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Hesperitin (Hesperetin)
Hesperitin (generic name: Hesperetin) is a hesperetin Small molecule drug developed by University of Vienna. It is currently in Phase 1 development. Also known as: (2S)-3',5,7-Trihydroxy-4'-methoxyflavan-4-one, CAS number 520-33-2.
Hesperitin works by blocking the enzyme carbonic anhydrase 7, which helps regulate the balance of fluids and electrolytes in the body.
Hesperetin is a small molecule flavanone that is a derivative of eriodictyol, with hesperidin being its 7-O-glycoside form found naturally in citrus fruits. Hesperetin has been studied in clinical trials for its potential ergogenic properties, including reducing exercise-induced fatigue and blood glucose fluctuations, as well as its effects on hunger and glucose intolerance.
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Baseline phase 1 → approval rate
+9.6pp
Industry-wide phase 1 drugs reach approval ~9.6% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
| Regulator | Country | Likely year | Lag vs FDA |
|---|---|---|---|
| FDA | US | 2033–2036 | — |
| EMA | EU | 2034–2037 | +0.7 yr |
| MHRA | GB | 2034–2037 | +0.7 yr |
| Health Canada | CA | 2034–2038 | +0.9 yr |
| TGA | AU | 2034–2038 | +1.2 yr |
| PMDA | JP | 2034–2038 | +1.5 yr |
| NMPA | CN | 2035–2039 | +2.3 yr |
| MFDS | KR | 2034–2038 | +1.4 yr |
| CDSCO | IN | 2034–2039 | +1.8 yr |
| ANVISA | BR | 2035–2039 | +2.3 yr |
Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).
Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.
At a glance
| Generic name | Hesperetin |
|---|---|
| Also known as | (2S)-3',5,7-Trihydroxy-4'-methoxyflavan-4-one, CAS number 520-33-2 |
| Sponsor | University of Vienna |
| Drug class | hesperetin |
| Target | Cytochrome P450 1B1, Lysine-specific histone demethylase 1A, Carbonic anhydrase 12 |
| Modality | Small molecule |
| Therapeutic area | Metabolic |
| Phase | Phase 1 |
Mechanism of action
Think of carbonic anhydrase 7 like a pump that helps move fluids and electrolytes in and out of cells. When Hesperitin blocks this pump, it can help regulate the balance of fluids and electrolytes in the body, which can be beneficial for people with certain medical conditions.
Approved indications
Common side effects
Key clinical trials
- Evaluation of the Ergogenic Properties of Hesperetin on Exercise-induced Fatigue (NA)
- Impact Hesperetin in Combination with Sucrose on Blood Glucose Regulation (EARLY_PHASE1)
- Impact of Hesperetin in Combination With Sucrose on Energy Metabolism (EARLY_PHASE1)
- Healthy Aging Through Functional Food (PHASE1,PHASE2)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Hesperitin CI brief — competitive landscape report
- Hesperitin updates RSS · CI watch RSS
- University of Vienna portfolio CI
Frequently asked questions about Hesperitin
What is Hesperitin?
How does Hesperitin work?
Who makes Hesperitin?
What is the generic name of Hesperitin?
Is Hesperitin also known as anything else?
What drug class is Hesperitin in?
What development phase is Hesperitin in?
What does Hesperitin target?
Related
- Drug class: All hesperetin drugs
- Target: All drugs targeting Cytochrome P450 1B1, Lysine-specific histone demethylase 1A, Carbonic anhydrase 12
- Manufacturer: University of Vienna — full pipeline
- Therapeutic area: All drugs in Metabolic
- Also known as: (2S)-3',5,7-Trihydroxy-4'-methoxyflavan-4-one, CAS number 520-33-2
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing