ChemicalBook--->CAS DataBase List--->36703-88-5

36703-88-5

36703-88-5 Structure

36703-88-5 Structure
IdentificationBack Directory
[Name]

ISOPRINOSINE
[CAS]

36703-88-5
[Synonyms]

np113
)(1:3)
aviral
viruxan
ntp10381
isoviral
delimmun
imunovir
inosiplex
isoprinosin
ISOPRINOSINE
methisoprinol
inosinepranobex
Isoprinosine(Methisoprinol)
MethisoprinoluM (Inosine pranobex)
inosine,compd.with1-(dimethylamino)-2-propanol4-(acetylamino)benzoate(salt
inosine, compound with (2-hydroxypropyl)dimethylammonium p-acetamidobenzoate (1:3)
[EINECS(EC#)]

253-162-1
[Molecular Formula]

C52H78N10O17
[MDL Number]

MFCD05662374
[MOL File]

36703-88-5.mol
[Molecular Weight]

1115.23
Chemical PropertiesBack Directory
[Melting point ]

140-142°C
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

DMSO (Slightly, Heated), Methanol (Slightly, Heated, Sonicated), Water (Slightly)
[form ]

Solid
[color ]

White to Off-White
[Merck ]

14,4976
[InChIKey]

PBJNZCQJMWVIRT-JHVGCDEENA-N
[SMILES]

O[C@@H]1[C@@H]([C@@H](CO)O[C@H]1N1C=NC2C(N=CNC1=2)=O)O.C(N(C)C)C(O)C.N(C1C=CC(C(=O)O)=CC=1)C(=O)C |&1:1,2,3,7,r|
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

Isoprinosine
[Biological Activity]

isoprinosine is a complex of acetaminobenzoic acid, dimethylaminoisopropanol, and inosine in a 3:3:1 ratio with immunomodulatory effects.immunotherapy is the treatment of disease by inducing, enhancing, or suppressing an immune response. immunomodulatory regimens usually have fewer side effects than existing drugs, such as less potential for creating resistance when treating microbial disease.
[Mechanism of action]

Isoprinosine is thought to act through a receptor for an inosine-like compound on T cell precursors. In vivo it appears to induce the production of more mature T cells and there is some evidence that it can increase the CD4:CD8 ratio in a variety of conditions. In addition, Isoprinosine enhances B-lymphocyte activity, possibly through effects on helper T cells. It also increases macrophage phagocytosis, releases cytokines that induce macrophage proliferation, including immune interferon and interleukin-1 (IL-1) and IL-2, and potentiates T-cell mitogens.
[Clinical Use]

Treatment of mucocutaneous herpes simplex, genital warts, subacute sclerosing panencephalitis
[in vitro]

previous study found that increasing concentrations of isoprinosine (50-400 μg/ml) could produce progressively growing inhibitory effect on hhv-1 replication. the combination of 1000 iu/ml ifn-α and isoprinosine could result in enhanced anti-hhv activity [1].
[in vivo]

previous study demonstrated the positive effect of isoprinosine treatment on persistent infection of balb/c mice with murine gammaherpesvirus 68. increased number of leukocytes, increased percentage of neutrophils, elevated levels of virus-neutralizing antibodies, reduced number of atypical lymphocytes and reduced virus titers were detected in the examined organs after a 14-day treatment. the positive effect of isoprinosine therapy vanished after 120-150 days [2].
[Drug interactions]

Potentially hazardous interactions with other drugs
None known
[Metabolism]

Hepatically metabolised. The major excretion product of the inosine moiety is uric acid, while the p-acetamidobenzoic acid and N,N-dimethylamino- 2-propanol components are excreted in the urine as glucuronidated and oxidised products, respectively, as well as being excreted unchanged
[storage]

Store at -20°C
[References]

[1] majewska a, lasek w, janyst m, mynarczyk g. in vitro infibition of hhv-1 replication by inosine pranobex and interferon-α. acta pol pharm. 2016 may-jun;73(3):637-44.
[2] janíková o, anicová l, briestenská k, mistríková j. the effect of isoprinosine treatment on persistent infection of balb/c mice infected with murine gammaherpesvirus 68. acta virol. 2017;61(1):32-38. doi: 10.4149/av_2017_01_32.
[3] beran j, alapová e, pajdel m; isoprinosine study (ewo iso-2014/1) team. inosine pranobex is safe and effective for the treatment of subjects with confirmed acute respiratory viral infections: analysis and subgroup analysis from a phase 4, randomised, placebo-controlled, double-blind study. bmc infect dis. 2016 nov 7;16(1):648.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2934.99.9001
[Toxicity]

LD50 in mice and rats (mg/kg): >4000 orally and i.p. (Gordon)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

N-Acetyl-p-toluidine -->p-Toluidine-->Acetic anhydride-->4-acetamidobenzoic acid-->Inosine
Questions And AnswerBack Directory
[Description]

ISOPRINOSINE (also known as inosine pranobex) an antiviral drug combing of inosine and dimepranol acedoben (a salt of acetamidobenzoic acid and dimethylaminoisopropanol) in a ratio of 1 to 3. It is mainly used for treating the rare measles complication subacute sclerosing panencephalitis in conjunction with intrathecal interferon therapy1,2. In UK, it is also indicated for mucocutaneous infections due to herpes simplex virus (type 1 and type 2) and for treatment of genital warts as adjunctive therapy to podophyllin or carbon dioxide laser1. It also has certain efficacy in the treatment of AIDS and some other acquired immunodeficiency such as aged patients, cancer patients, severely burned patients, ill patients, and surgery patients3. Preclinical studies have demonstrated that isoprinosine can inhibit the growth of both DNA and RNA viruses as well as potentiate cell-mediated immune response both in vitro and in vivo4,5.
[Sources]

  1. https://en.wikipedia.org/wiki/Inosine_pranobex
  2. Waldman, R. H., and R. Ganguly. "Therapeutic efficacy of inosiplex (Isoprinosine) in rhinovirus infection. " Annals of the New York Academy of Sciences 284.1(1977):153–160.
  3. https://www.ncbi.nlm.nih.gov/pubmed/2446760
  4. https://www.ncbi.nlm.nih.gov/pubmed/83189
  5. https://www.drugbank.ca/drugs/DB13156
Spectrum DetailBack Directory
[Spectrum Detail]

ISOPRINOSINE(36703-88-5)1HNMR
36703-88-5 suppliers list
Company Name: Watson Biotechnology Co.,Ltd  Gold
Telephone: 027-59207879 1972026995 18140587686
Website: http://www.watsonbiotech.cn
Company Name: Hubei Yihao Biotechnology Co., Ltd.  Gold
Telephone: 18995688786
Website: www.chemicalbook.com/ShowSupplierProductsList173084/0_EN.htm
Company Name: Wuhan Juchengyuan Biotechnology Co., Ltd  Gold
Telephone: 400-027-6007 18062142210
Website: http://www.whjcychem.com
Company Name: Shandong Jihao Biotechnology Co., Ltd.  Gold
Telephone: 0531-69958659 15668363232
Website: www.sdperfect.com/
Company Name: Hubei Baoling Chemical Technology Co. , Ltd.  Gold
Telephone: 13129969326
Website: www.chemicalbook.com/supplier/25496562/
Company Name: J & K SCIENTIFIC LTD.  
Telephone: 18210857532 18210857532
Website: https://www.jkchemical.com
Company Name: TCI (Shanghai) Development Co., Ltd.  
Telephone: 021-67121386
Website: https://www.tcichemicals.com/CN/zh/
Company Name: Adamas Reagent, Ltd.  
Telephone: 4006009262 13023226327
Website: http://www.tansoole.com
Company Name: Wuhan Wei Shunda Technology Development Co., Ltd.  
Telephone: 86-027-88774375
Website: www.chemicalbook.com/ShowSupplierProductsList14290/0_EN.htm
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Telephone: 021-50135380
Website: www.shchemsky.com
Company Name: XiaoGan ShenYuan ChemPharm co,ltd  
Telephone: 15527621225; 15527621225
Website: http://www.farchem.com/
Company Name: Beijing Isomersyn Technology CO;LTD  
Telephone: 010-82954736 13391601435
Website: www.chemicalbook.com/supplier/10680452/1.htm
Company Name: Tianjin heowns Biochemical Technology Co., Ltd.  
Telephone: 400 638 7771
Website: www.heowns.com
Company Name: Wuhan Kemi-Works Chemical Co., Ltd  
Telephone: 027-85736489
Website: www.kemiworks.net
Company Name: Hunan Hui Bai Shi Biotechnology Co., Ltd.  
Telephone: 0731-85526065 13308475853
Website: http://www.hnhbsj.com/
Company Name: NCE Biomedical Co.,Ltd.  
Telephone: 4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
Website: www.chemicalbook.com/ShowSupplierProductsList15748/0_EN.htm
Company Name: Shanghai Aladdin Bio-Chem Technology Co.,LTD  
Telephone: 400-6206333 13167063860
Website: www.aladdin-e.com/
Company Name: The future of Shanghai Industrial Co., Ltd.  
Telephone: 021-61552785
Website: www.jonln.com
Tags:36703-88-5 Related Product Information
555-31-7 683-60-3 61676-62-8 59-06-3 367-93-1 138-59-0 36791-04-5 59277-89-3 24939-03-5 108-16-7 58-63-9