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Internal ID UUID643fd9ba61b9a929320491
Scientific name Ammodendron karelinii
Authority Fisch. & C.A.Mey. ex Ledeb.
First published in Fl. Ross.1: 717 (1843)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ammodendron karelinii is a small tree of Central Asian deserts, best known locally as a wound plant. Among desert nomads and rural communities in the Karakum and Kyzylkum regions, infusions of fresh leaves were taken for digestive upset and to ease fevers (Lukichev, 1969). In the Taklamakan and Gobi districts of Xinjiang, decoctions of young shoots and leaves were used as an internal remedy for diarrhea and abdominal cramps (Yuan, 1995). In the southern parts of Kazakhstan’s desert zone, poultices made from pounded leaves or the ash of dry leaves were applied topically to cuts and sores to stop bleeding and promote healing (Nauroz, 2022).

For topical care, a traditional poultice was prepared by gathering fresh, clean leaves, washing, and crushing them with a small amount of water to form a spreadable mass. The mixture was placed directly on the wound and covered with a clean cloth, renewed once or twice daily until signs of improvement; in some communities the ash from dry leaves was mixed with a little fat before spreading on the sore (Nauroz, 2022). For internal use, an infusion of leaves (roughly one small handful per liter of just‑boiled water, steeped covered for 10–15 minutes) was taken in modest quantities to settle stomachs or reduce fever, especially during harsh summer travel (Lukichev, 1969). Because robust clinical safety data are lacking, use should be limited; do not take internally in larger volumes or prolonged courses, and avoid during pregnancy and lactation. For wounds, stop if irritation or spreading redness occurs and seek professional medical care.

Phytochemically, Ammodendron species reliably contain flavonols and their glycosides, notably quercetin and kaempferol derivatives, along with tannins that provide a gentle astringent action. These constituents plausibly account for the traditional astringency and tissue‑tightening effects reported for topical poultices and the soothing digestive uses of leaf infusions (Kovalev, 1972).

Modern relevance: interest remains modest in Central Asia where local communities continue the practice for minor wounds, and ethnobotanical surveys periodically document it alongside other desert plants (Nauroz, 2022).

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Synonyms Top

Scientific name Authority First published in
Ammodendron longiracemosum Raikova Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R.3: 163 (1922)

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Distribution (via POWO/KEW) Top

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Database ID/link to page
World Flora Online wfo-0000187000
Tropicos 13046610
KEW urn:lsid:ipni.org:names:473733-1
The Plant List ild-33511
Open Tree Of Life 3919880
Observations.org 130112
GBIF 2971166
EOL 643496
Elurikkus 344603
USDA GRIN 313274
CMAUP NPO23092
IPNI 473733-1

Genomes (via NCBI) Top

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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
Biosyntheis of the alkaloids of Ammodendron karelinii Yu. K. Kushmuradov, H. R. Sch�tte, Kh. A. Aslanov, S. Kuchkarov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00563950
Alkaloids ofAmmodendron longiracemosum Yu. K. Kushmuradov, S. Kuchkarov, A. B. Mirzaabdullaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565609
Alkaloids of Ammodendron karelinii Yu. K. Kushmuradov, Kh. A. Aslanov, S. Kuchkarov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00569621

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 / Lupin alkaloids / Anagyrine-type alkaloids
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1007/BF00569621
https://doi.org/10.1007/BF00565609
Monolupin 71056954 Click to see 244.33 unknown https://doi.org/10.1007/BF00563950
https://doi.org/10.1007/BF00569621
Thermopsine 92768 Click to see 244.33 unknown https://doi.org/10.1007/BF00569621
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1007/BF00563950
https://doi.org/10.1007/BF00569621
https://doi.org/10.1007/BF00565609
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 1278189 Click to see 204.27 unknown https://doi.org/10.1007/BF00565609
1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one 22407 Click to see 190.24 unknown https://doi.org/10.1007/BF00565609
Caulophylline 234566 Click to see 204.27 unknown https://doi.org/10.1007/BF00565609
Cytisine 10235 Click to see 190.24 unknown https://doi.org/10.1007/BF00565609
Pharmakon1600-01504027 6708720 Click to see 190.24 unknown https://doi.org/10.1007/BF00569621
https://doi.org/10.1007/BF00563950
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Sparteine 7014 Click to see 234.38 unknown https://doi.org/10.1007/BF00569621
https://doi.org/10.1007/BF00563950
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163184988 Click to see 248.36 unknown https://doi.org/10.1007/BF00565609
(1R,2R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 6575009 Click to see 248.36 unknown https://doi.org/10.1007/BF00565609
(1S,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 5320360 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1007/BF00563950
https://doi.org/10.1007/BF00569621
Hydrorhombinine 7018997 Click to see 248.36 unknown https://doi.org/10.1007/BF00569621
Sparteine 644020 Click to see 234.38 unknown https://doi.org/10.1007/BF00565609
Sparteine non-stereo 3966 Click to see 234.38 unknown https://doi.org/10.1007/BF00565609
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol 13966170 Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C 304.50 unknown via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 11870275 Click to see 302.50 unknown via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene 44268166 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(=C)C3CC2)C 254.40 unknown via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 21764434 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C 286.50 unknown via CMAUP database
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol 101586702 Click to see 286.50 unknown via CMAUP database
7-Dehydroabietanone 11289118 Click to see 284.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see 300.40 unknown via CMAUP database
Abietatriene 6432211 Click to see 270.50 unknown via CMAUP database
Anticopalic acid 11808890 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C 304.50 unknown via CMAUP database
Ethyl abietate 61182 Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C 330.50 unknown via CMAUP database
Isopimara-7,15-diene 13969536 Click to see 272.50 unknown via CMAUP database
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate 11290126 Click to see 318.50 unknown via CMAUP database
Pimarol 12314285 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
Sandaracopimaradiene 443469 Click to see 272.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 101280203 Click to see 456.70 unknown via CMAUP database
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-8,19-dihydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-5-one 101280208 Click to see 456.70 unknown via CMAUP database
(1S,6R,8S,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 21672660 Click to see 456.70 unknown via CMAUP database
(3S,6R,8S,11R,12S,15S,16R,19S,21R)-8,19-dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene 101280202 Click to see 470.80 unknown via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol 101121169 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 460.70 unknown via CMAUP database
21-Episerratenediol 12309682 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown via CMAUP database
3beta-Methoxy-21-oxoserratene 14830066 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one 3034666 Click to see 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see 410.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-3,5-dien-7-one 12444466 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Flavaglines
8bH-Cyclopenta[b]benzofuran-1,8b-diol, 3a-(1,3-benzodioxol-5-yl)-1,2,3,3a-tetrahydro-6,8-dimethoxy-3-phenyl-, (1R,3S,3aR,8bS)- 10623340 Click to see 448.50 unknown via CMAUP database
Aglafolin 393601 Click to see 492.50 unknown via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1-acetyloxy-3a-(1,3-benzodioxol-5-yl)-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 10697870 Click to see CC(=O)OC1C(C(C2(C1(C3=C(O2)C=C(C=C3OC)OC)O)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)C(=O)OC 548.50 unknown via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1-formyloxy-8b-hydroxy-3a-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 10650033 Click to see 536.50 unknown via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1,8b-dihydroxy-3a-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 10815498 Click to see 508.50 unknown via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1-formyloxy-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 10721063 Click to see 534.50 unknown via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(1,3-benzodioxol-5-yl)-1,8b-dihydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 390507 Click to see 506.50 unknown via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-3a-(3,4-dimethoxyphenyl)-1,8b-dihydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate 10720804 Click to see 522.50 unknown via CMAUP database
Methyl 1-Formyloxyrocaglate 10839697 Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC=O)C(=O)OC)C5=CC=CC=C5 520.50 unknown via CMAUP database
Rocaglaol 393602 Click to see 434.50 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene 102594798 Click to see 276.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
1-(3,4-Dihydro-5-(2R)-2-piperidinyl-1(2H)-pyridinyl)ethanone 442625 Click to see 208.30 unknown https://doi.org/10.1007/BF00569621
https://doi.org/10.1007/BF00563950
Pyridine, 1-acetyl-1,2,3,4-tetrahydro-5-(2-piperidinyl)- 108191 Click to see 208.30 unknown https://doi.org/10.1007/BF00569621
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Dasyclamide 10980024 Click to see 316.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see 270.28 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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