Martynoside - CAS 67884-12-2
Catalog number: 67884-12-2
Not Intended for Therapeutic Use. For research use only.
Molecular Formula:
C31H40O15
Molecular Weight:
652.7
COA:
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Chemical Family:
Phenols
Description:
Martynoside, a phenylpropanoid found in the herbs of Plantago asiatica L, is an important natural SERM. Martynoside exhibits the activities of anti-oxidative, anti-cancer and anti-metastatic. Martynoside has the potential of antagonizing sports anaemia, the mechanism of this effect might be related to preventing RBC from free radical damage.
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Purity:
>95%
Appearance:
Powder
Synonyms:
1-O-(3-Hydroxy-4-methoxyphenethyl)-3-O-(α-L-rhamnopyranosyl)-β-D-glucopyranose 4-(3-methoxy-4-hydroxy-trans-cinnamate);2-(3-Hydroxy-4-methoxyphenyl)ethyl 3-O-(α-L-rhamnopyranosyl)-4-O-[(E)-3-(4-hydroxy-3-methoxyphenyl)acryloyl]-β-D-glucopyranoside
MSDS:
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Application:
antioxidative; anti-cancer; anti-metastatic
Quality Standard:
Enterprise Standard
Quantity:
Milligrams-Grams
Density:
1.48g/cm3
1.Major constituents and cytotoxic effects of Ajuga chamaecistus ssp. tomentella.
Sadati N1, Jenett-Siems K, Siems K, Ardekani MR, Hadjiakhoondi A, Akbarzadeh T, Ostad SN, Khanavi M. Z Naturforsch C. 2012 May-Jun;67(5-6):275-81.
The n-butanolic fraction of a methanolic extract (80%) from aerial parts of Ajuga chamaecistus ssp. tomentella was analysed using different chromatographic methods. Column (CC) and high-performance liquid chromatography (HPLC) were used for isolation and purification. 13C, H NMR, H-H COSY, HSQC, HMBC, and ESI-MS were employed for identification of the compounds isolated from this fraction. The structures of the compounds were determined to be cis-melilotoside (1), trans-melilotoside (2), lavandulifolioside (3), 20-hydroxyecdysone (4), leonoside B (5), martynoside (6), ajugalactone (7), makisterone A (8), and 24-dehydroprecyasterone (9). This is the first report on the presence of cis- and trans-melilotoside in Ajuga species. Cytotoxic evaluation of the n-butanolic fraction, cis- and trans-melilotoside against cancer (T47D, HT-29, and Caco-2) and normal (NIH 3T3) cell lines by the mitochondrial tetrazolium test (MTT) showed no cytotoxic effects up to 400 microg/mL.
2.The effects of Acorus tatarinowii Schott on 5-HT concentrations, TPH2 and 5-HT1B expression in the dorsal raphe of exercised rats.
Zhu M1, Zhu H2, Tan N3, Zeng G3, Zeng Z2, Chu H2, Wang H2, Xia Z2, Wu R2. J Ethnopharmacol. 2014 Dec 2;158 Pt A:431-6. doi: 10.1016/j.jep.2014.10.026. Epub 2014 Nov 5.
ETHNOPHARMACOLOGICAL RELEVANCE: Acorus tatarinowii Schott (Shi Chang Pu) belongs to the family of Acoraceae. The plant is used as an important herb for prolonging life many years in traditional Chinese medicine. It is an ancient herbal tonic nutriment and can be used as anti-fatigue medicine. However, the effects of Acorus tatarinowii Schott on the endurance exercise in relation to central nervous system have not yet been clarified. In this study, the effects of Acorus tatarinowii Schott on treadmill running endurance, 5-HT concentrations, TPH2, 5-HT1B expression in the dorsal raphe of exercised rats were investigated.
3.Antinociceptive, free radical-scavenging, and cytotoxic activities of Acanthus hirsutus Boiss.
Harput US1, Arihan O, Iskit AB, Nagatsu A, Saracoglu I. J Med Food. 2011 Jul-Aug;14(7-8):767-74. doi: 10.1089/jmf.2010.0195. Epub 2011 Apr 11.
In vivo antinociceptive and in vitro radical scavenging and cytotoxic activities of Acanthus hirsutus Boiss. aqueous extract were investigated to give a new insight into plant usage in traditional medicine. The extract showed significant antinociceptive activity in acetic acid-induced writhing test in mice after oral application and did not change the hind-leg retraction period in the hot-plate test for any dose applied. In addition, the extract showed radical-scavenging activity against 2,2-diphenyl-1-picryl-hydrazyl, nitric oxide, and superoxide radicals similar to those of standard compounds 3-t-butyl-4-hydroxyanisole, ascorbic acid (vitamin C), and quercetin. The gallic acid equivalent total phenolic content of the plant was found to be 65.4 mg/g dry extract. Cytotoxic activity of the aqueous extract was tested against 3 different cancer cell lines-Hep-2 (human larynx epidermoid carcinoma), RD (human rhabdomyosarcoma), and L20B (transgenic murine L cells)-and 1 noncancerous cell line (VERO) using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide method.
4.Biological Activity and Phytochemical Study of Scutellaria platystegia.
Madani Mousavi SN1, Delazar A1, Nazemiyeh H2, Khodaie L3. Iran J Pharm Res. 2015 Winter;14(1):215-23.
This study aimed to determine biological activity and phytochemical study of Scutellaria platystegia (family Labiatae). Methanolic (MeOH) extract of aerial parts of S. platystegia and SPE fractions of methanolic extract (specially 20% and 40% methanolic fractions), growing in East-Azarbaijan province of Iran were found to have radical scavenging activity by DPPH (2, 2-diphenyl -1- pycryl hydrazyl) assay. Dichloromethane (DCM) extract of this plant exhibited animalarial activity by cell free method providing IC50 at 1.1876 mg/mL. Crude extracts did not exhibit any toxicity assessed by brine shrimp lethality assay. Phytochemical study of methanolic extract by using reverse phase HPLC method and NMR instrument for isolation and identification of pure compounds respectively, yielded 2-(4- hydroxy phenyl) ethyl-O-β-D- glucopyranoside from 10% and apigenin 7-O-glucoside, verbascoside and martynoside from 40% SPE fraction. Occurance of verbascoside and martynoside as biochemical markers appeared to be widespread in this genus.
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CAS 67884-12-2 Martynoside

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