Our product range includes a wide range of magnesium valproate api manufacturer india, memantine hcl api manufacturer india, mercurochrome merbromin api manufacturer india, metoclopramide hcl api, sodium chloride api manufacturer india and mosapride citrate api manufacturer india.
An antiepileptic and anti neoplastic drug, our offered Magnesium Valproate is magnesium salt of valproic acid. This drug is precisely formulated at our end by our team of seasoned professionals using finest grade chemical compounds and advanced techniques under hygienic conditions. The offered drug is used for treating various medical issues. Further, this drug is available for our esteemed clients in desired quantities to cater to their varied requirements at market leading prices.
Common salt produced by us is commonly used as a condiment and food preservative. It is one of the most commonly used edible salts so; it is kept away from all the other toxic salts at our plant, as well as supplied separately. It is also used as a flavor enhancer and for de-icing.
Used in biochemistry and molecular biology applications; a component of PBS and SSC buffers
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Mosapride Citrate API MANUFACTURER INDIA
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A selective SR-4 activator and a SR-3 inhibitor
Mosapride citrate is a selective SR-4 agonist and SR-3 antagonist.
An antibacterial agent that inhibits the activities of Topo II (DNA gyrase) and topoisomerase IV
Moxifloxacin Hydrochloride is the hydrochloride salt preparation of Moxifloxacin, an 8-methoxy-fluoroquinone compound with broad-spectrum bactericidal activity against gram-positive and gram-negative strains. 8-methoxy-fluoroquinones are described to inhibit the activities of Topo II (DNA gyrase) and topoisomerase IV. The 8-methoxy group of Moxifloxacin is suggested to confer a lowered propensity for resistance development as compared to other C-8 substituted quinolones, and Moxifloxacin demonstrates potent activity against wild-type and first-step gyrase- and topoisomerase IV-resistant mutants. Moxifloxacin shows activity against methicillin-susceptible staphylococci, penicillin-susceptible and penicillin-resistant pneumococci, penicillin-susceptible and penicillin-resistant viridans group streptococci, group A streptococci, M. catarrhalis, and H. influenzae in vitro.
An antineoplastic antimetabolite with immunosuppressant properties. It is an inhibitor of tetrahydrofolate dehydrogenase and prevents the formation of tetrahydrofolate, necessary for synthesis of thymidylate, an essential component of DNA.
A useful inhibitor of cGMP-mediated processes and a useful stain
Methylene Blue acts as a GCS (guanylyl cyclase) inhibitor, biological stain and redox indicator. Methylene Blue inhibits tau filament formation. Additionally, Methylene Blue is also reported to inhibit NOSs (nitric oxide synthase). Methylene Blue is widely used to inhibit cGMP-mediated processes. Methylene Blue has been observed to dose-dependently induce cytotoxicity in U-373 MG human astrocytoma and SK-N-MC human neuroblastoma cells. Furthermore Methylene Blue is reported to bind to the M2 subtype of muscarinic receptors in rat cardiac myocytes, and thus exhibit antimuscarinic effects on IK, ACh and ICa. Methylene Blue has also been reported to inhibit endothelium-dependent relaxation of isolated blood vessels.
Ci 52015; S No 1038; Swiss Blue; Chromosmon; Ci No 52015; D&Cblueno.1;Basic Blue 9; Methylene Blue; Ci Basic Blue 9; Methylenebluegr
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Nizatidine Powder API MANUFACTURER INDIA
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A histamine H2 receptor antagonist with low toxicity that inhibits gastric acid secretion. The drug is used for the treatment of duodenal ulcers.
Metaxalone (marketed by King Pharmaceuticals under the brand name Skelaxin) is a muscle relaxant used to relax muscles and relieve pain caused by strains, sprains, and other musculoskeletal conditions. Its exact mechanism of action is not known, but it may be due to general central nervous system depression. It is considered to be a moderately strong muscle relaxant, with relatively low incidence of side effects. Skelaxin comes in an 800 mg scored tablet. It previously came in both 400 mg and 800 mg tablets. The 400 mg tablet has been discontinued. Possible side effects include nausea, vomiting, drowsiness and CNS side effects such as dizziness, headache, and irritability.
Olmesartan Medoxomil is an angiotensin II receptor (AT1) antagonist. This compound also inhibits the negative regulatory feedback on renin secretion. The result of receptor inhibition is vasodilation and a reduction in peripheral resistance.
Mycophenolate sodium (Myfortic of Novartis) is an immunosuppressant drug used to prevent rejection in organ transplantation. It inhibits an enzyme needed for the growth of T cells and B cells. Mycophenolate sodium is indicated for the prevention of renal transplant rejection in adults. Mycophenolate sodium has also been used for the prevention of rejection in liver, heart, and/or lung transplants in children older than two years.An immunosuppressant that has drastically decreased the incidence of acute rejection in solid transplant recipients, Mycophenolate sodium is increasingly utilized as a steroid sparing treatment in immune-mediated disorders including immunoglobulin-A nephropathy, small vessel vasculitides, and psoriasis.
sodiummycophenolate; MYCOPHENOLATE SODIUM; mycophenolicmonosodiumsalt; mycophenolicacidmonosodiumsalt; 4-Hexenoic acid,6-(1,3-dihydro-4-hydroxy-6-Methoxy-7-Methyl-3-oxo-5-isobenzofuranyl)-4-Methyl-,sodiuM salt
Nimesulide is a relatively COX-2 selective, non-steroidal anti-inflammatory drug (NSAID) with analgesic and antipyretic properties. Its approved indications are the treatment of acute pain, the symptomatic treatment of osteoarthritis and primary dysmenorrhoea in adolescents and adults above 12 years old. Due to concerns about the risk of hepatotoxicity, nimesulide has been withdrawn from market in many countries.
For the treatment of acute pain, the symptomatic treatment of osteoarthritis and primary dysmenorrhoea in adolescents and adults above 12 years old.
Letrozole is an oral non-steroidal aromatase inhibitor that has been introduced for the adjuvant treatment of hormonally-responsive breast cancer Estrogens are produced by the conversion of androgens through the activity of the aromatase enzyme.
IUPAC name - 4-[(4-cyanophenyl)-(1,2,4-triazol-1-yl)methyl]benzonitrile
Triamcinolone topical is used to treat the itching, redness, dryness, crusting, scaling, inflammation, and discomfort of various skin conditions, including psoriasis (a skin disease in which red, scaly patches form on some areas of the body and eczema
Pentoxifylline, also known as oxpentifylline, is a xanthine derivative used as a drug to treat muscle pain in people with peripheral artery disease. It is generic and sold under many brand names worldwide
Lysergol is a achromatic aggravate clear or white apparent powder.It is odorless and tasteless.It is decaying in case of ablaze or air.However, lysergol can be activated as an average in the accomplish of some ergoloid medicines.
A selective ATP dependent K+ (Kir6) channel activator
Minoxidil (U-10858) is a selective ATP dependent K+ channel (Kir6) activator. As a result membrane permeability increases the flow of K+ across the membrane, which turns off voltage gated calcium channels. This inhibition in action potential causes a relaxation in arteriolar smooth muscle. Alternate studies indicate that Minoxidil (U-10858) activates the β-catenin pathway in human dermal papilla cells which results in accumulation of β-catenin in the nucleus.
Omeprazole is a cell-permeable, selective proton pump inhibitor. Omeprazole undergoes an acid-catalyzed rearrangement to a thiol-reactive cationic sulfenamide that inhibits (H+-K+)-ATPase in the gastric milieu. Omeprazole also acts as an aryl hydrocarbon-like inducer of cytochrome P450 secretion in human liver. This compound is an inhibitor a variety of CYP isoenzymes, including CYP2C19, CYP2C9 and CYP3A.
Alendronate is a nitrogen-containing, second generation bisphosphonate. Bisphosphonates were first used to treat Paget’s disease in 1971. This class of medications is comprised of inorganic pyrophosphate analogues that contain non-hydrolyzable P-C-P bonds. Similar to other bisphosphonates, alendronate has a high affinity for bone mineral and is taken up during osteoclast resorption. Alendronate inhibits farnesyl pyrophosphate synthetase, one of the enzymes in the mevalonic acid pathway involved in producing isoprenoid compounds that are essential for post-translational modification of small guanosine triphosphate (GTP)-binding proteins, such as Rho, Ras and Rab. Inhibition of this process interferes with osteoclast function and survival. Alendronate is used for the treatment of osteoporosis and Paget’s disease.
Nifedipine has been formulated as both a long- and short-acting 1,4-dihydropyridine calcium channel blocker. It acts primarily on vascular smooth muscle cells by stabilizing voltage-gated L-type calcium channels in their inactive conformation. By inhibiting the influx of calcium in smooth muscle cells, nifedipine prevents calcium-dependent myocyte contraction and vasoconstriction. A second proposed mechanism for the drug’s vasodilatory effects involves pH-dependent inhibition of calcium influx via inhibition of smooth muscle carbonic anhydrase. Nifedipine is used to treat hypertension and chronic stable angina.
For the management of vasospastic angina, chronic stable angina, hypertension, and Raynaud''s phenomenon. May be used as a first line agent for left ventricular hypertrophy and isolated systolic hypertension (long-acting agents).
Mebeverine Hydrochloride (Meh-bev-er-reen hi-droh-clor-ride) is a medicine which is used in irritable bowel syndrome. Mebeverine Hydrochloride is an antispasmodic which helps to relieve the pain and discomfort associated with gastrointestinal spasms.
An anti-inflammatory agent, structurally related to the salicylates, which is active in inflammatory bowel disease. It is considered to be the active moiety of sulphasalazine. MESALAMINE POWDER JAIRADHESALES
Metformin hydrochloride is an oral antihyperglycemic drug used in the management of type 2 diabetes. Metformin hydrochloride (N,N -dimethylimidodicarbonimidic diamide hydrochloride) is not chemically or pharmacologically related to any other classes of oral antihyperglycemic agents.
Metformin Hydrochloride Imp. D (Ep): 1,3,5-Triazine-2,4,6-Triamine (Melamine) Mm(Crm Standard)