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Ceratocapnos heterocarpa

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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 UUID6440105ebc286517991909
Scientific name Ceratocapnos heterocarpa
Authority Durieu
First published in Giorn. Bot. Ital. 1(1): 336 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ceratocapnos umbrosa Walp. Ann. Bot. Syst. (Walpers) 2(1): 30. 1851 [15-16 Dec 1851]
Corydalis heterocarpa (Durieu) Ball J. Linn. Soc., Bot. 16: 314 1877
Corydalis umbrosa (Durieu) Prantl & Kündig Nat. Pflanzenfam. 3(2): 144 (1889)

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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Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Canary Islands
    • Northern Africa
      • Algeria
      • Morocco

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000596338
Tropicos 24000392
KEW urn:lsid:ipni.org:names:671986-1
The Plant List kew-2711065
Open Tree Of Life 538846
Observations.org 127880
NCBI Taxonomy 1095359
IPNI 671986-1
GBIF 3603739
EPPO KKPHE
Elurikkus 382652

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
Environmental impact on the temporal production of chasmogamous and cleistogamous flowers in the mixed breeding system of Viola pubescens Sternberger AL, Ruhil AV, Rosenthal DM, Ballard HE, Wyatt SE PLoS One 11-Mar-2020
PMCID:PMC7065761
doi:10.1371/journal.pone.0229726
PMID:32160228
Zygomorphy evolved from disymmetry in Fumarioideae (Papaveraceae, Ranunculales): new evidence from an expanded molecular phylogenetic framework Sauquet H, Carrive L, Poullain N, Sannier J, Damerval C, Nadot S Ann Bot 26-Mar-2015
PMCID:PMC4407061
doi:10.1093/aob/mcv020
PMID:25814061
Alkaloids from Ceratocapnos heterocarpa plants and in vitro cultures Maria Valpuesta, Natalia Posadas, Inmaculada Ruiz, M. Victoria Silva, Ana I. Gomez, Rafael Suau, Buenaventura Perez, Fernando Pliego, Baltasar Cabezudo Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(94)00576-F
Cularine N-oxide alkaloids from Ceratocapnos heterocarpa Rafael Suau, Rafael Garcia-Segura, M.Victoria Silva, Maria Valpuesta Elsevier BV 05-Apr-2003
doi:10.1016/S0031-9422(96)00441-4
N-Benzylisoquinoline alkaloids from Ceratocapnos heterocarpa Rafael Suau, M.Victoria Silva, Inmaculada Ruiz, María Valpuesta Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97046-8
Structure and total synthesis of (-)-malacitanine. An unusual protoberberine alkaloid from ceratocapnos heterocarpa Rafael Suau, M. Victoria Silva, Maria Valpuesta Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)86777-6
(−)-Caseamine from Ceratocapnos heterocarpa: Structure and total synthesis Rafael Suau, Maria Valpuesta, M.Victoria Silva, Antonio Pedrosa Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80486-2
Cularine alkaloids from Ceratocapnos heterocarpa Rafael Suau, Maria Valpuesta, M.Victoria Silva Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80375-9
(±)-heterocarpine, a hydroxymethylated isoquinoline alkaloid from ceratocapnos heterocarpa Rafael Suau, Natalia Posadas, M.Victoria Silva, Maria Valpuesta Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00198-8
Quaternary protoberberine alkaloids from Ceratocapnos heterocarpa Rafael Suau, M. Victoria Silva, María Valpuesta Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)80045-T

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
> Alkaloids and derivatives / Cularin alkaloids and derivatives
(+)-cis-Cularine N-oxide 14337176 Click to see C[N+]1(CCC2=C3C1CC4=CC(=C(C=C4OC3=C(C=C2)OC)OC)OC)[O-] 357.40 unknown https://doi.org/10.1016/S0031-9422(96)00441-4
(10S)-4,5,17-trimethoxy-2-oxa-11-azatetracyclo[8.7.1.03,8.014,18]octadeca-1(17),3(8),4,6,14(18),15-hexaene 14194078 Click to see COC1=C2C3=C(CCNC3CC4=C(O2)C(=C(C=C4)OC)OC)C=C1 327.40 unknown https://doi.org/10.1016/0031-9422(89)80375-9
Cularidine 442203 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4OC3=C(C=C2)O)OC)OC 327.40 unknown https://doi.org/10.1016/0031-9422(89)80375-9
Norsacocapnine (+) hydrochloride 368266 Click to see COC1=C2C3=C(CCNC3CC4=C(O2)C(=C(C=C4)OC)OC)C=C1 327.40 unknown https://doi.org/10.1016/0031-9422(89)80375-9
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aS)-2,11-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-1,10-diol 101324786 Click to see COC1=C(C2=C(CCN3C2CC4=CC(=C(C=C4C3)O)OC)C=C1)O 327.40 unknown https://doi.org/10.1016/0031-9422(88)80486-2
https://doi.org/10.1016/0031-9422(94)00576-F
(7R,13aS)-2,10,11-trimethoxy-7-oxido-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-1-ol 163191235 Click to see COC1=C(C2=C(CC[N+]3(C2CC4=CC(=C(C=C4C3)OC)OC)[O-])C=C1)O 357.40 unknown https://doi.org/10.1016/0031-9422(93)80045-T
(8S,13aS)-8-(hydroxymethyl)-2,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-1,11-diol 21726228 Click to see COC1=C(C2=C(CCN3C2CC4=CC(=C(C=C4C3CO)OC)O)C=C1)O 357.40 unknown https://doi.org/10.1016/S0040-4020(01)86777-6
https://doi.org/10.1016/0031-9422(94)00576-F
2,10,11-trimethoxy-7-oxido-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-1-ol 163192799 Click to see COC1=C(C2=C(CC[N+]3(C2CC4=CC(=C(C=C4C3)OC)OC)[O-])C=C1)O 357.40 unknown https://doi.org/10.1016/0031-9422(93)80045-T
Caseadine 442188 Click to see COC1=C(C2=C(CCN3C2CC4=CC(=C(C=C4C3)OC)OC)C=C1)O 341.40 unknown https://doi.org/10.1016/0031-9422(94)00576-F
cis-Caseadine N-oxide 163184371 Click to see COC1=C(C2=C(CC[N+]3(C2CC4=CC(=C(C=C4C3)OC)OC)[O-])C=C1)O 357.40 unknown https://doi.org/10.1016/0031-9422(93)80045-T
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
4,5,17-Trimethoxy-2-oxa-11-azatetracyclo[8.7.1.03,8.014,18]octadeca-1(17),3(8),4,6,10,12,14(18),15-octaen-9-one 14892669 Click to see COC1=C2C3=C(C=C1)C=CN=C3C(=O)C4=C(O2)C(=C(C=C4)OC)OC 337.30 unknown https://doi.org/10.1016/0031-9422(89)80375-9
Oxocompostelline 13818256 Click to see COC1=C2C3=C(C=C1)C=CN=C3C(=O)C4=CC5=C(C=C4O2)OCO5 321.30 unknown https://doi.org/10.1016/0031-9422(89)80375-9
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1R)-2-[(3-hydroxy-4-methoxyphenyl)methyl]-1-(hydroxymethyl)-6-methoxy-3,4-dihydro-1H-isoquinolin-7-ol 100956100 Click to see COC1=C(C=C(C=C1)CN2CCC3=CC(=C(C=C3C2CO)O)OC)O 345.40 unknown https://doi.org/10.1016/S0031-9422(98)00198-8
6-Methoxy-2-(4-methoxybenzyl)-1,2,3,4-tetrahydroisoquinolin-7-ol 9839269 Click to see COC1=CC=C(C=C1)CN2CCC3=CC(=C(C=C3C2)O)OC 299.40 unknown https://doi.org/10.1016/S0031-9422(00)97046-8
6-methoxy-2-[(4-methoxy-3-phenylmethoxyphenyl)methyl]-7-phenylmethoxy-3,4-dihydro-1H-isoquinoline 163103321 Click to see COC1=C(C=C(C=C1)CN2CCC3=CC(=C(C=C3C2)OCC4=CC=CC=C4)OC)OCC5=CC=CC=C5 495.60 unknown https://doi.org/10.1016/S0031-9422(00)97046-8
7-methoxy-2-[(4-methoxyphenyl)methyl]-3,4-dihydro-1H-isoquinolin-6-ol 25073096 Click to see COC1=CC=C(C=C1)CN2CCC3=CC(=C(C=C3C2)OC)O 299.40 unknown https://doi.org/10.1016/S0031-9422(00)97046-8
Cambridge id 5259966 792291 Click to see COC1=C(C=C(C=C1)CN2CCC3=CC(=C(C=C3C2)OC)OC)O 329.40 unknown https://doi.org/10.1016/S0031-9422(00)97046-8

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