TH67350A - - Google Patents

Info

Publication number

TH67350A

TH67350A TH301002640A TH0301002640A TH67350A TH 67350 A TH67350 A TH 67350A TH 301002640 A TH301002640 A TH 301002640A TH 0301002640 A TH0301002640 A TH 0301002640A TH 67350 A TH67350 A TH 67350A

Authority

TH

Thailand

Prior art keywords

replaced

alkyls

phenyl

group

cycloalkyls

Prior art date

2003-07-16

Links

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• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 31
• 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims abstract 23
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract 19
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 14
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 13
• 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract 10
• NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims abstract 8
• FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims abstract 6
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims abstract 6
• 125000000217 alkyl group Chemical group 0.000 claims abstract 6
• -1 perrolidine Chemical compound 0.000 claims abstract 6
• 150000001875 compounds Chemical class 0.000 claims abstract 5
• 239000000126 substance Substances 0.000 claims abstract 5
• 239000002253 acid Substances 0.000 claims abstract 4
• 150000007513 acids Chemical class 0.000 claims abstract 4
• HONIICLYMWZJFZ-UHFFFAOYSA-N azetidine Chemical compound C1CNC1 HONIICLYMWZJFZ-UHFFFAOYSA-N 0.000 claims abstract 4
• 125000002541 furyl group Chemical group 0.000 claims abstract 4
• 125000005843 halogen group Chemical group 0.000 claims abstract 4
• 150000004677 hydrates Chemical class 0.000 claims abstract 4
• 125000001624 naphthyl group Chemical group 0.000 claims abstract 4
• 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract 4
• 125000004043 oxo group Chemical group O=* 0.000 claims abstract 4
• 125000004430 oxygen atom Chemical group O* 0.000 claims abstract 4
• 150000003839 salts Chemical class 0.000 claims abstract 4
• 229910052717 sulfur Inorganic materials 0.000 claims abstract 4
• 125000004434 sulfur atom Chemical group 0.000 claims abstract 4
• 125000004076 pyridyl group Chemical group 0.000 claims abstract 3
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 2
• NDTSRXAMMQDVSW-UHFFFAOYSA-N benzthiazide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(S(N2)(=O)=O)=C1N=C2CSCC1=CC=CC=C1 NDTSRXAMMQDVSW-UHFFFAOYSA-N 0.000 claims abstract 2
• 229960001541 benzthiazide Drugs 0.000 claims abstract 2
• 239000003814 drug Substances 0.000 claims abstract 2
• 229940079593 drug Drugs 0.000 claims abstract 2
• 229910052739 hydrogen Inorganic materials 0.000 claims abstract 2
• 239000001257 hydrogen Substances 0.000 claims abstract 2
• 230000001225 therapeutic effect Effects 0.000 claims abstract 2
• YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 6
• 229930192474 thiophene Natural products 0.000 claims 3
• 229910052736 halogen Inorganic materials 0.000 claims 1
• 150000002367 halogens Chemical class 0.000 claims 1
• 238000006467 substitution reaction Methods 0.000 claims 1
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
• YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 abstract 1
• DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 abstract 1
• JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical compound O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 abstract 1
• 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1