Ezhou Hengtong Weiye Chemical Co., Ltd.

Propranolol Hydrochloride is a widely used non-cardioselective beta-adrenergic antagonist. Target: beta- Adrenergic Receptor Propranolol is a sympatholytic non-selective beta blocker.

Carbenicillin Disodium is a broad-spectrum semisynthetic penicillin derivative used parenterally. Target: Antibacterial Carbenicillin is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of gram-negative bacteria while displaying low toxicity.

Buflomedil HCl is a vasodilator used to treat claudication or the symptoms of peripheral arterial disease. Target: Others Buflomedil is a vasoactive drug used to treat claudication or the symptoms of peripheral arterial disease.

Phenytoin is an inactive voltage-gated sodium channel stabilizer. Target: Sodium Channel Phenytoin is an antiepileptic drug.

Nitrendipine is a calcium channel blocker with marked vasodilator action. Target: Calcium Channel Nitrendipine is a dihydropyridine calcium channel blocker.

Captopril is a potent, competitive inhibitor of angiotensin-converting enzyme (ACE). Target: ACE Captopril has been shown to have similar morbidity and mortality benefits to those of diuretics and beta-blockers in hypertensive patients.

Enalapril Maleate, the active metabolite of enalapril, is an angiotensin-converting enzyme (ACE) inhibitor. Target: ACE Enalapril is a prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications.

Hydroxyurea is an antineoplastic agent that inhibits DNA synthesis through the inhibition of ribonucleoside diphosphate reductase. Target: DNA/RNA Synthesis Hydroxyurea(Cytodrox) is an antineoplastic agent that inhibits DNA synthesis through the inhibition of ribonucleoside diphosphate reductase.

Dipyridamole (Persantine) is a phosphodiesterase inhibitor that blocks uptake and metabolism of adenosine by erythrocytes and vascular endothelial cells. Target: Phosphodiesterase (PDE) Dipyridamole concentrations of 1 nmol/ml blood caused 90% inhibition of adenosine metabolism.

Nimodipine(Nimotop) is a dihydropyridine derivative and an analogue of the calcium channel blocker nifedipine, with antihypertensive activity.Nimodipine decreases intracellular free Ca2+,Beclin-1 and autophagy. Target: Calcium Channel Nimodipine is main use is in the prevention of cerebral vasospasm and resultant ischemia, a complica...

Glipizide is used to treat high blood sugar levels caused by a type of diabetes mellitus called type 2 diabetes. Target: Potassiun Channel Glipizide is an oral rapid- and short-acting anti-diabetic drug from the sulfonylurea class.

Hydrochlorothiazide is a diuretic drug of the thiazide class.

Chloramphenicol is a broad-spectrum antibiotic. Target: Antibacterial Chloramphenicol is a bacteriostatic drug that stops bacterial growth by inhibiting protein synthesis.

Epiandrosterone is a steroid hormone with weak androgenic activity, is a natural metabolite of DHEA.

Cyclophosphamide is a synthetic alkylating agent chemically related to the nitrogen mustards with antineoplastic and immunosuppressive activities.

Ifosfamide is a nitrogen mustard alkylating agent used in the treatment of cancer. IC50 Value: 1mM (in MCF-7 and MDA-MB231 cell lines, at 48 hr) [1] Target: DNA alkylating agent Ifosfamide (IF) is a prodrug requiring metabolic activation to produce 4-hydroxyifosfamide (4-OHIF), which breaks down to form isophosphoramide mustard.

Levamisole Hcl is an anthelmintic and immunomodulator belonging to a class of synthetic imidazothiazole derivatives. IC50 value: Target: Levamisole suppresses the production of white blood cells, resulting in neutropenia and agranulocytosis.

Zidovudine (Azidothymidine, AZT) is a nucleoside analog reverse-transcriptase inhibitor (NRTI), a type of antiretroviral drug used for the treatment of HIV/AIDS infection. IC50 value: Target: NRTI; reverse-transcriptase AZT is a thymidine analogue.

Tolterodine Tartrate(PNU-200583E; Kabi-2234) is a potent muscarinic receptor antagonists that show selectivity for the urinary bladder over salivary glands in vivo.