Haloxylon salicornicum is a shrub or undershrub belonging to the family Amaranthaceae. It is a desert shrub found in Israel, Jordan, Egypt, Saudi Arabia, Kuwait, Oman, United Arab Emirates, Afghanistan and Pakistan. It grows up to 60 cm (20 in) in height and has pale stems and minute triangular cup-shaped scales with membranous margins and woolly interiors. The flowers are in short spikes up to 6 cm (2 in) long and it is found in sandhills, sand ridges and other arid habitats.

Synonyms Top

Scientific name	Authority	First published in
Salsola articulata	Cav.	Icon. [Cavanilles] 3: 43 (-44; t. 284). 1795
Arthrophytum articulatum	(Moq.) Iljin	Mater. Istorii Fl. Rastitel'n. S.S.S.R. 2: 222 (1946)
Caroxylon articulatum	Moq.	Prodr. 13(2): 175 (1849)
Caroxylon salicornicum	Moq.	Prodr. 13(2): 174 (1849)
Haloxylon articulatum	(Moq.) Bunge	Beitr. Fl. Russl. : 293 (1852)
Haloxylon schweinfurthii	Asch. & Schweinf.	Mém. Inst. Égypt. 2: 128 (1887)
Hammada articulata	(Moq.) O.Bolòs & Vigo	Butl. Inst. Catalana Hist. Nat., Secc. Bot. 38(1): 89. 1974
Hammada elegans	(Bunge) Botsch.	Novosti Sist. Vyssh. Rast. 1: 362 (1964)
Hammada hispanica	Botsch.	Novosti Sist. Vyssh. Rast. 1: 363 (1964)
Hammada salicornica	(Moq.) Iljin	Bot. Zhurn. (Moscow & Leningrad) 33: 583 (1948)
Haloxylon elegans	Bunge	Trudy Imp. S.-Peterburgsk. Bot. Sada 6(2): 439 1880

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Arabic	رمث صفصافي
Arabic	ثرمد
German	caroxylon salicornicum
German	hammada salicornica
Persian	ترات (گیاه)
Chinese	柳枝梭梭

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Tunisia

Asia-temperate click to expand
- Arabian Peninsula
  - Gulf States
  - Kuwait
  - Oman
  - Saudi Arabia
- Western Asia
  - Afghanistan
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000715245
Tropicos	7201432
KEW	urn:lsid:ipni.org:names:165853-1
The Plant List	kew-2838922
Open Tree Of Life	499681
NCBI Taxonomy	454511
IPNI	165853-1
iNaturalist	474194
GBIF	3758958
EOL	2904176
USDA GRIN	5295
Wikipedia	Haloxylon_salicornicum
CMAUP	NPO20954

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

Ubenimex combined with Albendazole for the treatment of Echinococcus multilocularis-induced alveolar echinococcosis in mice

Zhou Z, Huayu M, Mu Y, Tang F, Ge RL

Front Vet Sci

15-Mar-2024

PMCID:	PMC10995866
doi:	10.3389/fvets.2024.1320308
PMID:	38585297

The sustainable use of diverse plants accustomed by different ethnic groups in Sibi District, Balochistan, Pakistan

Maria B, Saeed S, Ahmed A, Ahmed M, Rehman A

PLoS One

21-Feb-2024

PMCID:	PMC10880983
doi:	10.1371/journal.pone.0294989
PMID:	38381718

Structural and Functional Strategies in Cenchrus Species to Combat Environmental Extremities Imposed by Multiple Abiotic Stresses

Basharat S, Ahmad F, Hameed M, Ahmad MS, Asghar A, Fatima S, Ahmad KS, Shah SM, Hashem A, Avila-Quezada GD, Abd_Allah EF, Abbas Z

Plants (Basel)

11-Jan-2024

PMCID:	PMC10818359
doi:	10.3390/plants13020203
PMID:	38256756

Insights from the yield, protein production, and detailed alkaloid composition of white (Lupinus albus), narrow-leafed (Lupinus angustifolius), and yellow (Lupinus luteus) lupin cultivars in the Mediterranean region

Valente IM, Sousa C, Almeida M, Miranda C, Pinheiro V, Garcia-Santos S, Ferreira LM, Guedes CM, Maia MR, Cabrita AR, Fonseca AJ, Trindade H

Front Plant Sci

15-Dec-2023

PMCID:	PMC10755673
doi:	10.3389/fpls.2023.1231777
PMID:	38162308

Transcriptome and Proteome Association Analysis to Screen Candidate Genes Related to Salt Tolerance in Reaumuria soongorica Leaves under Salt Stress

Liu H, Chong P, Yan S, Liu Z, Bao X, Tan B

Plants (Basel)

12-Oct-2023

PMCID:	PMC10609793
doi:	10.3390/plants12203542
PMID:	37896006

Salinity-induced changes in plastoquinone pool redox state in halophytic Mesembryanthemum crystallinum L.

Pilarska M, Niewiadomska E, Kruk J

Sci Rep

10-Jul-2023

PMCID:	PMC10333315
doi:	10.1038/s41598-023-38194-7
PMID:	37430104

A comprehensive analysis of transcriptomic data for comparison of plants with different photosynthetic pathways in response to drought stress

Karami S, Shiran B, Ravash R, Fallahi H

PLoS One

27-Jun-2023

PMCID:	PMC10298789
doi:	10.1371/journal.pone.0287761
PMID:	37368898

Osmoprotectants play a major role in the Portulaca oleracea resistance to high levels of salinity stress—insights from a metabolomics and proteomics integrated approach

Rodrigues Neto JC, Salgado FF, Braga ÍD, Carvalho da Silva TL, Belo Silva VN, Leão AP, Ribeiro JA, Abdelnur PV, Valadares LF, de Sousa CA, Souza Júnior MT

Front Plant Sci

13-Jun-2023

PMCID:	PMC10296175
doi:	10.3389/fpls.2023.1187803
PMID:	37384354

Distinguishing features of Lycium L. species (family Solanaceae) distributed in Egypt based on their anatomical, metabolic, molecular, and ecological characteristics

Ragab OG, Mamdouh D, Bedair R, Smetanska I, Gruda NS, Yousif SK, Omer RM, Althobaiti AT, Abd El-Raouf HS, El-Taher AM, El-Sayed AS, Eldemerdash MM

Front Plant Sci

12-May-2023

PMCID:	PMC10213676
doi:	10.3389/fpls.2023.1162695
PMID:	37251766

Halophytes as new model plant species for salt tolerance strategies

Mann A, Lata C, Kumar N, Kumar A, Kumar A, Sheoran P

Front Plant Sci

11-May-2023

PMCID:	PMC10211249
doi:	10.3389/fpls.2023.1137211
PMID:	37251767

Antimicrobial, Antibiofilm, and Antioxidant Potentials of Four Halophytic Plants, Euphorbia chamaesyce, Bassia arabica, Fagonia mollis, and Haloxylon salicornicum, Growing in Qassim Region of Saudi Arabia: Phytochemical Profile and In Vitro and In Silico Bioactivity Investigations

Rugaie OA, Mohammed HA, Alsamani S, Messaoudi S, Aroua LM, Khan RA, Almahmoud SA, Altaleb AD, Alsharidah M, Aldubaib M, Al-Regaiey KA, Qureshi KA

Antibiotics (Basel)

02-Mar-2023

PMCID:	PMC10044527
doi:	10.3390/antibiotics12030501
PMID:	36978368

One-Step Phytofabrication Method of Silver and Gold Nanoparticles Using Haloxylon salicornicum for Anticancer, Antimicrobial, and Antioxidant Activities

Hamida RS, Ali MA, Alfassam HE, Momenah MA, Alkhateeb MA, Bin-Meferij MM

Pharmaceutics

04-Feb-2023

PMCID:	PMC9958700
doi:	10.3390/pharmaceutics15020529
PMID:	36839850

Soil structure influences proteins, phenols, and flavonoids of varied medicinal plants in Al Jubail, KSA

Alotaibi MO, Abd-Elgawad ME

Saudi J Biol Sci

23-Jan-2023

PMCID:	PMC9926020
doi:	10.1016/j.sjbs.2023.103567
PMID:	36798140

Plants from a semi-arid environment as a source of phytochemicals against Fusarium crown and foot rot in zucchini

Khalil AM, Saleh AM, Abo El-Souad SM, Mohamed MS

AMB Express

17-Jan-2023

PMCID:	PMC9845481
doi:	10.1186/s13568-023-01515-0
PMID:	36648547

The Life Cycle of the Xylophagous Beetle, Steraspis speciosa (Coleoptera, Buprestidae), Feeding on Acacia Trees in Saudi Arabia

Alanazi NA, Ghorbel M, Brini F, Mseddi K

Life (Basel)

02-Dec-2022

PMCID:	PMC9782656
doi:	10.3390/life12122015
PMID:	36556380

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
> Alkaloids and derivatives
Anabasine	205586	Click to see C1CCNC(C1)C2=CN=CC=C2	162.23	unknown	https://doi.org/10.2307/4117899
Pyridine, 3-(2-piperidinyl)-	2181	Click to see C1CCNC(C1)C2=CN=CC=C2	162.23	unknown	https://doi.org/10.2307/4117899
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
2-Hydroxy-3-methoxybenzoic acid	70140	Click to see COC1=CC=CC(=C1O)C(=O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid	7478	Click to see COC1=CC=C(C=C1)C(=O)O	152.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic acid	19	Click to see C1=CC(=C(C(=C1)O)O)C(=O)O	154.12	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron;phenoxide	20488062	Click to see [H+].C1=CC=C(C=C1)[O-]	94.11	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Hydrocarbons / Polycyclic hydrocarbons
(6aR,8aR,12S,14bS)-4,6a,8a,11,12,14b-hexamethyl-2,3,4,4a,5,6,6b,7,8,9,10,11,12,12a,14,14a-hexadecahydro-1H-picene	163188293	Click to see CC1CCCC2(C1CCC3(C2CC=C4C3CCC5(C4C(C(CC5)C)C)C)C)C	382.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
4,6a,6b,8a,11,12,14b-Heptamethyl-1,2,3,4,4a,5,6,7,8,9,10,11,12,12a,14,14a-hexadecahydropicene	75296743	Click to see CC1CCCC2(C1CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C	396.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	via CMAUP database
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	via CMAUP database
Hexacosanoic acid	10469	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	396.70	unknown	via CMAUP database
Tetracosanoic acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	via CMAUP database
Triacontanoic acid	10471	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	452.80	unknown	https://doi.org/10.1002/CHIN.200543209
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(24S)-24-hydroxyoctacosan-4-one	163191138	Click to see CCCCC(CCCCCCCCCCCCCCCCCCCC(=O)CCC)O	424.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
22-Cyclohexyldocosan-1-ol	49797775	Click to see C1CCC(CC1)CCCCCCCCCCCCCCCCCCCCCCO	408.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209
24-Cyclohexyltetracosan-1-ol	85787038	Click to see C1CCC(CC1)CCCCCCCCCCCCCCCCCCCCCCCCO	436.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209
24-Hydroxyoctacosan-4-one	49797799	Click to see CCCCC(CCCCCCCCCCCCCCCCCCCC(=O)CCC)O	424.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
1'-Hydroxydocasanyl cyclohexane	49797776	Click to see C1CCC(CC1)CCCCCCCCCCCCCCCCCCCCO	380.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
8,11,13-Abietatriene-3beta-ol	13996029	Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C	286.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Dihydrosolidagenone	101717490	Click to see CC1CC(=O)C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C	318.40	unknown	via CMAUP database
Rotundifuran	9841926	Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C	362.50	unknown	via CMAUP database
Vitetrifolin B	15543011	Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C	362.50	unknown	via CMAUP database
Vitetrifolin C	15543012	Click to see CC1C(C=C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C	360.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate	93317	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
gamma-Tocopherol	92729	Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O	416.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone	92785	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C	424.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1R,4aS,5R,7aR)-5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate	51346123	Click to see C1=COC(C2C1C(C=C2COC(=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	466.40	unknown	via CMAUP database
6'-O-p-Hydroxybenzoylmussaenosidic acid	23955877	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C4=CC=C(C=C4)O)O)O)O)O	496.50	unknown	via CMAUP database
Mussaenosidic acid	21633105	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O	376.36	unknown	via CMAUP database
Negundoside	9935561	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O	496.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(5S,6R,8R,9R,10S)-6-Acetoxy-9,15-dihydroxylabda-13-ene-16-oic acid 16,15-lactone	10022565	Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C	378.50	unknown	via CMAUP database
(8alpha)-9,16-Dihydroxylabda-13-ene-15-oic acid gamma-lactone	102105798	Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C	320.50	unknown	via CMAUP database
Previtexilactone	21636179	Click to see CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4)C)(C)C)OC(=O)C	378.50	unknown	via CMAUP database
Vitexilactone	21636178	Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)OC(=O)C	378.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate	345510	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) hexadecanoate	13915598	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	665.10	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
(4R,4aS,6aR,6bS,8aR,11R,12S,12aR,14aR,14bS)-4,6a,6b,8a,11,12,14b-heptamethyl-1,2,3,4,4a,5,6,7,8,9,10,11,12,12a,14,14a-hexadecahydropicene	15742794	Click to see CC1CCCC2(C1CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C	396.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
(4S,4aS,6aR,6bS,8aR,11R,12S,12aR,14aR,14bS)-4,6a,6b,8a,11,12,14b-heptamethyl-1,2,3,4,4a,5,6,7,8,9,10,11,12,12a,14,14a-hexadecahydropicene	49797798	Click to see CC1CCCC2(C1CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C	396.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
[(3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,4a,6a,6b,8a,11,11,12a,14b-decamethyl-1,2,3,5,6,7,8,9,10,12,14,14a-dodecahydropicen-3-yl] hexadecanoate	163188627	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CC=C4C(C3(CCC2(C1(C)C)C)C)(CCC5(C4(CC(CC5)(C)C)C)C)C)C	693.20	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
[(3S,4aR,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] hexadecanoate	13915597	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	665.10	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
[(3S,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] hexadecanoate	13915595	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	665.10	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
[(3S,6aR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate	5318302	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
3-Epiursolic acid	7163177	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	via CMAUP database
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
beta-Amyrin acetate	92156	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	via CMAUP database
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209
Lup-20(29)-en-3beta-ol, acetate	323074	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209
Lupeol acetate	92157	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Monogynol B (6CI)	44586882	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Olean-12-en-3beta-ol	225689	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
(1S,2R,6R,10R,13S,15S)-5-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadeca-8,18-dien-13-ol	163186444	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CC=C3C24C=CC5(C3(CCC(C5)O)C)OO4)C	426.60	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
(1S,2R,6R,9R,10R,13S,15S)-5-[(E,2R,5S)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol	5469431	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
(22E,24S)-5alpha,8alpha-epidioxy-24-methylcholesta-6,22-dien-3beta-ol	13830971	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
(22E,24S)-5alpha,8alpha-epidioxy-24-methylcholesta-6,9,22-trien-3beta-ol	70698275	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CC=C3C24C=CC5(C3(CCC(C5)O)C)OO4)C	426.60	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
5-(5,6-Dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol	633877	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	https://doi.org/10.1002/CHIN.200543209 https://doi.org/10.1016/J.BMCL.2010.05.061
5-(5,6-Dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadeca-8,18-dien-13-ol	5169735	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CC=C3C24C=CC5(C3(CCC(C5)O)C)OO4)C	426.60	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
5,8-Epidioxyergosta-6,9(11),22-trien-3-ol	11112737	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CC=C3C24C=CC5(C3(CCC(C5)O)C)OO4)C	426.60	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Ergosterol peroxide	5351516	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	https://doi.org/10.1002/CHIN.200543209 https://doi.org/10.1016/J.BMCL.2010.05.061
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
14-Methyl-15-(1-methylundecyl)-3,4,6,7,8,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ol	71588366	Click to see CCCCCCCCCCC(C)C1CCC2C1(C3CCC4=C(C3CC2)C=CC(C4)O)C	426.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4R,5R,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-methyloxane-3,4,5-triol	49797880	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(CCC34C)OC5C(C(C(C(O5)C)O)O)O)C)C(C)C	558.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11664211	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(CCC34C)OC5C(C(C(C(O5)CO)O)O)O)C)C(C)C	574.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209
(3R,4R,5R,6S)-2-[[(8S,9S,10R,13R,14S)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-methyloxane-3,4,5-triol	163185566	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(CCC34C)OC5C(C(C(C(O5)C)O)O)O)C)C(C)C	558.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
(3R,4S,5S,6R)-2-[[(3S,10R,13R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	44237224	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
(3R,4S,5S,6R)-2-[[(8S,9S,10R,13R,14R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-8,10,13-trimethyl-1,2,3,6,7,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163186709	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2(CCC4=CC(CCC34C)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	588.90	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73072970	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73046699	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(CCC34C)OC5C(C(C(C(O5)CO)O)O)O)C)C(C)C	574.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-methyloxane-3,4,5-triol	75251442	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4=CC(CCC34C)OC5C(C(C(C(O5)C)O)O)O)C)C(C)C	558.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209
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	via CMAUP database
Stigmasta-3,5-diene	13783149	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC=C4)C)C)C(C)C	396.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Stigmasta-3,5-diene, (24xi)-	157618	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC=C4)C)C)C(C)C	396.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Stigmastan-3,5-diene	525918	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC=C4)C)C)C(C)C	396.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
Stigmasterol glucoside	6602508	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(1R,2R,4aalpha,5'E)-2alpha,5,5,8abeta-Tetramethyl-4beta-acetoxy-4',5'-dihydrospiro[decalin-1,2'(3'H)-furan]-5'-ylidene]acetic acid	101357917	Click to see CC1CC(C2C(CCCC2(C13CCC(=CC(=O)O)O3)C)(C)C)OC(=O)C	364.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Isoambreinolide	15559824	Click to see CC1CCC2C(CCCC2(C13CCC(=O)O3)C)(C)C	264.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines / N-acylpiperidines
(2Z,4Z)-22-hydroxy-1-[(3S)-3-hydroxypiperidin-1-yl]docosa-2,4-dien-1-one	162976709	Click to see C1CC(CN(C1)C(=O)C=CC=CCCCCCCCCCCCCCCCCCO)O	435.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
22-Hydroxy-1-(3-hydroxypiperidin-1-yl)docosa-2,4-dien-1-one	72967383	Click to see C1CC(CN(C1)C(=O)C=CC=CCCCCCCCCCCCCCCCCCO)O	435.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1248/CPB.53.570
22-hydroxy-1-[(3R)-3-hydroxypiperidin-1-yl]docosa-2,4-dien-1-one	162976708	Click to see C1CC(CN(C1)C(=O)C=CC=CCCCCCCCCCCCCCCCCCO)O	435.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
22-Hydroxy-1-piperidin-1-yldocosa-2,4-dien-1-one	72817026	Click to see C1CCN(CC1)C(=O)C=CC=CCCCCCCCCCCCCCCCCCO	419.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1248/CPB.53.570
Haloxyline A	11362138	Click to see C1CCN(CC1)C(=O)C=CC=CCCCCCCCCCCCCCCCCCO	419.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209 https://doi.org/10.1248/CPB.53.570
Haloxyline B	11453345	Click to see C1CC(CN(C1)C(=O)C=CC=CCCCCCCCCCCCCCCCCCO)O	435.70	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061 https://doi.org/10.1002/CHIN.200543209 https://doi.org/10.1248/CPB.53.570
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
InChI=1/C6H6O4/c1-9-5-3-10-2-4(7)6(5)8/h2-3,7H,1H	10701923	Click to see COC1=COC=C(C1=O)O	142.11	unknown	https://doi.org/10.1021/NP990535+
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives
Isoniazid	3767	Click to see C1=CN=CC=C1C(=O)NN	137.14	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1	11208535	Click to see CC1CCC2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C	290.40	unknown	via CMAUP database
Vitex norditerpenoid 2	11462191	Click to see CC1CC(C2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C)OC(=O)C	348.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
6-Hydroxy-7,8-dimethoxycoumarin	11345068	Click to see COC1=C(C=C2C=CC(=O)OC2=C1OC)O	222.19	unknown	https://doi.org/10.1016/J.BMCL.2010.05.061
> 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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin	5280441	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6,3',4'-tetramethoxyflavone	5379563	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)OC	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin	5320351	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	via CMAUP database
Casticin	5315263	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	via CMAUP database
chrysoplenol D	5280699	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC	360.30	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Haloxylon salicornicum

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