Scientific name	Authority	First published in
Dithyrea griffithsii	Wooton & Standl.	Contr. U.S. Natl. Herb. 16: 124 (1913)
Dithyrea wislizeni	Engelm.	Mem. Tour N. Mexico : 95 (1848)
Dithyrea wislizeni var. griffithsii	Payson	Ann. Missouri Bot. Gard. 5: 148 (1918)

Common names Top

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Language	Common/alternative name
English	touristplant
nv	nahashtʼeʼiidą́ą́ʼ łibáhígíí
nv	nahatʼeʼiidą́ą́ʼ łibáhígíí

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

Northern America click to expand
- Mexico
  - Mexico Northeast
  - Mexico Northwest
- Northwestern U.S.A.
  - Colorado
- South-central U.S.A.
  - New Mexico
  - Texas
- Southwestern U.S.A.
  - Arizona
  - Nevada
  - Utah

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000647923
USDA Plants	DIWI2
Tropicos	4101222
KEW	urn:lsid:ipni.org:names:1154622-2
The Plant List	kew-2768728
Open Tree Of Life	364799
NCBI Taxonomy	98002
Nature Serve	2.132601
IPNI	1154622-2
iNaturalist	161924
GBIF	3047653
GBIF	3692639
Freebase	/m/05szct2
EOL	487905
USDA GRIN	414190
Wikipedia	Dimorphocarpa_wislizeni

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

Medicinal Plants in the Prevention and Treatment of Colon Cancer

Aiello P, Sharghi M, Mansourkhani SM, Ardekan AP, Jouybari L, Daraei N, Peiro K, Mohamadian S, Rezaei M, Heidari M, Peluso I, Ghorat F, Bishayee A, Kooti W

Oxid Med Cell Longev

04-Dec-2019

PMCID:	PMC7187726
doi:	10.1155/2019/2075614
PMID:	32377288

Plant evolution in alkaline magnesium-rich soils: A phylogenetic study of the Mediterranean genus Hormathophylla (Cruciferae: Alysseae) based on nuclear and plastid sequences

Salmerón-Sánchez E, Fuertes-Aguilar J, Španiel S, Pérez-García FJ, Merlo E, Garrido-Becerra JA, Mota J

PLoS One

21-Dec-2018

PMCID:	PMC6303028
doi:	10.1371/journal.pone.0208307
PMID:	30576314

Evolution of the Arabidopsis telomerase RNA

Beilstein MA, Brinegar AE, Shippen DE

Front Genet

24-Sep-2012

PMCID:	PMC3449308
doi:	10.3389/fgene.2012.00188
PMID:	23015808

Updated glucosinolate profile of Dithyrea wislizenii.

Montaut S, Grandbois J, Righetti L, Barillari J, Iori R, Rollin P

J Nat Prod

22-May-2009

doi:	10.1021/NP800738W
PMID:	19334740

Dithyreanitrile: an unusual insect antifeedant from Dithyrea wislizenii.

Powell RG, Mikolajczak KL, Zilkowski BW, Lu HS, Mantus EK, Clardy J

Experientia

15-Mar-1991

doi:	10.1007/BF01958168
PMID:	2009944

Phytochemical Profile Top

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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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-7-methylsulfanyl-N-sulfooxyheptanimidothioate	154496053	Click to see CSCCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	449.60	unknown	https://doi.org/10.1021/NP800738W
[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-6-methylsulfanyl-N-sulfooxyhexanimidothioate	159541159	Click to see CSCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	435.50	unknown	https://doi.org/10.1021/NP800738W
[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-N-sulfooxybut-3-enimidothioate	154497469	Click to see C=CCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	359.40	unknown	https://doi.org/10.1021/NP800738W
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-7-[(R)-methylsulfinyl]-N-sulfooxyheptanimidothioate	154497805	Click to see CS(=O)CCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	465.60	unknown	https://doi.org/10.1021/NP800738W
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-7-methylsulfanyl-N-sulfooxyheptanimidothioate	90657149	Click to see CSCCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	449.60	unknown	https://doi.org/10.1021/NP800738W
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1E)-8-methylsulfanyl-N-sulfooxyoctanimidothioate	44237369	Click to see CSCCCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	463.60	unknown	https://doi.org/10.1021/NP800738W
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-7-[(S)-methylsulfinyl]-N-sulfooxyheptanimidothioate	162952939	Click to see CS(=O)CCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	465.60	unknown	https://doi.org/10.1021/NP800738W
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 6-methylsulfanyl-N-sulfooxyhexanimidothioate	4479689	Click to see CSCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	435.50	unknown	https://doi.org/10.1021/NP800738W
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 7-methylsulfanyl-N-sulfooxyheptanimidothioate	75144756	Click to see CSCCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	449.60	unknown	https://doi.org/10.1021/NP800738W
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 8-methylsulfanyl-N-sulfooxyoctanimidothioate	74960823	Click to see CSCCCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	463.60	unknown	https://doi.org/10.1021/NP800738W
1-Methoxy-3-indolylmethyl glucosinolate	9576416	Click to see CON1C=C(C2=CC=CC=C21)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	478.50	unknown	https://doi.org/10.1021/NP800738W
3-[(2E)-2-sulfooxyimino-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]sulfanylethyl]indole-1-sulfonic acid	6913964	Click to see C1=CC=C2C(=C1)C(=CN2S(=O)(=O)O)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	528.50	unknown	https://doi.org/10.1021/NP800738W
3-Indolylmethyl glucosinolate	6602378	Click to see C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	448.50	unknown	https://doi.org/10.1021/NP800738W
4-Methoxy-3-indolylmethyl glucosinolate	9576738	Click to see COC1=CC=CC2=C1C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	478.50	unknown	https://doi.org/10.1021/NP800738W
Glucoberteroin	9548727	Click to see CSCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	435.50	unknown	https://doi.org/10.1021/NP800738W
Glucobrassicin	9601691	Click to see C1=CC=C2C(=C1)C(=CN2)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	448.50	unknown	https://doi.org/10.1021/NP800738W
Glucohesperin	134160269	Click to see CS(=O)CCCCCCC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O	465.60	unknown	https://doi.org/10.1021/NP800738W
Sulfoglucobrassicin	6828857	Click to see C1=CC=C2C(=C1)C(=CN2S(=O)(=O)O)CC(=NOS(=O)(=O)O)SC3C(C(C(C(O3)CO)O)O)O	528.50	unknown	https://doi.org/10.1021/NP800738W
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Dithyreanitrile	124971	Click to see COC1=CC=CC2=C1NC=C2C(C#N)(SC)SC	278.40	unknown	https://doi.org/10.1007/BF01958168

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Dimorphocarpa wislizeni

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