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| Product | Description | |
|---|---|---|
| 1-(2,2,2-Trifluoro-N-phenylethanimidate)-2,3,4-tri-O-acetyl-D-glucopyranuronic acid methyl ester | 1-(2,2,2-Trifluoro-N-phenylethanimidate)-2,3,4-tri-O-acetyl-D-glucopyranuronic acid methyl ester is a profoundly efficacious and multifaceted biomedical compound. With an intricate mode of action, it selectively interacts with targeted receptors and enzymes, effectively ameliorating the symptoms associated with inflammation, pain, and allergic responses. Group: Pharmaceutical. CAS No. 869996-05-4. Pack Sizes: 100 mg. Product ID: B1370-000042. Molecular formula: Custom synthesis is available. Send your inquiries for more information. |  London |
| 5-Carboxytetramethylrhodamine succinimidyl ester | 5-Carboxytetramethylrhodamine succinimidyl ester is an amine-reactive, orange-fluorescent dye used for labeling DNA and RNA. It also has been used to create bioconjugates with peptides, proteins and enzymes. Group: Pharmaceutical. CAS No. 150810-68-7. Pack Sizes: 250 mg. Product ID: B0001-331300. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| 6-Maleimidohexanoic Acid N-Hydroxysuccinimide Ester | 6-Maleimidohexanoic Acid N-Hydroxysuccinimide Ester is used for preparation of enzyme immunoconjugates and hapten carrier molecule conjugates. Uses: Adcs linker. Group: Pharmaceutical. CAS No. 55750-63-5. Pack Sizes: 100 g. Product ID: BAT-008147. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Acaterin | Acarbose is an acyl-CoA isolated from Pseudomonas species. A92. In the presence of oxidized low-density lipoprotein in macrophages J744, the synthesis of cholesterol enzymes is inhibited, with an IC50 of 45 μmol/L, and the IC50 for inhibiting ACAT in rat liver microsomes is 120 μmol/L. Inhibition of ACAT is non-competitive Sexual. Group: Pharmaceutical. CAS No. 144398-20-9. Pack Sizes: 1mg; 1g; 10g. Product ID: BBF-00539. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Acetyl coenzyme A-[13C2] lithium salt | Acetyl coenzyme A-[13C2] lithium salt, is the labelled analogue of Acetyl coenzyme A. Acetyl coenzyme A is the precursor to HMG CoA, an essential component in the synthesis of cholesterol and ketone. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Product ID: BLP-000009. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Amrinone | Amrinone is a selective cAMP phosphodiesterase (PDE-3) inhibitor with positive inotropic and vasodilatory activity. It is a simple, non-glycoside cardiotonic agent. It provides protection against ischemia-reperfusion injury in kidney, liver, and heart. It has the ability to stimulate calcium ion influx into the cardiac cell. It is used in the treatment of congestive heart failure. It increases cardiac contractility as a vasodilator. It acts by inhibiting the breakdown of both cAMP and cGMP by the phosphodiesterase (PDE3) enzyme. It is a drug that may improve the prognosis in patients with congestive heart failure. It has been shown to increase the contractions initiated in the heart by high gain calcium induced calcium release (CICR). It was developed by Sanofi and has been listed. Uses: Amrinone is a simple, non-glycoside cardiotonic agent. it provides protection against ischemia-reperfusion injury in kidney, liver, and heart. it is used in the treatment of congestive heart failure. it increases cardiac contractility as a vasodilator. Group: Pharmaceutical. CAS No. 60719-84-8. Pack Sizes: 2.5 g. Product ID: B0084-072903. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Atorvastatin N-(3,5-Dihydroxy-7-heptanoic Acid)amide | Atorvastatin N-(3,5-Dihydroxy-7-heptanoic Acid)amide is a prominent compound in the research of dyslipidemia and associated cardiovascular disorders. Its efficacious mechanism of action lies in its tremendous capacity to inhibit HMG-CoA reductase, a pivotal enzyme profoundly engaged in the intricate process of cholesterol biosynthesis. Uses: Atorvastatin (a791750) impurity. Group: Pharmaceutical. CAS No. 1105067-87-5. Pack Sizes: 10 mg. Product ID: B0190-258830. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Diosgenin | Diosgenin, a steroid sapogenin, is the product of hydrolysis by acids, strong bases, or enzymes of saponins, extracted from the tubers of Dioscorea wild yam, such as the Kokoro. The sugar-free (aglycone), diosgenin is used for the commercial synthesis of cortisone, pregnenolone, progesterone, and other steroid products. Diosgenin is an important medicine for the treatment of cardiovascular diseases, leukemia, encephalitis, skin diseases and tumors. Uses: Anti-inflammatory and anticancer. Group: Pharmaceutical. CAS No. 512-04-9. Pack Sizes: 250 g. Product ID: NP6077. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Fosinopril sodium salt | Fosinopril Sodium is the ester prodrug of an angiotensin-converting enzyme (ACE) inhibitor. Group: Pharmaceutical. CAS No. 88889-14-9. Pack Sizes: 5 g. Product ID: B2693-079000. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Ganoderol A | Ganoderol A,a natural triterpenoid found in the fruiting body of Ganoderma lucidum, has the activity of anti-inflammatory and protection against UVA damage, these founctions show that ganoderol A is a candidate for the development of a suitable product to protect skin from UV-induced photoaging. Ganoderol A exhibits potent inhibitory activity against angiotensin converting enzyme activity. Via conversion of acetate or mevalonate as a precursor of the compound, ganoderal A exhibits potent inhibitory activity against cholesterol biosynthesis. Uses: Anti-inflammatory. Group: Pharmaceutical. CAS No. 104700-97-2. Pack Sizes: 1 mg. Product ID: NP6284. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Irinotecan Hydrochloride Trihydrate | The hydrochloride salt of Irinotecan. Irinotecan is a prodrug that can be activated to 7-ethyl-10-hydroxy-camptothecin (SN-38) by the carboxylesterase-converting enzyme. SN-38 inhibits topoisomerase I to suppress DNA replication and promote cell death. Group: Pharmaceutical. CAS No. 136572-09-3. Pack Sizes: 1 g. Product ID: B0084-057943. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| L-α-Aspartyl-D-phenylalanine methyl ester | L-α-Aspartyl-D-phenylalanine methyl ester, a dipeptide compound, bears promise in the biomedical sector for its potential inhibitory impact on angiotensin converting enzyme (ACE), thus potentially reducing blood pressure levels. It has also shown potential in the treatment of hypertensive, cardiac failure, and other cardiovascular conditions. The study of its properties continues to generate interest and attention from academia and the scientific community. Group: Pharmaceutical. CAS No. 22839-65-2. Pack Sizes: 50 mg. Product ID: B2699-116576. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Mevastatin | It is produced by the strain of Penicillum brevicompactum. It has weak anti-fungal activity and can inhibit the key enzyme (3-hydroxy-3-methyl glutaryl coenzyme A(HMGCoA) reductase) in the cholesterol biosynthesis pathway. It has been shown to lower cholesterol in animals and humans. It led the discovery of statins, lipid-lowering drugs. It is now used as a biochemical reagent. Uses: Hydroxymethylglutaryl-coa reductase inhibitors. Group: Pharmaceutical. CAS No. 73573-88-3. Pack Sizes: 25 g. Product ID: BBF-01732. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Physostigmine salicylate | Physostigmine salicylate is a cholinesterase inhibitor that can cross blood-brain barrier. It forms slowly degrading carbamylated enzyme complex with acetylcholinesterase (AChE). It has been used to improve cognitive ability and treat glaucoma. Group: Pharmaceutical. CAS No. 57-64-7. Pack Sizes: 250 mg. Product ID: B0084-028331. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Rilapladib | Rilapladib is the third genomics-derived small molecule drug as a lipoprotein-associated phospholipase A2 (Lp-PLA2) inhibitor which is an enzyme associated with the formation of atherosclerotic plaques. Uses: 1-alkyl-2-acetylglycerophosphocholine esterase inhibitors. Group: Pharmaceutical. CAS No. 412950-08-4. Pack Sizes: 50 mg. Product ID: B1370-068407. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Sacubitril | Sacubitril, also known as AHU377 or LCZ696, is an angiotensin receptor neprilysin inhibitor being studied for use in combination with valsartan for heart failure. Sacubitril is a prodrug that is activated to LBQ657 by de-ethylation via esterases. LBQ657 inhibits the enzyme neprilysin, which is responsible for the degradation of atrial and brain natriuretic peptide, two blood pressure lowering peptides that work mainly by reducing blood volume. Group: Pharmaceutical. CAS No. 149709-62-6. Pack Sizes: 10 g. Product ID: B0084-458470. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Tannase | Tannase is an enzyme (EC 3.1.1.20) that catalyzes the hydrolysis of ester bonds present in gallotannins, complex tannins, and gallic acid esters. Group: Pharmaceutical. CAS No. 9025-71-2. Pack Sizes: 1 g. Product ID: B1370-154774. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Tretazicar | Tretazicar (CB1954) is a dinitrobenzamide prodrug that is converted in the presence of the enzyme NQO2 and co-substrate caricotamide (EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent. CB1954 has been proposed for use in enzyme-prodrug gene therapy systems with the Escherichia coli enzyme nitroreductase (Ntr). Ntr converts CB1954 to 2- and 4-hydroxylamino derivatives, whereupon the non-enzymatic reaction of the 4-hydroxylamino derivative with cellular thio- esters generates a potent cytotoxic bifunctional alkylating agent capable of cross-linking DNA. Ntr delivery has been achieved in vitro using retroviral and adenoviral vectors and confirmed by immunocytochemical demonstration of Ntr expression. The Ntr-expressing cells have been shown to be sensitized to CB1954 by up to 2000-fold. The Ntr-CB1954 system shows effective bystander killing in mixed populations of Ntr-expressing and non-expressing cells treated with CB1954. The efficacy of this enzyme-prodrug approach in model systems compared with other VDEPT approaches demonstrates the feasibility and future promise of this gene therapy strategy. Uses: Antineoplastic agents. Group: Pharmaceutical. CAS No. 21919-05-1. Pack Sizes: 1 g. Product ID: B2693-366889. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
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