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Succinic anhydride
Catalog No. A20536 nonclaevable ADC linkerSuccinic anhydride is a cyclic anhydride and a nonclaevable ADC linker extracted from patent WO2009064913A1. Succinic anhydride can react with compound 4 of the patent to link the prodrug to an amine or hydroxy 1 group of a targeting polypeptide. 了解更多 -
Docosatrienoic Acid
Catalog No. A20529 Docosatrienoic acid is a rare ??-3 fatty acid; inhibits LTB4 binding to pig neutrophil membranes with an Ki of 5 μM. 了解更多 -
Ecteinascidin 770
Catalog No. A20525 Ecteinascidin 770 (ET-770) is a 1,2,3,4-tetrahydroisoquinoline alkaloid with potent anti-cancer activities; inhibits U373MG cells with an IC50 of 4.83 nM. 了解更多 -
O-Acetylserine
Catalog No. A20524 O-Acetylserine (O-Acetyl-L-serine) is an intermediate in the biosynthesis of the amino acid cysteine in bacteria and plants. 了解更多 -
4-Acetamidobutanoic acid
Catalog No. A20514 4-Acetamidobutanoic acid (N-acetyl GABA) is a γ-aminobutyric acid (GABA) derivative. 了解更多 -
ICI 153110
Catalog No. A20513 phosphodiesterase inhibitorICI 153110 is an orally active phosphodiesterase inhibitor with both vasodilating and inotropic properties which is designed for the treatment of congestive cardiac failure. 了解更多 -
2-(Methylamino)-1H-purin-6(7H)-one
Catalog No. A20511 2-(Methylamino)-1H-purin-6(7H)-one (N2-Methylguanine) is a modified nucleoside. 2-(Methylamino)-1H-purin-6(7H)-one is an endogenous methylated nucleoside found in human fluids. 了解更多 -
Mivotilate
Catalog No. A20504 AhR activatorMivotilate is a nontoxic, potent activator of the aryl hydrocarbon receptor (AhR), and acts as a hepatoprotective agent. 了解更多 -
Coenzyme Q9
Catalog No. A20501 Coenzyme Q9, a nine isoprenyl group-containing member of the ubiquinone family, is a normal constituent of human plasma. 了解更多 -
Oxaquin
Catalog No. A20486 Oxaquin (MCB-3837) is a water-soluble, injectable prodrug that is rapidly converted to the active sub-stance MCB3681 in vivo following intravenous (i.v.) administration, active against Gram-positive bacterial species. Oxaquin (MCB-3837) itself has no antimicrobial effects. 了解更多 -
Agmatine sulfate
Catalog No. A20485 NO synthase inhibitorAgmatine sulfate exerts modulatory action at multiple molecular targets, such as neurotransmitter systems, ion channels and nitric oxide synthesis. It is an endogenous agonist at imidazoline receptor and a NO synthase inhibitor. 了解更多 -
GAL-021
Catalog No. A20480 -
TM5275 sodium
Catalog No. A20462 plasminogen activator inhibitorTM5275 sodium is a plasminogen activator inhibitor (PAI-1) with an IC50 of 6.95 μM. 了解更多 -
BRCA1-IN-1
Catalog No. A20459 BRCA1 inhibitorBRCA1-IN-1 is a novel small-molecule-like BRCA1 inhibitor with IC50 and Ki of 0.53 μM and 0.71 μM, respecrively. 了解更多 -
Trifarotene
Catalog No. A20458 RAR agonistTrifarotene (CD5789) is a retinoic acid receptor (RAR) agonist with Kdapp of 2, 15 and 500 nM for RARγ, RARβ and RARα, respectively. 了解更多 -
CGP 25454A
Catalog No. A20448 dopamine autoreceptor antagonistCGP 25454A is a novel and selective presynaptic dopamine autoreceptor antagonist. 了解更多 -
Ralfinamide
Catalog No. A20446 Na+ blockerRalfinamide (FCE-26742A) is an orally available Na+ blocker derived from α-aminoamide, with function of suppressing pain. 了解更多 -
beta-L-D4A
Catalog No. A20444 HIV-1 reverse transcriptase inhibitorbeta-L-D4A is a nucleoside HIV-1 reverse transcriptase inhibitor. 了解更多 -
Chymase-IN-1
Catalog No. A20404 chymase inhibitorChymase-IN-1 is a potent, selective, orally active, nonpeptide inhibitor of human mast cell chymase with an IC50 of 29 nM. 了解更多 -
Revizinone
Catalog No. A20398 PDE inhibitorRevizinone is a novel selective phosphodiesterase (PDE) inhibitor with IC50 values on this enzyme to 0.036 microM. 了解更多 -
Adenosine antagonist-1
Catalog No. A20383 AA3R antagonistAdenosine antagonist-1 is an adenosine A3 receptor (AA3R) antagonist. 了解更多 -
Naminidil
Catalog No. A20375 -
Bromobimane
Catalog No. A20366 Bromobimane is essentially nonfluorescent and converts into fluorescent products when reacts with small thiols. 了解更多 -
9-Propenyladenine
Catalog No. A20357 9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate. Tenofovir is an antiretroviral drug known as nucleotide analogue reverse transcriptase inhibitors, which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV. 了解更多
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