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Details

Stereochemistry MIXED
Molecular Formula C10H12N4O5.3C9H9NO3.3C5H13NO
Molecular Weight 1115.2325
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of INOSINE PRANOBEX

SMILES

CC(O)CN(C)C.CC(O)CN(C)C.CC(O)CN(C)C.CC(=O)NC1=CC=C(C=C1)C(O)=O.CC(=O)NC2=CC=C(C=C2)C(O)=O.CC(=O)NC3=CC=C(C=C3)C(O)=O.OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)N5C=NC6=C5N=CNC6=O

InChI

InChIKey=YLDCUKJMEKGGFI-QCSRICIXSA-N
InChI=1S/C10H12N4O5.3C9H9NO3.3C5H13NO/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18;3*1-6(11)10-8-4-2-7(3-5-8)9(12)13;3*1-5(7)4-6(2)3/h2-4,6-7,10,15-17H,1H2,(H,11,12,18);3*2-5H,1H3,(H,10,11)(H,12,13);3*5,7H,4H2,1-3H3/t4-,6-,7-,10-;;;;;;/m1....../s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/2431857

Inosine pranobex is an antiviral drug that is a combination of inosine and dimepranol acedoben (a salt of acetamidobenzoic acid and dimethylaminoisopropanol) in a ratio of 1 to 3. Inosine pranobex is used to treat mucocutaneous infections due to herpes simplex virus (type 1 and/or type II), genital warts as adjunctive therapy to podophyllin or carbon dioxide laser, and subacute sclerosing panencephalitis. The in vivo antiviral and activity of inosine pranobex is believed to result from an enhancement of host immune responses due to the drug. The drug does not by itself stimulate resting lymphocytes, but augments immunological processes by lymphocytes once they have been triggered by mitogens or viral antigens.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
IMUNOVIR

Approved Use

Imunovir tablets are indicated in the management of mucocutaneous infections due to herpes simplex virus (type 1 and/or type II), genital warts as adjunctive therapy to podophyllin or carbon dioxide laser, and subacute sclerosing panencephalitis.

Launch Date

4.37615985E11
Primary
IMUNOVIR

Approved Use

Imunovir tablets are indicated in the management of mucocutaneous infections due to herpes simplex virus (type 1 and/or type II), genital warts as adjunctive therapy to podophyllin or carbon dioxide laser, and subacute sclerosing panencephalitis.

Launch Date

4.37615985E11
Primary
IMUNOVIR

Approved Use

Imunovir tablets are indicated in the management of mucocutaneous infections due to herpes simplex virus (type 1 and/or type II), genital warts as adjunctive therapy to podophyllin or carbon dioxide laser, and subacute sclerosing panencephalitis.

Launch Date

4.37615985E11
PubMed

PubMed

TitleDatePubMed
In-vitro inhibition of LAV/HTLV-III infected lymphocytes by dithiocarb and inosine pranobex.
1985 Dec 21-28
Isoprinosine-induced modulation of T-helper-cell subsets and antigen-presenting monocytes (Leu M3 + Ia +) resulted in improvement of T- and B-lymphocyte functions, in vitro in ARC and AIDS patients.
1987 Nov
Influence of methisoprinol (isoprinosine) on HIV-infected human lymphocytes: in vitro immunological, virological, and ultrastructural studies.
1989
No effect of isoprinosine on HIV infection in vitro.
1990 Oct
Treatment of experimental pneumocystosis: review of 7 years of experience and development of a new system for classifying antimicrobial drugs.
1992 Sep
Activities of antifolate, antiviral, and other drugs in an immunosuppressed rat model of Pneumocystis carinii pneumonia.
1992 Sep
Patents

Sample Use Guides

Mucocutaneous herpes simplex: 1 g q.d.s. (4g daily), for 7 -14 days. Genital warts: 1g t.d.s. (3g daily), for 14-28 days as adjunctive therapy to podophyllin or carbon dioxide laser. Subacute sclerosing panencephalitis (SSPE): 50-100mg/kg daily, in divided does every 4 hours.
Route of Administration: Oral
In Vitro Use Guide
Inosine pranobex has been shown to stimulate various indices of metabolic activity of macrophages and monocytes. In vitro exposure to inosine pranobex or to 24-hour supernatants obtained from mononuclear cells pretreated with the drug restored chemotaxis to normal or near normal levels. Incubation with inosine pranobex in vitro stimulated the production of interleukin-l (lymphocyte activating factor) in human monocytes.
Name Type Language
INOSINE PRANOBEX
JAN   MART.   MI   WHO-DD  
Common Name English
INOSINE PRANOBEX [JAN]
Common Name English
IMUNOVIR
Brand Name English
INOSINE ACEDOBENE DIMEPRANOL
Common Name English
AVIRAL
Brand Name English
IAD
Common Name English
INOSINE-2-HYDROXYPROPYLDIMETHYLAMMONIUM 4-ACETAMIDOBENZOATE (1:3)
Common Name English
INOSIPLEX
Common Name English
ISOPRINOSINA
Brand Name English
PRANOSINA
Brand Name English
NP-113
Code English
Inosine pranobex [WHO-DD]
Common Name English
METHISOPRINOL
Common Name English
ISOPRINOSINE
Brand Name English
MODIMMUNAL
Brand Name English
INOSINE PRANOBEX [MI]
Common Name English
ISOVIRAL
Brand Name English
INOSINE PRANOBEX [MART.]
Common Name English
IMUNOVIRAL
Brand Name English
DELIMMUN
Brand Name English
VIRUXAN
Brand Name English
ISOPRINOSIN
Brand Name English
PRANOSINE
Brand Name English
NPT-10381
Code English
Classification Tree Code System Code
WHO-VATC QJ05AX05
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
NCI_THESAURUS C2139
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
FDA ORPHAN DRUG 26888
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
WHO-ATC J05AX05
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
Code System Code Type Description
RXCUI
6048
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY RxNorm
EVMPD
SUB14214MIG
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
MESH
D007542
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
SMS_ID
100000092431
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
DRUG BANK
DB13156
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
PUBCHEM
135449284
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
DRUG CENTRAL
4576
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
CAS
36703-88-5
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
MERCK INDEX
m6289
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
253-162-1
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
FDA UNII
W1SO0V223F
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
NCI_THESAURUS
C601
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
WIKIPEDIA
INOSINE PRANOBEX
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY
EPA CompTox
DTXSID401021342
Created by admin on Fri Dec 15 15:22:31 UTC 2023 , Edited by admin on Fri Dec 15 15:22:31 UTC 2023
PRIMARY