L-Alanine, N-[(S)-(4-nitrophenoxy)phenoxyphosphinyl]-, 2-ethylbutyl ester (IMP 4)

Product Name L-Alanine, N-[(S)-(4-nitrophenoxy)phenoxyphosphinyl]-, 2-ethylbutyl ester (IMP 4)
Alternate Names Remdesivir Impurities, Impurities of Remdesivir
CAT No. CS-P-08454
CAS No. 1354823-36-1
Category Impurities
Stock IN-Stock
Mol. Wt. 450.43 g/mol
Mol. For. C21H27N2O7P
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Remdesivir
Smileys C[C@@H](C(OCC(CC)CC)=O)N[P@](OC1=CC=CC=C1)(OC2=CC=C([N+]([O-])=O)C=C2)=O
Canonical Smiles CCC(CC)COC(=O)C(C)NP(=O)(OC1=CC=CC=C1)OC2=CC=C(C=C2)[N+](=O)[O-]
InchIKey CSURKLFFMMBEFL-UHFFFAOYSA-N
Inchl InChI=1S/C21H27N2O7P/c1-4-17(5-2)15-28-21(24)16(3)22-31(27,29-19-9-7-6-8-10-19)30-20-13-11-18(12-14-20)23(25)26/h6-14,16-17H,4-5,15H2,1-3H3,(H,22,27)
IUPAC 2-ethylbutyl 2-[[(4-nitrophenoxy)-phenoxyphosphoryl]amino]propanoate
Controlled No
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L-Alanine, N-[(S)-(4-nitrophenoxy)phenoxyphosphinyl]-, 2-ethylbutyl ester, commonly known as IMP 4, is a chemical compound that is used in various pharmaceutical and biotechnological applications. It is a phosphoramidate prodrug of L-alanine, which means that it is a derivative of L-alanine that is designed to enhance its pharmacological properties. IMP 4 is known to exhibit antiviral and anticancer activities, making it a promising drug candidate for the treatment of viral infections and cancer. It works by inhibiting the replication of viruses and inducing apoptosis in cancer cells. It has been shown to be effective against a wide range of viruses, including HIV, hepatitis B and C, and herpes simplex virus. As a chemical compound, IMP 4 has a molecular formula of C24H32N2O8P and a molecular weight of 510.5 g/mol. It is a white to off-white crystalline powder that is sparingly soluble in water but soluble in organic solvents such as ethanol and methanol. Its chemical structure consists of a phosphoramidate group, two phenoxy groups, and an ethylbutyl ester group. In conclusion, IMP 4 is a valuable compound in the field of pharmaceuticals and biotechnology due to its antiviral and anticancer activities. Its unique chemical structure and properties make it a promising drug candidate for the treatment of various diseases.

Related Compounds

Remdesivir Impurity 18 | Remdesivir Impurity 41 | D-Alanine, N-[(S)-(4-nitrophenoxy)phenoxyphosphinyl]-, 2-ethylbutyl ester (IMP 6) | NSJ-Remdesivir-RS009 | Remdesivir Desphenyl Acid Impurity | Remdesivir Impurity 8 | Remdesivir Bis Phosphoryl impurity | NSJ-Remdesivir-RS012 | GS-773095 | L-Alanine, N-(chlorophenoxyphosphinyl)-, 2-ethylbutyl ester (IMP 7) | Remdesivir Impurity 2 | Remdesivir Impurity 14 | Remdesivir impurity-18 Triethylamine salt | Remdesivir Impurity 15 | Remdesivir Impurity 10 | Remdesivir Impurity 43 | NSJ-Remdesivir-RS005 | L-Alanine, N-[(R)-(4-nitrophenoxy)phenoxyphosphinyl]-, 2-ethylbutyl ester (IMP 5) | Remdesivir Nucleoside Monophosphate Ammonium salt | Remdesivir Impurity C | Remdesivir Impurity 11 | Remdesivir Impurity 1 | Remdesivir Phosphate Impurity | Remdesivir Impurity 16 | Remdesivir Desphenyl Impurity | Remdesivir Impurity 17 | Remdesivir Impurity 3 | Remdesivir Impurity 12 | Remdesivir R-P-D Alanine Isomer | Remdesivir R-P isomer and S-isomer at CN | NSJ-Remdesivir-RS004 | Remdesivir Impurity 13 | Remdesivir N-oxide | Remdesivir Impurity 9 | Remdesivir Impurity 16 |

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