleoside analog, causes S phase cell cycle arrest and inhibits DNA polymerase. Cytarabine inhibits DNA synthesis with an IC50 of 16 nM. Cytarabine has antiviral effects against HSV. | ||||||||||||||||||||
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1-(β-D-Xylofuranosyl)uracil | 1-(β-D-Xylofuranosyl)uracil is a uridine analog. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents. | |||||||||||||||||||||
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6-Methyluridine | 99.02% | 6-Methyluridine is a uridine analogue. Uridine has potential antiepileptic effects, and its analogs can be used to study anticonvulsant and anxiolytic activities, as well as to develop new antihypertensive agents. | ||||||||||||||||||||
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1-β-D-Arabinofuranosyl-5-bromo-2,4(1H,3H)-pyrimidinedione | 1-β-D-Arabinofuranosyl-5-bromo-2,4(1H,3H)-pyrimidinedione is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. | |||||||||||||||||||||
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Cytidine-d2 | 98.4% | Cytidine-d2 is the deuterium labeled Cytidine. Cytidine is a pyrimidine nucleoside and acts as a component of RNA. Cytidine is a precursor of uridine. Cytidine controls neuronal-glial glutamate cycling, affecting cerebral phospholipid metabolism, catecholamine synthesis, and mitochondrial function. | ||||||||||||||||||||
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2'-Deoxyuridine-d2-1 | 2'-Deoxyuridine-d2-1 is the deuterium labeled 2'-Deoxyuridine. 2'-Deoxyuridine could increase chromosome breakage and results in a decreased thymidylate synthetase activity. A known use of 2'-Deoxyuridine is as a precursor in the synthesis of Edoxudine. | |||||||||||||||||||||
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1-beta-D-Arabinofuranosyluracil (Standard) | 99.91% | 1-beta-D-Arabinofuranosyluracil (Standard) is the analytical standard of 1-beta-D-Arabinofuranosyluracil. This product is intended for research and analytical applications. 1-beta-D-Arabinofuranosyluracil (Uracil 1-β-D-arabinofuranoside) isolated from the Caribbean sponge Tectitethya crypta, is a methoxyadenosine derivative. 1-beta-D-Arabinofuranosyluracil has demonstrated a diverse bioactivity profile including anti-inflammatory activity, analgesic and vasodilation properties. 1-beta-D-Arabinofuranosyluracil reduces a proliferation of mouse lymphoma cells. | ||||||||||||||||||||
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L-Uridine | 99.81% | L-Uridine is an enantiomer of the normal RNA constituent D-uridine. L-Uridine can be isolated from the Polyporaceae fungus Poria cocos (Schw.). L-uridine acts as a phosphate acceptor for nucleoside phosphotransferases. | ||||||||||||||||||||
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L-Uridine (Standard) | ≥98% | L-Uridine (Standard) is the analytical standard of L-Uridine (HY-W006429). This product is intended for research and analytical applications. L-Uridine is an enantiomer of the normal RNA constituent D-uridine. L-Uridine can be isolated from the Polyporaceae fungus Poria cocos (Schw.). L-uridine acts as a phosphate acceptor for nucleoside phosphotransferases. | ||||||||||||||||||||
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5-Bromouridine | 99.89% | 5-Bromouridine is a brominated uridine nucleoside. The triphosphate form of 5-Bromouridine, 5BrdUTP, can substitute for TTP as a substrate for DNA polymerase and be incorporated into nascent DNA strands, rendering the resulting 5-bromouridine-labeled DNA photosensitive to 300 nm UV irradiation; upon UV irradiation, the 5BrdU signal decreases and dU is generated, accompanied by DNA strand breaks and cross-link formation. 5-Bromouridine is useful for studies on nucleoside structure and halogenated nucleoside-labeled nucleic acids. | ||||||||||||||||||||
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5-Methyluridine-d4 | 99.96% | 5-Methyluridine-d4 is the deuterium labeled 5-Methyluridine. 5-Methyluridine is a is an endogenous methylated nucleoside found in human fluids. | ||||||||||||||||||||
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2'-Deoxy-2'-fluorouridine-d2 | 2'-Deoxy-2'-fluorouridine-d2 is the deuterium labeled 2'-Deoxy-2'-fluorouridine. 2'-Deoxy-2'-fluorouridine is a derivative of the pyrimidine nucleoside uridine. 2'-Deoxy-2'-fluorouridine is a nucleoside analog that inhibits the replication of wild-type viruses by binding to the viral RNA. Hepatitis C polyU/UC RNA strands containing 2'-Deoxy-2'-fluorouridine, bind to RIG-I but do not activate RIG-I signaling in a reporter assay using Huh7 cells. 2'-Deoxy-2'-fluorouridine also has been used as a starting material in the synthesis of respiratory syncytial virus (RSV) polymerase inhibitors. 2'-Deoxy-2'-fluorouridine can incorporate into DNA and RNA in rat and woodchuck model upon administration. 2'-Deoxy-2'-fluorouridine can be studied in anti-viral research. | |||||||||||||||||||||
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1-(a-D-ribofuranosyl)uracil | 97.0% | 1-(a-D-ribofuranosyl)uracil is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. | ||||||||||||||||||||
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