| DC71041 |
Fenadiazole |
Fenadiazole acts as a central nervous system agent to manage insomnia and dreaminess. |
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| DC71042 |
Fenquizone
Featured
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Fenquizone (MG-13054), a thiazide-like diuretic, exhibits chronic antihypertensive effect. Fenquizone can be used for the research of oedema and hypertension. |
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| DC71043 |
Flocoumafen |
Flocoumafen (WL 108366), a second-generation anticoagulant rodenticide (ARs), belongs to the family of vitamin K antagonist (VKA) molecules. |
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| DC71048 |
Glycolithocholic acid sodium |
Glycolithocholic acid sodium is the sodium salt of Glycolithocholic acid. Glycolithocholic acid is a glycine-conjugated secondary bile acid. Glycolithocholic acid can be used to diagnose ulcerative colitis (UC), non-alcoholic steatohepatitis (NASH) and primary sclerosing cholangitis (PSC). |
|
| DC71050 |
GP3269 |
GP3269 is a potent, selective, and orally active inhibitor of human adenosine kinase (AK) with an IC50 of 11 nM. GP3269 exhibits anticonvulsant activity in rats. |
|
| DC71051 |
Green CMFDA |
Green CMFDA (CMFDA) is a cell-permeable fluorescent probe that can be used a cell tracer. Green CMFDA can be cleaved by non-specific esterases common to living cells, producing a fluorescent compound, fluorescein, visible using a fluorescent microscope. |
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| DC71053 |
H-Glu(Met-OH)-OH |
H-Glu(Met-OH)-OH could induce oxidation of hydroxyl radical. |
|
| DC71058 |
Inositol nicotinate |
Inositol nicotinate, with vasodilatory effect, is used in the study of Peripheral arterial disease (PAD). |
|
| DC71065 |
Jineol |
Jineol is a cytotoxic alkaloid from the centipede Scolopendra subspinipes. Jineol exhibits modest cytotoxic activity in vitro against the growth of human tumor cell lines. |
|
| DC71072 |
Levatin |
Levatin is an 18-Norclerodane diterpene from Croton levatii. |
|
| DC71073 |
Linoleyl methane sulfonate |
Linoleyl methane sulfonate is a selective lipid-based vehicle for use in drug delivery systems. |
|
| DC71074 |
Loliolid |
Loliolide, a Carotenoid Metabolite, is a potential endogenous inducer of herbivore resistance. Loliolide also inhibits the seedling growth. |
|
| DC71078 |
Makisterone A |
Makisterone A, a 28-carbon moulting hormone, has been identified as the major free pupal ecdysteroid in the honey bee, Apis mellifera. |
|
| DC71080 |
Maresin 2 |
Maresin 2 is an anti-inflammatory and pro-resolving mediator from human macrophages. Maresins are a new family of anti-inflammatory and pro-resolving lipid mediators biosynthesized from docosahexaenoic acid (DHA) by macrophages. |
|
| DC71082 |
MitoPerOx |
MitoPerOx is a fluorescent ratio-probe of lipid peroxidation. MitoPerOx can be taken up very rapidly into mitochondria within cells, thereby responding to changes in mitochondrial lipid peroxidation. |
|
| DC71083 |
MitoTracker Green FM |
MitoTracker Green FM is a green-fluorescent dye that can selectively accumulate in the mitochondrial matrix. MitoTracker Green FM covalently binds to mitochondrial proteins by reacting with free thiol groups of cysteine residues. |
|
| DC71085 |
MoTP |
MoTP is a specific platelet activating factor receptor antagonist and can induce melanocyte ablation. MoTP can be used for the research of cancer. |
|
| DC71087 |
MRS4620 |
MRS4620 is a potent CD73 inhibitor, with a Ki of 0.436 nM. MRS4620 can be use for the research of cancer immunotherapy. |
|
| DC71093 |
Nonacosadiene |
Nonacosadiene is the pheromone of Drosophila melanogaster from a tetrahydrophyridine derivative. |
|
| DC71096 |
OB-24
Featured
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OB-24 is a potent inhibitor of heme oxygenase-1 (HO-1). Heme oxygenase-1, a member of the heat shock protein family, plays a key role as a sensor and regulator of oxidative stress. OB-24 significantly inhibited cell proliferation in vitro and tumor growth and lymph node/lung metastases in vivo. OB-24 has potential for the research of advanced prostate cancer (PCA). |
|
| DC71099 |
Paroxetine |
Paroxetine, a phenylpiperidine derivative, is a potent and selective serotonin reuptake inhibitor (SSRI). Paroxetine is a very weak inhibitor of norepinephrine (NE) uptake but it is still more potent at this site than the other SSRIs. |
|
| DC71105 |
Pseudoisocyanine iodide |
Pseudoisocyanine (iodide) is a pan inhibitor of monoamine transporters and organic cation transporters with antidepressant-like activity. |
|
| DC71107 |
Resolvin E2 |
Resolvin E2 ((-)-Resolvin E2), a proresolving lipid mediator, is useful as a lead for anti-inflammatory agent. |
|
| DC71113 |
Saponin PE |
Saponin PE is a saponin compound isolated from aerial part of Clematis tangutica. |
|
| DC71117 |
Sorbicillin |
Sorbicillin, a sorbicillinoid analogue, acts as a potent anti-inflammation agent. |
|
| DC71119 |
Suc-Gly-Pro-AMC |
Suc-Gly-Pro-AMC is a fibroblast activation protein (FAP)-specific substrate. Suc-Gly-Pro-AMC can be used to study the activity of FAP. |
|
| DC71120 |
Sulfo-GMBS |
Sulfo-GMBS is a cross-linker. Among the amine-sulfhydryl cross-linkers, Sulfo-GMBS generated the largest number of cross-links and covered most of the cross-links that were identified with AMAS and GMBS. |
|
| DC71133 |
UDP-GalNAz disodium
Featured
|
UDP-GalNAz disodium (UDP-N-azidoacetylgalactosamine disodium) is the analogue of UDP-GalNAc. UDP-GalNAc is the donor substrate of many N-acetylgalactosaminyltransferases, enzymes which transfer GalNAc from the nucleotide sugar to a saccharide or peptide acceptor. |
|
| DC71135 |
YZ9 |
Y29 is a potent PFKFB3 inhibitor with an IC50 of 0.183 µM, and acts as a competitive inhibitor against Fru-6-P with a Ki of 0.094 µM. Y29 also inhibits the HeLa cell growth with a GI50 of 2.7 µM. |
|
| DC71136 |
β-L-Fucopyranosyl phosphate |
β-L-Fucopyranosyl phosphate can be used for the research of carbohydrate metabolism. Glycosyl phosphates play crucial roles in carbohydrate metabolism as metabolic regulators or ubiquitous intermediates for glycoconjugate biosynthesis. |
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