Sodium Butyrate (丁酸钠) 被报道证实为HDAC抑制剂,从而导致组蛋白过乙酰化。
Sodium butyrate is the sodium salt of butyric acid and has long been known as an inhibitor of histone deacetylases (IC50 values are 0.3, 0.4, 0.3, mM for HDAC1, 2 and 7 respectively). This compound has been shown to cause induction of differentiation and gene expression and also prevent cell proliferation. Mechanistic studies suggest that the action of Sodium Butyrate is often mediated through Sp1/Sp3-associated HDAC activity which leads to transcriptional activation of the p21 gene.
动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数 | |
例如,已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法:将88 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到该药物用于大鼠的等效剂量44 mg/kg。
[1] Archer SY, et al. Proc Natl Acad Sci U S A, 1998, 95(12), 6791-6796.
[2] Davie, James R., et al., 2003. Inhibition of histone deacetylase activity by butyrate. The Journal of nutrition. 133(7 Suppl): 2485S-2493S.
[3] Joseph, Jeena., et al., 2004. Expression profiling of sodium butyrate (NaB)-treated cells: identification of regulation of genes related to cytokine signaling and cancer metastasis by NaB. Oncogene. 23(37): 6304-15.
[4] Sealy, L., et al., 1978. The effect of sodium butyrate on histone modification. Cell. 14(1): 115-21.
[5] Sekhavat, Anoushe., et al., 2007. Competitive inhibition of histone deacetylase activity by trichostatin A and butyrate. Biochemistry and cell biology = Biochimie et biologie cellulaire. 85(6): 751-8.
分子式 C4H7NaO2 |
分子量 110.09 |
CAS号 156-54-7 |
储存方式 ﹣20 ℃冷藏长期储存。冰袋运输 |
溶剂(常温) |
DMSO <1 mg/mL |
Water 20 mg/mL |
Ethanol <1 mg/mL |
体内溶解度
NCT Number | Conditions | Interventions | Sponsor/Collaborators | Phases | Start Date | Last Updated |
NCT02654405 | Schizophrenic Disorders|Cognitive Function | Dietary Supplement: Sodium Butyrate|Other: Placebo | Nathan Kline Institute for Psychiatric Research|Stanley Medical Research Institute | Phase 2|Phase 3 | 2016-04-01 | 2016-08-11 |
NCT03010865 | Schizophrenic Disorder|Cognitive Impairment | Drug: Sodium Butyrate|Drug: Placebo Oral Capsule | Shanghai Mental Health Center|Stanley Medical Research Institute | Phase 2|Phase 3 | 2017-02-01 | 2017-01-03 |
NCT00800930 | Shigellosis | Biological: Sodium Butyrate|Biological: Saline | International Centre for Diarrhoeal Disease Research, Bangladesh|Swedish International Development Cooperation Agency (SIDA)|Karolinska Institutet | Phase 2 | 2005-01-01 | 2011-12-06 |
NCT00693355 | Healthy | Other: Sodium butyrate|Other: NaCl | Maastricht University Medical Center|Top Institute Food and Nutrition | 2005-12-01 | 2017-02-22 | |
NCT00696098 | Gut Health | Other: sodium butyrate|Other: NaCl | Maastricht University Medical Center|Top Institute Food and Nutrition | 2007-05-01 | 2017-02-22 | |
NCT02271802 | SCFA Metabolism | Dietary Supplement: Sodium butyrate|Dietary Supplement: NaCl | Maastricht University Medical Center|Top Institute Food and Nutrition | 2009-06-01 | 2014-10-21 | |
NCT01757379 | Short Chain Fatty Acids Bioavailability | Dietary Supplement: 13C-labeled Acetate|Dietary Supplement: 13C-labeled propionate|Dietary Supplement: 13C-labeled butyrate|Dietary Supplement: Inulin | Katholieke Universiteit Leuven | 2011-04-01 | 2015-01-13 | |
NCT02090504 | Alcohol Withdrawal Syndrome|Alcohol Dependence | Drug: Sodium Oxybate (SMO)|Drug: Oxazepam | Catholic University of the Sacred Heart|CT Pharmaceutical Industries, Sanremo - Italy|University of Bologna|Medical University of Vienna | Phase 4 | 2002-02-01 | 2014-03-17 |
NCT01983046 | Obesity|Type 2 Diabetes | Drug: Three different mixture of acetate, butyrate and propionate and palcebo | Maastricht University Medical Center|Top Institute Food and Nutrition | 2013-09-01 | 2014-10-20 | |
NCT01518348 | Contact Dermatitis | Biological: Patch Test | Allerderm | Phase 3 | 2012-12-01 | 2013-02-26 |
NCT01797562 | Allergic Contact Dermatitis | Drug: T.R.U.E. Test Panel 3.2 | Allerderm | Phase 4 | 2012-12-01 | 2014-09-22 |
NCT00672308 | Cholera | Other: Benefiber|Other: Benefiber with ORS|Other: Benefiber with ORS|Other: Benefiber with ORS|Other: the reduced-osmolarity WHO-ORS without added Benefiber|Other: the reduced-osmolarity WHO-ORS without added Benefiber | International Centre for Diarrhoeal Disease Research, Bangladesh|University of Basel | Phase 2 | 2003-05-01 | 2008-05-05 |
NCT01862380 | Adrenal Hyperplasia, Congenital|21-hydroxylase Deficiency | Other: Functional explorations|Other: Functional explorations | Assistance Publique - H么pitaux de Paris | 2013-02-01 | 2016-09-28 | |
NCT00675272 | Brain Death | Drug: hydrocortisone|Drug: sodium chloride | Kuopio University Hospital|Tampere University Hospital | 2008-05-01 | 2015-04-03 | |
NCT00147004 | Shock, Septic | Drug: hydrocortisone sodium succinate|Drug: Placebo | Hadassah Medical Organization|European Society of Intensive Care Medicine|International Sepsis Forum|The Gorham Foundation | Phase 3 | 2002-03-01 | 2008-04-23 |
NCT01608945 | Some Studies Shows That the Steroid Can Reduce the Injury of the I/R of the Liver | Drug: Hydrocortisone sodium succinate | Eastern Hepatobiliary Surgery Hospital | 2008-04-01 | 2012-05-30 | |
NCT02549768 | Pituitary Neoplasms | Drug: Dexmedetomidine|Drug: Sodium Chloride 0.9% | Pontificia Universidad Catolica de Chile | Phase 4 | 2015-09-01 | 2016-10-10 |
NCT02152553 | Addison Disease | Drug: Hydrocortisone|Drug: Placebo | Vastra Gotaland Region | 2014-05-01 | 2016-01-04 | |
NCT00529841 | Adrenal Hyperplasia, Congenital | Drug: Hydrocortisone sodium acetate | Baylor College of Medicine | 2007-01-01 | 2015-09-10 | |
NCT02602210 | Liver Cirrhosis | Drug: Hydrocortisone|Drug: NaCL 0.9% | Universitaire Ziekenhuizen Leuven | Phase 3 | 2015-01-01 | 2015-11-09 |
NCT02691858 | Intussusception | Drug: Hydrocortisone|Drug: Saline | Cairo University | 2015-04-01 | 2017-02-05 |
注:以上所有数据均来自公开文献,并不保证对所有实验均有效,数据仅供参考。
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