Symplocos racemosa - Unknown
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Internal ID UUID64404f1fbc1d7472600314
Scientific name Symplocos racemosa
Authority Roxb.
First published in Fl. Ind. (Roxburgh) 2: 539. 1832

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Synonyms Top

Scientific name Authority First published in
Lodhra hamiltoniana Miers J. Linn. Soc., Bot. 17: 299 (1879)
Lodhra racemosa (Roxb.) Miers J. Linn. Soc., Bot. 17: 298 (1879)
Lodhra nervosa Miers J. Linn. Soc., Bot. 17: 299 (1879)
Symplocos nicobarica C.B.Clarke Fl. Brit. India 3: 580 (1882)
Symplocos orogenes Brand Pflanzenr. , IV, 242: 42 (1901)
Symplocos stocksii Brand Pflanzenr. , IV, 242: 59 (1901)
Symplocos petelotii Merr. Univ. Calif. Publ. Bot. 10: 429 (1924)
Symplocos beddomei C.B.Clarke Fl. Brit. India 3: 582 (1882)
Symplocos impressa H.R.Fletcher Bull. Misc. Inform. Kew 1937: 505 (1937)
Symplocos hamiltoniana Wall. & G.Don Gen. Hist. 4: 3 (1837)
Dicalix propinquus (Hance) Migo Bull. Shanghai Sci. Inst. 13: 204 (1943)
Eugenioides nicobaricum Kuntze Revis. Gen. Pl. 2: 975. 1891 [5 Nov 1891]
Hopea racemosa Dalzell & A.Gibson Bombay Fl. [Dalzell & Gibson] 140. 1861
Symplocos propinqua Hance J. Bot. 6: 329 (1868)
Symplocos macrostachya Brand Pflanzenr. , IV, 242: 36 (1901)
Symplocos macrostachya var. leducii Brand Repert. Spec. Nov. Regni Veg. 3(40–41): 217 1906
Symplocos intermedia Brand Repert. Spec. Nov. Regni Veg. 3: 217 (1906)
Symplocos intermedia var. trichantha Hand.-Mazz. Sinensia 5(1–2): 5–6 1934

Common names Top

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Language Common/alternative name
Arabic لطر
Arabic ارماك
Malayalam പൊടിപാടി
Malayalam പൊടിപാറി
Chinese 白檀
Chinese 珠仔树
Chinese 总序山矾

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Symplocos racemosa var. palauensis (Koidz.) Noot. Leiden Bot. Ser. 1: 274 (1975)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001141780
UNII O924S8B4SA
Tropicos 30900416
KEW urn:lsid:ipni.org:names:827266-1
The Plant List tro-30900416
Open Tree Of Life 5507837
NCBI Taxonomy 1340885
IPNI 827266-1
iNaturalist 602317
GBIF 7318861
USDA GRIN 432000

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
Plant-Origin Components: New Players to Combat Antibiotic Resistance in Klebsiella pneumoniae Luna-Pineda VM, Rodríguez-Martínez G, Salazar-García M, Romo-Castillo M Int J Mol Sci 10-Feb-2024
PMCID:PMC10888558
doi:10.3390/ijms25042134
PMID:38396811
Effects of natural products on polycystic ovary syndrome: From traditional medicine to modern drug discovery Jung W, Choi H, Kim J, Kim J, Kim W, Nurkolis F, Kim B Heliyon 11-Oct-2023
PMCID:PMC10589870
doi:10.1016/j.heliyon.2023.e20889
PMID:37867816
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
Contrasting sap flow characteristics between pioneer and late-successional tree species in secondary tropical montane forests of Eastern Himalaya, India Kumar M, Joseph G, Bhutia Y, Krishnaswamy J J Exp Bot 08-Jun-2023
PMCID:PMC10498023
doi:10.1093/jxb/erad207
PMID:37290031
Wound healing potential of Vakeri fortified KampillakadiTaila Dhawal PP, Gharpure M, Joshi MS, Khan RR, Barve SS J Ayurveda Integr Med 26-May-2023
PMCID:PMC10236188
doi:10.1016/j.jaim.2023.100721
PMID:37245340
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Preclinical evidence of polyherbal formulations on wound healing: A systematic review on research trends and perspectives Dubey S, Dixit AK J Ayurveda Integr Med 24-Feb-2023
PMCID:PMC9988554
doi:10.1016/j.jaim.2023.100688
PMID:36841194
An integrated management (Ayurveda and Modern medicine) of accidental burn injury: A case study Shindhe PS, K P, Killedar RS, Prasannan D, A K J Ayurveda Integr Med 24-Feb-2023
PMCID:PMC9988564
doi:10.1016/j.jaim.2023.100691
PMID:36841195
No ambiguity: Chemosensory-based ayurvedic classification of medicinal plants can be fingerprinted using E-tongue coupled with multivariate statistical analysis Jayasundar R, Ghatak S, Kumar D, Singh A, Bhosle P Front Pharmacol 02-Dec-2022
PMCID:PMC9755338
doi:10.3389/fphar.2022.1025591
PMID:36532778
Plants as Modulators of Melanogenesis: Role of Extracts, Pure Compounds and Patented Compositions in Therapy of Pigmentation Disorders Merecz-Sadowska A, Sitarek P, Stelmach J, Zajdel K, Kucharska E, Zajdel R Int J Mol Sci 26-Nov-2022
PMCID:PMC9736547
doi:10.3390/ijms232314787
PMID:36499134
Quinones as an Efficient Molecular Scaffold in the Antibacterial/Antifungal or Antitumoral Arsenal Dahlem Junior MA, Nguema Edzang RW, Catto AL, Raimundo JM Int J Mol Sci 15-Nov-2022
PMCID:PMC9697455
doi:10.3390/ijms232214108
PMID:36430585
“Wound healing activity of topical herbal aerosol sprays on diabetic and Varicose Ulcers: A randomized, controlled, open labelled, multi-centric clinical trial" Tamoli S, Ukhalkar V, Acharya GS, Gajre K, Pathak S, Pande S, Solanki Y, Jadhav R, Quadri MJ, Koli N J Ayurveda Integr Med 19-Jul-2022
PMCID:PMC9307666
doi:10.1016/j.jaim.2022.100594
PMID:35868135
Effect of an Ayurveda antidote Dooshivishari Agada in carboplatin induced myelosuppression in Male Wistar rats Patil SF, Shahapurkar VV, Khanal P J Ayurveda Integr Med 18-Jul-2022
PMCID:PMC9304609
doi:10.1016/j.jaim.2022.100599
PMID:35863084
Plant-Derived Toxin Inhibitors as Potential Candidates to Complement Antivenom Treatment in Snakebite Envenomations Adrião AA, dos Santos AO, de Lima EJ, Maciel JB, Paz WH, da Silva FM, Pucca MB, Moura-da-Silva AM, Monteiro WM, Sartim MA, Koolen HH Front Immunol 09-May-2022
PMCID:PMC9126284
doi:10.3389/fimmu.2022.842576
PMID:35615352
Herbal medicine AnoSpray suppresses proinflammatory cytokines COX-2 and RANTES in the management of hemorrhoids, acute anal fissures and perineal wounds Porwal A, Kundu GC, Bhagwat G, Butti R Exp Ther Med 25-Nov-2021
PMCID:PMC8688930
doi:10.3892/etm.2021.11009
PMID:34938368

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
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-3-(3,4-dihydroxy-5-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-hydroxy-6-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101701120 Click to see COC1=CC(=CC(=C1O)O)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)O 552.50 unknown https://doi.org/10.1002/MRC.1571
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,4aS,6aR,6aS,6bR,8aR,12aR)-1,2,6a,6b,9,9,12a-heptamethyl-10-oxo-2,3,4,5,6,6a,7,8,8a,11,12,13-dodecahydropicene-4a-carboxylic acid 101586330 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2=C1C)C)C(=O)O 452.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
(3S,4aS,6aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,14a-tetradecahydropicen-3-ol 154497735 Click to see CC1(CCC2(CCC3(C(C2C1)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00075-X
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(03)00075-X
(4S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 101586331 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C2C1)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
[(3S,4aR,6aR,6bS,8aS,11S,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,14,14a-dodecahydro-1H-picen-3-yl] acetate 101586329 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2=C1C)C)CO 482.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
[8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,14,14a-dodecahydro-1H-picen-3-yl] acetate 14707571 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2=C1C)C)CO 482.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
3-Oxo-12,18-ursadien-28-oic acid 14707579 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2=C1C)C)C(=O)O 452.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picen-3-one 14707588 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)C2C1)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(03)00075-X
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/0031-9422(90)85284-M
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(03)00075-X
https://doi.org/10.1016/0031-9422(90)85284-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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)00075-X
24-Ethylcholest-5-en-3beta-ol 22012 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)00075-X
Beta-Sitosterol 222284 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)00075-X
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1016/S0031-9422(03)00075-X
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 https://doi.org/10.1016/S0031-9422(03)00075-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Undecyl 3-[4-(3-oxo-3-undecoxypropyl)dithiadiazetidin-3-yl]propanoate 11656828 Click to see CCCCCCCCCCCOC(=O)CCN1N(SS1)CCC(=O)OCCCCCCCCCCC 546.90 unknown https://doi.org/10.3987/COM-05-10417
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Benzoylsalireposide 10369077 Click to see C1=CC=C(C=C1)C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)OC(=O)C4=CC=CC=C4)O 510.50 unknown https://doi.org/10.1016/S0031-9422(03)00075-X
https://doi.org/10.1016/J.FITOTE.2008.05.004
Salireposide 117440 Click to see C1=CC=C(C=C1)C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(03)00075-X
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[4-[(2S,3S,4S,5R,6R)-4-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-methoxyoxan-2-yl]-3,5-dihydroxyphenyl]methyl 4-hydroxy-3,5-dimethoxybenzoate 11679454 Click to see COC1C(C(C(OC1C2=C(C=C(C=C2O)COC(=O)C3=CC(=C(C(=C3)OC)O)OC)O)CO)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O 820.70 unknown https://doi.org/10.1002/CHIN.200629187
[4-[4-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-methoxyoxan-2-yl]-3,5-dihydroxyphenyl]methyl 4-hydroxy-3,5-dimethoxybenzoate 73059617 Click to see COC1C(C(C(OC1C2=C(C=C(C=C2O)COC(=O)C3=CC(=C(C(=C3)OC)O)OC)O)CO)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O 820.70 unknown https://doi.org/10.1002/CHIN.200629187

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