SA99190998B1 - شكل بلوري للأومبرازول omeprazole - Google Patents
شكل بلوري للأومبرازول omeprazole Download PDFInfo
- Publication number
- SA99190998B1 SA99190998B1 SA99190998A SA99190998A SA99190998B1 SA 99190998 B1 SA99190998 B1 SA 99190998B1 SA 99190998 A SA99190998 A SA 99190998A SA 99190998 A SA99190998 A SA 99190998A SA 99190998 B1 SA99190998 B1 SA 99190998B1
- Authority
- SA
- Saudi Arabia
- Prior art keywords
- omeprazole
- weak
- strong
- compound
- weight
- Prior art date
Links
- 229960000381 omeprazole Drugs 0.000 title claims abstract description 140
- SUBDBMMJDZJVOS-UHFFFAOYSA-N 5-methoxy-2-{[(4-methoxy-3,5-dimethylpyridin-2-yl)methyl]sulfinyl}-1H-benzimidazole Chemical compound N=1C2=CC(OC)=CC=C2NC=1S(=O)CC1=NC=C(C)C(OC)=C1C SUBDBMMJDZJVOS-UHFFFAOYSA-N 0.000 title claims abstract description 135
- 239000013078 crystal Substances 0.000 title abstract description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims abstract description 15
- 210000002784 stomach Anatomy 0.000 claims abstract description 9
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 4
- 210000000936 intestine Anatomy 0.000 claims abstract description 3
- 239000000126 substance Substances 0.000 claims description 7
- 238000002441 X-ray diffraction Methods 0.000 claims description 3
- 206010019375 Helicobacter infections Diseases 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 239000008186 active pharmaceutical agent Substances 0.000 claims 1
- 238000012512 characterization method Methods 0.000 claims 1
- 229940125904 compound 1 Drugs 0.000 claims 1
- 208000027866 inflammatory disease Diseases 0.000 claims 1
- -1 4-methoxy-3,5-dimethyl-2-pyridinyl Chemical group 0.000 abstract description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 239000000203 mixture Substances 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 14
- 239000000843 powder Substances 0.000 description 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 239000002552 dosage form Substances 0.000 description 3
- 230000001575 pathological effect Effects 0.000 description 3
- 230000028327 secretion Effects 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 238000001069 Raman spectroscopy Methods 0.000 description 2
- 238000004279 X-ray Guinier Methods 0.000 description 2
- 230000000767 anti-ulcer Effects 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000002050 diffraction method Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 208000000718 duodenal ulcer Diseases 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 208000021302 gastroesophageal reflux disease Diseases 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 description 2
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 2
- 238000000634 powder X-ray diffraction Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 206010061968 Gastric neoplasm Diseases 0.000 description 1
- 208000007882 Gastritis Diseases 0.000 description 1
- 241000589989 Helicobacter Species 0.000 description 1
- 208000032843 Hemorrhage Diseases 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 206010030216 Oesophagitis Diseases 0.000 description 1
- 201000004681 Psoriasis Diseases 0.000 description 1
- 208000007107 Stomach Ulcer Diseases 0.000 description 1
- 206010042220 Stress ulcer Diseases 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 201000008629 Zollinger-Ellison syndrome Diseases 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003159 antacid agent Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 208000034158 bleeding Diseases 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 230000037396 body weight Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000002648 combination therapy Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000002447 crystallographic data Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 206010013864 duodenitis Diseases 0.000 description 1
- 201000006549 dyspepsia Diseases 0.000 description 1
- 208000006881 esophagitis Diseases 0.000 description 1
- 210000004211 gastric acid Anatomy 0.000 description 1
- 201000005917 gastric ulcer Diseases 0.000 description 1
- 201000000052 gastrinoma Diseases 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 230000004968 inflammatory condition Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 208000019423 liver disease Diseases 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 208000000689 peptic esophagitis Diseases 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940126409 proton pump inhibitor Drugs 0.000 description 1
- 239000000612 proton pump inhibitor Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/SE1998/002028 WO1999008500A2 (fr) | 1998-11-10 | 1998-11-10 | Nouvelle forme cristalline d'omeprazole |
Publications (1)
Publication Number | Publication Date |
---|---|
SA99190998B1 true SA99190998B1 (ar) | 2006-03-25 |
Family
ID=43735642
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SA99190998A SA99190998B1 (ar) | 1998-11-10 | 1999-01-26 | شكل بلوري للأومبرازول omeprazole |
Country Status (5)
Country | Link |
---|---|
KR (1) | KR100572297B1 (fr) |
AR (1) | AR016700A1 (fr) |
MY (1) | MY118724A (fr) |
SA (1) | SA99190998B1 (fr) |
TN (1) | TNSN98221A1 (fr) |
-
1998
- 1998-11-10 KR KR1020017005830A patent/KR100572297B1/ko not_active IP Right Cessation
- 1998-11-24 MY MYPI98005336A patent/MY118724A/en unknown
- 1998-11-25 AR ARP980105984A patent/AR016700A1/es active IP Right Grant
- 1998-12-08 TN TNTNSN98221A patent/TNSN98221A1/fr unknown
-
1999
- 1999-01-26 SA SA99190998A patent/SA99190998B1/ar unknown
Also Published As
Publication number | Publication date |
---|---|
AR016700A1 (es) | 2001-07-25 |
KR20010107953A (ko) | 2001-12-07 |
MY118724A (en) | 2005-01-31 |
KR100572297B1 (ko) | 2006-04-24 |
TNSN98221A1 (fr) | 2005-03-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6150380A (en) | Crystalline form of omeprazole | |
TWI269795B (en) | Potassium salt of (S)-omeprazole | |
SA97180739B1 (ar) | الشكل البللوري للمتشاكل S - enantiomer للأومبرازول omeprazole | |
JP5315253B2 (ja) | ラセミ型イラプラゾールの固体形 | |
EP3443960A1 (fr) | Forme cristalline de complexe supramoléculaire de trisodium comprenant du valsartan et de l'ahu-377 et procédés associés | |
CZ296723B6 (cs) | Forma B sodné soli omeprazolu, zpusob její prípravy, farmaceutický prostredek obsahující tuto formua její pouzití | |
JP2015163623A (ja) | ベンズイミダゾール化合物の結晶 | |
JPWO2008075462A1 (ja) | 胃酸分泌抑制作用を併せ持つヘリコバクター・ピロリ除菌剤 | |
AU2008235668A1 (en) | Novel crystalline bepotastine metal salt hydrate, method for preparing same, and pharmaceutical composition comprising same | |
EP1375497B1 (fr) | Sel de magnésium de S-omeprazole | |
JPH04210982A (ja) | 半水和物 | |
SA99190998B1 (ar) | شكل بلوري للأومبرازول omeprazole | |
MXPA03005884A (es) | Hemimaleato de amlodipina. | |
US7514560B2 (en) | Crystalline form of omeprazole | |
TW202421127A (zh) | 5H-吡咯并〔2,3-d〕嘧啶-6(7H)-酮及其鹽體之結晶 | |
MXPA01004651A (es) | Nueva forma cristalina de omeprazol | |
KR20100101405A (ko) | 비결정형의 (+)-란소프라졸 제조방법 및 이에 사용되는 (+)-란소프라졸 알코올레이트 | |
CA2459012A1 (fr) | Forme cristalline z du rabeprazole sodique et procede pour sa preparation |