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Hypericin
Hypericin
Hypericin
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Hypericin[1]
Structural formula of hypericin
Ball-and-stick model of the hypericin molecule
Names
Preferred IUPAC name
1,3,4,6,8,13-Hexahydroxy-10,11-dimethylphenanthro[1,10,9,8-opqra]perylene-7,14-dione
Other names
4,5,7,4',5',7'-Hexahydroxy-2,2'-dimethylnaphthodianthrone
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.008.129 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C30H16O8/c1-7-3-9(31)19-23-15(7)16-8(2)4-10(32)20-24(16)28-26-18(12(34)6-14(36)22(26)30(20)38)17-11(33)5-13(35)21(29(19)37)25(17)27(23)28/h3-6,31-36H,1-2H3 checkY
    Key: BTXNYTINYBABQR-UHFFFAOYSA-N checkY
  • InChI=1/C30H16O8/c1-7-3-9(31)19-23-15(7)16-8(2)4-10(32)20-24(16)28-26-18(12(34)6-14(36)22(26)30(20)38)17-11(33)5-13(35)21(29(19)37)25(17)27(23)28/h3-6,31-36H,1-2H3
    Key: BTXNYTINYBABQR-UHFFFAOYAC
  • Cc0cc(O)c1C(=O)c2c(O)cc(O)c3c2c4c1c0c5c6c4c7c3c(O)cc(O)c7C(=O)c6c(O)cc5C
Properties
C30H16O8
Molar mass 504.450 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Hypericin is a carbopolycyclic compound derived from bisanthene with antidepressant properties, found in various Hypericum species, and is being studied for treating cutaneous T-cell lymphoma.[2]

Opinions differ on the extent to which hypericin exhibits antidepressant effects. According to some scholars, hypericin, along with other active compounds in Hypericum perforatum (St. John’s wort), contributes to the antidepressant effects of the total plant extract.[3] According to others, hypericin does not significantly inhibit monoamine oxidase and thus is unlikely to account for the antidepressant effects of Hypericum extract.[4] While another hypericin shows affinity mainly for NMDA receptors, suggesting that other plant constituents likely play a more significant role in its antidepressant effects.[5]

Hypericin is a structurally complex phenanthroperylene quinone with potential medical and photoreceptive applications.[6] It is red-colored, photosensitive compound whose biosynthesis is catalyzed by the gene Hyp-1, a Bet v 1-class allergen identified through red-color-based colony screening and shown to convert emodin to hypericin with high efficiency.[7] It is thought to be synthesized by the PR-10 protein Hyp-1 through emodin dimerization, but despite confirming Hyp-1’s structure and ligand-binding capability, its catalytic role in hypericin biosynthesis remains unproven.[8]

Biotechnological research is exploring in vitro culture methods to enhance and stabilize the production of hypericin.[9]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Hypericin

View on Grokipedia
from Grokipedia
Hypericin is a naturally occurring naphthodianthrone, a polycyclic derivative classified as an , primarily extracted from the yellow flowers and dark glands of (St. John's wort), a perennial herb in the family. This compound, characterized by its vibrant red pigmentation in plant oils, exhibits high photoreactivity due to its featuring four hydroxyl groups adjacent to two carbonyl groups, enabling hydrogen transfer under light exposure. With the molecular formula C₃₀H₁₆O₈ and a complex phenanthro[1,10,9,8-opqra] core, hypericin is lipophilic, possesses low aqueous solubility, and demonstrates good permeability across the blood-brain barrier, though its is limited. In St. John's wort extracts, where hypericin is a component, antidepressant effects are attributed to multiple mechanisms, including weak inhibition of (MAO-A and MAO-B) by hypericin and modulation of neurotransmitter reuptake (such as serotonin) primarily by , contributing to therapeutic use for mild to moderate depression; however, hypericin alone does not fully account for the activity. It also displays potent antiviral activity against enveloped viruses like , , and , particularly when activated by light, through mechanisms involving disruption and inhibition of replication. Furthermore, hypericin serves as a in (PDT) for antitumor applications, generating that induce in cancer cells, with demonstrated efficacy against malignancies such as , , and . Additional properties include immunostimulatory and effects, as well as potential neuroprotective benefits, though clinical translation remains under investigation due to challenges like . Despite its therapeutic promise, hypericin can cause , leading to skin irritation, , or ocular damage at high doses (e.g., ≥0.5 mg/kg), and St. John's wort extracts containing hypericin interact with numerous drugs, with hypericin inducing and other components like inducing enzymes (), potentially reducing the efficacy of medications like cyclosporine, , and antiretrovirals. In the dried plant material of St. John's wort, hypericin concentrations typically range from 0.03% to 0.09%, with pseudohypericin often present in higher amounts (0.03%–0.34%), while commercial extracts are standardized to approximately 0.3% total hypericins.

Chemical Characteristics

Molecular Structure

Hypericin is a naphthodianthrone with the molecular formula C30_{30}H16_{16}O8_{8} and a of 504.45 g/mol. Its preferred IUPAC name is 1,3,4,6,8,13-hexahydroxy-10,11-dimethylphenanthro[1,10,9,8-opqra]perylene-7,14-dione. This is a red-colored polycyclic formed by the coupling of two units via three bonds, resulting in an eight-ringed structure characterized by extensive conjugation. The core consists of a phenanthroperylene with seven fused aromatic rings and a central eight-membered ring linkage, bearing six phenolic hydroxyl groups at positions 1, 3, 4, 6, 8, and 13, two methyl groups at positions 10 and 11, and carbonyl functionalities at positions 7 and 14. Pseudohypericin serves as a of hypericin (C30_{30}H16_{16}O9_{9}), distinguished by a single difference where one of the methyl substituents is replaced by a .

Physical and Chemical Properties

Hypericin appears as a bright red crystalline powder, often described as dark red or reddish-black in solid form. It has a melting point of approximately 320 °C, at which it decomposes rather than fully melting. The compound is insoluble in water, where it forms non-fluorescent aggregates, but exhibits good solubility in polar organic solvents such as alcohols (e.g., ethanol and methanol), dimethyl sulfoxide (DMSO), acetone, pyridine, and alkaline solutions like 1 M NaOH (solubility ~10 mg/mL). It shows poor solubility in non-polar solvents due to its polar phenolic and quinone functionalities. Hypericin demonstrates high when stored in the dark at low temperatures (e.g., -20 °C), remaining viable for up to one year in solid form and three months in DMSO or solutions. However, it is light-sensitive and degrades under exposure to UV or in acidic environments, with being the primary factor accelerating breakdown. Due to its extended π-conjugation, hypericin is photosensitive, generating (quantum yield ΦΔ ≈ 0.28–0.5 in DMSO) upon light exposure, which contributes to its photodynamic properties. This photosensitivity is accompanied by , with excitation maxima around 560–590 nm and emission in the range of 600–650 nm (peak at ~603 nm in DMSO). The phenolic hydroxyl groups of hypericin confer weak acidity, with pKa values including ~2 for the most acidic site and ~7.8 for subsequent deprotonations, enabling solubility enhancements in basic media.

Occurrence and Production

Natural Sources

Hypericin is primarily sourced from plants in the genus Hypericum, with Hypericum perforatum L., commonly known as St. John's wort, serving as the main natural reservoir due to its relatively high concentrations of the compound. In H. perforatum, hypericin is biosynthesized and accumulated in specialized glandular structures called dark glands, which are most abundant on the flowers, leaves, and to a lesser extent, stems and pollen, where it contributes to the plant's pigmentation. Typical concentrations in H. perforatum range from 0.03% to 0.30% of dry weight, though values up to 0.5% have been reported in optimal conditions, with flowers often exhibiting the highest levels compared to other aerial parts. Several other Hypericum species also contain hypericin, albeit generally at lower or more variable levels than H. perforatum, making them secondary sources. For instance, Hypericum triquetrifolium Turra. has been found to possess hypericin concentrations of approximately 0.11% to 0.43% dry weight in aerial parts, with leaves showing the highest accumulation at up to 0.36%. In Hypericum hircinum L., hypericin occurs in trace amounts, primarily in flowers, often below detectable thresholds for commercial extraction. Other species, such as Hypericum montanum L., can exhibit elevated levels comparable to or exceeding those in H. perforatum, with hypericin reaching up to 0.25% dry weight, highlighting intraspecific variability across the genus. Hypericum perforatum is native to temperate , western and , and , where it thrives in sunny, well-drained meadows, roadsides, and disturbed habitats. The species has been widely introduced and naturalized in other temperate zones, including (from to ), , and parts of , often becoming invasive in grasslands and rangelands. Hypericin content in H. perforatum is influenced by ecological factors, with higher concentrations observed in exposed to increased and UV radiation, which promote in sunlit aerial parts. Seasonal variations also play a role, with peak levels typically occurring during the summer flowering period (June to August in the ), when glandular production is maximized, declining post-flowering as seeds mature. Beyond plants, hypericin occurs only in trace amounts in certain non-plant organisms, such as basidiomycete fungi like Dermocybe species, but these sources are negligible and not viable for practical isolation or commercial use. Endophytic fungi isolated from Hypericum tissues can produce hypericin analogs, yet their yields remain minimal compared to host plants.

Biosynthesis and Extraction

Hypericin is biosynthesized in certain Hypericum species through the polyketide pathway, initiating with the acetate-malonate route where type III polyketide synthases assemble an octaketide chain that cyclizes to form emodin anthrone. This intermediate undergoes oxidation to emodin, followed by dimerization to emodin dianthrone, oxidative coupling to protohypericin, and finally photochemical or enzymatic conversion to hypericin. Key precursors include emodin and protohypericin, with proto-pseudohypericin as a related intermediate formed via similar oxidative processes. The Hyp-1 gene, encoding a type III , has been implicated in the later stages of hypericin formation, potentially catalyzing the conversion from emodin to hypericin, though its precise catalytic role remains debated and unconfirmed experimentally. Another , HpPKS2 (an octaketide ), contributes to the initial assembly in glandular structures of H. perforatum. Seminal work by Brockmann et al. in 1957 elucidated the structural basis for this pathway through mimicking the biosynthetic steps. Extraction of hypericin from natural sources primarily involves solvent-based methods using dried flowers of , with or (often in hydroalcoholic mixtures) as common s to achieve efficient recovery through maceration, ultrasonication, or Soxhlet extraction. For higher purity, supercritical CO₂ extraction is employed, offering an alternative that minimizes residues while targeting lipophilic compounds like hypericin. Typical yields range from 0.2% to 0.3% w/w of hypericin from the dried material, depending on extraction conditions and variety. Synthetic production of hypericin includes chemical synthesis from , involving multi-step processes such as anthrone dimerization and oxidative cyclization, as pioneered by Brockmann et al. and refined by Falk et al. using microwave-assisted methods, though these routes suffer from low overall yields due to challenges in ring closure and purification. Recent advances include a for improved synthetic methods and successful cGMP of synthetic hypericin announced in July 2025 by Soligenix for potential clinical applications. microbial approaches, such as engineering or using endophytic fungi like Thielavia subthermophila isolated from H. perforatum, enable fermentation-based production by expressing biosynthetic genes, providing a sustainable alternative to extraction despite ongoing optimization needs. Commercial production of hypericin relies predominantly on cultivated H. perforatum, with extracts standardized to at least 0.3% hypericin content for use in St. John's wort supplements, ensuring consistency through controlled cultivation and validated extraction protocols.

Pharmacological Activity

Antidepressant Effects

Hypericin has been proposed as a contributor to the antidepressant effects of Hypericum perforatum (St. John's wort) extracts through weak inhibition of (MAO-A and MAO-B) and modest inhibition of the reuptake of serotonin, norepinephrine, and , though these actions are non-selective and occur primarily at concentrations exceeding therapeutic levels. In vitro studies indicate that hypericin inhibits MAO activity only at high concentrations greater than 10 μM, with 50% inhibition requiring 68 μM or higher, far above the plasma levels achieved in clinical use (~17 nM). Clinical evidence for hypericin's antidepressant role derives largely from trials of St. John's wort extracts standardized to 0.3% hypericin, which demonstrate efficacy in treating mild to moderate depression comparable to selective serotonin inhibitors (SSRIs) for short-term use (4-12 weeks), with response rates around 50-60% versus 30-40% for . However, isolated hypericin appears less potent than , another key component, in modulating systems, and extracts without hyperforin show reduced activity. Typical dosages in herbal supplements provide 0.3-0.9 mg of hypericin daily, often as 300 mg of extract taken three times per day. A 2023 of 27 randomized trials confirmed that these standardized extracts reduce Hamilton Depression Rating Scale scores by 5-7 points more than , with fewer adverse events than SSRIs. Limitations to hypericin's standalone use include its induction of photosensitivity, which increases the risk of sunburn and reactions upon sun exposure due to its photodynamic properties, occurring in up to 10% of users at therapeutic doses. Recent (2024-2025) highlight hypericin's potential in alleviating depression-like behaviors via the microbiota-gut-brain axis and signaling; for example, a 2025 study showed hypericin alleviates chronic restraint stress-induced depression-like behaviors in mice via the microbiota-gut-brain axis and improved 5-HT metabolism, but human reviews continue to question its primary role, attributing greater efficacy to while noting hypericin's contributions may be synergistic rather than dominant.

Antiviral and Antimicrobial Properties

Hypericin exhibits potent antiviral activity primarily against enveloped viruses, including human immunodeficiency virus (HIV), influenza, and herpes simplex virus (HSV), by disrupting their lipid envelopes through photodynamic mechanisms. In vitro studies demonstrate inhibitory concentrations (IC₅₀) typically in the low micromolar range (0.1–12 μM) for these viruses, varying by virus and assay conditions, with hypericin effectively inactivating viral particles and preventing infection in cell cultures such as Vero cells. The primary mechanism involves photoactivation of hypericin, which generates (ROS) that damage viral lipid membranes, leading to envelope disruption and loss of infectivity. Additionally, non-photodynamic effects contribute, such as inhibition of viral protein aggregation and interference with enzymes like integrase, allowing activity even in the absence of light. This dual action enhances hypericin's broad-spectrum efficacy against enveloped pathogens without requiring illumination for full effect in some contexts. Regarding antimicrobial properties, hypericin displays activity against , such as Staphylococcus aureus, and certain fungi, including Candida albicans and Exophiala dermatitidis, primarily through membrane permeabilization and ROS-mediated damage upon photoactivation. However, it is less effective against due to their protective outer , which limits penetration and reduces susceptibility. In vivo evidence from animal models, such as mice infected with HSV-1 or Friend leukemia virus (FLV), shows that hypericin treatment reduces viral loads when administered prior to or shortly after infection, with efficacy enhanced by incubation with viral particles. Human trials remain limited; for instance, topical hypericin formulations have been explored for HSV lesions, but phase II data from around 2022 indicate modest improvements without widespread adoption. No hypericin-based antivirals have received regulatory approval to date. Recent research from 2024–2025 has focused on hypericin and its structural analogues for potential use against , demonstrating envelope disruption and replication inhibition (IC50 ~0.5–1 μM), with synergistic effects when combined with existing antivirals targeting (RdRp) and 3CL protease. These studies highlight ongoing efforts to develop hypericin derivatives for emerging enveloped viruses like coronaviruses, though clinical translation is pending.

Therapeutic Applications and Research

Anticancer Potential

Hypericin demonstrates significant anticancer potential through its capacity to induce in malignant cells, primarily via the generation of (ROS) that cause oxidative damage. Upon photoactivation, hypericin localizes to mitochondria, where it disrupts the transmembrane potential, leading to release and subsequent activation of the cascade, particularly caspase-3. This process culminates in , with studies showing hypericin's effectiveness against multi-drug resistant cancer cells by downregulating proteins associated with chemotherapeutic resistance, such as those in lines. In vitro investigations have confirmed hypericin's cytotoxicity across multiple cancer types, including leukemia (e.g., K562 cells), melanoma, and breast cancer (e.g., MCF-7 cells), with IC50 values typically ranging from 0.5 to 5 μM. For instance, in K562 leukemia cells, hypericin achieved an IC50 of approximately 2 μg/mL (equivalent to ~4 μM), correlating with increased apoptosis markers. Hypericin also exhibits synergy with conventional chemotherapeutics like paclitaxel, amplifying ROS-mediated apoptosis and overcoming resistance in melanoma models. These effects highlight its selective targeting of rapidly proliferating cancer cells over normal tissues. Preclinical animal studies using xenograft models have shown hypericin, often in formulations, to inhibit tumor growth effectively, with reports of prolonged survival and tumor necrosis in various cancer models. Clinical evaluation includes phase 3 trials like FLASH for topical hypericin in early-stage (CTCL; ), showing response rates up to 49% after 18 weeks with visible light activation and minimal systemic toxicity. A 2025 phase 2 real-world study reported treatment success in 75% of patients after 18 weeks. However, broader systemic application remains constrained by hypericin-induced , prompting localized delivery strategies. As of 2025, these trials confirm tolerability and efficacy in lesion clearance without significant adverse events beyond mild skin reactions. In 2025, Soligenix successfully transferred manufacturing of synthetic hypericin to a U.S. facility, supporting larger-scale production for clinical trials. As of November 2025, Soligenix continues to advance synthetic hypericin programs, with ongoing preparations for potential regulatory submissions following positive trial outcomes.

Photodynamic Therapy Uses

Hypericin functions as a in (PDT), a treatment modality where it accumulates preferentially in diseased tissues and is activated by visible light in the 590-630 nm range to generate (ROS), including , which induce selective or in targeted cells while sparing surrounding healthy tissue. This light-dependent mechanism exploits hypericin's strong absorption in the orange-red spectrum, enabling precise localization of therapeutic effects through controlled illumination. Clinical investigations of hypericin-based PDT have primarily focused on dermatological conditions, including skin cancers such as (CTCL) and , with topical formulations demonstrating efficacy in reducing lesion severity. For instance, in a phase II placebo-controlled trial for early-stage CTCL and , twice-weekly applications of topical hypericin followed by visible light irradiation led to significant improvement in treated lesions for the majority of patients after six weeks, with response rates exceeding 50% in some cohorts. Ongoing phase II trials for mild-to-moderate , initiated in 2022 using synthetic hypericin (SGX302), reported an average lesion reduction of approximately 50% in PASI score in evaluable patients after 18 weeks of treatment. Compared to synthetic photosensitizers like porfimer sodium (Photofrin), hypericin offers advantages rooted in its natural derivation from , potentially lowering production costs and reducing synthetic impurities, while maintaining comparable ROS generation efficiency. However, its hydrophobic nature poses challenges, including limited skin penetration and prolonged systemic clearance, which can increase risks post-treatment. To overcome delivery limitations, hypericin is often formulated in liposomal encapsulation systems or conjugated with tetraether lipids, which enhance , stability, and targeted cellular uptake in tumor or inflamed tissues, improving PDT outcomes in preclinical models. These approaches allow for controlled release and better localization, minimizing off-target effects. Synthetic hypericin has secured FDA designation for (a form of CTCL) since 2021, with phase III trials like FLASH confirming sustained efficacy and in early-stage patients, paving the way for broader regulatory approvals.

Safety and

Adverse Effects

Hypericin exposure is primarily associated with , manifesting as sunburn-like skin reactions including and pruritus upon (UV) light exposure. This phototoxic effect is dose-dependent, with clinical studies reporting incidences of 42% at oral doses of 0.05 mg/kg/day and 86% at 0.10 mg/kg/day in patients with chronic hepatitis C. Such reactions typically occur particularly in light-skinned individuals or with prolonged sun exposure. Gastrointestinal disturbances, such as and , are among the most frequently reported adverse effects of hypericin-containing preparations, though they are generally mild and transient. These symptoms tend to arise at higher oral doses greater than 2 mg/day and may resolve with dose reduction or discontinuation. Neurological effects from hypericin are uncommon and typically mild, including rare instances of , , or , which have been noted in short-term use without evidence of severe outcomes. No significant has been observed in short-term human studies or controlled trials. In , hypericin demonstrates minimal transplacental passage, with placental perfusion studies indicating no detectable transfer to the fetal circuit and thus low fetal exposure throughout . Adverse effects of hypericin are dose-dependent, indicating low based on available data, with recent predictions estimating an oral LD₅₀ of 1000 mg/kg in ( IV). Human data on long-term effects remain limited.

Drug Interactions

Hypericin, a naphthodianthrone found in , has been shown in studies to inhibit key enzymes, including and , potentially increasing the plasma concentrations and efficacy (or toxicity) of co-administered metabolized by these pathways. For instance, hypericin competitively inhibits with a Ki value of 4.2 μM and with a Ki of 1.4 μM, which may elevate levels of substrates such as oral contraceptives, cyclosporine, and by 20-50% in terms of area under the curve (AUC) based on estimated [I]/Ki ratios ranging from 0.35-1.04 for . This inhibition contrasts with the induction effects observed in whole-plant extracts, highlighting hypericin's specific role in pharmacokinetic modulation. Hypericin also acts as a substrate and inhibitor of (P-gp), an efflux transporter, with values around 30 μM for markers like , potentially enhancing the absorption and systemic exposure of P-gp substrates such as and increasing the risk of toxicity from under-clearance. assays demonstrate dose-dependent reduction in P-gp-mediated efflux, suggesting caution with drugs reliant on this transporter for elimination. Pharmacodynamic interactions arise from hypericin's weak inhibition of monoamine oxidase (MAO) and serotonin reuptake, which can potentiate serotonergic effects when combined with selective serotonin reuptake inhibitors (SSRIs), raising the risk of characterized by agitation, hyperthermia, and autonomic instability. This stems from hypericin's affinity for neurotransmitter transporters, similar to its mechanisms involving enhanced monoamine availability. Case reports document such syndromes with extracts, attributing contributions to hypericin alongside other constituents. Clinical evidence for hypericin's interactions remains limited, primarily derived from and studies, with broader data from 1990s-2020s trials on extracts showing altered in up to 30% of users involving CYP substrates. Pure hypericin trials, such as those for antiviral in the 1990s (doses 0.05-0.1 mg/kg), reported no major interactions but lacked comprehensive monitoring. As of 2025, guidelines from sources like and recommend avoiding or monitoring concomitant use with /P-gp substrates and serotonergic agents, suggesting a 2-week washout period when switching to mitigate risks. Contraindications include concurrent administration with protease inhibitors (e.g., ), where inhibition may substantially increase drug levels (potentially by over 50% AUC), risking toxicity, though specific hypericin data are sparse and contrast with extract-based reductions. Similar caution applies to agents like , as hypericin inhibits carboxylesterase 2 (hCE2) with Ki values of 10.53-81.77 μM, potentially elevating exposure by 2-69%. Healthcare providers should advise dose adjustments or avoidance based on individual risk profiles.

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