2016年5月31日星期二

Mouse liver cells(IAR20) price


Product Name: mouse liver cells (IAR20)

Model: 75ml / bottle

Type: Normal cells

Specifications: strains

Medium: Eagle's minimum essential medium with 10% fetal calf serum

Morphology: epithelial

Features: non-transformed rat liver cell line epitherial adult liver. No tumorigenic in newborn rats and nude mice metabolized benzo (a) pyrene.

Buy Gefitinib

Product Name:Gefitinib
CAS:184475-35-2

Molecular Formula:C22H24ClFN4O3
Molecular Weight:446.9024
Description:GEFITINIB; AKOS 91371; n-(3-chloro-4-fluoro-phenyl)-7-methoxy-6-(3-morpholin-4-ylpropoxy)quinazolin-4-amine; N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-[3-(4-morpholinyl)propoxy]-4-quinazolinamine; ZD 1839; 4-Quinazolinamine, N-(3-chloro-4-fluorophenyl)-7-methoxy-6-[3-(4-morpholinyl)propoxy]-; Gefitinib(TINIBS); Gefitinib, Iressa, ZD1839; Gefitinib Base

From:http://www.chemicals-chemicals.net/Intermediates/Gefitinib/

Phenylacetone price


Product Name: phenylacetone
CAS: 103-79-7
Molecular formula: C9H10O
Molecular weight: 134.18g / mol
Description: phenylacetone is an organic compound. There is a clear oil with a refractive index of 1.5168. This substance is used in the manufacture of methamphetamine and amphetamine.

Sodium oxide for sale


Product Name: sodium
CAS: 1313-59-3
Molecular formula: Na2O
Molecular Weight: 61.9789
Product Description: flakes or amorphous white powder. Sensitive to wet. If melt at over 400 ℃ dark red when decomposed into metal sodium and sodium. Until the reaction dramatic combination to form sodium hydroxide in water. 2.27 relative density. Not flammable, corrosive, very exciting, the human body can cause burns. Having a strong driver and corrosive used on human body.Mainly for the production of sodium compounds or as bleaching agents, disinfectants, a dehydrogenating agent is used, a chemical reaction of the curing agent, condensing agents, etc. .

Cefadroxil price


Product Name: Cefadroxil
CAS: 50370-12-2
Molecular formula: C16H17N3O5S
Molecular Weight: 363.39
Product Description: The role of the product similar to benzyl ammonia cephalosporin on Staphylococcus aureus, hemolytic streptococcus, pneumococcus, Escherichia coli, Proteus, Klebsiella pneumoniae, white bacillus, etc. have an antibacterial effect. Oral absorption is good. Mainly used in the urinary tract, biliary tract and respiratory infections. to obtain an effective concentration in the body for a long straight, 12 hours can be measured. There are more than 90% of the drug in the urine, a prototype, a 0.5 g oral, peak urinary concentration up to 1800 um g / ml, an effective concentration maintained for 20 hours.

Trivastal for sales


Product Name: Trivastal
CAS: 3605-01-4
Molecular formula: C16H18N4O2
Molecular Weight: 298.34
Product Description: dopamine agonists, a single drug or a treatment with levodopa combination of Parkinson's disease, improving the former chip caused by some defect symptoms such as attention and memory decline, dizziness, lower extremity artery embolism by claudication caused disease (2) adjuvant therapy. Defective retinal attack, to improve visual acuity, acts like dopamine, similar side effects to L-dopa. Moreover, to improve our products and peripheral blood circulation, have some curative effect on obstructive or embolic ophthalmology.

What is Leuprorelin


Leuprorelin (leuprolide acetate) is a gonadotropin releasing hormone (GnRH) is used analogously to treat a wide range of sexual disorders associated with hormone, including advanced prostate cancer, endometriosis and precocious puberty. It is mainly in the anterior pituitary to induce transient increase in gonadotropin early release. With continued use causes desensitization leuprolide pituitary and / or regulation, which, to a suppression of circulating levels of gonadotropins and sex hormones Clinical studies in men with advanced prostate cancer as leuprolide (usually monthly for deposit injections of 3.75 or 7.5 mg) is less likely to cause serious cardiovascular side effects such as diethylstilbestrol, and has comparable efficacy to other bilateral orchiectomy or GnRH analogues. the choice between leuprolide and orchiectomy can be made based on the preference of the patient treatment, as well as particular characteristics of the patient, and consequently, affects the cost. monthly intramuscular or subcutaneous depot leuprolide 3.75 mg was superior to placebo and comparable to oral danazol 800 mg / day or intranasal buserelin 900 micrograms / day, in the realization of the objective and subjective responses in women with endometriosis. Leuprolide and is an effective alternative to other treatments for women with endometriosis, but the recommended duration of its use in this clinical setting is limited to 6 months because it decreases bone density. In children with central precocious puberty, leuprolide (usually intramuscular injections or monthly subcutaneous depot leuprolide 3.75 to 15mg), the growth rate decreased average and signs of sexual maturation and increased predicted adult height compared to reference measurements. Although the impact on final adult height of available data can be predicted and must be confirmed by long-term follow-up studies, the lack of alternatives to GnRH analogues leuprolide a first line therapy for children with this rare disease. In women with uterine leiomyomas monthly intramuscular depot leuprolide reduced by 3.75 mg for 6 months significantly uterine volume and fibroid symptoms, but, like other GnRH analogues, these effects dissipate after stopping the drug. As adjunctive therapy in women in preventing premature luteinizing vitro fertilization or gamete intra-fallopian transfer, leuprolide (usually 0.5 to 1 mg / day subcutaneously) reduces the risk of aborted cycles for sampling oocyte. Although some studies retrieved improved intermediate parameters such as increasing the number of mature oocytes and embryos to demonstrate the transfer available, did not show a significant effect on the live birth rate per stimulated cycle.