DE6227T1 - - Google Patents
Info
- Publication number
- DE6227T1 DE6227T1 DE1979101934 DE79101934T DE6227T1 DE 6227 T1 DE6227 T1 DE 6227T1 DE 1979101934 DE1979101934 DE 1979101934 DE 79101934 T DE79101934 T DE 79101934T DE 6227 T1 DE6227 T1 DE 6227T1
- Authority
- DE
- Germany
- Prior art keywords
- group
- formula
- namely
- chain
- dithiobis
- Prior art date
- 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.)
- Pending
Links
- 239000003814 drug Substances 0.000 claims 27
- -1 cyclohexylamino group Chemical group 0.000 claims 25
- 150000001875 compounds Chemical class 0.000 claims 16
- 125000004432 carbon atom Chemical group C* 0.000 claims 14
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 10
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 6
- 239000005977 Ethylene Substances 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 125000003277 amino group Chemical group 0.000 claims 3
- SDNJNDFHCODQDQ-UHFFFAOYSA-N n-(2-ethylphenyl)-2-[[2-[(2-ethylphenyl)carbamoyl]phenyl]disulfanyl]benzamide Chemical compound CCC1=CC=CC=C1NC(=O)C1=CC=CC=C1SSC1=CC=CC=C1C(=O)NC1=CC=CC=C1CC SDNJNDFHCODQDQ-UHFFFAOYSA-N 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000001691 aryl alkyl amino group Chemical group 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims 2
- 125000004986 diarylamino group Chemical group 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000005191 hydroxyalkylamino group Chemical group 0.000 claims 2
- NQKAXKSLWJHSEC-UHFFFAOYSA-N n-(3-morpholin-4-ylpropyl)-2-[[2-(3-morpholin-4-ylpropylcarbamoyl)phenyl]disulfanyl]benzamide Chemical compound C=1C=CC=C(SSC=2C(=CC=CC=2)C(=O)NCCCN2CCOCC2)C=1C(=O)NCCCN1CCOCC1 NQKAXKSLWJHSEC-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- ZMPGQRAMAKWWIJ-UHFFFAOYSA-N 2-(2,2-dimethoxyethyl)benzamide Chemical compound COC(CC1=C(C(=O)N)C=CC=C1)OC ZMPGQRAMAKWWIJ-UHFFFAOYSA-N 0.000 claims 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 101710095395 Histidine decarboxylase proenzyme Proteins 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 230000002785 anti-thrombosis Effects 0.000 claims 1
- 239000003146 anticoagulant agent Substances 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000001769 aryl amino group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000000440 benzylamino group Chemical group [H]N(*)C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- UDMOIPYMZQQHPE-UHFFFAOYSA-N n-(2,2-dimethoxyethyl)benzamide Chemical compound COC(OC)CNC(=O)C1=CC=CC=C1 UDMOIPYMZQQHPE-UHFFFAOYSA-N 0.000 claims 1
- ZKSYUNLBFSOENV-UHFFFAOYSA-N n-(2-hydroxyethyl)benzamide Chemical compound OCCNC(=O)C1=CC=CC=C1 ZKSYUNLBFSOENV-UHFFFAOYSA-N 0.000 claims 1
- ODUBEYQKYAQFNS-UHFFFAOYSA-N n-(2-hydroxypropyl)-2-[[2-(2-hydroxypropylcarbamoyl)phenyl]disulfanyl]benzamide Chemical compound CC(O)CNC(=O)C1=CC=CC=C1SSC1=CC=CC=C1C(=O)NCC(C)O ODUBEYQKYAQFNS-UHFFFAOYSA-N 0.000 claims 1
- HVEKOIABBLJFPQ-UHFFFAOYSA-N n-(2-hydroxypropyl)benzamide Chemical compound CC(O)CNC(=O)C1=CC=CC=C1 HVEKOIABBLJFPQ-UHFFFAOYSA-N 0.000 claims 1
- YFCAIOHLFKWWGE-UHFFFAOYSA-N n-(3-hydroxypropyl)-2-[[2-(3-hydroxypropylcarbamoyl)phenyl]disulfanyl]benzamide Chemical compound OCCCNC(=O)C1=CC=CC=C1SSC1=CC=CC=C1C(=O)NCCCO YFCAIOHLFKWWGE-UHFFFAOYSA-N 0.000 claims 1
- 125000005184 naphthylamino group Chemical group C1(=CC=CC2=CC=CC=C12)N* 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000006308 propyl amino group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7296578 | 1978-06-16 | ||
| JP15411478 | 1978-12-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE6227T1 true DE6227T1 (enExample) | 1981-01-22 |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MY113693A (en) | Erythromycin derivatives having an enterokinesis stimulating action | |
| DE68920125D1 (de) | Pyrimidindion-Derivate, Verfahren zu deren Herstellung und diese enthaltende antiarrythmische Mittel. | |
| DE137145T1 (de) | Camptothecin-derivate und verfahren zu deren herstellung. | |
| US2924609A (en) | (1-alkylamino-2-anthraquinonylcar-bonylamido) alkyl trialkyl ammonium salts as disperse dyes for acrylic fibers | |
| DE69015244D1 (de) | Peptidverbindungen, Verfahren zu deren Herstellung und pharmazeutische Präparate, die diese enthalten. | |
| DE69324217D1 (de) | Komplexe eines Übergangsmetalls mit 2,2-Bipyridin-Liganden, die mit mindestens einer Ammoniumalkylgruppe substituiert sind, Verfahren zu ihrer Herstellung und ihre Anwendung als Redoxvermittler | |
| MX9606382A (es) | Derivados de n,n'-bis(quinolin-4-il)diamina, su preparacion y su uso como compuestos antimalaria. | |
| CA2190765A1 (en) | Novel potent inducers of terminal differentiation and methods of use thereof | |
| ATE54667T1 (de) | Kosmetische mittel auf der basis von nhydroxypropylchitosanen, neue n-hydroxypropylchitosane sowie verfahren zu ihrer herstellung. | |
| EP0216357A3 (en) | Phosphoramidite compounds and process for production thereof | |
| ES2089204T3 (es) | Compuestos de quinoxalina y su preparacion y uso. | |
| DE6227T1 (enExample) | ||
| AR248067A1 (es) | Composiciones repelentes de los insectos y los acaros, procedimiento para su obtencion y derivados utiles en dichas composiciones excluyendo su uso en o sobre seres humanos o animales superiores. | |
| GB2002758A (en) | Neuromuscular blocking agents | |
| GR900100035A (el) | Παράγωγα υδροξυαλκανοκαρβονικού οξέος, η παρασευή και η χρησιμοπποίηση τους. | |
| GB1370599A (en) | Agents for wet fastness properties | |
| AR245688A1 (es) | Compuestos trigliceridos de amonio cuaternario, su preparacion y su uso. | |
| ES8705357A1 (es) | Procedimiento para preparar nuevos derivados del 1,1,2,2-tetrametil-1,2-bis-(2-fluoro-4-hidroxi-fenil)-etano | |
| ES476166A1 (es) | Procedimiento para la preparacion de nuevas imidazo-isoqui- nolein-dionas | |
| JPS56169614A (en) | Hair cosmetic | |
| CA2022451A1 (en) | Anti-psychotic piperidynl benzimidazole compounds | |
| ES2015026B3 (es) | Agente secante autobrillante | |
| ES435420A1 (es) | Procedimiento para preparar sales cuaternizadas de poliami- nas. | |
| ES454383A1 (es) | Procedimiento para la preparacion de colorantes cationicos. | |
| DE3260015D1 (en) | Novel bis- and poly-disulfides having immunostimulant activity |