Oxazinanes
TARGETMOL CHEMICALS INC AMSACRINE HYDROCHLORIDE 200MG
Also available in 10 mg 25 mg 50 mg 100 mg 500 mg 1000 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Amsacrine hydrochloride (acridinyl anisidide hydrochloride) is topoisomerase II inhibitor is used in the treatment of acute myelogenous leukemia. purity: 99%
Medchemexpress LLC Brilliant black BN | 2519-30-4 | 10 MG
Brilliant black BN (E151) is an azo dye and a food colorant with potential as an antiviral agent against EV71 infection. It operates by inhibiting the interaction between EV71 and its cellular uncoating factor cyclophilin A. This substance holds promise for the investigation of contagious diseases.
- Inhibits interaction between EV71 and cyclophilin A.
- Inhibits EV71-GFP infection in vitro.
- Exhibits dose-dependent inhibition of EV71-GFP in infected RD cells.
- Able to inhibit all tested 28 EV71, CVA16, and CVA6 strains.
- Shows protective effect in EV71 challenged AG129 mice in vivo.
eMolecules AstaTech RAC-(2R4S)-24-DIMETHYLPYRROLIDINE HYDROCHLORIDE 1g 261437568 87744 95.000 866412-04-6 MFCD28133601 135.640 C6H14ClN
AstaTech RAC-(2R4S)-24-DIMETHYLPYRROLIDINE HYDROCHLORIDE 1g 261437568 87744 95.000 866412-04-6 MFCD28133601 135.640 C6H14ClN
Apexbio Technology LLC 5,6-Dihydro-UTP(Synonyms: 5,6-Dihydrouridine-5'-triphosphate, DHU-TP, 5,6-DHUTP, Dihydrouridine triphosphate), 100ul (100 mM).
5 6-Dihydro-UTP is a base-modified ribonucleoside triphosphate utilized in biochemical research Acting primarily as an acceptor substrate during enzymatic synthesis of dinucleoside polyphosphates this compound participates in phosphorylation reactions catalyzed by nucleotide-utilizing enzymes Due to its altered nucleobase structure 5 6-Dihydro-UTP serves as a strategic molecular probe in studies examining nucleotide synthesis pathways enzyme specificity and nucleic acid biochemistry
Sigma Aldrich Fine Chemicals Biosciences Landiolol hydrochloride >=98% (HPLC) | 144481-98-1 | MFCD01937430 | 5MG
Landiolol hydrochloride >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 546.05 | 144481-98-1 | MFCD01937430 | 5MG
eMolecules Combi-Blocks 2-(Morpholin-4-yl)-8-phenylchromen-4-one 100mg 303339417 QI-9914 95 000 154447-36-6 MFCD00270881 307 349 C19H17NO3
Combi-Blocks 2-(Morpholin-4-yl)-8-phenylchromen-4-one 100mg 303339417 QI-9914 95 000 154447-36-6 MFCD00270881 307 349 C19H17NO3
Medchemexpress LLC 7-Ethylcamptothecin | 78287-27-1 | 250 MG
7-Ethylcamptothecin is a derivative of Camptothecin and a DNA topoisomerase I inhibitor. It exhibits significant antitumor activity against tumor cells and serves as a key precursor for the synthesis of 20 (S)-O-substituted benzoyl-7-ethylcamptothecin compounds. It is widely used in various tumor-related scientific studies.
- Functions as a DNA topoisomerase I inhibitor.
- Exhibits significant antitumor activity against tumor cells.
- Serves as a precursor for synthesizing 20 (S)-O-substituted benzoyl-7-ethylcamptothecin compounds.
- Utilized in various tumor-related scientific studies.
- Starting material for developing E-ring modified water-soluble camptothecin derivatives.
- Appears as a light yellow to yellow solid.
- Has a purity of 99.58%.
eMolecules Advanced ChemBlocks - In Stock 1-methylazetidin-3-one hydrochloride 250mg 381422434 L18430 97 000 1818847-43-6 MFCD29060167 121 560 C4H8ClNO
Advanced ChemBlocks - In Stock 1-methylazetidin-3-one hydrochloride 250mg 381422434 L18430 97 000 1818847-43-6 MFCD29060167 121 560 C4H8ClNO
Medchemexpress LLC Iadademstat (dihydrochloride) | 1431303-72-8 | 99.98% | 1 ML
Product Overview
Iadademstat (ORY-1001) is a highly potent, orally active, and selective LSD1 (KDM1A) inhibitor that exhibits antileukemic activity. It is intended for research use, particularly in studies concerning relapsed or refractory acute myeloid leukemia.Features and Benefits
- Highly potent, orally active, and selective LSD1 (KDM1A) inhibitor.
- Exhibits antileukemic activity.
- Can be used for research on relapsed or refractory acute myeloid leukemia.
- Inhibits the proliferation of cancer cells (H1299 and A549), arrests the cell cycle at G1 phase, and induces apoptosis in vitro.
- Decreases glycolysis in H1299 and A549 cells by reducing HK2 protein levels in vitro.
- Demonstrates antitumor activity and increases survival rate in glioblastoma xenograft mouse models in vivo.
Medchemexpress LLC 4-Phenyl-7,8-dihydroxycoumarin | 842-01-3 | 99.4% | 10 MG
4-Phenyl-7,8-dihydroxycoumarin is a coumarin derivative for research use only, and can be used for bronchiectasis research.
- Chemical formula: C15H10O4
- Molecular weight: 254.24
- Appearance: Solid, off-white to yellow
- Solubility: 100 mg/mL in DMSO
- Powder storage: -20°C for 3 years, 4°C for 2 years
- In solvent storage: -80°C for 6 months, -20°C for 1 month
- Related disease areas: Neurological, Eye or Ear Disease, Inflammation or Immune System Disease, Neurodegenerative Disease, Parkinson's Disease
- Signaling pathways: Inflammation/Immunology, Metabolic Enzyme/Protease, Neuronal Signaling, COMT
TARGETMOL CHEMICALS INC BELOTECAN HYDROCHLORIDE 25MG
Also available in 1 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Belotecan hydrochloride (CKD-602) is a synthetic water-soluble camptothecin derivative and topoisomerase I inhibitor with potential antitumor activitypurity: 98%