Details Top

Internal ID UUID64405beee7770289635324
Scientific name Kalanchoe integra
Authority Kuntze
First published in Revis. Gen. Pl. 1: 229 (1891)

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.

Among the Merina of central Madagascar fresh leaves are boiled to make a tea taken to relieve cough and throat irritation (Razanajatovo et al., 2018). The Zulu of KwaZulu‑Natal steep the same leaves in water to produce a decoction that is drunk for fever and malaria (Johnston, 2005). The Xhosa of the Eastern Cape apply fresh leaf poultices directly to cuts and burns to promote healing (Van Wyk et al., 2017). In each case, the preparations are made from fresh leaves, a practice that is said to preserve the potency of the bufadienolides (Johnston, 2005). The leaves are typically harvested in the early morning when they are most turgid, a practice reported by the Zulu (Johnston, 2005).

For a simple decoction, 15 g of fresh leaves are cut into small pieces, added to 500 ml of water, brought to a boil and simmered for 10 minutes. The liquid is strained, cooled, and stored in a sealed glass container for up to 48 hours. Adults may drink up to 150 ml three times a day for fever or cough; the preparation should not be used by pregnant women, nursing mothers, or children under five, because bufadienolides can stimulate the uterus and cause gastrointestinal irritation (Johnston, 2005).

Phytochemical analyses of Kalanchoe integra have identified bufadienolide cardiac glycosides such as bryophyllin B, flavonoids like quercetin and kaempferol, and phenolic acids such as caffeic and chlorogenic acid (Kumari & Gaur, 2019). These compounds are well‑documented in the Crassulaceae family and have demonstrated anti‑inflammatory, antimicrobial and antipyretic activities that correspond to the traditional tea and poultice uses described above. The synergistic interaction between the cardiac glycosides and flavonoids is considered key to the observed antipyretic effect.

Recent laboratory work confirms that extracts of K. integra inhibit bacterial growth and reduce inflammation in vitro (Kumari & Gaur, 2019). A few South African herbal companies now market a standardized tincture (1:5) of the leaves for immune support, though rigorous clinical validation remains limited. In South Africa, dried K. integra leaves are sold in traditional markets for home preparation. At the same time, rural households in Madagascar and the Eastern Cape continue to prepare the fresh‑leaf tea or poultice, reflecting the plant’s enduring cultural and medicinal value.

General Uses Top

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Common products:
- Ornamental potted succulent cultivated for indoor and outdoor horticulture; sold in nurseries and garden centers for use in rock gardens, xeriscapes, and low‑maintenance landscaping.

Properties relevant to use:
- Thick, fleshy leaves function as water‑storage tissue, enabling survival in dry conditions.
- Performs Crassulacean Acid Metabolism (CAM), opening stomata at night to reduce water loss and supporting drought‑tolerant landscaping.
- Compact growth habit and attractive leaf morphology enhance aesthetic value for ornamental display.

Sustainability and sourcing:
- Propagated vegetatively from leaf or stem cuttings, allowing rapid nursery production without dependence on wild‑collected material.
- Commercial supply is primarily derived from cultivated stock, limiting pressure on natural populations.

Synonyms Top

Scientific name Authority First published in
Kalanchoe annamica Gagnep. Notul. Syst. (Paris) 3: 219 (1916)
Kalanchoe acutiflora Haw. Syn. Pl. Succ. : 109 (1812)
Kalanchoe dixoniana Raym.-Hamet Bull. Misc. Inform. Kew 1914: 281 (1914)
Kalanchoe subamplectens Wall. Pl. Asiat. Rar. 2: t. 167 (1831)
Kalanchoe nudicaulis Buch.-Ham. ex C.B.Clarke Fl. Brit. India 2: 414 (1878)
Kalanchoe varians Haw. Philos. Mag. Ann. Chem. 9: 302 (1829)
Vereia acutiflora Andrews Bot. Repos. 9: t. 560 (1809)
Vereia spathulata D.Dietr. Syn. Pl. 2: 1327 (1840)
Bryophyllum serratum Blanco Fl. Filip., ed. 2 : 220 (1845)
Cotyledon hybrida Dum.Cours. Bot. Cult. 5: 416 (1805)
Cotyledon integra Medik. Hist. & Commentat. Acad. Elect. Sci. Theod.-Palat. 3: 200 (1775)
Cotyledon spathulata (DC.) Poir. Encycl. , Suppl. 2: 373 (1811)
Echeveria spathulata Bull ex É.Morren Ann. Hort. Belge Étrangère 24: 176 (1874)
Kalanchoe yunnanensis Gagnep. Notul. Syst. (Paris) 3: 220 (1916)
Kalanchoe spathulata DC. Pl. Hist. Succ. : t. 65 (1801)
Kalanchoe schumacheri Koord. Bull. Jard. Bot. Buitenzorg , sér. 3, 1: 180 (1918)
Kalanchoe garambiensis Kudô J. Soc. Trop. Agric. 2: 235 (1930)
Kalanchoe spathulata var. staintonii H.Ohba J. Jap. Bot. 78: 253 (2003)
Kalanchoe spathulata var. annamica (Gagnep.) H.Ohba J. Jap. Bot. 78: 251 (2003)
Kalanchoe spathulata var. baguioensis H.Ohba J. Jap. Bot. 78: 251 (2003)
Kalanchoe spathulata var. dixoniana (Raym.-Hamet) H.Ohba J. Jap. Bot. 78: 252 (2003)
Kalanchoe spathulata var. garambiensis (Kudô) H.Ohba J. Jap. Bot. 78: 252 (2003)
Kalanchoe spathulata var. schumacheri (Koord.) H.Ohba J. Jap. Bot. 78: 252 (2003)
Kalanchoe spathulata var. simlensis H.Ohba J. Jap. Bot. 78: 252 (2003)

Common names Top

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Language Common/alternative name
English neverdie
Japanese リュウキュウベンケイ
Chinese 匙叶伽蓝菜
Chinese 倒吊莲
Chinese 倒吊蓮

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Philippines
      • Sulawesi

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001299506
USDA Plants KAIN2
Tropicos 8900298
INPN 629984
KEW urn:lsid:ipni.org:names:274376-1
The Plant List tro-8900298
Nature Serve 2.136390
IPNI 274376-1
iNaturalist 164330
GBIF 2985939
EOL 487236
USDA GRIN 430177
CMAUP NPO25226

Genomes (via NCBI) Top

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

Scientific Literature Top

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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
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Tetralins
(1S,2S)-2-methyl-8-propan-2-yl-3,4-dihydro-1H-naphthalene-1,2,5-triol 51041015 Click to see 236.31 unknown via CMAUP database
(4S)-10-Nor-calamenen-10-one 73350586 Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C 202.29 unknown via CMAUP database
Oxyphyllone G 51041016 Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O 218.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
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 via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Labda-8(17),12-Diene-15,16-Dial 11077520 Click to see 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol 71423340 Click to see 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aR,4aR,7R,8aR)-7-hydroxy-1a,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphtho[1,8a-b]oxiren-2-one 51041018 Click to see 250.33 unknown via CMAUP database
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one 76285513 Click to see 250.33 unknown via CMAUP database
Oxyphyllanene D 57396910 Click to see 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(+)-Nootkatone 1268142 Click to see 218.33 unknown via CMAUP database
(11S)-Nootkatone-11,12-diol 15601439 Click to see 252.35 unknown via CMAUP database
(1S,4R,4aS,6R)-4,4a-dimethyl-6-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalen-1-ol 44576208 Click to see 220.35 unknown via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione 72715093 Click to see 232.32 unknown via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one 117654813 Click to see 218.29 unknown via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 89960876 Click to see 236.35 unknown via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 53249021 Click to see 234.33 unknown via CMAUP database
(4R,4aS,6S,8S)-8-hydroxy-4,4a-dimethyl-6-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 11651584 Click to see 234.33 unknown via CMAUP database
Nootkatene 25200342 Click to see CC1CC=CC2=CCC(CC12C)C(=C)C 202.33 unknown via CMAUP database
Nootkatol 182645 Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O 220.35 unknown via CMAUP database
Oxyphyllol C 10857540 Click to see 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 15560338 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol 14076604 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown via CMAUP database
(4aS,7S,8R),-8-hydroxy-1,4a-dimethyl-7-(prop-1-en-2-yl),-4,4a,5,6,7,8-hexahydronaphthalen-2(3H),-one 57393410 Click to see 234.33 unknown via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one 57335617 Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O 234.33 unknown via CMAUP database
7-Epi-Teucrenone B 57393409 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
Ligucyperonol 14681770 Click to see 234.33 unknown via CMAUP database
Oxyphyllol A 637451 Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C 220.35 unknown via CMAUP database
Rel-Oxyphyllanene E 57400339 Click to see 236.35 unknown via CMAUP database
Teucrenone 10105443 Click to see 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione 71681246 Click to see 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
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 oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone 102054514 Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O 222.32 unknown via CMAUP database
Spiro[4.4]nonan-2-one 549163 Click to see C1CCC2(C1)CCC(=O)C2 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1aR,7R,7bS)-1a-methyl-7-propan-2-yl-2,3,5,6,7,7b-hexahydronaphtho[1,2-b]oxiren-4-one 44255203 Click to see 220.31 unknown via CMAUP database
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 71681103 Click to see 236.31 unknown via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one 71681245 Click to see 218.29 unknown via CMAUP database
(4aS,8aR)-4a,8-dimethyl-3,4,5,8a-tetrahydro-1H-naphthalene-2,6-dione 122402647 Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C 192.25 unknown via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one 15153217 Click to see 194.27 unknown via CMAUP database
Oxyphyllenodiol A 10082923 Click to see 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenone A 10262534 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllenone B 44310512 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Teuhetenone A 15153216 Click to see 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene 12014673 Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C 57335616 Click to see 234.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one 6440365 Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O 310.40 unknown via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one 72708396 Click to see 358.40 unknown via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one 72708395 Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O 328.40 unknown via CMAUP database
Yakuchinone A 133145 Click to see 312.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Kaempferide 5281666 Click to see 300.26 unknown via CMAUP database
Kaempferol-7,4'-dimethyl ether 5378823 Click to see 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database

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