FIELD: medicine, pharmaceutics.
SUBSTANCE: claimed invention relates to compounds of formula (IC-2), to their pharmaceutically acceptable salts, N- oxides or solvates. In formula (IC-2) Z represents carbomoyl group, which can be replaced with C1-4 alkyl or hydroxy; R1 represents C1-8 alkyl or C1-8 alkoxy; R4 and R4-1 each independently represent hydrogen atom or C1-8 alkyl; m represents integer number from 1 to 5, when m equals 2 or larger number, all R1 can have same or different values. Invention also relates to compounds, representing 1-({6-[(2-methoxy-4-propylbenzyl)oxy]-1-methyl-3,4-dihydro-2-napthlenyl}methyl)-3-azetidinecarbonic acid, 1-({6-[(4-isobutyl-2-methoxybenzyl)oxy]-1-methyl-3,4-dihydro-2-naphthalinyl}methyl)-3- azetidinecarbonic acid and other, given in formula of claimed invention.
EFFECT: obtaining pharmaceutical composition, which has agonistic activity with respect to EDG-1, EDG-6 and/or EDG-8, containing as active component invention compound, to method of prevention and/or treatment of disease, conditioned by EDG-1, EDG-6 and/or EDG-8 invention compounds, to method of prevention and/or treatment of disseminated sclerosis and method of immune reaction suppression and/or induction of lymphopenia, to application of invention compounds for obtaining medication for prevention and/or treatment of disease, conditioned by EDG-1, EDG-6 and/or EDG-8, to application of compounds for obtaining medication for prevention and/or treatment of disseminated sclerosis, to application of compounds for obtaining immunodepresant and/or medication inducing lymphopenia and to crystal forms of some individual compounds.
17 cl, 10 dwg, 5 tbl, 251 ex
Title |
Year |
Author |
Number |
COMPOUND CAPABLE OF BONDING WITH S1P RECEPTOR AND PHARMACEUTICAL APPLICATION THEREOF |
2004 |
- Nakade Sindzi
- Mizuno Khirotaka
- Ono Takedzi
- Minami Masasi
- Saga Khirosi
- Khagija Khirosi
- Komija Takaki
- Khabasita Khiromu
- Kurata Kharuto
- Okhtsuki Kazukhiro
- Kusumi Kensuke
|
RU2390519C2 |
NITROGEN-CONTAINING HETEROCYCLIC DERIVATIVES AND MEDICAMENTS THEREOF AS ACTIVE INGREDIENT |
2004 |
- Nisizava Rena
- Takaoka Josikazu
- Sibajama Siro
|
RU2366655C2 |
DERIVATIVES OF CARBOXYLIC ACIDS AND PHARMACEUTICAL AGENT COMPRISING THEIR AS ACTIVE COMPONENT |
2002 |
- Tani Kosuke
- Asada Masaki
- Kobajasi Kaoru
- Narita Masami
- Ogava Mikio
|
RU2315746C2 |
SULPHONAMIDE COMPOUND OR SALT THEREOF |
2017 |
- Miyahara, Seiji
- Ueno, Hiroyuki
- Hara, Shoki
- Ogino, Yoshio
|
RU2732572C2 |
COMPOUNDS BASED ON BENZOXAZINE AND INDOLE, WITH ANTAGONISTIC EFFECT ON cysLT RECEPTOR |
2004 |
- Takeuti Dzun
- Itadani Satosi
- Nakajama Josisuke
- Tatsumi Tadasi
- Takakhasi Sinia
- Fudzita Manabu
|
RU2371436C2 |
DERIVATIVE OF CARBOXYLIC ACID, PHARMACEUTICAL COMPOSITION AND MEDICINE OF PREVENTING AND/OR CURING DISEASES, CAUSED BY ACTIVATION OF DP RECEPTOR, USE OF SUCH DERIVATIVE FOR MAKING SUCH MEDICINE, METHOD OF PREVENTING AND/OR CURING DISEASES, CAUSED BY ACTIVATION OF DP RECEPTORS |
2003 |
- Ivakhasi Maki
- Kobajasi Kaoru
- Nambu Fumio
|
RU2329256C2 |
ANTITUMOR AGENT |
2018 |
- Ueno, Hiroyuki
- Hoshino, Takuya
|
RU2770824C2 |
TETRAHYDROCARBOLINE DERIVATIVE |
2011 |
- Okhata Akira
- Nakatani Singo
- Sugijama Tetsuja
- Morimoto Takasi
|
RU2572818C2 |
DERIVATIVES OF 3,4-DIHYDROISOQUINOLINE AND PHARMACEUTICAL AGENT COMPRISING ITS AS ACTIVE COMPONENT |
2001 |
- Ogava Mikio
- Takaoka Esikazu
- Okhkhata Akira
|
RU2272030C2 |
N-PHENYLARYLSULFONYLAMIDE, PHARMACEUTICAL COMPOSITION CONTAINING INDICATED SUBSTANCE AS ACTIVE COMPONENT, COMPOUND AS INTERMEDIATE IN SYNTHESIS OF INDICATED COMPOUND AND METHOD FOR ITS PREPARING |
2002 |
- Naganava Atsusi
- Saitokh Tetsudzi
- Kobajasi Kaoru
- Marujama Takajuki
- Nakai Esikhiko
- Khasimoto Sinsuke
|
RU2299202C2 |