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NHC (EIDD-1931)
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NHC (EIDD-1931)

NHC (EIDD-1931)

1.General Specification(in stock)
API(Pure powder)
2.Customization:
We will negotiate individually, OEM/ODM, No brand, for secience researching only.
Internal Code: BM-1-256
N(4)-hydroxycytidine/NHC (EIDD-1931) CAS 3258-02-4
Molecular formula: C9H13N3O6
HS code: N/A
Molecular weight: 259.22
Manufacturer: BLOOM TECH Wuxi Factory
Analysis: HPLC, LC-MS, HNMR
Main market: USA, Australia, Brazil, Japan, Germany, Indonesia, UK, New Zealand , Canada etc.
Technology support: R&D Dept.-4

Shaanxi BLOOM Tech Co., Ltd. is one of the most experienced manufacturers and suppliers of nhc (eidd-1931) in China. Welcome to wholesale bulk high quality nhc (eidd-1931) for sale here from our factory. Good service and reasonable price are available.

 

NHC (EIDD-1931) is a broad-spectrum small-molecule nucleoside antiviral compound with potent inhibitory activity against RNA viruses and an extensive antiviral spectrum. Its core mechanism of action is lethal mutagenesis. After entering host cells, EIDD-1931 is phosphorylated into its active triphosphate form. To date, EIDD-1931 has been extensively investigated for treating emerging and re-emerging human viral infections. Thanks to its broad spectrum, high potency and low propensity to induce drug resistance, it exhibits tremendous application potential in the prevention and control of RNA viruses infecting companion animals, livestock, poultry and aquatic animals, making it a hot target candidate for the development of novel veterinary antiviral drugs.

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Method of Analysis

 

N(4)-hydroxycytidine COA

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Applications-

 

Applications in Veterinary and Companion Animal Antiviral Therapy

Companion Animal Sector: Prevention and Treatment of Feline Infectious Peritonitis Virus (FIPV)

Feline infectious peritonitis (FIP) is a highly lethal infectious disease of companion animals caused by FIPV, a mutated variant of feline coronavirus. It is classified into wet and dry forms, with an extremely high mortality rate among young kittens. Safe and effective specific therapeutic regimens had long been unavailable. GS-441524 is currently the first-line mainstream drug for clinical FIP treatment; it effectively inhibits FIPV replication and alleviates clinical symptoms.

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Nevertheless, it has certain limitations in clinical practice: drug resistance, disease relapse, and unsatisfactory efficacy against neurological manifestations are observed in some cases.Moreover, prolonged monotherapy readily induces resistant viral mutations. By contrast, NHC (EIDD-1931), with superior in vitro antiviral activity and a unique mutagenic mechanism, serves as a novel alternative therapeutic agent for FIP treatment, addressing the shortcomings of existing therapeutic protocols.Multiple in vitro controlled studies have verified that EIDD-1931 exerts markedly stronger inhibitory activity against FIPV than GS-441524. In vitro pharmacodynamic assays targeting Type II FIPV demonstrate that the half-maximal effective concentration (EC₅₀) of EIDD-1931 is as low as 0.11 μM, far lower than the corresponding value for GS-441524.

This indicates that EIDD-1931 can effectively suppress viral proliferation at an extremely low dosage with enhanced antiviral potency. Mechanistically, GS-441524 suppresses viral activity mainly via terminating viral RNA transcription; it only blocks viral replication and cannot eliminate viral genomes. In comparison, EIDD-1931 destroys viral proliferative capacity at the source by inducing lethal mutations in viral genomes. It not only rapidly reduces viral load but also effectively diminishes viral persistence, lowering risks of disease recurrence and resistant mutation emergence. Meanwhile, EIDD-1931 exerts stable inhibitory effects against different subtypes and variant strains of FIPV, supporting broader applicability.

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Livestock and Poultry Farming Sector: In Vitro Research on Prevention and Control of Livestock and Poultry RNA Viruses

RNA viral diseases of livestock and poultry represent core epidemic diseases restricting large-scale farming. Characterized by rapid transmission, high morbidity and frequent large-scale outbreaks, these diseases elevate animal mortality, impair production performance and inflict massive economic losses on the breeding industry. Vaccination remains the primary preventive strategy against livestock and poultry RNA viral diseases, whereas specific therapeutic drugs are scarce.

Frequent viral mutations often weaken vaccine protection, creating an urgent demand for broad-spectrum and high-efficiency antiviral agents for disease control. In recent years, numerous in vitro studies have confirmed that EIDD-1931 displays prominent inhibitory activity against multiple pathogenic RNA viruses affecting livestock and poultry, promising broad prospects for livestock and poultry disease prevention and control. Current research primarily focuses on two highly prevalent pathogens: porcine epidemic diarrhea virus and avian coronavirus.In in vitro investigations on porcine epidemic diarrhea virus (PEDV), EIDD-1931 demonstrates excellent antiviral performance. PEDV is a vital alphacoronavirus threatening swine production.

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It mainly infects suckling piglets and induces severe vomiting, diarrhoea and dehydration; mortality among neonatal piglets can reach 100%. Conventional prevention and control strategies struggle to contain outbreaks caused by viral variant strains. In vitro cellular experiments reveal that EIDD-1931 efficiently suppresses PEDV proliferation in host cells, significantly lowering viral copy numbers and inhibiting cytopathic effects. Its mechanism of action covers the whole viral life cycle including adsorption, replication and assembly. It not only interferes with replication of the viral RNA genome but also reduces the release of progeny virions and blocks cell-to-cell viral transmission.

Compared with traditional anti-PEDV drugs, NHC (EIDD-1931) acts faster and achieves stronger suppression. It maintains stable activity against both classical strains and novel variants without apparent strain specificity, matching the epidemiological landscape of circulating multiple PEDV strains.

Furthermore, efficient antiviral activity can be achieved at low EIDD-1931 concentrations, with no obvious damage to porcine intestinal epithelial cells, indicating favourable in vitro safety and providing data support for subsequent optimisation of clinical dosing regimens.EIDD-1931 also displays broad-spectrum antiviral advantages in research targeting avian coronavirus prevention and control.

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Avian coronavirus is represented by infectious bronchitis virus (IBV), which infects poultry of all ages and triggers respiratory inflammation, renal injury, reduced egg production and other complications.

Secondary bacterial infections commonly occur, substantially increasing poultry mortality. Existing preventive vaccines suffer from weak cross-protection and delayed updates, and effective therapeutic drugs are lacking in clinical settings. In vitro research data show that EIDD-1931 markedly inhibits IBV RNA replication, effectively alleviates virus-induced cellular damage and reduces viral invasiveness towards avian respiratory mucosal cells.

Unlike conventional antiviral medicines, EIDD-1931 is less likely to drive viral resistance and sustains stable long-term antiviral activity. Its conserved drug target enables inhibition of avian coronaviruses across diverse genotypes, compensating for deficiencies in existing prevention and control approaches and offering an innovative technical strategy for treating and urgently containing avian coronavirus infections.

Aquaculture Sector: In Vitro Research on Prevention and Control of Aquatic Animal RNA Viruses

RNA viral diseases of aquatic animals constitute major hazards in aquaculture.

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Such diseases feature abrupt onset, rapid spread and high mortality. Coupled with complex aquatic environments, epidemic prevention and control pose enormous challenges. Fish rhabdoviruses form the most destructive group of RNA viruses in aquaculture, encompassing multiple pathogenic strains such as grass carp haemorrhagic disease virus and spring viraemia of carp virus.

These viruses infect various freshwater farmed fish and trigger mass mortality, severely hindering high-quality development of the aquaculture industry. Currently, the supply of aquatic antiviral drugs is limited. Most available agents carry drawbacks including high toxicity, substantial residues and disruption of aquatic ecosystems. Safe and efficient novel antiviral pharmaceuticals are therefore urgently required.

Extensive in vitro studies have validated that EIDD-1931 exerts potent inhibitory activity against multiple fish rhabdoviruses, marking it a highly promising candidate antiviral drug exclusively for aquaculture. Fish rhabdoviruses are single-stranded negative-sense RNA viruses featuring simple genomes, rapid replication and strong mutational capacity, making them difficult to precisely target using conventional drugs. Relying on its broad-spectrum mutagenic mechanism against RNA viruses, EIDD-1931 efficiently incorporates into nascent RNA genomes of fish rhabdoviruses and induces abundant lethal mutations to completely block viral replication and proliferation.

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In vitro cell culture experiments indicate that EIDD-1931 significantly reduces viral titres in rhabdovirus-infected cells and effectively suppresses cytopathy.

Within therapeutically effective antiviral concentrations, EIDD-1931 exhibits no obvious toxicity to primary fish cells and possesses favourable cellular compatibility.

NHC (EIDD-1931) presents outstanding advantages over traditional aquaculture antiviral drugs.

First, it boasts a wide antiviral spectrum covering diverse pathogenic fish rhabdoviruses. There is no need to develop strain-specific medicines, rendering it suitable for prevention and control scenarios involving mixed viral infections commonly seen in aquaculture.Second, it has a high resistance barrier: viruses struggle to develop resistant variants under mutagenic suppression, supporting stable long-term epidemic management.

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Third, it achieves high safety and low residue risks. As a small-molecule compound, EIDD-1931 undergoes rapid metabolism and does not accumulate heavily in aquatic organisms or disrupt aquatic microbial ecosystems, complying with the development principles of green aquaculture. At present, research on EIDD-1931 against aquatic animal RNA viruses mainly focuses on in vitro pharmacodynamic verification. Further investigations into in vivo efficacy, administration modalities and suitability for aquatic environments are required to lay a foundation for its large-scale application in aquatic disease prevention and control.

Discovering History

 

NHC was developed under the leadership of the Drug Innovation Ventures at Emory (DRIVE) team at Emory University, United States. It is a nucleoside candidate drug obtained via targeted screening for broad-spectrum control of RNA viruses. The research initiative originated from the industry challenge of limited specific therapies for highly pathogenic, rapidly mutating RNA viruses.

 

Around 2010, the research team carried out small-molecule compound screening against various RNA viruses including coronaviruses, rhabdoviruses and influenza viruses, and discovered that N4-hydroxycytidine derivatives possess a unique viral mutagenic inhibitory mechanism.

 

Between 2016 and 2018, following structural optimisation and activity validation, EIDD-1931 was formally identified as the core active monomer, and its non-chain-terminating antiviral mechanism, distinct from traditional nucleoside drugs, was characterised.

 

Circa 2020, alongside rising research interest in broad-spectrum antiviral agents, the antiviral spectrum and pharmacological properties of EIDD-1931 were systematically defined. Subsequent research gradually expanded into the field of animal epidemic prevention and control, establishing theoretical support for its application as an antiviral agent in veterinary medicine and aquaculture.

References

  • An In-depth Technical Guide to β-D-N4-hydroxycytidine (EIDD-1931)[R]. BenchChem, 2025.
  • Niu M, et al. Nucleoside analogue EIDD-1931 in the treatment of naturally occurring feline infectious peritonitis[J]. PMC, 2024, 12(1): 2957568.
  • Zhang Y, et al. An Optimized Bioassay for Screening Combined Anticoronaviral Compounds for Efficacy against Feline Infectious Peritonitis Virus[J]. PMC, 2023, 11(1): 9697187.
  • DRIVE Team, Emory University. Research on Development and Activity Mechanism of Broad-spectrum Nucleoside Antiviral Agent EIDD-1931[R]. 2018.
  • Wang L, et al. In vitro antiviral activity of EIDD-1931 against animal RNA viruses[J]. Frontiers in Veterinary Science, 2024.

 

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