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Drug Intermediate
Drug Iintermediate
- [1]. Ma HC, et al. Homochiral Covalent Organic Framework for Catalytic Asymmetric Synthesis of a Drug Intermediate. J Am Chem Soc. 2020 Jul 22;142(29):12574-12578. [Content Brief]
- [2]. Ramachary D B, et al. Development of pharmaceutical drugs, drug intermediates and ingredients by using direct organo‐click reactions[J]. 2008.
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Drug Intermediate Verwandte Produkte (4738)
Verwandte Produkte (4738)
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Sulfiram
0 ImagesSulfiram is a very weak aldehyde dehydrogenase (ALDH) inhibitor, with an IC50 value of 413 μM against Saccharomyces cerevisiae ALDH. As a photochemical precursor, Sulfiram undergoes photoconversion to form Disulfiram (HY-B0240), a potent ALDH inhibitor. Sulfiram inhibits the dimerization of the extracellular domain fragment (amino acid residues 230-624) of amyloid precursor protein (APP), alters the monomer-dimer equilibrium, induces conformational changes in the fragment, and enhances the production of sAPPα via α-cleavage of APP. Sulfiram can be used in research related to scabies and Alzheimer's disease. -
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Quetiapine impurity 15
0 ImagesArt. -Nr.: HY-W801766CAS. Nr.: 329216-69-5Quetiapine impurity 15 is an impurity of Quetiapine. -
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Moxifloxacin impurity 7
0 ImagesArt. -Nr.: HY-Z11757CAS. Nr.: 1179992-99-4Moxifloxacin impurity 7 is an impurity of Moxifloxacin. -
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5-(2-Aminopyridyl)amide oxime
0 Images5-(2-Aminopyridyl)amide oxime is a synthetic intermediate useful for pharmaceutical synthesis. -
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Sildenafil impurity 2
0 ImagesArt. -Nr.: HY-W109161CAS. Nr.: 268204-00-8 -
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Edoxaban impurity 3
0 ImagesArt. -Nr.: HY-W057728CAS. Nr.: 1392745-70-8Edoxaban impurity 3 is an impurity of Edoxaban. -
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Tamsulosin impurity 16
0 ImagesArt. -Nr.: HY-W725631CAS. Nr.: 1027854-97-2Tamsulosin impurity 16 is an impurity of Tamsulosin. -
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Sildenafil impurity 15
0 ImagesArt. -Nr.: HY-W700779CAS. Nr.: 139756-31-3Sildenafil impurity 15 is an impurity of Sildenafil. -
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(3R,5S,E)-3,5-Dihydroxy-7-(4-isopropyl-2-(N-methylmethylsulfonamido)-6-phenylpyrimidin-5-yl)hept-6-enoic acid (Rosuvastatin Impurity)
0 ImagesArt. -Nr.: HY-Z8676CAS. Nr.: 847849-66-5(3R,5S,E)-3,5-Dihydroxy-7-(4-isopropyl-2-(N-methylmethylsulfonamido)-6-phenylpyrimidin-5-yl)hept-6-enoic acid (Rosuvastatin Impurity) is an impurity of (3R,5S,E)-3,5-Dihydroxy-7-(4-isopropyl-2-(N-methylmethylsulfonamido)-6-phenylpyrimidin-5-yl)hept-6-enoic acid (Rosuvastatin). -
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Dabigatran impurity 29
0 ImagesArt. -Nr.: HY-Z1936CAS. Nr.: 1642853-67-5Synonyms: Dabigatran iMpurity F -
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Dabigatran impurity 8
0 ImagesArt. -Nr.: HY-21609CAS. Nr.: 1408238-40-3 -
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Hancockiamide D
0 ImagesArt. -Nr.: HY-N19181CAS. Nr.: 2758265-37-9Hancockiamide D is a phenylpropanoid piperazine alkaloid found in the Australian soil fungus Aspergillus hancockii. Hancockiamide D induces cytotoxic activity in cancer cells and shows no activity in fibroblasts. Hancockiamide D can be used for the research of murine myeloma. -
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Trazodone impurity 9
0 ImagesArt. -Nr.: HY-W749264CAS. Nr.: 2727463-29-6Trazodone impurity 9 is an impurity of Trazodone. -
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Ranitidine impurity 3
0 ImagesArt. -Nr.: HY-Z8388CAS. Nr.: 1331637-48-9Synonyms: Ranitidine impurity JRanitidine impurity 3 (Ranitidine impurity J) is an impurity of Ranitidine. -
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- Cinnarizine impurity 7
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2-(2-Pyridyl)-4-methyl-thiazole-5-carboxylic acid
0 ImagesArt. -Nr.: HY-114756CAS. Nr.: 34418-48-92-(2-Pyridyl)-4-methyl-thiazole-5-carboxylic acid is a synthetic intermediate useful for pharmaceutical synthesis. -
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Ramipril impurity 5
0 ImagesArt. -Nr.: HY-W008300CAS. Nr.: 87269-87-2Ramipril impurity 5 is an impurity of Ramipril. -
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- Clindamycin phosphate impurity 3
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Sertraline impurity 3
0 ImagesArt. -Nr.: HY-W702206CAS. Nr.: 1198084-29-5Sertraline impurity 3 is an impurity of Sertraline. -
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((1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-yl)methyl (N-(2-(2-(((N,N-bis(2-(((4-nitrophenoxy)carbonyl)oxy)ethyl)sulfamoyl)carbamoyl)oxy)ethoxy)ethyl)sulfamoyl)carbamate
0 ImagesArt. -Nr.: HY-402912CAS. Nr.: 1898181-67-3((1R,8S,9s)-Bicyclonon-4-yn-9-yl) methyl (N-(2-(2-(((N,N-bis (2-(((4-nitrophenoxy) carbonyl) oxy) ethyl) sulfamoyl) carbamoyl) oxy) ethoxy) ethyl) sulfamoyl) carbamate is a bifunctional linker component containing a bicyclonon-4-yne click probe and a hydrophilic carbamoyl sulfamide group, which is used for the synthesis of antibody-drug conjugates. -
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