Kalmia latifolia - Unknown
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Details Top

Internal ID UUID643ff3987f6ab829352336
Scientific name Kalmia latifolia
Authority L.
First published in Sp. Pl. : 391 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Kalmia myrtifolia André Rev. Hort. (Paris) 55: 10 (1883)
Kalmia nitida J.Forbes Hort. Woburn. : 93 (1833)
Chamaedaphne latifolia (L.) Kuntze Revis. Gen. Pl. 2: 388 (1891)
Kalmia latifolia f. obtusata (Rehder) Rehder Rhodora 12: 2. 1910
Kalmia latifolia f. alba (Mouill.) Rehder Rhodora 12: 2. 1910
Kalmia latifolia f. polypetala (G.Nicholson) Rehder Rhodora 12: 1. 1910
Kalmia latifolia f. fuscata (Rehder) Rehder Rhodora 12: 2. 1910
Kalmia latifolia var. polypetala G.Nicholson Hand-List Trees Shrubs 2: 49 (1896)
Kalmia latifolia var. obtusata Rehder Möller's Deutsche Gärtn.-Zeitung 18: 577 (1903)
Kalmia latifolia var. fuscata Rehder Möller's Deutsche Gärtn.-Zeitung 18: 578 (1903)
Kalmia latifolia var. alba Mouill.

Common names Top

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Language Common/alternative name
English calico bush
English mountain-laurel
English clamoun
English ivybush
English lambkill
English mountain laurel
English calico-bush
English sheep laurel
English spoonwood
English american laurel
Arabic غار الجبل
Arabic كلمية عريضة الأوراق
Bulgarian американски лавър
Bulgarian планински лавър
Catalan laurier des montagnes
Welsh calmia llydanddail
Danish bredbladet kalmia
German laurier des montagnes
Persian کالمیا لاتیفولیا
Finnish leveälehtikalmia
French laurier des montagnes
French laurier d'amérique
French kalmie
Hebrew קלמיה לאטיפוליה
Croatian gorski lovor
Lithuanian laurier des montagnes
Dutch lepelboom
Polish kalmia szerokolistna
Russian chamaedaphne latifolia
Russian Кальмия широколистная
Swedish laurier des montagnes
Swedish bredbladig kalmia
Chinese 山月桂
Chinese 宽叶山月桂

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Southeastern U.S.A.
      • Alabama
      • Delaware
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000356132
UNII P1SWF7DK1Y
Florida Plant Atlas 3648
Flora of Alabama 1740
Cornell Woody Plants 129
Canadensys 5530
USDA Plants KALA
UConn 236
Tropicos 12300612
KEW urn:lsid:ipni.org:names:279164-2
The Plant List kew-2333573
Missouri Botanical Garden 279967
PFAF Kalmia latifolia
Open Tree Of Life 743767
NCBI Taxonomy 45902
NBN Atlas NHMSYS0100001861
Nature Serve 2.159823
IUCN Red List 62002834
IPNI 279164-2
iNaturalist 49397
GBIF 2883005
Freebase /m/04bxc
FEIS plants/shrub/kallat
EPPO KAMLA
EOL 595778
Elurikkus 5323
USDA GRIN 21115
Wikipedia Kalmia_latifolia
CMAUP NPO19198

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
Bat activity is related to habitat structure and time since prescribed fire in managed pine barrens in New England Kay N, Sadlon A, Bakermans MH PeerJ 12-Sep-2023
PMCID:PMC10503498
doi:10.7717/peerj.15888
PMID:37719121
White-tailed deer (Odocoileus virginianus) fawn survival and the influence of landscape characteristics on fawn predation risk in the Southern Appalachian Mountains, USA Edge AC, Rosenberger JP, Yates CJ, Little AR, Killmaster CH, Johannsen KL, Osborn DA, Kilgo JC, Miller KV, D’Angelo GJ PLoS One 31-Aug-2023
PMCID:PMC10470973
doi:10.1371/journal.pone.0288449
PMID:37651350
Camera Trap Methods and Drone Thermal Surveillance Provide Reliable, Comparable Density Estimates of Large, Free-Ranging Ungulates Baldwin RW, Beaver JT, Messinger M, Muday J, Windsor M, Larsen GD, Silman MR, Anderson TM Animals (Basel) 05-Jun-2023
PMCID:PMC10252056
doi:10.3390/ani13111884
PMID:37889800
Spatial Ecology, Movements, and Habitat Selection of Clemmys guttata in a Temporally Dynamic Wetland System in North Carolina, USA Roe JH Herpetol Conserv Biol 30-Apr-2023
PMCID:PMC10655762
PMID:37981954
Current Scenario and Future Prospects of Endophytic Microbes: Promising Candidates for Abiotic and Biotic Stress Management for Agricultural and Environmental Sustainability Anand U, Pal T, Yadav N, Singh VK, Tripathi V, Choudhary KK, Shukla AK, Sunita K, Kumar A, Bontempi E, Ma Y, Kolton M, Singh AK Microb Ecol 14-Mar-2023
PMCID:PMC10497456
doi:10.1007/s00248-023-02190-1
PMID:36917283
Risks for human health related to the presence of grayanotoxins in certain honey Schrenk D, Bignami M, Bodin L, Chipman JK, del Mazo J, Grasl‐Kraupp B, Hogstrand C, Hoogenboom L(, Leblanc J, Nebbia CS, Nielsen E, Ntzani E, Petersen A, Sand S, Schwerdtle T, Vleminckx C, Dusemund B, Hart A, Mulder P, Viviani B, Anastassiadou M, Cascio C, Riolo F, Wallace H EFSA J 02-Mar-2023
PMCID:PMC9978999
doi:10.2903/j.efsa.2023.7866
PMID:36875862
Climate‐mediated population dynamics of a migratory songbird differ between the trailing edge and range core Lewis WB, Cooper RJ, Chandler RB, Chitwood RW, Cline MH, Hallworth MT, Hatt JL, Hepinstall‐Cymerman J, Kaiser SA, Rodenhouse NL, Sillett TS, Stodola KW, Webster MS, Holmes RT Ecol Monogr 04-Jan-2023
PMCID:PMC10078169
doi:10.1002/ecm.1559
PMID:37035418
Modulation of Cytoskeleton, Protein Trafficking, and Signaling Pathways by Metabolites from Cucurbitaceae, Ericaceae, and Rosaceae Plant Families Patel A, Rasheed A, Reilly I, Pareek Z, Hansen M, Haque Z, Simon-Fajardo D, Davies C, Tummala A, Reinhardt K, Bustabad A, Shaw M, Robins J, Vera Gomez K, Suphakorn T, Camacho Gemelgo M, Law A, Lin K, Hospedales E, Haley H, Perez Martinez JP, Khan S, DeCanio J, Padgett M, Abramov A, Nanjundan M Pharmaceuticals (Basel) 10-Nov-2022
PMCID:PMC9698530
doi:10.3390/ph15111380
PMID:36355554
Woody species do not differ in dormancy progression: Differences in time to budbreak due to forcing and cold hardiness Kovaleski AP Proc Natl Acad Sci U S A 02-May-2022
PMCID:PMC9171508
doi:10.1073/pnas.2112250119
PMID:35500120
Avian Toxins and Poisoning Mechanisms Yeung KA, Chai PR, Russell BL, Erickson TB J Med Toxicol 26-Apr-2022
PMCID:PMC9492810
doi:10.1007/s13181-022-00891-6
PMID:35474563
High‐speed video and plant ultrastructure define mechanisms of gametophyte dispersal Mitchell N, Piatczyc NP, Wang DD, Edwards J Appl Plant Sci 20-Apr-2022
PMCID:PMC9039801
doi:10.1002/aps3.11463
PMID:35495193
Effects of Rhododendron removal and prescribed fire on bees and plants in the southern Appalachians Ulyshen M, Elliott K, Scott J, Horn S, Clinton P, Liu N, Miniat CF, Caldwell P, Oishi C, Knoepp J, Bolstad P Ecol Evol 01-Mar-2022
PMCID:PMC8888263
doi:10.1002/ece3.8677
PMID:35261754
Persistent calyces increase floral longevity and female fitness in Salvia miltiorrhiza (Lamiaceae) Li DF, Yu Y, Yang HJ, Yan XC AoB Plants 27-Jan-2022
PMCID:PMC8903887
doi:10.1093/aobpla/plac004
PMID:35273787
Abiotic Stress and Belowground Microbiome: The Potential of Omics Approaches Sandrini M, Nerva L, Sillo F, Balestrini R, Chitarra W, Zampieri E Int J Mol Sci 19-Jan-2022
PMCID:PMC8835006
doi:10.3390/ijms23031091
PMID:35163015
Land-use history impacts spatial patterns and composition of woody plant species across a 35-hectare temperate forest plot Orwig DA, Aylward JA, Buckley HL, Case BS, Ellison AM PeerJ 03-Jan-2022
PMCID:PMC8734465
doi:10.7717/peerj.12693
PMID:35036094

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 / Grayanoids
[(3R,4R,6R,8S,9R,10R,11R,15R)-2,4,10,15-tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-3-yl] acetate 6325559 Click to see CC(=O)OC1C(C23CC(CCC2C(C4C1(C(C5C4O5)(C)C)O)(C)O)C(C3)(C)O)O 410.50 unknown https://doi.org/10.1021/NP50011A016
Kalmitoxin IV 44584062 Click to see CC(=O)OC1C(C23CC(C(C2O)CCC3C(C4C1(C(C5C4O5)(C)C)O)(C)O)(C)O)O 426.50 unknown https://doi.org/10.1021/NP50011A016
kalmitoxin V 44584060 Click to see CC(=O)OC1C(C2(C(C3C(C2(C)C)O3)C(C4C15CC(C(C5O)CC4)(C)O)(C)O)O)OC(=O)C 468.50 unknown https://doi.org/10.1021/NP50011A016
Lyoniol-A 161699 Click to see CC(=O)OC1C(C2(C(C3C(C2(C)C)O3)C(C4C15CC(CC4)C(C5)(C)O)(C)O)O)O 410.50 unknown https://doi.org/10.1021/NP50011A016
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids / Leucothol and grayanotoxane diterpenoids
(1R,3S,4S,6R,8R,9S,10S,13S,14R,16S)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,8]hexadecane-3,4,6,9,14,16-hexol 73051 Click to see CC1(C(CC2C1(C(CC34CC(C(C3O)CCC4C2(C)O)(C)O)O)O)O)C 370.50 unknown https://doi.org/10.1021/NP50011A016
(1S,4R,8S,9R,10S,13S,14R,16R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,8]hexadecane-3,4,6,9,14,16-hexol 138113481 Click to see CC1(C(CC2C1(C(CC34CC(C(C3O)CCC4C2(C)O)(C)O)O)O)O)C 370.50 unknown https://doi.org/10.1021/NP50011A016
Grayanotoxin I 9548612 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown https://doi.org/10.1021/NP50005A008
Kalmitoxin I 44559353 Click to see CC1(C(CC2C1(C(C(C34CC(C(C3O)CCC4C2(C)O)(C)O)O)O)O)O)C 386.50 unknown https://doi.org/10.1021/NP50011A016
Kalmitoxin III 44559352 Click to see CC(=O)OC1C(C23CC(C(C2O)CCC3C(C4C1(C(C(C4)O)(C)C)O)(C)O)(C)O)O 428.50 unknown https://doi.org/10.1021/NP50011A016
Kalmitoxin VI 44559347 Click to see CC(=O)OC1C2CCC3C1(CC2(C)O)C(C(C4(C(C3(C)O)C(C(C4(C)C)O)O)O)O)OC(=O)C 486.60 unknown https://doi.org/10.1021/NP50011A016
Rhodotoxine 442034 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown https://doi.org/10.1021/NP50005A008
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1R,2S,3S,4R,6S,8S,10S,13R,14R,16R)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.01,10.04,8]hexadecane-2,3,4,6,14,16-hexol 139597063 Click to see CC1(C(CC2C1(C(C(C34CC(C(C3O)CCC4C2=C)(C)O)O)O)O)O)C 368.50 unknown https://doi.org/10.1021/NP50011A016
(1S,3R,4R,6S,8S,10S,13R,14R)-5,5,14-trimethyl-9-methylidenetetracyclo[11.2.1.01,10.04,8]hexadecane-3,4,6,14,16-pentol 107976 Click to see CC1(C(CC2C1(C(CC34CC(C(C3O)CCC4C2=C)(C)O)O)O)O)C 352.50 unknown https://doi.org/10.1021/NP50011A016
CID 137092549 137092549 Click to see CC1(C(CC2C1(C(CC34CC(CCC3C2=C)C(C4)(C)O)O)O)O)C 336.50 unknown https://doi.org/10.1021/NP50011A016
Grayanotoxin II 14060930 Click to see CC1(C(CC2C1(C(CC34CC(C(C3O)CCC4C2=C)(C)O)O)O)O)C 352.50 unknown https://doi.org/10.1021/NP50011A016
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2',6'-Dihydroxy-4'-methoxyacetophenone 24135 Click to see CC(=O)C1=C(C=C(C=C1O)OC)O 182.17 unknown https://doi.org/10.1021/NP50005A008
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Capparin B 24813533 Click to see COC1=CC2=C(C=C1)C(=C(N2)SC)C=O 221.28 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
6-Methoxyindoline-2,3-dione 10374972 Click to see COC1=CC2=C(C=C1)C(=O)C(=O)N2 177.16 unknown via CMAUP database
Capparin A 101457836 Click to see COC1=CC2=C(C=C1)C3(CN=C(S3)SC)C(=O)N2 280.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP50012A008
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP50012A008
> 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 via CMAUP database
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 / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1021/NP50012A008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3-Hydroxyphloretin 2'-O-glucoside 102068587 Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O)O 452.40 unknown https://doi.org/10.1021/NP50012A008
CID 11190157 11190157 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)CCC3=CC=C(C=C3)O)O 450.40 unknown via CMAUP database
CID 12308643 12308643 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)C(=O)CCC3=CC=C(C=C3)O)O 450.40 unknown https://doi.org/10.1021/NP50005A008
phloretin 2'-O-glucoside 46926173 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)[O-])O 435.40 unknown via CMAUP database
Phlorizin 6072 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1021/NP50012A008
https://doi.org/10.1021/NP50005A008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 44259215 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1021/NP50012A008
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1021/NP50012A008
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/NP50012A008
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Oroxylin A 5320315 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
6,8-Di-C-methylkaempferol 3,7-dimethyl ether 14353450 Click to see CC1=C(C2=C(C(=C1OC)C)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 342.30 unknown https://doi.org/10.1515/ZNC-1984-7-804
8-Demethyllatifolin 14353449 Click to see CC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC 328.30 unknown https://doi.org/10.1515/ZNC-1984-7-804
8-Desmethylkalmiatin 44259656 Click to see CC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)OC)OC)OC 342.30 unknown https://doi.org/10.1515/ZNC-1984-7-804
Kalmiatin 44259657 Click to see CC1=C(C2=C(C(=C1OC)C)OC(=C(C2=O)OC)C3=CC=C(C=C3)OC)O 356.40 unknown https://doi.org/10.1515/ZNC-1984-7-804
Sideroxylin 3083788 Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC=C(C=C3)O)O 312.30 unknown https://doi.org/10.1515/ZNC-1981-11-1201
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
3-(3,4-Dihydroxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one 11778945 Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O)O 290.27 unknown https://doi.org/10.1021/NP50012A008
Phloretin 4788 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O 274.27 unknown https://doi.org/10.1021/NP50005A008

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