Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty
Filter
Applied FilterClear all
TargetMol | Tags By Target
  • Carbonic Anhydrase
    (208)
  • Apoptosis
    (14)
  • Cholinesterase (ChE)
    (9)
  • Antibacterial
    (8)
  • Autophagy
    (5)
  • CDK
    (5)
  • Calcium Channel
    (5)
  • Potassium Channel
    (5)
  • Sodium Channel
    (5)
  • Others
    (90)
Filter
Search Result
Results for "

hydrase

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    211
    TargetMol | All_Pathways
  • Inhibitory Antibodies
    1
    TargetMol | Inhibitory_Antibodies
  • Dye Reagents
    1
    TargetMol | All_Dye_Reagents
  • PROTAC Products
    1
    TargetMol | PROTAC
  • Natural Products
    11
    TargetMol | Natural_Products
  • Recombinant Protein
    48
    TargetMol | Recombinant_Protein
  • Isotope Products
    3
    TargetMol | Isotope_Products
  • Antibody Products
    56
    TargetMol | Antibody_Products
  • Cell Research
    5
    TargetMol | Cell_Research_Reagents
  • Reference Standards
    2
    TargetMol | Standard_Products
Seneciphylline
TN1078480-81-9
Seneciphylline, one of the hepatotoxic pyrolizidine alkaloids, has mutagenic activity in Drosophila and their transfer into rat milk.Seneciphylline can significantly increased the activities of epoxide hydrase and glutathione-S-transferase but cause reduc
  • $48
In Stock
Size
QTY
Punicalin
T4S171865995-64-4
Punicalin exerts anti-inflammatory, antioxidative, and anti-hepatotoxic activities, it shows inhibitory activity on HIV-1 reverse transcriptase in a dose-dependent manner, with an IC50 of 0.11 microg/ml (0.14 microM).
  • $43
In Stock
Size
QTY
TargetMol | Inhibitor Hot
TargetMol | Citations Cited
Ellagic acid
Gallogen, Elagostasine
T0465476-66-4
Ellagic acid (Gallogen), a thickened tetracyclic natural product, is a potent CK2 inhibitor (IC50=40 nM; Ki=20 nM) with ATP-competitive properties. Ellagic acid is an antioxidant and also possesses antiproliferative activity.
  • $44
In Stock
Size
QTY
TargetMol | Citations Cited
Urea
Ureophil, E-Cardamoni, Carbonyldiamide, Carbamide
T073857-13-6
Urea (Carbonyldiamide) is formed in the liver from ammonia produced by the deamination of amino acids. It is the principal end metabolite of protein catabolism and accounts for about one-half of the total urinary solids.
  • $30
In Stock
Size
QTY
Methyl 2,4-dihydroxybenzoate
TN67072150-47-2
Methyl 2,4-dihydroxybenzoate is a natural product.
  • $34
In Stock
Size
QTY
Pyrocatechol
T4847120-80-9
Pyrocatechol, often known as catechol or benzene-1,2-diol, is a benzenediol, Pyrocatechol was produced at a large scale industrially, mainly as precursors to pesticides, flavors, and fragrances. Its sulfonic acid is often present in the urine of many mammals.
  • $29
In Stock
Size
QTY
TargetMol | Inhibitor Sale
6-Hydroxycoumarin
6-hydroxychromen-2-one
T2S03576093-68-1
6-Hydroxycoumarin (6-hydroxychromen-2-one) exhibits cytotoxicity against human HL60, HCT116, COLO205 cells with activity value of 35 uM, 42 uM, 37 respectively. 6-Hydroxycoumarin is a human CA9, CA12 inhibitor.
  • $29
In Stock
Size
QTY
(E)-Dehydrodiconiferyl alcohol
T40611528814-97-3
(E)-Dehydrodiconiferyl alcohol is a potent dual inhibitor of hCA IX and hCA XII, effectively impeding the catalytic activity of both carbonic anhydrase isoforms. Additionally, (E)-Dehydrodiconiferyl alcohol exerts inhibitory effects on the nuclear translocation of NF-κB in the connective tissue of the healing area.
  • $970
Inquiry
Size
QTY
Dimethylfraxetin
Fraxetin dimethyl ether, 6,7,8-Trimethoxycoumarin
T4S23546035-49-0
Dimethylfraxetin (6,7,8-Trimethoxycoumarin) is a Carbonic anhydrase inhibitor(Ki:0.0097 μM)
  • $35
In Stock
Size
QTY
Eriocitrin
Eriodictyol-7-O-Rutinoside, Eriodictyol glycoside, eriodictyol 7-rutinoside, Eriodictioside
T6S022113463-28-0
1. Eriocitrin (Eriodictyol-7-O-Rutinoside) is powerful antioxidative flavonoid; (1) Prevents oxidative damages caused by acute exercise-induced oxidative stress.(2) Lipid-lowering effects in a rat model of high-fat diet. 2. Dietary Eriocitrin ameliorates diet-induced hepatic steatosis with activation of mitochondrial biogenesis. 3. Eriocitrin and Apigenin were identified as new potent inhibitors of human carbonic anhydrase VA isozyme.
  • $31
In Stock
Size
QTY
TargetMol | Citations Cited
Seneciphylline (Standard)
TMSM-2623480-81-9
Seneciphylline (Standard) is a reference standard for research and analysis in studies involving Seneciphylline. Seneciphylline, one of the hepatotoxic pyrolizidine alkaloids, has mutagenic activity in Drosophila and their transfer into rat milk.Seneciphylline can significantly increased the activities of epoxide hydrase and glutathione-S-transferase but cause reduction of cytochrome P-450 and related monooxygenase activities.
  • $397
7-10 days
Size
QTY