BIOMAT Database Logo BIOMAT Database Logo

Antitumor activity of aromatic acyl derivatives of amino acids. 1977

N Lichtenstein, and N Grossowicz, and M Schlesinger

UI MeSH Term Description Entries
D010648 Phenylacetates Derivatives of phenylacetic acid. Included under this heading are a variety of acid forms, salts, esters, and amides that contain the benzeneacetic acid structure. Note that this class of compounds should not be confused with derivatives of phenyl acetate, which contain the PHENOL ester of ACETIC ACID. Benzeneacetates,Benzeneacetic Acids,Phenylacetic Acids,Acids, Benzeneacetic,Acids, Phenylacetic
D010666 Phenylpropionates Derivatives of 3-phenylpropionic acid, including its salts and esters.
D002286 Carcinoma, Ehrlich Tumor A transplantable, poorly differentiated malignant tumor which appeared originally as a spontaneous breast carcinoma in a mouse. It grows in both solid and ascitic forms. Ehrlich Ascites Tumor,Ascites Tumor, Ehrlich,Ehrlich Tumor Carcinoma,Tumor, Ehrlich Ascites
D004987 Ethers Organic compounds having two alkyl or aryl groups bonded to an oxygen atom, as in the formula R1–O–R2.
D005561 Formates Derivatives of formic acids. Included under this heading are a broad variety of acid forms, salts, esters, and amides that are formed with a single carbon carboxy group. Formic Acids,Acids, Formic
D000596 Amino Acids Organic compounds that generally contain an amino (-NH2) and a carboxyl (-COOH) group. Twenty alpha-amino acids are the subunits which are polymerized to form proteins. Amino Acid,Acid, Amino,Acids, Amino
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D000970 Antineoplastic Agents Substances that inhibit or prevent the proliferation of NEOPLASMS. Anticancer Agent,Antineoplastic,Antineoplastic Agent,Antineoplastic Drug,Antitumor Agent,Antitumor Drug,Cancer Chemotherapy Agent,Cancer Chemotherapy Drug,Anticancer Agents,Antineoplastic Drugs,Antineoplastics,Antitumor Agents,Antitumor Drugs,Cancer Chemotherapy Agents,Cancer Chemotherapy Drugs,Chemotherapeutic Anticancer Agents,Chemotherapeutic Anticancer Drug,Agent, Anticancer,Agent, Antineoplastic,Agent, Antitumor,Agent, Cancer Chemotherapy,Agents, Anticancer,Agents, Antineoplastic,Agents, Antitumor,Agents, Cancer Chemotherapy,Agents, Chemotherapeutic Anticancer,Chemotherapy Agent, Cancer,Chemotherapy Agents, Cancer,Chemotherapy Drug, Cancer,Chemotherapy Drugs, Cancer,Drug, Antineoplastic,Drug, Antitumor,Drug, Cancer Chemotherapy,Drug, Chemotherapeutic Anticancer,Drugs, Antineoplastic,Drugs, Antitumor,Drugs, Cancer Chemotherapy
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus

Related Publications

N Lichtenstein, and N Grossowicz, and M Schlesinger
Synthesis and antitumor activity of boronated dipeptides containing aromatic amino acids.
January 1997, Anticancer research,
N Lichtenstein, and N Grossowicz, and M Schlesinger
Amino-acids, acyl-amino-acids, dipeptides, acyl-dipeptides and derivatives of these compounds: Absorption spectra.
January 1937, The Biochemical journal,
N Lichtenstein, and N Grossowicz, and M Schlesinger
N-Acyl derivatives of Asn, new bacterial N-acyl D-amino acids with surfactant activity.
March 2004, Amino acids,
N Lichtenstein, and N Grossowicz, and M Schlesinger
New derivatives of CNC-amino acids and -oligopeptides: experimental antitumor activity.
January 1986, Journal of cancer research and clinical oncology,
N Lichtenstein, and N Grossowicz, and M Schlesinger
[N-PHENYLACETYL-AMINO ACIDS AND THEIR DERIVATIVES. N-ACYL AMINO ACIDS. I].
April 1965, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
N Lichtenstein, and N Grossowicz, and M Schlesinger
[Aliphatic acyl-amino acids. N-Acyl-amino acids. II].
October 1966, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
N Lichtenstein, and N Grossowicz, and M Schlesinger
Synthesis and characterisation of acyl coenzyme A derivatives of aromatic carboxylic acids.
January 1974, Zeitschrift fur Naturforschung. Section C, Biosciences,
N Lichtenstein, and N Grossowicz, and M Schlesinger
Bulky aromatic amino acids increase the antibacterial activity of 15-residue bovine lactoferricin derivatives.
August 2001, Journal of peptide science : an official publication of the European Peptide Society,
N Lichtenstein, and N Grossowicz, and M Schlesinger
[Antiviral potentials. 8. Highter N-acyl derivatives of various amino acids].
August 1968, Bollettino chimico farmaceutico,
N Lichtenstein, and N Grossowicz, and M Schlesinger
THE ENZYMATIC ACTIVATION OF AMINO ACIDS VIA THEIR ACYL-ADENYLATE DERIVATIVES.
June 1956, Proceedings of the National Academy of Sciences of the United States of America,
Copied contents to your clipboard!