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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC32615 | Talinolol Featured |
Talinolol is a beta(1)-adrenergic receptor antagonist and a probe drug for P-glycoprotein (P-gp) activity in humans.
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| DC23978 | hPGDS-IN-1 Featured |
hPGDS-IN-1 is a potent, selective hPGDS inhibitor with IC50 of 12 nM in FP or EIA assays..
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| DC21610 | Tafenoquine succinate Featured |
Tafenoquine succinate (SB-252263, Tafenoquine, WR 238605) is a long-acting, orally active anti-malarial agent to prevent malaria that is holoendemic for Plasmodium falciparum..
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| DC10064 | GSK-F1 Featured |
GSK-F1 is a potent inhibitor of PI4KA.
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| DC23895 | AY-9944 Featured |
AY 9944 is a specific cholesterol biosynthesis inhibitor. AY 9944 inhibits the 7-dehydro cholesterol Δ7-reductase (DHCR7) enzyme (IC50=13 nM). AY 9944 causes hypocholesterolemia and accumulation of 7DHC. At high doses, AY 9944 inhibits also in cultured embryos sterol Δ7-Δ8 isomerase, which causes the accumulation of cholest-8-en-3β-ol.
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| DC22191 | PBT434 Featured |
PBT434 is a novel quinazolinone compound with effect of lowering cellular iron levels, prevents iron mediated neurodegeneration and α-synuclein toxicity in multiple models of Parkinson disease; inhibits iron-mediated redox activity and iron-mediated aggregation of α-synuclein, a protein that aggregates in the neuropathology; prevents loss of substantia nigra pars compacta neurons (SNpc), lowers nigral α-synuclein accumulation, and rescues motor performance in mice model of PD.
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| DC42212 | 1,3-Oxazolidine-2-thione |
1,3-Oxazolidine-2-thione, a free oxazolidinethione, increases thyroid size and severely depresses hepatic trimethylamine oxidase activity in the laying diet domestic fowl.
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| DC42194 | 1-Phenylpropane-1,2-dione |
1-Phenylpropane-1,2-dione, isolated from young Ephedra sinica Stapf (Ephedraceae), is biosynthetic precursors of the ephedrine alkaloids.
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| DC42146 | Isoquinoline |
Isoquinoline is an analog of?pyridine. Isoquinoline structural-based alkaloids, such as tropoloisoquinoline, phthalideisoquinoline, and naphthylisoquinoline has anti-cancer activities.
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| DC42133 | Methyl palmitoleate |
Methyl palmitoleate ((Z)-Methyl hexadec-9-enoate), a fatty acid methyl ester, is an analogue of Palmitoleate with cytoprotective and growth-promoting properties.
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| DC42120 | cis-3-Hexen-1-ol |
cis-3-Hexen-1-ol ((Z)-3-Hexen-1-ol) is a green grassy smelling compound found in many fresh fruits and vegetables. cis-3-Hexen-1-ol is widely used as an added flavor in processed food to provide a fresh green quality. cis-3-Hexen-1-ol is an attractant to various insects.
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| DC42111 | β-Cyclocitral |
β-Cyclocitral, a volatile oxidized derivative of β-carotene, is a grazer defence signal unique to the Cyanobacterium Microcystis. β-Cyclocitral, one of the predominant volatile terpenoid compounds, can upregulate the expression of defence genes to enhance excess light (EL) acclimation. β-Cyclocitral is a powerful repellent.
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| DC42108 | Diethyl fumarate |
Diethyl fumarate is a decomposition product of Malathion (an insecticide). Diethyl fumarate is a reputed skin irritant. Diethyl fumarate can causes non-immunologic contact urticaria on skin.
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| DC42100 | Methyl behenate |
Methyl behenate (Methyl docosanoate) is a naturally fatty acid methyl ester isolated from the plant of Aspidopterys obcordata Lemsl.
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| DC41484 | Pennogenin |
Pennogenin is a bioactive component which can be isolated from T. govanianum rhizomes. Pennogenin exhibits significant in vitro inhibitory effect on release of ROS.
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| DC41479 | Debenzoylpaeoniflorgenin |
Debenzoylpaeoniflorgenin is a natural compound from Paeonial lactiflora in Guizhitang.
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| DC41470 | Isotoosendanin |
Isotoosendanin is a limonoid isolated from Melia toosendan fruit. Isotoosendanin displays significant anti-inflammatory and analgesic activities.
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| DC41466 | Podophyllol |
Podophyllol, a derivative of podophyllotoxin esters, has antitumor activity.
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| DC41458 | Euphorbetin |
Euphorbetin, isolated from the ethyl acetate extract of the dried whole plants of Viola yedoensis Makino, exhibits anticoagulant activities.
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| DC41457 | Saikogenin F |
Saikogenin F is isolated from the chloroform extract of the Chinese medicine formula Shenqi San. Anti-cancer activity.
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| DC41456 | Taccalonolide C |
Taccalonolides C, isolated from T. plantaginea, is an anti-cancer agent.
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| DC41452 | Neoanhydropodophyllol |
Neoanhydropodophyllol is a cyclolignan derivative, with antineoplastic activity. Neoanhydropodophyllol displays cytotoxicity against several cancer cells (leukemia, lung carcinoma, colon carcinoma).
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| DC41446 | Deoxylimonin |
Desoxylimonin is a triterpenoid compound isolated from grapefruit seed. Desoxylimonin derivatives has better anticancer, analgesic and anti-inflammatory activitythan the lead compound.
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| DC41445 | Dihydrolapachenole |
Dihydrolapachenole is a naturally occurring quinone.
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| DC41437 | Acetylatractylodinol |
Acetylatractylodinol, isolated from Atractylodes lancea, possesses antioxidant activity.
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| DC41428 | Safranal |
Safranal is an orally active main component of Saffron (Crocus sativus) and is responsible for the unique aroma of this spice. Safranal has neuroprotective and anti-inflammatory effects and has the potential for Parkinson’s disease research.
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| DC41426 | Cognac oil |
Cognac oil, mainly found in wine lees, has unique fatty acid profiles, including Palmitic acid (59.26%), Linoleic acid (11.92%), Myristic acid (8.97%), Oleic acid (8.3%) and other fatty acids. Cognac oil leads to a general increase in the permeation of R6G (Rhodamine 6G) across all the membranes.
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| DC41412 | 2-(Hydroxymethyl)anthraquinone |
2-(Hydroxymethyl)anthraquinone is used as a photoremovable protecting group (PRPG) to chemically cage sex pheromone (e.g. (Z)-11-hexadecen-1-ol (sex pheromone of?Chilo infuscatellussnellen)).
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| DC41409 | Pentacosane |
Pentacosane is one of the major components in the acetone extract from Curcuma raktakanda and is also in the essential oil from the leaves of Malus domestica. Pentacosane exhibit anti-cancer activities.
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| DC41408 | Anhydroerythromycin A |
Anhydroerythromycin A is a degradation product of the macrolide antibiotic erythromycin. Anhydroerythromycin A is formed via degradation of erythromycin in acidic aqueous solutions in vitro as well as in vivo. Anhydroerythromycin A is active against S. aureus and B. cereus in vitro (MICs = 12.5 and 6.25 μg/ml, respectively). Anhydroerythromycin A also inhibits steroid 6β-hydroxylase activity associated with the cytochrome P450 (CYP) isoform CYP3A in human liver microsomes.
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