TH13113A - ซัลโฟนามีดชนิดใหม่ - Google Patents
ซัลโฟนามีดชนิดใหม่Info
- Publication number
- TH13113A TH13113A TH9201000818A TH9201000818A TH13113A TH 13113 A TH13113 A TH 13113A TH 9201000818 A TH9201000818 A TH 9201000818A TH 9201000818 A TH9201000818 A TH 9201000818A TH 13113 A TH13113 A TH 13113A
- Authority
- TH
- Thailand
- Prior art keywords
- alkyl
- halogen
- lower alkyl
- phenyl
- pyridyl
- Prior art date
Links
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 title 1
- 229940124530 sulfonamide Drugs 0.000 claims abstract 7
- 150000003839 salts Chemical class 0.000 claims abstract 6
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract 5
- 150000003456 sulfonamides Chemical class 0.000 claims abstract 3
- 239000008280 blood Substances 0.000 claims abstract 2
- 210000004369 blood Anatomy 0.000 claims abstract 2
- 208000028867 ischemia Diseases 0.000 claims abstract 2
- -1 hydrogen halogen Chemical class 0.000 claims 174
- 125000000217 alkyl group Chemical group 0.000 claims 124
- 229910052739 hydrogen Inorganic materials 0.000 claims 62
- 239000001257 hydrogen Substances 0.000 claims 62
- 229910052736 halogen Inorganic materials 0.000 claims 60
- 150000002367 halogens Chemical group 0.000 claims 39
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 39
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 35
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 20
- 150000001875 compounds Chemical class 0.000 claims 15
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims 15
- 125000000623 heterocyclic group Chemical group 0.000 claims 14
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 14
- 241000156724 Antirhea Species 0.000 claims 13
- 150000001204 N-oxides Chemical class 0.000 claims 13
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 claims 12
- 125000003545 alkoxy group Chemical group 0.000 claims 12
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 claims 11
- 239000000126 substance Substances 0.000 claims 9
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims 8
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 7
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 7
- 125000004414 alkyl thio group Chemical group 0.000 claims 6
- 125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 6
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 6
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 6
- 125000001041 indolyl group Chemical group 0.000 claims 6
- 210000003734 kidney Anatomy 0.000 claims 6
- 229910052760 oxygen Inorganic materials 0.000 claims 6
- 229910052717 sulfur Inorganic materials 0.000 claims 6
- ORZMSMCZBZARKY-UHFFFAOYSA-N 1,3,2$l^{6}-benzodioxathiole 2,2-dioxide Chemical compound C1=CC=C2OS(=O)(=O)OC2=C1 ORZMSMCZBZARKY-UHFFFAOYSA-N 0.000 claims 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 5
- 239000005977 Ethylene Substances 0.000 claims 5
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 5
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 4
- RWGFKTVRMDUZSP-UHFFFAOYSA-N isopropyl-benzene Natural products CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 claims 4
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims 2
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims 2
- 150000008331 benzenesulfonamides Chemical class 0.000 claims 2
- MHCVCKDNQYMGEX-UHFFFAOYSA-N 1,1'-biphenyl;phenoxybenzene Chemical compound C1=CC=CC=C1C1=CC=CC=C1.C=1C=CC=CC=1OC1=CC=CC=C1 MHCVCKDNQYMGEX-UHFFFAOYSA-N 0.000 claims 1
- JCIXLSHBTLKMCB-UHFFFAOYSA-N 1-ethenoxy-2-methoxybenzene Chemical group COC1=CC=CC=C1OC=C JCIXLSHBTLKMCB-UHFFFAOYSA-N 0.000 claims 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims 1
- UUDRRSKRJPTTOK-UHFFFAOYSA-N 2-methylidene-1,4-dioxane Chemical compound C=C1COCCO1 UUDRRSKRJPTTOK-UHFFFAOYSA-N 0.000 claims 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- 125000001137 3-hydroxypropoxy group Chemical group [H]OC([H])([H])C([H])([H])C([H])([H])O* 0.000 claims 1
- UUYZWKALKMYIOV-UHFFFAOYSA-N COC(C=CC(F)=C1)=C1ON1C=CC(OCCO)=NC1 Chemical compound COC(C=CC(F)=C1)=C1ON1C=CC(OCCO)=NC1 UUYZWKALKMYIOV-UHFFFAOYSA-N 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 1
- 206010020772 Hypertension Diseases 0.000 claims 1
- HCUARRIEZVDMPT-UHFFFAOYSA-N Indole-2-carboxylic acid Chemical compound C1=CC=C2NC(C(=O)O)=CC2=C1 HCUARRIEZVDMPT-UHFFFAOYSA-N 0.000 claims 1
- KNGOGERIDJTUTD-UHFFFAOYSA-N NS(C(C(OCCO)=C1OC2=CC=CC=C2)=CC=C1C1=NC=CC=N1)(=O)=O Chemical class NS(C(C(OCCO)=C1OC2=CC=CC=C2)=CC=C1C1=NC=CC=N1)(=O)=O KNGOGERIDJTUTD-UHFFFAOYSA-N 0.000 claims 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical group [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000004494 ethyl ester group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 claims 1
- 239000003814 drug Substances 0.000 abstract 2
- 206010008479 Chest Pain Diseases 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
Abstract
ซัลโฟนาไมด์ชนิดใหม่ที่มีสูตร I ที่ซึ่งสัญลักษณ์ R1-R9,Ra,Rb,X,Y,Z และ n มีความสำคัญที่ระบุในคำอธิบายและเกลือของมันสามารถใช้เป็นส่วนประกอบออกฤทธิ์สำหรับการผลิตเครื่องยาเพื่อการบำบัดความผิดปกติทางการหมุนเวียนโลหิต โดยเฉพาะ ความดันโลหิตสูง ภาวะการขาดเลือดเฉพาะแห่ง ภาวะหลอดโลหิตบีบเกร็งและการปวดเค้นหน้าอก สิทธิบัตรยา
Claims (1)
1.การใช้ตามข้อถือสิทธิ 20 ที่ซึ่ง R4 คือ ไฮโดรเจน 2-ไพริมิดิล 2-ไพริมิดิล 2-หรือ 3-ฟิวริล 2-หรือ 3-ไธอีนิลมอร์ฟอลิโน หรือ p-เมทธอกซีฟีนิล
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TH13113A true TH13113A (th) | 1993-09-10 |
| TH9708B TH9708B (th) | 2000-07-04 |
Family
ID=
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