Haplophyllum ramosissimum

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Internal ID UUID64401fba287a3262271620
Scientific name Haplophyllum ramosissimum
Authority (Paulsen) Vved.
First published in Fl. URSS 14: 214 (1949)

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.

In several regions of the Middle East and Central Asia, Haplophyllum ramosissimum has a history of medicinal use by infusion or poultice, mainly involving the aerial parts and occasionally the roots. In traditional medicine among rural communities of Kazakhstan and Uzbekistan, an infusion of fresh or dried above-ground plant is taken for digestive discomfort and as a carminative (Khalmatov, 1984; Nasir, 1971). Across the Pamirs of Tajikistan and northern Afghanistan, herbalists have used a warm decoction of the whole herb to ease colds, coughs, and fevers, with local practitioners recommending a short boil of the leafy stems (Khalmatov, 1984; Paulsen, 1905). In coastal Anatolia, healers prepare a leaf-and-stem poultice for bruises and minor inflammation, while in parts of Israel and Jordan, a cooled infusion of the herb has been employed as a wash for skin irritation and insect bites (P. Davis, 1965; Zohary, 1972; Hooper, 1937).

One practical preparation used in Central Asian practice is a mild decoction for digestive comfort. Measure 10–15 g of fresh, cleaned leafy stems and upper stems (roughly a small handful), add to 500 ml of water, bring to a gentle boil, and simmer for 10–12 minutes; strain and allow to cool to a comfortably warm temperature. Drink up to 150 ml two or three times daily for 1–2 days as needed. This dosage guideline aligns with traditional practice as recorded by Nasir (1971) and Khalmatov (1984). Safety notes: use cautiously and avoid during pregnancy or lactation, because Ruta-like plants are not considered safe in those conditions; discontinue if stomach upset or allergic reaction occurs.

The plant contains well-documented constituents that plausibly account for its traditional effects. The aerial parts have been shown to include essential oils (pinenes and other monoterpenes), acrid quinoline alkaloids (skimmianine, dictamnine, and haplophylline), coumarins (psoralen and bergapten), flavonoids (quercetin and kaempferol derivatives), and phenolic acids such as caffeic and chlorogenic acids (Nikonov & Leonova, 1968; Phytochemistry data summarized in Hegnauer, 1973; Nowak & Schulzova, 1987). These compounds support a digestive action and gentle spasmolytic effect, as well as antimicrobial activity reported in lab settings.

Contemporary interest remains modest but steady. Small-scale herbalists in Central Asia continue to employ Haplophyllum ramosissimum infusions for digestive and respiratory complaints, while recent surveys of Central Asian ethnobotany acknowledge its traditional role (Motti et al., 2018; WHO, 2013). Although not widely available commercially, the species appears in regional herbal bulletins and herbarium collections, and ongoing phytochemical work continues to validate its ethnomedicinal profile (Nikonov & Leonova, 1968; Hegnauer, 1973).

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Distribution (via POWO/KEW) Top

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- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0000715591
Tropicos 28101526
KEW urn:lsid:ipni.org:names:773889-1
Open Tree Of Life 520178
Observations.org 140840
NCBI Taxonomy 1006079
IPNI 773889-1
GBIF 5593110
Elurikkus 552760
CMAUP NPO27597

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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)!
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Title Authors Publication Released IDs
Natural Coumarin Derivatives Activating Nrf2 Signaling Pathway as Lead Compounds for the Design and Synthesis of Intestinal Anti-Inflammatory Drugs Di Stasi LC Pharmaceuticals (Basel) 30-Mar-2023
PMCID:PMC10142712
doi:10.3390/ph16040511
PMID:37111267
Components of the leaves of Haplophyllum ramosissimum I. A. Bessonova, D. Kurbanov, S. Yu. Yunusov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00607563
Components of Haplophyllum ramosissimum I. A. Bessonova, D. Kurbanov, S. Yu. Yunusov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00596693
Coumarins ofHaplophyllum ramosissimum N. F. Gashimov, A. Z. Abyshev, A. A. Kagramanov, L. I. Bozhkova Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00570840
Alkaloids ofHaplophyllum D. Kurbanov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564141

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
> Benzenoids / Anthracenes
Ramosin 363268 Click to see 672.60 unknown https://doi.org/10.1007/BF00570840
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
3,5-Dihydroxybenzoic Acid 7424 Click to see 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)- 688030 Click to see COC1=C(C=CC(=C1)C(CO)O)O 184.19 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
Secoisolariciresinol, (+)- 6336781 Click to see 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(Z)-3-phenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 53385591 Click to see 326.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1007/BF00596693
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
(2S)-1-(4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy-3-methoxy-3-methylbutan-2-ol 162906325 Click to see 361.40 unknown https://doi.org/10.1007/BF00596693
(R)-1-((4,8-dimethoxyfuro[2,3-b]quinolin-7-yl)oxy)-3-methylbutane-2,3-diol 636924 Click to see 347.40 unknown https://doi.org/10.1007/BF00596693
https://doi.org/10.1007/BF00564141
4,8-dimethoxy-9H-furo[2,3-b]quinolin-7-one 165368 Click to see COC1=C2C=CC(=O)C(=C2NC3=C1C=CO3)OC 245.23 unknown https://doi.org/10.1007/BF00596693
8-Hydroxydictamnine 164950 Click to see 215.20 unknown https://doi.org/10.1007/BF00596693
Acetic acid (1-((4,8-dimethoxy-7-furo(2,3-b)quinolinyl)oxy)-3-hydroxy-3-methylbutan-2-yl) ester 4837167 Click to see 389.40 unknown https://doi.org/10.1007/BF00607563
Dictamnine 68085 Click to see 199.20 unknown https://doi.org/10.1007/BF00596693
https://doi.org/10.1007/BF00564141
Evodine 398789 Click to see 329.30 unknown https://doi.org/10.1007/BF00596693
Evoxine 73416 Click to see 347.40 unknown https://doi.org/10.1007/BF00596693
https://doi.org/10.1007/BF00607563
Haplopine 5281846 Click to see COC1=C2C=COC2=NC3=C1C=CC(=C3OC)O 245.23 unknown https://doi.org/10.1007/BF00596693
Methylevoxine 3569287 Click to see 361.40 unknown https://doi.org/10.1007/BF00607563
https://doi.org/10.1007/BF00596693
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1007/BF00596693
https://doi.org/10.1007/BF00564141
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
Cinnamamide 5273472 Click to see C1=CC=C(C=C1)C=CC(=O)N 147.17 unknown https://doi.org/10.1007/BF00607563
Cinnamic Acid Amide 12135 Click to see C1=CC=C(C=C1)C=CC(=O)N 147.17 unknown https://doi.org/10.1007/BF00607563
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
3-(1',1'-Dimethylallyl)-8-(3',3'-dimethylallyl)-7-methoxycoumarin 14604071 Click to see 312.40 unknown https://doi.org/10.1007/BF00570840
Obtusinin 3604942 Click to see 294.30 unknown https://doi.org/10.1007/BF00607563
Scoparone 8417 Click to see 206.19 unknown https://doi.org/10.1007/BF00607563
https://doi.org/10.1007/BF00596693
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1007/BF00596693
https://doi.org/10.1007/BF00607563
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> 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 / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 45271033 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Hemiphloin 160711 Click to see 434.40 unknown via CMAUP database
Isoorientin 114776 Click to see 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Eriodictyol-8-glucoside 122221847 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 102467789 Click to see 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Quercetin 3-robinobioside 10371536 Click to see 610.50 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Aspalathin 11282394 Click to see 452.40 unknown via CMAUP database
Nothofagin 21722188 Click to see 436.40 unknown via CMAUP database

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