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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1698 | Carvedilol EP IMpurity E | Carvedilol USP E,Carvedilol Impurity E | Others |
Carvedilol EP IMpurity E (Carvedilol USP E) is used as a pharmaceutical intermediate. | |||
T1733 | Ciprofloxacin EP IMpurity A | Q-Acid,Fluoroquinolonic Acid,Ciprofloxacin Impurity A | Antibiotic |
Ciprofloxacin EP IMpurity A (Fluoroquinolonic Acid) is an antibiotic and antimicrobial agent. | |||
T8752 | BAR 501 impurity | GPCR19 | |
BAR501 impurity is an impurity found in the preparation of BAR501 that acts as an agonist of the G protein-coupled bile acid-activated receptor (GP-BAR1). BAR501 impurity (10 μM) induces a 150% increase in luciferase act... | |||
T11007L | Levofloxacin Hydrochloride Impurity A | Levofloxacin Hydrochloride Impurity A(117707-40-1 Free base) | Antibacterial |
Levofloxacin Hydrochloride Impurity A I, one of the quinolones, has a broad spectrum of antibacterial action. | |||
T31204 | Darapladib-impurity | Others | |
Darapladib-impurity is the impurity of Darapladib. Darapladib inhibits lipoprotein-associated phospholipase A2 (Lp-PLA2). | |||
T9042 | Teriflunomide impurity 3 | 4-Amino-N-(4-trifluoromethylphenyl)benzamide | COX |
Teriflunomide impurity 3 (4-Amino-N-(4-trifluoromethylphenyl)benzamide) is a selective COX-1 inhibitor(IC50 of 30 μM). It is less active against COX-2 (IC50>100 μM). | |||
T12962 | Sofosbuvir impurity G | HCV Protease | |
Sofosbuvir impurity G is a diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity. | |||
T0667 | Flecainide Impurity D | Others | |
Flecainide Impurity D is used as an intermediate in industry. | |||
T1690 | BroMhexine IMpurity B | Others | |
Bromhexine Impurity B reagent used in the preparation of Ambroxol and Bromhexine (B678600) metabolites Ambroxol EP Impurity E. | |||
T67853 | Rivaroxaban Impurity | Rivaroxaban-10 | Factor Xa |
Rivaroxaban Impurity (Rivaroxaban-10) is a potent Blood-coagulation factor Xa inhibitor, IC50= 66 nM. | |||
T0550 | Domperidone EP Impurity A | Others | |
Domperidone EP Impurity A is used as pharmaceutical intermediates. | |||
T1357 | TriMetazidine EP IMpurity-D | Others | |
TriMetazidine EP Impurity-D is the starting material for the synthesis of TriMetazidine and an intermediate for the synthesis of various compounds. | |||
T3097 | Mycophenolic Acid Impurity | 5,7-dihydroxy-4-methylphthalide | Others |
Mycophenolic Acid Impurity (5,7-dihydroxy-4-methylphthalide) is an an immunosuppresant drug and potent anti-proliferative, and can be used in place of the older anti-proliferative azathioprine. It is usually used as part... | |||
T4196 | Betahistine EP Impurity C | NSC19005 | Others , Histamine Receptor |
Betahistine EP Impurity C (NSC19005) is structurally related to Betahistine. Betahistine EP Impurity C is a dimer of Betahistine. | |||
T1689 | Enalapril IMpurity B | (+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine | Others |
Enalapril IMpurity B ((+)-N-[1-(S)-Ethoxycarbonxyl-3-phenylpropyl]-L-alanine) is Moexipril intermediate and is the main metabolite of Imidapril. | |||
T12961 | Sofosbuvir impurity F | Sofosbuvir 3',5'-Bis-(S)-phosphate | HCV Protease |
Sofosbuvir impurity F (Sofosbuvir 3',5'-Bis-(S)-phosphate) is both a diastereomer of Sofosbuvir and an impurity of Sofosbuvir which is an inhibitor of HCV RNA replication. | |||
T9084 | Cetirizine Impurity B dihydrochloride | De(carboxymethoxy) Cetirizine Acetic Acid Dihydrochloride | Histamine Receptor |
Cetirizine Impurity B dihydrochloride (De(carboxymethoxy) Cetirizine Acetic Acid Dihydrochloride) is an impurity of Cetirizine dihydrochloride. Cetirizine is a second-generation antihistamine. Cetirizine is a specific, o... | |||
T32550 | Lamivudine impurity A RS | Lamivudine impurity A,Lamivudine specified impurity A | |
Lamivudine impurity A RS is a bioactive chemical. | |||
T21113 | N2-Acetylaciclovir | Aciclovir EP Impurity F | Antibacterial |
N2-Acetylaciclovir (Aciclovir EP Impurity F) is a derivative of the antiviral compound Aciclovir, which has selective T-cell immunotoxicity. | |||
T39031 | Olmesartan impurity | ||
Olmesartan impurity, a compound related to Olmesartan, is an angiotensin II receptor (AT1R) antagonist utilized in the study of high blood pressure. Olmesartan (RNH-6270) is the parent compound with similar properties an... |