Language	Common/alternative name
English	false hellebore
English	green false hellebore
English	indian poke
Spanish	veratrum eschscholtzii
Spanish	veratrum eschscholtzii var. incriminatum
Spanish	falso eleboro verde
Spanish	falso eléboro verde
Spanish	veratrum eschscholtzianum
Spanish	veratrum eschscholtzii var incriminatum
Azerbaijani	yaşıl asırqal
azb	یاشیل آسیرقال
Persian	وراتروم ویرید
French	vératre vert
Swedish	grön nysrot

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Veratrum viride var. eschscholtzianum	(Schult. & Schult.f.) Breitung	Canad. Field-Naturalist 71: 49 (1957)
Veratrum viride var. viride		Unknown

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

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.

seed very poisonous, wash hands after handling; store @ 4°C; sow 20°C x 4 weeks, then -7°C x 6 weeks, 10°C to germinate

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Eastern Canada
  - Labrador
  - New Brunswick
  - Québec
- Northeastern U.S.A.
  - Connecticut
  - Maine
  - Massachusetts
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Idaho
  - Montana
  - Oregon
  - Washington
- Southeastern U.S.A.
  - Delaware
  - Georgia
  - Maryland
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California
- Subarctic America
  - Alaska
  - Northwest Territorie
  - Yukon
- Western Canada
  - Alberta
  - British Columbia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000751734
UNII	36K54AW5KX
Canadensys	6665
USDA Plants	VEVI
Tropicos	18400395
KEW	urn:lsid:ipni.org:names:543543-1
The Plant List	kew-291258
Open Tree Of Life	453154
NCBI Taxonomy	72650
NBN Atlas	NBNSYS0000014612
Nature Serve	2.158937
IPNI	543543-1
iNaturalist	79484
GBIF	2742131
Freebase	/m/05wq65
EPPO	VEAVI
EOL	1083443
Calflora (Californian flora)	8223
USDA GRIN	41142
Wikipedia	Veratrum_viride

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

New Plants, New Resources, New Knowledge: Early Introductions of Exotic Plants to Indigenous Territories in Northwestern North America

Turner NJ

Plants (Basel)

28-Aug-2023

PMCID:	PMC10490097
doi:	10.3390/plants12173087
PMID:	37687334

2023 ACMT Annual Scientific Meeting Abstracts – San Diego, CA

N/A

J Med Toxicol

23-Mar-2023

PMCID:	PMC10035466
doi:	10.1007/s13181-023-00930-w
PMID:	36952114

Scale‐dependent effects of marine subsidies on the island biogeographic patterns of plants

Obrist DS, Fitzpatrick OT, Brown NE, Hanly PJ, Nijland W, Reshitnyk LY, Wickham SB, Darimont CT, Reynolds JD, Starzomski BM

Ecol Evol

09-Sep-2022

PMCID:	PMC9461347
doi:	10.1002/ece3.9270
PMID:	36177118

Chemistry and bioactivities of natural steroidal alkaloids

Xiang ML, Hu BY, Qi ZH, Wang XN, Xie TZ, Wang ZJ, Ma DY, Zeng Q, Luo XD

Nat Prod Bioprospect

15-Jun-2022

PMCID:	PMC9198197
doi:	10.1007/s13659-022-00345-0
PMID:	35701630

Plant-Derived Pesticides as an Alternative to Pest Management and Sustainable Agricultural Production: Prospects, Applications and Challenges

Souto AL, Sylvestre M, Tölke ED, Tavares JF, Barbosa-Filho JM, Cebrián-Torrejón G

Molecules

10-Aug-2021

PMCID:	PMC8400533
doi:	10.3390/molecules26164835
PMID:	34443421

Shikimic acid as intermediary model for the production of drugs effective against influenza virus

Priyanka Singh, Gupta E, Neha Mishra, Mishra P

Phytochemicals as Lead Compounds for New Drug Discovery

24-Jan-2020

PMCID:	PMC7153330
doi:	10.1016/B978-0-12-817890-4.00016-0

Marketing medicines: charting the rise of modern therapeutics through a systematic review of adverts in UK medical journals (1950–1980)

Green AR, Haddad PM, Aronson JK

Br J Clin Pharmacol

25-Mar-2018

PMCID:	PMC6046508
doi:	10.1111/bcp.13549
PMID:	29442380

Hikers poisoned: Veratrum steroidal alkaloid toxicity following ingestion of foraged Veratrum parviflorum

Anwar M, Turner M, Farrell N, Zomlefer WB, McDougal OM, Morgan BW

Clin Toxicol (Phila)

28-Feb-2018

PMCID:	PMC6086754
doi:	10.1080/15563650.2018.1442007
PMID:	29490507

The effects of herbal medicine on epilepsy

Liu W, Ge T, Pan Z, Leng Y, Lv J, Li B

Oncotarget

03-Apr-2017

PMCID:	PMC5564656
doi:	10.18632/oncotarget.16801
PMID:	28423368

Twenty years of ecosystem response after clearcutting and slashburning in conifer forests of central British Columbia, Canada

Chandler JR, Haeussler S, Hamilton EH, Feller M, Bradfield G, Simard SW

PLoS One

24-Feb-2017

PMCID:	PMC5325286
doi:	10.1371/journal.pone.0172667
PMID:	28234960

Testing predator–prey theory using broad‐scale manipulations and independent validation

Serrouya R, McLellan BN, Boutin S

J Anim Ecol

11-Aug-2015

PMCID:	PMC4744978
doi:	10.1111/1365-2656.12413
PMID:	26101058

Medicinal history of North American Veratrum

Chandler CM, McDougal OM

Phytochem Rev

15-Oct-2013

PMCID:	PMC4217314
doi:	10.1007/s11101-013-9328-y
PMID:	25379034

Edward D. Freis—A True Pioneer

Ventura HO

J Clin Hypertens (Greenwich)

31-Jan-2007

PMCID:	PMC8109578
doi:	10.1111/j.1524-6175.2005.05404.x
PMID:	16596033

Gitksan medicinal plants-cultural choice and efficacy

Johnson LM

J Ethnobiol Ethnomed

21-Jun-2006

PMCID:	PMC1564001
doi:	10.1186/1746-4269-2-29
PMID:	16790066

Rustom Jal Vakil: His Contributions to Cardiology

Isharwal S, Gupta S

Tex Heart Inst J

01-Jan-2006

PMCID:	PMC1524711
PMID:	16878618

Phytochemical Profile Top

Add a new one!

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
> Benzenoids / Fluorenes
14,15,16,17-Tetradehydroveratraman-3,23-diol	229854	Click to see CC1CC(C(NC1)C(C)C2=C(C3=C(C=C2)C4CC=C5CC(CCC5(C4C3)C)O)C)O	409.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E https://doi.org/10.1002/JPS.3030411014
Veratramine	6070	Click to see CC1CC(C(NC1)C(C)C2=C(C3=C(C=C2)C4CC=C5CC(CCC5(C4C3)C)O)C)O	409.60	unknown	https://doi.org/10.1002/JPS.3030411014 https://doi.org/10.1016/0031-9422(94)00825-E
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
(3S,8R,9S,10R,12R,13S,14S,17R)-10,13-dimethyl-17-[(1S)-1-[(2S,5S)-5-methylpiperidin-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol	101919103	Click to see CC1CCC(NC1)C(C)C2CCC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C	415.70	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
(3S,8R,9S,10R,12S,13R,14S,17R)-10,13-dimethyl-17-[(1S)-1-[(2S,5S)-5-methylpiperidin-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol	162936272	Click to see CC1CCC(NC1)C(C)C2CCC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C	415.70	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
10,13-dimethyl-17-[1-(5-methylpiperidin-2-yl)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol	162936271	Click to see CC1CCC(NC1)C(C)C2CCC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C	415.70	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(10,12,13,14,23-Pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl) 2-methylbut-2-enoate	78410119	Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C	575.70	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
(16,22-Diacetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-13-yl) 2-methylbutanoate	12305686	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C)O)C)OC(=O)C)O)O	677.80	unknown	https://doi.org/10.1021/JA01132A027
(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23R,25R)-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosane-10,12,13,14,16,22,23-heptol	23616919	Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)C(CC7C5(CCC(C7(O6)O)O)C)O)(C)O	509.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,18S,19S,22S,23R,25R)-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosane-10,12,13,14,22,23-hexol	163185348	Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)O)C)(C)O	493.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
(22-Acetyloxy-10,12,14,16,23-pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-13-yl) 2-methylbutanoate	23290444	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C)O)C)O)O)O	635.80	unknown	https://doi.org/10.1021/JA01132A027
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-10,12,14,16,23-pentahydroxy-6,10,19-trimethyl-13-[(2R)-2-methylbutanoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (2R,3R)-2,3-dihydroxy-2-methylbutanoate	162912692	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(C(C)O)O)O)C)O)O)O	709.90	unknown	https://doi.org/10.1021/JA01617A058
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-10,12,14,16,23-pentahydroxy-6,10,19-trimethyl-13-[(2R)-2-methylbutanoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (2S,3R)-2,3-dihydroxy-2-methylbutanoate	162912695	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(C(C)O)O)O)C)O)O)O	709.90	unknown	https://doi.org/10.1021/JA01617A058
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-10,12,14,16,23-pentahydroxy-6,10,19-trimethyl-13-[(2R)-2-methylbutanoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (2S)-2-hydroxy-2-methylbutanoate	163194108	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(CC)O)O)C)O)O)O	693.90	unknown	https://doi.org/10.1021/JA01132A027
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-16-acetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-13-[(2R)-2-methylbutanoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (2S)-2-hydroxy-2-methylbutanoate	163003057	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(CC)O)O)C)OC(=O)C)O)O	735.90	unknown	https://doi.org/10.1021/JA01132A027
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-22-acetyloxy-10,12,14,16,23-pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-13-yl] (2R)-2-methylbutanoate	131879509	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C)O)C)O)O)O	635.80	unknown	https://doi.org/10.1021/JA01132A027
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16S,17R,18R,19S,22S,23S,25R)-17-acetyloxy-10,12,14,16,23-pentahydroxy-6,10,19-trimethyl-13-[(2R)-2-methylbutanoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (2R,3R)-2,3-dihydroxy-2-methylbutanoate	163019773	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(C(C6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(C(C)O)O)O)C)OC(=O)C)O)O)O	767.90	unknown	https://doi.org/10.1021/JA01617A058
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,18S,19S,22S,23R,25R)-10,12,13,14,23-pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (Z)-2-methylbut-2-enoate	134145571	Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4CC3)O)O)O)(C)O)C)O)C	575.70	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
[10,12,14,16,23-Pentahydroxy-6,10,19-trimethyl-13-(2-methylbutanoyloxy)-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] 2-hydroxy-2-methylbutanoate	78410929	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(CC)O)O)C)O)O)O	693.90	unknown	https://doi.org/10.1002/ARDP.19552881005 https://doi.org/10.1021/JA01132A027
[10,12,14,16,23-Pentahydroxy-6,10,19-trimethyl-13-(2-methylbutanoyloxy)-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] 2,3-dihydroxy-2-methylbutanoate	3818601	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(C(C)O)O)O)C)O)O)O	709.90	unknown	https://doi.org/10.1021/JA01617A058
[16-Acetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-13-(2-methylbutanoyloxy)-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] 2-hydroxy-2-methylbutanoate	74369277	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(CC)O)O)C)OC(=O)C)O)O	735.90	unknown	https://doi.org/10.1021/JA01132A027
[16,17-Diacetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-13-(2-methylbutanoyloxy)-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] 2,3-dihydroxy-2-methylbutanoate	4975	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(C(C6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(C(C)O)O)O)C)OC(=O)C)OC(=O)C)O)O	809.90	unknown	https://doi.org/10.1002/HLCA.19530360326
[17-Acetyloxy-10,12,14,16,23-pentahydroxy-6,10,19-trimethyl-13-(2-methylbutanoyloxy)-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] 2,3-dihydroxy-2-methylbutanoate	163019772	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(C(C6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(C(C)O)O)O)C)OC(=O)C)O)O)O	767.90	unknown	https://doi.org/10.1021/JA01617A058
6,10,19-Trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosane-10,12,13,14,22,23-hexol	4486612	Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)O)C)(C)O	493.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
6,10,23-Trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-17-ene-10,12,20-triol	12444725	Click to see CC1CCC2C(C3C(CC4C5CC=C6CC(CCC6(C5CC4C3CN2C1)C)O)O)(C)O	429.60	unknown	https://doi.org/10.1076/PHBI.34.3.161.13210
Germin	409814	Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)C(CC7C5(CCC(C7(O6)O)O)C)O)(C)O	509.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
Neogermitrine	91799750	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C)O)C)OC(=O)C)O)O	677.80	unknown	https://doi.org/10.1021/JA01132A027
protoveratrine A	8931	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(C(C6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(CC)O)O)C)OC(=O)C)OC(=O)C)O)O	793.90	unknown	https://doi.org/10.1002/ARDP.19552881005 https://doi.org/10.1021/JA01617A058
protoveratrine B	222158	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(C(C6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(C(C)O)O)O)C)OC(=O)C)OC(=O)C)O)O	809.90	unknown	https://doi.org/10.1002/HLCA.19530360326
Puroverine	4974	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(C(C6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(CC)O)O)C)OC(=O)C)OC(=O)C)O)O	793.90	unknown	https://doi.org/10.1021/JA01617A058 https://doi.org/10.1002/ARDP.19552881005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Jerveratrum-type alkaloids
Iervin	222153	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)O)C)NC1	425.60	unknown	https://doi.org/10.1002/JPS.3030411014 https://doi.org/10.1039/CT8793500421 https://doi.org/10.1016/0031-9422(94)00825-E
Jervine	10098	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)O)C)NC1	425.60	unknown	https://doi.org/10.1039/CT8793500421 https://doi.org/10.1002/JPS.3030411014 https://doi.org/10.1016/0031-9422(94)00825-E
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(1S,2R,7S,10R,11S,13R,14S,15R,16S,17R,20S,23S)-14-(hydroxymethyl)-10,16,20-trimethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-ene-7,13-diol	101919102	Click to see CC1CCC2C(C3C(N2C1)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)CO)C	429.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
Rubijervine	253295	Click to see CC1CCC2C(C3C(N2C1)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C	413.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
Solanid-5-en-3beta,12alpha-diol	591288	Click to see CC1CCC2C(C3C(N2C1)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C	413.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
Solanidine base + 2O	139292073	Click to see CC1CCC2C(C3C(N2C1)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)CO)C	429.60	unknown	https://doi.org/10.1016/0031-9422(94)00825-E
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
11-Oxo-17,23-epoxyveratraman-3-yl hexopyranoside	3605588	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)OC7C(C(C(C(O7)CO)O)O)O)C)NC1	587.70	unknown	https://doi.org/10.1016/0031-9422(94)00825-E https://doi.org/10.1039/CT8793500421
Pseudojervine	16398499	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)OC7C(C(C(C(O7)CO)O)O)O)C)NC1	587.70	unknown	https://doi.org/10.1039/CT8793500421 https://doi.org/10.1016/0031-9422(94)00825-E

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Veratrum viride

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