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  • 西红花苷

    Crocin

    西红花苷
    产品编号 CFN90227
    CAS编号 42553-65-1
    分子式 = 分子量 C44H64O24 = 976.96
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Diterpenoids
    植物来源 The stigmas of Crocus sativus L.
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
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    产品名称 产品编号 CAS编号 包装 QQ客服
    西红花苷 CFN90227 42553-65-1 10mg QQ客服:1457312923
    西红花苷 CFN90227 42553-65-1 20mg QQ客服:1457312923
    西红花苷 CFN90227 42553-65-1 50mg QQ客服:1457312923
    西红花苷 CFN90227 42553-65-1 100mg QQ客服:1457312923
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    ChemFaces的产品在许多优秀和顶级科学期刊中被引用

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • Wageningen University (Netherlands)
  • University of Beira Interior (Portugal)
  • University of Leipzig (Germany)
  • University of British Columbia (Canada)
  • Center for protein Engineering (CIP) (Belgium)
  • University of Perugia (Italy)
  • Universidad Industrial de Santander (Colombia)
  • University of South Australia (Australia)
  • Amity University (India)
  • Stanford University (USA)
  • S.N.D.T. Women's University (India)
  • Medizinische Universit?t Wien (Austria)
  • Max Rubner-Institut (MRI) (Germany)
  • Complutense University of Madrid (Spain)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • J. of The Korean Society of Food Culture2017, 144-149
  • Curr Med Sci.2024, 44(2):355-368.
  • Pharmacognosy Journal.2022, 14,4,327-337.
  • In Vitro Cellular & Developmental Biology - Plant 2021, 57:874–882.
  • Nat Prod Commun.2018, 10.1177
  • Food Chem.2019, 290:286-294
  • Plants (Basel).2021, 10(11):2317.
  • Food Quality and Safety2018, 2:213-219
  • Eur J Pharmacol.2020, 889:173589.
  • J Sci Food Agric.2017, 97(5):1656-1662
  • University of Central Lancashire2017, 20472
  • Natural Product Communications2021, 16(9):1-10.
  • Phytomedicine.2019, 59:152785
  • Life Sci.2018, 209:498-506
  • J of Engineering Science&Technology2018, 13(9):2820-2828
  • Molecules.2024, 29(5):1048.
  • BMC Complement Altern Med.2017, 17(1):384
  • Nutr Metab (Lond).2019, 16:31
  • Sci Rep.2023, 13(1):21690.
  • J Agric Food Chem.2023, 71(47):18510-18523.
  • Phytomedicine.2020, 79, 153351
  • Int J Mol Sci.2023, 25(1):283.
  • J Appl Biol Chem2021, 64(3):245-251.
  • ...
  • 生物活性
    Description: Crocin is a water-soluble carotenoid pigment of saffron (Crocus sativus L.), it has been used as a spice for flavoring and coloring food preparations. Crocin has anti-inflammatory, anti-oxidative, anti-apoptotic, anti-asthma, anti-cancer, and hypolipidemic effects. Crocin improves toxic effects of diazinon via reducing lipid peroxidation and restoring altered contractile and relaxant responses in rat aorta; it also protects retinal photoreceptors against light-induced cell death. Crocin can also promote ovarian cancer HO-8910 cell apoptosis, most likely by increasing p53 and Fas/APO-1 expression, and then activating the apoptotic pathway regulated by Caspase-3.
    Targets: PGE | TNF-α | IL Receptor | Caspase | ERK | JNK | p38MAPK | p53 | AChR | LDL | Fas | APO-1
    In vitro:
    Nat Prod Commun. 2015 Feb;10(2):249-52.
    Ovarian cancer HO-8910 cell apoptosis induced by crocin in vitro.[Pubmed: 25920253]
    The effect and mechanism of ovarian cancer HO-8910 cell apoptosis induced by crocin.
    METHODS AND RESULTS:
    MTT assay was performed to detect the inhibitory action of crocin on the proliferation of HO-8910 cells. Flow cytometry was used to test the cell cycle distribution and apoptosis rate of ovarian cancer HO-8910 cells. Western blot analysis was utilized to measure the levels of apoptotic proteins such as p53, Fas/APO-1, and Caspase-3. MTT analysis revealed that crocin significantly inhibited the growth of HO-8910 cells. Additionally, flow cytometry illustrated that crocin raised the proportion of HO-8910 cells in the G0/G1 phase and increased their apoptosis rate. Furthermore, Western blot analysis revealed that crocin up-regulated the expression of p53, Fas/APO-1, and Caspase-3.
    CONCLUSIONS:
    The results of this study showed that crocin can significantly inhibit the growth of HO-8910 cells and arrest them in the G0/G1 phase. Crocin can also promote ovarian cancer HO-8910 cell apoptosis, most likely by increasing p53 and Fas/APO-1 expression, and then activating the apoptotic pathway regulated by Caspase-3.
    Invest Ophthalmol Vis Sci. 2006 Jul;47(7):3156-63.
    Protective effect of crocin against blue light- and white light-mediated photoreceptor cell death in bovine and primate retinal primary cell culture.[Pubmed: 16799063 ]
    The present study was performed to investigate the effect of crocin on blue light- and white light-induced rod and cone death in primary retinal cell cultures.
    METHODS AND RESULTS:
    Primary retinal cell cultures were prepared from primate and bovine retinas. Fifteen-day-old cultures were exposed to blue actinic light or to white fluorescent light for 24 hours. Cultures were treated by the addition of different concentrations of crocin for 24 hours before light exposure or for 8 hours after light exposure. Cultures kept in the dark were used as controls. Green nucleic acid stain assay was used to evaluate cell death. Rods and cones were immunolabeled with specific antibodies and counted. TUNEL labeling was used to detect fragmented DNA in fixed cells after light exposure. Primary retinal cell cultures contained a mixture of retinal cells enriched in photoreceptors, bipolar cells, and Müller cells. Twenty-four-hour exposure to blue and white light induced death in 70% to 80% of the photoreceptors in bovine and primate retinal cell cultures. Crocin protected the photoreceptors against blue light- or white light-mediated damage in a concentration-dependent manner with an EC50 of approximately 30 microM. TUNEL assays confirmed that crocin protected photoreceptors from light damage.
    CONCLUSIONS:
    These results show that blue and white light selectively induce rod and cone cell death in an in vitro model. Crocin protects retinal photoreceptors against light-induced cell death.
    In vivo:
    Immunopharmacol Immunotoxicol. 2015 Jun;37(3):236-43.
    Anti-asthma potential of crocin and its effect on MAPK signaling pathway in a murine model of allergic airway disease.[Pubmed: 25753844]
    Crocin, a diterpenoid glucoside, has multitudinous activities such as anti-inflammation, anti-allergy, anti-oxidation and relaxing smooth muscles. In this study, the potential of crocin as an anti-asthma agent was investigated in a murine model.
    METHODS AND RESULTS:
    BALB/c mice were sensitized and challenged by ovalbumin (OVA) to induce allergic airway inflammation, with crocin administered one hour before every OVA challenge. Airway hyper-reactivity was evaluated by lung function analysis systems. Leukocyte counts in bronchoalveolar lavage fluid (BALF) were measured by a hemocytometer and Diff-Quick-stained smears. Lung tissues were stained with hematoxylin-eosin, Congo red and methylene blue for histopathological inspection. Inflammatory mediators in serum, BALF and lung were measured by ELISA or RT-PCR. Effects of crocin on MAPK signaling pathways were investigated by western blot analysis. Crocin significantly suppressed airway inflammation and hyper-reactivity, reduced levels of BALF interleukin (IL-4), IL-5, IL-13 and tryptase, lung eosinophil peroxidase and serum OVA-specific IgE, and inhibited the expression of lung eotaxin, p-ERK, p-JNK and p-p38 in the OVA-challenged mice.
    CONCLUSIONS:
    These results demonstrated that the suppression of crocin on airway inflammation and hyper-reactivity in a murine model, thus crocin might have a great potential to be a candidate for the treatment of asthma.
    Drug Chem Toxicol. 2014 Oct;37(4):378-83.
    Protective effect of crocin on diazinon induced vascular toxicity in subchronic exposure in rat aorta ex-vivo.[Pubmed: 24392635]
    Diazinon (DZN) is a widely used organophosphate insecticide. Although mechanism of DZN cardiovascular toxicity is primarily mediated through inhibition of acetylcholinesterase, however, DZN causes remarkable atropine-insensitive hypotension in rats. It has been proved that oxidative stress is an important mechanism of DZN toxicity especially in chronic exposure. Crocin, an active ingredient of saffron, has been found to antagonize the hypotensive effects of DZN in rats, but do not reverse acetylcholinesterase inhibition. In this study the effects of DZN on contractile and relaxant responses in rat aorta as well as ex-vivo antioxidant actions of crocin have been investigated.
    METHODS AND RESULTS:
    Rats were divided into 7 groups: corn oil (control), DZN (15 mg/kg/day, gavage), crocin (12.5, 25 and 50 mg/kg/day, i.p.) plus DZN, vitamin E (200 IU/kg, i.p., three days a week) plus DZN and crocin (50 mg/kg/day, i.p.) groups. Treatments were continued for 4 weeks. Contractile and relaxant responses were evaluated on the isolated aorta. Our results showed that DZN not only decreased the contractile responses to KCl and Phenylephrine (PE) (p < 0.001), but also attenuated the relaxant response to acetylcholine (ACh) (p < 0.01). Crocin and vitamin E attenuated lipid peroxidation, improved the reduction of contractile responses by KCl and PE and restored the decrease in ACh relaxation in rat aorta.
    CONCLUSIONS:
    DZN induced vascular toxicity which may be due to oxidative stress and not to a cholinergic mechanism. Crocin improved toxic effects of DZN via reducing lipid peroxidation and restoring altered contractile and relaxant responses in rat aorta.
    Life Sci . 2019 Oct 15;235:116794.
    Crocin attenuates lung inflammation and pulmonary vascular dysfunction in a rat model of bleomycin-induced pulmonary fibrosis[Pubmed: 31465731]
    Abstract Amongst the various forms of lung injury; pulmonary fibrosis remains the most intricate form with limited therapeutic options to both the patient and the physicians. Bleomycin (BLM) is a chemotherapeutic agent used for the treatment of various carcinomas; however, its therapeutic value is significantly limited by its associated pulmonary fibrosis. The current study highlights the prominent antioxidant, anti-inflammatory and anti-fibrotic effect of crocin against BLM-induced pulmonary fibrosis. Intratracheal BLM instillation induced significant biochemical, structural, functional and vascular pulmonary injury. BLM instillation increased oxidant load with quenching of antioxidant defenses together with increase inflammatory and fibrotic cytokines expression. Crocin significantly attenuated BLM-induced lung injury and its effect was comparable to the standard anti-fibrotic; halofuginone. The observed anti-inflammatory and anti-fibrotic and antioxidant impacts are thought to be embroiled in the therapeutic impacts of crocin. Down-regulation of TLR4, IL-10 expression is the major pathway involved in the observed anti-inflammatory effects and finally, down-regulation of tissue expression of TNF-α and TGF-β1 is the major pathways implicated in the observed anti-fibrotic activities and modulation of Nrf2 and HO-1 pathways is the main mechanism involved in the observed antioxidant effects. Keywords: Bleomycin; Crocin; HO-1; Halofuginone; NrF2; TGF-β1.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.0236 mL 5.1179 mL 10.2358 mL 20.4717 mL 25.5896 mL
    5 mM 0.2047 mL 1.0236 mL 2.0472 mL 4.0943 mL 5.1179 mL
    10 mM 0.1024 mL 0.5118 mL 1.0236 mL 2.0472 mL 2.559 mL
    50 mM 0.0205 mL 0.1024 mL 0.2047 mL 0.4094 mL 0.5118 mL
    100 mM 0.0102 mL 0.0512 mL 0.1024 mL 0.2047 mL 0.2559 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
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