Coumarins and derivatives
Br-Mmc (=4-Bromomethyl-7-methoxycoumarin) 98.0+%, TCI America™
CAS: 35231-44-8 Molecular Formula: C11H9BrO3 Molecular Weight (g/mol): 269.09 MDL Number: MFCD00006869 InChI Key: CTENSLORRMFPDH-UHFFFAOYSA-N Synonym: 4-bromomethyl-7-methoxycoumarin,4-bromomethyl-7-methoxy-2h-chromen-2-one,br-mmc,ccris 7996,4-bromomethyl-7-methoxychromen-2-one,2h-1-benzopyran-2-one, 4-bromomethyl-7-methoxy,4-bromomethyl-7-methoxy-2-oxo-2h-benzopyran,acmc-1agnd,4-brommethyl-7-methoxy-2h-chromen-2-on,4-bromomethyl-7-methoxy coumarin PubChem CID: 121894 IUPAC Name: 4-(bromomethyl)-7-methoxy-2H-chromen-2-one SMILES: COC1=CC=C2C(CBr)=CC(=O)OC2=C1
N-Succinimidyl 7-Methoxycoumarin-3-carboxylate 98.0+%, TCI America™
CAS: 150321-92-9 Molecular Formula: C15H11NO7 Molecular Weight (g/mol): 317.253 MDL Number: MFCD00467593 InChI Key: JMQAALOXLOSYCQ-UHFFFAOYSA-N Synonym: 7-Methoxycoumarin-3-carboxylic Acid N-Succinimidyl Ester PubChem CID: 2760554 IUPAC Name: (2,5-dioxopyrrolidin-1-yl) 7-methoxy-2-oxochromene-3-carboxylate SMILES: COC1=CC2=C(C=C1)C=C(C(=O)O2)C(=O)ON3C(=O)CCC3=O
Sigma Organic Chemistry 6,7-Dihydroxycoumarin | 5G | 305-01-1 | MFCD00006874 | 0.98
6,7-Dihydroxycoumarin, 5G
About This Item:
Storage: room temp
EINECS Number: 206-161-5
Sigma Organic Chemistry 8-Methoxycoumarin | 1G | 2445-81-0 | MFCD00016708
8-Methoxycoumarin, 1G
About This Item:
Linear Formula: C10H8O3
FUJIFILM IRVINE SCIENTIFIC INC 7-AMINO-4-METHYL-3-COUMARINYLA
*Orders for this supplier are non-cancellable/non-returnable once they are processed.* 7-Amino-4-methyl-3-coumarinylacetic Acid 500ME
Indofine Chemical 7-Hydroxycoumarin, 99%, 5 Gm
7-HYDROXYCOUMARIN 5 GM, Coumarin, Umbelliferone, C9H6O3, MW: 162.14, 99+%, 93-35-6, MFCD00006878
Selleck Chemical LLC Esculetin S4711-1g
Esculetin (Cichorigenin Aesculetin) is a coumarin derivative found in various natural plant products with various biological and pharmaceutical properties including anti-edema anti-inflammatory and anti-tumour effects It inhibits lipoxygenases (LOs)
Selleck Chemical LLC 4-Methylesculetin S4966-25mg
4-methylesculetin is one of the coumarin derivatives with great anti-oxidant and anti-inflammatory activities 4-Methylesculetin inhibits myeloperoxidase (MPO) activity and reduces IL-6 level
Selleck Chemical LLC Palomid 529 (P529) S2238-1g
Palomid 529 (P529 SG 00529) inhibits both the mTORC1 and mTORC2 complexes reduces phosphorylation of pAktS473 pGSK3 S9 and pS6 Phase 1
Cayman Chemical CoumarIn hydrazIn 10mg
A fluorescent probe for a-keto acids reacts with aldehydes to produce highly fluorescent benzimidazole derivatives ex/em spectra 361/448 nm can be reacted with ketones and carbonyls to form fluorescent adducts that can be separated and quantitated by reversed-phase high-performance liquid chromatography
Cayman Chemical 7hydroy CoumarIn GlucuRND 10mg
A tertiary amine that complexes with and stabilizes Cu(I) to accelerate azide-alkyne cycloadditions as used in click chemistry
Cayman Chemical 7-ethoxy-4-MethylcoumarIn 1g
A PPARa and PPARY dual agonist increases transcriptional activity of PPARa and PPARY in a luciferase reporter assay in AC2F rat liver cells at 5 UM reduces serum glucose triglyceride and insulin levels and improves hepatic steatosis in db/db mice and 20-month-old rats at 3mg/kg reduces peroxynitrite and COX-2 levels ROS production and Akt phosphorylation in 20-month-old rat kidney at 3 mg/kg inhibits mushroom tyrosinase (IC50 8 19 UM) inhibits increases in melanin content in a-melanocyte stimulating hormone-induced B16/F10 murine melanoma cells at 10 UM
Sigma Organic Chemistry Coumarin-3-carboxylic a | 25gr | 531-81-7 | MFCD00006852
Coumarin-3-carboxylic a , 25G
About this Item:
CAS #: 531-81-7
MDL #: MFCD00006852
Molecular Weight: 190.15
UNSPSC Code: 12352100
Chemical Formula: C10H6O4
Chem-Impex International, Inc. 7-Diethylamino-4-methylcoumarin | MFCD00006864 | 250G
7-Diethylamino-4-methylcoumarin, MFCD00006864, 250G
Cayman Chemical 7-EthoxycoumarIn 100mg
A plant growth and plant circadian rhythm regulator inhibits hypocotyl elongation in lettuce seedlings at 100 Ug/L inhibits primary root growth in Arabidopsis seedlings disrupts the transcription of plant circadian rhythm regulatory genes in Arabidopsis seedlings active against P falciparum with an IC50 value of 35 mg/ml