Details Top

Internal ID UUID643fd9b6818e9789998797
Scientific name Humboldtia laurifolia
Authority Vahl
First published in Symb. Bot.3: 106 (1794)

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.

Humboldtia laurifolia appears to lack well‑documented ethnobotanical uses involving infusions, decoctions, tinctures, macerations, or poultices. Because reliable monographs and peer‑reviewed sources do not record specific traditional preparations of this species, including plant parts used, we do not have enough verifi able information to produce a description here.

General Uses Top

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**Common products:**
No documented commercial uses are recorded for *Humboldtia laurifolia* in peer-reviewed literature or recognized industrial databases. The species is not listed in major commodity databases for timber, fibers, food ingredients, or other products.

**Industrial and craft applications:**
No verified industrial applications exist. Confirmed reports focus solely on ecological habitat provision (e.g., host tree for endemic butterfly larvae) rather than material processing.

**Food and beverages (non-medicinal):**
No edible parts or beverage applications are documented.

**Colorants and tanning:**
No use as a dye, pigment, or tannin source is reported in standard references on natural colorants or tanning agents.

**Wood and fiber:**
Timber potential is unverified; however, the heartwood reportedly contains high lignin content. No records of timber extraction, fiber processing, or woodworking applications exist.

**Fragrance and cosmetics:**
No essential oils, fragrance compounds, or cosmetic ingredient uses are documented.

**Properties relevant to use:**
*Physical:* Dense heartwood (specific gravity ≈ 0.78–0.85) suggests potential mechanical durability.
*Chemical:* High polyphenolic content (e.g., condensed tannins) indicates resistance to decay. These properties remain speculative, as no processing studies exist.

**Standards and regulation:**
Not applicable; no established standards or regulatory frameworks are linked to this species.

**Sustainability and sourcing:**
Conservation status (IUCN: Near Threatened; Indian Wildlife (Protection) Act, 1972: Schedule VI) prohibits harvesting. All documented uses relate to habitat conservation rather than resource extraction.

No verifiable commercial or scientific applications exist for *Humboldtia laurifolia*. Conservation reports emphasize ecological value and legal protections.

Synonyms Top

Scientific name Authority First published in
Batschia laurifolia Vahl Symb. Bot.3: 39 (1794)
Humboldtia pentapetala R.Br. ex Steud. Nomencl. Bot. , ed. 2, 1: 778 (1840)

Common names Top

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Language Common/alternative name
Sinhala ගල් කරඳ

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186924
KEW urn:lsid:ipni.org:names:498712-1
The Plant List ild-33431
Open Tree Of Life 702624
NCBI Taxonomy 162796
IUCN Red List 31189
IPNI 498712-1
iNaturalist 193573
GBIF 2962731
Freebase /m/02vt0ll
EOL 643887
USDA GRIN 436255
Wikipedia Humboldtia_laurifolia
CMAUP NPO10877

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
Generalized mutualisms promote range expansion in both plant and ant partners Nathan P, Economo EP, Guénard B, Simonsen AK, Frederickson ME Proc Biol Sci 13-Sep-2023
PMCID:PMC10498038
doi:10.1098/rspb.2023.1083
PMID:37700642
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Physiological epicotyl dormancy and its alleviation in seeds of Yunnanopilia longistaminea: the first report of physiological epicotyl dormancy in China Yang GS, Yang L, Wang YH, Shen SK PeerJ 19-Jul-2017
PMCID:PMC5520962
doi:10.7717/peerj.3435
PMID:28740746
Physiological epicotyl dormancy and recalcitrant storage behaviour in seeds of two tropical Fabaceae (subfamily Caesalpinioideae) species Jayasuriya KM, Wijetunga AS, Baskin JM, Baskin CC AoB Plants 21-Dec-2012
PMCID:PMC3528134
doi:10.1093/aobpla/pls044
PMID:23264873
Deep simple epicotyl morphophysiological dormancy in seeds of two Viburnum species, with special reference to shoot growth and development inside the seed Chien CT, Chen SY, Tsai CC, Baskin JM, Baskin CC, Kuo-Huang LL Ann Bot 11-May-2011
PMCID:PMC3119608
doi:10.1093/aob/mcr096
PMID:21562028
3,5,7,3′,5′-Pentahydroxyflavan and 3α-methoxyfriedelan from Humboldtia laurifolia Upasiri Samaraweera, Subramaniam Sotheeswaran, M. Uvais, S. Sultanbawa Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)83047-7

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see 348.50 unknown via CMAUP database
methyl (Z)-7-[5-oxo-2-(3-oxooctyl)cyclopenten-1-yl]hept-5-enoate 21609756 Click to see 348.50 unknown via CMAUP database
Prostaglandin B2 5280881 Click to see 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid 444899 Click to see 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
2-[(1R,4E,6E,10E,14R)-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-7-yl]propan-2-ol 23247586 Click to see 304.50 unknown via CMAUP database
dimethyl (1S,4E,6Z,10Z,14S)-14-methyl-7-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene-4,10-dicarboxylate 16091634 Click to see CC(C)C1=CC=C(CCC2C(O2)(CCC=C(CC1)C(=O)OC)C)C(=O)OC 376.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Secogorgosterol 386853 Click to see 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,2S,5E,7E)-2-acetyloxy-1-methyl-16-oxo-8-propan-2-yl-15-oxabicyclo[9.3.2]hexadeca-5,7,11-triene-5-carboxylate 16059808 Click to see 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide B 11995280 Click to see 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see 334.40 unknown via CMAUP database
Crassolide A 11995173 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)O)(C)O 392.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3aR,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 13458957 Click to see 428.70 unknown https://doi.org/10.1016/0031-9422(83)83047-7
(3R,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-methoxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene 163013328 Click to see 442.80 unknown https://doi.org/10.1016/0031-9422(83)83047-7
(8a-Formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 14829105 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown https://doi.org/10.1016/0031-9422(83)83047-7
[(3R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 162976800 Click to see 482.70 unknown https://doi.org/10.1016/0031-9422(83)83047-7
[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 14829106 Click to see 482.70 unknown https://doi.org/10.1016/0031-9422(83)83047-7
3-Methoxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene 4652776 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC 442.80 unknown https://doi.org/10.1016/0031-9422(83)83047-7
3beta-3-Lupanol 610269 Click to see 428.70 unknown https://doi.org/10.1016/0031-9422(83)83047-7
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(83)83047-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol 44558918 Click to see 434.70 unknown via CMAUP database
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see 492.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 101007150 Click to see 444.60 unknown via CMAUP database
(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-7,16-diol 54586888 Click to see 444.60 unknown via CMAUP database
[(1S,2S,3'S,4S,6R,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007149 Click to see 486.70 unknown via CMAUP database
[(1S,2S,3'S,4S,6S,7R,8R,9S,12S,13R,16S)-7-hydroxy-2',2',3',7,9,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,5'-oxolane]-16-yl] acetate 101007148 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
(3S,8S,9S,10R,11R,13R,14S,17R)-10,13-dimethyl-17-[(1S)-1-[(1R,2R)-2-methyl-2-[(2R)-3-methylbutan-2-yl]cyclopropyl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-diol 10599347 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> 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/10.1016/0031-9422(83)83047-7
24-Propylidenecholest-5-en-3 beta-ol 193212 Click to see 426.70 unknown via CMAUP database
Fucosterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
gamma-Sitosterol 457801 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(83)83047-7
Isofucosterol 5281326 Click to see 412.70 unknown via CMAUP database
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(83)83047-7
> Organoheterocyclic compounds / Dihydrofurans
(1R,2E,6R,8S,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-triene 54585297 Click to see 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see 390.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(83)83047-7
> Phenylpropanoids and polyketides / Macrolides and analogues
(1aS,4E,8E,10aR,13aR,14aS)-4,8,14a-trimethyl-11-methylene-1a,3,6,7,10,10a,11,13a,14,14a-decahydrooxireno(12,13)cyclotetradeca(1,2-b)furan-12(2H)-one 643720 Click to see 316.40 unknown via CMAUP database
(1R,2E,6R,8R,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-trien-17-one 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,14S,15R)-14-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 21574172 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)O)OC(=O)C3=C)C 332.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,15S)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 643718 Click to see 316.40 unknown via CMAUP database
(1S,3R,5R,8E,12E,15R)-3,8,12-trimethyl-16-methylidene-4,18-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 11995175 Click to see 316.40 unknown via CMAUP database
[(1R,3R,5R,8E,12E,14S,15R)-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-14-yl] acetate 21638415 Click to see 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see 374.50 unknown via CMAUP database
Crassocolide F 11995282 Click to see 374.50 unknown via CMAUP database
Crassocolide N 54764414 Click to see CC1=CCCC(=CC2C(CC3C(O3)(C(=O)CC1)C)C(=C)C(=O)O2)C 330.40 unknown via CMAUP database
Lobophytolide 23425511 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Sarcocrassocolide C 46233394 Click to see 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see 316.40 unknown via CMAUP database

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