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Sunshine Biopharma and University of Arizona Publish Significant New Research Findings

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Sunshine Biopharma (NASDAQ:SBFM) announced peer‑reviewed publication in the Journal of Medicinal Chemistry of research on MR1‑114, a novel noncovalent PLpro inhibitor for SARS‑CoV‑2. MR1‑114 showed nanomolar potency in vitro across multiple variants, including the Washington strain, Delta and Omicron BA.5.

According to Sunshine Biopharma, MR1‑114 demonstrated broad‑spectrum activity, favorable ADME properties, high oral bioavailability and preferential lung enrichment in mice and rats. In the K18‑hACE2 mouse model, repeated oral dosing matched the therapeutic efficacy of Nirmatrelvir by significantly suppressing pulmonary viral replication and preventing disease‑associated weight loss.

The work, conducted with the University of Arizona, is described as an important milestone in Sunshine Biopharma’s PLpro inhibitor program for SARS Coronavirus infections. The company also highlights a commercial portfolio of 60 generic prescription drugs in Canada, with about 12 additional launches planned for 2026 and a K1.1 mRNA program for liver cancer.

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Positive

  • MR1-114 nanomolar potency against PLpro in multiple SARS-CoV-2 variants in vitro
  • Oral MR1-114 matched Nirmatrelvir efficacy in K18-hACE2 SARS-CoV-2 mouse model
  • Favorable PK profile with high oral bioavailability and lung enrichment in mice and rats
  • 60 generic prescription drugs currently marketed in Canada
  • ~12 additional generics scheduled for launch during the remainder of 2026

Negative

  • None.

Market reaction after PLpro preclinical data: SBFM -3.89% in the Jul 20 session

-3.89%
4 alerts
-3.89% Session close to close
+9.5% Peak Tracked
-6.0% Trough Tracked
$3.82M Market Cap
1.1x Rel. Volume

In the Jul 20 session, SBFM declined 3.89%, reflecting a moderate negative market reaction. Argus tracked a peak move of +9.5% during that session. Argus tracked a trough of -6.0% from its starting point during tracking. Our momentum scanner triggered 4 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

Recent history included 4.9% and -5.94% reactions to Canadian approvals, so the platform record is m...
Analysis

Recent history included 4.9% and -5.94% reactions to Canadian approvals, so the platform record is mixed rather than uniform. The study's preclinical status and low short positioning provide context; clinical advancement and follow-through remain items to watch.

Key Figures

Virus variants tested: at least three variants Potency: nanomolar potency Publication citation: 2026, Vol. 69, pp. 8433–8450 +4 more
7 metrics
Virus variants tested at least three variants MR1-114 in vitro research
Potency nanomolar potency MR1-114 against SARS-CoV-2 variants in vitro
Publication citation 2026, Vol. 69, pp. 8433–8450 Journal of Medicinal Chemistry
Generic drugs marketed 60 drugs Canada
Additional drugs scheduled approximately 12 drugs Remainder of 2026
University research expenditures more than $1 billion annually University of Arizona
University economic impact $4.1 billion annually University of Arizona

Historical Context

5 past events · Latest: Jun 25 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jun 25 Canadian drug approval Positive +4.9% Canadian approval of generic Anastrozole tablets and planned distribution through Nora Pharma
Jun 01 Canadian drug approval Positive -5.9% Canadian approval of generic Rivaroxaban tablets across four dosage strengths
May 29 Coronavirus patent issuance Positive -19.8% U.S. patent issued for proprietary PLpro inhibitor compounds targeting coronavirus infection
May 28 Reverse stock split Negative -25.3% Company approved a 1-for-10 reverse split to address Nasdaq bid-price compliance
May 21 Canadian drug approval Positive +40.6% Canadian approval of generic Amoxicillin with planned August 2026 pharmacy shipments

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

SBFM's recent news reactions were mixed, with positive reactions to some approvals but sharp declines after other corporate and development announcements.

Key Terms

plpro, nanomolar potency, adme profile, oral bioavailability
4 terms
plpro medical
"The published data demonstrate a novel PLpro inhibitor, MR1-114"
PLpro is an enzyme produced by certain viruses that acts like a pair of scissors to cut viral proteins into working pieces and also helps the virus hide from the body’s defenses. For investors, PLpro matters because drugs or tests that block or measure this enzyme can stop virus replication or improve treatments, so developments involving PLpro can affect the value and prospects of biotech companies developing antivirals.
nanomolar potency medical
"with nanomolar potency in at least three variants of the SARS-CoV-2 virus"
Nanomolar potency describes how strong a drug or compound is by the concentration needed to produce a measurable biological effect, expressed in nanomoles per liter (nM). A nanomolar value means the compound works at very low concentrations — like a tiny pinch of spice flavoring a large pot — and can signal potential advantages in dosing, manufacturing scale, and competitive positioning that investors watch when judging a drug's development and commercial prospects.
adme profile medical
"It exhibited desirable ADME profile, had high oral bioavailability"
An ADME profile summarizes how a drug is absorbed into the body, how it spreads to tissues, how the body breaks it down (metabolism), and how it is eliminated (excretion). Think of it like tracking a package through a delivery system—when it arrives, where it goes, how it’s repackaged, and when it leaves—and those characteristics affect dosing, safety, interactions, and the likelihood of regulatory approval. Investors use ADME data to gauge development risk and potential clinical success.
oral bioavailability medical
"had high oral bioavailability and it was preferentially enriched in the lungs"
Oral bioavailability is the share of a pill or liquid medicine that survives the digestive system and reaches the bloodstream to have an effect. It matters to investors because low bioavailability can mean higher doses, more side effects, tougher manufacturing, and greater clinical or regulatory risk, all of which affect a drug’s cost, pricing and commercial prospects—like ordering a package and finding only part of it arrives.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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FORT LAUDERDALE, FL / ACCESS Newswire / July 20, 2026 / Sunshine Biopharma Inc. (NASDAQ:SBFM) (the "Company"), a leading pharmaceutical company specializing in generic and specialty prescription medications today announced the publication of new research results in the Journal of Medicinal Chemistry. The published data demonstrate a novel PLpro inhibitor, MR1-114, with nanomolar potency in at least three variants of the SARS-CoV-2 virus in vitro. MR1-114 was found to be efficacious in a mouse model of SARS-CoV-2 infection by repeated oral administration. This peer-reviewed study marks an important milestone for Sunshine Biopharma in its effort to develop an effective treatment for SARS Coronavirus infections. A copy of the publication (J. Med. Chem. 2026, 69, 8433−8450) is available on the Company website at www.sunshinebiopharma.com/scientific-publications/.

There are still unmet medical needs to combat SARS-CoV-2 infection. SARS-CoV-2 undergoes mutation at a rapid rate, which leads to the continuous emergence of variants of concern (VOC) posing an ongoing significant threat to public health. In addition, certain populations, such as immunocompromised patients who are susceptible to severe and prolonged infections, may not respond well to current therapies or vaccines. For high-risk patients, blocking early infection at home may prevent disease rapid progression and reduce hospitalization.

PLpro is a compelling therapeutic target for developing antiviral compounds against SARS-CoV-2. It is a virus encoded protease essential for viral replication and is responsible for suppression of the human immune system following infection by the virus. PLpro eluded scientist for many years due to its featureless active site. To address the challenges posed by PLpro's indistinct active site, we designed and synthesized a library of noncovalent inhibitors targeting two vulnerabilities remote from the catalytic site: the BL2 groove and the cryptic Val70Ub pocket.

One of the rationally designed PLpro inhibitors library, MR1-114, displayed nanomolar potency against the enzyme targets and had broad-spectrum activity against SARS-CoV-2 variants, including the original Washington Strain, Delta and Omicron BA.5, with nanomolar potency in vitro. It exhibited desirable ADME profile, had high oral bioavailability and it was preferentially enriched in the lungs of both mice and rats. In the K18-hACE2 mouse model, oral administration of MR1-114 matched the therapeutic efficacy of Nirmatrelvir (the viral enzyme inhibitor in Paxlovid®), significantly suppressing pulmonary viral replication and preventing disease-associated weight loss.

"The support of Sunshine Biopharma has allowed exploration and testing of antiviral agents that may be important for any future outbreaks," said Dr. Gregory Thatcher, pharmacology professor at the University of Arizona.

"MR1-114 and its analogs provide a promising new strategy for targeting PLpro and may offer a complementary therapeutic approach to existing SARS-CoV-2 antivirals," added Dr. Rui Xiong, assistant professor in the Department of Pharmacology & Toxicology at the University of Arizona.

"We are delighted to be working with world renowned Dr. Gregory Thatcher and Dr. Rui Xiong at the University of Arizona in the Department of Pharmacology & Toxicology. The publication of these results in the Journal of Medicinal Chemistry reflects our commitment to advancing science and improving patient outcomes," said Dr. Steve Slilaty, CEO of Sunshine Biopharma and a co-author of the publication. "These findings underscore the potential of MR1-114 to transform the treatment landscape for SARS Coronavirus infections, and we look forward to further exploring its capabilities and clinical development in the future."

About The University of Arizona

The University of Arizona, a land-grant university with two independently accredited medical schools, is one of the nation's top 50 public universities, according to U.S. News & World Report. Established in 1885, the university is widely recognized as a student-centric university and has been designated as a Hispanic Serving Institution by the U.S. Department of Education. The University ranked in the top 20 in 2026 in research expenditures among all public universities, according to the National Science Foundation, and is a leading Research Institution with more than $1 billion in annual research expenditures. The university advances the frontiers of interdisciplinary scholarship and entrepreneurial partnerships as a member of the Association of American Universities, the 66 leading public and private research universities in the U.S. It benefits the state with an estimated economic impact of $4.1 billion annually.

About Sunshine Biopharma Inc.

Sunshine Biopharma currently has 60 generic prescription drugs on the market in Canada and approximately 12 additional drugs scheduled to be launched in the remainder of 2026. In addition, Sunshine Biopharma is conducting a proprietary drug development program which is comprised of (i) K1.1 mRNA, an mRNA-Lipid Nanoparticle targeted for liver cancer, and (ii) PLpro protease inhibitor, a small molecule for treatment of SARS Coronavirus infections. For more information, please visit: www.sunshinebiopharma.com.

Safe Harbor Forward-Looking Statements

This press release contains forward-looking statements which are based on current expectations, forecasts, and assumptions of Sunshine Biopharma Inc. (the "Company") that involve risks as well as uncertainties that could cause actual outcomes and results to differ materially from those anticipated or expected. These statements appear in this release and include all statements that are not statements of historical fact regarding the intent, belief or current expectations of the Company, including statements related to the Company's drug development activities, financial performance, and future growth. These risks and uncertainties are further described in filings and reports by the Company with the U.S. Securities and Exchange Commission (SEC). Actual results and the timing of certain events could differ materially from those projected in or contemplated by the forward-looking statements due to a number of factors detailed from time to time in the Company's filings with the SEC. Reference is hereby made to cautionary statements and risk factors set forth in the Company's most recent SEC filings.

For more information, please contact:

Camille Sebaaly, CFO
Direct Line: 514-814-0464
camille.sebaaly@sunshinebiopharma.com

SOURCE: Sunshine Biopharma Inc.



View the original press release on ACCESS Newswire

FAQ

What did Sunshine Biopharma (NASDAQ:SBFM) announce on July 20, 2026?

Sunshine Biopharma announced publication of new MR1‑114 antiviral research in the Journal of Medicinal Chemistry. According to Sunshine Biopharma, the study details a novel PLpro inhibitor for SARS‑CoV‑2 with nanomolar potency in vitro and efficacy after oral dosing in a mouse infection model.

What is MR1-114 in Sunshine Biopharma’s SARS-CoV-2 research program (SBFM)?

MR1‑114 is a rationally designed noncovalent PLpro inhibitor targeting SARS‑CoV‑2. According to Sunshine Biopharma, it shows nanomolar enzyme inhibition, broad‑spectrum activity against Washington, Delta and Omicron BA.5 variants, high oral bioavailability and preferential lung enrichment in mice and rats.

How effective was Sunshine Biopharma’s MR1-114 compared with Nirmatrelvir in preclinical models?

In a K18‑hACE2 mouse SARS‑CoV‑2 model, oral MR1‑114 matched the therapeutic efficacy of Nirmatrelvir. According to Sunshine Biopharma, MR1‑114 significantly suppressed pulmonary viral replication and prevented disease‑associated weight loss after repeated oral administration, supporting its potential as an oral antiviral candidate.

What collaboration does Sunshine Biopharma (SBFM) have with the University of Arizona?

Sunshine Biopharma is collaborating with University of Arizona researchers, including Dr. Gregory Thatcher and Dr. Rui Xiong, on PLpro inhibitors. According to Sunshine Biopharma, this partnership produced the MR1‑114 study now published in the Journal of Medicinal Chemistry, advancing its antiviral drug development program.

What are Sunshine Biopharma’s main drug programs and generic portfolio as of 2026?

Sunshine Biopharma reports marketing 60 generic prescription drugs in Canada, with about 12 more planned for 2026. According to Sunshine Biopharma, its proprietary pipeline includes the K1.1 mRNA program for liver cancer and a PLpro protease inhibitor program for SARS Coronavirus infections.

Why is PLpro a key antiviral target in Sunshine Biopharma’s MR1-114 research?

PLpro is a SARS‑CoV‑2 protease essential for viral replication and immune suppression. According to Sunshine Biopharma, MR1‑114 was designed to bind vulnerabilities in the BL2 groove and Val70Ub pocket, offering a strategy to inhibit PLpro and potentially complement existing SARS‑CoV‑2 antivirals.