ethyl ester

Compound 5936-0108 may has modulationg effect on β-Amyloid.

(2-AMINO-PHENYL)-ACETIC ACID ETHYL ESTER, with CAS No. 64460-85-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. (2-AMINO-PHENYL)-ACETIC ACID ETHYL ESTER provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

6-Hydroxy-1,2,3,4-tetrahydro-isoquinoline-1-carboxylic acid ethyl ester hydrochloride ,with CAS No. 128073-50-7, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. 6-Hydroxy-1,2,3,4-tetrahydro-isoquinoline-1-carboxylic acid ethyl ester hydrochloride provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.

Atorvastatin ethyl ester, a derivative of Atorvastatin, exhibits potent inhibition of 9-cis-RA-induced Gal4 reporter activity.

Dabigatran ethyl ester hydrochloride is an effective inhibitor of ribosyl dihydronicotinic acid amide dehydrogenase (NQO2) with an IC50 value of 0.8 μM and is a thrombin inhibitor.

7-Methoxy-1-naphthaleneacetic acid ethyl ester is a useful organic compound for research related to life sciences. The catalog number is T124411 and the CAS number is 6836-21-1.

3-Nitro-L-tyrosine ethyl ester hydrochloride [catalog number T124433] is a valuable compound for life sciences research.

Apigenin-7-O-glucuronide-6'-ethyl ester is a useful organic compound for research related to life sciences and the catalog number is T124530.

beta-Resorcylic acid, Ethyl ester is a useful organic compound for research related to life sciences and the catalog number is T131526.

Valsartan Ethyl Ester is an impurity of Valsartan, an angiotensin II receptor antagonist used for the treatment of high blood pressure and heart failure.

Zaurategrast ethyl ester sulfate is a α4β1/α4β7 integrin antagonist, and used for the treatment of inflammatory and autoimmune disorders.

Zaurategrast ethyl ester is the ethyl ester prodrug of CT7758 and is an α4β1/α4β7 integrin antagonist. It is used for the treatment of inflammatory and autoimmune disorders.

Azido-PEG3-phosphonic acid ethyl ester, a PEG-based PROTAC linker, enables the synthesis of PROTACs[1].

Boc-PEG4-phosphonic acid ethyl ester is a polyethylene glycol (PEG) derived linker compound used in the synthesis of PROteolysis TArgeting Chimeras (PROTACs) [1].

Carboxy-PEG4-phosphonic acid ethyl ester is a PEG-based PROTAC linker used in the synthesis of PROTACs, serving as an integral compound [1].

m-PEG4-C6-phosphonic acid ethyl ester, a polyethylene glycol (PEG)-based linker compound, is used for synthesizing proteolysis-targeting chimeras (PROTACs)[1].

m-PEG4-phosphonic acid ethyl ester is a PEGylation-based linker used in the design and synthesis of PROTACs, which are heterobifunctional molecules that facilitate targeted protein degradation[1].

m-PEG5-phosphonic acid ethyl ester, a polyethylene glycol (PEG)-derived linker, is commonly used in constructing proteolysis targeting chimeras (PROTACs) [1].

m-PEG6-C6-phosphonic acid ethyl ester is a PEG-based PROTAC linker used in the synthesis of PROTACs[1].

m-PEG8-(CH2)12-phosphonic acid ethyl ester is a polyethylene glycol (PEG)-based PROTAC linker, ideal for synthesizing PROTAC compounds[1].

m-PEG9-phosphonic acid ethyl ester, a PEG-based PROTAC linker, facilitates the synthesis of PROTACs[1].

S-acetyl-PEG3-phosphonic acid ethyl ester is a polyethylene glycol (PEG)-based linker utilized in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].

Thiol-PEG3-phosphonic acid ethyl ester, a PEG-based linker, serves as a valuable component in the synthesis of PROTACs[1].

5-Azidopentanoic acid ethyl ester is an azide compound used in the synthesis of other substances. It has been shown to inhibit cancer cell proliferation both in vitro and in vivo. This compound reacts with amines to form conjugates, which can then serve as probes for identifying amine-containing proteins.