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non-alcoholic fatty liver disease/protease

Odkaz je uložen do schránky
15 Výsledek

Interleukin-1 beta converting enzyme like apoptotic protease-6

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
FIELD OF INVENTION This invention relates, in part, to newly identified polynucleotides and polypeptides; variants and derivatives of the polynucleotides and polypeptides; processes for making the polynucleotides and the polypeptides, and their variants and derivatives; agonists and antagonists of

Interleukin-1.beta. converting enzyme like apoptotic protease-6

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
FIELD OF INVENTION This invention relates, in part, to newly identified polynucleotides and polypeptides; variants and derivatives of the polynucleotides and polypeptides; processes for making the polynucleotides and the polypeptides, and their variants and derivatives; agonists and antagonists of

Interleukin-1.beta. converting enzyme like apoptotic protease-6

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
FIELD OF INVENTION This invention relates, in part, to newly identified polynucleotides and polypeptides; variants and derivatives of the polynucleotides and polypeptides; processes for making the polynucleotides and the polypeptides, and their variants and derivatives; agonists and antagonists of

Interleukin-1 beta converting enzyme like apoptotic protease-7

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND OF THE INVENTION Apoptosis, or programmed cell death (PCD), is a genetically regulated mechanism with a central role in both metazoan development and homeostasis. (Raff, 1992; Steller, 1995). The cell death machinery is conserved throughout evolution (Vaux et al., 1994) and is composed of

Interleukin-1 .beta. converting enzyme like apoptotic protease-6

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
FIELD OF INVENTION This invention relates, in part, to newly identified polynucleotides and polypeptides; variants and derivatives of the polynucleotides and polypeptides; processes for making the polynucleotides and the polypeptides, and their variants and derivatives; agonists and antagonists of

Process for manufacturing soybean proteins

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a process for manufacturing soybean proteins and, more particularly, to a process for manufacturing soybean proteins particularly suitable as edible proteins. 2. Description of the Prior Art Heretofore, processes

Amino-substituted 3-heteroaroylamino-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The present invention relates to compounds of the formula I, ##STR00002## wherein A, D, E, G, R.sup.10, R.sup.11, R.sup.30, R.sup.40, R.sup.50 and R.sup.60 have the meanings indicated below, which are valuable pharmaceutical active compounds. They are inhibitors of the protease cathepsin A, and are

Oxygen-substituted 3-heteroaroylamino-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The present invention relates to compounds of the formula I, ##STR00002## wherein A, D, E, G, R.sup.10, R.sup.30, R.sup.40, R.sup.50 and R.sup.60 have the meanings indicated below, which are valuable pharmaceutical active compounds. They are inhibitors of the protease cathepsin A, and are useful for

Biaryl-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
This application claims the benefit of European Application No. EP13305402.3, filed Mar. 28, 2013, the disclosure of which is herein incorporated by reference in its entirety. The present invention relates to compounds of the formula I, ##STR00002## wherein X, R, R1, R2, D, E.sub.1, E.sub.2,

Biaryl-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
This application claims the benefit of European Application No. EP13305401.5, filed Mar. 28, 2013, the disclosure of which is herein incorporated by reference in its entirety. The present invention relates to compounds of the formula I, ##STR00002## wherein X, R, R1, R2, D, E.sub.1, E.sub.2,

3-heteroaroylamino-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The present invention relates to compounds of the formula I, ##STR00002## wherein Ht, G, R.sup.10, R.sup.30, R.sup.40, R.sup.50 and R.sup.60 have the meanings indicated below, which are valuable pharmaceutical active compounds. They are inhibitors of the protease cathepsin A, and are useful for the

Substituted 3-heteroaroylamino-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The present invention relates to compounds of the formula I, ##STR00002## wherein A, D, E, L, G, R.sup.10, R.sup.30, R.sup.40, R.sup.50 and R.sup.60 have the meanings indicated below, which are valuable pharmaceutical active compounds. They are inhibitors of the protease cathepsin A, and are useful

Substituted 3-heteroaroylamino-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The present invention relates to compounds of the formula I, ##STR00002## wherein A, D, E, L, G, R.sup.10, R.sup.30, R.sup.40, R.sup.50 and R.sup.60 have the meanings indicated below, which are valuable pharmaceutical active compounds. They are inhibitors of the protease cathepsin A, and are useful

Substituted 3-heteroaroylamino-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The present invention relates to compounds of the formula I, ##STR00002## wherein A, D, E, L, G, R.sup.10, R.sup.30, R.sup.40, R.sup.50 and R.sup.60 have the meanings indicated below, which are valuable pharmaceutical active compounds. They are inhibitors of the protease cathepsin A, and are useful

Substituted 3-thiazoloamino-propionic acid derivatives and their use as pharmaceuticals

Články mohou překládat pouze registrovaní uživatelé
Přihlášení Registrace
The present invention relates to compounds of the formulae Ia and Ib, ##STR00002## wherein R1, R2, G, R.sup.10, R.sup.30, R.sup.40, R.sup.50 and R.sup.60 have the meanings indicated below, which are valuable pharmaceutical active compounds. They are inhibitors of the protease cathepsin A, and are
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