Kalanchoe daigremontiana - Unknown
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Internal ID UUID64405beed7667179454370
Scientific name Kalanchoe daigremontiana
Authority Raym.-Hamet & H.Perrier
First published in Ann. Mus. Colon. Marseille , sér. 3, 2: 128 (1914)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bryophyllum daigremontianum A.Berger Nat. Pflanzenfam. ed. 2 , 18a: 412 (1930)

Common names Top

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Language Common/alternative name
English devil's backbone
English alligator plant
English mother of thousands
Arabic طحلبية القبعة المكسيكية
Persian کالانکوئه دایگریمونتیا
Hebrew ניצנית משוננת
Hungarian sarjika
Hungarian elevenszülő korallvirág
Indonesian cocor bebek anak banyak
Japanese コダカラベンケイ
Latvian degremona kalanhoja
Dutch broedblad
Polish Żyworódka daigremonta
Russian Каланхоэ Дегремона
Swedish livsblad
Tonga faʻēʻaemano
Tonga bryophyllum tubiflorum
Tonga bryophyllum delagoense
Ukrainian Каланхое Дайгремонта
Ukrainian Каланхоє Дайгремонта
Uzbek degremon kalanxoesi
Chinese 锦蝶
Chinese 銳葉掌上珠
Chinese 大叶落地生根
Chinese 不死鸟

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
  • Africa
    • Macaronesia
      • Canary Islands
      • Cape Verde
      • Madeira
    • Middle Atlantic Ocean
      • Saint Helena
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
    • West Tropical Africa
      • Senegal
    • Western Indian Ocean
      • Madagascar
  • Europe
    • Southeastern Europe
      • Sicilia
    • Southwestern Europe
      • Baleares
      • Spain
  • Northern America
    • Mexico
      • Mexico Southwest
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Florida
  • Pacific
    • South-central Pacific
      • Cook Islands
    • Southwestern Pacific
      • New Caledonia
      • Niue
  • Southern America
    • Caribbean
      • Bahamas
      • Cuba
      • Dominican Republic
      • Puerto Rico
    • Central America
      • Guatemala
      • Nicaragua
    • Southern South America
      • Argentina Northeast
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001299505
UNII 9KEA668IM5
Florida Plant Atlas 243
USDA Plants KADA
Tropicos 8900296
INPN 629982
Flora of Italy 1714
KEW urn:lsid:ipni.org:names:274315-1
The Plant List tro-8900296
Open Tree Of Life 7978
NCBI Taxonomy 23013
IUCN Red List 88507997
IPNI 274315-1
iNaturalist 164327
GBIF 2985936
Freebase /m/0crd2k
EPPO KANDA
EOL 487234
USDA GRIN 21026
Wikipedia Kalanchoe_daigremontiana

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
Endophytic Bacillus vallismortis and Bacillus tequilensis bacteria isolated from medicinal plants enhance phosphorus acquisition and fortify Brassica napus L. vegetative growth and metabolic content Nagah A, El-Sheekh MM, Arief OM, Alqahtani MD, Alharbi BM, Dawwam GE Front Plant Sci 22-Mar-2024
PMCID:PMC10995350
doi:10.3389/fpls.2024.1324538
PMID:38584952
The influence of exotic and native plants on illnesses with physical and spiritual causes in the semiarid region of Piauí, Northeast of Brazil da Silva PH, Ferreira Júnior WS, Zank S, do Nascimento AL, de Abreu MC J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895823
doi:10.1186/s13002-024-00667-y
PMID:38409039
Analyzing the Antihyperglycemic Effect of Cissus quadrangularis and Bacopa monnieri on 3T3-L1 Cell Lines R K, S M, IGK I, J S, S V Cureus 21-Jan-2024
PMCID:PMC10877220
doi:10.7759/cureus.52661
PMID:38380214
Identification and Functional Characterization of Oxidosqualene Cyclases from Medicinal Plant Hoodia gordonii Parveen I, Wang M, Lee J, Zhao J, Zhu Y, Chittiboyina AG, Khan IA, Pan Z Plants (Basel) 14-Jan-2024
PMCID:PMC10818575
doi:10.3390/plants13020231
PMID:38256784
Recent advances in nanoflowers: compositional and structural diversification for potential applications Lee SJ, Jang H, Lee DN Nanoscale Adv 04-Sep-2023
PMCID:PMC10521310
doi:10.1039/d3na00163f
PMID:37767032
A Review of the Popular Uses, Anatomical, Chemical, and Biological Aspects of Kalanchoe (Crassulaceae): A Genus of Plants Known as “Miracle Leaf” Assis de Andrade E, Machinski I, Terso Ventura AC, Barr SA, Pereira AV, Beltrame FL, Strangman WK, Williamson RT Molecules 21-Jul-2023
PMCID:PMC10383218
doi:10.3390/molecules28145574
PMID:37513446
Cryo-EM structure of the Agrobacterium tumefaciens type IV secretion system-associated T-pilus reveals stoichiometric protein-phospholipid assembly Kreida S, Narita A, Johnson MD, Tocheva EI, Das A, Ghosal D, Jensen GJ Structure 03-Mar-2023
PMCID:PMC10168017
doi:10.1016/j.str.2023.02.005
PMID:36870333
Plant-Derived Compounds and Extracts as Modulators of Plasmin Activity—A Review Kolodziejczyk-Czepas J, Czepas J Molecules 09-Feb-2023
PMCID:PMC9965408
doi:10.3390/molecules28041677
PMID:36838662
Green Synthesis of Flower-Like Carrageenan-Silver Nanoparticles and Elucidation of Its Physicochemical and Antibacterial Properties Jaffar SS, Saallah S, Misson M, Siddiquee S, Roslan J, Lenggoro W Molecules 16-Jan-2023
PMCID:PMC9860806
doi:10.3390/molecules28020907
PMID:36677963
The Modification of Substrate in the Soilless Cultivation of Raspberries (Rubus Idaeus L.) as a Factor Stimulating the Biosynthesis of Selected Bioactive Compounds in Fruits Balawejder M, Matłok N, Piechowiak T, Szostek M, Kapusta I, Niemiec M, Komorowska M, Wróbel M, Mudryk K, Szeląg-Sikora A, Neuberger P, Kuboń M Molecules 23-Dec-2022
PMCID:PMC9822297
doi:10.3390/molecules28010118
PMID:36615315
Species-Specific Plant-Derived Nanoparticle Characteristics Viršilė A, Samuolienė G, Laužikė K, Šipailaitė E, Balion Z, Jekabsone A Plants (Basel) 16-Nov-2022
PMCID:PMC9698261
doi:10.3390/plants11223139
PMID:36432868
Systematic Identification and Analysis of OSC Gene Family of Rosa rugosa Thunb Wang J, Wang P, Xu M, Chen Y, Feng L Int J Mol Sci 11-Nov-2022
PMCID:PMC9698161
doi:10.3390/ijms232213884
PMID:36430363
Free and Esterified Tocopherols, Tocotrienols and Other Extractable and Non-Extractable Tocochromanol-Related Molecules: Compendium of Knowledge, Future Perspectives and Recommendations for Chromatographic Techniques, Tools, and Approaches Used for Tocochromanol Determination Górnaś P, Baškirovs G, Siger A Molecules 04-Oct-2022
PMCID:PMC9573122
doi:10.3390/molecules27196560
PMID:36235100
Neurofuzzy logic predicts a fine-tuning metabolic reprogramming on elicited Bryophyllum PCSCs guided by salicylic acid García-Pérez P, Lozano-Milo E, Zhang L, Miras-Moreno B, Landin M, Lucini L, Gallego PP Front Plant Sci 23-Sep-2022
PMCID:PMC9541431
doi:10.3389/fpls.2022.991557
PMID:36212372
Inorganic Nanoflowers—Synthetic Strategies and Physicochemical Properties for Biomedical Applications: A Review Lee SJ, Jang H, Lee DN Pharmaceutics 06-Sep-2022
PMCID:PMC9505446
doi:10.3390/pharmaceutics14091887
PMID:36145635

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1515/ZNC-1997-7-805
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
Gibberellin A20 5280481 Click to see CC12CCCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O 332.40 unknown https://doi.org/10.1007/BF00385554
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosterol acetate 5354503 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
Stigmast-5-en-3-yl acetate 521199 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
2,15-Dimethyl-14-(6-methylheptan-2-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol 304 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylene,25-methylcholesta-5-en-3beta-ol 5283645 Click to see CC(CCC(=C)C(C)(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
24-Methylenecholesterol 92113 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
24,24-Dimethyl-25,26-didehydrocholesterol 14312353 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
25-Methyl-24-methylenecholesterol 13889669 Click to see CC(CCC(=C)C(C)(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
Ergosta-5,24(28)-dien-3beta-ol 314582 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
[(1R,3S,5S,8R,9S,10R,13R,14S,17R)-10-formyl-3,5,14-trihydroxy-13-methyl-17-(6-oxopyran-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-1-yl] acetate 21768174 Click to see CC(=O)OC1CC(CC2(C1(C3CCC4(C(CCC4(C3CC2)O)C5=COC(=O)C=C5)C)C=O)O)O 474.50 unknown https://doi.org/10.1515/ZNB-1985-0920
https://doi.org/10.1016/S0031-9422(01)00199-6
https://doi.org/10.1002/HLCA.19860690215
[(1R,3S,5S,8R,9S,10S,13R,14S,17R)-1,5,14-trihydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 21768175 Click to see CC(=O)OC1CC(C2(C3CCC4(C(CCC4(C3CCC2(C1)O)O)C5=COC(=O)C=C5)C)C)O 460.60 unknown https://doi.org/10.1515/ZNB-1985-0920
https://doi.org/10.1002/HLCA.19860690215
[1,5,14-trihydroxy-10,13-dimethyl-17-(6-oxopyran-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 73833577 Click to see CC(=O)OC1CC(C2(C3CCC4(C(CCC4(C3CCC2(C1)O)O)C5=COC(=O)C=C5)C)C)O 460.60 unknown https://doi.org/10.1002/HLCA.19860690215
https://doi.org/10.1515/ZNB-1985-0920
[10-formyl-3,5,14-trihydroxy-13-methyl-17-(6-oxopyran-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-1-yl] acetate 73833576 Click to see CC(=O)OC1CC(CC2(C1(C3CCC4(C(CCC4(C3CC2)O)C5=COC(=O)C=C5)C)C=O)O)O 474.50 unknown https://doi.org/10.1002/HLCA.19860690215
https://doi.org/10.1016/S0031-9422(01)00199-6
https://doi.org/10.1515/ZNB-1985-0920
5-[(1S,4R,5S,8R,9R,11R,12S,13R,14R,16R,18S)-5,11-dihydroxy-13-(hydroxymethyl)-9,16-dimethyl-15,17,20-trioxahexacyclo[14.3.1.114,18.01,13.04,12.05,9]henicosan-8-yl]pyran-2-one 101049584 Click to see CC12CC(C3C(C1(CCC2C4=COC(=O)C=C4)O)CCC56C3(C7CC(C5)OC(O7)(O6)C)CO)O 474.50 unknown https://doi.org/10.1016/S0031-9422(01)00199-6
5,11-Dihydroxy-9,16-dimethyl-8-(6-oxopyran-3-yl)-15,17,20-trioxahexacyclo[14.3.1.114,18.01,13.04,12.05,9]henicosane-13-carbaldehyde 4482623 Click to see CC12CC(C3C(C1(CCC2C4=COC(=O)C=C4)O)CCC56C3(C7CC(C5)OC(O7)(O6)C)C=O)O 472.50 unknown https://doi.org/10.1016/S0031-9422(01)00199-6
Bersaldegenin 1,5-orthoacetate 282021 Click to see CC12CCC3C(C1(CCC2C4=COC(=O)C=C4)O)CCC56C3(C7CC(C5)OC(O7)(O6)C)C=O 456.50 unknown https://doi.org/10.1002/HLCA.19860690215
https://doi.org/10.1016/S0031-9422(01)00199-6
https://doi.org/10.1515/ZNB-1985-0920
Bersaldegenin 3-acetate 21768173 Click to see CC(=O)OC1CC(C2(C3CCC4(C(CCC4(C3CCC2(C1)O)O)C5=COC(=O)C=C5)C)C=O)O 474.50 unknown https://doi.org/10.1002/CHIN.198624332
https://doi.org/10.1002/HLCA.19860690215
https://doi.org/10.1016/S0031-9422(01)00199-6
https://doi.org/10.1515/ZNB-1985-0920
Bersaldegenin 3-acetate 282020 Click to see CC(=O)OC1CC(C2(C3CCC4(C(CCC4(C3CCC2(C1)O)O)C5=COC(=O)C=C5)C)C=O)O 474.50 unknown https://doi.org/10.1515/ZNB-1985-0920
https://doi.org/10.1002/HLCA.19860690215
Bersalldegenin-1,3,5-orthoacetate 101717792 Click to see CC12CCC3C(C1(CCC2C4=COC(=O)C=C4)O)CCC56C3(C7CC(C5)OC(O7)(O6)C)C=O 456.50 unknown https://doi.org/10.1002/HLCA.19860690215
https://doi.org/10.1016/S0031-9422(01)00199-6
https://doi.org/10.1515/ZNB-1985-0920
Bryophyllin A 5488801 Click to see CC12CC(C3C(C1(CCC2C4=COC(=O)C=C4)O)CCC56C3(C7CC(C5)OC(O7)(O6)C)C=O)O 472.50 unknown https://doi.org/10.1016/S0031-9422(01)00199-6
CID 127105 127105 Click to see CC12C(CCC1(C3CCC45CC6CC(C4(C3C(C2=O)O)C=O)OC(O6)(O5)C)O)C7=COC(=O)C=C7 486.50 unknown https://doi.org/10.1055/S-2007-969441
https://doi.org/10.1271/BBB.65.947
https://doi.org/10.1515/ZNB-1985-0920
https://doi.org/10.1016/S0031-9422(01)00199-6
Daigremontianin 101717793 Click to see CC12C(CCC1(C3CCC45CC6CC(C4(C3C(C2=O)O)C=O)OC(O6)(O5)C)O)C7=COC(=O)C=C7 486.50 unknown https://doi.org/10.1016/S0031-9422(01)00199-6
https://doi.org/10.1271/BBB.65.947
https://doi.org/10.1515/ZNB-1985-0920
https://doi.org/10.1002/HLCA.19860690215
https://doi.org/10.1055/S-2007-969441
https://doi.org/10.1002/CHIN.198624332
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
10,13-dimethyl-17-(5-propan-2-ylhept-5-en-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86747 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
17-(5-ethyl-6-methylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 9801810 Click to see CCC(=C(C)C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
17-(5-ethyl-6-methylhepta-3,6-dien-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 73200193 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
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(90)85251-A
22-Dehydroclerosterol 15608667 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
24-Ethylcholesta-5,24-dien-3beta-ol 5283643 Click to see CCC(=C(C)C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
5,25-Stigmastadienol 286499 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
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/10.1016/0031-9422(90)85251-A
Clerosterol 5283638 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85251-A
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(2R,4aS,4bR,6R,7R,10aR)-6-hydroxy-7-[(2S,4S,5R,6R)-5-[(2S,4R,5R,6S)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4S,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one 16093718 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3OC)OC4C(OC(CC4OC)OC5CC6=CCC7C(C6(CC5O)C)CCC(C7=O)C8=C(OC=C8)C)C)C)C)OC)O 893.10 unknown https://doi.org/10.1016/0031-9422(90)85251-A
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
7,8-Dihydroxy-3-(2-hydroxypentyl)-6-methoxy-3,4-dihydroisochromen-1-one 76010681 Click to see CCCC(CC1CC2=CC(=C(C(=C2C(=O)O1)O)O)OC)O 296.31 unknown https://doi.org/10.1515/ZNB-1985-0920
https://doi.org/10.1016/S0031-9422(01)00199-6
https://doi.org/10.1002/HLCA.19860690215

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