Cat. No. | Product Name | Field of Application | Chemical Structure |
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DCN-005 | Butylparaben Featured |
Butylparaben is an organic compound that has proven to be a very successful antimicrobial preservative in cosmetics, can also be used in active molecule suspensions, and as a food flavoring additive.
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DC33202 | Benzethonium Chloride Featured |
Benzethonium Chloride, also known as Hyamine, is synthetic quaternary ammonium salt that has surfactant, antiseptic, and anti-infective properties. Benzethonium Chloride is commonly used as a topical antimicrobial agent. Benzethonium chloride exhibited concentration-dependent inhibitions of HERG channel currents with IC(50) values of 4nM and 17nM, respectively, which were also voltage-dependent and use-dependent. Benzethonium Chloride shifted the channel activation I-V curves in a hyperpolarized direction for 10-15mV and accelerated channel activation and inactivation processes by 2-fold.
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DCY-156 | cis-9-Octadecenoic acid Featured |
cis-9-Octadecenoic acid is an abundant monounsaturated fatty acid. Oleic acid is a Na+/K+ ATPase activator.
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DCG-043 | Triolein Featured |
Triolein is a symmetric triacylglycerol that reduces upregulation of MMP-1 and has strong antioxidant and anti-inflammatory activities.
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DC37279 | Cetylpyridinium chloride Featured |
Cetylpyridinium chloride is a Germicide, Bactericide, and Disinfectant.
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DC31074 | Isopropyl myristate Featured |
Isopropyl myristate is the ester of isopropyl alcohol and myristic acid.
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DCW-004 | Citric acid Featured |
Citric acid is a natural preservative and food tartness enhancer. Citric acid induces apoptosis and cell cycle arrest at G2/M phase and S phase in HaCaT cells. Citric acid cause oxidative damage of the liver by means of the decrease of antioxidative enzyme activities. Citric acid causes renal toxicity in mice.
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DC12469 | CYH33 Featured |
CYH33 (CYH-33) is a novel potent, PI3Kα-selective inhibitor with IC50 of 5.9 nM/598 nM/ 78.7 nM/225 nM aginst class I PI3K isoform α/β/δ/γ, respectively.
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DC31669 | Dydrogesterone Featured |
Dydrogesterone is a synthetic progestin. Dydrogesterone alone or in combination with estrogen to endothelial cells results in neutral effects on NO synthesis and on the activity and expression of eNOS. Unlike many other progestational compounds, dydrogesterone produces no increase in temperature and does not inhibit ovulation.
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DCC2242 | GFB-12811 Featured |
GFB-12811 is a high selective and orally active CDK5 inhibitor with an IC50 of 2.3 nM. GFB-12811 is highly selective over the other tested kinases (CDK1/2/6/7/9).
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DC24085 | Rigosertib sodium Featured |
Rigosertib sodium (ON 01910.Na) is a potent, non-ATP-competitive PLK1 inhibitor (IC50=9-10 nM), selectively induces mitotic G2/M arrest and apoptosis in cancer cells.
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DC7267 | Riociguat (BAY 63-2521) Featured |
Riociguat (BAY 63-2521) is a stimulator of soluble guanylate cyclase (sGC).
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DC24050 | Anamorelin hydrochloride Featured |
A non-peptide, centrally-penetrant and selective agonist of GHSR with appetite-enhancing and anabolic effects.
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DC36997 | Acth (4-10) Featured |
ACTH (4-10) is a water soluble potent melanocortin receptor agonist.
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DC31537 | Amisulpride Featured |
Amisulpride is an atypical antipsychotic used to treat psychosis in schizophrenia and episodes of mania in bipolar disorder. In Italy, it is also used as a treatment for dysthymia. It was introduced by Sanofi-Aventis in the 1990s. Its patent had expired by 2008 and hence generic formulations are now available.Amisulpride function primarily as a D2 and D3 receptor antagonist. It has high affinity for these receptors with dissociation constants of 2.2 nM and 2.4 nM, respectively. Although standard doses used to treat psychosis inhibit dopaminergic neurotransmission, low doses preferentially block inhibitory pre-synaptic autoreceptors.
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DCQ-064 | Penicillinase |
Penicillinase is a beta-lactamase. beta-lactamase enzymes inactivate beta-lactam antibiotics by hydrolyzing the peptide bond of the characteristic four-membered beta-lactam ring rendering the antibiotic ineffective.
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DC20123 | EC0489 |
EC0489, a conjugate of folic acid and desacetyl vinblastine hydrazide, is a high-affinity ligand for the folate receptor (FR). Refractory or metastatic Tumor. Small molecule-drug conjugate (SMDC).
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DCZ-284 | Allosecurinine |
Allosecurinine (Phyllochrysine) is a Securinega alkaloid isolated from Phyllanthus glaucus .
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DCQ-080 | Dehydrotrametenolic acid |
Dehydrotrametenolic acid is a sterol isolated from the sclerotium of Poria cocos. Dehydrotrametenolic acid induces apoptosis through caspase-3 pathway. Dehydrotrametenolic acid has anti-tumor activity, anti-inflammatory, anti-diabetic effects.
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DCZ-048 | ligupurpuroside B |
Ligupurpuroside B is a glycoside isolated from Ligustrum robustum, with antioxidant activity.
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DCZ-047 | Ligupurpuroside A |
Ligupurpuroside A is an active product that can be extracted from Ligustrum robustum. Ligupurpuroside A acts as a natural inhibitor of lipase in a competitive manner.
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DCJ-063 | 10-Methoxycamptothecin |
10-Methoxycamptothecin is a natural bioactive derivative of camptothecin (CPT) isolated from Camptotheca acuminata, and has been confirmed to possess high anti-cancer properties. 10-Methoxycamptothecin has higher cytotoxicity than 10-hydroxycamptothecin by testing antitumor activity against 2774 cell lines.
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DCZ-049 | Ligupurpuroside C |
Ligupurpuroside C is a natural phenylethanoid glycoside isolated from Kudingcha.
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DCZ-050 | Ligupurpuroside D |
Ligupurpuroside D is a phenylethanoid glycoside that can be isolated from Ligustrum purpurascens. Ligupurpuroside D has antioxidant activity.
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DCZ-051 | cis- Ligupurpuroside B |
cis-Ligupurpuroside B is a phenylethanoid glycoside that can be found L. purpurascens.
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DCL-064 | Foresaconitine |
Foresaconitine(Vilmorrianine C) is a norditerpenoid alkaloid isolated from the processed tubers of Aconitum carmichaeli.
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DCQ-069 | Dehydrodicentrine |
Dehydrodicentrine is an alkaloid inhibitor of acetylcholinesterase (AChE) (IC50=2.98 μM). Dehydrodicentrine.
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DCR-042 | Lonicerin |
Lonicerin is an anti-algE (alginate secretion protein) flavonoid with inhibitory activity for P. aeruginosa. Lonicerin prevents inflammation and apoptosis in LPS-induced acute lung injury.
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DCY-111 | Heteroclitin D |
Heteroclitin D is a lignin from Kadsura medicinal plants with anti-liqid peroxidation. Heteroclitin D inhibits L-type calcium channels.
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DCC-080 | Waltonitone |
Waltonitone is a ursane-type pentacyclic triterpene isolated from Gentian waltonii Burkill. Waltonitone significantly inhibits hepatocellular carcinoma cells growth and induces apoptosis in vitro and in vivo.
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