ペプチド
抗体
色素試薬
PROTAC
バーチャルスクリーニング
TargetMolキット
Cell Counting Kit-8 (CCK-8)
Inhibitor Cocktails
天然化合物
フェノール類
アルカロイド類
フラボノイド類
阻害剤
血管新生
アポトーシス
オートファジー
細胞周期・チェックポイント
クロマチン・エピジェネティック
細胞骨格シグナル
DNA損傷・DNA修復
内分泌・ホルモン
GPCR/Gタンパク質
免疫・炎症
JAK・STATシグナル
Coumarins (1-benzopyran-2-one) are chemical compounds in the benzopyrone class of organic compounds found in many plants. Coumarins possess a variety of biological properties, including antimicrobial, antiviral, antiinflammatory, antidiabetic, antioxidant, and enzyme inhibitory activity.
| Cat. No. | 製品名 | CAS No. | Purity | Chemical Structure |
|---|---|---|---|---|
| T20510 | Novobiocin | 303-81-1 | 98% |
|
| Novobiocin is an orally active and potent antibiotic.Novobiocin is a DNA gyrase inhibitor and heat shock protein 90 (Hsp90) antagonist with inhibitory effects on... | ||||
| TJS0315 | 4-Methyldaphnetin | 2107-77-9 | 98% |
|
| 1. 4-Methyldaphnetin is a potent inhibitor (low micromolar) of lipid peroxidation and scavengers of superoxide anion radicals and of aqueous alkylperoxyl radical... | ||||
| T5070 | LC3-mHTT-IN-AN2 | 7758-73-8 | 98% |
|
| 5,7-dihydroxy-4-phenyl coumarin is found in the plant Passiflora serratodigitata with the antibacterial activity. | ||||
| Fr12290 | 4-Methoxycoumarine | 20280-81-3 | 98% |
|
| 4-Methoxycoumarine has antitumour effects. | ||||
| T7049 | Herniarin | 531-59-9 | 98% |
|
| Herniarin is a natural coumarin with antitumor effect. | ||||
| Fr12277 | 4-Hydroxy-6-methylcoumarin | 13252-83-0 | 98% |
|
| 4-Hydroxy-6-methylcoumarin (4-HMC) is a naturally occurring phenolic compound, a derivative of coumarin, found in a variety of plants, fungi, and bacteria. It ha... | ||||
| Fr12596 | 3-Acetylcoumarin | 3949-36-8 | 98% |
|
| 3-Acetylcoumarin as a practical ligand for copper-catalyzed CN coupling reactions at room temperature. It has neuroprotective and acaricidal properties. | ||||
| T8038 | 7-Ethoxy-4-Methylcoumarin | 87-05-8 | 98% |
|
| 7-Ethoxy-4-Methylcoumarin is a natural organic compound, aromatic compound with a distinctive odor. It is considered an inhibitor of enzymes in cells and has bee... | ||||
| T7934 | 7-Methylcoumarin | 2445-83-2 | 98% |
|
| 7-Methylcoumarin with strong hepatoprotective activity. | ||||
| T18927 | Br-Mmc | 35231-44-8 | 98% |
|
| Br-Mmc is used as a new fluorescence label for fatty acids. It is used for the determination of fatty acids by HPLC or TLC. | ||||
| TN1048 | Cnidilin | 14348-22-2 | 98% |
|
| Cnidilin is found in association with Angelica dahurica roots, has high BBB permeability and has pharmacokinetic potential in the treatment of CNS disorders. | ||||
| T7696 | 3-Cyano-7-ethoxycoumarin | 117620-77-6 | 98% |
|
| 3-Cyano-7-ethoxycoumarin is cytochrome P450 (CYP) isoforms CYP1A1 and CYP1A2 . | ||||
| TJS0328 | Nordalbergin | 482-82-6 | 98% |
|
| TN1905 | Magnolioside | 20186-29-2 | 98% |
|
| Magnolioside has anti-plasmodial activity, shows notable growth inhibitory activity against chloroquine-sensitive strains of P. falciparum. It also shows a moder... | ||||
| TN1328 | 7-Amino-4-methylcoumarin-3-acetic acid | 106562-32-7 | 98% |
|
| 7-Amino-4-methylcoumarin is more suitable as a substrate for enteropeptidase than GD(4)K-NA. | ||||
| T8113 | 4-Methyl-6-Methoxycoumarin | 6295-35-8 | 98% |
|
| 4-Methyl-6-Methoxycoumarin is a natural product isolated from Eupatorium pauciflorum. | ||||
| TJS0341 | 7-Amino-4-(trifluoromethyl)coumarin | 53518-15-3 | 98% |
|
| 7-Amino-4-(trifluoromethyl)coumarin is a 5-Hydroxytryptamine Receptor Subtype 1E (HTR1E) antagonist. 7-Amino-4-(trifluoromethyl)coumarin is a Galanin Receptor 2 ... | ||||
| T2S0357 | 6-Hydroxycoumarin | 6093-68-1 | 98% |
|
| 6-Hydroxycoumarin exhibits cytotoxicity against human HL60, HCT116, COLO205 cells with activity value of 35 uM, 42 uM, 37 respectively. 6-Hydroxycoumarin is a hu... | ||||
| TN1702 | Glycycoumarin | 94805-82-0 | 98% |
|
| Glycycoumarin is an estrogen agonist, it shows moderate inhibitory effects against CYP1A2 and CYP2B6. | ||||
| T7970 | 7-Ethoxycoumarin | 31005-02-4 | 98% |
|
| 7-Ethoxycoumarin, a typical human P450 substrate, is catalyzed by both wild-type and mutant forms of CYP102A1. | ||||
