Hydrazines and derivatives
Sigma Aldrich Fine Chemicals Biosciences Mineral oil, 8042-47-5, MFCD00131611, 100 mL
Light oil ((neat)), BioXtra, suitable for mouse embryo cell culture. Mineral oil has been commonly used and recommended for overlaying mouse embryo cultures to prevent drying during the procedure.
Medchemexpress LLC Semicarbazide hydrochloride | 563-41-7 | MFCD00013009 | 98.0% | 111.53 | CH6ClN3O | 100g
Semicarbazide hydrochloride is an orally active urea derivative Semicarbazide hydrochloride binds to copper or iron in cells Semicarbazide hydrochloride inhibits the activity of soluble semicarbazide sensitive amine oxidase (SSAO) Semicarbazide hydrochloride damages cartilage blood vessels ovaries testicles and thyroid follicles[1][2][3][4][5][6][7][8][9]
Medchemexpress LLC Semicarbazide hydrochloride | 563-41-7 | MFCD00013009 | 98.0% | 111.53 g/mol | CH6ClN3O | 10g
Semicarbazide hydrochloride is an orally active urea derivative Semicarbazide hydrochloride binds to copper or iron in cells Semicarbazide hydrochloride inhibits the activity of soluble semicarbazide sensitive amine oxidase (SSAO) Semicarbazide hydrochloride damages cartilage blood vessels ovaries testicles and thyroid follicles[1][2][3][4][5][6][7][8][9]
Medchemexpress LLC Semicarbazide hydrochloride | 563-41-7 | MFCD00013009 | 98.0% | 111.53 g/mol | CH6ClN3O | 1mL
Semicarbazide hydrochloride is an orally active urea derivative Semicarbazide hydrochloride binds to copper or iron in cells Semicarbazide hydrochloride inhibits the activity of soluble semicarbazide sensitive amine oxidase (SSAO) Semicarbazide hydrochloride damages cartilage blood vessels ovaries testicles and thyroid follicles[1][2][3][4][5][6][7][8][9]
Medchemexpress LLC Semicarbazide (hydrochloride) | 563-41-7 | MFCD00013009 | 98.0% | 111.53 | CH6ClN3O | 50g
Semicarbazide hydrochloride is an orally active urea derivative Semicarbazide hydrochloride binds to copper or iron in cells Semicarbazide hydrochloride inhibits the activity of soluble semicarbazide sensitive amine oxidase (SSAO) Semicarbazide hydrochloride damages cartilage blood vessels ovaries testicles and thyroid follicles[1][2][3][4][5][6][7][8][9]
Medchemexpress LLC Benzaldehyde, 4-methyl- | 104-87-0 | 99.16% | 120.15 | 250 G
p-Tolualdehyde is an active small molecule functioning as a crucial drug intermediate. It is also utilized in the synthesis of isoxazole derivatives, which show promise as multidrug resistance (MDR) reversal agents, and serves as a model for forming fluorescent compounds for aldehyde determination.
- Used as a drug intermediate
- Applied in the synthesis of isoxazole derivatives
- Potential in developing multidrug resistance reversal agents
- Forms fluorescent compounds for aldehyde determination
- Exhibits an IC50 of 70.74 μM against B16-F10 cells
Apexbio Technology LLC SEMICARBAZIDE-HYDROCHLORIDE
Semicarbazide hydrochloride (CAS No 563-41-7) is a chemical compound used in biomedical research primarily within the biochemistry and pharmacology fields It originates as a derivative of semicarbazide and exhibits activity through the inhibition of certain enzyme pathways affecting cellular processes Its mechanism of action involves interference with enzymes such as monoamine oxidases impacting neurotransmitter activity Commonly its in vitro activity is measured in the nanomolar to low micromolar range making it useful in detailed mechanistic studies Typical applications include use in cell models for cancer research metabolic studies and neuropharmacology as well as in animal studies for drug screening and toxicology assessments Experimental concentrations typically depend on the specific research design accommodating various biological models and objectives ensuring flexibility in experimental setups
Apexbio Technology LLC SEMICARBAZIDE-HYDROCHLORIDE
Semicarbazide hydrochloride (CAS No 563-41-7) is a chemical compound used in biomedical research primarily within the biochemistry and pharmacology fields It originates as a derivative of semicarbazide and exhibits activity through the inhibition of certain enzyme pathways affecting cellular processes Its mechanism of action involves interference with enzymes such as monoamine oxidases impacting neurotransmitter activity Commonly its in vitro activity is measured in the nanomolar to low micromolar range making it useful in detailed mechanistic studies Typical applications include use in cell models for cancer research metabolic studies and neuropharmacology as well as in animal studies for drug screening and toxicology assessments Experimental concentrations typically depend on the specific research design accommodating various biological models and objectives ensuring flexibility in experimental setups