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Cat. No.: HY-N8060

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Orotidine 5′-monophosphate

(Synonyms: Orotidine monophosphate; Orotidylic acid)

2 Cited Publications

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Based on 2 publication(s) in Google Scholar

Orotidine 5′-monophosphate is a pyrimidine ribonucleoside and plays a role as an endogenous metabolite of human, E. coli or mouse. Orotidine 5′-monophosphate is an intermediate in the biosynthesis of?uridine monophosphate (UMP). Orotidine 5′-monophosphate can be used for the study of mechanism of orotidine 5′-monophosphate decarboxylase.

For research use only. We do not sell to patients.

CAS No.: 2149-82-8
Formula: C₁₀H₁₃N₂O₁₁P
Molecular Weight:368.19

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (274 KB)

Orotidine 5′-monophosphate Chemical Structure

CAS No.: 2149-82-8

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Biological Activity
- Description
- IC₅₀ & Target
- In Vitro
Chemical Information
Publications (2)
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
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Biological Activity

Description

IC₅₀ & Target

Human Endogenous Metabolite

All Endogenous Metabolite Isoforms :

In Vitro

Orotidine 5′-monophosphate is formed from?orotate?and?phosphoribosyl pyrophosphate?by the enzyme?orotate phosphoribosyltransferase. The enzyme?UMP synthase can convert OMP into?uridine 5'- monophosphate^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

CAS No. 2149-82-8
Molecular Weight 368.19
Formula C₁₀H₁₃N₂O₁₁P
SMILES

O[C@H]([C@@H]1O)[C@@](N(C(N2)=O)C(C(O)=O)=CC2=O)([H])O[C@@H]1CO[P](O)(O)=O
Synonyms

Orotidine monophosphate; Orotidylic acid
Structure Classification
- Ketones, Aldehydes, Acids
Initial Source
- Endogenous metabolite
- Human Gut Microbiota Metabolites
- Microorganisms
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Publications (2)

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J Adv Res

Antimycin A inhibits alpha-herpesvirus replication by disrupting the formation of pyrimidinosomes. [Abstract]

2025 May 10:S2090-1232(25)00309-1. PMID: 40354935
Acta Pharm Sin B

2026 May 22.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (274 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. R Jund, et al. Regulation of orotidylic acid pyrophosphorylase in Saccharomyces cerevisiae. J Bacteriol. 1972 Jan;109(1):196-202. [Content Brief]

[2]. From Wikipedia. Orotidine 5'-monophosphate

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Keywords

Orotidine 5′-monophosphate

2 Cited Publications

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Biological Activity
- Description
- IC₅₀ & Target
- In Vitro
Chemical Information
Publications (2)
Purity & Documentation
References

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Orotidine 5′-monophosphate

Publications Citing Use of MedChemExpress (MCE) Orotidine 5′-monophosphate

All Endogenous Metabolite Isoforms

Biological Activity

Chemical Information

Publications (2)

Purity & Documentation

References

Calculators

Help & FAQs

Orotidine 5′-monophosphate Related Classifications

HY-N8060 Related Classifications