A Deep Dive into the Botanical and Medicinal Heritage of Taxus
Abstract
:1. Introduction
1.1. Historical and Cultural Significance of Taxus
1.2. Pharmacological Importance and Discovery of Taxanes
1.3. Sustainability Concerns and Research Trends
1.4. Scope of This Review
2. Botanical Overview of Taxus Species
3. Traditional Uses in Folk Medicine
4. Phytochemistry of Taxus Species
5. Pharmacological and Therapeutic Applications
5.1. Medicinal Benefits
5.2. Nutritional Value and Food Potential of Taxus Arils
- α-Linolenic acid (ALA), a key omega-3 fatty acid with cardioprotective and anti-inflammatory effects, was identified at ~1800 mg/100 g in Taxus arils. This level, while lower than in chia (17,500 mg/100 g) or flaxseed (22,800 mg/100 g) [150,151], greatly exceeds ALA levels found in conventional nuts such as walnuts (900 mg/100 g) or almonds (~1.5 mg/100 g) [152], and is almost absent in most fruits and vegetables.
- Sciadonic acid, a rare polymethylene-interrupted fatty acid (PMI-FA) with emerging anti-inflammatory potential, is present at ~276 mg/100 g in the aril, a feature not shared by typical food plants [32].
- Total protein content in the aril (~9.5%) surpasses that of most fruits (e.g., avocado: 2%, banana: 1.1%) and aligns with levels seen in legumes like cooked quinoa (~8%) or green peas (5.4%) [153,154,155,156]. More importantly, the essential amino acid (EAA) to total amino acid ratio of 40.5% is on par with high-quality proteins such as egg (43%) or soy (36–38%) [32,157].
- Mineral content is also notable. The potassium concentration (~500 mg/100 g) exceeds that of banana (358 mg/100 g) [154] and compares favorably with avocado (485 mg/100 g) [153] and sweet potato (337 mg/100 g) [158]. The iron content (3.0 mg/100 g) surpasses that of spinach (1.05 mg/100 g) [159], but is lower than that in lentils (7.1 mg/100 g) [159].
5.3. Dermatological Applications
- A cosmetic composition incorporating cultured cells from the cambial or procambium regions of Taxus stems: This invention pertains to a formulation exhibiting antioxidant, anti-inflammatory, and anti-aging properties. It comprises one or more cell lines derived from the cambial or procambium tissues of Taxus stems, alongside their respective extracts, lysates, and culture media. The authors of this invention have endeavored to formulate compositions grounded in natural compounds that demonstrate significant antioxidant and anti-inflammatory efficacy. The inventors have established that cell lines derived from Taxus cambium and Taxus procambium, as well as their extracts, possess remarkable capabilities to mitigate inflammation and impede the aging process of the skin, which constitutes the core premise of this invention. The extract and cell line culture medium derived from the cell lines described in the present invention demonstrate a significant capacity to inhibit the synthesis of matrix metalloproteinase 1 (MMP-1), exhibiting effects comparable to those of retinoic acid, which is widely recognized for its potent anti-aging properties. This finding implies that the invention effectively mitigates collagen degradation, thereby contributing to the prevention of skin aging and the reduction of wrinkles, positioning it as a valuable candidate for anti-aging applications. Furthermore, the invention has been shown to inhibit melanogenesis in mouse melanoma cells, indicating its potential as a depigmenting agent [161]. The outcomes presented in this patent hold considerable significance, with the inventors having successfully developed functional formulations based on these findings.
- 2.
- Goat’s milk soap incorporating Taxus chinensis extract: This invention pertains to a daily cleansing product, specifically a goat’s milk soap infused with Taxus chinensis extract. The formulation of the soap is as follows: 3–5 g of Taxus chinensis extract, 20–28 g of fresh goat’s milk, 0.8–1.2 g of virgin olive oil, 0.8–1.2 g of palm oil, 0.8–1.2 g of coconut oil, 0.8–1.2 g of mustard oil, and 45–50 g of soap base. The extract of Taxus chinensis is known to contain various skin-protective nutrients, while fresh goat’s milk is recognized for its skin-whitening properties. This soap formulation is designed to effectively cleanse the skin, promote whitening and moisturization, and retain moisture, thereby mitigating the risk of intracellular water loss [167].
6. Conclusions and Future Directions
- Exploration of underutilized plant parts, such as arils, to uncover novel bioactives with pharmacological potential.
- Development of green synthesis methods for taxanes, including metabolic engineering in microbial systems and tissue culture optimization.
- Investigation into combinatorial therapies, leveraging taxane synergy with other plant-derived compounds or modern drug delivery platforms, especially nanocarriers.
- Clinical translation of lesser-known compounds, such as biflavonoids and polymethylated fatty acids, for use in oncology, neurology, and immunology.
- Integrative omics approaches to map species-specific metabolic pathways and understand interspecies variability in phytochemical content.
Supplementary Materials
Author Contributions
Funding
Data Availability Statement
Acknowledgments
Conflicts of Interest
Abbreviations
ADA | Adenosine Deaminase |
Al | Aluminum |
Cd | Cadmium |
DNA | Deoxyribonucleic Acid |
ED₅₀ | Median Effective Dose |
FDA | Food and Drug Administration |
GC-MS | Gas Chromatography–Mass Spectrometry |
GLUT4 | Glucose Transporter Type 4 |
GPX4 | Glutathione Peroxidase 4 |
HDL | High-Density Lipoprotein |
HIV | Human Immunodeficiency Virus |
HPLC-MS/MS | High-Performance Liquid Chromatography–Tandem Mass Spectrometry |
IC₅₀ | Half-Maximal Inhibitory Concentration |
IL-1β | Interleukin 1-Beta |
IUCN | International Union for Conservation of Nature |
LDL | Low-Density Lipoprotein |
MMP-1 | Matrix Metalloproteinase 1 |
MRSA | Methicillin-Resistant Staphylococcus aureus |
NCI | National Cancer Institute |
Ni | Nickel |
NSCLC | Non-Small Cell Lung Cancer |
P-gp | P-Glycoprotein |
PMI-FAs | Polymethylated Fatty Acids |
RDA | Recommended Dietary Allowance |
RNA | Ribonucleic Acid |
ROS | Reactive Oxygen Species |
SARS-CoV-2 | Severe Acute Respiratory Syndrome Coronavirus 2 |
SOD | Superoxide Dismutase |
TNF-α | Tumor Necrosis Factor-Alpha |
UPLC-ESI-MS/MS | Ultra-Performance Liquid Chromatography Coupled with Electrospray Ionization Tandem Mass Spectrometry |
UV | Ultraviolet |
WHO | World Health Organization |
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Species | IUCN Status | Geographic Distribution |
---|---|---|
Taxus wallichiana | Endangered | Himalayas: Afghanistan, India, Nepal, Bhutan, southern China |
Taxus chinensis | Endangered | Southern China (Yunnan, Guizhou, Sichuan), northern Vietnam |
Taxus calcicola | Vulnerable | China (Yunnan, Guizhou) |
Taxus baccata | Least concern | Europe, North Africa, Western Asia |
Taxus brevifolia | Near threatened | Pacific Northwest (USA: California to Alaska), British Columbia |
Taxus canadensis | Least concern | Eastern Canada, Northeastern USA (Appalachians, Great Lakes region) |
Taxus mairei | Vulnerable | Southern and eastern China, Vietnam, Taiwan |
Taxus contorta | Endangered | Western Himalayas (Pakistan, India, Nepal) |
Taxus floridana | Critically endangered | Northern Florida (Gadsden and Liberty Counties) |
Taxus globosa | Endangered | Mexico and Central America (Sierra Madre Oriental) |
Taxus cuspidata | Least concern | Northeast China, Korea, Japan, Russian Far East |
Species and Region: | Plant Part Used: | Administration: | Traditional Uses: | References: |
---|---|---|---|---|
Taxus wallichiana (India—Bhotiya tribe) | Bark | Tea |
| [26] |
Decoction |
| |||
Decoction with jaggery |
| |||
Paste |
| |||
Young branches | Tincture |
| ||
Decoction |
| |||
Leaves | Decoction/juice |
| ||
Powder |
| |||
Extract/juice |
| |||
Taxus wallichiana (India) | Bark, seeds | Extract (oral) |
| [37] |
Bark | Tea |
| ||
Tea |
| |||
Paste |
| |||
Tea mixed with salt and ghee |
| |||
Paste mixed with egg yolk |
| |||
Decoction |
| |||
Leaves | Juice from the leaves |
| ||
Decoction |
| |||
Decoction of leaves with honey |
| |||
Tea |
| |||
Bark, leaves | Tea |
| ||
Young branches | Tincture |
| ||
Stem | Decoction |
| ||
The entire plant | — |
| ||
Taxus baccata (India—Pauri district, Uttarakhand) | Bark, leaves | — |
| [60] |
Taxus contorta, Taxus mairei, Taxus wallichiana (Hindu Kush-Himalayan region) | Arils | Consumed as is |
| [35] |
Taxus contorta, Taxus mairei, Taxus wallichiana (Hindu Kush-Himalayan region) | Leaves | Juice from leaves with honey |
| |
Taxus contorta, Taxus mairei, Taxus wallichiana (Hindu Kush-Himalayan region) | Leaves | Juice or decoction (oral) |
| |
Aril | Consumed as is |
| ||
Leaves, bark | Juice |
| ||
Bark | Tea |
| ||
Taxus wallichiana (Hindu Kush-Himalayan region) | Leaves, bark | Paste with honey |
| |
Taxus contorta, Taxus wallichiana (Hindu Kush-Himalayan region) | Leaves | Leaf juice (oral) |
| |
Bark | Paste (external use) |
| ||
Decoction |
| |||
Taxus wallichiana | — | Decoction, tea, juice |
| [51,61] |
— | Poultice |
| ||
Bark | Paste |
| ||
Bark, leaves | Steam baths |
| ||
Stem | Decoction—in Pakistan |
| ||
Bark, leaves | Unani Medicine |
| ||
Young branches | Ayurvedic tincture |
| ||
Taxus baccata | — | Asturias, León |
| [5] |
Aril | Aril pulp—syrup (Northern Spain) |
| ||
Taxus wallichiana (Indian Ayurvedic Pharmacopoeia) | Leaves | Powder |
| [26] |
Taxus baccata (Ukraine, Bukovina) | Bark | Bark decoction |
| [4] |
Taxus baccata (Narew River, Northeast Poland) | Bark | Bark powder |
| |
Taxus baccata (Central Balkan Peninsula) | Bark | Crushed bark |
| |
Taxus baccata (Poland—Wólka Jagielczynska village, Częstochowa) | Bark | Infusion with milk or fumigation of the wood |
|
Plant Part | Chemical Compound | Pharmacological Properties | References | ||
---|---|---|---|---|---|
ALKALOIDS | |||||
Bark, leaves, roots | Paclitaxel (Taxol A) 0.007–0.01% | Anticancer effect: widely used to treat various types of cancer (lung, breast, blood, liver, brain, kidney, prostate, colon, cervical, gastric, pancreatic, Kaposi’s sarcoma). Antiviral effect (HIV, SARS-CoV-2). Low doses: treatment of liver, lung, and kidney fibrosis (0.3 mg/kg, 2×/week), coronary artery restenosis (1.3–10 µg/mm2), Alzheimer’s disease. | [25,27,28,29,104] | ||
Leaves | 10-Deacetylbaccatin III (1.76%) | Ethyl acetate extract: benefits against insulin resistance associated with inflammation and high-fat diet in C57BL/6 mice; significantly improves glucose uptake in skeletal muscle cells with inflammation-induced insulin resistance; dose-dependent reduction in lipid accumulation; decreased LDL, triglycerides, and total cholesterol, increased HDL; reduction of pro-inflammatory cytokines (TNF-α, IL-6, IL-1β); enhanced GLUT4 expression and distribution; no cytotoxicity at effective dose. | [56,81] | ||
Leaves | Brevifoliol (7.59%) | [56] | |||
Bark | 4-Deacetylbaccatin III | Anti-inflammatory, analgesic effect (in vitro). | [51] | ||
Bark | Tasumatrol B | Pronounced anti-inflammatory effect, remarkable analgesic effect. | [25,51,65] | ||
Bark | Taxusabietane A | Significant anti-inflammatory effect (in vivo, 5–10 mg/kg), via 5-lipoxygenase inhibition at IC50 = 57 ± 0.31 μmol/L. | [25,51,65] | ||
Bark | Taxusabietane C | Significant anti-inflammatory effect (IC50 = 69 ± 0.31 μmol/L). | [65] | ||
Bark | Taxamairin F | Significant anti-inflammatory effect (IC50 = 73 ± 0.14 μmol/L). | [65] | ||
Bark | Taxawallin I | Methanolic extract: strong cytotoxic activity in vitro against various cancer cell lines (A498, MDR 2780AD, NCI-H226, HepG2). | [25,65] | ||
Bark | 1-Hydroxy-2-deacetoxy-5-decinnamoyltaxinine J | Significant, dose-dependent anticancer effect against Colo 320DM, MCF-7, KB PA1, WRL-68 cell lines; immunomodulatory activity (1 µg/mL), enhances concanavalin A effects. | [25,65] | ||
Bark | Taxusine | Ethanolic extract: anti-inflammatory, antinociceptive properties. | [68] | ||
Bark | Baccatin VI | ||||
Bark | 1-Hydroxybaccatin I | ||||
FLAVONOIDS | |||||
Branches, leaves | Flavone | Apigenin | Antioxidant (0.5–32 µg/mL—strong inhibition of reactive oxygen species); anticancer (synergistic with paclitaxel in HeLa cervical carcinoma cells, reducing cell viability by 29% and increasing apoptosis by 24%); antidepressant (in mice at 50 mg/kg—increased immobility, swimming, and climbing time); anti-inflammatory (50–200 µmol/L—inhibits nitric oxide production and phagocytosis); potential protective effect in UV-induced cutaneous tumors. | [64,66,105,106,107,108] | |
Branches | Luteolin | Antioxidant (0.5–32 µg/mL); anticancer (synergistic effect with paclitaxel in human colorectal carcinoma cells); anti-inflammatory. | [64,105,106,108] | ||
Leaves | Tricin | High potential as a functional agent in glycemic control; anti-inflammatory and anticancer effects. | [66,109] | ||
Leaves | Chrysoeriol | Exhibits anti-inflammatory, anticancer, and anti-osteoporotic activity. | [66,108] | ||
Leaves, branches | Biflavone | Bilobetin | Antibacterial and significant antifungal activity (against Alternaria alternata, Cladosporium oxysporum, Fusarium culmorum—median effective doses ED₅₀ = 14, 11, and 17 mmol/L, respectively; inhibited growth of C. oxysporum and F. culmorum at 100 mmol/L); acts as an efflux transporter inhibitor of P-glycoprotein (P-gp) and CYP3A4, enhancing the oral absorption of paclitaxel by limiting P-gp activity at a concentration of 50 mg/mL; concurrently, it reduced both the expression and activity of CYP3A4 at 100 µg/mL. | [64,110] | |
Leaves | 4‴-O-methyl amentoflavone | Anticancer effect (human breast carcinoma MCF-7 cells were dramatically suppressed at ED₅₀ = 4.56–16.24 µg/mL → cellular apoptosis). | [64,111] | ||
Leaves | 7-O-methyl amentoflavone | Shows significant antifungal activity (especially against Alternaria alternata at 100 µmol/L). | [64] | ||
Leaves, branches, bark | Sciadopitysin | Antibacterial effect; anti-Alzheimer’s activity (95% ethanolic extract: inhibits β-amyloid fibril aggregation); neuroprotective action at concentrations ranging from 0.4 to 50 μM—neuronal cell viability (SK-N-MC cells) increased at 400 μM, and cellular apoptosis was inhibited at 0.1–1 μM → this suggests potential as a novel therapeutic compound for Alzheimer’s disease; significant antifungal activity (potent inhibitory effect particularly against Cladosporium oxysporum, with ED₅₀ = 9 μM); as a P-glycoprotein (P-gp) and CYP3A4 inhibitor, it enhances the oral absorption of paclitaxel by limiting P-gp activity at a concentration of 50 mg/mL, while simultaneously reducing both expression and activity of CYP3A4 at 100 μg/mL. | [64,82,110,112] | ||
Leaves, bark, branches, aril | Ginkgetin | Antibacterial and anticancer effects (inhibitory activity against HepG2 hepatocellular carcinoma cell line at 50 µmol/mL, resulting in reduced cell viability and decreased number of cancer cells); significant antifungal activity (particularly against Alternaria alternata at 100 µmol/L); acts as an efflux transporter inhibitor of P-glycoprotein (P-gp) and CYP3A4, enhancing the oral absorption of paclitaxel by limiting P-gp activity at a concentration of 50 mg/mL; simultaneously, it reduced both the expression and activity of CYP3A4 at a concentration of 100 µg/mL. | [64,110,113] | ||
Leaves, branches | Amentoflavone | Antibacterial and anti-leishmanial effects (IC₅₀ = 28.5 ± 2 µmol/L, inducing mitochondrial disruption in Leishmania amazonensis); antiviral activity (inhibitory effect against SARS-CoV-2); significant antifungal activity. Acts as an efflux transporter inhibitor of P-glycoprotein (P-gp) and CYP3A4, enhancing the oral absorption of paclitaxel by limiting P-gp activity at a concentration of 50 mg/mL; simultaneously, it reduced both the expression and activity of CYP3A4 at a concentration of 100 µg/mL. | [64,110,114,115] | ||
Leaves, branches | Sequoiaflavone | Antibacterial activity; functions as an efflux transporter inhibitor of P-glycoprotein (P-gp) and CYP3A4, enhancing the oral absorption of paclitaxel by limiting P-gp activity at a concentration of 50 mg/mL; simultaneously, it reduced both the expression and activity of CYP3A4 at a concentration of 100 µg/mL. | [64,110] | ||
Leaves, branches | Isoginkgetin | Exhibits anti-inflammatory and anticancer activity (apparent inhibitory effect on A549 lung cancer cells at concentrations ranging from 2.5 to 20 µmol/L). | [64,116] | ||
Leaves, branches | Putraflavone | Anti-inflammatory activity (inhibits reactive oxygen species production and CD69 expression). | [64,117] | ||
Leaves | Sotetsuflavone | Anticancer activity (apparent inhibitory effect on A549 lung cancer cells at 200 mmol/L, associated with increased E-cadherin expression and decreased N-cadherin expression). | [64,118] | ||
Leaves, branches | Kayaflavone | Antiviral activity (inhibitory effect against SARS-CoV-2). | [64,115] | ||
Leaves, branches | Flavonols | Kaempferol | Antioxidant activity (0.5–32 µg/mL); antiviral effects (strong antiviral activity through inhibition of HIV-1 reverse transcriptase at 100 µg/mL); anti-inflammatory properties. | [64,105,119] | |
Leaves | Myricetin | Antiviral activity (limited effect against infectious bronchitis virus at 100 µmol/mL, with approximately 50% viral activity reduction observed at 10 µmol/mL). | [64,120] | ||
Leaves, bark, branches | Quercetin | Antioxidant, anti-inflammatory, and antiallergic activity (intravenous administration: inhibits mast cell degranulation); hepatoprotective effect. | [64,83,105,121] | ||
Leaves, bark | Isorhamnetin | Antiviral activity (suppressed the growth and invasion of SARS-CoV-2 in the human body). | [64,122] | ||
Leaves | Aromadendrin | Neuroprotective effect (enhanced cell viability at 20 µmol/L and increased confluency at 2 mmol/L in SH-SY5y neuronal cells). | [64,123] | ||
Leaves | Fisetin | Significantly reduces renal hypertrophy and albuminuria in diabetic mouse models, primarily by inhibiting the progression of glycation; shows beneficial effects in diabetes mellitus. | [64] | ||
Leaves, branches | Flavonol glycosides | Kaempferol-3-O-rutinoside | Antioxidant effect (hydroxyl radical scavenging activity, IC₅₀ = 351.46 ± 2.30 µg/mL); potent anti-aging effect (hyaluronidase inhibition at IC₅₀ = 84.07 ± 10.46 µg/mL). | [64,124] | |
Leaves, branches | Kaempferol-7-O-glucoside | Antiviral activity (strong antiviral effects through inhibition of HIV-1 reverse transcriptase at 100 µg/mL). | [64,119] | ||
Leaves, branches | Quercetin-3-O-rutinoside (rutin) | Anticancer activity (radioprotective effect on intestinal cancer by modulating ROS levels and antioxidant proteins, and inhibiting inflammasome activation at a dose of 10.25 mg/kg). | [64,125] | ||
Leaves | Quercetin-7-O-glucoside | Antiviral activity (strong inhibitory effect against influenza virus strains at IC₅₀ = 3.1–8.19 µg/mL, associated with reduced ROS levels and suppression of virus-induced autophagy). | [64,126] | ||
Leaves | Quercetin-3-O-α-L-arabinopyranosyl-β-D-glucopyranoside | Antidiabetic effect (enhances glucose uptake and glycogen synthesis at 20 µmol/L). | [64,127] | ||
Leaves, branches | Quercetin-3-O-glucoside | Anticancer activity (significant antitumor effects against MCF-7 and HeLa cancer cell lines with IC₅₀ values of 36.4 µmol/L and 52.5 µmol/L, respectively). | [57,64] | ||
Leaves, branches | Quercetin-3-rhamnoside | Antilipase activity (inhibits lipase activity at concentrations ranging from 0 to 3 × 10⁻⁵ mol/L). | [64,128] | ||
Leaves | Flavanone glycosides | Prunin | Strong ROS-inhibitory activity; shows medicinal potential against UV-induced cutaneous tumorigenesis. | [66,129] | |
Leaves | Neohesperidin | Exhibits antioxidant, anti-inflammatory, and antiallergic activities, especifically effective in preventing immediate and delayed allergic diseases caused by mast cell degranulation. | [66,130] | ||
Branches | Dihydroflavones | Pinocembrin | Antiviral activity (significant suppression of Zika virus invasion at IC₅₀ = 17.4 µmol/L, by reducing viral RNA and protein expression). | [64,131] | |
Branches | Eriodictyol | Antidiabetic effect (enhances cell viability and superoxide dismutase activity, while reducing ROS generation at concentrations of 5, 10, and 20 µmol/L in diabetic mice). | [64,132] | ||
Branches | Butin | Antidiabetic effect (at 10 and 20 mg/kg: significantly reduces blood glucose levels, oxidative stress, and neuroinflammation; enhances neurobehavioral parameters and metabolic levels). | [64,132] | ||
Branches | Naringenin | Anticancer activity (as nanoparticles: reduces proliferation and migration of A549 lung cancer cells); anti-inflammatory effect (nanoparticles: attenuates pro-inflammatory cytokines and their expression levels); antiallergic activity (intravenous administration: inhibits mast cell degranulation). | [64,121,133] | ||
Branches | Pinostrobin | Promotes melanogenesis (inhibits tyrosinase activity with an IC₅₀ value of 700 µmol/L). | [64,134] | ||
Leaves | Dihydroflavonols | Taxifolin | Antidiabetic activity (IC₅₀ = 0.038–0.647 mg/mL: inhibits α-amylase and α-glucosidase; regulates postprandial hyperglycemia); significant antioxidant and anti-inflammatory activity (40 mg/kg); chemopreventive, hepatoprotective, and cardioprotective properties (100 µg/kg/day: inhibits angiotensin II-converting enzyme and suppresses ROS formation; 3.3 mg/kg: lowers elevated blood pressure). Anti-Alzheimer’s potential (prevents and/or treats cognitive dysfunction related to β-amyloid fibril aggregation); antiviral activity (against hepatitis A virus at 59 µg/mL); antibacterial action (Propionibacterium acnes; Toxoplasma gondii in combination with pyrimethamine, IC₅₀ = 1.39 µg/mL); antilipase and antityrosinase effects; inhibits ROS production. Enhances the efficacy of ceftazidime and levofloxacin in treating methicillin-resistant Staphylococcus aureus (MRSA) infections; suppresses osteoclast activity and mitigates ovariectomy-induced bone loss (potential alternative to estrogen therapy). Demonstrates therapeutic potential in treating bacterial infections (including acne and toxoplasmosis), liver disorders (including autoimmune hepatitis), cardiovascular diseases, inflammation, cancer, viral infections, Alzheimer’s disease, diabetes, allergic reactions, and immune deficiencies. | [64,83,135] | |
Leaves, bark, branches, roots | Flavanols | (+)-Catechin | Antioxidant activity (inhibits autooxidation at 0.01 mol/L; IC₅₀ = 16.88 µg/mL compared to ascorbic acid at 14.48 µg/mL); antidiabetic effect (significantly inhibits α-amylase at IC₅₀ = 0.752 mg/mL and α-glucosidase); anticancer activity (significant antitumor effects against MCF-7, HeLa, and HepG2 cancer cell lines); hepatoprotective properties. | [57,64,83,136,137,138,139] | |
Leaves, bark, branches, roots | (−)-Epicatechin | Antioxidant activity (inhibits autooxidation at 0.01 mol/L; IC₅₀ = 20.20 µg/mL compared to ascorbic acid at 14.48 µg/mL); antidiabetic effect (significantly inhibits α-amylase at IC₅₀ = 0.655 mg/mL and α-glucosidase). Anticancer activity (significant antitumor effects against MCF-7, HeLa, and HepG2 cancer cell lines; reduces radiation resistance and enhances therapeutic effects by activating cyclooxygenase in pancreatic cancer cells at 200 µmol/L); also demonstrates radioprotective effects in human fibroblasts at 20 µmol/L. | [57,64,136,138,139,140,141] | ||
Leaves | Gallocatechin | Antidiabetic and antiviral activity (suppresses SARS-CoV-2 replication with an IC₅₀ = 13.14 ± 2.081 µmol/L). | [64,139,142] | ||
Leaves | Epigallocatechin | Antidiabetic activity. | [64,139] | ||
Leaves | Procyanidin B2 | Antidiabetic activity (protected endothelial progenitor cell function, reduced oxidative damage, and promoted wound healing and angiogenesis in diabetic mice). | [64,136,143] | ||
Branches | Chalcones | Pinocembrin chalcone | Antibacterial activity (moderate inhibitory effect against Neisseria gonorrhoeae at 128 µg/mL). | [64,144] | |
Branches | Isoliquiritigenin | Significant hepatoprotective activity (at 10 µmol/L, reduced transaminase and inflammatory cytokine levels while enhancing catalase activity). | [64,145] | ||
Branches | Butein | Significant anti-inflammatory and antinociceptive effects, demonstrated by reduced nociception in thermal and paw edema tests in mice at 10–20 mg/kg, accompanied by decreased levels of inflammatory cytokines. | [64,146] | ||
Branches | Naringenin chalcone | Anti-inflammatory and antiallergic activity (intravenous administration: inhibits mast cell degranulation). | [64,121] | ||
Leaves | Isoflavones | Glycitin (glycitein-7-O-glucoside) | Protective effect against UV-induced skin photoaging in primary human dermal fibroblasts and against lipopolysaccharide-induced acute lung injury. | Exhibits beneficial effects in the fight against cancer, in the treatment of cardiovascular diseases, as well as in the prevention and management of Alzheimer’s disease. | [66,147] |
Leaves | Genistin (genistein-7-O-glucoside) | Protective effect of genistin on wild-type p53 cells against taxol-induced cytotoxicity in the combined treatment of lung cancer. | [66,148] | ||
LIGNANS | |||||
Bark, leaves | Taxiresinol | Anticancer activity (methanolic extracts). | Anticancer, antiulcer activities. | [25,26,65,80] | |
Roots | (−)-7-O-methyltanegool | α-glucosidase inhibitory effects. | |||
Roots | 13α-Conidendrin | ||||
Roots | 4-Formosanol | ||||
Roots | 14(+)-Tsugacetal | ||||
Roots | 14α-Intermedianol | ||||
Roots | 14-Oxabicyclooctalignan | ||||
Roots | Lanceolatanin C | ||||
Roots | Lanceolatanin D | ||||
Roots | Matairesinol | ||||
Roots | 147-Methoxymatairesinol | ||||
Roots | 17-Oxomatairesinol | ||||
Bark | Taxiresinol I | Ethanolic extract exhibits anticancer activity (in vitro) against ovarian, colon, breast, and liver cancer cells; also shows anti-inflammatory and antinociceptive properties; antiulcer effects; and antifungal activity against Nigrospora oryzae, Epidermophyton floccosum, Curvularia lunata, and Pleurotus ostreatus. | |||
Bark | Isotaxiresinol | Exhibits therapeutic potential in postmenopausal osteoporosis by promoting bone formation and inhibiting bone resorption. | |||
Bark | Lariciresinol | Exhibits anti-inflammatory and antinociceptive properties, as well as antifungal activity against Nigrospora oryzae, Epidermophyton floccosum, Curvularia lunata, and Pleurotus ostreatus. | [38,68,80] | ||
Bark | Isolariciresinol | ||||
Bark | 30-demethyl-isolariciresinol-9′-hydroxyisopropyl ether | ||||
Bark | 3-demethyl-isolariciresinol | ||||
PHYTOSTEROLS | |||||
Bark | Daucosterol | Exhibits cytotoxic activity against various cancer cell lines, including HepG2 (liver cancer), MCF-7 (breast cancer), HeLa (cervical cancer), and A549 (lung cancer). | [26,37,65] | ||
Bark, seeds | β-Sitosterol | Exhibits antiviral, anti-inflammatory, antipyretic, and uterotrophic effects. |
Body Lotion Based on Taxus Cambium and Procambium | Cream Based on Taxus Cambium and Procambium |
|
|
The formulations described in the present invention demonstrate efficacy in the prevention and delay of skin aging. Furthermore, these formulations exhibit notable depigmenting and anti-inflammatory properties. |
Type of Extract/Chemical Compound | Therapeutic Action | References |
---|---|---|
Hydro-methanolic extract | Exhibits antibacterial activity against Pectobacterium sp. and Dickeya chrysanthemi, with a minimum inhibitory concentration (MIC) ranging from 1000 to 1500 µg/mL. | [33] |
Ethanolic Extract (Rhodoxanthin) | Demonstrated significant antiproliferative and pro-apoptotic effects on murine melanoma B16F10 cells in vitro. Oral administration of 7 mg rodoxanthin/kg body weight for 21 days significantly reduced tumor growth (by 42.18%) and tumor weight (by 15.74%) in CD57BL/6J mice bearing B16F10 melanoma; also significantly increased erythrocyte count, hemoglobin, and hematocrit levels in treated tumor-bearing mice. Showed dose-dependent in vitro cytotoxic activity on metastatic murine melanoma B16F10 cell line—the highest tested concentration (C1 = 0.18 µmol/mL) reduced cell viability to 32.29%, while the lowest concentration (C5 = 0.025 µmol/mL) reduced viability to 48.58%, indicating an inverse correlation between rodoxanthin concentration and melanoma cell viability. Exhibited cytoprotective effects against hydrogen peroxide-induced oxidative stress in human HaCaT epidermal keratinocytes and human retinal epithelial cells, improving cell viability by 12.55%, 13%, and 9.66%, respectively. | [34,80] |
Ethanolic Extract (Phenolic Compounds) | Exhibits moderate antioxidant activity (IC₅₀ = 68.46 mg/mL), with an antioxidant capacity (10.7 µmol/100 mL) comparable to that of blackcurrant fruits (Ribes nigrum) (10 µmol/100 mL). | [77] |
Methanolic Extract | Exhibits antifungal activity against Candida albicans and Aspergillus brasiliensis. | [80] |
Methanolic, Acetone, and Distilled Water Extracts | Antioxidant activity (the methanolic extract showed the highest potency, followed by the distilled water extract; the acetone extract was the least effective). Hypoglycemic activity (inhibition of α-amylase and α-glucosidase)—the methanolic extract was the most potent, followed by the distilled water extract, with the acetone extract showing the weakest effect. | [30] |
Carotenoids | Reduce the harmful effects of reactive oxygen species (ROS), contributing to the prevention and mitigation of degenerative diseases, macular degeneration, cardiovascular conditions, and several types of cancer, including lung, gastric, pancreatic, breast, and prostate cancers. | [77] |
Terpenoids | Exhibit antimicrobial activity (limonene, p-cymene, α/β-pinene), anti-inflammatory and chemopreventive effects (limonene), antioxidant and hepatoprotective properties, as well as antiulcer activity (α-pinene, limonene) and antispasmodic action (α-pinene). | [31,84] |
Ferulic acid, p-Coumaric acid, Caffeic acid | Exhibit immunomodulatory, cytoprotective, and antioxidant effects. | [31,32] |
Ascorbic Acid | The aril of Taxus species provides the full recommended dietary allowance (RDA) of vitamin C for healthy adults. | [31,32] |
Carbohydrates | A total of 100 g of aril yields approximately 106 kilocalories, making it suitable as a low-calorie snack option. | [31,32] |
Amino Acids | The aril can serve as a high-quality protein source in human nutrition, containing 43% essential amino acids (according to WHO, foods with over 40% essential amino acids are considered ideal protein sources). The content of branched-chain amino acids (leucine, isoleucine, valine) in the aril (18.4%) is comparable to that found in animal-derived proteins (20%). | [31,32] |
Macroelements and Microelements | The potassium content of the aril is comparable to that of bananas, which are widely considered a typical dietary source of potassium. A 100 g serving of aril provides 11–15% of the recommended daily intake of zinc, 9–15% of iron, and 30–50% of chromium. | [31,32] |
Aril Juice | It alleviates Alzheimer’s disease by modulating several biological processes, including oxidative stress, inflammatory responses, neuronal apoptosis, insulin secretion, amyloid fibril formation, and T-cell co-stimulation. | [88,149] |
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Jîjie, A.-R.; Iliescu, D.; Sbârcea, L.; Boru, C.; Pătrașcu, D.; Iftode, O.A.; Minda, I.-D.; Avram, Ș.; Trandafirescu, C.-M.; Dehelean, C.A.; et al. A Deep Dive into the Botanical and Medicinal Heritage of Taxus. Plants 2025, 14, 1439. https://doi.org/10.3390/plants14101439
Jîjie A-R, Iliescu D, Sbârcea L, Boru C, Pătrașcu D, Iftode OA, Minda I-D, Avram Ș, Trandafirescu C-M, Dehelean CA, et al. A Deep Dive into the Botanical and Medicinal Heritage of Taxus. Plants. 2025; 14(10):1439. https://doi.org/10.3390/plants14101439
Chicago/Turabian StyleJîjie, Alex-Robert, Dan Iliescu, Laura Sbârcea, Casiana Boru, Dalia Pătrașcu, Oana Andrada Iftode, Ionela-Daliana Minda, Ștefana Avram, Cristina-Maria Trandafirescu, Cristina Adriana Dehelean, and et al. 2025. "A Deep Dive into the Botanical and Medicinal Heritage of Taxus" Plants 14, no. 10: 1439. https://doi.org/10.3390/plants14101439
APA StyleJîjie, A.-R., Iliescu, D., Sbârcea, L., Boru, C., Pătrașcu, D., Iftode, O. A., Minda, I.-D., Avram, Ș., Trandafirescu, C.-M., Dehelean, C. A., & Moacă, E.-A. (2025). A Deep Dive into the Botanical and Medicinal Heritage of Taxus. Plants, 14(10), 1439. https://doi.org/10.3390/plants14101439