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Antiviral API
- Arenavirus
- Cytomegalovirus (CMV)
- Dengue virus
- Endogenous Metabolite
- Enterovirus (EV)
- Epstein-Barr virus (EBV)
- Filovirus
- Flavivirus
- HCV Protease
- Hepatitis B Virus (HBV)
- Hepatitis C Virus (HCV)
- Herpes simplex Virus (HSV)
- HIF/HIF Prolyl-Hydroxylase
- HIV Integrase
- HIV Protease
- Human immunodeficiency Virus (HIV)
- Human papillomavirus (HPV)
- Influenza Virus
- Nipah virus
- Orthopoxvirus
- Others
- Rabies virus (RABV)
- Respiratory syncytial Virus (RSV)
- Reverse Transcriptases (RTs)
- SARS-CoV
- Tobacco mosaic virus (TMV)
- Vesicular stomatitis virus (VSV)
- Virus Protease
- West Nile virus
- Antiviral intermediates
Diclofenac EP Impurity E
Category | Human immunodeficiency Virus (HIV) |
CAS | 59-48-3 |
Description | Diclofenac EP Impurity E is an impurity of Diclofenac, which is a non-selective COX inhibitor used as a non-steroidal anti-inflammatory drug (NSAID). |
Product Information
Synonyms | Diclofenac sodium EP impurity E; Diclofenac potassium EP impurity E; 1,3-dihydro-2H-indol-2-one; 2H-Indol-2-one, 1,3-dihydro-; 1,3-Dihydro-2H-indol-2-one; 2-Indolinone; Oxindole; 2,3-Dihydro-1H-indol-2-one; 2-Indolone; 2-Oxindole; 2-Oxo-2,3-dihydroindole; 2-Oxoindole; 2-Oxoindoline; Indol-2(3H)-one; Indoline-2-one; NSC 274863; Oxindol |
IUPAC Name | 1,3-dihydroindol-2-one |
Molecular Weight | 133.15 |
Molecular Formula | C8H7NO |
Canonical SMILES | C1C2=CC=CC=C2NC1=O |
InChI | InChI=1S/C8H7NO/c10-8-5-6-3-1-2-4-7(6)9-8/h1-4H,5H2,(H,9,10) |
InChIKey | JYGFTBXVXVMTGB-UHFFFAOYSA-N |
Boiling Point | 227°C |
Melting Point | 128°C |
Flash Point | 190.0±18.0 °C |
Purity | ≥95% |
Density | 1.198±0.06 g/cm3 |
Solubility | Soluble in Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) |
Appearance | Light Brown to Brown Solid |
Storage | Store at 2-8°C for short term (days to weeks) or -20°C for long term (months to years) |
Complexity | 155 |
Exact Mass | 133.052763847 |
Index Of Refraction | 1.640 |
In Vitro | Oxindole (Indolin-2-one) is a bicyclic structure consisting of a benzene ring fused to 2-pyrrolidone. Substituted indolinones can be referred as 'privileged structures' owing to their excellent binding affinity for many receptors and to the number of approved drugs containing this scaffold. Oxindole has been found in tissues and fluids of mammals as well as natural products produced by a range of plants, bacteria and invertebrates. 2-indolinone derivatives possess diverse range of pharmacological activities including anti-cancer, anti-HIV, anti-diabetic, antibacterial, antioxidant, kinase inhibitory, AChE inhibitory, anti-leishmanial, b3 adrenergic receptor agonistic, phosphatase inhibitory, analgesic, spermicidal, vasopressin antagonists, progesterone antagonists, neuroprotection, NMDA blocker and sleep inducing activities. |
PSA | 29.10000 |
Target | HIV |
Vapor Pressure | 0.0±0.7 mmHg at 25°C |
XLogP3-AA | 1.2 |