GB1091252A - Pharmaceutical compositions containing cholanic acid derivatives - Google Patents

Info

Publication number

GB1091252A

GB1091252A GB2920666A GB2920666A GB1091252A GB 1091252 A GB1091252 A GB 1091252A GB 2920666 A GB2920666 A GB 2920666A GB 2920666 A GB2920666 A GB 2920666A GB 1091252 A GB1091252 A GB 1091252A

Authority

GB

United Kingdom

Prior art keywords

acid

pharmaceutical compositions

alkyl

hydroxy

diketocholanic

Prior art date

1965-06-30

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

Links

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• 239000008194 pharmaceutical composition Substances 0.000 title abstract 3
• 239000003763 cholanic acid derivative Substances 0.000 title 1
• 150000001830 cholanoic acids Chemical class 0.000 title 1
• MAFJMPFLJJCSTB-CGNYGZBVSA-N (4r)-4-[(3r,8r,9s,10s,13r,14s,17r)-3-hydroxy-10,13-dimethyl-7,12-dioxo-2,3,4,5,6,8,9,11,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-17-yl]pentanoic acid Chemical class C1C[C@@H](O)CC2CC(=O)[C@H]3[C@@H]4CC[C@H]([C@@H](CCC(O)=O)C)[C@@]4(C)C(=O)C[C@@H]3[C@]21C MAFJMPFLJJCSTB-CGNYGZBVSA-N 0.000 abstract 2
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
• 229910052739 hydrogen Inorganic materials 0.000 abstract 2
• 239000011777 magnesium Substances 0.000 abstract 2
• 229910052749 magnesium Inorganic materials 0.000 abstract 2
• 229910052700 potassium Inorganic materials 0.000 abstract 2
• 239000011734 sodium Substances 0.000 abstract 2
• 229910052708 sodium Inorganic materials 0.000 abstract 2
• 125000004080 3-carboxypropanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C(O[H])=O 0.000 abstract 1
• DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
• FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
• OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
• ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
• 239000002253 acid Substances 0.000 abstract 1
• 239000013543 active substance Substances 0.000 abstract 1
• 125000002252 acyl group Chemical group 0.000 abstract 1
• 125000005907 alkyl ester group Chemical group 0.000 abstract 1
• 125000000217 alkyl group Chemical group 0.000 abstract 1
• 230000001989 choleretic effect Effects 0.000 abstract 1
• BHQCQFFYRZLCQQ-OELDTZBJSA-N cholic acid Chemical class C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-OELDTZBJSA-N 0.000 abstract 1
• 229940117975 chromium trioxide Drugs 0.000 abstract 1
• WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 abstract 1
• GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 abstract 1
• 150000001875 compounds Chemical class 0.000 abstract 1
• 239000008298 dragée Substances 0.000 abstract 1
• 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
• 239000008187 granular material Substances 0.000 abstract 1
• 239000001257 hydrogen Substances 0.000 abstract 1
• 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
• 239000000203 mixture Substances 0.000 abstract 1
• 150000002763 monocarboxylic acids Chemical class 0.000 abstract 1
• 230000001590 oxidative effect Effects 0.000 abstract 1
• 239000011591 potassium Chemical group 0.000 abstract 1
• 239000000829 suppository Substances 0.000 abstract 1
• 239000003826 tablet Substances 0.000 abstract 1

Cited By (1)