GB1520441A - Di-(substituted alkyl) amino-benzenes with cytostatic activity - Google Patents

Di-(substituted alkyl) amino-benzenes with cytostatic activity

Info

Publication number
GB1520441A
GB1520441A GB29218/75A GB2921875A GB1520441A GB 1520441 A GB1520441 A GB 1520441A GB 29218/75 A GB29218/75 A GB 29218/75A GB 2921875 A GB2921875 A GB 2921875A GB 1520441 A GB1520441 A GB 1520441A
Authority
GB
United Kingdom
Prior art keywords
alkyl
amino
residue
substituted alkyl
group
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB29218/75A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
THIEMANN CHEM PHARM FAB
Original Assignee
THIEMANN CHEM PHARM FAB
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by THIEMANN CHEM PHARM FAB filed Critical THIEMANN CHEM PHARM FAB
Publication of GB1520441A publication Critical patent/GB1520441A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06008—Dipeptides with the first amino acid being neutral
    • C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06026—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/06—Dipeptides
    • C07K5/06008—Dipeptides with the first amino acid being neutral
    • C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
    • C07K5/06034—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0802—Tripeptides with the first amino acid being neutral
    • C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
    • C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Abstract

1520441 Di-(substituted alkyl)amino-benzenes CHEM PHARMAZ FABRIK DR HERMANN THIEMANN GmbH 11 July 1975 [16 July 1974] 29218/75 Heading C3H [Also in Division C2] Novel compounds I in which R1 is Y is N or N#O, each of X1 and X2 is H or C1-6 alkyl, X3 is halogen or C1-6 alkanesulphonyloxy, n is 0-6, R2 is C1-6 alkyl, R3 is OH (when n # 0), an alpha-amino acid residue or a polypeptide residue (when X1 is C1-6 alkyl or the group -NH-CH(R4)-COR5 (when X1 is H or C1-6 alkyl), where R4 is optionally substituted alkyl and R5 is OH (when n # 0), an alpha-aminoacid residue or a polypeptide residue, and esters and salts thereof, are prepared by hydroxyalkylating a compound II in which X is C1-6 alkyl, to convert the amino group into a di-(hydroxyalkyl)amino group, replacing the hydroxy groups by halogen atoms or alkanesulphonyloxy groups, if necessary after hydrolysis of the ester group to the carboxylic acid, followed by coupling a resultant carboxylic acid to an amino-acid or polypeptide or converting it to a salt or ester. Cytostatic compositions comprise a compound I together with a pharmaceutical carrier.
GB29218/75A 1974-07-16 1975-07-11 Di-(substituted alkyl) amino-benzenes with cytostatic activity Expired GB1520441A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE2434231A DE2434231A1 (en) 1974-07-16 1974-07-16 N-LOST AROMATIC COMPOUNDS, PROCEDURES FOR THEIR PRODUCTION AND MEDICINAL PRODUCTS CONTAINING N-LOST COMPOUNDS

Publications (1)

Publication Number Publication Date
GB1520441A true GB1520441A (en) 1978-08-09

Family

ID=5920727

Family Applications (1)

Application Number Title Priority Date Filing Date
GB29218/75A Expired GB1520441A (en) 1974-07-16 1975-07-11 Di-(substituted alkyl) amino-benzenes with cytostatic activity

Country Status (13)

Country Link
JP (1) JPS5134123A (en)
BE (1) BE831380A (en)
DD (1) DD119211A5 (en)
DE (1) DE2434231A1 (en)
DK (1) DK308275A (en)
ES (1) ES439437A1 (en)
FI (1) FI752004A (en)
FR (1) FR2278333A1 (en)
GB (1) GB1520441A (en)
IL (1) IL47607A0 (en)
NL (1) NL7507494A (en)
SE (1) SE7508075L (en)
ZA (1) ZA754092B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108047099A (en) * 2017-12-19 2018-05-18 江苏欣诺科催化剂有限公司 A kind of amides organonitrogen ligands compound and its synthetic method

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4186194A (en) * 1973-10-23 1980-01-29 Agence Nationale De Valorisation De La Recherche (Anvar) Water soluble agents effective as immunological adjuvants for stimulating, in the host the immune response to various antigens and compositions, notably vaccines containing said water soluble agents
US4370265A (en) * 1974-10-22 1983-01-25 Agence Nationale De Valorisation Water soluble agents effective as immunological adjuvants for stimulating in the host the immune response to various antigens and compositions, notably vaccines containing said water soluble agents
DE69825555D1 (en) * 1997-12-22 2004-09-16 Konishiroku Photo Ind Compound releasing iodide ion and light-sensitive silver halide material containing this compound

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108047099A (en) * 2017-12-19 2018-05-18 江苏欣诺科催化剂有限公司 A kind of amides organonitrogen ligands compound and its synthetic method

Also Published As

Publication number Publication date
FI752004A (en) 1976-01-17
FR2278333A1 (en) 1976-02-13
DK308275A (en) 1976-01-17
JPS5134123A (en) 1976-03-23
ZA754092B (en) 1976-05-26
NL7507494A (en) 1976-01-20
BE831380A (en) 1976-01-15
IL47607A0 (en) 1975-11-25
DE2434231A1 (en) 1976-02-05
ES439437A1 (en) 1977-02-16
FR2278333B1 (en) 1978-11-10
DD119211A5 (en) 1976-04-12
SE7508075L (en) 1976-01-19

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee