AR057776A1 - Derivados de 1,4-benzotiazepinas para prevenir y tratar trastornos que in-volucran la modulacion de los receptores ryr; procesos de obtencion y composiciones farmaceuticas - Google Patents
Derivados de 1,4-benzotiazepinas para prevenir y tratar trastornos que in-volucran la modulacion de los receptores ryr; procesos de obtencion y composiciones farmaceuticasInfo
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- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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Abstract
La presente se refiere a sus sales, hidratos, solvatos, complejos y prodrogas. Se proveen además, métodos para sintetizar. Composiciones farmacéuticas que comprenden los compuestos y métodos para usar las composiciones farmacéuticas de la formula (1) para el tratamiento y prevencion de trastornos y enfermedades asociados con los receptores RyR que regulan al funcionamiento de los canales de calcio en las células. Reivindicacion 1: Un compuesto de formula (1), en donde, n es 0, 1 o 2; q es 0, 1, 2, 3 o 4; cada R se selecciona, de forma independiente, del grupo formado por halogeno, -OH, -NH2, -NO2, -CN, -CF3, -OCF3, -N3, -SO3H, -S(=O)2alquilo, -S(=O)alquilo, -OS(=O)2CF3, acilo, -O-acilo, alquilo, alcoxilo, alquilamino, alquilarilamino, alquiltio, cicloalquilo, alquilarilo, arilo, heteroarilo, heterociclilo, heterociclilalquilo, alquenilo, alquinilo, (hetero-)arilo, (hetero-)ariltio, y (hetero-)arilamino; en donde cada acilo, -O-acilo, alquilo, alcoxilo, alquilamino, alquilarilamino, alquiltio, cicloalquilo, alquilarilo, arilo, heteroarilo, heterociclilo, heterociclilalquilo, alquenilo, alquinilo, (hetero-)arilo, (hetero-)ariltio, y (hetero-) arilamino puede estar sustituido o no sustituido; R1 se selecciona del grupo formado por H, oxo, alquilo, alquenilo, arilo, alquilarilo, cicloalquilo, heteroarilo y heterociclilo; en donde cada alquilo, alquenilo, arilo, alquilarilo, cicloalquilo, heteroarilo y heterociclilo puede estar sustituido o no sustituido; R2 se selecciona del grupo formado por H, -C(=O)R5, -C(=S)R6, -SO2R7, -P(=O)R8R9, -(CH2)m-R10, alquilo, arilo, alquilarilo, heteroarilo, cicloalquilo, cicloalquilalquilo, y heterociclilo; en donde cada alquilo, arilo, alquilarilo, heteroarilo, cicloalquilo, cicloalquilalquilo, y heterociclilo puede estar sustituido o no sustituido; R3 se selecciona del grupo formado por H, -CO2Y, C(=O)NHY, acilo, -O-acilo, alquilo, alquenilo, arilo, alquilarilo, cicloalquilo, heteroarilo y heterociclilo; en donde cada acilo, alquilo, alquenilo, arilo, alquilarilo, cicloalquilo, heteroarilo y heterociclilo puede estar sustituido o no sustituido; y en donde Y se selecciona del grupo formado por H, alquilo, arilo, alquilarilo, cicloalquilo, heteroarilo y heterociclilo; y en donde cada alquilo, arilo, alquilarilo, cicloalquilo, heteroarilo y heterociclilo puede estar sustituido o no sustituido; R4 se selecciona del grupo formado por H, alquilo, alquenilo, arilo, alquilarilo, cicloalquilo, heteroarilo y heterociclilo; en donde cada alquilo, alquenilo, arilo, alquilarilo, cicloalquilo, heteroarilo y heterociclilo puede estar sustituido o no sustituido; R5 se selecciona del grupo formado por -NR15R16, - (CH2)qNR15R16, -NHNR15R16, NHOH, -OR15, -C(=O)NHNR15R16, -CO2R15, -C(=O)NR15R16, CH2X, acilo, alquilo, alquenilo, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo; en donde cada acilo, alquilo, alquenilo, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo puede estar sustituido o no sustituido, y en donde q es 1, 2, 3, 4, 5 o 6; R6 se selecciona del grupo formado por -OR15, NHNR15R16, - NHOH, -NR15R16, -CH2X, acilo, alquenilo, alquilo, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo; en donde cada acilo, alquenilo, alquilo, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo puede estar sustituido o no sustituido; R7 se selecciona del grupo formado por -OR15, -NR15R16, NHNR15R16, -NHOH, -CH2X, alquilo, alquenilo, alquinilo, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo; en donde cada alquilo, alquenilo, alquinilo, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo puede estar sustituido o no sustituido; R8 y R9 se seleccionan, de forma independiente, del grupo formado por OH, acilo, alquenilo, alcoxilo, alquilo, alquilamino, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo; en donde cada acilo, alquenilo, alcoxilo, alquilo, alquilamino, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo puede estar sustituido o no sustituido; R10 se selecciona del grupo formado por -NR15R16, OH, -SO2R11, - NHSO2R11, C(=O)(R12), NHC=O(R12), -OC=O(R12), y -P(=O)R13R14; R11, R12, R13, y R14 se seleccionan, de forma independiente, del grupo formado por H, OH, NH2, -NHNH2, -NHOH, acilo, alquenilo, alcoxilo, alquilo, alquilamino, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo; en donde cada acilo, alquenilo, alcoxilo, alquilo, alquilamino, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo puede estar sustituido o no sustituido; X se selecciona del grupo formado por halogeno, -CN, -CO2R15, -C(=O)NR15R16, -NR15R16, -OR15, -SO2R7, y -P(=O)R8R9; y R15 y R16 se seleccionan, de forma independiente, del grupo formado por H, acilo, alquenilo, alcoxilo, OH, NH2, alquilo, alquilamino, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo; en donde cada acilo, alquenilo, alcoxilo, alquilo, alquilamino, arilo, alquilarilo, cicloalquilo, cicloalquilalquilo, heteroarilo, heterociclilo, y heterociclilalquilo puede estar sustituido o no sustituido; y opcionalmente R15 y R16 junto con el N al cual están unidos, pueden formar un heterociclo que puede estar sustituido; el nitrogeno en el anillo benzotiazepina puede ser opcionalmente un nitrogeno cuaternario; y enantiomeros, diastereomeros, tautomeros, sales, hidratos, solvatos, complejos y prodrogas aceptables para uso farmacéutico de los mismos; con la condicion que cuando q es 0 y n es 0, entonces R2 no es H, Et, -C(=O)NH2, (=O)NHPh, -C(=S)NH-nButilo, -C(=O)NHC(= O)CH2Cl, -C(=O)H, -C(=O)Me, -C(=O)Et, -C(=O)CH=CH2, -S(=O)2Me o -S(=O)2Et; con la condicion que cuando q es 0 y n es 1 o 2, entonces R2 no es -C(=O)Me, -C(=O)Et, -S(=O)2Et; con la condicion adicional que cuando q es 1, y R es Me, Cl o F en la posicion 6 del anillo benzotiazepeno, entonces R2 no es H, Me, -C(=O)H, -C(=O)Me, -C(=O)Et, -C(=O)Ph, -S(=O)2Me o -S(=O)Et; y con la condicion adicional que cuando q es 1, n es 0, y R es OCT3, OH, alcoxilo C1-3 en la posicion 7 del anillo benzotiazepeno, entonces R2 no es H, -C(=O)CH=CH2, o un resto de formula (2).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US11/212,413 US7704990B2 (en) | 2005-08-25 | 2005-08-25 | Agents for preventing and treating disorders involving modulation of the RyR receptors |
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AR057776A1 true AR057776A1 (es) | 2007-12-19 |
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Application Number | Title | Priority Date | Filing Date |
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ARP060103693A AR057776A1 (es) | 2005-08-25 | 2006-08-24 | Derivados de 1,4-benzotiazepinas para prevenir y tratar trastornos que in-volucran la modulacion de los receptores ryr; procesos de obtencion y composiciones farmaceuticas |
Country Status (35)
Country | Link |
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US (1) | US7704990B2 (es) |
EP (4) | EP2764867A1 (es) |
JP (1) | JP5342877B2 (es) |
KR (2) | KR20080037741A (es) |
CN (2) | CN102558093B (es) |
AP (1) | AP3091A (es) |
AR (1) | AR057776A1 (es) |
AU (1) | AU2006283534C1 (es) |
BR (1) | BRPI0615097B1 (es) |
CA (1) | CA2620183C (es) |
CR (1) | CR9812A (es) |
CY (3) | CY1113974T1 (es) |
DK (3) | DK2177224T3 (es) |
EA (1) | EA014941B1 (es) |
EC (1) | ECSP088306A (es) |
ES (3) | ES2405765T3 (es) |
GE (1) | GEP20105134B (es) |
HK (3) | HK1119705A1 (es) |
HN (1) | HN2008000299A (es) |
HR (3) | HRP20130353T1 (es) |
IL (1) | IL189675A (es) |
MA (1) | MA29785B1 (es) |
MY (1) | MY144622A (es) |
NO (1) | NO20081421L (es) |
NZ (1) | NZ566822A (es) |
PL (3) | PL2311464T3 (es) |
PT (3) | PT2177224E (es) |
RS (3) | RS52780B (es) |
SI (3) | SI2177224T1 (es) |
SV (1) | SV2008002828A (es) |
TN (1) | TNSN08078A1 (es) |
TW (1) | TWI486338B (es) |
UA (1) | UA93388C2 (es) |
WO (1) | WO2007024717A2 (es) |
ZA (1) | ZA200802338B (es) |
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US20040048780A1 (en) * | 2000-05-10 | 2004-03-11 | The Trustees Of Columbia University In The City Of New York | Method for treating and preventing cardiac arrhythmia |
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US20040229781A1 (en) * | 2000-05-10 | 2004-11-18 | Marks Andrew Robert | Compounds and methods for treating and preventing exercise-induced cardiac arrhythmias |
US7879840B2 (en) * | 2005-08-25 | 2011-02-01 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
US7393652B2 (en) * | 2000-05-10 | 2008-07-01 | The Trustees Of Columbia University In The City Of New York | Methods for identifying a chemical compound that directly enhances binding of FKBP12.6 to PKA-phosphorylated type 2 ryanodine receptor (RyR2) |
US6489125B1 (en) * | 2000-05-10 | 2002-12-03 | The Trustees Of Columbia University In The City Of New York | Methods for identifying chemical compounds that inhibit dissociation of FKBP12.6 binding protein from type 2 ryanodine receptor |
US20060293266A1 (en) * | 2000-05-10 | 2006-12-28 | The Trustees Of Columbia | Phosphodiesterase 4D in the ryanodine receptor complex protects against heart failure |
US8022058B2 (en) * | 2000-05-10 | 2011-09-20 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
US7544678B2 (en) * | 2002-11-05 | 2009-06-09 | The Trustees Of Columbia University In The City Of New York | Anti-arrythmic and heart failure drugs that target the leak in the ryanodine receptor (RyR2) |
AU2004220548A1 (en) * | 2003-03-07 | 2004-09-23 | The Trustees Of Columbia University, In The City Of New York | Type 1 ryanodine receptor-based methods |
US8710045B2 (en) * | 2004-01-22 | 2014-04-29 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the ryanodine receptors |
US7704990B2 (en) | 2005-08-25 | 2010-04-27 | The Trustees Of Columbia University In The City Of New York | Agents for preventing and treating disorders involving modulation of the RyR receptors |
WO2008144483A2 (en) * | 2007-05-18 | 2008-11-27 | Armgo Pharma, Inc. | Agents for treating disorders involving modulation of ryanodine receptors |
NZ587767A (en) | 2008-03-03 | 2012-05-25 | Servier Lab | Process for preparing benzothiazepines from gamma-aminoalkylbenzenes |
AU2008243144A1 (en) * | 2008-11-06 | 2010-05-20 | Quark Technologies Australia Pty Ltd | Improvements in Radiopharmaceutical Purification |
CN102333774B (zh) * | 2009-02-25 | 2014-04-23 | 金子升 | 1,4-苯并硫氮杂*-1-氧化物衍生物及使用该衍生物的医药组合物 |
US8933129B2 (en) | 2009-04-15 | 2015-01-13 | State Of Oregon By And Through The State Board Of Higher Education On Behalf Of Portland State University | Compounds and methods for modulating activity of calcium release channels |
CN101812523B (zh) * | 2010-04-09 | 2012-08-22 | 广州益善生物技术有限公司 | Ryr1基因snp检测特异性引物、液相芯片和检测方法 |
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