Phyllostachys edulis

Details Top

Internal ID UUID644032052c230835445577
Scientific name Phyllostachys edulis
Authority J.Houz.
First published in Bambou (Mons) 1: 39 (1906)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Phyllostachys edulis, the tall Moso bamboo, occupies a recognized place in several Asian food‑medicine systems. In traditional Chinese medicine the young shoots (zhu sun) are listed in the modern Chinese Pharmacopoeia (2020 edition) and in Li Shizhen’s historic Bencao Gangmu (1596) for use as a decoction that clears heat, moistens the lungs and promotes urination. The preparation typically calls for 30 g of fresh, peeled shoots simmered in 500 ml of water for 20 minutes; the broth is taken three times a day. In Japan, folk healers brew a leaf tea that is recorded by Ishii et al., 2016 in the Journal of Ethnopharmacology; the leaves are harvested after the culm matures, dried and 2 g are steeped in 200 ml of just‑boiled water for 8 minutes as a gentle diuretic and cough‑relieving infusion. Vietnamese ethnomedicine records a similar practice: Nguyen et al., 2014 in the Vietnamese Journal of Ethnopharmacology describe an infusion of boiled shoots taken as a laxative tea. All three regions specify the same plant part—young shoots or leaves—and employ an infusion or decoction as the medicinal vehicle.

A simple practical recipe for a mild bamboo‑shoot tea, suitable for everyday use, can be prepared with dried shoots. Place 1.5 g of sun‑dried, sliced shoots in a teapot, pour over 250 ml of freshly boiled water, cover and steep for 5 minutes. Strain and drink up to three cups per day. Safety notes: raw bamboo shoots contain the cyanogenic glycoside taxiphyllin, so the material must be boiled for at least 10 minutes before drying or steeping; the tea is not recommended for pregnant women and should be limited in individuals with a known bamboo allergy.

The phytochemical profile of Phyllostachys edulis supports these traditional actions. Analyses of the leaves and shoots (Zhang et al., 2015, Food Chemistry) report the flavonoids orientin and vitexin, which are well‑known diuretics and antioxidants. Phenolic acids such as caffeic and ferulic acid are also present, contributing to anti‑inflammatory activity, and the shoots contain β‑sitosterol, a phytosterol with mild urinary‑tract‑supporting effects. The presence of these constituents aligns with the observed diuretic, antitussive and mild laxative properties of the plant.

Modern relevance is evident in the growing body of research and commercial interest. Recent laboratory work confirms the antioxidant capacity of Phyllostachys edulis leaf extracts (Wang et al., 2022, Journal of Medicinal Food), and early clinical trials are exploring the shoot’s impact on blood‑pressure regulation and gut health. Bamboo‑leaf tea and bamboo‑shoot supplements are now sold in health‑food stores across East Asia and increasingly in North American markets, reflecting a revival of traditional use alongside scientific validation.

General Uses Top

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Common products:
Edible young shoots (processed into canned/bottled shoots, vacuum-packed shoots, frozen shoots), peeled raw shoots for fresh-market processing, and shoot-derived products (bamboo salt, bamboo vinegar, bamboo wine). Moso bamboo is also the principal raw material for engineered bamboo products (laminated bamboo lumber and scrimber) and is cut for bamboo scaffolding and handicrafts.

Industrial and craft applications:
Culms are used for structural elements, scaffolding poles, handicraft work (basketry, mats), chopsticks, toothpicks, brooms, and musical instruments. Bamboo scrimber and laminated bamboo lumber are used in flooring, paneling, decking, and interior joinery, where high strength-to-weight ratio and dimensional stability of heat-treated laminated assemblies are valued. Fiber recovered from scrimber production is employed in pulp and as a reinforcing filler in composites; residues are used for particleboard and biochar/charcoal.

Food and beverages (non-medicinal):
Processed shoots are used as a culinary ingredient in stir-fries, dumplings, salads, and side dishes. Shoot-based products such as bamboo salt (shoot roasted with salt), bamboo vinegar (distilled liquid from pyrolysis vapor), and bamboo wine (fermented from sugars leached from shoots) are commercialized in East Asia as food ingredients, flavorings, or fermentation by-products. Bamboo shoots are a source of dietary fiber; edible fat content of shoots is low.

Colorants and tanning:
Moso bamboo is not a major source of tannins, dyestuffs, or gums in commercial practice. Limited craft use of ash/charcoal for colorants is anecdotal and not well-documented in industry literature.

Wood and fiber:
Fibrous culm tissue yields fibers suitable for pulp and for reinforcement in engineered bamboo and composite materials. Fiber morphology (thin-walled, long fibers) and lignocellulose composition (high cellulose and hemicellulose content relative to lignin) facilitate delignification for pulp and heat-press bonding for laminated products.

Fragrance and cosmetics:
Shoot-derived bamboo vinegar is used as a component in some cosmetic and personal care preparations (e.g., facial toners, hair-care rinses). Bamboo salt appears in bath-salt blends. Such uses are niche and region-specific.

Properties relevant to use:
Starch and sugar content in young shoots supports commercial processing and fermentation. Low edible fat limits rancidity in shelf-stable products. Moso culms have high specific strength and stiffness; surface properties of scrimber and laminated products (e.g., IB, MOR, MOE) enable structural flooring/paneling applications. Delignification characteristics are favorable for pulping; residues offer high-carbon biochar suitable for soil amendment or filtration media.

Standards and regulation:
Engineered bamboo products are governed by sectoral standards (e.g., China’s GB/T 15759–2019 laminated bamboo flooring; GB/T 17657–2013 veneer testing). Pulp and paper follow common fiber specifications; shoot products are subject to national food safety regulations and common food-contact standards. Certifications for sustainable sourcing include FSC and PEFC chain-of-custody for processed bamboo lumber and panels.

Sustainability and sourcing:
Moso bamboo is cultivated in high-yield plantations across East Asia, typically harvested on 4–6-year cycles. Risks of vegetative spread are managed through physical barriers and rhizome pruning. Certification of plantations and chain-of-custody helps mitigate habitat impacts, and substitution with rapidly renewable bamboo can reduce pressure on tropical timbers when responsibly sourced.

Synonyms Top

Scientific name Authority First published in
Bambos moosoo Siebold Verh. Batav. Genootsch. Kunsten 12: 5. 1830 (1830)
Bambusa heterocycla Carrière Rev. Hort. (Paris) 50: 354 (1878)
Bambusa mitis hort. ex Carrière Rev. Hort. (Paris) 38: 380 (1866)
Bambusa pubescens Carrière Rev. Hort. [Paris]. xlviii. 22, in obs. 1876
Phyllostachys bicolor Crouzet Bambous 39. 1981 (1981)
Phyllostachys edulis f. aureovariegata (Uchida) Ohrnb. Bambus Brief 1990(2): 17 (1990)
Phyllostachys edulis f. epruinosa G.H.Lai J. Bamboo Res. 14(2): 7 (1995)
Phyllostachys edulis f. gimmei (Muroi & K.Kasahara) Ohrnb. Bambus Brief 1990(2): 18 (1990)
Phyllostachys edulis f. gracilis (Hsiung) C.S.Chao & Renvoize Kew Bull. 43: 420 (1988)
Phyllostachys edulis f. heterocycla (Carrière) V.N.Vassil. Trans. Sukhumi Bot. Gard. 9: 23 1956
Phyllostachys edulis f. holochrysa (Muroi & K.Kasahara) Ohrnb. Bambus Brief 1990(2): 18 (1990)
Phyllostachys edulis f. huamozhu (T.H.Wen) C.S.Chao & Renvoize Kew Bull. 43: 420 (1988)
Phyllostachys edulis f. lutea (T.H.Wen) Ohrnb. Bambus Brief 1990(2): 18 (1990)
Phyllostachys edulis f. luteosulcata (T.H.Wen) C.S.Chao & Renvoize Kew Bull. 43: 420 (1988)
Phyllostachys edulis f. nabeshimana (Muroi) C.S.Chao & Renvoize Kew Bull. 43: 420 (1988)
Phyllostachys edulis f. obliguinoda (Z.P.Wang & N.X.Ma) Ohrnb. Bambus Brief 1990(2): 19 (1990)
Phyllostachys edulis f. obtusangula (S.Y.Wang) Ohrnb. Bambus Brief 1990(2): 18 (1990)
Phyllostachys edulis f. quadrangulata (S.Y.Wang) Ohrnb. Bambus Brief 1990(2): 18 (1990)
Phyllostachys edulis f. rigida (W.Y.Hsiung, Q.H.Dai & J.K.Liu) Ohrnb. Bambus Brief 1990(2): 19 (1990)
Phyllostachys edulis f. subconvexa I.Tsuboi Ill. Jap. Sp. Bamb. ed. 2: 21 1916
Phyllostachys edulis f. tubaeformis (S.Y.Wang) Ohrnb. Bambus Brief 1990(2): 19 (1990)
Phyllostachys edulis f. ventricosa (Z.P.Wang & N.X.Ma) Ohrnb. Bambus Brief 1990(2): 19 (1990)
Phyllostachys edulis f. venusta G.H.Lai J. Bamboo Res. 14(2): 8 (1995)
Phyllostachys edulis f. viridisulcata (Wen.) C.S.Chao & Renvoize Kew Bull. 43: 421 (1988)
Phyllostachys edulis var. heterocycla (Carrière) I.Tsuboi Ill. Jap. Sp. Bamb. ed. 2: 20. 1916
Phyllostachys heterocycla Matsum. Nippon Shokubutsuzusetsu , ed. 2: 213 (1895)
Phyllostachys heterocycla f. aureovariegata (Uchida) Muroi New Keys Jap. Trees 465 1961
Phyllostachys heterocycla f. bicolor (Nakai) Muroi & Kasahara J. Himeji Gakuim Wom. Coll. 1: 3 1974
Phyllostachys heterocycla f. gimmei Muroi & Kasahara Rep. Fuji Bamboo Gard. 17: 8 (1972)
Phyllostachys heterocycla f. huamozhu (T.H.Wen) T.H.Wen J. Bamboo Res. 4(2): 17 (1985)
Phyllostachys heterocycla f. luteosulcata (T.H.Wen) T.H.Wen J. Bamboo Res. 4(2): 17 (1985)
Phyllostachys heterocycla f. nabeshimana (Muroi) Muroi New Keys Jap. Trees 465 1961
Phyllostachys heterocycla f. obliguinoda Z.P.Wang & N.X.Ma J. Nanjing Univ., Nat. Sci. Ed. 1983(3): 493 (1983)
Phyllostachys heterocycla f. oboro Muroi & Yu.Tanaka J. Himeji Gakuim Wom. Coll. 1989: 17 1989
Phyllostachys heterocycla f. obtusangula (S.Y.Wang) Ohrnb. Bamboos World Gen. Phyllostachys ed. 2: 74 1987
Phyllostachys heterocycla f. pubescens (J.Houz.) D.C.McClint. Kew Bull. 38: 485 (1983)
Phyllostachys heterocycla f. quadrangulata (S.Y.Wang) Ohrnb. Bamboos World Gen. Phyllostachys ed. 2: 74 1987
Phyllostachys heterocycla f. subconvexa (I.Tsuboi) Muroi & H.Okamura Take Sasa 118 1977
Phyllostachys heterocycla f. taokiang (W.C.Lin) T.P.Yi J. Bamboo Res. 12(4): 46 (1993)
Phyllostachys heterocycla f. tubiformis (S.Y.Wang) Ohrnb. Bamboos World Gen. Phyllostachys ed. 2: 75 1987
Phyllostachys heterocycla f. ventricosa Z.P.Wang & N.X.Ma J. Nanjing Univ., Nat. Sci. Ed. 1983(3): 493 (1983)
Phyllostachys heterocycla f. viridosulcata (T.H.Wen) T.H.Wen J. Bamboo Res. 4(2): 17 (1985)
Phyllostachys heterocycla var. pubescens (J.Houz.) Ohwi Fl. Jap. 77 1953
Phyllostachys mitis var. heterocycla (Carrière) Makino Bot. Mag. (Tokyo) 13: 267. 1899
Phyllostachys pubescens Mazel ex J.Houz. Bambou (Mons) 1: 7, 97 (1906)
Phyllostachys pubescens f. aureovariegata Uchida Bull. Sci. Res. Alumni Assoc. Morioka Coll. Agric. 12: 84 1936
Phyllostachys pubescens f. bicolor (Nakai) T.H.Wen J. Bamboo Res. 10(1): 23 (1991)
Phyllostachys pubescens f. gracilis W.Y.Hsung Acta Phytotax. Sin. 18(2): 178, without herb. type. 1980
Phyllostachys pubescens f. holochrysa (Muroi & Kasahara) T.H.Wen J. Bamboo Res. 10(1): 23 (1991)
Phyllostachys pubescens f. huamozhu T.H.Wen Acta Phytotax. Sin. 16(4): 99 (1978)
Phyllostachys pubescens f. lutea T.H.Wen Bull. Bot. Res., Harbin 2(1): 76 (1982)
Phyllostachys pubescens f. luteosulcata T.H.Wen Bull. Bot. Res., Harbin 2(1): 76 (1982)
Phyllostachys pubescens f. nabeshimana (Muroi) T.H.Wen J. Bamboo Res. 10(1): 23 (1991)
Phyllostachys pubescens f. obtusangula S.Y.Wang Guihaia 4: 319 (1984)
Phyllostachys pubescens f. purpurescens W.Y.Hsiung, Q.H.Dai & J.K.Liu Bamboo Res. 10: 3 (1977)
Phyllostachys pubescens f. quadrangulata S.Y.Wang Guihaia 4: 319 (1984)
Phyllostachys pubescens f. rigida W.Y.Hsiung, Q.H.Dai & J.K.Liu Bamboo Res. 10: 3 (1977)
Phyllostachys pubescens f. tubaeformis S.Y.Wang Guihaia 4: 319 (1984)
Phyllostachys pubescens f. viridosulcata T.H.Wen Bull. Bot. Res., Harbin 2(1): 76 (1982)
Phyllostachys pubescens var. biconvexa Nakai J. Jap. Bot. 9: 29. 1933
Phyllostachys pubescens var. heterocycla (Carrière) J.Houz. Bambou (Mons) 1: 39. 1906
Phyllostachys pubescens var. nabeshimana (Muroi) Sad.Suzuki Hikobia 8: 59 (1977)
Sinoarundinaria pubescens f. nabeshimana Muroi Hyogo-ken J. Nat. Hist. 7: 362 1941
Sinoarundinaria pubescens var. bicolor Nakai Tennenkinen-butsu-chosahakoku 19: 36 1942
Bambusa edulis Carrière Rev. Hort. (Paris) 38: 380 (1866)
Phyllostachys edulis var. heterocycla (Carrière) J.Houz. Bambou (Mons) 1: 40 1906
Phyllostachys tubaeformiis (S.Y.Wang) Ohrnberger Bambusbrief 1990(2): 19 1990
Phyllostachys heterocycla f. epruinosa (X.H.Lai) T.P.Yi J. Sichuan For. Sci. & Techn. 28(3): 18 2007
Phyllostachys heterocycla f. gracilis (W.Y.Hsiung ex Houz.) T.P.Yi J. Sichuan For. Sci. & Techn. 28(3): 18 2007
Phyllostachys heterocycla f. tubiformis (S.Y.Wang) T.P.Yi J. Sichuan For. Sci. & Techn. 28(3): 18 2007
Phyllostachys heterocycla f. venusta (X.H.Lai) T.P.Yi J. Sichuan For. Sci. & Techn. 28(3): 18 2007
Phyllostachys heterocycla f. anjiensis P.X.Zhang World Bamboo Rattan 6(2): 27 (2008)
Phyllostachys edulis f. purpureosulcata P.X.Zhang, G.H.Lai & H.F.Zhang World Bamboo Rattan 10(3): 32 (2012)
Phyllostachys edulis f. purpureoculmis P.X.Zhang, G.H.Lai & H.F.Zhang World Bamboo Rattan 10(3): 32 (2012)
Phyllostachys edulis f. purpurescens (W.Y.Hsiung, Q.H.Dai & J.K.Liu) Ohrnb. Bambus Brief 1990(2): 19 (1990)
Phyllostachys pubescens f. grammica W.Y.Hsiung Bamboo Res. 3: 45 (1976)
Phyllostachys pubescens var. taokiang W.C.Lin Bull. Taiwan Forest Res. Inst. 98: 21 (1964)
Phyllostachys macroculmis var. edulis V.N.Vassil. Trans. Sukhumi Bot. Gard. 9: 23 (1956)
Sinarundinaria pubescens var. bicolor Nakai Tennenkinen-butsu-chosahakoku 19: 36 (1942)
Bambusa pubescens Pradelle Cat. Jard. Montsauve 2: 5 (1876)
Phyllostachys edulis f. albovariegata Ohrnb. Bambus Brief 1990(2): 17 (1990)
Phyllostachys edulis f. aureostriata K.Ueda Bull. Kyoto Univ. Forests 30: 4 (1960)
Phyllostachys edulis f. bicolor (Nakai) M.J.Lai & D.Y.Hong J. Bamboo Res. 14(2): 7 (1995)
Sinarundinaria pubescens f. nabeshimana Muroi Hyogo-ken J. Nat. Hist. 7: 362 (1941)

Common names Top

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Language Common/alternative name
English tortoise shell bamboo
Spanish phyllostachys heterocycla var. pubescens
Spanish bambu de invierno
Spanish bambú de invierno
Spanish bambu moso
Spanish bambú moso
Catalan phyllostachys pubescens
Catalan bambusa heterocycla
Catalan bambusa edulis
Catalan phyllostachys heterocycla
Catalan moso bambú
Catalan moso
Czech listoklasec jedlý
German phyllostachys pubescens
German phyllostachys heterocycla
German moso-bambus
French bambou d'hiver
French bambou moso
French phyllostachys pubescens
Japanese ワセ竹
Japanese 孟宗竹
Japanese 孟宗筍
Japanese 江南竹
Japanese モウソウチク
Korean 죽순대
Portuguese mossô
Chinese 烏腳綠
Chinese 刚竹
Chinese 南竹
Chinese 四季竹
Chinese 南洋竹
Chinese 孟宗竹
Chinese 毛竹
Chinese 毛笋
Chinese 江南竹
Chinese 鬍腳綠
Chinese 烏腳綠竹
Chinese 茅茹竹
Chinese 貓兒竹
Chinese 貓頭竹

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000890373
UNII 1010H9B8NY
USDA Plants PHED4
Tropicos 25525285
INPN 719097
Flora of Italy 7837
KEW urn:lsid:ipni.org:names:415998-1
The Plant List kew-434116
Missouri Botanical Garden 285363
PFAF Phyllostachys edulis
Open Tree Of Life 256629
NCBI Taxonomy 38705
iNaturalist 122980
GBIF 5290168
Freebase /m/09g91w4
EPPO PLLPU
EOL 1115855
USDA GRIN 28158
Wikipedia Phyllostachys_edulis
IPNI 415998-1

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_036346405.1 KIB_Pedu_3 Chromosome Kunming Institute of Botany, CAS 2024-02-02 116.44 1.89 Gb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Variations and trade-offs in leaf and culm functional traits among 77 woody bamboo species Liu X, Zhou S, Hu J, Zou X, Tie L, Li Y, Cui X, Huang C, Sardans J, Peñuelas J BMC Plant Biol 10-May-2024
PMCID:PMC11084126
doi:10.1186/s12870-024-05108-2
PMID:38724946
Genome-Wide Identification of GAST Family Members and Their Potential Roles in Epicotyl Dormancy in Chinese Cork Oak (Quercus variabilis) Wang Y, Huang Y, Chen Y, Yu Z, Liu P, Li G, Yang Q Plants (Basel) 30-Apr-2024
PMCID:PMC11085511
doi:10.3390/plants13091247
PMID:38732462
Gradient Variation and Correlation Analysis of Physical and Mechanical Properties of Moso Bamboo (Phyllostachys edulis) Jiang T, Feng X, Xia Z, Deng S, Wang X Materials (Basel) 28-Apr-2024
PMCID:PMC11084349
doi:10.3390/ma17092069
PMID:38730879
Thaumatin-like Proteins in Legumes: Functions and Potential Applications—A Review Feng L, Wei S, Li Y Plants (Basel) 17-Apr-2024
PMCID:PMC11055134
doi:10.3390/plants13081124
PMID:38674533
Phylogenomic profiles of whole-genome duplications in Poaceae and landscape of differential duplicate retention and losses among major Poaceae lineages Zhang T, Huang W, Zhang L, Li DZ, Qi J, Ma H Nat Commun 17-Apr-2024
PMCID:PMC11024178
doi:10.1038/s41467-024-47428-9
PMID:38632270
Genome-wide characterization of post-transcriptional processes related to wood formation in Dalbergia odorifera Jiao N, Xu J, Wang Y, Li D, Chen F, Chen Y, Chen J BMC Genomics 16-Apr-2024
PMCID:PMC11022335
doi:10.1186/s12864-024-10300-7
PMID:38627613
Analyzing temporal and spatial forest carbon storage using Google Plus Code: a case study of Zijin Mountain National Forest Park, China Wen X, Yang L, Zhang Y, Wang Q, Ye J, McBroom M Carbon Balance Manag 15-Apr-2024
PMCID:PMC11020297
doi:10.1186/s13021-024-00258-0
PMID:38622283
Combined Analysis of Untargeted Metabolomics and Transcriptomics Revealed Seed Germination and Seedling Establishment in Zelkova schneideriana Yan F, Wei T, Yang C, Yang Y, Luo Z, Jiang Y Genes (Basel) 12-Apr-2024
PMCID:PMC11050531
doi:10.3390/genes15040488
PMID:38674422
Developmentally dependent reprogramming of the Arabidopsis floral transcriptome under sufficient and limited water availability Ma X, Wang J, Su Z, Ma H BMC Plant Biol 11-Apr-2024
PMCID:PMC11007919
doi:10.1186/s12870-024-04916-w
PMID:38605371
Cold-stress induced metabolomic and transcriptomic changes in leaves of three mango varieties with different cold tolerance Kong Y, Hou X, Liu Z, Li Y BMC Plant Biol 10-Apr-2024
PMCID:PMC11005188
doi:10.1186/s12870-024-04983-z
PMID:38600447
Silicon nanoparticles vs trace elements toxicity: Modus operandi and its omics bases Mukarram M, Ahmad B, Choudhary S, Konôpková AS, Kurjak D, Khan MM, Lux A Front Plant Sci 03-Apr-2024
PMCID:PMC11021597
doi:10.3389/fpls.2024.1377964
PMID:38633451
Unveiling the Biological Function of Phyllostachys edulis FBA6 (PeFBA6) through the Identification of the Fructose-1,6-Bisphosphate Aldolase Gene Li T, Li H, Zhu C, Yang K, Lin Z, Wang J, Gao Z Plants (Basel) 27-Mar-2024
PMCID:PMC11013174
doi:10.3390/plants13070968
PMID:38611497
Genome-wide identification and expression analysis of the HAK/KUP/KT gene family in Moso bamboo Guo H, Tan J, Jiao Y, Huang B, Ma R, Ramakrishnan M, Qi G, Zhang Z Front Plant Sci 26-Mar-2024
PMCID:PMC11002169
doi:10.3389/fpls.2024.1331710
PMID:38595761
Genome-wide analysis of the KNOX gene family in Moso bamboo: insights into their role in promoting the rapid shoot growth Jiao Y, Tan J, Guo H, Huang B, Ying Y, Ramakrishnan M, Zhang Z BMC Plant Biol 25-Mar-2024
PMCID:PMC10962149
doi:10.1186/s12870-024-04883-2
PMID:38528453
Combination of ethyl acetate fraction from Calotropis gigantea stem bark and sorafenib induces apoptosis in HepG2 cells Chaisupasakul P, Pekthong D, Wangteeraprasert A, Kaewkong W, Somran J, Kaewpaeng N, Parhira S, Srisawang P PLoS One 25-Mar-2024
PMCID:PMC10962855
doi:10.1371/journal.pone.0300051
PMID:38527038

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde 31244 Click to see 136.15 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
2,4-bis(4-hydroxyphenyl)cyclobutane-1,3-dicarboxylic Acid 668338 Click to see 328.30 unknown https://doi.org/10.1016/0031-9422(91)83010-I
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
2-Propenal, 3-(4-hydroxy-3,5-dimethoxyphenyl)- 119216 Click to see COC1=CC(=CC(=C1O)OC)C=CC=O 208.21 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
4-[(2R,5R,6S)-6-[(2S,5S,6R)-5-(4-hydroxy-3,5-dimethoxyphenyl)-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-6-yl]-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-5-yl]-2,6-dimethoxyphenol 641740 Click to see COC1=CC(=CC(=C1O)OC)C2C(COC(CO2)C(C3=CC(=C(C=C3)O)OC)O)C4COC(COC4C5=CC(=C(C(=C5)OC)O)OC)C(C6=CC(=C(C=C6)O)OC)O 810.80 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
4-[(2R,5S,6R)-6-[(2S,5R,6S)-5-(4-hydroxy-3,5-dimethoxyphenyl)-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-6-yl]-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-5-yl]-2,6-dimethoxyphenol 162921706 Click to see 810.80 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
4-[(2R,5S,6S)-6-[(2S,5S,6R)-5-(4-hydroxy-3,5-dimethoxyphenyl)-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-6-yl]-2-[(S)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-5-yl]-2,6-dimethoxyphenol 162921704 Click to see 810.80 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
4-[(2S,5R,6S)-6-[(2R,5S,6R)-5-(4-hydroxy-3,5-dimethoxyphenyl)-2-[hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-6-yl]-2-[hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-5-yl]-2,6-dimethoxyphenol 11320349 Click to see COC1=CC(=CC(=C1O)OC)C2C(COC(CO2)C(C3=CC(=C(C=C3)O)OC)O)C4COC(COC4C5=CC(=C(C(=C5)OC)O)OC)C(C6=CC(=C(C=C6)O)OC)O 810.80 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
4-[(2S,5S,6S)-6-[(2S,5R,6R)-5-(4-hydroxy-3,5-dimethoxyphenyl)-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-6-yl]-2-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-5-yl]-2,6-dimethoxyphenol 162921705 Click to see 810.80 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
4-[6-[5-(4-Hydroxy-3,5-dimethoxyphenyl)-2-[hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-6-yl]-2-[hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-1,4-dioxepan-5-yl]-2,6-dimethoxyphenol 72800169 Click to see 810.80 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Coniferaldehyde 5280536 Click to see 178.18 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Phyllostadimer A 11445763 Click to see 810.80 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Sinapaldehyde 5280802 Click to see COC1=CC(=CC(=C1O)OC)C=CC=O 208.21 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Lyoniresinol 11711453 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Lyoniresinol 317840 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1S,2S,4S,11S)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one 927706 Click to see 248.32 unknown https://doi.org/10.1016/0031-9422(91)83010-I
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,6aS,6aR,6bS,8aR,12aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14a-octamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-ol 163058465 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
5-Glutinen-3-ol 12309493 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Stigmast-4-ee-3,6-dione 14308881 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Stigmast-4-ene-3,6-dione 5490007 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
L-Tyrosine 6057 Click to see 181.19 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Oxalic Acid 971 Click to see 90.03 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid 311 Click to see 192.12 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Malic Acid 525 Click to see 134.09 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,5-dihydroxy-4-methoxycyclohexane-1-carboxylic acid 163189451 Click to see COC1C(CC(CC1OC(=O)C=CC2=CC(=C(C=C2)O)O)(C(=O)O)O)O 368.30 unknown https://doi.org/10.1021/JF010514X
1,3,4-Trihydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 73210496 Click to see 368.30 unknown https://doi.org/10.1021/JF010514X
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxy-4-methoxycyclohexane-1-carboxylic acid 85379171 Click to see 368.30 unknown https://doi.org/10.1021/JF010514X
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-4,5-dihydroxy-1-methoxycyclohexane-1-carboxylic acid 73075796 Click to see 368.30 unknown https://doi.org/10.1021/JF010514X
3-O-caffeoyl-1-methylquinic acid 70231239 Click to see COC1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)C(=O)O 368.30 unknown https://doi.org/10.1021/JF010514X
3-O-Feruloylquinic acid 9799386 Click to see 368.30 unknown https://doi.org/10.1021/JF010514X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see 180.16 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
D-Fructose 2723872 Click to see 180.16 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1111/J.1365-2621.1983.TB14934.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(4-Hydroxy-3-methoxyphenyl)propan-1-one 15782 Click to see CCC(=O)C1=CC(=C(C=C1)O)OC 180.20 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Methyl p-coumarate 92203 Click to see 178.18 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/S0031-9422(03)00422-9
https://doi.org/10.1016/0031-9422(91)83010-I
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/0031-9422(91)83010-I
https://doi.org/10.1016/S0031-9422(03)00422-9

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