AR088781A1 - Compuestos antimicrobianos y metodos para prepararlos y utilizarlos - Google Patents
Compuestos antimicrobianos y metodos para prepararlos y utilizarlosInfo
- Publication number
- AR088781A1 AR088781A1 ARP120101303A ARP120101303A AR088781A1 AR 088781 A1 AR088781 A1 AR 088781A1 AR P120101303 A ARP120101303 A AR P120101303A AR P120101303 A ARP120101303 A AR P120101303A AR 088781 A1 AR088781 A1 AR 088781A1
- Authority
- AR
- Argentina
- Prior art keywords
- unsaturated
- saturated
- group
- sulfur
- nitrogen
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 230000000845 anti-microbial effect Effects 0.000 title 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 24
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 14
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 13
- 125000005842 heteroatom Chemical group 0.000 abstract 13
- 229910052757 nitrogen Inorganic materials 0.000 abstract 13
- 229910052760 oxygen Inorganic materials 0.000 abstract 13
- 239000001301 oxygen Chemical group 0.000 abstract 13
- 229910052717 sulfur Chemical group 0.000 abstract 13
- 239000011593 sulfur Chemical group 0.000 abstract 13
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 12
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 8
- 125000001424 substituent group Chemical group 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 7
- 125000002837 carbocyclic group Chemical group 0.000 abstract 5
- 229910052799 carbon Inorganic materials 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 4
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 150000001721 carbon Chemical group 0.000 abstract 3
- 239000011203 carbon fibre reinforced carbon Substances 0.000 abstract 3
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- -1 (i) -OCH3 Chemical class 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 101100006939 Zea mays CNR11 gene Proteins 0.000 abstract 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A61P31/06—Antibacterial agents for tuberculosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
- C07D239/36—One oxygen atom as doubly bound oxygen atom or as unsubstituted hydroxy radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Pulmonology (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Materials For Medical Uses (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
Abstract
Reivindicación 1: Un compuesto caracterizado porque tiene la fórmula (1) o un tautómero del mismo, o una sal, éster o profármaco de dicho compuesto o tautómero farmacéuticamente aceptable, donde X¹ es CR¹ o N; X² es CR² o N; X³ es CR³ o N; X⁴ es CR⁴ o N; X⁵ es CR⁵ o N; con la condición de que X¹, X², X³, X⁴, y X⁵ no sean todos N; Y⁶ es CR⁶ o N; Y⁷, es CR⁷ o 6N; Y⁸ es CR⁸ o N; Y⁹ es CR⁹ o N; Y¹⁰ es CR¹⁰ o N; con la condición de que Y⁶, Y⁷, Y⁸, Y⁹, e Y¹⁰ no sean todos N; donde R¹, R², R⁴, R⁵, R⁶, R⁷, R⁸ y R¹⁰ se seleccionan, cada uno, independientemente de (a) hidrógeno, (b) F, (c) Cl, (d) Br, (e) I, (f) -CF₃, (g) -CF₂H, (h) -CFH₂, (i) -OCF₃, (j) -OCF₂H, (k) -OCFH₂, (l) -OCH₃, (m) -CN, (n) -N₃, (o) -NO₂, (p) -NR¹¹R¹¹, (q) -NR¹¹C(O)R¹¹, (r) -C(O)NR¹¹R¹¹, (s) -OR¹¹, (t) -COH, (u) -CO(alquilo C₁₋₈), (v) -COR¹¹, (w) -NR¹¹(CNR¹¹)NR¹¹R¹¹, (x) -S(O)ₚR¹¹, (y) -NR¹¹S(O)PR¹¹, (z) -SR¹¹, (aa) -SCF₃, (bb) -C(CF₃)H-NH-CHR¹¹R¹¹, (cc) -COOR¹¹, (dd) -(OCH₂CH₂)ₜR¹¹, (ee) -(OCH₂CH₂)ₜOR¹¹, (ff) -alquilo C₁₋₈, (gg) -alquenilo C₂₋₈, (hh) -alquinilo C₂₋₈, (ii) -(alquilo C₁₋₈)-(heterociclo saturado, insaturado o aromático de 3 - 14 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre), (jj) -(alquilo C₁₋₈)-(carbociclo saturado, insaturado o aromático de 3 - 14 miembros), (kk) -haloalquilo, (ll) -heterociclo saturado, insaturado o aromático de 3 - 14 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre, (mm) -carbociclo saturado, insaturado o aromático de 3 - 14 miembros, y (nn) -CHR¹¹-NH-(heterociclo saturado, insaturado o aromático de 3 - 14 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre); donde cada (ff) hasta (nn) está opcionalmente sustituido con uno o más R¹²; alternativamente, donde dos sustituyentes seleccionados entre R⁶, R⁷, y R⁸ se toman junto con el átomo de carbono al que están ligados para formar (a) un carbocíclico saturado o insaturado de 3 - 7 miembros o (b) un anillo heterocíclico saturado o insaturado de 3 - 7 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre; donde cada (a) hasta (b) está opcionalmente sustituido con uno o más R¹²; cada R¹¹ se selecciona independientemente entre (a) hidrógeno, (b) halógeno, (c) -OH, (d) -SH, (e) -(alquilo C₁₋₈)OH, (f) -OCF₃, (g) -OCF₂H, (h) -OCFH₂, (i) -OCH₃, (j) -OR¹², (k) -COR¹², (l) -CN, (m) -NO₂, (n) -CONH₂, (o) -CONR¹²R¹², (p) -COCH₃, (q) -S(O)ₚCH₃, (r) -S(O)ₚNR¹²R¹², (s) -SR¹², (t) -C(O)OH, (u) -C(O)OR¹², (v) -N₃, (w) -NH₂, (x) -NR¹²C(O)R¹², (y) -NH(alquilo C₁₋₈), (z) -N(alquilo C₁₋₈)₂, (aa) -alquilo C₁₋₈, (bb) -alquenilo C₂₋₈, (cc) -alquinilo C₂₋₈, (dd) -haloalquilo, (ee) -(alquilo C₁₋₈)-(heterociclo saturado, insaturado o aromático de 3 - 14 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre), (ff) -(alquilo C₁₋₈)-(carbociclo saturado, insaturado o aromático de 3 - 14 miembros), (gg) -heterociclo saturado, insaturado o aromático de 3 - 14 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre, (hh) -carbociclo saturado, insaturado o aromático de 3 - 14 miembros, y (ii) -(C=NH)NR¹²R¹²; donde cada (y) hasta (hh) está opcionalmente sustituido con uno o más R¹²; alternativamente dos sustituyentes R¹¹ se toman juntos para formar (a) un carbocíclico saturado o insaturado de 3 - 7 miembros o (b) un anillo heterocíclico saturado o insaturado de 3 - 7 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre, donde cada (a) hasta (b) está opcionalmente sustituido con uno o más R¹²; R³ se selecciona entre el grupo de formulas (2), donde R³ᵃ, R³ᵇ, R³ᶜ, R³ᵈ, R³ᵉ, R³ᶠ, R³ᵍ, R³ʰ, R³ⁱ, R³ʲ, R³ᵏ, y R³ˡ se seleccionan, cada uno, independientemente de (a) hidrógeno, (b) halógeno, (c) -CN, (d) -N₃, (e) -NO₂, (f) -OCF₃, (g) -OCF₂H, (h) -OCFH₂, (i) -OCH₃, (j) -OR¹¹, (k) -C(O)R¹¹, (l) -C(O)NR¹¹R¹¹, (m) -NH₂, (n) -NR¹¹R¹¹, (o) -NR¹¹C(O)R¹¹, (p) -S(O)ₚR¹¹, (q) -C(O)OH, (r) -C(O)OR¹¹, (s) -alquilo C₁₋₈, (t) -alquenilo C₂₋₈, (u) -alquinilo C₂₋₈, (v) haloalquilo, (w) -heterociclo saturado, insaturado o aromático de 3 - 14 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre, y (x) -carbociclo saturado, insaturado o aromático de 3 - 14 miembros; donde cada (s) hasta (x) está opcionalmente sustituido con uno o más R¹²; alternativamente, uno o más pares de sustituyentes seleccionados entre R³ᵃ, R³ᵇ, R³ᶜ, R³ᵈ, R³ᵉ y R³ᶠ, R³ᵍ y R³ʰ, R³ⁱ y R³ʲ, y R³ᵏ y R³ˡ se toman junto con el átomo de carbono al que están ligados para formar (a) un carbocíclico saturado o insaturados de 3 - 7 miembros, (b) un anillo heterocíclico saturado o insaturado de 3 - 7 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre, (c) un enlace doble carbono-carbono exo, (d) un grupo carbonilo o (e) un grupo tiocarbonilo; donde cada (a) hasta (b) está opcionalmente sustituido con uno o más R¹²; alternativamente, donde dos sustituyentes seleccionados entre R³ᵃ, R³ᵇ, R³ᶜ, R³ᵈ, R³ᵉ, R³ᶠ, R³ᵍ, R³ʰ, R³ⁱ, R³ʲ, R³ᵏ, y R³ˡ en diferentes átomos de carbono se toman junto con los átomos que intervienen a los que están ligados para formar (a) un carbocíclico saturado o insaturado de 3 - 7 miembros o (b) un anillo heterocíclico saturado o insaturado de 3 - 7 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre; donde cada (a) hasta (b) está opcionalmente sustituido con uno o más R¹²; alternativamente, donde dos sustituyentes seleccionados entre R³ᵃ, R³ᵇ, R³ᶜ, R³ᵈ, R³ᵉ, R³ᶠ, R³ᵍ, R³ʰ, R³ⁱ, R³ʲ, R³ᵏ, y R³ˡ en dos átomos de carbono adyacentes se toman junto con el enlace entre dichos átomos de carbono adyacentes para formar un doble enlace carbono-carbono sustituido o insustituido, o donde cuatro sustituyentes seleccionados entre R³ᵃ, R³ᵇ, R³ᶜ, R³ᵈ, R³ᵉ, R³ᶠ, R³ᵍ, R³ʰ, R³ⁱ, R³ʲ, R³ᵏ, y R³ˡ en dos átomos de carbono adyacentes se toman junto con el enlace entre dichos átomos de carbono adyacentes para formar un enlace triple carbono-carbono; U se selecciona entre -O-, -S(O)ₚ-, -NR¹¹-, -(C=O)-, -NR¹¹(C=O)-, -(C=O)NR¹¹, -S(O)ₚNR¹¹-, -NR¹¹S(O)ₚ-, -NR¹¹S(O)ₚNR¹¹-, y -NR¹¹C(O)NR¹¹-; T se selecciona entre -NR¹¹R¹¹, -NR¹¹(C=O)OR¹¹, -NR¹¹(C=NR¹¹)NR¹¹R¹¹, y OR¹¹; alternativamente, un R¹¹ y un sustituyente seleccionado entre R³ᵃ, R³ᵇ, R³ᶜ, R³ᵈ, R³ᵉ, R³ᶠ, R³ᵍ, R³ʰ, R³ⁱ, R³ʲ, R³ᵏ, y R³ˡ se toman junto con los átomos que intervienen a los que están ligados para formar (a) un carbocíclico saturado o insaturado de 3 - 7 miembros o (b) un anillo heterocíclico saturado o insaturado de 3 - 7 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre; donde cada (a) hasta (b) está opcionalmente sustituido con uno o más R¹²; R⁹ se selecciona del grupo de formulas (3), donde R⁹ᵏ, R⁹ˡ, R⁹ᵐ, R⁹ⁿ, R⁹ᵒ, R⁹ᵖ, R⁹q, R⁹ʳ, R⁹ˢ, y R⁹ᵗ se seleccionan, cada uno, independientemente de (a) hidrógeno, (b) halógeno, (c) -CN, (d) -N₃, (e) -NO₂, (f) -OCF₃, (g) -OCH₃, (h) -OCF₂H, (i) -OCFH₂, (j) -OR¹¹, (k) -NH₂, (l) -NR¹¹R¹¹, (m) -C(O)R¹¹, (n) -C(O)OR¹¹, (o) -C(O)NR¹¹R¹¹, (p) -NR¹¹C(O)R¹¹, (q) -S(O)ₚR¹¹, (r) -alquilo C₁₋₈, (s) -alquenilo C₂₋₈, (t) -C₁₋₈ alquinilo, (u) haloalquilo, (v) -heterociclo saturado, insaturado o aromático de 3 - 14 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre, y (w) -carbociclo saturado, insaturado o aromático de 3 - 14 miembros; donde cada (r) hasta (w) está opcionalmente sustituido con uno o más R¹²; alternativamente, uno o más pares de sustituyentes seleccionados entre R⁹ᵏ y R⁹ˡ, R⁹ᵐ y R⁹ⁿ, R⁹ᵒ y R⁹ᵖ, R⁹q y R⁹ʳ, R⁹ˢ y R⁹ᵗ se toman junto con el átomo de carbono al que están ligados para formar (a) un carbocíclico saturado o insaturado de 3 - 7 miembros, (b) un anillo heterocíclico saturado o insaturado de 3 - 7 miembros que contiene uno o más heteroátomos seleccionados del grupo formado por nitrógeno, oxígeno y azufre, (c) un enlace doble carbono-carbono exo, (d) un grupo carbonilo o (e) un grupo t
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161476138P | 2011-04-15 | 2011-04-15 | |
| US201161535118P | 2011-09-15 | 2011-09-15 | |
| US201261610363P | 2012-03-13 | 2012-03-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR088781A1 true AR088781A1 (es) | 2014-07-10 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP120101303A AR088781A1 (es) | 2011-04-15 | 2012-04-16 | Compuestos antimicrobianos y metodos para prepararlos y utilizarlos |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US9221827B2 (es) |
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| NZ599291A (en) | 2009-10-16 | 2014-06-27 | Melinta Therapeutics Inc | Antimicrobial compounds and methods of making and using the same |
| MY173518A (en) | 2011-04-15 | 2020-01-30 | Melinta Therapeutics Inc | Antimicrobial compounds and methods of making and using the same |
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| CN111254091B (zh) * | 2020-01-20 | 2022-04-19 | 浙江工业大学 | 一种嗜麦芽窄食单胞菌gyh及其在降解氯代烃类污染物中的应用 |
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- 2012-04-11 CN CN201280029215.5A patent/CN103958514B/zh not_active Expired - Fee Related
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