TH13358A - Indole, which was replaced by 3- piperidinyl methyl carboxy-silate - Google Patents
Indole, which was replaced by 3- piperidinyl methyl carboxy-silateInfo
- Publication number
- TH13358A TH13358A TH9201001169A TH9201001169A TH13358A TH 13358 A TH13358 A TH 13358A TH 9201001169 A TH9201001169 A TH 9201001169A TH 9201001169 A TH9201001169 A TH 9201001169A TH 13358 A TH13358 A TH 13358A
- Authority
- TH
- Thailand
- Prior art keywords
- alkyl
- group
- hydrogen atom
- hydroxyl
- indole
- Prior art date
Links
- -1 3- piperidinyl methyl Chemical group 0.000 title claims abstract 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 title abstract 4
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 title abstract 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 title abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 4
- 239000000126 substance Substances 0.000 claims abstract 3
- 125000003342 alkenyl group Chemical group 0.000 claims abstract 2
- 125000005466 alkylenyl group Chemical group 0.000 claims abstract 2
- 150000001875 compounds Chemical class 0.000 claims abstract 2
- 239000003814 drug Substances 0.000 claims abstract 2
- 229940079593 drug Drugs 0.000 claims abstract 2
- 125000005843 halogen group Chemical group 0.000 claims abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 2
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 abstract 5
- CUCJJMLDIUSNPU-UHFFFAOYSA-N 1-oxidopiperidin-1-ium Chemical compound [O-][NH+]1CCCCC1 CUCJJMLDIUSNPU-UHFFFAOYSA-N 0.000 abstract 1
- 239000002246 antineoplastic agent Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229940076279 serotonin Drugs 0.000 abstract 1
Abstract
อนุพันธ์ของอินโดลสูตร (I);**สูตรเคมี** ซึ่ง R1 แทนไฮโดรเจรหรือเฮโลเจนอะตอม,หรือหมู่ C1-6 แอลคิล, C1-6 แอลคอกซิหรือไฮดรอกซิ; R2 แทนไฮโดรเจนอะตอม หรือหมู่ C1-6 แอลคิล -CH2-C2-5 แอลเค นิล หรือ-CH2-C2-5 แอลไคนิล; R3 แทนไฮโดรเจนอะตอม หรือหมู่ C1-6 แอลคิล หรือ C1-6 แอล คอกซิ; N แทน 2 หรือ 3 ; R4 แทนหมู่ที่เลือกจากไซแอโน,ไฮดรอกซิล, C1-6 แอลคอกซิ,เฟ นอกซิ,C(O)C1-6 แอลคิล, C(O)C6H5,-CONR5R6,-SO2NR5R6 หรือ -NR5SO2R6( ซึ่ง R5 และ R6 แต่ละหมู่เป็นอิสระต่อกันแทน ไฮโดรเจนอะตอม,หมู่ C1-6 แอลคิลหรือเฟนิล); และอนุพันธ์ควอ เทอร์แนรี แอมโมเนียม,พิเพอริดีน N-ออกไซด์ และเกลือและโซล เวทของสารเหล่านั้นซึ่งเป็นที่ยอมรับทางเสภสัชศาสตร์; ซึ่ง สารประกอบเหล่านี้มีศักยภาพที่ดีและเป็นสารต้านฤทธิ์ที่ดี และเป็นสารต้านฤทธิ์ที่เฉพาะเจาะจงของ 5- ไฮดรอกซิทริพทา มีน(5-HT; เซอโรโทนิน) สิทธิบัตรยา The derivative of the indole formula (I); ** Chemical formula ** where R1 represents hydrogre or halogen atom, or C1-6 alkyl group, C1-6 alkyl or hydroxyl; R2 represents the hydrogen atom or group C1-6 Alkyl-CH2-C2-5 Alkylenyl or -CH2-C2-5 Alkenyl; R3 represents the hydrogen atom or group C1-6 alkyl or C1-6 alkyl; N represents 2 or 3; R4 represents the selected group from cyano, hydroxyl, C1-6 Lcoxin, Feoxi, C (O) C1-6 alkyl, C (O). C6H5, -CONR5R6, -SO2NR5R6, or -NR5SO2R6 (where R5 and R6 are independent of each other Hydrogen atom, group C1-6 alkyl or phenyl); And quaternary ammonium, piperidine N-oxide and salt and sol. The magic of those substances, which is technically acceptable; These compounds have great potential and are good anti-activity agents. And is a specific antitumor agent of 5-hydroxytriptamine (5-HT; Serotonin), drug patent
Claims (1)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TH13358A true TH13358A (en) | 1993-11-15 |
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