Cholic acid–quinoxaline (2/1)

نویسندگان

  • Barbara Wicher
  • Maria Gdaniec
چکیده

In the title inclusion compound, 2C(24)H(40)O(5)·C(8)H(6)N(2), the unit cell contains two mol-ecules of cholic acid (3α,7α,12α-trihydr-oxy-5β-cholan-24-oic acid) and one mol-ecule of quinoxaline which implies disorder of the quinoxaline in the space group P2(1). The amphiphilic mol-ecules of cholic acid assemble, in an anti-parallel arrangement, via O-H⋯O hydrogen bonds, into typical corrugated host bilayers which are lipophilic on the outside and lipophobic on the inside. The host framework belongs to the so called α-trans subtype. The quinoxaline mol-ecules are accommodated in lipophilic channels formed between neighboring bilayers with only van der Waals inter-actions between host and guest. There is a crystallographic twofold screw axis directed along an empty channel in the host framework; however, neighboring guests in any one channel are related by a unit-cell translation along the b axis. Thus, the overall structure is a 1:1 superposition of two such channels related by the crystallographic twofold screw axis.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Bile Acids and Steroids LXXXIII. ON THE IKTERCONVERSION OF CHOLIC AND DEOXYCHOLIC ACID IN THE RAT

Cholic acid and chenodeoxycholic acid are the main bile acids in rat bile, occurring in the approximate proportion of 8:2 (1). The occurrence of minor amounts of metabolites of cholic and chenodeoxycholic acid, formed by the action of intestinal microorganisms and liver enzymes, has recently been reported (2, 3). The transformation of labeled cholic acid during the enterohepatic circulation has...

متن کامل

Bile acids and steroids. LXXXIII. On the inter-conversion of cholic and deoxycholic acid in the rat.

Cholic acid and chenodeoxycholic acid are the main bile acids in rat bile, occurring in the approximate proportion of 8:2 (1). The occurrence of minor amounts of metabolites of cholic and chenodeoxycholic acid, formed by the action of intestinal microorganisms and liver enzymes, has recently been reported (2, 3). The transformation of labeled cholic acid during the enterohepatic circulation has...

متن کامل

Oxidoreduction of different hydroxyl groups in bile acids during their enterohepatic circulation in man.

The extent of oxidoreduction of the 3 alpha-, 7 alpha- and 12 alpha-hydroxyl groups in bile acids during the enterohepatic circulation in man was studied with the use of [3 beta-3H]-labeled deoxycholic acid and cholic acid, [7 beta-3H]-labeled cholic acid, and [12 beta-3H]-labeled deoxycholic acid and cholic acid. Each [3H]-labeled bile acid was given per os to healthy volunteers, together with...

متن کامل

Protoporphyrin hepatopathy. Effects of cholic acid ingestion in murine griseofulvin-induced protoporphyria.

Short-term effects of cholic acid ingestion on hepatic accumulation, fecal excretion, and blood levels of protoporphyrin were studied in vivo in griseofulvin-induced protoporphyric mice. Experimental mice that received feed with 2% griseofulvin and 0.5% cholic acid were compared with control mice that received feed with 2% griseofulvin for 4 wk. Five mice from each group were assessed each week...

متن کامل

Zwitterionic imidazolium salt of [MOEI]-BSA: An efficient solid acid catalyst-promoted green synthesis of quinoxaline derivatives

Easily synthesized1-methyl-3-(2-oxyethyl)-1H-imidazol-3-ium-borate sulfonic acid {[MOEI]-BSA} as a novel catalyst efficiently promoted the synthesis of quinoxaline derivatives via condensation of various diamines with 1,2-dicarbonyl compounds at room temperature conditions in ethanol. This research provides a new method for the synthesis of quinoxalines in good to excellent yields with little c...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 64  شماره 

صفحات  -

تاریخ انتشار 2008