| Weight | 348.208 g/mol |
|---|---|
| Formula | C10H13N4O8P |
| Hydrogen Acceptors | 9 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
Inosinic acid (131-99-7, 30918-54-8)
IMP · Inosine Monophosphate · Inosinic Acids
Score:
#1069 in Biochemistry
,
#2766 in Biology
,
#3470 in Chemistry
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- Magnetic loop behind an interplanetary shock: Voyager, Helios, and IMP 8 observations (Journal of Geophysical Research, 1981)
- Quantifying Local Cerebral Blood Flow by N-Isopropyl-p-[123I]Iodoamphetamine (IMP) Tomography (The Journal of Nuclear Medicine, 1982)
- Initial results of the imp 1 magnetic field experiment (Journal of Geophysical Research, 1964)
- Structure and Mechanism of Inosine Monophosphate Dehydrogenase in Complex with the Immunosuppressant Mycophenolic Acid (Cell, 1996)
- Characterization of human type I and type II IMP dehydrogenases. (Journal of Biological Chemistry, 1993)
- IMP dehydrogenase, an enzyme linked with proliferation and malignancy (Nature, 1975)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - IMP
- Inosine Monophosphate
- Inosinic Acids
- Sodium Inosinate
- Ribosylhypoxanthine Monophosphate
-
SMILESC1=NC(=O)C2=C(N1)N(C=N2)C3C(C(C(O3)COP(=O)(O)O)O)O
-
InChIKeyGRSZFWQUAKGDAV-UHFFFAOYSA-N
- Pubchem - Inosinic acid
- Wikipedia - inosinic acid
Inosinic acid or inosine monophosphate (IMP) is a nucleoside monophosphate. Widely used as a flavor enhancer, it is typically obtained from chicken byproducts or other meat industry waste. Inosinic acid is important in metabolism.
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