Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Monika Klimt"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2085-2091 (2019)
Atorvastatin calcium (Lipitor®, Sortis®) is a well-established cholesterol synthesis enzyme (CSE) inhibitor commonly used in the therapy of hypercholesterolemia. This drug is known to be sensitive to acid treatment, but only little data has been pu
Externí odkaz:
https://doaj.org/article/a0bee547b15b4b6dac7df48c6eeec64a
Autor:
Jürgen Krauß, Christoph Müller, Monika Klimt, Leandro Jorquera Valero, José Francisco Martínez, Martin Müller, Karin Bartel, Ulrike Binder, Franz Bracher
Publikováno v:
Molecules, Vol 26, Iss 23, p 7208 (2021)
The aliphatic heterocycles piperidine and morpholine are core structures of well-known antifungals such as fenpropidin and fenpropimorph, commonly used as agrofungicides, and the related morpholine amorolfine is approved for the treatment of dermal m
Externí odkaz:
https://doaj.org/article/a0f65cc090474ba8b727559d6d19935f
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2085-2091 (2019)
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2085-2091 (2019)
Atorvastatin calcium (Lipitor®, Sortis®) is a well-established cholesterol synthesis enzyme (CSE) inhibitor commonly used in the therapy of hypercholesterolemia. This drug is known to be sensitive to acid treatment, but only little data has been pu
Autor:
Monika Klimt, José Francisco Martínez, Karin Bartel, Ulrike Binder, Martin Müller, Franz Bracher, Christoph Müller, Leandro Jorquera Valero, Jürgen Kraus
Publikováno v:
Molecules
Molecules, Vol 26, Iss 7208, p 7208 (2021)
Molecules; Volume 26; Issue 23; Pages: 7208
Molecules, Vol 26, Iss 7208, p 7208 (2021)
Molecules; Volume 26; Issue 23; Pages: 7208
The aliphatic heterocycles piperidine and morpholine are core structures of well-known antifungals such as fenpropidin and fenpropimorph, commonly used as agrofungicides, and the related morpholine amorolfine is approved for the treatment of dermal m
Publikováno v:
ChemInform. 33
Derivatives of 1-[2-(4-carboxyphenoxy)ethyl]-3-dodecanoylindole-2-carboxylic acid (4) with modified substituents at the indole-1-position were synthesized and evaluated for their ability to inhibit the arachidonic acid release in human platelets medi
Publikováno v:
ChemInform. 34
A series of 3-dodecanoylindole-2-carboxylic acid derivatives with varied carboxylic acid substituents at the indole 1-position were synthesized and evaluated for their ability to inhibit arachidonic acid release in human platelets mediated by the cyt
Publikováno v:
Bioorganicmedicinal chemistry letters. 11(19)
Derivatives of 1-[2-(4-carboxyphenoxy)ethyl]-3-dodecanoylindole-2-carboxylic acid (4) with modified substituents at the indole-1-position were synthesized and evaluated for their ability to inhibit the arachidonic acid release in human platelets medi