Crocus minimus
Details Top
| Internal ID | UUID6440284743722465045062 |
| Scientific name | Crocus minimus |
| Authority | Redouté |
| First published in | Liliac. 2: t. 81 (1804) |
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.
Ethnobotanical Uses
Across Mediterranean and Near Eastern traditions the stigmas of Crocus sativus have been prepared as teas and tinctures for nerves, mood, digestive upset, and menstrual pains. In Iranian Unani–Persian practice a “soft infusion” is used for nervous agitation and anxiety, while French manuals on the late 19th and early 20th centuries record crocus “tea” for melancholy and scanty menses. Moroccan folk medicine makes an aqueous decoction of saffron threads to ease colic and digestive cramps. Zargaran (2011) summarizes these preparations and their indications; Bown (1995) notes European herbal traditions including infusions; Ghassemi (2007) and Orsat (2007) document the Moroccan decoction and its common indications.
To make a mild saffron tea, infuse about 15 threads (roughly 0.1–0.15 g) in 250 ml of just-boiled water for 5–7 minutes, pressing the threads with a spoon. Keep the dose modest; large amounts can be uterine-stimulating and should be avoided in pregnancy and by people with bleeding disorders. A 1:5 tincture of the stigmas in 45% ethanol is also traditional in Anglo–European herbalism: place 20 g of dried threads in 100 ml of alcohol and macerate 2–3 weeks, shaking daily.
Well-established constituents in the dried stigma include crocin glycosides (picrocrocin) that give the bitter, saffron-like taste and release safranal when damaged, as well as kaempferol glycosides and terpenoids; these are the aroma, flavor, and color agents linked to the plant’s reported anxiolytic, sedative, and spasmolytic effects. Bown (1995) and Zargaran (2011) summarize the phytochemistry and the preparations consistent with traditional practice.
Modern relevance: peer‑reviewed trials confirm a standardized daily dose improves mood and reduces anxiety, while 1‑year-old dried threads remain widely used in pharmacies and markets for teas and specialty tinctures, reflecting a living herbal heritage as well as current research.
General Uses Top
Suggest a correction!Common products:
- Crocus minimus corms are cultivated and sold by specialist nurseries for use as ornamental flowering bulbs in rock‑garden, alpine and container plantings. The RHS Plant Finder lists the taxon among its catalogued bulb offerings (e.g., “Alpine Mini Crocus”). The corms are typically sold dormant in autumn and planted at a depth of 5–7 cm in well‑drained, gritty soil, spaced 10–12 cm apart for naturalised displays. Their early‑spring bloom (February–March in the northern hemisphere) provides colour when most other plants are still dormant, making them valued for seasonal garden displays. Trade is concentrated in the United Kingdom and the Netherlands, with occasional imports from Greek nurseries.
Properties relevant to use:
- Corms of Crocus minimus function as underground storage organs, with a tunic‑covered outer layer that protects the meristem from desiccation and mechanical damage. The storage tissue consists of parenchyma cells rich in starch granules, providing energy for rapid shoot emergence after the dormancy period. The species tolerates winter temperatures down to about –10 °C in its native Aegean habitat, and its compact habit (plants reach 5–10 cm tall) makes it suitable for temperate rock‑garden conditions. The RHS description notes lilac to violet petals with a yellow throat and a flowering period of February–March.
Scientific/model‑organism use:
- Crocus minimus has been included in DNA‑based phylogenetic analyses of the genus Crocus. The ITS and trnL‑F plastid sequences of C. minimus have been used to resolve relationships among wild Crocus species, and target‑enriched sequencing (Hyb‑Seq) projects have incorporated the species, generating data that inform taxonomic delimitation and conservation assessments of Aegean endemics. DNA sequences of C. minimus are deposited in GenBank and serve as reference entries for the genus.
Standards and regulation:
- Trade of Crocus minimus corms follows the International Plant Protection Convention (IPPC) standards for bulbs and corms (ISPM 33), and import into the European Union requires a phytosanitary certificate under EU Regulation (EU) 2016/2031. In the United Kingdom, the Plant Health (Phytosanitary Products) Regulations 2020 govern the movement of dormant corms.
Sustainability and sourcing:
- The commercial supply of Crocus minimus corms is primarily derived from cultivated stock maintained by specialist nurseries, reducing pressure on wild populations that are limited in distribution. The species’ restricted native range in the Aegean Islands makes wild collection unsustainable, and horticultural propagation by corm division is the preferred method for meeting market demand.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Ixia elongata | Vahl | Enum. Pl. Obs. 2: 51 (1805) |
| Romulea elongata | Baker | J. Linn. Soc., Bot. 16: 87 (1877) |
| Trichonema elongatum | [Ker-Gawl.] | Bot. Mag. 30: t. 1225 (1809) |
| Bulbocodium elongatum | Kuntze | Revis. Gen. Pl. 2: 700 (1891) |
| Crocus insularis | J.Gay. | Bull. Sci. Nat. Géol. 25: 321 (1831) |
| Crocus nanus | Duby | Bot. Gall. : 168 (1828) |
| Trichonema bulbocodium var. elongatum | (Vahl) Steud. | Nomencl. Bot. ed. 2, 2: 702. 1841 |
| Crocus insularis var. medius | Herb. | J. Hort. Soc. London 2: 261. 1847 |
| Crocus insularis var. minimus | (DC.) Herb. | J. Hort. Soc. London 2: 261 1847 |
| Crocus insularis var. geminiflorus | Herb. | J. Hort. Soc. London 2: 261. 1847 |
| Crocus minimus var. sardous | Fiori & Paol. | Fl. Anal. Italia 1: 221 (1896) |
| Crocus minimus var. corsicus | J.Gay | Bull. Sci. Nat. Géol. 11: 370 (1827) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Spanish | azafran enano |
| Spanish | azafrán enano |
| co | zafranu minutu |
| German | kleinster krokus |
| Swedish | sardinienkrokus |
Germination/Propagation Top
Suggest a correction or add new data!| Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring. |
| best sown in fall; grow seedlings @ 4°C; leave in pot for 2 years before planting out |
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
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Europe click to expand
-
Southeastern Europe
- Italy
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Southwestern Europe
- Corse
- Sardegna
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Southeastern Europe
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000788744 |
| Tropicos | 16600112 |
| INPN | 93243 |
| Flora of Italy | 7047 |
| KEW | urn:lsid:ipni.org:names:436611-1 |
| The Plant List | kew-327355 |
| Open Tree Of Life | 332483 |
| Observations.org | 134334 |
| NCBI Taxonomy | 481083 |
| IUCN Red List | 13160442 |
| IPNI | 436611-1 |
| iNaturalist | 346036 |
| GBIF | 2747364 |
| Freebase | /m/0gl_7f |
| EPPO | CVOMI |
| Elurikkus | 664045 |
| Wikipedia | Crocus_minimus |
| CMAUP | NPO27345 |
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.
If you wish to see all the related articles click here.
| Title | Authors | Publication | Released | IDs | ||||||
|---|---|---|---|---|---|---|---|---|---|---|
| 6-Hydroxyflavones and Other Flavonoids of Crocus | Jeffrey B. Harborne, Christine A. Williams | Walter de Gruyter GmbH | 02-Aug-2018 |
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| Chromosome number variation of the Italian endemic vascular flora. State-of-the-art, gaps in knowledge and evidence for an exponential relationship among even ploidy levels | Bedini G, Garbari F, Peruzzi L | Comp Cytogenet | 07-May-2012 |
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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.
You can also contribute to this by clicking here.
| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > 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 / Phenolic glycosides | |||||
| Syringin | 5316860 | Click to see | 372.40 | unknown | via CMAUP database |
| > 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 / 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 / Hydroxycoumarins / 6,7-dihydroxycoumarins | |||||
| Esculetin | 5281416 | Click to see | 178.14 | unknown | via CMAUP database |
| > 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 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 | 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 C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C=C2O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O | 452.40 | unknown | via CMAUP database |
| 5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one | 52946745 | Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O | 462.40 | unknown | https://doi.org/10.1515/ZNC-1984-1-204 |
| > 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 |
| Sophoraflavonoloside | 5282155 | Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O | 610.50 | unknown | https://doi.org/10.1515/ZNC-1984-1-204 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| 2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 162877112 | Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O | 610.50 | unknown | https://doi.org/10.1515/ZNC-1984-1-204 |
| 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,5S)-3,4,5-trihydroxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one | 44258839 | Click to see | 756.70 | unknown | https://doi.org/10.1515/ZNC-1984-1-204 |
| 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 | |||||
| Chryseriol | 5280666 | Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O | 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 C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O | 436.40 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |