Dian Di Mei
StarAndrosace umbellata (Lour.) Merr.
Synonyms: Drosace umbellata Lour., Androsace saxifragifolia Bunge
Also known as: Tien Ti Mei · Wade–Giles
Safety at a glance
No rule in our tables for this herb: pregnancy, breastfeeding, incompatible pairs (十八反 / 十九畏), herb–drug, dose ceiling. This is not a safety clearance.
Not graded — No toxicity grade is recorded. Most herbs in the catalogue carry none.
Traditionally used for
- Headaches
- Eye health
- Nose & throat
- Teeth & mouth
- Cough & breathing
- Urinary & fluids
- Pain & joints
- Skin
☯ TCM Properties
Clears Heat, removes toxicity, resolve swelling, Clears the chest and throat and alleviates pain
Traditional Chinese Uses
Dian Di Mei is the whole herb of Androsace umbellata (Herba Androsaces Umbellatae), the umbellate rock-jasmine. Bitter and pungent with a cold nature, entering the Lung, Liver and Spleen channels, it clears Heat and resolves toxicity, reduces swelling, benefits the chest and throat, and alleviates pain. It is used for sore and swollen throat, mouth ulcers (aphtha) and toothache, sores and boils, acute conjunctivitis, headache, rheumatic joint pain, cough and asthma, cloudy painful urination, and topically for traumatic injury, burns and snakebite. It is typically decocted (about 9–15 g) or powdered.
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Botanical Description
Dian Di Mei (点地梅) is the whole herb of Androsace umbellata (Lour.) Merr. (Primulaceae), a small overwintering annual forming a flat basal rosette. The many long-stalked leaves are rounded to broadly ovate, 0.5-2 cm across, with shallowly toothed margins and fine white hairs. In spring several slender, leafless scapes rise 3-15 cm and carry an umbel of small white, five-lobed flowers with a yellow eye, followed by tiny globose capsules. It grows in open grassland, roadsides and moist meadows throughout China and much of East and Southeast Asia. The plant is collected in spring and summer and used to clear heat, relieve toxicity, reduce swelling, and ease sore throat and pain.
Open grassy slopes, meadows, roadsides and moist waste ground from lowlands to montane elevations.
Active Constituents
Saxifragifolin A
Cyclamiretin A-type triterpenoid saponinOne of four saxifragifolin saponins isolated by cytotoxicity-guided fractionation of the methanol extract of the whole plant. Together with saxifragifolins B, C and D it was cytotoxic to a panel of human tumour cell lines with IC50 values of 0.19-2.37 microM, and induced Annexin V binding and nuclear condensation consistent with apoptosis.
Saxifragifolin B
Cyclamiretin A-type triterpenoid saponinCytotoxic in the same sub-micromolar to low-micromolar range as the other saxifragifolins. Notably, multidrug-resistant cell lines (MES-SA/DX5, HCT15/CLO2) were no less sensitive than their parent lines, although they were highly resistant to doxorubicin, suggesting these saponins are not P-glycoprotein substrates.
Saxifragifolin C
Cyclamiretin A-type triterpenoid saponinThe major cytotoxic saponin recovered from the n-butanol soluble fraction. Like related Primulaceae saponins it is surface-active, which is the usual explanation for the irritancy of saponin-rich crude extracts applied to mucosa.
Saxifragifolin D
Cyclamiretin A-type triterpenoid saponinCytotoxic against both drug-sensitive and multidrug-resistant human tumour lines and, with saxifragifolin B, one of the two compounds shown to produce apoptotic nuclear condensation in RAW 264.7 macrophages.
3-O-[beta-D-xylopyranosyl-(1-2)-beta-D-glucopyranosyl-(1-4)-[beta-D-glucopyranosyl-(1-2)]-alpha-L-arabinopyranosyl]-3beta-hydroxy-13beta,28-epoxy-16-oxo-oleanan-30-al
Oleanane triterpenoid saponinOne of two saponins first described from the ethanol extract of the whole plant; reported cytotoxic to human hepatoma cells. Structurally it belongs to the same 13beta,28-epoxy oleanane series as the saxifragifolins.
Kaempferol 3-O-alpha-L-rhamnopyranoside
Flavonol glycosideOne of ten flavonol glycosides characterised from the whole plant, alongside several 2-O- and 3-O-acetylated rhamnosides and 3,7-di-rhamnosides of kaempferol. These are the plant's main polar phenolics; no specific pharmacology has been reported for them in this species.
Quercetin 3-O-beta-D-glucopyranoside
Flavonol glycosideReported from the whole plant together with quercetin 3-O-alpha-L-rhamnopyranoside and myricetin 3-O-beta-D-glucopyranoside. Contributes to the antioxidant character of aqueous-alcoholic extracts.
Dosage Calculator
⚖ Dosage Calculator
A weight-based mathematical estimate for Dian Di Mei. Not a prescription.
Evidence Tier
2 studies on recordRecorded studies by study design, strongest design at the top. This is a study-design tier only, not a GRADE rating: it does not weigh risk of bias, consistency or precision.
Systematic review / meta-analysis
0
Randomized controlled trial
0
Other clinical trial
0
Observational / case report
0
In vitro / animal
2
0 verified · 2 unverified
Other / unclassified
0
Verified: design read from PubMed for a DOI that resolves to the cited paper Unverified: taken from the study's recorded description
Clinical Studies
Cytotoxic effects of triterpenoid saponins from Androsace umbellata against multidrug resistance (MDR) and non-MDR cells
Cytotoxicity-guided fractionation of a methanol extract of Androsace umbellata yielded saxifragifolins C, A, B and D. In the sulforhodamine B assay all four were strongly cytotoxic against non-MDR human tumour lines (A549, SK-OV-3, SK-MEL-2, MES-SA, HCT15) with IC50 values of 0.19-2.37 microM, and the MDR lines MES-SA/DX5 and HCT15/CLO2 were equally sensitive even though they were highly resistant to doxorubicin. The compounds induced Annexin V binding and nuclear condensation in RAW 264.7 cells. This is cell-culture work only; no animal or human data support an anticancer use of the herb.
Triterpenoid Saponins fromAndrosace umbellataand their Anti-proliferative Activities in Human Hepatoma Cells
Two previously undescribed 13beta,28-epoxy-16-oxo-oleanan-30-al saponins were isolated from an ethanol extract of the whole plant along with five known saponins, and all showed significant cytotoxic activity in human hepatoma cells. The paper reports structure elucidation and cell-line cytotoxicity only.
Historical Texts
Shanghai Zhong Cao Yao (Shanghai Herbal Medicines)
Modern, People's Republic of China (1970s)References
- Jun L. Flavonoid glycosides from Androsace umbellata . China Journal of Chinese Materia Medica (2011) [DOI]
This information is for educational purposes only and is not intended to replace professional medical advice. Always consult a qualified healthcare provider before using any herbal remedy, especially if you are pregnant, nursing, or taking medications.
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