Venetoclax Manufacturer

Our well-equipped facilities and superb good quality control throughout all stages of manufacturing enables us to guarantee total buyer gratification for Venetoclax Manufacturer, Credence Trial Canagliflozin, Brilinta Ticagrelor, Sofosbuvir 400 Mg, We welcome you to definitely inquire us by simply call or mail and hope to develop a prosperous and cooperative connection. With advanced technologies and facilities, strict high-quality handle, reasonable rate, superior services and close co-operation with prospects, we are devoted to furnishing the best price for our customers for Venetoclax Manufacturer, With the best technological support, we have tailored our website for the best user experience and kept in mind your ease of shopping. we ensure that the best reaches you at your doorstep, in the shortest possible time and with the help of our efficient logistical partners i.e DHL and UPS. We promise quality, living by the motto of promising only what we can deliver.


  • Venetoclax 1257044-40-8

    Venetoclax 1257044-40-8

    API’s Name Indication Innovator Patent Expiry Date(The U.S)
    Venetoclax 1257044-40-8 CLL Abbvie Jun.27,2031
  • Professional Design Doxycycline Hyclate And Doxycycline Monohydrate - Enalapril Maleate  – CPF

    Professional Design Doxycycline Hyclate And Doxycycline Monohydrate - Enalapril Maleate – CPF

    Background Enalapril Maleate Description Enalapril (maleate) (MK-421 (maleate)), the active metabolite of enalapril, is an angiotensin-converting enzyme (ACE) inhibitor. In Vivo Enalapril (MK-421) is a prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications. It is rapidly metabolized in the liver to enalaprilat following oral administration. Enalapril (MK-421) is a potent, competitive inhibitor of ACE, the enzyme responsible for the conversion of angio...
  • Factory Price Doxycycline Hyclate Español - Captopril  – CPF

    Factory Price Doxycycline Hyclate Español - Captopril – CPF

    Description Captopril (SQ-14534) is a potent, competitive inhibitor of angiotensin-converting enzyme (ACE). In Vitro Captopril (SQ-14534) has been shown to have similar morbidity and mortality benefits to those of diuretics and beta-blockers in hypertensive patients. Captopril (SQ-14534) has been shown to delay the progression of diabetic nephropathy, and enalapril and lisinopril prevent the development of nephropathy in normoalbuminuric patients with diabetes[1]. An equimolar ratio of the c...
  • China Wholesale Rosuvastatin Calcium Tablets Manufacturers - Venetoclax 1257044-40-8  – CPF

    China Wholesale Rosuvastatin Calcium Tablets Manufacturers - Venetoclax 1257044-40-8 – CPF

    维奈妥拉 Venetoclax 1257044-40-8 In-House     VCL-6A 98549-88-3 In-House     VCL-7A 1235865-75-4 In-House     VCLM2 1228780-72-0 In-House     VCLM2-2HCl 1628047-87-9 In-House     VCLM3 1228779-96-1 In-House Generic Name: venetoclax (ven ET oh klax) Brand Name: Venclexta, Venclexta Starting Pack Venetoclax is used to treat chronic lymphocytic leukemia or small lymphocytic leukemia in adults. Venetoclax is used alone or in combination with other cancer medicines to trea...
  • Leading Manufacturer for Daclatasvir Prescribing Information - Niraparib 1038915-60-4  – CPF

    Leading Manufacturer for Daclatasvir Prescribing Information - Niraparib 1038915-60-4 – CPF

    Description Niraparib (MK-4827) is a highly potent and orally bioavailable PARP1 and PARP2 inhibitor with IC50s of 3.8 and 2.1 nM, respectively. Niraparib leads to inhibition of repair of DNA damage, activates apoptosis and shows anti-tumor activity.   In Vitro Niraparib (MK-4827) inhibits PARP activity with EC50=4 nM and EC90=45 nM in a whole cell assay. MK-4827 inhibits proliferation of cancer cells with mutant BRCA-1 and BRCA-2 with CC50 in the 10-100 nM range. MK-4827 displays exce...
  • China Wholesale Rosuvastatin Calcium Generic Suppliers - Bictegravir 1611493-60-7  – CPF

    China Wholesale Rosuvastatin Calcium Generic Suppliers - Bictegravir 1611493-60-7 – CPF

    Description Bictegravir is a novel, potent inhibitor of HIV-1 integrase with an IC50 of 7.5 nM. In Vitro Bictegravir (BIC) inhibits the strand transfer activity with an IC50 of 7.5± 0.3 nM. Relative to its inhibition of strand transfer activity, Bictegravir is a much weaker inhibitor of 3′-processing activity of HIV-1 IN, with an IC50 of 241±51 nM. Bictegravir enhances the accumulation of 2-LTR circles ~5-fold relative to the mock-treated control and reduces the amount of authentic integrati...
  • New Arrival China Obeticholic Acid Nash - Baloxavir Marboxil 1985606-14-1  – CPF

    New Arrival China Obeticholic Acid Nash - Baloxavir Marboxil 1985606-14-1 – CPF

    Background Baloxavir marboxil is an antiviral drug and is an endonuclease inhibitor. In rats and monkeys, the blood concentration of the drug is lower than the minimum detection amount in a single oral administration of the drug. In preclinical influenza A and B infection models (including strains that are resistant to existing antiviral drugs), Baloxavir marboxil has a certain effect. Chemical Properties Storage Store at -20°C M.Wt 571.55 Cas No. 1985606-14-1 Formula C27H23F2N3O7S ...
  • New Arrival China Sofosbuvir Tablets 400 Mg - Doxycycline Hyclate  – CPF

    New Arrival China Sofosbuvir Tablets 400 Mg - Doxycycline Hyclate – CPF

    Background Doxycycline hyclate is an antibiotic [1]. Doxycycline hyclate is a derivative of tetracycline and possesses the activities of anti-inflammatory and antimicrobial. Doxycycline inhibits dengue virus replication in vitro with a temperature-dependent manner. The IC50 value is 52.3μM at 37°C and 26.7μM at 40°C. It inhibits the dengue virus via inhibiting the NS2B-NS3 serine protease of the virus. 60μM doxycycline reduces the CPE of the DNEV2-infected cells [1]. Doxycycline is found to b...
  • 2020 wholesale price Canagliflozin Ppt - Pregabalin  – CPF

    2020 wholesale price Canagliflozin Ppt - Pregabalin – CPF

    Pregabalin is not a GABAA or GABAB receptor agonist. Pregabalin is a gabapentinoid and acts by inhibiting certain calcium channels. Specifically it is a ligand of the auxiliary α2δ subunit site of certain voltage-dependent calcium channels (VDCCs), and thereby acts as an inhibitor of α2δ subunit-containing VDCCs. There are two drug-binding α2δ subunits, α2δ-1 and α2δ-2, and pregabalin shows similar affinity for (and hence lack of selectivity between) these two sites. Pregabalin is selective i...
  • Leading Manufacturer for Bictegravir Cost - Ledipasvir Actone /PVP  – CPF

    Leading Manufacturer for Bictegravir Cost - 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 ...
  • Cheap PriceList for Canagliflozin Metformin - Agomelatine  – CPF

    Cheap PriceList for Canagliflozin Metformin - Agomelatine – CPF

    Background Agomelatine is an agonist of melatonin receptors and an antagonist of the serotonin 5-HT2C receptor with Ki values of 0.062nM and 0.268nM and IC50 value of 0.27μM, respectively for MT1, MT2 and 5-HT2C [1]. Agomelatine is a unique antidepressant and is developed for treatment of major depressive disorder (MDD). Agomelatine is selective against 5-HT2C. It shows low affinities to cloned human 5-HT2A and 5-HT1A. For melatonin receptors, agomelatine shows similar affinities to cloned hu...
  • 2020 New Style Ticagrelor Supplier - Ezetimibe  – CPF

    2020 New Style Ticagrelor Supplier - 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...