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Kalanchoe pinnata

Kalanchoe pinnata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ff3cc4d6f1805969304
Scientific name Kalanchoe pinnata
Authority (Lam.) Pers.
First published in Syn. Pl. 1: 446 (1805)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vereia pinnata Spreng. Syst. Veg. 2: 260 (1825)
Bryophyllum calcicola (H.Perrier) V.V.Byalt Novosti Sist. Vyssh. Rast. 32: 51 (2000)
Bryophyllum calycinum Salisb. Parad. Lond. 1: t. 3 (1805)
Bryophyllum germinans Blanco Fl. Filip., ed. 2 : 220 (1845)
Bryophyllum pinnatum (Lam.) Oken Allg. Naturgesch. iii. (3) 1966 (1841); fide Merrill in Journ. Arn. Arb. xxxi.272 (1950).
Cotyledon calycina Roth Nov. Pl. Sp. : 217 (1821)
Cotyledon calyculata Sol. ex Sims Bot. Mag. 34: t. 1409 (1811)
Cotyledon pinnata Lam. Encycl. 2: 141 (1786)
Cotyledon rhizophylla Roxb. Fl. Ind. 2: 456 (1824)
Crassula pinnata L.f. Suppl. Pl. : 191 (1782)
Crassuvia floripendia Comm. ex Lam. Encycl. 2: 141 (1786)
Kalanchoe pinnata var. brevicalyx Raym.-Hamet & H.Perrier Ann. Mus. Colon. Marseille, sér. 3, 3: 88–90 1915
Kalanchoe calcicola (H.Perrier) Boiteau Kalanchoe Madagascar : 132 (1995)
Kalanchoe brevicalyx (Raym.-Hamet & H.Perrier) Boiteau in P. Boiteau & L. Allorge-Boiteau, Kalanchoe de Madagascar 133 (1995), without basionym ref.
Sedum madagascariense Clus. Exot. 4: 91, cap. 22
Crassuvia floripenula Comm.
Kalanchoe pinnata var. floripendula Pers. Syn. Pl. t. 1: 446 1805
Cotyledon calyculata Solander Prodr. 3: 396 1828
Kalanchoe pinnata var. calcicola H.Perrier Arch. Bot. Bull. Mens. 2: 21 1928

Common names Top

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Language Common/alternative name
English air plant
English cathedral bells
English goethe plant
English maternity plant
English curtain plant
English mexican loveplant
English life plant
English good luck leaf
English floppers
English tree of life
English mother in law
English miracle leaf
Spanish bryophyllum pinnatum
Spanish crassula pinnata
Spanish hoja de aire
Spanish kalanchoe pinnata var calcicola
Spanish kalanchoe pinnata var. calcicola
Spanish pinnata de cotiledón
Spanish sedum madagascaricum
Spanish bryophyllum calycinum
bcl katakataka
Bengali পাথরকুচি
German goethepflanze
German goethe-pflanze
German echte goethepflanze
Estonian crassuvia floripendia
Estonian sulgjas kalanhoe
Estonian sedum madagascaricum
Estonian crassula pinnata
Estonian cotyledon pinnata
Estonian cotyledon calyculata
Estonian cotyledon calycina
Estonian bryophyllum calycinum
Estonian bryophyllum germinans
Estonian cotyledon rhizophylla
Estonian bryophyllum pinnatum
Persian بریوفیلوم پیناتوم
Finnish sulkaitulehti
French bryophyllum pinnatum
Hindi पथरचटा
Indonesian cocor bebek
ilo abistrana
ilo bryophyllum pinnatum
ilo bryophyllum calycinum
ilo abisrana
Japanese ゲーテ草
Japanese セイロンベンケイ
Japanese ハカラメ
Japanese セイロンベンケイソウ
Japanese セイロンベンケイ草
jv cocor bèbèk
jv cocor bebek
Lithuanian plunksninė kalankė
Lithuanian plunksninė spurguolė
Latvian plūksnainā kalanhoja
mad ghâmet
min sidingin
Malayalam ഇലമുളച്ചി
Marathi पानफुटी
Burmese ရွက်ကျပင်ပေါက်
Oriya ଅମରପୋଇ
Polish kalanchoe pierzaste
Polish briofilum pierzaste
Polish bryophillum pinnatum
Polish płodnolist pierzasty
Polish Żyworódka pierzasta
Portuguese bryophyllum calycinum
Quechua ch'uqri yuyu
Quechua chukri yuyu
Quechua chukriyuyu
Quechua chuqri yuyu
Quechua chuqriyuyu
Quechua ch'uqriyuyu
Russian Каланхоэ перистое
Sango zözömbö
Sinhala අක්කපාන
su buntiris
Tamil பிரையோபில்லம்
tcy ಕಾಟ್ ಬಸಲೆ(ಕಾಡ ಬಸಲೆ)
Thai คว่ำตายหงายเป็น
Thai kalanchoe pimata
Tonga pipivao
Tonga bryophyllum pinnatum
Tonga bryophyllum calycinum
Ukrainian Каланхоє пірчасте
Ukrainian Каланхое пірчасте
Vietnamese cây lá bỏng
Vietnamese cây thuốc bỏng
Vietnamese bryophyllum pinnatum
Vietnamese bryophyllum calycinum
za gociengzseng
Chinese 落地生根
Chinese 灯笼草

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000357656
UNII D2TTE8F2Z3
Florida Plant Atlas 1571
USDA Plants KAPI
Tropicos 8900302
INPN 445593
KEW urn:lsid:ipni.org:names:274438-1
The Plant List kew-2336037
Open Tree Of Life 726046
Observations.org 138744
NCBI Taxonomy 80913
IPNI 164558-3
iNaturalist 164333
GBIF 2985930
Freebase /m/03c84py
EPPO KANPI
EOL 487240
USDA GRIN 21076
Wikipedia Kalanchoe_pinnata

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
Exploring the therapeutic mechanism of potential phytocompounds from Kalanchoe pinnata in the treatment of diabetes mellitus by integrating network pharmacology, molecular docking and simulation approach Halayal RY, Bagewadi ZK, Aldabaan NA, Shaikh IA, Khan AA Saudi Pharm J 13-Mar-2024
PMCID:PMC10973190
doi:10.1016/j.jsps.2024.102026
PMID:38550331
Syrupy herbal formulation of green bean pod extract of Phaseolus vulgaris L.: Formulation optimization by central composite design, and evaluation for anti-urolithiatic activity Noorulla KM, Doyo Dalecha D, Jemal Haji M, S R, Arumugam M, Zafar A, Gadisa Gobena W, Mekit S, Haji Negawo H, Hussein M, Fekadu Demessie H, Yasir M Heliyon 29-Feb-2024
PMCID:PMC10943400
doi:10.1016/j.heliyon.2024.e27330
PMID:38495171
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
Sea Buckthorn Flavonoid Extracted by High Hydrostatic Pressure Inhibited IgE-Stimulated Mast Cell Activation through the Mitogen-Activated Protein Kinase Signaling Pathway Yan Z, Feng X, Li X, Gao Z, Wang Z, Ren G, Long F Foods 12-Feb-2024
PMCID:PMC10887968
doi:10.3390/foods13040560
PMID:38397537
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Comparative Anti-inflammatory Activity of Silver and Zinc Oxide Nanoparticles Synthesized Using Ocimum tenuiflorum and Ocimum gratissimum Herbal Formulations Varghese RM, S AK, Shanmugam R Cureus 26-Jan-2024
PMCID:PMC10894022
doi:10.7759/cureus.52995
PMID:38406168
Development of Antibacterial Thermoplastic Starch with Natural Oils and Extracts: Structural, Mechanical and Thermal Properties López Terán JL, Cabrera Maldonado EV, Araque Rangel JD, Poveda Otazo J, Beltrán Rico MI Polymers (Basel) 08-Jan-2024
PMCID:PMC10818525
doi:10.3390/polym16020180
PMID:38256979
In Vitro Hypoglycemic and Antioxidant Activities of Dichloromethane Extract of Xerophyta spekei Ndile MM, Makori WA, Kibiti CM, Ngugi MP Scientifica (Cairo) 29-Dec-2023
PMCID:PMC10769734
doi:10.1155/2023/6652112
PMID:38188987
Targeting key RNA methylation enzymes to improve the outcome of colorectal cancer chemotherapy (Review) Shao C, Han Y, Huang Y, Zhang Z, Gong T, Zhang Y, Tian X, Fang M, Han X, Li M Int J Oncol 19-Dec-2023
PMCID:PMC10783943
doi:10.3892/ijo.2023.5605
PMID:38131226
Effects of light spectra on morphological characteristics, primary and specialized metabolites of Thymus vulgaris L Seyedi FS, Nafchi MG, Reezi S Heliyon 01-Dec-2023
PMCID:PMC10750077
doi:10.1016/j.heliyon.2023.e23032
PMID:38148820
Effects of Ottonia anisum plant extract on local anesthetic, analgesic, anti-inflammatory and HCl‑induced acute lung injury activities: a study in animal models Liu M, Wang H, Yue Q, Liu J Bioresour Bioprocess 30-Nov-2023
PMCID:PMC10992343
doi:10.1186/s40643-023-00706-8
The mechanism of traditional medicine in alleviating ulcerative colitis: regulating intestinal barrier function Xu Q, Yao Y, Liu Y, Zhang J, Mao L Front Pharmacol 09-Oct-2023
PMCID:PMC10590899
doi:10.3389/fphar.2023.1228969
PMID:37876728
Anti-inflammatory natural products modulate interleukins and their related signaling markers in inflammatory bowel disease: A systematic review Gandhi GR, Mohana T, Athesh K, Hillary VE, Vasconcelos AB, Farias de Franca MN, Montalvão MM, Ceasar SA, Jothi G, Sridharan G, Gurgel RQ, Xu B J Pharm Anal 22-Sep-2023
PMCID:PMC10785269
doi:10.1016/j.jpha.2023.09.012
PMID:38223446
Phytochemical analysis and bioactivity assessment of five medicinal plants from Pakistan: Exploring polyphenol contents, antioxidant potential, and antibacterial activities Rao H, Rao I, Saeed L, Aati HY, Aati S, Zeeshan M, ur Rehman Khan K Saudi J Biol Sci 22-Aug-2023
PMCID:PMC10480623
doi:10.1016/j.sjbs.2023.103783
PMID:37680976
BDMediLeaves: A leaf images dataset for Bangladeshi medicinal plants identification Islam S, Ahmed MR, Islam S, Rishad MM, Ahmed S, Utshow TR, Siam MI Data Brief 11-Aug-2023
PMCID:PMC10450835
doi:10.1016/j.dib.2023.109488
PMID:37636130

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/10.1055/S-0028-1099426
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1055/S-0028-1099426
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1080/10575639708041195
> Benzenoids / Dibenzocycloheptenes
23-Methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.9.2.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-22-one 23642748 Click to see CN1C2CC3=CC4=C(C=C3C(C1=O)C5=CC6=C(C=C25)OCO6)OCO4 337.30 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
> Benzenoids / Phenanthrenes and derivatives
2-Dec-9-enylphenanthrene 129682058 Click to see C=CCCCCCCCCC1=CC2=C(C=C1)C3=CC=CC=C3C=C2 316.50 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
2-Undec-10-enylphenanthrene 163097550 Click to see C=CCCCCCCCCCC1=CC2=C(C=C1)C3=CC=CC=C3C=C2 330.50 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
2-Undec-9-enylphenanthrene 163192410 Click to see CC=CCCCCCCCCC1=CC2=C(C=C1)C3=CC=CC=C3C=C2 330.50 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1016/S0031-9422(00)90117-1
Triacontane 12535 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 422.80 unknown https://doi.org/10.1016/S0031-9422(00)90117-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1055/S-0028-1097931
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown https://doi.org/10.1055/S-0028-1097931
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-oct-1-en-3-yloxy-6-[[(3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 163194749 Click to see CCCCCC(C=C)OC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O 422.50 unknown https://doi.org/10.1590/S0102-695X2006000400008
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
(4aR,6aR,6aR,6bR,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol 138113838 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
(4aR,6aS,6aR,6bR,8aR,12aS,14aS,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicene 162930219 Click to see CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
18alpha-Oleanane 12306152 Click to see CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
18alpha(H)-OLEANANE 12306151 Click to see CC1(CCC2(CCC3(C(C2C1)CCC4C3(CCC5C4(CCCC5(C)C)C)C)C)C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)90117-1
https://doi.org/10.1016/S0031-9422(00)97999-8
alpha-Amyrin acetate 293754 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
https://doi.org/10.1016/S0031-9422(00)90117-1
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)90117-1
https://doi.org/10.1016/S0031-9422(00)97999-8
Urs-12-en-3beta-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)90117-1
https://doi.org/10.1016/S0031-9422(00)97999-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
[(3S,5S,6R,8R,9S,10R,13R,14R,17R)-3,14-dihydroxy-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-yl] acetate 162898173 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2CC(C4C3(CCC(C4)O)C)OC(=O)C)C)O 462.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
[3,14-Dihydroxy-10,13-dimethyl-17-(6-methylheptan-2-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-yl] acetate 162898172 Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2CC(C4C3(CCC(C4)O)C)OC(=O)C)C)O 462.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1007/BF02536432
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/10.1007/BF02536432
Codisterol 13833114 Click to see CC(CCC(C)C(=C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1007/BF02536432
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
(1S,4R,5S,8R,9R,11R,12S,13R,14R,16S,18S)-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 162962641 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
[(1R,4R,6R,7R,10S,11R,14S,16S,18R,19S)-2,10,14,16-tetrahydroxy-6-methyl-7-(6-oxopyran-3-yl)-3-oxapentacyclo[9.7.1.01,14.04,19.06,10]nonadecan-18-yl] acetate 101424435 Click to see CC(=O)OC1CC(CC2(C13C4C(CC2)C5(CCC(C5(CC4OC3O)C)C6=COC(=O)C=C6)O)O)O 490.50 unknown https://doi.org/10.1021/NP50065A025
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/10.1271/BBB.65.947
https://doi.org/10.1271/BBB.64.1310
5-[(1S,4R,5S,8R,9R,11R,12S,13S,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 162939551 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-[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 162939550 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/10.1271/BBB.64.1310
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/10.1271/BBB.64.1310
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/10.1271/BBB.65.947
https://doi.org/10.1248/CPB.36.1615
https://doi.org/10.1021/NP50065A025
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/10.1248/CPB.36.1615
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/10.1271/BBB.65.947
https://doi.org/10.1248/CPB.36.1615
https://doi.org/10.1271/BBB.64.1310
https://doi.org/10.1021/NP50065A025
CID 5462418 5462418 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-hydroxy-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 162878073 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)(C)O 430.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
17-(5-ethyl-6-hydroxy-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 77716181 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)(C)O 430.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
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/10.1007/BF02536432
https://doi.org/10.1016/S0031-9422(00)90117-1
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF02536432
https://doi.org/10.1016/S0031-9422(00)90117-1
24-Ethylcholest-5-en-3beta,25-diol 69781079 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)(C)O 430.70 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
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/10.1007/BF02536432
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/10.1007/BF02536432
Clionasterol 457801 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF02536432
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/10.1007/BF02536432
Peposterol 5321504 Click to see CCC(=C(C)C)CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C 412.70 unknown https://doi.org/10.1007/BF02536432
Stigmasta-5,25-dien-3ss-ol 185472 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 412.70 unknown https://doi.org/10.1007/BF02536432
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/10.1007/BF02536432
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols
2-Aminooctadecane-1,3-diol 3126 Click to see CCCCCCCCCCCCCCCC(C(CO)N)O 301.50 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Alpha-branched alpha,beta-unsaturated ketones
5,7-Dihydroxytricosa-4,7,10,12-tetraene-3,6,9-trione 162915412 Click to see CCCCCCCCCCC=CC=CC(=O)C=C(C(=O)C(=CC(=O)CC)O)O 390.50 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aS,6aR,6bS,8aS,12aS,14aR,14bR)-1,6a,6b,9,9,12a-hexamethyl-4-oxo-3,5,6,7,8,8a,10,11,12,14,14a,14b-dodecahydropicene-4a-carboxylic acid 162898317 Click to see CC1=CCC(=O)C2(C1C3CC=C4C5(CCCC(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 438.60 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
1,6a,6b,9,9,12a-Hexamethyl-4-oxo-3,5,6,7,8,8a,10,11,12,14,14a,14b-dodecahydropicene-4a-carboxylic acid 162898316 Click to see CC1=CCC(=O)C2(C1C3CC=C4C5(CCCC(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 438.60 unknown https://doi.org/10.1016/S0031-9422(00)97999-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1055/S-0028-1099426
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1055/S-0028-1099426
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1055/S-0028-1099426
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1515/ZNC-1997-7-805
https://doi.org/10.1055/S-0028-1099426
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1055/S-0028-1099426
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1055/S-0028-1099426
https://doi.org/10.1515/ZNC-1997-7-805
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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 https://doi.org/10.1080/10575639708041195
> 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 https://doi.org/10.1055/S-0028-1099426
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/10.1055/S-0028-1099426
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-(beta-D-Arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one 21722017 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/10.1007/BF00568608
3-[(2R,3R,4R,5S,6S)-3-[(2R,4R,5S)-4,5-dihydroxyoxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 162935930 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5CC(C(CO5)O)O)O)O 564.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.027
3-[(2R,3R,4R,5S,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 162989289 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5C(C(C(CO5)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.027
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 16085191 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC5C(C(C(CO5)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.027
3-[3-(4,5-Dihydroxyoxan-2-yl)oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 162935929 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5CC(C(CO5)O)O)O)O 564.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.027
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-0028-1099718
quercetin-3-O-deoxyhexosyl(1-2)pentoside 13784485 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5C(C(C(CO5)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.027
Reynoutrin 5878729 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/10.1007/BF00568608
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1055/S-0028-1099718
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
3',7-Dimethoxy-4',5,8-trihydroxyflavone 8-glucoside 131752831 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.027
8-(beta-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one 162947821 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.06.027

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