Kamagra enthält Sildenafilcitrat als pharmakologisch aktiven Bestandteil. Dieser hemmt selektiv die Phosphodiesterase-5 und erhöht dadurch die Konzentration von cGMP im Corpus cavernosum. Der Effekt ist zeitlich begrenzt, da die Halbwertszeit von Sildenafil etwa vier Stunden beträgt. In der galenischen Form als Mundgel erfolgt die Resorption besonders rasch, was zu einem schnelleren Wirkeintritt führt. Der Abbau erfolgt überwiegend hepatisch über CYP3A4, wobei ein aktiver Metabolit entsteht, der zur Gesamtwirkung beiträgt. Typische Nebenwirkungen ergeben sich aus der Vasodilatation, darunter leichte Kopfschmerzen und nasale Kongestion. In klinischen Beschreibungen wird kamagra oral jelly im Zusammenhang mit der schnelleren Absorption erwähnt.
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Dortmund Data Bank (DDB) Data for Pharmaceuticals
Software & Separation Technology GmbH
Table of Contents Introduction.2 Data Bank Content. 2
Summary. 2Pure Component Properties.2Components.3
DDBST Software & Separation Technology GmbH
Introduction The Dortmund Data Bank contains a variety of data for pharmaceuticals like solubilities, vapor-liquid equilibrium data and more. The purpose of this paper to to provide a statistics on available pharmaceu- ticals and amount of available related data. For detailed information please contact DDBST (contact information is available on the title page). Data Bank Content The Dortmund Data Bank contains thermodynamic data for a variety of pure pharmaceuticals and of pharmaceuticals in mixtures with other components. The tables below give an overview on the amount of data separated by properties. Summary Databank Description Data Sets Data Points References
Activity Coefficients at Infinite Dilution
Pure Component Properties (several properties)
Densities, Volumes, Volume Effects of Mixing
Vapor-Liquid Equilibria (high-boiling components) 59
Vapor-Liquid Equilibria (low-boiling components) 437
DDBST Software & Separation Technology GmbH
Pure Component Properties Property Compounds References Data Sets Data Points
DDBST Software & Separation Technology GmbH
Components CAS Registry Empirical Formula
2,2-Dichloro-1,1-difluoro-1-methoxyethane
DDBST Software & Separation Technology GmbH
CAS Registry Empirical Formula
3,7-Dihydro-3,7-dimethyl-1H-purine-2,6-dione
4-Amino-N-(aminoiminomethyl)benzenesulfonamide 57-67-0
3,7-Dihydro-1,3,7-trimethyl-1H-purine-2,6-dione
DDBST Software & Separation Technology GmbH
CAS Registry Empirical Formula
2-Acetoxybenzoic acid <Acetylsalicylic acid>
1-Propanesulfonamide, 3-(4-nitrophenoxy)-
1-(4-Hydroxy-3-methoxyphenyl)-2-amino-ethanol
1,2-Benzenediol, 4-(2-amino-1-hydroxypropyl)-
DDBST Software & Separation Technology GmbH
CAS Registry Empirical Formula
3-(p-Aminobenzenesulfamido)-6-methoxypyridazine 80-35-3
N-(6-Methyl-2-pyridinyl) benzenesulfonamide
N1-(4,6-Dimethyl-2-pyrimidinyl)-sulfanilamide
Sulfanilic acid (2,6-dimethoxy-pyrimidine-4-ylamide) 122-11-2
DDBST Software & Separation Technology GmbH
CAS Registry Empirical Formula
n-(5-Bromo-8-quinolinyl)benzenesulfonamide
N-(2-Methyl-4-quinolinyl)benzenesulfonamide
N-(2-Methyl-8-quinolinyl)benzenesulfonamide
N-(6-Methoxy-8-quinolinyl)benzenesulfonamide
6-[D-(-)-alpha-Amino-alpha-phenylacetamidol]-peni- 69-53-4
6-[Amino-(4-hydroxyphenyl)-acetamido]-penicillan
DDBST Software & Separation Technology GmbH
CAS Registry Empirical Formula
4,4'-(1,2-Diethyl-1,2-ethenediyl)bisphenol
11-alpha-Hydroxy-16-alpha,17-alpha-epoxyproges-
DDBST Software & Separation Technology GmbH
CAS Registry Empirical Formula
21-Acetoxy-4-pregnene-11,beta,17,alpha-diol-3,20-
2-(3,4Dimethoxyphenyl)-ethyl-(3-4-(2-isopropylin-
dolizine-1-sulfonyl)-phenoxypropylmethylamin
DDBST Software & Separation Technology GmbH
CAS Registry Empirical Formula
[12] The side product related to 6 was also formed, but the optical purityof O-allyl-l-tyrosine (2) into proteins in E. coli. The alkenefunctional group of this unnatural amino acid should provide[13] M. Shimazaki, H. Haram, K. Suzuki, G.-i. Tsuchihashi, Tetrahedronnew chemical methods for the selective modification ofLett. 1987, 28, 5891; K. Suzuki, E. Katayama, G.-i. Tsuchihashi,[14] R
J. Appl. Ent. 127, 481–488 (2003)Ó 2003 Blackwell Verlag, BerlinISSN 0931-2048Effects of ivermectin and doramectin faecal residueson the invertebrate colonization of cattle dungV. H. Suarez1, A. L. Lifschitz2, J. M. Sallovitz2 and C. E. Lanusse21Estacio´n Experimental Agropecuaria Anguil, INTA, Anguil, La Pampa, Argentina; 2Laboratorio deFarmacologı´a, Dpto. Fisiopatologı´a, Facultad de