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Crotalaria laburnifolia

Crotalaria laburnifolia - 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 UUID643fdd77091e9293820052
Scientific name Crotalaria laburnifolia
Authority L.
First published in Sp. Pl.: 715 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Clavulium laburnifolium (L.) M.R.Almeida Fl. Maharashtra2: 28 (1998)

Common names Top

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No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Crotalaria laburnifolia subsp. australis (Baker f.) Polhill Kew Bull.22: 213 (1968)
Crotalaria laburnifolia subsp. eldomae (Baker f.) Polhill Kew Bull.22: 211 (1968)
Crotalaria laburnifolia subsp. laburnifolia L. Unknown
Crotalaria laburnifolia subsp. petiolaris (Franch.) Polhill Kew Bull.22: 211 (1968)
Crotalaria laburnifolia subsp. tenuicarpa Polhill Kew Bull.22: 212 (1968)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Burundi
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Seychelles
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Sri Lanka
    • Indo-China
      • Thailand
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000206634
USDA Plants CRLA17
Tropicos 13029248
KEW urn:lsid:ipni.org:names:488337-1
The Plant List ild-5284
Open Tree Of Life 1025283
NCBI Taxonomy 992673
IPNI 488337-1
iNaturalist 369997
GBIF 2942065
EOL 689748
USDA GRIN 12332
Wikipedia Crotalaria_laburnifolia
CMAUP NPO21482

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
The dynamics of vegetation diversity and biomass under traditional grazing in Ethiopia's Somali rangeland Gebremedhn HH, Dejene SW, Tuffa S, Tesfay Y, Mensah S, Devenish AJ Plant Environ Interact 07-Nov-2023
PMCID:PMC10711641
doi:10.1002/pei3.10127
PMID:38089846
Medicinal Uses of the Fabaceae Family in Zimbabwe: A Review Maroyi A Plants (Basel) 10-Mar-2023
PMCID:PMC10051751
doi:10.3390/plants12061255
PMID:36986943
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Medicinal plants used for the management of respiratory diseases in Zimbabwe: Review and perspectives potential management of COVID-19 Nyagumbo E, Pote W, Shopo B, Nyirenda T, Chagonda I, Mapaya RJ, Maunganidze F, Mavengere WN, Mawere C, Mutasa I, Kademeteme E, Maroyi A, Taderera T, Bhebhe M Phys Chem Earth (2002) 21-Sep-2022
PMCID:PMC9489988
doi:10.1016/j.pce.2022.103232
PMID:36161239
Herb-Induced Liver Injury—A Challenging Diagnosis Nunes DR, Monteiro CS, dos Santos JL Healthcare (Basel) 31-Jan-2022
PMCID:PMC8872293
doi:10.3390/healthcare10020278
PMID:35206892
Current Knowledge and Perspectives of Pyrrolizidine Alkaloids in Pharmacological Applications: A Mini-Review Wei X, Ruan W, Vrieling K Molecules 31-Mar-2021
PMCID:PMC8037423
doi:10.3390/molecules26071970
PMID:33807368
B N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771680
doi:10.1016/B978-0-7020-7463-9.50010-0
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
Insight into HIV of IFN-Induced Myxovirus Resistance 2 (MX2) Expressed by Traditional Chinese Medicine Hung TC, Lee WY, Chen KB, Chan YC, Chen CY Biomed Res Int 18-Jun-2014
PMCID:PMC4086518
doi:10.1155/2014/871576
PMID:25045710
Adverse drug reactions in some African herbal medicine: literature review and stakeholders’ interview Kamsu-Foguem B, Foguem C Integr Med Res 23-May-2014
PMCID:PMC5481732
doi:10.1016/j.imr.2014.05.001
PMID:28664088
Medicinal plants potential and use by pastoral and agro-pastoral communities in Erer Valley of Babile Wereda, Eastern Ethiopia Belayneh A, Asfaw Z, Demissew S, Bussa NF J Ethnobiol Ethnomed 22-Oct-2012
PMCID:PMC3549935
doi:10.1186/1746-4269-8-42
PMID:23082858
A survey of plants and plant products traditionally used in livestock health management in Buuri district, Meru County, Kenya Gakuubi MM, Wanzala W J Ethnobiol Ethnomed 08-Oct-2012
PMCID:PMC3539861
doi:10.1186/1746-4269-8-39
PMID:23044218
Pyrrolizidine Alkaloids from <i>Crotalaria laburnifolia</i> subspec. <i>australis</i> E. Röder, K. Pegel, H. Wiedenfeld, N. Krey Informa UK Limited 20-Nov-2007
doi:10.3109/13880209209053988
Pyrrolizidine and seco-pyrrolizidine alkaloids of Crotalaria laburnifolia L. subspecies eldomae. Crout DH J Chem Soc Perkin 1 01-Jan-1972
doi:10.1039/P19720001602
PMID:5066465
Phytochemical studies on Crotalaria laburnifolia. Subramanian SS, Nagarajan S Planta Med 01-Jan-1970
doi:10.1055/S-0028-1099931
PMID:5734382

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 / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Crotonate 6971246 Click to see CC=CC(=O)[O-] 85.08 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,3S,5S,7R,8S,9S,10S,11R,12R)-12-(hydroxymethyl)-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-3,7,9,10-tetrol 102298137 Click to see CC1(CCCC23C1C(C(C45C2C(CC(C4)C(=C)C5O)O)(OC3)O)O)CO 366.40 unknown via CMAUP database
(1S,2S,5S,7R,8S,9S,10S,11R,12R)-7,9,10-trihydroxy-12-(hydroxymethyl)-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadec-14-en-3-one 102298136 Click to see CC1(CC=CC23C1C(C(C45C2C(=O)CC(C4)C(=C)C5O)(OC3)O)O)CO 362.40 unknown via CMAUP database
1alpha,6beta,7beta,11alpha,15beta-Pentahydroxy-7alpha,20-epoxy-ent-kaur-16-ene 101677459 Click to see CC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5O)O)(OC3)O)O)O)C 366.40 unknown via CMAUP database
Kaurane-7beta,16,17-triol 101676167 Click to see CC1(CCCC2(C1CC(C34C2CCC(C3)C(C4)(CO)O)O)C)C 322.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
7-Megastigmene-3,5,6,9-tetraol 637237 Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)O 244.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,3E,5S,9R,12E)-3,12-dimethyl-8-methylidene-6,18-dioxatricyclo[14.2.1.05,9]nonadeca-3,12,16(19)-triene-7,17-dione 6451060 Click to see CC1=CCCC2=CC(CC(=CC3C(CC1)C(=C)C(=O)O3)C)OC2=O 328.40 unknown via CMAUP database
(1S,2'R,5R,6S,9R,10S)-2'-(hydroxymethyl)-10-(methoxymethyl)-3',3'-dimethylspiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,1'-cyclohexane]-2,11-dione 49870970 Click to see CC1(CCCC2(C1CO)COC(=O)C34C2CCC(C3)C(C4=O)COC)C 364.50 unknown via CMAUP database
(1S,2'R,5R,6S,9R)-2'-(hydroxymethyl)-3',3'-dimethyl-10-methylidenespiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,1'-cyclohexane]-2,11-dione 49870969 Click to see CC1(CCCC2(C1CO)COC(=O)C34C2CCC(C3)C(=C)C4=O)C 332.40 unknown via CMAUP database
(1S,2S,3R,5R,7R,8S,11S,14R,17S,20R)-3,5,7-trihydroxy-14-methyl-6-methylidene-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one 72947649 Click to see CC12CCC3C4(C1C(OC2)OC4)C5C(CC6(CC5(C(C6=C)O)C(=O)O3)O)O 378.40 unknown via CMAUP database
(1S,2S,3R,5S,7R,8S,11S,14R,17S,20R)-3,7-dihydroxy-14-methyl-6-methylidene-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one 20056294 Click to see CC12CCC3C4(C1C(OC2)OC4)C5C(CC6CC5(C(C6=C)O)C(=O)O3)O 362.40 unknown via CMAUP database
(1S,4S,6R,8R,9R,12S,13S,14R,16S,17S)-6,9,14,17-tetrahydroxy-7,7,17-trimethyl-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione 72947650 Click to see CC1(C(CC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5(C)O)C(=O)O2)O)O)C 396.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,14S,16R,17R,19R)-9,19-dihydroxy-7,7-dimethyl-18-methylidene-3,10,15-trioxahexacyclo[15.2.1.01,13.04,12.08,12.014,16]icosan-2-one 72947453 Click to see CC1(CCC2C3(C1C(OC3)O)C4C5C(O5)C6CC4(C(C6=C)O)C(=O)O2)C 362.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,14S,16S,17S,18S)-9,14,17,18-tetrahydroxy-7,7,17-trimethyl-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-2-one 72947651 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(C5(C)O)O)C(=O)O2)O)C 382.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,16R,18R)-9,18-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-2-one 76309974 Click to see CC1(CCC2C3(C1C(OC3)O)C4CCC5CC4(C(C5=C)O)C(=O)O2)C 348.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,16S,18R)-9,18-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadec-14-en-2-one 72947454 Click to see CC1(CCC2C3(C1C(OC3)O)C4C=CC5CC4(C(C5=C)O)C(=O)O2)C 346.40 unknown via CMAUP database
(6R,9S,13R,16S)-1alpha,6,11alpha-Trihydroxy-15-oxo-6,20:12beta,17-diepoxy-6,7-secokaurane-7-oic acid 7,1-lactone 24764126 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(C5C6CC4(C(=O)C6CO5)C(=O)O2)O)C 378.40 unknown via CMAUP database
Enemin 352542 Click to see CC1(C(CC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown via CMAUP database
Epinodosin 9975896 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown via CMAUP database
Longirabdolide C 101670648 Click to see CC1(C(CC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)O)C 378.40 unknown via CMAUP database
Macrocalin A 11382408 Click to see CC1(CCC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)C 346.40 unknown via CMAUP database
Maoyecrystal D 46883375 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5CO)C(=O)O2)O)C 380.40 unknown via CMAUP database
Nodosin 10248089 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown via CMAUP database
Sculponeatin A 15922655 Click to see CC12CCC3C4(C1C(OC2)OC4)C5C(CC6CC5(C(=O)C6=C)C(=O)O3)O 360.40 unknown via CMAUP database
Sculponin F 44557721 Click to see CC(=O)OC1C(=C)C2CC(C3C1(C2)C(=O)OC4C35COC(C5C(C(C4)O)(C)C)O)O 422.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,1'S,4S,4'S,6S,7'R,8R,9R,10'S,12S,13S,13'S,14'S,15'R,16R,17S,17'S,25'R)-6,9,15'-trihydroxy-7,7,7'-trimethylspiro[3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-17,21'-3,9,11,22-tetraoxaheptacyclo[15.6.1.17,10.01,14.04,13.018,23.013,25]pentacos-18(23)-ene]-2,2',18-trione 44557720 Click to see CC1(C(CC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C56CCC7=C(O6)C89CC7CC(C8C13COC4C1C(CCC3OC9=O)(CO4)C)O)C(=O)O2)O)C 722.80 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Sculponin D 44557719 Click to see CC12CCC3C4(C1C(OC2)OC4)C5C(CC6CC5(C7=C6CCC8(O7)C9CC(C1C(C9)(C8=O)C(=O)OC2C11COC4C1C(CC2)(CO4)C)O)C(=O)O3)O 720.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
[(2S)-2-acetamido-3-phenylpropyl] (2S)-2-benzamido-3-phenylpropanoate 46222163 Click to see CC(=O)NC(CC1=CC=CC=C1)COC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
Senkyunolide A 3085257 Click to see CCCCC1C2=C(C=CCC2)C(=O)O1 192.25 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
4-Methylene-5beta-hydroperoxyovatodiolide 24970924 Click to see CC1=CC2C(CCC(=C)C(CCC3=CC(C1)OC3=O)OO)C(=C)C(=O)O2 360.40 unknown via CMAUP database
4alpha-Hydroperoxy-5-enovatodiolide 24970923 Click to see CC1=CC2C(CCC(C=CCC3=CC(C1)OC3=O)(C)OO)C(=C)C(=O)O2 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Cedrusin 11210164 Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)O 346.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Martynoside 5319292 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 652.60 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-0028-1099931
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4E,6R,7S,11Z)-4-ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 6442572 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown via CMAUP database
(1R,4Z,6R,7S,11Z)-4-ethylidene-7-hydroxy-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 163190470 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)O)C 351.40 unknown https://doi.org/10.1039/P19720001602
(1R,4Z,6R,7S,11Z)-4-ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 12041879 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(CO)O)C 381.40 unknown https://doi.org/10.1039/P19720001602
(1R,6R,7S)-4-ethylidene-7-hydroxy-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 163081802 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)O)C 351.40 unknown https://doi.org/10.1039/P19720001602
(1S,4E,6R,7R,16R,17R)-4-Ethylidene-7,16-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 16058066 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(C(C3)O)OC1=O)(C)O)C 351.40 unknown https://doi.org/10.1039/P19720001602
(8R,9R,11E,14S,15R,16S)-11-ethylidene-8,15-dihydroxy-8,9-dimethyl-6,13-dioxa-1-azatricyclo[12.2.1.04,16]heptadec-3-ene-7,12-dione 101606296 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(C(C3)OC1=O)O)(C)O)C 351.40 unknown https://doi.org/10.3109/13880209209053988
(8R,9R,11Z,14R,15S,16R)-11-ethylidene-8,15-dihydroxy-8,9-dimethyl-6,13-dioxa-1-azatricyclo[12.2.1.04,16]heptadec-3-ene-7,12-dione 162964920 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(C(C3)OC1=O)O)(C)O)C 351.40 unknown https://doi.org/10.1039/P19720001602
11-Ethylidene-8,15-dihydroxy-8,9-dimethyl-6,13-dioxa-1-azatricyclo[12.2.1.04,16]heptadec-3-ene-7,12-dione 168485 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(C(C3)OC1=O)O)(C)O)C 351.40 unknown https://doi.org/10.1039/P19720001602
4-Ethylidene-7-hydroxy-6,7,14-trimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 259733 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1039/P19720001602
4-Ethylidene-7-hydroxy-7-(hydroxymethyl)-6,14-dimethyl-2,9-dioxa-14-azabicyclo[9.5.1]heptadec-11-ene-3,8,17-trione 85433052 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(CO)O)C 381.40 unknown https://doi.org/10.1039/P19720001602
4-Ethylidene-7,16-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 271154 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(C(C3)O)OC1=O)(C)O)C 351.40 unknown https://doi.org/10.1039/P19720001602
Anacrotine 5281720 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(C(C3)O)OC1=O)(C)O)C 351.40 unknown https://doi.org/10.1039/P19720001602
https://doi.org/10.3109/13880209209053988
Madurensine 5459074 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(C(C3)OC1=O)O)(C)O)C 351.40 unknown https://doi.org/10.3109/13880209209053988
Senkirkine 5281752 Click to see CC=C1CC(C(C(=O)OCC2=CCN(CCC(C2=O)OC1=O)C)(C)O)C 365.40 unknown https://doi.org/10.1039/P19720001602

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