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Colchicum ritchiei

Colchicum ritchiei - 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 UUID644025a81b6e4753825527
Scientific name Colchicum ritchiei
Authority R.Br.
First published in Narr. Travels Africa , App.: 241 (1826)

Description Top

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Synonyms Top

Scientific name Authority First published in
Colchicum aegyptiacum Boiss. Diagn. Pl. Orient. 5: 66 (1844)
Colchicum stenopetalum Boiss. & Buhse ex Stef. Sborn. B'lghar. Akad. Nauk 22: 30 (1926)
Colchicum ritchii var. pusillum Bég. & A.Vacc. Contr. Fl. Lib. 21. 1913

Common names Top

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Language Common/alternative name
Arabic لحلاح ريتشي
Arabic خميرة
Arabic عكنة
Arabic فرج الأرض

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • Western Asia
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000764009
Tropicos 100170726
KEW urn:lsid:ipni.org:names:533382-1
The Plant List kew-302941
Open Tree Of Life 111345
NCBI Taxonomy 1094113
IPNI 533382-1
iNaturalist 848315
GBIF 2739732
Freebase /m/010fch7j
EOL 1087041
USDA GRIN 11145
Wikipedia Colchicum_ritchii

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
Notizen: New Colchicine and Homoaporphine- N-Oxide Alkaloids from Colchicum Ritchii: The First Homoaporphine TV-Oxide Found in Nature Musa H. Abu Zarga, Raed A. Al-Qawasmeh, Salim S. Sabri, Taleb H. Al-Tel, Wolfgang Voelter Walter de Gruyter GmbH 11-Feb-2015
doi:10.1515/ZNB-1995-0923
Central-to-Axial Chirality Transfer in the Benzannulation Reaction of Optically Pure Fischer Carbene Complexes in the Synthesis of Allocolchicinoids Vorogushin AV, Wulff WD, Hansen HJ Tetrahedron 28-Jan-2008
PMCID:PMC2344159
doi:10.1016/j.tet.2007.10.115
PMID:19180172
New Natural Colchicinoids: Indications of Two Possible Catabolic Routes for the Colchicine Alkaloids Taleb H. Al-Tel, Musa H. Abu Zarga, Salim S. Sabri, Alan J. Freyer, Maurice Shamma American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50069A013
Effects of the flavone luteolin, isolated from <i>Colchicum richii</i>, on guinea‐pig isolated smooth muscle and heart and on blood pressure and blood flow S. Abdalla, M. Abu Zarga, S. Sabri Wiley 18-Oct-2006
doi:10.1002/PTR.2650080503
Five New Alkaloids from Colchicum ritchii Alan J. Freyer, Musa H. Abu Zarga, Sadiqa Firdous, Hélène Guinaudeau, Maurice Shamma American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50052A018
High resolution NMR Studies of the Homoaporphine Alkaloids fromColchicum decaisnei Musa H. Abu Zarga Wiley 07-Jan-2005
doi:10.1002/PRAC.199533701141

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 / Allocolchicine alkaloids
(-)-Androbiphenyline 10927179 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=C1C(=C(C=C3)OC)O)OC)OC)OC 387.40 unknown https://doi.org/10.1021/NP50069A013
> Alkaloids and derivatives / Androcymbine alkaloids
Androcymbine 5462452 Click to see CN1CCC23C=C(C(=O)C=C2C1CCC4=CC(=C(C(=C34)OC)O)OC)OC 371.40 unknown https://doi.org/10.1021/NP50052A018
O-methylandrocymbine 15286666 Click to see CN1CCC23C=C(C(=O)C=C2C1CCC4=CC(=C(C(=C34)OC)OC)OC)OC 385.50 unknown https://doi.org/10.1021/NP50052A018
> Alkaloids and derivatives / Homoaporphines
Kreysigine 15560400 Click to see CN1CCC2=CC(=C(C3=C2C1CCC4=CC(=C(C(=C43)OC)OC)OC)O)OC 385.50 unknown https://doi.org/10.1515/ZNB-1995-0923
> Alkaloids and derivatives / Lumicolchicine alkaloids
(10S,12R,16S)-3,4,5,14-tetramethoxy-10-(methylamino)tetracyclo[9.5.0.02,7.012,16]hexadeca-1(11),2,4,6,14-pentaen-13-one 163051987 Click to see CNC1CCC2=CC(=C(C(=C2C3=C1C4C3C=C(C4=O)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1515/ZNB-1995-0923
3,4,5,14-Tetramethoxy-10-(methylamino)tetracyclo[9.5.0.02,7.012,16]hexadeca-1(11),2,4,6,14-pentaen-13-one 12311431 Click to see CNC1CCC2=CC(=C(C(=C2C3=C1C4C3C=C(C4=O)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1515/ZNB-1995-0923
> Alkaloids and derivatives / Phenethylisoquinoline alkaloids
(S)-autumnaline 13878324 Click to see CN1CCC2=CC(=C(C=C2C1CCC3=CC(=C(C(=C3)OC)OC)O)O)OC 373.40 unknown https://doi.org/10.1021/NP50052A018
Isoautumnaline 183312 Click to see CN1CCC2=CC(=C(C=C2C1CCC3=CC(=C(C(=C3)OC)OC)O)OC)O 373.40 unknown https://doi.org/10.1021/NP50052A018
> Benzenoids / Phenol ethers / Anisoles
N-(6,13-dihydroxy-5,14,15-trimethoxy-8-tricyclo[9.4.0.02,7]pentadeca-1(15),2(7),3,5,11,13-hexaenyl)acetamide 14655861 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=C1C(=C(C=C3)OC)O)OC)OC)O 373.40 unknown https://doi.org/10.1021/NP50069A013
> Hydrocarbon derivatives / Tropones
(7S)-1,2,3,10-tetramethoxy-7-[(2-methoxyphenyl)methyl-methylamino]-6,7-dihydro-5H-benzo[a]heptalen-9-one 162958167 Click to see CN(CC1=CC=CC=C1OC)C2CCC3=CC(=C(C(=C3C4=CC=C(C(=O)C=C24)OC)OC)OC)OC 491.60 unknown https://doi.org/10.1515/ZNB-1995-0923
(7S)-3-hydroxy-1,2,10-trimethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 14413737 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 357.40 unknown https://doi.org/10.1021/NP50052A018
1,2,3,10-tetramethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 2832 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1021/NP50052A018
1,2,3,10-tetramethoxy-7-[(2-methoxyphenyl)methyl-methylamino]-6,7-dihydro-5H-benzo[a]heptalen-9-one 162958166 Click to see CN(CC1=CC=CC=C1OC)C2CCC3=CC(=C(C(=C3C4=CC=C(C(=O)C=C24)OC)OC)OC)OC 491.60 unknown https://doi.org/10.1515/ZNB-1995-0923
2-Demthyldemecolcine 146030 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)O)OC 357.40 unknown https://doi.org/10.1021/NP50052A018
3-Desmethylcolchicine 299664 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)O 385.40 unknown https://doi.org/10.1021/NP50052A018
Colchicine 6167 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 399.40 unknown https://doi.org/10.1021/NP50052A018
Colchifoline 100132 Click to see COC1=CC=C2C(=CC1=O)C(CCC3=CC(=C(C(=C32)OC)OC)OC)NC(=O)CO 415.40 unknown https://doi.org/10.1021/NP50052A018
Deacetylamino-7-oxocolchicine 97092 Click to see COC1=CC=C2C(=CC1=O)C(=O)CCC3=CC(=C(C(=C32)OC)OC)OC 356.40 unknown https://doi.org/10.1021/NP50069A013
Demecolcine 220401 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1021/NP50052A018
Specioritchine 183313 Click to see CN(CC1=CC=CC=C1O)C2CCC3=CC(=C(C(=C3C4=CC=C(C(=O)C=C24)OC)OC)OC)O 463.50 unknown https://doi.org/10.1021/NP50052A018
Speciosine 330188 Click to see CN(CC1=CC=CC=C1O)C2CCC3=CC(=C(C(=C3C4=CC=C(C(=O)C=C24)OC)OC)OC)OC 477.50 unknown https://doi.org/10.1515/ZNB-1995-0923
> Hydrocarbon derivatives / Tropones / Tropolones
(7S)-10-hydroxy-1,2,3-trimethoxy-7-(methylamino)-6,7-dihydro-5H-benzo[a]heptalen-9-one 235315 Click to see CNC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)O)OC)OC)OC 357.40 unknown https://doi.org/10.1021/NP50052A018
Colchiceine 234105 Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)O)OC)OC)OC 385.40 unknown https://doi.org/10.1021/NP50052A018
> Organoheterocyclic compounds / Benzodioxoles
(-)-Cornigerine 10000015 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=CC=C(C(=O)C=C14)OC)OC)OCO3 383.40 unknown https://doi.org/10.1021/NP50052A018
Heptaleno(2',1':4,5)benzo(1,2-d)(1,3)dioxole-4,6-dione, 7,8-dihydro-3,13-dimethoxy- 181423 Click to see COC1=CC=C2C(=CC1=O)C(=O)CCC3=CC4=C(C(=C32)OC)OCO4 340.30 unknown https://doi.org/10.1021/NP50069A013
N-(5,19-dimethoxy-6-oxo-15,17-dioxapentacyclo[10.7.0.02,8.03,7.014,18]nonadeca-1(19),2(8),4,12,14(18)-pentaen-9-yl)acetamide 162955104 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=C1C5C4C=C(C5=O)OC)OC)OCO3 383.40 unknown https://doi.org/10.1515/ZNB-1995-0923
N-[(3R,7R,9S)-5,19-dimethoxy-6-oxo-15,17-dioxapentacyclo[10.7.0.02,8.03,7.014,18]nonadeca-1(19),2(8),4,12,14(18)-pentaen-9-yl]acetamide 162955105 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=C1C5C4C=C(C5=O)OC)OC)OCO3 383.40 unknown https://doi.org/10.1002/PRAC.199533701141
N-[(3R,9S)-5,19-dimethoxy-6-oxo-15,17-dioxapentacyclo[10.7.0.02,8.03,7.014,18]nonadeca-1(19),2(8),4,12,14(18)-pentaen-9-yl]acetamide 163193471 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=C1C5C4C=C(C5=O)OC)OC)OCO3 383.40 unknown https://doi.org/10.1002/PRAC.199533701141
N-[(3S,7R,9S)-5,19-dimethoxy-6-oxo-15,17-dioxapentacyclo[10.7.0.02,8.03,7.014,18]nonadeca-1(19),2(8),4,12,14(18)-pentaen-9-yl]acetamide 162955106 Click to see CC(=O)NC1CCC2=CC3=C(C(=C2C4=C1C5C4C=C(C5=O)OC)OC)OCO3 383.40 unknown https://doi.org/10.1515/ZNB-1995-0923
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Colchiritchine 5491721 Click to see COC1=CC23CCNC(C2=CC1=O)CCC4=CC5=C(C(=C34)OC)OCO5 355.40 unknown https://doi.org/10.1021/NP50052A018
> 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/10.1002/PTR.2650080503

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