Crene Biotechnology,API,pharmaceutical intermediates,small molecules,prostaglandins,chemicals

+ AII PRODUCTS

- Prostaglandins - Custom Synthesis - PARP Inhibitors - PI3K Inhibitors - FAK Inhibitors - AKT Inhibitors - C-Kit Inhibitors - VEGFR Inhibitors - c-Met Inhibitors - CDK Inhibitors - CYP17 Inhibitors - DNA/RNA Inhibitors - mTOR Inhibitors - SRC Inhibitors - Others - Veterinary APIs

Catalog No	CAS NO	Product name
CR1496	25316-40-9	Doxorubicin HCl Doxorubicin is an anthracycline antibiotic with antineoplastic activity. Doxorubicin, isolated from the bacterium Streptomyces peu..
CR1495	23541-50-6	Daunorubicin hydrochloride Daunorubicin hydrochloride is the hydrochloride salt of an anthracycline antineoplastic antibiotic with therapeutic effects simila..
CR1494	111358-88-4	CEP701 Lesraurtinib Lesraurtinib, also known as CEP701; KT 5555; SP 924, is an orally bioavailable indolocarbazole derivative with antineoplastic prop..
CR1493	156897-06-2	Licofelone Licofelone is a dual COX/LOX inhibitor being considered as a treatment for osteoarthritis and which is under development by Merckl..
CR1492	83480-29-9	Voglibose Voglibose is an alpha-glucosidase inhibitor used for lowering post-prandial blood glucose levels in people with diabetes mellitus...
CR1491	19356-17-3	Calcifediol Calcifediol, also known as 25-hydroxy Vitamin D3, 25-OH Vitamin D3 or 25-hydroxy Cholecalciferol, is an intermediate in the pathwa..
CR1490	63283-36-3	Calcifediol monohydrate Calcifediol is a prehormone that is produced in the liver. Physicians worldwide measure this metabolite to determine a patient'..
CR1489	801312-28-7	GSK256066 GSK256066 is a potent and selective PDE4 inhibitor that can be given by inhalation, minimising the potential for side effects. GSK..
CR1488	1020172-07-9	DCC-2036 Rebastinib Rebastinib, also known as DCC-2036, is an orally bioavailable small-molecule inhibitor of multiple tyrosine kinases with potential..
CR1487	850173-95-4	ADL-5859 ADL5859 is a δ-opioid receptor agonist with Ki of 0.8 nM, selectivity against opioid receptor κ, μ, and weak inhibitory activit..

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