Podocarpus neriifolius - Unknown
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Internal ID UUID64400291b6de5874137257
Scientific name Podocarpus neriifolius
Authority D.Don
First published in Descr. Pinus 2: 21 (1824)

Description Top

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Podocarpus neriifolius is a conifer species that typically grows between 10-15m tall in tropical and subtropical wet forests at altitudes of 650m to 1600m. In Cambodia, it grows in a dwarf form of 2-4m tall at an elevation of 1000m. This species can be found in various countries such as India, Bangladesh, Nepal, China, Myanmar, Thailand, Laos, Cambodia, Vietnam, Malaysia, Indonesia, Brunei, the Philippines, Papua New Guinea, Solomon Islands, Fiji, and Bhutan. In Khmer, it is known as "srô:l" and has a yellowish wood that is commonly used in construction, graded as a 2nd category wood.

Synonyms Top

Scientific name Authority First published in
Nageia neriifolia Kuntze Revis. Gen. Pl. 2: 800 (1891)
Nageia endlicheriana Kuntze Revis. Gen. Pl. 2: 800 (1891)
Margbensonia neriifolia (D.Don) A.V.Bobrov & Melikyan Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 103(1): 60 (1998)
Podocarpus endlicherianus Carrière Traité Gén. Conif. : 468 (1855)
Podocarpus neriifolius var. staintonii Silba J. Int. Conifer Preserv. Soc. 7: 36 (2000)
Podocarpus polyanthus (Wasscher) Gaussen Trav. Lab. Forest. Toulouse 1(1, 1(2))21: 212 (1976)
Podocarpus macrophyllus var. acuminatissimus E.Pritz. Bot. Jahrb. Syst. 29: 213. 1900
Podocarpus neriifolius var. linearis Wasscher Blumea 4: 452. 1941
Podocarpus neriifolius var. membranaceus Wasscher Blumea 4: 450. 1941
Podocarpus neriifolius var. polyanthus Wasscher Blumea 4: 455. 1941
Podocarpus neriifolius subsp. staintonii (Silba) Silba J. Int. Conifer Preserv. Soc. 17: 16 (2010)
Podocarpus annamiensis var. hainanensis Gaussen Trav. Lab. Forest. Toulouse 1(1, 1(2))21: 210 (1976)

Common names Top

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Language Common/alternative name
English brown pine
Bulgarian зокумолистен подокарпус
Bengali বাঁশপাতি
Catalan podocarp
Indonesian ki putri
Burmese သစ်မင်းဖိုပင်
Burmese သစ်မင်းဖို
Burmese သစ်မင်း
Nepali गुन्सी
Thai พญาไม้
Chinese 脉叶罗汉松
Chinese 缨珞柏
Chinese 竹柏松
Chinese 桃柏松
Chinese 大叶竹柏松
Chinese 鸡毛松
Chinese 竹叶松
Chinese 百日青
Chinese 竹柏根
Chinese 油松
Chinese 白松

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
      • Nepal
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000485162
UNII A1HKS2R89E
USDA Plants PONE21
Tropicos 25600056
KEW urn:lsid:ipni.org:names:263545-1
The Plant List kew-2567549
Open Tree Of Life 203268
NCBI Taxonomy 61307
IUCN Red List 42521
IPNI 263545-1
iNaturalist 135672
GBIF 5286088
Freebase /m/02vv09l
EPPO PODNE
EOL 1033700
USDA GRIN 29124
Wikipedia Podocarpus_neriifolius

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
Distribution Patterns of Gymnosperm Species along Elevations on the Qinghai–Tibet Plateau: Effects of Climatic Seasonality, Energy–Water, and Physical Tolerance Variables Umair M, Hu X, Cheng Q, Ali S, Ni J Plants (Basel) 04-Dec-2023
PMCID:PMC10708526
doi:10.3390/plants12234066
PMID:38068701
Phytochemical and metabolic profiling of the different Podocarpus species in Egypt: Potential antimicrobial and antiproliferative activities Mohamed NZ, Shaaban L, Safan S, El-Sayed AS Heliyon 09-Sep-2023
PMCID:PMC10559778
doi:10.1016/j.heliyon.2023.e20034
PMID:37810029
Discovery and development of botanical natural products and their analogues as therapeutics for ovarian cancer Mize BK, Salvi A, Ren Y, Burdette JE, Fuchs JR Nat Prod Rep 19-Jul-2023
PMCID:PMC10448539
doi:10.1039/d2np00091a
PMID:37387219
Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S Pharmaceuticals (Basel) 15-Jun-2023
PMCID:PMC10302623
doi:10.3390/ph16060881
PMID:37375828
Diversity, Distribution, Systematics and Conservation Status of Podocarpaceae Khan R, Hill RS, Liu J, Biffin E Plants (Basel) 03-Mar-2023
PMCID:PMC10005643
doi:10.3390/plants12051171
PMID:36904033
Assessment of ITS2 Region Relevance for Taxa Discrimination and Phylogenetic Inference among Pinaceae Sokołowska J, Fuchs H, Celiński K Plants (Basel) 15-Apr-2022
PMCID:PMC9029031
doi:10.3390/plants11081078
PMID:35448806
Assessing the effectiveness of community managed forests for plant diversity conservation in Meghalaya, Northeast India Mir AH, Sarma K, Upadhaya K Plant Divers 15-Dec-2021
PMCID:PMC9209898
doi:10.1016/j.pld.2021.11.010
PMID:35769587
Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM Plants (Basel) 04-Jul-2021
PMCID:PMC8309379
doi:10.3390/plants10071367
PMID:34371570
A computer-aided method for identifying the presence of softwood growth ring boundaries Lin Q, He T, Sun Y, He X, Qiu J PLoS One 18-Sep-2020
PMCID:PMC7500654
doi:10.1371/journal.pone.0235727
PMID:32946443
The tropical-subtropical evergreen forest transition in East Asia: An exploration Ashton P, Zhu H Plant Divers 25-May-2020
PMCID:PMC7567766
doi:10.1016/j.pld.2020.04.001
PMID:33094198
Bioactivity-Guided Isolation of Totarane-Derived Diterpenes from Podocarpus neriifolius and Structure Revision of 3-Deoxy-2α-hydroxynagilactone E Benatrehina PA, Chen WL, Czarnecki AA, Kurina S, Chai HB, Lantvit DD, Ninh TN, Zhang X, Soejarto DD, Burdette JE, Kinghorn AD, Rakotondraibe LH Nat Prod Bioprospect 19-Feb-2019
PMCID:PMC6426912
doi:10.1007/s13659-019-0198-x
PMID:30783922
The Repeat Sequences and Elevated Substitution Rates of the Chloroplast accD Gene in Cupressophytes Li J, Su Y, Wang T Front Plant Sci 20-Apr-2018
PMCID:PMC5920036
doi:10.3389/fpls.2018.00533
PMID:29731764
A Multiscale Vibrational Spectroscopic Approach for Identification and Biochemical Characterization of Pollen Bağcıoğlu M, Zimmermann B, Kohler A PLoS One 16-Sep-2015
PMCID:PMC4574200
doi:10.1371/journal.pone.0137899
PMID:26376486
Antimicrobial activity, toxicity and selectivity index of two biflavonoids and a flavone isolated from Podocarpus henkelii (Podocarpaceae) leaves Bagla VP, McGaw LJ, Elgorashi EE, Eloff JN BMC Complement Altern Med 08-Oct-2014
PMCID:PMC4197215
doi:10.1186/1472-6882-14-383
PMID:25293523
Effects of Competition and Facilitation on Species Assemblage in Two Types of Tropical Cloud Forest Long W, Zang R, Ding Y, Huang Y PLoS One 02-Apr-2013
PMCID:PMC3615009
doi:10.1371/journal.pone.0060252
PMID:23565209

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
4b,8,8-Trimethyl-3-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-2-ol 12442760 Click to see CC(C)C1=C(C=C2CCC3C(CCCC3(C2=C1)C)(C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
4beta-Carboxy-19-nortotarol 15694359 Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C(=O)O)C)O 316.40 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
6-(8-Carboxy-2-hydroxy-4b,8-dimethyl-1-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl)-7-hydroxy-1,4a-dimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 12312651 Click to see CC(C)C1=C(C(=CC2=C1CCC3C2(CCCC3(C)C(=O)O)C)C4=CC5=C(CCC6C5(CCCC6(C)C(=O)O)C)C(=C4O)C(C)C)O 630.90 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
7-(1,3-Dihydroxypropan-2-yl)-6-hydroxy-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid 20056646 Click to see CC12CCCC(C1CCC3=CC(=C(C=C23)O)C(CO)CO)(C)C(=O)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
Pododacric acid 20055005 Click to see CC12CCCC(C1CCC3=CC(=C(C=C23)O)C(CO)CO)(C)C(=O)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
Sempervirol 12442761 Click to see CC(C)C1=C(C=C2CCC3C(CCCC3(C2=C1)C)(C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(00)80328-3
> Organoheterocyclic compounds / Naphthopyrans
(1S,2R,4R,5R,10S,11R,13S,14R,15R,18R)-5-ethenyl-14-hydroxy-10,15-dimethyl-3,6,12,17-tetraoxahexacyclo[8.7.1.02,4.04,9.011,13.015,18]octadec-8-ene-7,16-dione 101593067 Click to see CC12C3C(C4C5(O4)C(OC(=O)C=C5C3(C6C(C1O)O6)C)C=C)OC2=O 346.30 unknown https://doi.org/10.1007/BF01928670
(1S,2R,4S,5R,10S,11S,13R,14R,15R,18R)-5-[(2R)-1,2-dihydroxypropan-2-yl]-14-hydroxy-10,15-dimethyl-3,6,12,17-tetraoxahexacyclo[8.7.1.02,4.04,9.011,13.015,18]octadec-8-ene-7,16-dione 162869050 Click to see CC12C3C(C4C5(O4)C(OC(=O)C=C5C3(C6C(C1O)O6)C)C(C)(CO)O)OC2=O 394.40 unknown https://doi.org/10.1021/JO00876A023
(1S,2R,4S,5R,10S,11S,13R,14R,18R)-5-[(2R)-1,2-dihydroxypropan-2-yl]-14-hydroxy-10,15-dimethyl-3,6,12,17-tetraoxahexacyclo[8.7.1.02,4.04,9.011,13.015,18]octadec-8-ene-7,16-dione 163194234 Click to see CC12C3C(C4C5(O4)C(OC(=O)C=C5C3(C6C(C1O)O6)C)C(C)(CO)O)OC2=O 394.40 unknown https://doi.org/10.1021/JO00876A023
(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2S)-1,2-dihydroxypropan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.02,4.04,9.012,14.015,18]octadec-8-ene-7,16-dione 101289543 Click to see CC12CC3C(O3)C4(C1C(C5C6(C2=CC(=O)OC6C(C)(CO)O)O5)OC4=O)C 378.40 unknown https://doi.org/10.1021/JO00876A023
(1S,2R,4S,5R,10S,12S,14R,15R,18R)-5-[(2S)-2-hydroxy-1-[(S)-methylsulfinyl]propan-2-yl]-10,15-dimethyl-3,6,13,17-tetraoxahexacyclo[8.7.1.02,4.04,9.012,14.015,18]octadec-8-ene-7,16-dione 162913226 Click to see CC12CC3C(O3)C4(C1C(C5C6(C2=CC(=O)OC6C(C)(CS(=O)C)O)O5)OC4=O)C 424.50 unknown https://doi.org/10.1021/JO00876A023
(1S,2R,4S,5R,10S,14R,17R)-5-[(2S)-2-hydroxy-1-[(R)-methylsulfinyl]propan-2-yl]-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione 162869487 Click to see CC12CC=CC3(C1C(C4C5(C2=CC(=O)OC5C(C)(CS(=O)C)O)O4)OC3=O)C 408.50 unknown https://doi.org/10.1021/JO00876A023
(1S,2R,4S,5R,14R,17R)-5-[(2S)-2-hydroxy-1-[(R)-methylsulfinyl]propan-2-yl]-10,14-dimethyl-3,6,16-trioxapentacyclo[8.6.1.02,4.04,9.014,17]heptadeca-8,12-diene-7,15-dione 163194215 Click to see CC12CC=CC3(C1C(C4C5(C2=CC(=O)OC5C(C)(CS(=O)C)O)O4)OC3=O)C 408.50 unknown https://doi.org/10.1021/JO00876A023
(1S,2R,4S,5R,6R,9S,12R,17R)-12-ethenyl-5-hydroxy-1,6-dimethyl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-10,15-diene-7,14-dione 163011375 Click to see CC12C3C(C=C4C(OC(=O)C=C4C3(C5C(C1O)O5)C)C=C)OC2=O 330.30 unknown https://doi.org/10.1007/BF01928670
(1S,2S,4R,5R,6R,9S,12R,17R)-12-ethenyl-5-hydroxy-1,6-dimethyl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-10,15-diene-7,14-dione 163011376 Click to see CC12C3C(C=C4C(OC(=O)C=C4C3(C5C(C1O)O5)C)C=C)OC2=O 330.30 unknown https://doi.org/10.1021/JO00876A023
(1S,2S,4R,5R,9S,12R,17R)-12-ethenyl-5-hydroxy-1,6-dimethyl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-10,15-diene-7,14-dione 163190176 Click to see CC12C3C(C=C4C(OC(=O)C=C4C3(C5C(C1O)O5)C)C=C)OC2=O 330.30 unknown https://doi.org/10.1021/JO00876A023
12-Ethenyl-5-hydroxy-1,6-dimethyl-3,8,13-trioxapentacyclo[7.7.1.02,4.06,17.011,16]heptadeca-10,15-diene-7,14-dione 75049146 Click to see CC12C3C(C=C4C(OC(=O)C=C4C3(C5C(C1O)O5)C)C=C)OC2=O 330.30 unknown https://doi.org/10.1007/BF01928670
5-Ethenyl-14-hydroxy-10,15-dimethyl-3,6,12,17-tetraoxahexacyclo[8.7.1.02,4.04,9.011,13.015,18]octadec-8-ene-7,16-dione 186146 Click to see CC12C3C(C4C5(O4)C(OC(=O)C=C5C3(C6C(C1O)O6)C)C=C)OC2=O 346.30 unknown https://doi.org/10.1007/BF01928670
Podolactone B 442078 Click to see CC12C3C(C4C5(O4)C(OC(=O)C=C5C3(C6C(C1O)O6)C)C(C)(CO)O)OC2=O 394.40 unknown https://doi.org/10.1021/JO00876A023
Podolactone C 336287 Click to see CC12CC3C(O3)C4(C1C(C5C6(C2=CC(=O)OC6C(C)(CS(=O)C)O)O5)OC4=O)C 424.50 unknown https://doi.org/10.1021/JO00876A023
Podolactone E 3084650 Click to see CC12C3CC(=O)OC(C3=CC4C1C(C(C5C2O5)O)(C(=O)O4)C)C=C 332.30 unknown https://doi.org/10.1021/JO00876A023

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