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Crotalaria crispata

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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 UUID643fd956f03c1109395812
Scientific name Crotalaria crispata
Authority F.Muell. ex Benth.
First published in Fl. Austral.2: 179 (1864)

Description Top

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Synonyms Top

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Common names Top

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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
  • Australasia
    • Australia
      • Northern Territory
      • Queensland
      • Western Australia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185074
Tropicos 13029082
KEW urn:lsid:ipni.org:names:487992-1
The Plant List ild-31212
Open Tree Of Life 3927758
NCBI Taxonomy 1978203
IPNI 487992-1
iNaturalist 564302
GBIF 2941818
EOL 644221
USDA GRIN 410518
CMAUP NPO3630

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
ON THE PRESENCE OF CITRININ IN CROTALARIA CRISPATA. F.V.M. A. J. EWART Oxford University Press (OUP) 03-Feb-2017
doi:10.1093/OXFORDJOURNALS.AOB.A090425
Alkaloids of Crotalaria crispata F. Muell. ex Benth., The Structures of Crispatine and Fulvine CCJ Culvenor, LW Smith CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9630239
Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968 R. Melville, J. J. Willaman, Hui-Lin Li JSTOR 27-Nov-2007
doi:10.2307/4117899

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Elwesine 70697964 Click to see C1CC23CCN(C2CC1O)CC4=CC5=C(C=C34)OCO5 273.33 unknown via CMAUP database
(+)-epi-Vittatine 12304132 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
(11S,13beta,19S)-1,2-Didehydrocrinan-3alpha,11-diol 5282088 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
(1R,13S,15R,18R)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 92211489 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown via CMAUP database
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
11-Epicrinamine 5281172 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
11-O-Methylcrinamine 101493050 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)OC 315.40 unknown via CMAUP database
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown via CMAUP database
Crinamin 73620 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
Powellin 443669 Click to see COC1=C2CN3CCC4(C3CC(C=C4)O)C2=CC5=C1OCO5 301.34 unknown via CMAUP database
Vittatine 443693 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
[(1S,12S,14R)-4-acetyl-9-methoxy-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraen-14-yl] acetate 21826143 Click to see CC(=O)N1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)OC(=O)C 357.40 unknown via CMAUP database
Epinorgalanthamine 443721 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
Galantamine 9651 Click to see CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown via CMAUP database
Norgalanthamine 9838394 Click to see COC1=C2C3=C(CNCCC34C=CC(CC4O2)O)C=C1 273.33 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
(1S,17S,18S,19R)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraene-17,18-diol 7060909 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown via CMAUP database
[(1S,17S,18S,19S)-17-hydroxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraen-18-yl] hexadecanoate 54764247 Click to see CCCCCCCCCCCCCCCC(=O)OC1C(C=C2CCN3C2C1C4=CC5=C(C=C4C3)OCO5)O 525.70 unknown via CMAUP database
Lycorine O1,O2-di-(beta-D-glucopyranoside) 101529183 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5OC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)OCO4 611.60 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Phenanthridine- and phenanthridone-type amaryllidaceae alkaloids
Crinasiadine 442850 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC=C4NC3=O 239.23 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16,19-Dimethoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,13,15,17,19-octaene 25051817 Click to see COC1=C2C=C3C4=CC5=C(C=C4CC[N+]3=CC2=C(C=C1)OC)OCO5 336.40 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben 8434 Click to see CCOC(=O)C1=CC=C(C=C1)O 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Aminobenzaldehyde 11158 Click to see C1=CC(=CC=C1C=O)N 121.14 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
alpha-Glyceryl linoleate 6436630 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(CO)O 354.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans
(3R,4S)-7-(dihydroxymethylidene)-3,4,5-trimethyl-3,4-dihydroisochromene-6,8-dione 219203 Click to see CC1C(OC=C2C1=C(C(=O)C(=C(O)O)C2=O)C)C 250.25 unknown https://doi.org/10.1093/OXFORDJOURNALS.AOB.A090425
> Organoheterocyclic compounds / Pyrrolizines
(1R,4S,5R,6S,16R)-5-hydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione 101773684 Click to see CC1C(=O)OCC2=CCN3C2C(CC3)OC(=O)C(C1(C)O)C 309.36 unknown https://doi.org/10.2307/4117899
(1S,4S,5R,6R,16S)-5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione 53298479 Click to see CC1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)O)(C)O 325.36 unknown https://doi.org/10.1071/CH9630239
(4R,5R,6R,16R)-5,6-dihydroxy-4,5,6-trimethyl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione 56840789 Click to see CC1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)O)(C)O 325.36 unknown via CMAUP database
Isocromadurine 442726 Click to see CC1C(=O)OCC2=CCN3C2C(CC3)OC(=O)C(C1(C)O)C 309.36 unknown https://doi.org/10.1071/CH9630239
https://doi.org/10.2307/4117899
Monocrotalin 4246 Click to see CC1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)O)(C)O 325.36 unknown https://doi.org/10.1071/CH9630239
Unii-txc0AS8ulr 185881 Click to see CC1C(=O)OCC2=CCN3C2C(CC3)OC(=O)C(C1(C)O)C 309.36 unknown https://doi.org/10.2307/4117899
https://doi.org/10.1071/CH9630239
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(-)-8-Demethylmaritidine 443683 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown via CMAUP database
(4aS,10bR)-Noroxomaritidine 11184826 Click to see COC1=C(C=C2CN3CCC4(C3CC(=O)C=C4)C2=C1)O 271.31 unknown via CMAUP database
1-Epideacetylbowdensine 443673 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown via CMAUP database
1-Epijosephinine 70697961 Click to see CC(=O)OC1CCC2C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5 331.40 unknown via CMAUP database
1-O-Acetylbulbisine 70698017 Click to see CC(=O)OC1C(CCC2C13CCN2CC4=C(C5=C(C=C34)OCO5)OC)O 361.40 unknown via CMAUP database
2-O-Acetylbulbisine 56928078 Click to see CC(=O)OC1CCC2C3(C1O)CCN2CC4=C(C5=C(C=C34)OCO5)OC 361.40 unknown via CMAUP database
2-O-Acetylcrinamabine 70697942 Click to see CC(=O)OC1CCC2(C3(C1O)CCN2CC4=CC5=C(C=C34)OCO5)O 347.40 unknown via CMAUP database
3-O-Acetyl-8-O-demethylmaritidine 52937473 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC(=C(C=C43)OC)O)C=C1 315.40 unknown via CMAUP database
4a-Dehydroxycrinamabine 398935 Click to see C1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O 289.33 unknown via CMAUP database
7-Methoxycrinamabine 70698020 Click to see COC1=C2CN3CCC4(C2=CC5=C1OCO5)C3(CCC(C4O)O)O 335.40 unknown via CMAUP database
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy- 5488695 Click to see COC1=C(C=C2C3=CC=CC4=C3N(C=C4)C(=O)C2=C1)O 265.26 unknown via CMAUP database
9-Methoxy-10-hydroxy-4aalpha,6-dihydro-5alpha,10balpha-ethanophenanthridine-3(4H)-one 11140214 Click to see COC1=C(C2=C(CN3CCC24C3CC(=O)C=C4)C=C1)O 271.31 unknown via CMAUP database
CID 3738100 3738100 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)[O-])OCO4 265.26 unknown via CMAUP database
Crinamabine 15378991 Click to see C1CC2(C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O)O 305.32 unknown via CMAUP database
Hippacine 10015025 Click to see C1=CC2=C3C(=C1)C4=CC(=C(C=C4C(=O)N3C=C2)O)O 251.24 unknown via CMAUP database
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown via CMAUP database
Maritinamine 11818191 Click to see COC1=C(C=C2CN3CCC4(C3CC(CC4)O)C2=C1)O 275.34 unknown via CMAUP database
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown via CMAUP database
Siculine 11208052 Click to see COC1=C(C=C2CN3CCC4(C3CC(C=C4)O)C2=C1)O 273.33 unknown via CMAUP database
Ungeremine 159646 Click to see C1C[N+]2=CC3=CC4=C(C=C3C5=CC(=CC1=C52)O)OCO4 266.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-Caffeoyltyramine 9994897 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O 299.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine 5372945 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(2,6-dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-, (2S)- 157671 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=CC=C3O)O 288.25 unknown https://doi.org/10.1093/OXFORDJOURNALS.AOB.A090425
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(S)-2-(3-Hydroxy-4-methoxyphenyl)chroman-7-ol 44257179 Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-Hydroxy-7-methoxyflavan 185609 Click to see COC1=CC2=C(CCC(O2)C3=CC=C(C=C3)O)C=C1 256.30 unknown via CMAUP database

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