RU96115933A - PHARMACEUTICAL COMPOSITIONS CONTAINING POLYTIOMAURIN AND METHOD OF THEIR APPLICATION - Google Patents
PHARMACEUTICAL COMPOSITIONS CONTAINING POLYTIOMAURIN AND METHOD OF THEIR APPLICATIONInfo
- Publication number
- RU96115933A RU96115933A RU96115933/04A RU96115933A RU96115933A RU 96115933 A RU96115933 A RU 96115933A RU 96115933/04 A RU96115933/04 A RU 96115933/04A RU 96115933 A RU96115933 A RU 96115933A RU 96115933 A RU96115933 A RU 96115933A
- Authority
- RU
- Russia
- Prior art keywords
- oligomer
- pharmaceutical composition
- hydrogen
- pharmaceutically acceptable
- specified
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title claims 6
- 150000004984 aromatic diamines Chemical class 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 3
- 206010000565 Acquired immunodeficiency syndrome Diseases 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- SIISYXWWQBUDOP-UHFFFAOYSA-N bis(1H-imidazol-2-yl)methanethione Chemical compound N=1C=CNC=1C(=S)C1=NC=CN1 SIISYXWWQBUDOP-UHFFFAOYSA-N 0.000 claims 2
- 239000003599 detergent Substances 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 239000012039 electrophile Substances 0.000 claims 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- -1 C 1 -C 4 -alkyl Chemical group 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 229920002396 Polyurea Polymers 0.000 claims 1
- 210000002356 Skeleton Anatomy 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 150000001768 cations Chemical class 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 230000000875 corresponding Effects 0.000 claims 1
- 238000003745 diagnosis Methods 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000006210 lotion Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 125000000542 sulfonic acid group Chemical group 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Claims (1)
где X представляет собой двухвалентный ароматический гидрокарбиленовый радикал, замещенный по меньшей мере одной группой сульфоновой кислоты.1. Water soluble, having a rigid skeleton, a polyurea oligomer containing repeating radicals, derivatives of compounds represented by the formula
where X represents a bivalent aromatic hydrocarbylene radical, substituted by at least one sulfonic acid group.
где R представляет собой водород, C1-C4-алкил, фенил или фенил, замещенный 0 - 2 группами R1 и содержащий до трех заместителей, независимо выбранных из атома хлора или брома, или C1-C4-алкильной группы;
R1 представляет собой -SO3R2, -CO2R2, -PO3R2 или -OPO3R2;
R2 представляет собой водород или фармацевтически приемлемый катион;
R3 представляет собой -R или -X-NHR, где R указан выше;
X представляет собой
Y представляет собой -CO2-, -C=C-, -N=N-,
m равен целому числу 0 или 1, при условии, что, когда m равен 0, R1 представляет собой атом водорода, и n равен целому числу от 3 до 50.4. The oligomer according to claim 1, corresponding to the formula:
where R represents hydrogen, C 1 -C 4 -alkyl, phenyl or phenyl, substituted with 0-2 groups of R 1 and containing up to three substituents, independently selected from a chlorine or bromine atom, or a C 1 -C 4 alkyl group;
R 1 represents -SO 3 R 2, -CO 2 R 2, -PO 3 R 2 or -OPO 3 R 2;
R 2 is hydrogen or a pharmaceutically acceptable cation;
R 3 is —R or —X — NHR, wherein R is as defined above;
X is
Y represents -CO 2 -, -C = C-, -N = N-,
m is an integer of 0 or 1, provided that when m is 0, R 1 is a hydrogen atom, and n is an integer from 3 to 50.
6. Олигомер по п.4, где m равно 1, R и R3 представляют собой 4-метилфенил; n равно от 3 до 15; а X представляет собой
7. Фармацевтическая композиция для диагностики и/или лечения СПИД и/или ССК, содержащая эффективное количество олигомера, указанного в пп.1 - 6, и фармацевтически приемлемый носитель и/или детергент.5. The oligomer according to claim 4, where R is hydrogen, m is 1, the substituents R and R 3 are 4-methylphenyl; n is from 3 to 15; and X represents
6. The oligomer according to claim 4, where m is 1, R and R 3 are 4-methylphenyl; n is from 3 to 15; and X is
7. Pharmaceutical composition for the diagnosis and / or treatment of AIDS and / or SSC, containing an effective amount of the oligomer specified in paragraphs 1 - 6, and a pharmaceutically acceptable carrier and / or detergent.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/176586 | 1994-01-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
RU96115933A true RU96115933A (en) | 1998-12-10 |
Family
ID=
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