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Cat. No. Product Name Field of Application Chemical Structure
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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