Coumarin

DEAC, SE can be used for relevant research in the field of life sciences. Its product number is T64949 and CAS number is 139346-57-9.

7-BFC (7-Benzyloxy-4-(trifluoromethyl)coumarin) is a coumarin-like fluorescent substrate that serves as a biomarker for cytochrome P 450 and can be used to study CYP isoforms and cytochrome P 450 metabolism.

7-Hydroxycoumarin-3-carboxylic acid (7-HC-3-CA) is a safe anti-browning agent that inhibits tyrosinase activity, used in food preservation and human pigmentation research.

Coumarin hydrazine is a fluorophore containing an aromatic hydrazine moiety that serves as a fluorescent chemical probe for labeling intracellular protein- and lipid-bound carbonyls, and as a fluorescent sensor in living cells for the detection of carbonylated biomolecules produced following oxidative stress.

Coumarin102 (Exciton 480) is a fluorescent dye.Coumarin102 has weak inhibitory activity against Monoamine oxidase B, MAO-B and MAO-A and can be used to study neurological disorders.

7ACC1 (D 142) selectively affects a single part of the MCT symporter translocation cycle, leading to strict inhibition of lactate influx. This singular activity is associated with antitumor effects less prone to resistance and side effects.

3-Cyano-7-hydroxycoumarin (3-Cyanoumbelliferone) is a macrophage inhibitor of macrophage inhibitory factor (MIF) interconjugate isomerase with a Ki of 2.9 μM. 3-Cyano-7-hydroxycoumarin belongs to the group of coumarin derivatives, which can be used as molecular probes and fluorescent dyes.

Coumarin343 inhibits monocarboxylic acid transporter protein 4 with IC50 values in the range of 0.01-100 µM.Coumarin343 exhibits anticancer and antibacterial activity.Coumarin343 is a coumarin dye.

3-Cyano-7-ethoxycoumarin is cytochrome P450 (CYP) isoforms CYP1A1 and CYP1A2 .

7-(Diethylamino)-4-methyl-2H-chromen-2-one is a useful organic compound for research related to life sciences. The catalog number is T66262 and the CAS number is 91-44-1.

MDCC is a multifunctional dye that serves as a crucial tool in biological experiments, assisting researchers in observing and analyzing cell structures, tracking biomolecules, evaluating cell functions, distinguishing cell types, detecting biomolecules, studying tissue pathology, and monitoring microorganisms. Its applications span from fundamental scientific research to a wide range of clinical diagnostics. Additionally, dyes are extensively utilized in traditional fields like textile dyeing and in emerging areas such as functional textile processing, food pigments, and dye-sensitized solar cells.

'O'-(carboxymethyl)fluoresceinamide is a multifunctional dye used in biological experiments to observe and analyze cell structures, track biomolecules, evaluate cell functions, distinguish cell types, detect biomolecules, study tissue pathology, and monitor microorganisms. It has applications in basic research, clinical diagnostics, textile dyeing, functional textile processing, food pigments, and dye-sensitized solar cells.

AMCA-X, N-succinimidyl ester is an amine-reactive, UV-excitable, blue fluroscent dye.

1-(Dichloro-1,3,5-triazinyl)-pyrene (1-(4,6-Dichloro-1,3,5-triazin-2-yl)pyrene) serves as a multifunctional dye with diverse applications in both traditional and emerging fields. In biological experiments, dyes facilitate the observation and analysis of cell structures, tracking of biomolecules, evaluation of cell functions, distinction of cell types, detection of biomolecules, examination of tissue pathology, and monitoring of microorganisms. Their utilization spans from foundational scientific research to extensive clinical diagnostics. Additionally, dyes are integral to the textile industry for coloring purposes, and find innovative uses in functional textile processing, food coloring, and dye-sensitized solar cells.

MCA succinimidyl ester, a derivative of MCA, selectively reacts with amines and serves as a peptide substrate for fluorescence resonance energy transfer (FRET) [1].

7-Amino-4-methylcoumarin hydrogensulfate (Coumarin 120 hydrogensulfate; AMC hydrogensulfate) serves as a versatile dye extensively utilized across various domains. This compound plays a crucial role in biological experiments, aiding in the observation and analysis of cell structures, tracking of biomolecules, evaluation of cell functions, differentiation of cell types, detection of biomolecules, examination of tissue pathology, and monitoring of microorganisms. Its applications extend beyond basic scientific research, encompassing both traditional uses in textile dyeing and contemporary usages in functional textile processing, food pigments, and dye-sensitized solar cells.

2-(7-Methoxy-2-oxo-2H-chromen-4-yl)acetic acid is a useful organic compound for research related to life sciences. The catalog number is T64951 and the CAS number is 62935-72-2.

7-Diethylaminocoumarin-3-carbohydrazide, a type of coumarin, can be utilized for detecting sugar chains and quantifying biological carbonyl compounds [1].

6,7-Dimethoxy-4-coumarinylacetic acid (2-(6,7-Dimethoxy-2-oxo-2H-chromen-4-yl)acetic acid) serves as a multifunctional dye with diverse applications in both scientific and traditional domains. This compound facilitates the observation and analysis of cell structures in biological experiments, enabling researchers to track biomolecules, assess cell functions, categorize cell types, identify biomolecules, investigate tissue pathology, and monitor microorganisms. Beyond its scientific utility, 6,7-Dimethoxy-4-coumarinylacetic acid is also employed in industries including textile dyeing, functional textile processing, food pigments, and dye-sensitized solar cells. Its broad utility spans from fundamental research to clinical diagnostics, highlighting its importance across multiple fields.

7-Diethylamino-3-N-(4-maleimidopropyl)carbamoylcoumarin is a versatile dye utilized across various fields. This compound is primarily important in biological experiments for observing and analyzing cell structures, tracking biomolecules, evaluating cell functions, distinguishing cell types, detecting biomolecules, studying tissue pathology, and monitoring microorganisms. Its applications extend beyond basic scientific research into clinical diagnostics. Additionally, it is employed in traditional industries like textile dyeing and in innovative areas including functional textile processing, food pigments, and dye-sensitized solar cells.

N-(4-Methylumbelliferyl)-maleinimid serves as a multifunctional dye utilized extensively across various domains. In biological experiments, dyes are pivotal for observing and analyzing cell structures, tracking biomolecules, assessing cell functions, differentiating cell types, detecting biomolecules, exploring tissue pathology, and monitoring microorganisms. Their utilization spans from fundamental scientific research to a broad spectrum of clinical diagnostics. Additionally, dyes find applications in conventional industries like textile dyeing and in emerging sectors, including functional textile processing, food pigments, and dye-sensitized solar cells.

2-(7-Hydroxy-2-oxo-2H-chromen-4-yl)acetic acid is a useful organic compound for research related to life sciences. The catalog number is T65277 and the CAS number is 6950-82-9.

Pro-AMC is a multifunctional dye pivotal in biological experiments, aiding researchers in observing and analyzing cell structures, tracking biomolecules, evaluating cell functions, distinguishing cell types, detecting biomolecules, studying tissue pathology, and monitoring microorganisms. Its applications span basic scientific research to clinical diagnostics, traditional fields like textile dyeing, and emerging fields such as functional textile processing, food pigments, and dye-sensitized solar cells.

The amine-reactive AMCA, SE (7-amino-4-methylcoumarin-3-acetic acid, succinimidyl ester) and its conjugates yield blue-fluorescence (approximate excitation emission maxima ~353 442) that can be used as a contrasting color in multicolor applications.