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Isoprinosine CAS 36703-88-5 Raw Materials Powder
Product Overview:
Isoprinosine Powder is a 1:3 complex of inosine and dimethylaminoisopropanol ester of acetamido benzoate, which is a chemically synthesized immunomodulator used in the pharmaceutical industry to treat viral disease infections such as influenza virus, herpes virus, and immunodeficiency virus.Isoprinosine CAS 36703-88-5 is a white powder, odorless and Odorless. It is soluble in water. Isoprinosine has antiviral effects and is effective against herpes, influenza and nasal infections in humans. Isoprinosine Raw Materials is an antiviral drug that increases peripheral blood lymphocytes, lymphocyte transformation rate and IFN levels in children with herpes simplex virus infection.
Isoprinosine CAS 36703-88-5 Raw Materials Powder Attributes
CAS: 36703-88-5
MF: C24H34N6O9
MW: 550.57
EINECS: 253-162-1
Specification: 99% min Isoprinosine
Sample: Isoprinosine Powder
Brand: Henrikang
Appearance: White Powder
Storage: Cool Dry Place
Shelf Life: 2 Years
Test Method: HPLC
Isoprinosine CAS 36703-88-5 Raw Materials Powder Details
Isoprinosine Powder Usage and Synthesis.
Isoprinosine Powder is a 1:3 complex of inosine and dimethylaminoopropisanol ester of acetamido benzoate, which is a chemically synthesized immunomodulator used in the pharmaceutical industry to treat viral disease infections such as influenza virus, herpes virus, and immunodeficiency
Isoprinosine CAS 36703-88-5 is a white powder, odorless and Odorless. It is soluble in water. Isoprinosine has antiviral effects and is effective Isoprinosine has antiviral effects and is effective against herpes, influenza and nasal infections in humans.
Isoprinosine Raw Materials is an antiviral drug that increases peripheral blood lymphocytes, lymphocyte transformation rate and IFN levels in Isoprinosine Raw Materials is an antiviral drug that increases peripheral blood lymphocytes, lymphocyte transformation rate and IFN levels in children with herpes simplex virus infection.
Application/Function of Isoprinosine Powder.
- (1) Isoprinosine can promote the proliferation of lymphocytes induced by phytohaemagglutinin (PHA), cutin A (ConA), tetanus toxoid, influenza virus, etc.
- (2) Enhances the delayed allergic response induced by dinitrochlorobenzene and normalizes the delayed allergic response inhibited by cyclophosphamide.
- (3) Restores the proliferative response of mouse spleen lymphocytes inhibited by cyclophosphamide to ConA.
- (4) It also promotes the production of interleukin 1 (IL-1), interleukin 2 (IL-2) and interferon, and enhances the activity of mononuclear macrophages and natural killer cells (NK).
It also restores normal immune function due to aging, including decreased lymphocyte proliferative response due to aging, cytotoxicity of NK, monocyte chemotaxis and vacuole-forming cell count to normal or near-normal levels.
Isoproterenol has antiviral effects and is effective against herpes, influenza and nasal infections in humans. It is more effective in patients with herpes simplex virus infection.
In addition to its direct antiviral effect, it has immune enhancing effect, mainly enhancing cellular immune function.
Clinical studies have shown that it can increase the proliferation of lymphocytes due to mitogenic factors, increase the production of antibodies, and increase the production of cytokines, such as interleukin-2. This product has high efficacy and low toxic side effects.
Isoproterenol is an antiviral drug that increases peripheral blood lymphocytes, lymphocyte transformation rate and IFN level in children with SSPE. It has been used for SSPE for nearly 20 years. Most studies have shown that the drug can improve or stabilize symptoms and increase survival rate in some children, and is mostly used in combination with IFN.
It is mainly used for herpes simplex virus infection and genital warts, and also leads to improved immune function in patients with primary tumors such as lung cancer, breast cancer, and melanoma. Immune function is usually maintained for 2 months after each dose.
Isoproterenol is also effective in autoimmune diseases such as rheumatoid arthritis, including slowed blood sedimentation, reduced fibrinogen, decreased number of swollen joints, and reduced morning stiffness. It also has efficacy in polymicrobial stomatitis and focal genititis.
Veterinary medicine clinically isoproterenol can be used as an immune enhancer to assist in the treatment of various viral disease infections, especially respiratory disorder syndrome caused by viral infections.
Use characteristics: Isoproterenol is convenient and widely used, and can be used simultaneously with many drugs, according to the synergistic or additive effect. The product has no species specificity and can be widely used on poultry, pigs, cattle and other animals.
- (1) The use of the product can improve the antibody level of the body, which can be used to prevent frequent viral diseases and avoid the high antibody level and vaccine stress caused by booster immunization.
- (2) It has a wide antiviral spectrum, low toxicity and a large safety range. It can be used at the same time with vaccine, which can make up for the immunity gap, reduce the vaccine stress and enhance the immunity effect.
Recommended formula: The product is recommended to be compounded with suitable drugs for the treatment of viral diseases:
- (1) It is used for the treatment of atypical Newcastle disease, porcine reproductive and respiratory disorder syndrome and other immunosuppressive diseases in combination with purple chrysanthemum polysaccharide and astragalus polysaccharide.
- (2) It is made into feed premix with vitamin C and astragalus polysaccharide to improve the immune function of animal organism.
- (3) It is used in combination with Chinese herbal medicines such as Panax quinquefolium, Astragalus, Goldenseal, Forsythia, Scutellaria, etc. to make special antiviral drugs.
Production Method of Isoprinosine Powder
This product is rapidly absorbed and metabolized after oral or intravenous administration. The blood concentration peaks after 1 hour of oral administration and decreases to disappear after 2 hours. The main excretion product is uric acid, while other metabolites are excreted in urine after oxidation or glucuronidation. The plasma half-life is 50 minutes for oral administration and 3 minutes for sedation.