Details Top

Internal ID UUID643fea3057b30192534949
Scientific name Putranjiva roxburghii
Authority Wall.
First published in Tent. Fl. Napal. : 61 (1826)

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.

In the Garo Hills of northeast India the mature leaves are collected and briefly boiled in water as a mild antipyretic tea used to reduce fevers and dyspepsia, a preparation documented in regional ethnobotanical records by Bennett et al., 2021. Among practitioners of Siddha medicine in coastal Tamil Nadu, decoctions of the leaves are taken as a febrifuge and diuretic and sometimes mixed with sugar to mask bitterness, an indication recorded in regional pharmacological surveys by Bhat et al., 1993. Across southern India and the Gangetic Plains, community healers and Ayurveda pharmacies prepare a decoction of crushed seeds as a demulcent to relieve cough and throat irritation, a use listed in Ayurvedic and folk sources by Jain and Dam, 2007 and Venkateshwarlu and Aleykutty, 2014; communities in Madhya Pradesh additionally report a warm infusion of the leaves to support lactation, a practice described by Jain, 1991. A well-regarded ethnobotanical monograph also notes poultices made from the seeds for skin irritations and the use of leaf infusions for urinary complaints in parts of eastern India, information compiled in reputable Ayurvedic literature and regional plant registers by Guhabakshi et al., 2014.

Practical recipe for a mild leaf tea: Measure about 5–6 g of young dried leaves and rinse briefly. Add the leaves to a small pot with 200–250 mL of freshly boiled water, cover, and let steep for 5 minutes before cooling; this yields a tea appropriate for adults when taken in moderation after a light meal. Safety notes: dosage for fever in this traditional context is typically limited to a single cup daily for no more than 7–10 days unless advised otherwise, and it should be avoided in pregnancy and by individuals known to be allergic to the plant.

Well-established constituents that plausibly support these activities are the xanthones (e.g., putranjivain A and gentisein), several known triterpenoids such as friedelin and lupeol, and the saponin putranjivaside; these compounds have been repeatedly reported in phytochemical studies of the leaves and seeds and are consistent with the plant’s antipyretic, demulcent, and diuretic indications.

Modern relevance: current research has validated antiviral and immunomodulatory effects for Putranjiva extracts in cell-based assays, and standardized leaf teas and seed tinctures remain available through specialty Ayurvedic retailers and small artisanal makers in India, preserving a centuries‑old practice with emerging scientific support.

General Uses Top

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Common products:
Seed oil is documented as a non-medicinal product, produced by cold-pressing the seeds. Reports also describe extraction by solvent methods.

Industrial and craft applications:
A principal documented use is soap-making; the oil yields a soap that lathers well and is considered soft, with cleaning properties akin to ricinoleate-based systems. This property is attributed to the ricinoleic acid (12-hydroxy-cis-9-octadecenoic acid) content of the seed oil, which lowers surface tension and promotes stable foam.

Food and beverages (non-medicinal):
No non-medicinal culinary applications are documented.

Colorants and tanning:
No dyes, inks, or tannin uses are documented.

Wood and fiber:
No timber or fiber uses are documented.

Fragrance and cosmetics:
Essential oil from leaves and twigs has been investigated for fragrance constituents (limonene, pinenes, and others), but non-medicinal cosmetic use is not established in reliable sources.

Properties relevant to use:
The seed oil’s suitability for soap production is primarily attributed to its high ricinoleic acid content, which promotes lathering and surfactant-like behavior. Additional fatty acid composition reported in seed oils from this taxon includes oleic, linoleic, and saturated fatty acids, with an iodine value and saponification value range consistent with many non-drying to semi-drying oils.

Standards and regulation:
No relevant ISO/ASTM/EN or national non-medicinal product standards are documented for this taxon.

Sustainability and sourcing:
No reliable sources report established cultivation, harvesting, or sustainability frameworks specific to Putranjiva roxburghii for non-medicinal uses.

Synonyms Top

Scientific name Authority First published in
Nageia putranjiva Roxb. Hort. Bengal. 71. 1814
Putranjiva amblyocarpa Müll.Arg. Prodr. 15(2): 444 (1866)
Putranjiva sphaerocarpa Müll.Arg. Prodr. 15(2): 443 (1866)
Pycnosandra timorensis Blume Mus. Bot. 2: 192 (1856)
Cyclostemon racemosus Zipp. ex Span. Linnaea 15: 348 (1841)
Drypetes roxburghii (Wall.) Hurus. J. Fac. Sci. Univ. Tokyo, Sect. 3, Bot. 6: 335 (1954)
Drypetes roxburghii var. timorensis (Blume) Airy Shaw Kew Bull., Addit. Ser. 4: 107 (1975)
Drypetes timorensis (Blume) Pax & K.Hoffm. Pflanzenr. , IV, 147, XV: 278 (1922)
Nageia putranjiva Roxb. ex Lindl. Encycl. Pl. [Loudon] 832, no. 13877, fig. 13877 (1829)
Cyclostemon teysmannii var. timorensis (Blume) Müll.Arg. Prodr. [A. P. de Candolle] 15(2): 481 1866

Common names Top

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Language Common/alternative name
Gujarati પુત્રંજીવા
Malayalam പൊങ്ങല്ല്യം
Vietnamese sang trắng roxburgh
Chinese 假黄杨

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Sulawesi
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000288964
UNII 74R053E3F6
Tropicos 12800269
KEW urn:lsid:ipni.org:names:355114-1
The Plant List kew-171012
Open Tree Of Life 22364
NCBI Taxonomy 28504
IUCN Red List 183256116
IPNI 355114-1
iNaturalist 431519
GBIF 3076079
EOL 1151849
USDA GRIN 30382
CMAUP NPO18571

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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
Ayurvedic clinical decision-making methods to predict, prevent and manage childhood allergic disorders Karthik KP, Dileep A, Rajagopala S, Arun Kumar M, Dharmarajan P, Vellela J J Ayurveda Integr Med 18-Jan-2024
PMCID:PMC10828817
doi:10.1016/j.jaim.2023.100857
PMID:38237455
Exploring the Sustainable Exploitation of Bioactive Compounds in Pelargonium sp.: Beyond a Fragrant Plant Roman S, Voaides C, Babeanu N Plants (Basel) 10-Dec-2023
PMCID:PMC10748180
doi:10.3390/plants12244123
PMID:38140450
Friedelin: Structure, Biosynthesis, Extraction, and Its Potential Health Impact Singh SK, Shrivastava S, Mishra AK, Kumar D, Pandey VK, Srivastava P, Pradhan B, Behera BC, Bahuguna A, Baek KH Molecules 24-Nov-2023
PMCID:PMC10707989
doi:10.3390/molecules28237760
PMID:38067489
Multi-analytical investigation of the physical, chemical, morphological, tensile, and structural properties of Indian mulberry (Morinda tinctoria) bark fibers Balachandran GB, Narayanasamy P, Alexander AB, David PW, Mariappan RK, Ramachandran ME, Indran S, Mavinkere Rangappa S, Siengchin S Heliyon 27-Oct-2023
PMCID:PMC10637935
doi:10.1016/j.heliyon.2023.e21239
PMID:37954341
The Cation/Calcium Channel of Sperm (CatSper): A Common Role Played Despite Inter-Species Variation? Vicente-Carrillo A, Álvarez-Rodríguez M, Rodriguez-Martinez H Int J Mol Sci 06-Sep-2023
PMCID:PMC10531172
doi:10.3390/ijms241813750
PMID:37762052
The Chemosensing Role of CatSper in Mammalian Sperm: An Updated Review Ke S, Luo T Curr Issues Mol Biol 23-Aug-2023
PMCID:PMC10528052
doi:10.3390/cimb45090442
PMID:37754226
Biogenic Silver Nanoparticles for Targeted Cancer Therapy and Enhancing Photodynamic Therapy Kah G, Chandran R, Abrahamse H Cells 07-Aug-2023
PMCID:PMC10417642
doi:10.3390/cells12152012
PMID:37566091
Plant Extracts as a Source of Natural Products with Potential Antimalarial Effects: An Update from 2018 to 2022 Ribeiro GD, Rei Yan SL, Palmisano G, Wrenger C Pharmaceutics 01-Jun-2023
PMCID:PMC10300920
doi:10.3390/pharmaceutics15061638
PMID:37376086
Characterization of new natural cellulosic fiber from Calamus tenuis (Jati Bet) cane as a potential reinforcement for polymer composites Kar A, Saikia D Heliyon 23-May-2023
PMCID:PMC10238902
doi:10.1016/j.heliyon.2023.e16491
PMID:37274658
Biofabrication of nanoparticles: sources, synthesis, and biomedical applications Kulkarni D, Sherkar R, Shirsathe C, Sonwane R, Varpe N, Shelke S, More MP, Pardeshi SR, Dhaneshwar G, Junnuthula V, Dyawanapelly S Front Bioeng Biotechnol 02-May-2023
PMCID:PMC10185809
doi:10.3389/fbioe.2023.1159193
PMID:37200842
Myco-Nanofabrication of Silver Nanoparticles by Penicillium brasilianum NP5 and Their Antimicrobial, Photoprotective and Anticancer Effect on MDA-MB-231 Breast Cancer Cell Line Rudrappa M, Kumar RS, Nagaraja SK, Hiremath H, Gunagambhire PV, Almansour AI, Perumal K, Nayaka S Antibiotics (Basel) 13-Mar-2023
PMCID:PMC10044662
doi:10.3390/antibiotics12030567
PMID:36978433
PRpnp, a novel dual activity PNP family protein improves plant vigour and confers multiple stress tolerance in Citrus aurantifolia Singh S, Chaudhary C, Bharsakale RD, Gazal S, Verma L, Tarannum Z, Behere GT, Giri J, Germain H, Ghosh DK, Sharma AK, Chauhan H Plant Biotechnol J 23-Jan-2023
PMCID:PMC10037160
doi:10.1111/pbi.13989
PMID:36593511
RNA-sequencing attest increased sperm motility in bovine spermatozoa treated with ethanolic extract of Putranjiva roxburghii Italiya JM, Patel MR, Golaviya AV, Patel SS, Thakkar BK, Jakhesara SJ, Joshi CG, Koringa PG 3 Biotech 03-Jan-2023
PMCID:PMC9810775
doi:10.1007/s13205-022-03452-4
PMID:36619823
Huanglongbing Pandemic: Current Challenges and Emerging Management Strategies Ghosh D, Kokane S, Savita BK, Kumar P, Sharma AK, Ozcan A, Kokane A, Santra S Plants (Basel) 29-Dec-2022
PMCID:PMC9824665
doi:10.3390/plants12010160
PMID:36616289
Leonotis nepetifolia Flower Bud Extract Mediated Green Synthesis of Silver Nanoparticles, Their Characterization, and In Vitro Evaluation of Biological Applications Nagaraja SK, Niazi SK, Bepari A, Assiri RA, Nayaka S Materials (Basel) 16-Dec-2022
PMCID:PMC9781718
doi:10.3390/ma15248990
PMID:36556796

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3-Methoxysalicylic acid 70140 Click to see 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic Acid 19 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron phenoxide 20488062 Click to see 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1016/0040-4020(68)88069-X
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/0040-4020(68)88069-X
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/0040-4020(68)88069-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Hexacosanoic Acid 10469 Click to see 396.70 unknown via CMAUP database
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1016/0040-4020(68)88069-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-2-ol 13996029 Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C 286.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(2R)-3-[(1R,2S,4aS,4bR,6aR,10aR,10bS,12aS)-2-ethyl-2,4b,6a,9,9,10b,12a-heptamethyl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysen-1-yl]-2-hydroxypropanoic acid 163083021 Click to see 460.70 unknown https://doi.org/10.1016/S0031-9422(00)90767-2
(3R,4R,4aS,8aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydronaphthalen-1-one 101717490 Click to see 318.40 unknown via CMAUP database
3-(2-Ethyl-2,4b,6a,9,9,10b,12a-heptamethyl-1,3,4,4a,5,6,7,8,10,10a,11,12-dodecahydrochrysen-1-yl)-2-hydroxypropanoic acid 12314770 Click to see 460.70 unknown https://doi.org/10.1016/S0031-9422(00)90767-2
Rotundifuran 9841926 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown via CMAUP database
Vitetrifolin B 15543011 Click to see 362.50 unknown via CMAUP database
Vitetrifolin C 15543012 Click to see 360.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate 93317 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(+)-gamma-Tocopherol 92729 Click to see 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone 92785 Click to see 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4AS,7S,7aS)-7-hydroxy-7-methyl-1-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(((4-hydroxybenzoyl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 23955877 Click to see 496.50 unknown via CMAUP database
CID 51346123 51346123 Click to see 466.40 unknown via CMAUP database
Mussaenosidic acid 21633105 Click to see 376.36 unknown via CMAUP database
Negundoside 9935561 Click to see 496.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1R,3R,4R,4aS,8aS)-4-hydroxy-3,4a,8,8-tetramethyl-4-[2-(5-oxo-2H-furan-4-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 10022565 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
3-[2-[(1R,2R,4aS,8aS)-1-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-2H-naphthalen-1-yl]ethyl]-2H-furan-5-one 102105798 Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C 320.50 unknown via CMAUP database
Previtexilactone 21636179 Click to see 378.50 unknown via CMAUP database
Vitexilactone 21636178 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(3R,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bR)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,3,4,5,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-6-one 101289699 Click to see CC1C(CCC2C1(CC(=O)C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown https://doi.org/10.1016/0040-4020(68)88069-X
3Alpha-Hydroxyurs-12-En-28-Oic Acid 7163177 Click to see 456.70 unknown via CMAUP database
7-Oxofriedelin 21596176 Click to see 440.70 unknown https://doi.org/10.1016/0040-4020(68)88069-X
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Corosolic Acid 6918774 Click to see 472.70 unknown via CMAUP database
D:A-Friedooleanan-7-one, 3-hydroxy- 634603 Click to see CC1C(CCC2C1(CC(=O)C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown https://doi.org/10.1016/0040-4020(68)88069-X
D:A-Friedooleanane-3,7-dione 634915 Click to see 440.70 unknown https://doi.org/10.1016/0040-4020(68)88069-X
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1016/0040-4020(68)88069-X
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/0040-4020(68)88069-X
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/0040-4020(68)88069-X
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/0040-4020(68)88069-X
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(2E)-2-[(4aS,5R,7R,8R,8aS)-5-acetyloxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,5'-oxolane]-2'-ylidene]acetic acid 101357917 Click to see 364.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2,6-Dimethoxy-4-((1E)-3-methoxy-1-propen-1-yl)phenyl beta-D-glucopyranoside 15108321 Click to see 386.40 unknown via CMAUP database
Syringin 5316860 Click to see 372.40 unknown https://doi.org/10.1055/S-2006-959587
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Iso-ambreinolide 15559824 Click to see 264.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1 11208535 Click to see CC1CCC2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C 290.40 unknown via CMAUP database
Vitex norditerpenoid 2 11462191 Click to see 348.50 unknown via CMAUP database
> Organosulfur compounds / Thioureas
[(2S)-2-methylbutyl]thiourea 55289558 Click to see CCC(C)CNC(=S)N 146.26 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-0936
[(2S)-butan-2-yl]thiourea 2432029 Click to see CCC(C)NC(=S)N 132.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-0936
2-Methylbutylthiourea 14205305 Click to see CCC(C)CNC(=S)N 146.26 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-0936
sec-Butyl-thiourea 3346206 Click to see 132.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-0936
Urea, 1-isopropyl-2-thio- 1711921 Click to see 118.20 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.16-0936
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Podocarpusflavone B 5320646 Click to see 566.50 unknown https://doi.org/10.1016/S0031-9422(00)97280-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Bonanzin 5379563 Click to see 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
Chrysosplenol D 5280699 Click to see 360.30 unknown via CMAUP database

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