Pitavastatin Manufacturer

"Quality first, Honesty as base, Sincere service and mutual profit" is our idea, in order to develop continuously and pursue the excellence for Pitavastatin Manufacturer, Doxycycline Monohydrate For Pneumonia, Amiloride And Hydrochlorothiazide, Doxycycline Hyclate 100mg For Ear Infection, We focus on to make excellent quality products to supply service for our clients to establish long-term win-win relationship. We will devote ourselves to giving our esteemed buyers using the most enthusiastically thoughtful services for Pitavastatin Manufacturer, In order to meet our market demands, we have paied more attention to the quality of our products and services. Now we can meet customers' special requirements for special designs. We persistently develop our enterprise spirit "quality lives the enterprise, credit assures cooperation and keep the motto in our minds: customers first.


  • Pitavastatin Calcium

    Pitavastatin Calcium

    API’s Name Indication Specification US DMF  EU DMF  CEP
    Pitavastatin Calcium Hypercholesterolemia In-House      
  • OEM Manufacturer Doxycycline Hyclate 100mg Español - Tofacitnib Citrate  – CPF

    OEM Manufacturer Doxycycline Hyclate 100mg Español - Tofacitnib Citrate – CPF

    Background Tofacitinib citrate, also known as CP-690550 citrate, is a potent inhibitor of janus kinase 3 (JAK3), a hematopoetic cell-restricted tyrosine kinase involved in signal transduction regulating lymphocyte survival, proliferation, differentiation, and apoptosis.  The inhibition is JAK3 specific with a selectivity 1000-fold more than other non-JAK family kinases. Besides inhibiting JAKS (IC50 = 1 nM), tofacitinib citrate also inhibits janus kinase 2 (JAK2) and janus kinase 1 (JAK1) wit...
  • China Wholesale Rosuvastatin Calcium 20 Manufacturers - Ledipasvir Actone /PVP  – CPF

    China Wholesale Rosuvastatin Calcium 20 Manufacturers - Ledipasvir Actone /PVP – CPF

    雷迪帕韦丙酮/聚维酮 Ledipasvir actone/PVP 1256388-51-8 In-House     LPSM1   1256387-87-7 In-House     LPSM1-5   291775-59-2 In-House     LPSM2   1129634-44-1 In-House     LPS-6   1441670-89-8 In-House Ledipasvir acetone (GS-5885 acetone) is the active ingredient of Ledipasvir. Ledipasvir is an inhibitor of the hepatitis C virus NS5A, with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon. In Vitro Ledipasvir acetone is considered the active ingredient, which ...
  • China OEM Obeticholic Acid Supplier - LCZ696(Sacubitril + Valsartan)  – CPF

    China OEM Obeticholic Acid Supplier - LCZ696(Sacubitril + Valsartan) – CPF

    Description LCZ696 (Sacubitril/Valsartan), comprised Valsartan (an ARB) and Sacubitril (AHU377) in 1:1 molar ratio, is a first-in-class, orally bioavailable, and dual-acting angiotensin receptor-neprilysin (ARN) inhibitor for hypertension and heart failure[1][2][3]. LCZ696 ameliorates diabetic cardiomyopathy by inhibiting inflammation, oxidative stress and apoptosis.   Background LCZ696 is a first in class ARNi (angiotensin receptor neprilysin inhibitor) comprising anionic moieties of AR...
  • China Gold Supplier for Canagliflozin Prescribing Information - Rivaroxaban  – CPF

    China Gold Supplier for Canagliflozin Prescribing Information - Rivaroxaban – CPF

    Background Rivaroxaban, 5-chloro-N-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide, is a potent small-molecule inhibitor of factor Xa which is a coagulation factor at a critical juncture in the blood coagulation pathway resulting in the generation of thrombin and the formation of clot. Rivaroxaban binds to the Tyr288 in S1 pocket of factor Xa through the interaction of Tyr288 and the chlorine substituent of the chlorothiophene moiety. The inhi...
  • China Wholesale Rosuvastatin Supplier Factory - Canagliflozin  – CPF

    China Wholesale Rosuvastatin Supplier Factory - Canagliflozin – CPF

    Background Canagliflozin is a novel, potent, and highly selective sodium glucose co-transporter (SGLT) 2 inhibitor [1]. It has been proved that Canagliflozin can increase urine glucose excretion by reducing the renal glucose threshold and by decreasing the filtered glucose re-absorption [2]. Canagliflozin has been shown to inhibit the Na+-mediated 14C-AMG intakes in CHO-hSGLT2, CHO-rat SGLT2 and CHO-mouse SGLT2 with IC50 values of 4.4, 3.7 and 2.0 nM, respectively [1]. Canagliflozin has been ...
  • Wholesale Dealers of Hydrochlorothiazide 25 Mg Uses - LOXO-101 1223403-58-4  – CPF

    Wholesale Dealers of Hydrochlorothiazide 25 Mg Uses - LOXO-101 1223403-58-4 – CPF

    Background IC50: low nanomolar range for inhibition of all TRK family members LOXO-101 is a tropomyosin receptor kinases (TRK) inhibitor. The TRK family of neurotrophin receptors and their neurotrophin ligands regulate neuron growth, differentiation and survival. In vitro: In previous study, LOXO-101 was evaluated for off-target kinase enzyme inhibition against a panel of non-TRK kinases at a concentration of 1,000 nM and ATP concentrations around the Km. Results showed that LOXO-101 had grea...
  • OEM Supply Is Hydrochlorothiazide - Apixaban  – CPF

    OEM Supply Is Hydrochlorothiazide - Apixaban – CPF

    Background Apixaban is a highly selective and reversible inhibitor of Factor Xa with Ki values of 0.08 nM and 0.17 nM in human and rabbit, respectively[1]. Factor X, also known by the eponym Stuart–Prower factor, is an enzyme of the coagulation cascade. Factor X is activated, by hydrolysis, into factor Xa by both factor IX. Factor Xa is the activated form of the coagulation factorthrombokinase.Inhibiting Factor Xa could offer an alternate method for anticoagulation. Direct Xa inhibitors are p...
  • Discount wholesale Hydrochlorothiazide - LCZ696(Sacubitril + Valsartan)  – CPF

    Discount wholesale Hydrochlorothiazide - LCZ696(Sacubitril + Valsartan) – CPF

    Description LCZ696 (Sacubitril/Valsartan), comprised Valsartan (an ARB) and Sacubitril (AHU377) in 1:1 molar ratio, is a first-in-class, orally bioavailable, and dual-acting angiotensin receptor-neprilysin (ARN) inhibitor for hypertension and heart failure[1][2][3]. LCZ696 ameliorates diabetic cardiomyopathy by inhibiting inflammation, oxidative stress and apoptosis.   Background LCZ696 is a first in class ARNi (angiotensin receptor neprilysin inhibitor) comprising anionic moieties of AR...
  • Big discounting Doxycycline Monohydrate 50 Mg Tablet - Velpatasvir(PVP)  – CPF

    Big discounting Doxycycline Monohydrate 50 Mg Tablet - Velpatasvir(PVP) – CPF

    Foreign Names Velpatasvirum (Latin) Velpatasvir (German) Velpatasvir (French) Velpatasvir (Spanish) Generic Names Velpatasvir (OS: USAN) GS-5816 (IS) UNII-KCU0C7RS7Z (IS) Multi-ingredient medications containing velpatasvir:sofosbuvir/velpatasvir systemic Brand names: Epclusa Drug class(es): antiviral combinations Sofosbuvir/velpatasvir systemic is used in the treatment of:Hepatitis C sofosbuvir/velpatasvir/voxilaprevir systemic Brand names: Vosevi Drug class(es): antiviral combinations Sofosb...
  • Factory making Sofosbuvir Dosage - Rivaroxaban  – CPF

    Factory making Sofosbuvir Dosage - Rivaroxaban – CPF

    Background Rivaroxaban, 5-chloro-N-[[(5S)-2-oxo-3-[4-(3-oxomorpholin-4-yl)phenyl]-1,3-oxazolidin-5-yl]methyl]thiophene-2-carboxamide, is a potent small-molecule inhibitor of factor Xa which is a coagulation factor at a critical juncture in the blood coagulation pathway resulting in the generation of thrombin and the formation of clot. Rivaroxaban binds to the Tyr288 in S1 pocket of factor Xa through the interaction of Tyr288 and the chlorine substituent of the chlorothiophene moiety. The inhi...
  • Free sample for Pregabalin 100 Mg - Ezetimibe  – CPF

    Free sample for Pregabalin 100 Mg - Ezetimibe – CPF

    Background Ezetimibe is a potent and novel inhibitor of cholesterol absorption [1]. Cholesterol is a lipid molecule and is required to build and maintain membranes structural integrity and fluidity. Also, it serves as a precursor of vitamin D, bile acids and steroid hormones. In differentiated Caco-2 cells incubated with a carotenoid (1 μM), ezetimibe (10 mg/L) inhibited carotenoid transport with 50% inhibition for ɑ-carotene and β-carotene. Also, it inhibited the transport of β-cryptoxanthin...