Amsonia elliptica

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Details Top

Internal ID	UUID64403c0a53413167999719
Scientific name	Amsonia elliptica
Authority	(Thunb.) Roem. & Schult.
First published in	Syst. Veg., ed. 15 bis 4: 432 (1819)

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Synonyms Top

Scientific name	Authority	First published in
Ansonia elliptica	Raf.	New Fl. 4: 58 (1838)
Tabernaemontana elliptica	Thunb.	Syst. Veg. ed. 14 : 255 (1784)
Amsonia sinensis	Tsiang & P.T.Li	Acta Phytotax. Sin. 11: 368 (1973)

Common names Top

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Language	Common/alternative name
Japanese	ホソバチョウジソウ
Japanese	チョウジソウ
Korean	정향풀
Swedish	japansk amsonia
Chinese	水甘草

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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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Maintain seeds at 20°C for 3 months, then transfer to 4°C for another 3 months.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China Southeast
- Eastern Asia
  - Japan
  - Korea

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000967098
Tropicos	1801586
KEW	urn:lsid:ipni.org:names:76906-1
The Plant List	kew-8447
Open Tree Of Life	173548
NCBI Taxonomy	403098
IPNI	76906-1
iNaturalist	708085
GBIF	3619167
Freebase	/m/0nbd37r
EPPO	AMVEL
EOL	2898443

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

Editorial: Seed-environment interactions

Xu F, Asghar MA

Front Plant Sci

04-May-2023

PMCID:	PMC10195042
doi:	10.3389/fpls.2023.1201047
PMID:	37215288

Characterization of the complete chloroplast genome of Amsonia elliptica (Apocynaceae)

Kim Y, Nam BM, Kim I, Deng T, Kim C

Mitochondrial DNA B Resour

29-Mar-2023

PMCID:	PMC10062215
doi:	10.1080/23802359.2023.2192834
PMID:	37006955

Lupeol Accumulation Correlates with Auxin in the Epidermis of Castor

Li D, Pan C, Lu J, Zaman W, Zhao H, Zhang J, Lü S

Molecules

17-May-2021

PMCID:	PMC8156332
doi:	10.3390/molecules26102978
PMID:	34067825

Studies on plants containing indole alkaloids. VII. Isolation of several Aspidosperma- and Vincamine-type alkaloids from the seeds of Amsonia elliptica Roem. et Schult.

NORIO AIMI, YOSHIHISA ASADA, SHINICHIRO SAKAI, JOJU HAGINIWA

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.26.1182

Biosynthesis of the 24-methylcholesterols dihydrobrassicasterol and campesterol in cultured cells of Amsonia elliptica: incorporation of [1,2-13C2]acetate and [2-13C,2H3]acetate

Shujiro Seo, Atsuko Uomori, Yohko Yoshimura, Ken'ichi Takeda, Hiroshi Noguchi, Yutaka Ebizuka, Ushio Sankawa, Haruo Seto

Royal Society of Chemistry (RSC)

26-Apr-2004

doi:	10.1039/P19920000569

New indole alkaloids from Alstonia macrophylla.

Kam TS, Choo YM

J Nat Prod

01-Apr-2004

doi:	10.1021/NP034041V
PMID:	15104482

Biosynthesis of campesterol and dihydrobrassicasterol in cultured cells of Amsonia elliptica

Atsuko Uomori, Yuzo Nakagawa, Shinya Yoshimatsu, Shujiro Seo, Ushio Sankawa, Ken'ichi Takeda

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(92)83108-B

Indole alkaloids in hairy roots of Amsonia elliptica

Martina Sauerwein, Kanji Ishimaru, Koichiro Shimomura

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)95193-8

17α-O-Methylyohimbine and vallesiachotamine from roots ofAmsonia elliptica

Martina Sauerwein, Koichiro Shimomura

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(90)80225-6

Degradation of 17α-O-methylyohimbine in Amsonia elliptica roots

Martina Sauerwein, Koichiro Shimomura

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(91)84183-S

New Indole Alkaloids from Amsonia sinensis.

Liu HM, Wu B, Zheng QT, Feng XZ

Planta Med

01-Dec-1991

doi:	10.1055/S-2006-960207
PMID:	17226203

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 / Akuammilan and related alkaloids
Strictamine	21159178	Click to see CC=C1CN2CCC34C(C1CC2C3=NC5=CC=CC=C45)C(=O)OC	322.40	unknown	https://doi.org/10.1021/NP034041V
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
Lochnericine	11382599	Click to see CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=CC=CC=C6N3)C(=O)OC	352.40	unknown	https://doi.org/10.1055/S-2006-960207 https://doi.org/10.1021/NP034041V
methyl (1R,12R)-12-(1-hydroxyethyl)-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate	118701461	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)O	354.40	unknown	https://doi.org/10.1021/NP034041V
Minovincinine	443401	Click to see CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)O	354.40	unknown	https://doi.org/10.1055/S-2006-960207
Vincadifformine	94255	Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC	338.40	unknown	https://doi.org/10.1055/S-2006-960207 https://doi.org/10.1021/NP034041V
> Alkaloids and derivatives / Eburnan-type alkaloids
Dehydroepivincamine	182094	Click to see CCC12CC(N3C4=CC=CC=C4C5=C3C1N(CC5)CC=C2)(C(=O)OC)O	352.40	unknown	https://doi.org/10.1248/CPB.26.1182
Eburnamine	101699	Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O	296.40	unknown	https://doi.org/10.1021/NP034041V
> Alkaloids and derivatives / Pleiocarpaman alkaloids
Pleiocarpamine	5385014	Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC	322.40	unknown	https://doi.org/10.1016/0031-9422(91)84183-S https://doi.org/10.1016/S0031-9422(00)95193-8 https://doi.org/10.1016/0031-9422(90)80225-6
> Alkaloids and derivatives / Plumeran-type alkaloids
methyl (1R,12R,16R,19S)-12-ethyl-16-oxido-8-aza-16-azoniapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate	163188582	Click to see CCC12CC(=C3C4(C1[N+](CC4)(CC=C2)[O-])C5=CC=CC=C5N3)C(=O)OC	352.40	unknown	https://doi.org/10.1248/CPB.26.1182
methyl (1R,12R,19S)-12-ethyl-15-oxo-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate	10915101	Click to see CCC12CC(=C3C4(C1N(CC4)C(=O)C=C2)C5=CC=CC=C5N3)C(=O)OC	350.40	unknown	https://doi.org/10.1248/CPB.26.1182
methyl (1R,12R,19S)-12-ethyl-16-oxido-8-aza-16-azoniapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9,13-pentaene-10-carboxylate	163195513	Click to see CCC12CC(=C3C4(C1[N+](CC4)(CC=C2)[O-])C5=CC=CC=C5N3)C(=O)OC	352.40	unknown	https://doi.org/10.1248/CPB.26.1182
Tabersonine	20485	Click to see CCC12CC(=C3C4(C1N(CC4)CC=C2)C5=CC=CC=C5N3)C(=O)OC	336.40	unknown	https://doi.org/10.1021/NP034041V
> Alkaloids and derivatives / Strychnos alkaloids
(11S,12Z,17S)-12-ethylidene-6-hydroxy-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2(7),3,5,9-tetraene-10-carbaldehyde	101627612	Click to see CC=C1CN2CCC34C2CC1C(=C3NC5=C4C=CC=C5O)C=O	308.40	unknown	https://doi.org/10.1021/NP034041V
> Alkaloids and derivatives / Yohimbine alkaloids
CID 5458418	5458418	Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O	354.40	unknown	https://doi.org/10.1021/NP034041V
methyl (1S,15R,16R,19R,20S)-16-hydroxy-16-methyl-17-oxa-3,13-diazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8-tetraene-19-carboxylate	5318152	Click to see CC1(C2CN3CCC4=C(C3CC2C(CO1)C(=O)OC)NC5=CC=CC=C45)O	370.40	unknown	https://doi.org/10.1021/NP034041V
Tetrahydroalstonine	72340	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1021/NP034041V
Yohimbine	8969	Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O	354.40	unknown	https://doi.org/10.1016/0031-9422(91)84183-S
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(92)83108-B https://doi.org/10.1039/P19920000569
22,23-Dihydrobrassicasterol	5283637	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(92)83108-B https://doi.org/10.1039/P19920000569
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1039/P19920000569 https://doi.org/10.1016/0031-9422(92)83108-B
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1021/NP034041V
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
methyl (1R,9R,11S,14E,17S)-14-ethylidene-18-oxa-2,12-diazahexacyclo[9.6.1.19,15.01,9.03,8.012,17]nonadeca-3,5,7-triene-19-carboxylate	102004475	Click to see CC=C1CN2C3CC1C(C45C3(NC6=CC=CC=C64)OC2C5)C(=O)OC	338.40	unknown	https://doi.org/10.1021/NP034041V
Vallesiachotamine	5384527	Click to see CC=C(C=O)C1CC2C3=C(CCN2C=C1C(=O)OC)C4=CC=CC=C4N3	350.40	unknown	https://doi.org/10.1016/0031-9422(91)84183-S https://doi.org/10.1016/0031-9422(90)80225-6
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Rhazimine	6443646	Click to see CC=C1CN2CCC34C5=CC=CC=C5N=CC3(C1CC2C4=O)C(=O)OC	350.40	unknown	https://doi.org/10.1021/NP034041V

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Amsonia elliptica

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top