MX2008001336A - Uso de derivados de 5-amino-1h-pirrol-2-carbonitrilo sustituidos como moduladores del receptor de progesterona. - Google Patents

Info

Publication number

MX2008001336A

MX2008001336A MX2008001336A MX2008001336A MX2008001336A MX 2008001336 A MX2008001336 A MX 2008001336A MX 2008001336 A MX2008001336 A MX 2008001336A MX 2008001336 A MX2008001336 A MX 2008001336A MX 2008001336 A MX2008001336 A MX 2008001336A

Authority

MX

Mexico

Prior art keywords

methyl

cyano

pyrrol

alkyl

phenyl

Prior art date

2005-07-29

Links

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• Global Dossier
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• LWXSBBWYHZHVIM-UHFFFAOYSA-N 5-amino-1h-pyrrole-2-carbonitrile Chemical class NC1=CC=C(C#N)N1 LWXSBBWYHZHVIM-UHFFFAOYSA-N 0.000 title 1
• 239000002379 progesterone receptor modulator Substances 0.000 title 1
• 229940095745 sex hormone and modulator of the genital system progesterone receptor modulator Drugs 0.000 title 1
• 150000001875 compounds Chemical class 0.000 claims abstract description 152
• 208000024891 symptom Diseases 0.000 claims abstract description 34
• 150000003839 salts Chemical class 0.000 claims abstract description 33
• 201000010260 leiomyoma Diseases 0.000 claims abstract description 8
• 206010046798 Uterine leiomyoma Diseases 0.000 claims abstract description 7
• 230000012173 estrus Effects 0.000 claims abstract description 7
• 238000002657 hormone replacement therapy Methods 0.000 claims abstract description 7
• 206010004446 Benign prostatic hyperplasia Diseases 0.000 claims abstract description 6
• 208000005171 Dysmenorrhea Diseases 0.000 claims abstract description 6
• 206010013935 Dysmenorrhoea Diseases 0.000 claims abstract description 6
• 201000009273 Endometriosis Diseases 0.000 claims abstract description 6
• 208000004403 Prostatic Hyperplasia Diseases 0.000 claims abstract description 6
• 210000000481 breast Anatomy 0.000 claims abstract description 6
• 210000001072 colon Anatomy 0.000 claims abstract description 6
• 206010027191 meningioma Diseases 0.000 claims abstract description 6
• 230000002632 myometrial effect Effects 0.000 claims abstract description 6
• 210000001672 ovary Anatomy 0.000 claims abstract description 6
• 230000001817 pituitary effect Effects 0.000 claims abstract description 6
• 210000002307 prostate Anatomy 0.000 claims abstract description 6
• 201000000736 Amenorrhea Diseases 0.000 claims abstract description 5
• 206010001928 Amenorrhoea Diseases 0.000 claims abstract description 5
• 201000009030 Carcinoma Diseases 0.000 claims abstract description 5
• 206010013908 Dysfunctional uterine bleeding Diseases 0.000 claims abstract description 5
• 206010027514 Metrorrhagia Diseases 0.000 claims abstract description 5
• 208000027030 Premenstrual dysphoric disease Diseases 0.000 claims abstract description 5
• 206010036618 Premenstrual syndrome Diseases 0.000 claims abstract description 5
• 231100000540 amenorrhea Toxicity 0.000 claims abstract description 5
• 210000004696 endometrium Anatomy 0.000 claims abstract description 5
• 208000009956 adenocarcinoma Diseases 0.000 claims abstract description 4
• 230000001939 inductive effect Effects 0.000 claims abstract 2
• -1 O- (CHmXn) zCHpXq Chemical group 0.000 claims description 83
• 125000000217 alkyl group Chemical group 0.000 claims description 69
• YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 51
• JZAVMYVQBMKQNC-UHFFFAOYSA-N 5-(4-aminophenyl)-1-methylpyrrole-2-carbonitrile Chemical compound CN1C(C#N)=CC=C1C1=CC=C(N)C=C1 JZAVMYVQBMKQNC-UHFFFAOYSA-N 0.000 claims description 28
• 229910052736 halogen Inorganic materials 0.000 claims description 26
• 150000002367 halogens Chemical class 0.000 claims description 26
• 125000003118 aryl group Chemical group 0.000 claims description 24
• 239000000583 progesterone congener Substances 0.000 claims description 24
• 125000000623 heterocyclic group Chemical group 0.000 claims description 22
• 125000001072 heteroaryl group Chemical group 0.000 claims description 19
• 229910052739 hydrogen Inorganic materials 0.000 claims description 19
• 229910052799 carbon Inorganic materials 0.000 claims description 18
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
• WWYNJERNGUHSAO-XUDSTZEESA-N (+)-Norgestrel Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](CC)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 WWYNJERNGUHSAO-XUDSTZEESA-N 0.000 claims description 16
• 229960004400 levonorgestrel Drugs 0.000 claims description 16
• 125000003342 alkenyl group Chemical group 0.000 claims description 15
• 239000000262 estrogen Substances 0.000 claims description 15
• 229940011871 estrogen Drugs 0.000 claims description 15
• RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical class C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 claims description 14
• 125000000304 alkynyl group Chemical group 0.000 claims description 12
• 239000000902 placebo Substances 0.000 claims description 12
• 229940068196 placebo Drugs 0.000 claims description 12
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 10
• 230000000708 anti-progestin effect Effects 0.000 claims description 10
• 239000003418 antiprogestin Substances 0.000 claims description 10
• 239000008194 pharmaceutical composition Substances 0.000 claims description 10
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 10
• 230000001072 progestational effect Effects 0.000 claims description 10
• 229910052801 chlorine Inorganic materials 0.000 claims description 7
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 7
• 230000001419 dependent effect Effects 0.000 claims description 7
• 125000006125 ethylsulfonyl group Chemical group 0.000 claims description 7
• 229910052731 fluorine Inorganic materials 0.000 claims description 7
• 229940088597 hormone Drugs 0.000 claims description 7
• 239000005556 hormone Substances 0.000 claims description 7
• GYNKGXYJQCGQIF-UHFFFAOYSA-N 5-[4-amino-3-(trifluoromethoxy)phenyl]-1-methylpyrrole-2-carbonitrile Chemical compound CN1C(C#N)=CC=C1C1=CC=C(N)C(OC(F)(F)F)=C1 GYNKGXYJQCGQIF-UHFFFAOYSA-N 0.000 claims description 6
• 239000003433 contraceptive agent Substances 0.000 claims description 6
• 125000004051 hexyl group Chemical class [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
• 125000005647 linker group Chemical group 0.000 claims description 6
• FTTCQTKVYBUBMB-UHFFFAOYSA-N 5-(4-amino-2,5-difluorophenyl)-1-methylpyrrole-2-carbonitrile Chemical compound CN1C(C#N)=CC=C1C1=CC(F)=C(N)C=C1F FTTCQTKVYBUBMB-UHFFFAOYSA-N 0.000 claims description 5
• MGFMZAUPZJHQAW-UHFFFAOYSA-N 5-(4-amino-2-fluorophenyl)-1-methylpyrrole-2-carbonitrile Chemical compound CN1C(C#N)=CC=C1C1=CC=C(N)C=C1F MGFMZAUPZJHQAW-UHFFFAOYSA-N 0.000 claims description 5
• OGFHZLPBRQKMLY-UHFFFAOYSA-N 5-(4-amino-3-fluorophenyl)-1-methylpyrrole-2-carbonitrile Chemical compound CN1C(C#N)=CC=C1C1=CC=C(N)C(F)=C1 OGFHZLPBRQKMLY-UHFFFAOYSA-N 0.000 claims description 5
• KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 5
• 241000124008 Mammalia Species 0.000 claims description 5
• 230000002254 contraceptive effect Effects 0.000 claims description 5
• 125000003107 substituted aryl group Chemical group 0.000 claims description 5
• 229910052717 sulfur Inorganic materials 0.000 claims description 5
• IXOGTWWGFMXXIT-UHFFFAOYSA-N 5-(4-amino-2,6-difluorophenyl)-1-methylpyrrole-2-carbonitrile Chemical compound CN1C(C#N)=CC=C1C1=C(F)C=C(N)C=C1F IXOGTWWGFMXXIT-UHFFFAOYSA-N 0.000 claims description 4
• PUCDWBFWHOLURA-UHFFFAOYSA-N 5-(4-amino-2-cyanophenyl)-1-methylpyrrole-2-carbonitrile Chemical compound CN1C(C#N)=CC=C1C1=CC=C(N)C=C1C#N PUCDWBFWHOLURA-UHFFFAOYSA-N 0.000 claims description 4
• VZCNXMRTPVJLMG-UHFFFAOYSA-N 5-[4-amino-2-(trifluoromethyl)phenyl]-1-methylpyrrole-2-carbonitrile Chemical compound CN1C(C#N)=CC=C1C1=CC=C(N)C=C1C(F)(F)F VZCNXMRTPVJLMG-UHFFFAOYSA-N 0.000 claims description 4
• QCSWQKGZIZVCSO-UHFFFAOYSA-N [4-(5-cyano-1-methylpyrrol-2-yl)-2-propan-2-ylphenyl]cyanamide Chemical compound C1=C(NC#N)C(C(C)C)=CC(C=2N(C(C#N)=CC=2)C)=C1 QCSWQKGZIZVCSO-UHFFFAOYSA-N 0.000 claims description 4
• LUOOLNPIHBNSAG-UHFFFAOYSA-N [4-(5-cyano-1-methylpyrrol-2-yl)-3-methoxyphenyl]cyanamide Chemical compound COC1=CC(NC#N)=CC=C1C1=CC=C(C#N)N1C LUOOLNPIHBNSAG-UHFFFAOYSA-N 0.000 claims description 4
• 239000000539 dimer Substances 0.000 claims description 4
• 201000010099 disease Diseases 0.000 claims description 4
• 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 4
• ZCRZCMUDOWDGOB-UHFFFAOYSA-N ethanesulfonimidic acid Chemical compound CCS(N)(=O)=O ZCRZCMUDOWDGOB-UHFFFAOYSA-N 0.000 claims description 4
• QHLYHKQLBQGUHK-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]propanamide Chemical compound C1=CC(NC(=O)CC)=CC=C1C1=CC=C(C#N)N1C QHLYHKQLBQGUHK-UHFFFAOYSA-N 0.000 claims description 4
• VLUDBBFJPLCBJQ-UHFFFAOYSA-N n-[4-(5-cyano-1h-pyrrol-2-yl)phenyl]ethanesulfonamide Chemical compound C1=CC(NS(=O)(=O)CC)=CC=C1C1=CC=C(C#N)N1 VLUDBBFJPLCBJQ-UHFFFAOYSA-N 0.000 claims description 4
• BCLHPXBEMVAJAF-UHFFFAOYSA-N 1,3-bis[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]urea Chemical compound CN1C(C#N)=CC=C1C(C=C1)=CC=C1NC(=O)NC1=CC=C(C=2N(C(C#N)=CC=2)C)C=C1 BCLHPXBEMVAJAF-UHFFFAOYSA-N 0.000 claims description 3
• 206010028980 Neoplasm Diseases 0.000 claims description 3
• LFRQWGZNCKPYCH-UHFFFAOYSA-N [2-chloro-4-(5-cyano-1-methylpyrrol-2-yl)phenyl]cyanamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(NC#N)C(Cl)=C1 LFRQWGZNCKPYCH-UHFFFAOYSA-N 0.000 claims description 3
• FZBIMASXXBCBBD-UHFFFAOYSA-N [4-(5-cyano-1-methylpyrrol-2-yl)-2-fluorophenyl]cyanamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(NC#N)C(F)=C1 FZBIMASXXBCBBD-UHFFFAOYSA-N 0.000 claims description 3
• ULSOEHVKDWHXKM-UHFFFAOYSA-N [4-(5-cyano-1-methylpyrrol-2-yl)-2-methoxyphenyl]cyanamide Chemical compound C1=C(NC#N)C(OC)=CC(C=2N(C(C#N)=CC=2)C)=C1 ULSOEHVKDWHXKM-UHFFFAOYSA-N 0.000 claims description 3
• FMALLCKEZNKLBP-UHFFFAOYSA-N [4-(5-cyano-1-methylpyrrol-2-yl)-2-propylphenyl]cyanamide Chemical compound C1=C(NC#N)C(CCC)=CC(C=2N(C(C#N)=CC=2)C)=C1 FMALLCKEZNKLBP-UHFFFAOYSA-N 0.000 claims description 3
• UDBAIWBVUZPWLR-UHFFFAOYSA-N [4-(5-cyano-1-methylpyrrol-2-yl)phenyl]methylcyanamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(CNC#N)C=C1 UDBAIWBVUZPWLR-UHFFFAOYSA-N 0.000 claims description 3
• 238000004519 manufacturing process Methods 0.000 claims description 3
• USHJUWFAOFMGNQ-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]-2-methylprop-2-enamide Chemical compound C1=CC(NC(=O)C(=C)C)=CC=C1C1=CC=C(C#N)N1C USHJUWFAOFMGNQ-UHFFFAOYSA-N 0.000 claims description 3
• GKDVKPGBVTYGCC-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]-2-methylpropanamide Chemical compound C1=CC(NC(=O)C(C)C)=CC=C1C1=CC=C(C#N)N1C GKDVKPGBVTYGCC-UHFFFAOYSA-N 0.000 claims description 3
• KIQORVZTLMGMOA-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]-3-methylbutanamide Chemical compound C1=CC(NC(=O)CC(C)C)=CC=C1C1=CC=C(C#N)N1C KIQORVZTLMGMOA-UHFFFAOYSA-N 0.000 claims description 3
• WINRLKMXNQDAOS-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]acetamide Chemical compound C1=CC(NC(=O)C)=CC=C1C1=CC=C(C#N)N1C WINRLKMXNQDAOS-UHFFFAOYSA-N 0.000 claims description 3
• YLBIRAWBRJYPQQ-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]benzamide Chemical compound CN1C(C#N)=CC=C1C(C=C1)=CC=C1NC(=O)C1=CC=CC=C1 YLBIRAWBRJYPQQ-UHFFFAOYSA-N 0.000 claims description 3
• LFXXQZFFCMOSKT-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]furan-2-carboxamide Chemical compound CN1C(C#N)=CC=C1C(C=C1)=CC=C1NC(=O)C1=CC=CO1 LFXXQZFFCMOSKT-UHFFFAOYSA-N 0.000 claims description 3
• 206010000060 Abdominal distension Diseases 0.000 claims description 2
• 208000019901 Anxiety disease Diseases 0.000 claims description 2
• 206010006313 Breast tenderness Diseases 0.000 claims description 2
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
• 206010056465 Food craving Diseases 0.000 claims description 2
• 206010022998 Irritability Diseases 0.000 claims description 2
• 206010027951 Mood swings Diseases 0.000 claims description 2
• WOWBVKKIFGYNQZ-UHFFFAOYSA-N [4-(5-cyano-1-methylpyrrol-2-yl)-2-ethylphenyl]cyanamide Chemical compound C1=C(NC#N)C(CC)=CC(C=2N(C(C#N)=CC=2)C)=C1 WOWBVKKIFGYNQZ-UHFFFAOYSA-N 0.000 claims description 2
• 125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
• 230000036506 anxiety Effects 0.000 claims description 2
• 230000003247 decreasing effect Effects 0.000 claims description 2
• 206010016256 fatigue Diseases 0.000 claims description 2
• 239000011737 fluorine Substances 0.000 claims description 2
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
• UGLNZYAMAVOBSG-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)-2,5-difluorophenyl]propane-1-sulfonamide Chemical compound C1=C(F)C(NS(=O)(=O)CCC)=CC(F)=C1C1=CC=C(C#N)N1C UGLNZYAMAVOBSG-UHFFFAOYSA-N 0.000 claims description 2
• PALDPPQXEQQEEN-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)-2-fluorophenyl]ethanesulfonamide Chemical compound C1=C(F)C(NS(=O)(=O)CC)=CC=C1C1=CC=C(C#N)N1C PALDPPQXEQQEEN-UHFFFAOYSA-N 0.000 claims description 2
• AUKVLDKBBZQWBT-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)-2-fluorophenyl]methanesulfonamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(NS(C)(=O)=O)C(F)=C1 AUKVLDKBBZQWBT-UHFFFAOYSA-N 0.000 claims description 2
• MZUYPFIOEIBRRF-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)-3-(trifluoromethyl)phenyl]ethanesulfonamide Chemical compound FC(F)(F)C1=CC(NS(=O)(=O)CC)=CC=C1C1=CC=C(C#N)N1C MZUYPFIOEIBRRF-UHFFFAOYSA-N 0.000 claims description 2
• YDNXSGWPZKYTGY-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)-3-(trifluoromethyl)phenyl]propane-1-sulfonamide Chemical compound FC(F)(F)C1=CC(NS(=O)(=O)CCC)=CC=C1C1=CC=C(C#N)N1C YDNXSGWPZKYTGY-UHFFFAOYSA-N 0.000 claims description 2
• SQXJRHMGTHTNHO-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)-3-fluorophenyl]butane-1-sulfonamide Chemical compound FC1=CC(NS(=O)(=O)CCCC)=CC=C1C1=CC=C(C#N)N1C SQXJRHMGTHTNHO-UHFFFAOYSA-N 0.000 claims description 2
• SWLJOQFFIVIKMD-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)-3-fluorophenyl]ethanesulfonamide Chemical compound FC1=CC(NS(=O)(=O)CC)=CC=C1C1=CC=C(C#N)N1C SWLJOQFFIVIKMD-UHFFFAOYSA-N 0.000 claims description 2
• UYROQEMFTDNRIY-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)-3-fluorophenyl]methanesulfonamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(NS(C)(=O)=O)C=C1F UYROQEMFTDNRIY-UHFFFAOYSA-N 0.000 claims description 2
• WMVKGPPFFNOKOW-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]-2,2,2-trifluoroethanesulfonamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(NS(=O)(=O)CC(F)(F)F)C=C1 WMVKGPPFFNOKOW-UHFFFAOYSA-N 0.000 claims description 2
• SQAKCCOKXHKQED-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=C(C=2N(C(C#N)=CC=2)C)C=C1 SQAKCCOKXHKQED-UHFFFAOYSA-N 0.000 claims description 2
• AXMPUJAZUBSBOV-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]-4-propan-2-ylbenzenesulfonamide Chemical compound C1=CC(C(C)C)=CC=C1S(=O)(=O)NC1=CC=C(C=2N(C(C#N)=CC=2)C)C=C1 AXMPUJAZUBSBOV-UHFFFAOYSA-N 0.000 claims description 2
• ZGNLOIZNQPSIBQ-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]-n-methylsulfonylmethanesulfonamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(N(S(C)(=O)=O)S(C)(=O)=O)C=C1 ZGNLOIZNQPSIBQ-UHFFFAOYSA-N 0.000 claims description 2
• NXCIMYDGFDRLFP-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]benzenesulfonamide Chemical compound CN1C(C#N)=CC=C1C(C=C1)=CC=C1NS(=O)(=O)C1=CC=CC=C1 NXCIMYDGFDRLFP-UHFFFAOYSA-N 0.000 claims description 2
• LIAYYMAKCKBDJR-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]butanamide Chemical compound C1=CC(NC(=O)CCC)=CC=C1C1=CC=C(C#N)N1C LIAYYMAKCKBDJR-UHFFFAOYSA-N 0.000 claims description 2
• YVXWZPHAJXHQIZ-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]butane-1-sulfonamide Chemical compound C1=CC(NS(=O)(=O)CCCC)=CC=C1C1=CC=C(C#N)N1C YVXWZPHAJXHQIZ-UHFFFAOYSA-N 0.000 claims description 2
• DIUADYZIHJCFKC-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]cyclobutanecarboxamide Chemical compound CN1C(C#N)=CC=C1C(C=C1)=CC=C1NC(=O)C1CCC1 DIUADYZIHJCFKC-UHFFFAOYSA-N 0.000 claims description 2
• GBAUHXPGPWTPFT-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]cyclohexanecarboxamide Chemical compound CN1C(C#N)=CC=C1C(C=C1)=CC=C1NC(=O)C1CCCCC1 GBAUHXPGPWTPFT-UHFFFAOYSA-N 0.000 claims description 2
• ANODMLLRRSJHOJ-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]ethanesulfonamide Chemical compound C1=CC(NS(=O)(=O)CC)=CC=C1C1=CC=C(C#N)N1C ANODMLLRRSJHOJ-UHFFFAOYSA-N 0.000 claims description 2
• GMHRJLKGYBNGKA-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]methanesulfonamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(NS(C)(=O)=O)C=C1 GMHRJLKGYBNGKA-UHFFFAOYSA-N 0.000 claims description 2
• BKJARJTZZXCKKA-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]propane-1-sulfonamide Chemical compound C1=CC(NS(=O)(=O)CCC)=CC=C1C1=CC=C(C#N)N1C BKJARJTZZXCKKA-UHFFFAOYSA-N 0.000 claims description 2
• XSJZNLVVOVDASQ-UHFFFAOYSA-N n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]propane-2-sulfonamide Chemical compound C1=CC(NS(=O)(=O)C(C)C)=CC=C1C1=CC=C(C#N)N1C XSJZNLVVOVDASQ-UHFFFAOYSA-N 0.000 claims description 2
• RNKLDLHPMJXHCG-UHFFFAOYSA-N n-[4-[5-cyano-1-(3-phenylpropyl)pyrrol-2-yl]phenyl]ethanesulfonamide Chemical compound C1=CC(NS(=O)(=O)CC)=CC=C1C1=CC=C(C#N)N1CCCC1=CC=CC=C1 RNKLDLHPMJXHCG-UHFFFAOYSA-N 0.000 claims description 2
• 230000001850 reproductive effect Effects 0.000 claims description 2
• 230000035946 sexual desire Effects 0.000 claims description 2
• 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
• 206010006187 Breast cancer Diseases 0.000 claims 1
• 208000026310 Breast neoplasm Diseases 0.000 claims 1
• 206010033128 Ovarian cancer Diseases 0.000 claims 1
• 206010061535 Ovarian neoplasm Diseases 0.000 claims 1
• DKPRREAGWJNWGD-UHFFFAOYSA-N ethyl n-[4-(5-cyano-1-methylpyrrol-2-yl)phenyl]carbamate Chemical compound C1=CC(NC(=O)OCC)=CC=C1C1=CC=C(C#N)N1C DKPRREAGWJNWGD-UHFFFAOYSA-N 0.000 claims 1
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
• XWVOMJKOXKPRBH-UHFFFAOYSA-N n-[2-cyano-4-(5-cyano-1-methylpyrrol-2-yl)phenyl]methanesulfonamide Chemical compound CN1C(C#N)=CC=C1C1=CC=C(NS(C)(=O)=O)C(C#N)=C1 XWVOMJKOXKPRBH-UHFFFAOYSA-N 0.000 claims 1
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