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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 (4595)
Related Products (4595)
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m-Tolylacetic acid (Standard)
0 ImagesSynonyms: 3-Methylbenzeneacetic acid (Standard)m-Tolylacetic acid (3-Methylbenzeneacetic acid) (Standard) is the analytical standard of m-Tolylacetic acid (HY-W053507). This product is intended for research and analytical applications. m-Tolylacetic acid is a hydroaromatic dicarboxylic acids excreted in the urine as metabolite of tolueneacetic acid. m-Tolylacetic acid can be used for drug intermediate for synthesising more complex molecules. -
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POLRMT-IN-3
0 ImagesCat. No.: HY-181071POLRMT-IN-3 is a photosensitive inhibitor of mitochondrial RNA polymerase (POLRMT). POLRMT-IN-3 is biologically inactive in the dark but rapidly releases the active parent compound LJ03 upon illumination with 405 nm light, enabling spatiotemporally precise inhibition of POLRMT. POLRMT-IN-3 exhibits antitumor activity and can be used in research on tumors such as pancreatic cancer and ovarian cancer. -
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Cyclosporin impurity 2
0 ImagesCat. No.: HY-W793067CAS No.: 138957-23-0Synonyms: Acetoxy cyclosporin A acetateCyclosporin impurity 2 (Acetoxy cyclosporin A acetate) is an impurity of Cyclosporin. -
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XL388-C2-amide-PEG9-NH2 TFA
0 ImagesCat. No.: HY-139085BXL388-C2-amide-PEG9-NH2 TFA is an intermediate used in the synthesis of C26-linked Rapamycin analog. -
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7-Aminodeacetoxycephalosporanic acid (Standard)
0 ImagesCat. No.: HY-W014217RCAS No.: 22252-43-3Synonyms: 7-ADCA (Standard)7-Aminodeacetoxycephalosporanic acid (Standard) is the analytical standard of 7-Aminodeacetoxycephalosporanic acid. This product is intended for research and analytical applications. 7-Aminodeacetoxycephalosporanic acid (7-ADCA) is a key intermediate in the synthesis of cephalosporins. -
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GA44
0 ImagesCat. No.: HY-W746957CAS No.: 36434-15-8GA44 is a C20-gibberellin and is an intermediate in the early 13-hydroxylation pathway. -
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BMS-135-L-Lys dihydrochloride
0 ImagesCat. No.: HY-184414BBMS-135-L-Lys dihydrochloride is a dual-cation prodrug derived from CK2 inhibitor BMS-135 (HY-181022) through esterification with L-lysine using a secondary alcohol. BMS-135-L-Lys dihydrochloride achieves enhanced solubility by maintaining protonation of the ε-amino group of the Lys side chain at intestinal pH. BMS-135-L-Lys dihydrochloride is released in situ by intestinal wall esterase from the parent drug, significantly increasing the oral bioavailability of the parent drug and overcoming the non-linear pharmacokinetic problem when the dose of the parent drug is increased. BMS-135-L-Lys dihydrochloride can be used in related research on colon cancer and lung cancer. -
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- Tropinone (Standard)
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3,4,5-Trimethoxybenzoic acid-d3
0 ImagesCat. No.: HY-Y0084SCAS No.: 84759-05-7Synonyms: Eudesmic acid-d3; Trimethylgallic acid-d33,4,5-Trimethoxybenzoic acid-d3 is the deuterium labeled 3,4,5-Trimethoxybenzoic acid[1]. 3,4,5-Trimethoxybenzoic acid (Eudesmic acid;Trimethylgallic Acid) is a benzoic acid derivative. A building block in medicine and organic synthesis. 3,4,5-Trimethoxybenzoic acid exhibits antibacterial activity against S. aureus with MIC of 0.97 μg/mL. -
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Acorbine
0 ImagesCat. No.: HY-P12115CAS No.: 860314-33-6Acorbine is an orally active, hepatoprotective tripeptide present in the brackish-water bivalve Corbicula japonica. Hydrolysis of Acorbine yields free β-alanine and ornithine, which mediate the host defense system of Corbicula japonica in response to biological stress and changes in growth conditions. Acorbine inhibits ethanol-induced hepatocyte death and liver injury. Acorbine can be used in studies related to liver diseases. -
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PNU 101850
0 ImagesCat. No.: HY-105373CAS No.: 852336-59-5PNU 101850 is an Eperezolid (HY-10393) ester prodrug. PNU 101850 acquires antibacterial activity after conversion to the parent drug Eperezolid. -
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DL-Cystathionine dihydrochloride
0 ImagesCat. No.: HY-W009749BDL-Cystathionine dihydrochloride is a mixture of 4 isomers of cystathionine and allocystathionine. DL-Cystathionine dihydrochloride also is an intermediate in the biosynthesis of amino acid cysteine. DL-Cystathionine dihydrochloride serves as a standard for quantifying tissue cystathionine. -
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- 6-Methoxytryptamine
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Scrophuloside A
0 ImagesCat. No.: HY-N19942CAS No.: 886061-50-3Scrophuloside A is a phenylpropanoid glycoside identified from the rhizome of Neopicrorhiza scrophulariiflora. Scrophuloside A induces cytotoxicity in leukemia cells with a IC50 of 0.58 μg/mL. Scrophuloside A is applicable to leukemia-related research. -
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H-Pro-His-OH
0 ImagesCat. No.: HY-W716776CAS No.: 92027-43-5H-Pro-His-OH is a commonly used amino acid building block in biochemistry and peptide synthesis. -
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GalNA-PEG6-azido
0 ImagesCat. No.: HY-184771CAS No.: 2766875-91-4GalNA-PEG6-azido (P192 Compound 11) is a compound derived from N-acetylgalactosamine, bearing a PEG6 linker arm and an azido group, and serves as a drug linker. -
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Fumiquinazoline A
0 ImagesCat. No.: HY-N19916CAS No.: 140715-85-1Fumiquinazoline A is a peptidyl quinazolinone indole alkaloid isolated from Aspergillus fumigatus, with antifungal activity. Fumiquinazoline A serves as a substrate for the flavoenzyme Af12070 and FAD-dependent amide oxidase Af12070, which oxidizes it into the seven-membered spiroaminal Fumiquinazoline C. Fumiquinazoline A is applicable to studies related to fungal infections. -
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Cyclopropylmethyl bromide-d3
0 ImagesCat. No.: HY-Y1100S1CAS No.: 1219799-17-3Cyclopropylmethyl bromide-d3 is the deuterium labeled Cyclopropylmethyl bromide (HY-Y1100). Cyclopropylmethyl bromide is an intermediate. Cyclopropylmethyl bromide can be used in the preparation of Firocoxib (HY-14670). Firocoxib (ML 1785713) is a potent, selective, orally active COX-2 inhibitor. -
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D-Lyxose-13C-2
0 ImagesCat. No.: HY-128753S3CAS No.: 70849-22-8D-Lyxose-13C-2 is the 13C labeled D-Lyxose. D-Lyxose is an endogenous metabolite. D-Lyxose is a rare pentose sugar with significant potential for drug synthesis. D-Lyxose can be used as a starting material for anti-tumor drugs such as alpha galactose ceramide immunostimulants. D-Lyxose can be used as a precursor for L-nucleoside analogs for the development of antiviral drugs. D-Lyxose can be used as a synthetic intermediate for other rare sugars such as L-ribose. -
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Licoagrocarpin
0 ImagesCat. No.: HY-186188CAS No.: 202815-29-0 -
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