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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 Related Products (4714)
Related Products (4714)
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(1R,2S)-1-tert-Butoxycarbonylamino-2-vinylcyclopropanecarboxylic acid
0 Images(1R,2S)-1-tert-Butoxycarbonylamino-2-vinylcyclopropanecarboxylic acid is a drug intermediate for synthesis of various active compounds. -
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Methyl 3-((tert-butoxycarbonyl)amino)-5-iodothiophene-2-carboxylate
0 ImagesMethyl 3-((tert-butoxycarbonyl)amino)-5-iodothiophene-2-carboxylate is a drug intermediate for synthesis of various active compounds. -
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4-Hydroxy-N,N,2-trimethyl-1H-benzimidazole-6-carboxamide
0 Images4-Hydroxy-N,N,2-trimethyl-1H-benzimidazole-6-carboxamide is a drug intermediate for synthesis of various active compounds. -
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Methyl 2-bromo-4-fluorobenzo[d]thiazole-6-carboxylate
0 ImagesMethyl 2-bromo-4-fluorobenzo[d]thiazole-6-carboxylate is a drug intermediate for synthesis of various active compounds. -
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4-Hydroxy-3-methoxy-5-nitrobenzoic acid
0 ImagesSynonyms: 3-Nitro-4-hydroxy-5-methoxybenzoic acid; 5-Nitrovanillic acid; 3-Methoxy-4-hydroxy-5-nitrobenzoic acid4-Hydroxy-3-methoxy-5-nitrobenzoic acid (3-Nitro-4-hydroxy-5-methoxybenzoic acid) is a drug intermediate for synthesis of various active compounds. -
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((3aR,4R,6R,6aR)-6-((E)-4-(Hydroxyimino)-2-oxo-3,4-dihydropyrimidin-1(2H)-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl isobutyrate
0 ImagesSynonyms: Uridine,2',3'-o-(1-methylethylidene)-,4-oxidechemicalbook,5'-(2-methylpropanoate)((3aR,4R,6R,6aR)-6-((E)-4-(Hydroxyimino)-2-oxo-3,4-dihydropyrimidin-1(2H)-yl)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methyl isobutyrate (Uridine,2',3'-o-(1-methylethylidene)-,4-oxidechemicalbook,5'-(2-methylpropanoate)) is a drug intermediate for synthesis of various active compounds. -
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5-Methyl-2-(pyrimidin-2-yl)benzoicacid
0 Images5-Methyl-2-(pyrimidin-2-yl)benzoicacid is a drug intermediate for synthesis of various active compounds. -
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1-(4-Chloro-2-hydroxyphenyl)ethan-1-one
0 Images1-(4-Chloro-2-hydroxyphenyl)ethan-1-one is a drug intermediate for synthesis of various active compounds. -
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2-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxaldehyde
0 ImagesCat. No.: HY-42451CAS No.: 1211443-55-82-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxaldehyde is a drug intermediate for synthesis of various active compounds. -
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1,4-Cyclohexanedione
0 Images1,4-Cyclohexanedione is a drug intermediate. 1,4-Cyclohexanedione is an accepted substrate of EryKR1 domain which takes on a certain biocatalyst activity and stereospecificity. -
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5-(Piperazin-1-yl)isoquinoline hydrochloride
0 Images5-(Piperazin-1-yl)isoquinoline hydrochloride is a drug intermediate for synthesis of various active compounds. -
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Thiosalicylic acid
0 ImagesThiosalicylic acid (2-Mercaptobenzoic acid) is an organosulfur compound bearing both sulfhydryl and carboxyl functional groups. Thiosalicylic acid acts as a desulfurizing agent. Thiosalicylic acid also serves as a ligand to synthesize azosulfonamide derivatives with antibacterial and antifungal activities, as well as their Fe3+, Cu2+ and Hg2+ chelates. -
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6,7-Dimethoxy-2-tetralone
0 Images6,7-Dimethoxy-2-tetralone is a drug intermediate for synthesis of various active compounds. -
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Elsulfavirine
0 ImagesSynonyms: R-1206Elsulfavirine (R-1206) is an orally active human carbonic anhydrase (carbonic anhydrase, CA) inhibitor and an allosteric inhibitor of HIV-1 non-nucleoside reverse transcriptase (NNRT). Elsulfavirine also targets and blocks the interaction between adenylosuccinate lyase (ADSL) and insulin-induced gene proteins INSIG1/2, blocks SREBP-1-mediated de novo lipid synthesis, and inhibits the proliferation of liver cancer cells. The combination of Elsulfavirine and Lenvatinib (HY-10981) produces a synergistic anti-tumor effect. Elsulfavirine is converted into the active metabolite VM1500A in vivo, blocks the DNA polymerase activity of reverse transcriptase, and inhibits HIV-1 replication. Elsulfavirine exhibits a Ki of 1960 nM-52400 nM against human carbonic anhydrase isoforms including I, VII, VI, VA, VB, IX, XIII, XIV. Elsulfavirine is used in studies related to HIV-1 infection and liver cancer. -
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5’-O-(4,4’-Dimethoxytrityl)-2’-O-methyluridine
0 ImagesCat. No.: HY-W025438CAS No.: 103285-22-95’-O-(4,4’-Dimethoxytrityl)-2’-O-methyluridine is a 2'-O-methyluridine derivative bearing a 5'-O-(4,4'-dimethoxytrityl) protecting group.5’-O-(4,4’-Dimethoxytrityl)-2’-O-methyluridine serves as a starting material for synthesis of a conformationally rigid cyclic uridylic acid derivative. -
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N-Methoxy-N-methylacetamide
0 ImagesN-Methoxy-N-methylacetamide can efficiently acetylate polycarbonyl compounds. As an important intermediate, N-Methoxy-N-methylacetamide can be used for the synthesis of other active compounds. -
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7-Bromoisoquinoline
0 Images7-Bromoisoquinoline is a brominated isoquinoline and synthetic precursor that constructs the isoquinoline functional group at the C17 position of target molecules. 7-Bromoisoquinoline serves as a key synthetic intermediate for the synthesis of cortistatin A-derived anti-angiogenic steroidal analogs (e.g., 7-tributylstannyl isoquinoline). 7-Bromoisoquinoline. -
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Olivetolic acid
0 ImagesOlivetolic acid is a biosynthetic precursor of cannabinol acid (CBGA). Olivetolic acid exhibits a modest anticonvulsant effect in a mouse model of Dravet syndrome. Olivetolic acid can be used for the study of convulsion. -
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(R)-Tetrahydropapaverine hydrochloride
0 Images(R)-Tetrahydropapaverine hydrochloride is the isomer of Tetrahydropapaverine hydrochloride (HY-N0137), and can be used as an experimental control. Tetrahydropapaverine hydrochloride is one of the Tetrahydroisoquinolines. Tetrahydropapaverine hydrochloride has neurotoxic effects on dopamine neurons. -
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Cyclohexanecarboxylic acid
0 ImagesCyclohexanecarboxylic acid is a Valproate structural analogue. Cyclohexanecarboxylic acid is an essential intermediate for the aromatization of Shikimic acid (HY-N0130) by mammals. Cyclohexanecarboxylic acid has anticonvulsant action. -
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