2016年3月7日星期一

Muscle glycogen concept


The importance of carbohydrates as an energy source during endurance training is known for 60 years. With the advent of needle muscle biopsy in the 1960s, it was found that the main source of carbohydrates during exercise are the glycogen reserves. It was shown that the capacity between 65 to 75% VO2max exercised at intensities of pre-exercise glycogen levels in the muscle bound, ie more glycogen reserves, more exercise time to exhaustion. Because of the critical importance of muscle glycogen during prolonged, intense exercise, a considerable amount of research has been conducted in order to design the best diet to increase muscle glycogen stores prior to the competition and the most effective means of replenishment quickly determining the glycogen after training. The rate determining step in the glycogen synthesis is the transfer of glucose from uridine diphosphate-glucose on an amylose chain. This reaction is catalyzed by the enzyme glycogen synthase, which in a glucose 6-phosphate-dependent, inactive form (form D) and an active form of glucose 6-phosphate can independent (I-form) exist. The conversion of glycogen synthase from one form to the other is controlled by phosphorylation-dephosphorylation reactions. The concentration of muscle glycogen can vary greatly depending on the level of conditioning, exercise routines and diet. The pattern of muscle glycogen re-synthesis after exercise-induced exhaustion is biphasic. After completion of movement and adequate glycogen muscle carbohydrate consumption is rapidly resynthesized to close before training levels within 24 hours. Muscle glycogen then increased very gradually to normal in the coming days. A contribution to the rapid phase of the re-synthesis is to increase the proportion of glycogen synthase I, an increase in muscle cell membrane permeability to glucose and an increased sensitivity of muscle to insulin. The slow phase of the glycogen synthesis is under the control of the intermediate form of glycogen synthase, which is very sensitive to the activation of the glucose 6-phosphate. The conversion of the enzyme can be attributed to this intermediate to form a plasma insulin concentration elevated after several days of high consumption of carbohydrates constantly exposed to muscle tissue. For optimal performance of the exercise, muscle glycogen stores must be replenished on a daily basis again. For athletes daily average endurance of a carbohydrate consumption of 500 to 600 g is required. This leads to a maximum glycogen from 80 to 100 micromol / g wet weight.

L-Cysteine HCL anhydrous for sale


Product name:L-Cysteine HCL anhydrous

Molecular Formula
:C3H8ClNO2S

Formula Weight:157.61912g/mol

Description:It is a white or colorless HCl crystals.L-cysteine (hydrochloride) - anhydrous (E920) used in cooking and preparation flavours.It strong sour taste and very soluble in water.It is a promoter for fermentation.It bread used to prevent the natural fruit juice vitamin C-oxide. It has a detoxification for poison of acrylonitrile aromafic acid. It is to protect against radiation damage and the treatment of bronchitis and liquefy sputum used.

Remifentanil


Remifentanil has a rapid onset and short duration of action, predictable pharmacokinetics / pharmacodynamics, and unlike fentanyl, does not accumulate with repeated or prolonged administration. In this study, predictors of use of remifentanil in surgical patients with impaired hepatic or renal or obesity in the United States, remifentanil was, fentanyl, or the combination.

Testosterone propionate


Product name: Testosterone propionate 
CAS no.: 
1255-49-8 ,57-85-2
Molecular Formula: C22H32O3 
Molecular Weight: 
344.49 
Appearance: White crystal or white crystalline powder 
Product description: For the treatment of breast cancer, ovarian cancer, uterine fibroids, multiple myeloma and renal cell carcinoma.
For more, please click:http://www.chemicalspharm.com/New-Products/

Biapenem Side Chain price


Product name: Biapenem Side Chain
CAS no.: 
153851-71-9
Molecular Formula: C5H8ClN3S
Molecular Weight: 
177.66
Appearance: White or off-white crystalline powder
Purity: ≥98%(HPLC)
Product description: In Apei south side chain framework in medicine and pharmaceutical raw materials, can be used as Apei antibiotic-producing south. As Apei South (biapenem, 10627 YOA) by the Japanese company Lederle and developed in 1989 with ammonia in the United States by penicillin injection with alkenes antibiotics finished carbon now Ⅲ clinical trials in Japan Awaiting Approval ,

2016年3月6日星期日

Thebaine content and Plant


Four varieties of thebaine-rich P. bracteatum grown outdoors on two seasons and distribution of thebaine in the aerial parts considered the most suitable raw material for commercial production to be determined. The leaves contain only 0-1 to 0-15%; capsules 0-5 to 3-0% and 28-53% latex bled. The maximum for the latter occurred about 3-4 weeks after the opening of the petals and during the day, at about 15.00 pm. A product 'bractium' just prepared as opium of P. somniferum contain up to 55% thebaine and calculations of the 1974 results provided theoretical yields of up to 58 k of thebaine per hectare. However, this method is very labor; more latex bled represents only 46% of the total thebaine of the capsule. Also contain significant amounts of thebaine stalks so that the seed heads can be recommended as a starting material. In the capsule of thebaine content peaked at 3 to 4 weeks after the opening of the petals and again two weeks later. At this stage, mature, there is a theoretical yield of 50 kg per hectare. Two other advantages result from the collection at that time mature seeds can probably be used for similar purposes in a poppy; and fruit walls at this stage does not contain thebaine bound '(i, e, thebaine insoluble in MeOH but soluble in acetic acid; NH4OH - linked in immature capsules thebaine 18-36% of the total thebaine represents. ). There is some evidence that, as these perennial increases in age, the ability of thebaine increase seems to continue production. Storage of the raw material, even under ideal conditions, resulting in a loss of thebaine between 12 and 20% in one year.

Organization of an activator


Initiation of transcription requires the conversion of complexes formed promoters consist of the RNA polymerase (RNAP) and double-stranded DNA to open promoter complex in which the enzyme is able to access to the DNA template in a single-stranded form. The complex between RNAP and sigma factor variant .sigma 54 in hydrolysis of ATP-dependent remodeling by activating proteins as a closure remains complex occurs. This conversion facilitates DNA background and made the transition to the open complex. We present cryo-electron microscopy bacterial RNAP reconstructions in complex with σ54alone and σ54 of RNAP with a AAA + activator. With photoréticulation data establishing the position of the promoter DNA in the complex, we explain why the σ54 RNAP gated complex is not able to provide the DNA template for access and how structural changes activator induced binding can initiate conformational changes that ultimately result in the formation of the open complex.