Basic Description

Synonyms	Isoprinosine \| INOSINE PRANOBEX \| 36703-88-5 \| Inosiplex \| Delimmun \| Methisoprinol \| Imunovir \| Isoviral \| Viruxan \| Isoprinosin \| Isoprinosina \| Aviral \| Inosine Acedobene Dimepranol \| Imunoviral \| Modimmunal \| Immunovir \| Pranosina \| Pranosine \| NP 113 \| NPT-10381 \| W1SO0V223F \| NP-113 \| Inosine
Specifications & Purity	10mM in DMSO
Storage Temp	Store at -80°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Nucleosides, nucleotides, and analogues
  - Class Purine nucleosides

Kingdom	Organic compounds
Superclass	Nucleosides, nucleotides, and analogues
Class	Purine nucleosides
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Purine nucleosides
Alternative Parents	Glycosylamines 6-oxopurines Pentoses Hypoxanthines Benzoic acids Benzoyl derivatives Pyrimidones N-substituted imidazoles Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Trialkylamines Secondary alcohols 1,2-aminoalcohols Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Oxacyclic compounds Carboximidic acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Primary alcohols Hydrocarbon derivatives
Molecular Framework	Not available
Substituents	Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Pentose monosaccharide - Purinone - Hypoxanthine - Imidazopyrimidine - Benzoic acid or derivatives - Purine - Benzoic acid - Benzoyl - Pyrimidone - Benzenoid - Pyrimidine - N-substituted imidazole - Monocyclic benzene moiety - Monosaccharide - Tetrahydrofuran - Heteroaromatic compound - Imidazole - Azole - Vinylogous amide - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-aminoalcohol - Oxacycle - Azacycle - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid derivative - Carboxylic acid - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Alcohol - Amine - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Primary alcohol - Organooxygen compound - Organic oxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	4-acetamidobenzoic acid;9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one;1-(dimethylamino)propan-2-ol
INCHI	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;31-6(11)10-8-4-2-7(3-5-8)9(12)13;31-5(7)4-6(2)3/h2-4,6-7,10,15-17H,1H2,(H,11,12,18);32-5H,1H3,(H,10,11)(H,12,13);35,7H,4H2,1-3H3/t4-,6-,7-,10-;;;;;;/m1....../s1
InChIKey	YLDCUKJMEKGGFI-QCSRICIXSA-N
Smiles	CC(CN(C)C)O.CC(CN(C)C)O.CC(CN(C)C)O.CC(=O)NC1=CC=C(C=C1)C(=O)O.CC(=O)NC1=CC=C(C=C1)C(=O)O.CC(=O)NC1=CC=C(C=C1)C(=O)O.C1=NC2=C(C(=O)N1)N=CN2C3C(C(C(O3)CO)O)O
Isomeric SMILES	CC(CN(C)C)O.CC(CN(C)C)O.CC(CN(C)C)O.CC(=O)NC1=CC=C(C=C1)C(=O)O.CC(=O)NC1=CC=C(C=C1)C(=O)O.CC(=O)NC1=CC=C(C=C1)C(=O)O.C1=NC2=C(C(=O)N1)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O
PubChem CID	135449284
Molecular Weight	1115.25

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Chemical and Physical Properties

Sensitivity	Hygroscopic
Specific Rotation[α]	-11° (C=1,H2O)
Molecular Weight	1115.200 g/mol
XLogP3
Hydrogen Bond Donor Count	13
Hydrogen Bond Acceptor Count	22
Rotatable Bond Count	14
Exact Mass	1114.55 Da
Monoisotopic Mass	1114.55 Da
Topological Polar Surface Area	399.000 Å²
Heavy Atom Count	79
Formal Charge	0
Complexity	658.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	4
Undefined Atom Stereocenter Count	3
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	7

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Song Zhu, Jian Li, Ai-Guo Huang, Ji-Qiu Huang, Yong-Quan Huang, Gao-Xue Wang. (2019) Anti-betanodavirus activity of isoprinosine and improved efficacy using carbon nanotubes based drug delivery system. AQUACULTURE, 512 (734377).

Solution Calculators

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Inosine Pranobex - 10mM in DMSO, high purity , CAS No.36703-88-5