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Crioceras dipladeniiflorus

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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 UUID644036576b8bf774551878
Scientific name Crioceras dipladeniiflorus
Authority (Stapf) K.Schum.
First published in Nat. Pflanzenfam. , Nachtr. 2: 56 (1900)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tabernaemontana dipladeniflora Stapf Bull. Misc. Inform. Kew 1894: 121 (1894)
Crioceras longiflorus Pierre Bull. Mens. Soc. Linn. Paris 2: 1312 (1897)
Crioceras longiflora Stapf

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000927094
Tropicos 1805248
KEW urn:lsid:ipni.org:names:78181-1
The Plant List kew-49082
Observations.org 275104
IPNI 78181-1
GBIF 8097978
Freebase /m/010pfmrn
Elurikkus 642506
Wikipedia Crioceras_dipladeniiflorus
Open Tree Of Life 937758

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)!
Title Authors Publication Released IDs
La criocerine: Nouvel alcaloide isole des tiges de Crioceras dipladeniiflorus Jean Bruneton, Christiane Kan-Fan, André Cavé Elsevier BV 12-Feb-2003
doi:10.1016/0031-9422(75)85130-2
La méthoxy-12Δ14-vincamine, nouvel alcaloïde isole du Crioceras dipladeniiflorus (Staff) K. Schumann (Apocynacées) J. Bruneton, Ad. Cavé, A. Cavé Elsevier BV 25-Jul-2002
doi:10.1016/0040-4020(73)80073-0

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 / Eburnan-type alkaloids
14,15-Didehydro-12-methoxyvincamine 181142 Click to see CCC12CC(N3C4=C(CCN(C41)CC=C2)C5=C3C(=CC=C5)OC)(C(=O)OC)O 382.50 unknown https://doi.org/10.1016/0031-9422(75)85130-2
Dehydroepivincamine 182094 Click to see CCC12CC(N3C4=CC=CC=C4C5=C3C1N(CC5)CC=C2)(C(=O)OC)O 352.40 unknown https://doi.org/10.1016/0031-9422(75)85130-2
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
methyl (1S,16R,18S,20S)-20-ethyl-17-oxa-3,13-diazahexacyclo[11.7.0.02,10.03,18.04,9.016,20]icosa-2(10),4,6,8,14-pentaene-18-carboxylate 163089080 Click to see CCC12CC3(N4C5=CC=CC=C5C6=C4C1N(CC6)C=CC2O3)C(=O)OC 350.40 unknown https://doi.org/10.1016/0031-9422(75)85130-2
> Alkaloids and derivatives / Schizozygine alkaloids
(1R,14S,18S,19R,22S)-22-hydroxy-8,10-dioxa-4,17-diazaheptacyclo[15.4.3.01,18.04,19.05,13.07,11.014,19]tetracosa-5,7(11),12-trien-3-one 163018146 Click to see C1CN2CCC(C34C2C5(C1C6=CC7=C(C=C6N5C(=O)C3)OCO7)CC4)O 354.40 unknown https://doi.org/10.1016/0040-4020(73)80073-0

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