MedChem Express

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MedChemExpress has an experienced team of custom synthesis chemists, led by an impressive group of Ph.D.'s. With this team, we have the capability of supporting all kinds of chemistry projects of multiple step syntheses of complex labeled molecules, including metabolites and steroids. Following scientific and technological innovation, challenging traditional thinking, MedChemExpress has always been committed to develop quality products that exceed international standards on cost and reliability, to create the most advanced synthetic route. With high experiences in preparing a large numbers of different biologically active molecules, we provide rapid synthesis of new products. That is why we can consistently deliver your custom synthesis compounds faster than any other company.

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ADT-007 | MedChemExpress (MCE) 5 mg  | ≥98.0%

MedChem Express

ADT-007 is a potent and orally active pan-RAS inhibitor with strong anticancer effects. ADT-007 binds RAS in a nucleotide-free conformation to block GTP activation. ADT-007 potently and selectively inhibits the growth of cancer cells with mutated or hyper-activated wild-type RAS isozymes[1].

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ADT-007 | MedChemExpress (MCE) 10 mg  | ≥98.0%

MedChem Express

ADT-007 is a potent and orally active pan-RAS inhibitor with strong anticancer effects. ADT-007 binds RAS in a nucleotide-free conformation to block GTP activation. ADT-007 potently and selectively inhibits the growth of cancer cells with mutated or hyper-activated wild-type RAS isozymes[1].

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ADT-007 | MedChemExpress (MCE) 25 mg  | ≥98.0%

MedChem Express

ADT-007 is a potent and orally active pan-RAS inhibitor with strong anticancer effects. ADT-007 binds RAS in a nucleotide-free conformation to block GTP activation. ADT-007 potently and selectively inhibits the growth of cancer cells with mutated or hyper-activated wild-type RAS isozymes[1].

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ADT-007 | MedChemExpress (MCE) 50 mg  | ≥98.0%

MedChem Express

ADT-007 is a potent and orally active pan-RAS inhibitor with strong anticancer effects. ADT-007 binds RAS in a nucleotide-free conformation to block GTP activation. ADT-007 potently and selectively inhibits the growth of cancer cells with mutated or hyper-activated wild-type RAS isozymes[1].

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AE-ITU dihydrobromide | MedChemExpress (MCE) 100 mg  | ≥98.0%

MedChem Express

AE-ITU dihydrobromide is the dihydrobromide form of AE-ITU. AE-ITU dihydrobromide is a selective inhibitor for inducible NO synthase (iNOS), and attenuates the liver dysfunction caused by endotoxaemia in rats[1].

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Aerothionin | MedChemExpress (MCE) 1 mg  | ≥98.0%

MedChem Express

Aerothionin is an antibiotic with potent antimicrobial efficacy against bacteria and fungi. Aerothionin exhibits antitumor efficacy against adrenal pheochromocytomas and extra-adrenal paragangliomas (PPGLs)[1][2].

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AF 594 azide triethylamine | MedChemExpress (MCE) 1 mg  | ≥98.0%

MedChem Express

AF 594 azide (triethylamine) is an azide derivative of the red fluorescent dye AF 594, which has high fluorescence quantum yield and high photostability (maximum absorption wavelength of 586 nm, maximum emission wavelength of 613 nm). AF 594 azide (triethylamine) forms stable adducts by reaction of the azide group with alkynyl derivatives (terminal alkynes and […]

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AF 594 azide triethylamine | MedChemExpress (MCE) 5 mg  | ≥98.0%

MedChem Express

AF 594 azide (triethylamine) is an azide derivative of the red fluorescent dye AF 594, which has high fluorescence quantum yield and high photostability (maximum absorption wavelength of 586 nm, maximum emission wavelength of 613 nm). AF 594 azide (triethylamine) forms stable adducts by reaction of the azide group with alkynyl derivatives (terminal alkynes and […]

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AF 594 azide triethylamine | MedChemExpress (MCE) 10 mg  | ≥98.0%

MedChem Express

AF 594 azide (triethylamine) is an azide derivative of the red fluorescent dye AF 594, which has high fluorescence quantum yield and high photostability (maximum absorption wavelength of 586 nm, maximum emission wavelength of 613 nm). AF 594 azide (triethylamine) forms stable adducts by reaction of the azide group with alkynyl derivatives (terminal alkynes and […]

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AF299 | MedChemExpress (MCE) 1 mg  | ≥98.0%

MedChem Express

AF299 can reduce collagen-related peptide-induced platelet Ca2+ rises and collagen-induced platelet aggregation. AF299 can be used for research of antiplatelet research[1].

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AF488 NHS ester diTEA | MedChemExpress (MCE) 1 mg  | ≥98.0%

MedChem Express

AF488 NHS ester diTEA is a multifunctional dye. Dyes are important tools in biological experiments. They can help researchers observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology and monitor microorganisms. Their applications range from basic scientific research to clinical A wide range of diagnostics. Dyes […]

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Aflatoxin B1/BSA | MedChemExpress (MCE) 1 mg  | ≥98.0%

MedChem Express

Aflatoxin B1/BSA is one of protein/peptide and small molecule drug conjugates (PDCs), consisting of Aflatoxin B1 (HY-N6615) and BSA. PCDs are promising targeted therapeutics with better cell permeability and drug selectivity than antibody-drug conjugates (ADCs). PDCs have been widely used in research on cancer, COVID-19, and metabolic diseases[1].

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Aflatoxin B1/KLH | MedChemExpress (MCE) 1 mg  | ≥98.0%

MedChem Express

Aflatoxin B1/KLH is one of protein/peptide and small molecule drug conjugates (PDCs), consisting of Aflatoxin B1 (HY-N6615) and KLH. PCDs are promising targeted therapeutics with better cell permeability and drug selectivity than antibody-drug conjugates (ADCs). PDCs have been widely used in research on cancer, COVID-19, and metabolic diseases[1].

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AG-041R | MedChemExpress (MCE) 1 mg  | ≥98.0%

MedChem Express

AG-041R is a potent and selective CCK2 Receptor/Gastrin antagonist. AG-041R inhibits gastrin-evoked secretion of pancreastatin with an IC50 of 2.2 nM. AG-041R inhibits cell growth of Mastomys ECL carcinoid tumor cells[1][2].

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