ChemicalBook--->CAS DataBase List--->314-50-1

314-50-1

314-50-1 Structure

314-50-1 Structure
IdentificationBack Directory
[Name]

OROTIDINE
[CAS]

314-50-1
[Synonyms]

OROTIDINE
Orotidine ,98%
6-Carboxyuridine
URIDIN-6-CARBOXYLIC ACID
URIDINE-6-CARBOXYLIC ACID
orotidine free acid approx. 90%
Orotidine (Uridine-6-carboxylic acid)
1,2,3,6-Tetrahydro-2,6-dioxo-3-β-D-ribofuranosyl-4-pyrimidinecarboxylic acid
4-Pyrimidinecarboxylicacid, 1,2,3,6-tetrahydro-2,6-dioxo-3-b-D-ribofuranosyl-
4-Pyrimidinecarboxylic acid, 1,2,3,6-tetrahydro-2,6-dioxo-3-β-D-ribofuranosyl-
3-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-2,6-dioxopyrimidine-4-carboxylic acid
3-[(2R,3R,4S,5R)-3,4-dihydroxy-5-methylol-tetrahydrofuran-2-yl]-2,6-diketo-pyrimidine-4-carboxylic acid
[Molecular Formula]

C10H12N2O8
[MDL Number]

MFCD00057418
[MOL File]

314-50-1.mol
[Molecular Weight]

288.21
Chemical PropertiesBack Directory
[Melting point ]

>400 °C
[density ]

1.847±0.06 g/cm3(Predicted)
[storage temp. ]

−20°C
[solubility ]

DMSO (Slightly), Methanol (Slightly), Water (Slightly)
[form ]

Solid
[pka]

2.62±0.20(Predicted)
[color ]

White to Off-White
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

29349990
Hazard InformationBack Directory
[Uses]

Orotidine is a metabolite of Orotic Acid (O691500); a compound used in the preparation of therapeutic agents for chronic obstructive pulmonary disease (COPD) treatment.
[Definition]

ChEBI: A nucleoside formed by attaching orotic acid to a ribose ring via a beta1N(1)-glycosidic bond.
[Enzyme inhibitor]

This water-soluble ribonucleoside (FWfree-acid = 288.21 g/mol; CAS 314-50- 1; lmax of 267 nm in 0.1 N HCl (e = 9570 cm–1M–1; another report lists 9800) and 265 nm in 0.1 N methanolic NaOH (e = 8960 cm–1M–1; another report lists 7800)), first observed in Neurospora crassa, is also foound in the urine of cancer patients treated with 6-azauridine, Orotidine is most likely formed from OMP, its 5’-monophosphate ester and the direct precursor of UMP. Orotidine is readily hydrolyzed in dilute mineral acids. Target(s): orotate phosphoribosyltransferase; orotidine-5’-phosphate decarboxylase.
[storage]

Store at -20°C
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