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Inosinic acid

CAT: 0804-HY-108213-01Size: 25 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-108213-01Size:25 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Inosinic acid is an endogenous metabolite. Inosinic acid is used as umami tastant, or as the dietary supplement to improve the yield and meat quality of pigs[1].
CAS Number
131-99-7
Product Name Alternative
5'-IMP; IMP; Inosine 5'- (dihydrogen phosphate)
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
Endogenous Metabolite
Type
Natural Products
Related Pathways
Metabolic Enzyme/Protease
Applications
Metabolism-sugar/lipid metabolism
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/Inosinic_acid.html
Purity
99.93
Solubility
H2O : 116.67 mg/mL (ultrasonic)
Smiles
O=P(O)(O)OC[C@@H]1[C@@H](O)[C@@H](O)[C@H](N2C3=C(C(N=CN3)=O)N=C2)O1
Molecular Formula
C10H13N4O8P
Molecular Weight
348.21
Precautions
H302, H315, H319, H335
References & Citations
[1]Bonagurio LP, et al., Effects of different levels of inosine-5'-monophosphate (5'-IMP) supplementation on the growth performance and meat quality of finishing pigs (75 to 100 kg) . Meat Sci. 2023 Feb;196:109016.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C, 3 years (Powder)
Scientific Category
Natural Products
Clinical Information
Phase 2
Isoform
Human Endogenous Metabolite; Microbial Metabolite
Citation 01
Nature. 2025 Jul;643 (8070) :192-200.|SSRN. 2025 Sep 8.|Talanta. 2024 Jan 15:267:125171.|Mol Ther Oncolytics. 2021 Aug 28:23:107-123.

Chemical Information

Inosinic Acid

IMP is a purine ribonucleoside 5'-monophosphate having hypoxanthine as the nucleobase. It has a role as a mouse metabolite, an Escherichia coli metabolite and a human metabolite. It is an inosine phosphate and a purine ribonucleoside 5'-monophosphate. It is a conjugate acid of an IMP(2-).

CAS Number131-99-7
PubChem CID135398640
IUPAC Name[(2R,3S,4R,5R)-3,4-dihydroxy-5-(6-oxo-1H-purin-9-yl)oxolan-2-yl]methyl dihydrogen phosphate
Molecular FormulaC10H13N4O8P
Molecular Weight348.21
XLogP-3
Topological Polar Surface Area176
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count10
Rotatable Bond Count4
Heavy Atom Count23
Formal Charge0
Complexity555
SMILES
C1=NC2=C(C(=O)N1)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O
InChI
InChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
GRSZFWQUAKGDAV-KQYNXXCUSA-N
Chemical Structure
2D Structure
2D structure of Inosinic Acid
CAS: 131-99-7
CID: 135398640
Formula: C10H13N4O8P
MW: 348.21
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight348.21
XLogP3-3
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count10
Rotatable Bond Count4
Exact Mass348.04710038
Monoisotopic Mass348.04710038
Topological Polar Surface Area176 Ų
Heavy Atom Count23
Formal Charge0
Complexity555
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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