Sweet flavor modifier
The present invention includes compounds having structural formula (I), or pharmaceutically acceptable salts, solvate, and/or ester thereof. These compounds are useful as sweet flavor modifiers. The present invention also includes compositions comprising the present compounds and methods of enhancing the sweet taste of ingestible compositions. Furthermore, the present invention provides methods for preparing the compounds.
1. An ingestible composition comprising
a compound having a structure of Formula (IIIa) or (IIIa′),
or a tautomer, and/or salt thereof; and
an ingestibly acceptable excipient,
wherein:
A is —NH 2 ;
B is hydrogen, alkyl, —CN, —OR 4 , —S(O) a R 4 , —NR 4 R 5 , —C(O)NR 4 R 5 , —CO 2 R 4 , —NR 4 CO 2 R 5 , —NR 4 C(O)NR 5 R 6 , —NR 4 C(S)NR 5 R 6 , —NR 4 C(═NH)NR 5 R 6 , —SO 2 NR 4 R 5 , —NR 4 SO 2 R 5 , —NR 4 SO 2 NR 5 R 6 , —B(OR 4 )(OR 5 ), —P(O)(OR 4 )(OR 5 ), or —P(O)(R 4 )(OR 5 );
C is —CO 2 R 7 ;
a is 0, 1 or 2;
R 4 , R 5 , R 6 , and R 7 are independently hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, acyl, substituted acyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl or substituted heteroarylalkyl; or alternatively, R 4 and R 5 , or R 5 and R 6 , together with the atoms to which they are bonded, form a cycloheteroalkyl or substituted cycloheteroalkyl ring;
R 21 is hydrogen;
R 22 is hydrogen, alkyl, substituted alkyl, halo, —CN, or —OR 27 ;
R 23 is hydrogen, alkyl, substituted alkyl, —CN, OR 29 , —S(O) f R 29 , —OC(O)R 29 , —NR 29 R 30 , —C(O)NR 29 R 30 , —C(O)R 29 , —CO 2 R 29 , —SO 2 NR 29 R 30 , or —NR 29 SO 2 R 30 ;
R 24 is —O-L 1 -L 2 -R 33 or OR 33 ;
L 1 is alkylene or substituted alkylene;
L 2 is —NR 34 —, —O—, —S—, —NR 34 —C(O)—, —C(O)—NR 34 —, —O—C(O)—, —C(O)—O—, —NR 34 —C(O)—O—, —O—C(O)—NR 34 —, —NR 34 —C(O)—NR 35 —, —O—C(O)—O—, -heterocyclylene-C(O)—, or -(substituted heterocyclylene)-C(O)—;
R 33 is alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocyclyl, substituted heterocyclyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, or substituted heteroarylalkyl; and
R 34 and R 35 are independently hydrogen, alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocyclyl, substituted heterocyclyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, or substituted heteroarylalkyl;
f is 0, 1 or 2; and
R 27 , R 29 , and R 30 are independently hydrogen, or alkyl;
wherein substituted, when used to modify a specified group or radical, means that one or more hydrogen atoms of the specified group or radical are each independently replaced with one or more substituent group(s);
wherein substituent groups on saturated carbon atoms in the substituted group or radical include one or more of —R a , halo, ═O, —OR b , —SR b , ═S, —NR c R c , ═NR b , ═N—OR b , trihalomethyl, —CF 3 , —CN, —OCN, —SCN, —NO, —NO 2 , N 2 , —N 3 , —S(O) 2 R b , —S(O) 2 NR b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ,
wherein each R a is independently selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, cycloheteroalkyl, aryl, arylalkyl, heteroaryl and heteroarylalkyl; each R b is independently hydrogen or R a ; and each R c is independently R b or alternatively, the two R c s may be taken together with the nitrogen atom to which they are bonded form a 4-, 5-, 6- or 7-membered cycloheteroalkyl which may optionally include from 1 to 4 of the same or different additional heteroatoms selected from the group consisting of O, N and S;
wherein the one or more substituent groups, taken together with the atoms to which they are bonded, may form a cyclic ring including cycloalkyl and cycloheteroalkyl;
wherein substituent groups on unsaturated carbon atoms in the specified group or radical include —R a , halo, —OR b , —SR b , —NR c R c , trihalomethyl, —CF 3 , —CN, —OCN, —SCN, —NO, —NO 2 , —N 3 , —S(O) 2 R b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)O − , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ;
wherein substituent groups on nitrogen atoms in heteroatom-containing groups include —R a , —OR b , —SR b , trihalomethyl, —CF 3 , —CN, —NO, —NO 2 , —S(O) 2 R b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ; and
wherein substituents used to substitute a specified group can be further substituted with one or more of the same or different substituent groups.
2. The ingestible composition of claim 1 , further comprising one or more sweeteners.
3. The ingestible composition of claim 2 , wherein the sweetener is selected from the group consisting of sucrose, fructose, glucose, galactose, mannose, lactose, tagatose, maltose, corn syrup, D-tryptophan, glycine, erythritol, isomalt, lactitol, mannitol, sorbitol, xylitol, maltodextrin, maltitol, isomalt, hydrogenated glucose syrup (HGS), hydrogenated starch hydrolyzate (HSH), stevioside, rebaudioside A, other sweet Stevia-based glycosides, carrelame, other guanidine-based sweeteners, saccharin, acesulfame-K, cyclamate, sucralose, alitame, mogroside, neotame, aspartame, other aspartame derivatives, and combinations thereof.
4. The ingestible composition of claim 1 , which has an increased sweet taste as compared to the ingestible composition not containing the compound of claim 1 , as judged by a majority of a panel of at least eight human taste testers.
5. The ingestible composition of claim 1 , which is in form of a food or beverage product, a pharmaceutical composition, a nutritional product, a dietary supplement, over-the-counter medication, or oral care product.
6. The ingestible composition of claim 5 , wherein the food or beverage product is for human or animal consumption.
7. The ingestible composition of claim 1 , wherein the food or beverage product is selected from the group consisting of the Soup category; the Dried Processed Food category; the Beverage category; the Ready Meal category; the Canned or Preserved Food category; the Frozen Processed Food category; the Chilled Processed Food category; the Snack Food category; the Baked Goods category; the Confectionary category; the Dairy Product category; the Ice Cream category; the Meal Replacement category; the Pasta and Noodle category; the Sauces, Dressings, Condiments category; the Baby Food category; the Spreads category; sweet coatings, frostings, or glazes; and combinations thereof.
8. A method of enhancing the sweet taste of an ingestible composition comprising contacting the ingestible composition thereof with a compound having the structure of Formula (IIIa or (IIIa′),
or a tautomer, and/or salt thereof, to form a modified ingestible composition,
wherein:
A is —NH 2 ;
B is hydrogen, alkyl, —CN, —OR 4 , —S(O) a R 4 , —NR 4 R 5 , —C(O)NR 4 R 5 , —CO 2 R 4 , —NR 4 CO 2 R 5 , —NR 4 C(O)NR 5 R 6 , —NR 4 C(S)NR 5 R 6 , —NR 4 C(═NH)NR 5 R 6 , —SO 2 NR 4 R 5 , —NR 4 SO 2 R 5 , —NR 4 SO 2 NR 5 R 6 , —B(OR 4 )(OR 5 ), —P(O)(OR 4 )(OR 5 ), or —P(O)(R 4 )(OR 5 );
C is —CO 2 R 7 ;
a is 0, 1 or 2;
R 4 , R 5 , R 6 , and R 7 are independently hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, acyl, substituted acyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl or substituted heteroarylalkyl; or alternatively, R 4 and R 5 , or R 5 and R 6 , together with the atoms to which they are bonded, form a cycloheteroalkyl or substituted cycloheteroalkyl ring;
R 21 is hydrogen;
R 22 is hydrogen, alkyl, substituted alkyl, halo, —CN, or —OR 27 ;
R 23 is hydrogen, alkyl, substituted alkyl, —CN, OR 29 , —S(O) f R 29 , —OC(O)R 29 , —NR 29 R 30 , —C(O)NR 29 R 30 , —C(O)R 29 , —CO 2 R 29 , —SO 2 NR 29 R 30 , or —NR 29 SO 2 R 30 ;
R 24 is —O-L 1 -L 2 -R 33 or —OR 33 ;
L 1 is alkylene or substituted alkylene;
L 2 is —NR 34 —, —O—, —S—, —NR 34 —C(O)—, —C(O)—NR 34 —, —O—C(O)—, —C(O)—O—, —NR 34 —C(O)—O—, —O—C(O)—NR 34 —, —NR 34 —C(O)—NR 35 —, —O—C(O)—O—, -heterocyclylene-C(O)—, or -(substituted heterocyclylene)-C(O)—;
R 33 is alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocyclyl, substituted heterocyclyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, or substituted heteroarylalkyl; and
R 34 and R 35 are independently hydrogen, alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocyclyl, substituted heterocyclyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, or substituted heteroarylalkyl;
f is 0, 1 or 2; and
R 27 , R 29 , and R 30 are independently hydrogen, or alkyl;
wherein substituted, when used to modify a specified group or radical, means that one or more hydrogen atoms of the specified group or radical are each independently replaced with one or more substituent group(s);
wherein substituent groups on saturated carbon atoms in the substituted group or radical include one or more of —R a , halo, ═O, —OR b , —SR b , ═S, —NR c R c , ═NR b , ═N—OR b , trihalomethyl, —CF 3 , —CN, —OCN, —SCN, —NO, —NO 2 , N 2 , —N 3 , —S(O) 2 R b , —S(O) 2 NR b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ,
wherein each R a is independently selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, cycloheteroalkyl, aryl, arylalkyl, heteroaryl and heteroarylalkyl; each R b is independently hydrogen or R a ; and each R c is independently R b or alternatively, the two R c s may be taken together with the nitrogen atom to which they are bonded form a 4-, 5-, 6- or 7-membered cycloheteroalkyl which may optionally include from 1 to 4 of the same or different additional heteroatoms selected from the group consisting of O, N and S;
wherein the one or more substituent groups, taken together with the atoms to which they are bonded, may form a cyclic ring including cycloalkyl and cycloheteroalkyl;
wherein substituent groups on unsaturated carbon atoms in the specified group or radical include —R a , halo, —OR b , —SR b , —NR c R c , trihalomethyl, —CF 3 , —CN, —OCN, —SCN, —NO, —NO 2 , —N 3 , —S(O) 2 R b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)O − , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ;
wherein substituent groups on nitrogen atoms in heteroatom-containing groups include —R a , —OR b , —SR b , trihalomethyl, —CF 3 , —CN, —NO, —NO 2 , —S(O) 2 R b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ; and
wherein substituents used to substitute a specified group can be further substituted with one or more of the same or different substituent groups.
9. A sweet enhancing composition, comprising a compound having the structure of Formula (IIIa or (IIIa′),
Or a tautomer, and/or salt thereof, in an amount effective to provide sweetening in combination with a first amount of sweetener, wherein the sweetening is more than the sweetening provided by the first amount of sweetener without the compound,
wherein:
A is —NH 2 ;
B is hydrogen, alkyl, —CN, —OR 4 , —S(O) a R 4 , —NR 4 R 5 , —C(O)NR 4 R 5 , —CO 2 R 4 , —NR 4 CO 2 R 5 , —NR 4 C(O)NR 5 R 6 , —NR 4 C(S)NR 5 R 6 , —NR 4 C(═NH)NR 5 R 6 , —SO 2 NR 4 R 5 , —NR 4 SO 2 R 5 , —NR 4 SO 2 NR 5 R 6 , —B(OR 4 )(OR 5 ), —P(O)(OR 4 )(OR 5 ), or —P(O)(R 4 )(OR 5 );
C is —CO 2 R 7 ;
a is 0, 1 or 2;
R 4 , R 5 , R 6 , and R 7 are independently hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, acyl, substituted acyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl or substituted heteroarylalkyl; or alternatively, R 4 and R 5 , or R 5 and R 6 , together with the atoms to which they are bonded, form a cycloheteroalkyl or substituted cycloheteroalkyl ring;
R 21 is hydrogen;
R 22 is hydrogen, alkyl, substituted alkyl, halo, —CN, or —OR 27 ;
R 23 is hydrogen, alkyl, substituted alkyl, —CN, OR 29 , —S(O) f R 29 , —OC(O)R 29 , —NR 29 R 30 , —C(O)NR 29 R 30 , —C(O)R 29 , —CO 2 R 29 , —SO 2 NR 29 R 30 , or —NR 29 SO 2 R 30 ;
R 24 is —O-L 1 -L 2 -R 33 or OR 33 ;
L 1 is alkylene or substituted alkylene;
L 2 is —NR 34 —, —O—, —S—, —NR 34 —C(O)—, —C(O)—NR 34 —, —O—C(O)—, —C(O)—O—, —NR 34 —C(O)—O—, —O—C(O)—NR 34 —, —NR 34 —C(O)—NR 35 —, —O—C(O)—O—, -heterocyclylene-C(O)—, or -(substituted heterocyclylene)-C(O)—;
R 33 is alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocyclyl, substituted heterocyclyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, or substituted heteroarylalkyl; and
R 34 and R 35 are independently hydrogen, alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocyclyl, substituted heterocyclyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, or substituted heteroarylalkyl;
f is 0, 1 or 2; and
R 27 , R 29 , and R 30 are independently hydrogen, or alkyl;
wherein substituted, when used to modify a specified group or radical, means that one or more hydrogen atoms of the specified group or radical are each independently replaced with one or more substituent group(s);
wherein substituent groups on saturated carbon atoms in the substituted group or radical include one or more of —R a , halo, ═O, —OR b , —SR b , ═S, —NR c R c , ═NR b , ═N—OR b , trihalomethyl, —CF 3 , —CN, —OCN, —SCN, —NO, —NO 2 , N 2 , —N 3 , —S(O) 2 R b , —S(O) 2 NR b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ,
wherein each R a is independently selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, cycloheteroalkyl, aryl, arylalkyl, heteroaryl and heteroarylalkyl; each R b is independently hydrogen or R a ; and each R c is independently R b or alternatively, the two R c s may be taken together with the nitrogen atom to which they are bonded form a 4-, 5-, 6- or 7-membered cycloheteroalkyl which may optionally include from 1 to 4 of the same or different additional heteroatoms selected from the group consisting of O, N and S;
wherein the one or more substituent groups, taken together with the atoms to which they are bonded, may form a cyclic ring including cycloalkyl and cycloheteroalkyl;
wherein substituent groups on unsaturated carbon atoms in the specified group or radical include —R a , halo, —OR b , —SR b , —NR c R c , trihalomethyl, —CF 3 , —CN, —OCN, —SCN, —NO, —NO 2 , —N 3 , —S(O) 2 R b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)O − , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ;
wherein substituent groups on nitrogen atoms in heteroatom-containing groups include —R a , —OR b , —SR b , trihalomethyl, —CF 3 , —CN, —NO, —NO 2 , —S(O) 2 R b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ; and
wherein substituents used to substitute a specified group can be further substituted with one or more of the same or different substituent groups.
10. An ingestible composition comprising the sweet enhancing composition of claim 9 .
11. The ingestible composition of claim 10 , which is in form of a food or beverage product, a pharmaceutical composition, a nutritional product, a dietary supplement, over-the-counter medication, or oral care product.
12. A flavoring concentrate formulation comprising
i) as flavor modifying ingredient, a compound having the structure of Formula (IIIa or (IIIa′),
or a tautomer, and/or salt thereof;
ii) a carrier; and
iii) optionally at least one adjuvant,
wherein:
A is —NH 2 ;
B is hydrogen, alkyl, —CN, —OR 4 , —S(O) a R 4 , —NR 4 R 5 , —C(O)NR 4 R 5 , —CO 2 R 4 , —NR 4 CO 2 R 5 , —NR 4 C(O)NR 5 R 6 , —NR 4 C(S)NR 5 R 6 , —NR 4 C(═NH)NR 5 R 6 , —SO 2 NR 4 R 5 , —NR 4 SO 2 R 5 , —NR 4 SO 2 NR 5 R 6 , —B(OR 4 )(OR 5 ), —P(O)(OR 4 )(OR 5 ), or —P(O)(R 4 )(OR 5 );
C is —CO 2 R 7 ;
a is 0, 1 or 2;
R 4 , R 5 , R 6 , and R 7 are independently hydrogen, alkyl, substituted alkyl, aryl, substituted aryl, arylalkyl, substituted arylalkyl, acyl, substituted acyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl or substituted heteroarylalkyl; or alternatively, R 4 and R 5 , or R 5 and R 6 , together with the atoms to which they are bonded, form a cycloheteroalkyl or substituted cycloheteroalkyl ring;
R 21 is hydrogen;
R 22 is hydrogen, alkyl, substituted alkyl, halo, —CN, or —OR 27 ;
R 23 is hydrogen, alkyl, substituted alkyl, —CN, OR 29 , —S(O) f R 29 , —OC(O)R 29 , —NR 29 R 30 , —C(O)NR 29 R 30 , —C(O)R 29 , —CO 2 R 29 , —SO 2 NR 29 R 30 , or —NR 29 SO 2 R 30 ;
R 24 is —O-L 1 -L 2 -R 33 or OR 33 ;
L 1 is alkylene or substituted alkylene;
L 2 is —NR 34 —, —O—, —S—, —NR 34 —C(O)—, —C(O)—NR 34 —, —O—C(O)—, —C(O)—O—, —NR 34 —C(O)—O—, —O—C(O)—NR 34 —, —NR 34 —C(O)—NR 35 —, —O—C(O)—O—, -heterocyclylene-C(O)—, or -(substituted heterocyclylene)-C(O)—;
R 33 is alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocyclyl, substituted heterocyclyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, or substituted heteroarylalkyl; and
R 34 and R 35 are independently hydrogen, alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; aryl, substituted aryl, arylalkyl, substituted arylalkyl, heterocyclyl, substituted heterocyclyl, heteroalkyl, substituted heteroalkyl, heteroaryl, substituted heteroaryl, heteroarylalkyl, or substituted heteroarylalkyl;
f is 0, 1 or 2; and
R 27 , R 29 , and R 30 are independently hydrogen, or alkyl;
wherein substituted, when used to modify a specified group or radical, means that one or more hydrogen atoms of the specified group or radical are each independently replaced with one or more substituent group(s);
wherein substituent groups on saturated carbon atoms in the substituted group or radical include one or more of —R a , halo, ═O, —OR b , —SR b , ═S, —NR c R c , ═NR b , ═N—OR b , trihalomethyl, —CF 3 , —CN, —OCN, —SCN, —NO, —NO 2 , N 2 , —N 3 , —S(O) 2 R b , —S(O) 2 NR b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ,
wherein each R a is independently selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, cycloheteroalkyl, aryl, arylalkyl, heteroaryl and heteroarylalkyl; each R b is independently hydrogen or R a ; and each R c is independently R b or alternatively, the two R c s may be taken together with the nitrogen atom to which they are bonded form a 4-, 5-, 6- or 7-membered cycloheteroalkyl which may optionally include from 1 to 4 of the same or different additional heteroatoms selected from the group consisting of O, N and S;
wherein the one or more substituent groups, taken together with the atoms to which they are bonded, may form a cyclic ring including cycloalkyl and cycloheteroalkyl;
wherein substituent groups on unsaturated carbon atoms in the specified group or radical include —R a , halo, —OR b , —SR b , —NR c R c , trihalomethyl, —CF 3 , —CN, —OCN, —SCN, —NO, —NO 2 , —N 3 , —S(O) 2 R b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)O − , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ;
wherein substituent groups on nitrogen atoms in heteroatom-containing groups include —R a , —OR b , —SR b , trihalomethyl, —CF 3 , —CN, —NO, —NO 2 , —S(O) 2 R b , —S(O) 2 OR b , —OS(O) 2 R b , —OS(O) 2 OR b , —P(O)(OR b )(OR b ), —C(O)R b , —C(S)R b , —C(NR b )R b , —C(O)OR b , —C(S)OR b , —C(O)NR c R c , —C(NR b )NR c R c , —OC(O)R b , —OC(S)R b , —OC(O)OR b , —OC(S)OR b , —NR b C(O)R b , —NR b C(S)R b , —NR b C(O)OR b , —NR b C(S)OR b , —NR b C(O)NR c R c , —NR b C(NR b )R b or —NR b C(NR b )NR c R c ; and
wherein substituents used to substitute a specified group can be further substituted with one or more of the same or different substituent groups.
13. The flavoring concentrate formulation of claim 12 , wherein the at least one adjuvant comprises one or more flavoring agents.
14. The flavoring concentrate formulation of claim 13 , wherein the at least one adjuvant comprises one or more sweeteners.
15. The flavoring concentrate formulation of claim 14 , wherein the at least one adjuvant comprises one or more ingredients selected from the group consisting of a emulsifier, a stabilizer, an antimicrobial preservative, an antioxidant, vitamins, minerals, fats, starches, protein concentrates and isolates, salts, a freezing point depressant, nucleating agent, and combinations thereof.
16. The flavoring concentrate formulation of claim 15 , which is in a form selected from the group consisting of liquid, solid, semi-solid, foamy material, paste, gel, cream, lotion, and combinations thereof.
17. The flavoring concentrate formulation of claim 16 , wherein the compound is in a concentration that is at least 2 times of the concentration in a ready-to-use composition.
18. The ingestible composition of claim 1 , wherein R 21 , R 22 , and R 23 are all hydrogen.
19. The ingestible composition of claim 1 , wherein R 21 and R 22 are all hydrogen.
20. The ingestible composition of claim 1 , wherein the compound has a structure of Formula (IIIb) or (IIIb′),
or a tautomer, and/or salt thereof.
21. The ingestible composition of claim 1 , wherein the compound has a structure of Formula (IIIc) or (IIIc′),
or a tautomer, and/or salt thereof.
22. The ingestible composition of claim 21 , wherein R 33 is alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; heterocyclyl, substituted heterocyclyl, heteroalkyl, or substituted heteroalkyl.
23. The ingestible composition of claim 21 , wherein B is hydrogen or alkyl.
24. The ingestible composition of claim 20 , wherein
B is hydrogen, or alkyl;
L 2 is —NR 34 —, —O—, —NR 34 —C(O)—, —C(O)—NR 34 —, —O—C(O)—, —C(O)—O—, -hetercyclylene-C(O)—, or -(substituted hetercyclylene)-C(O)—; and
R 34 is hydrogen, alkyl, or substituted alkyl.
25. The ingestible composition of claim 21 , wherein
B is hydrogen, or alkyl;
R 33 is alkyl, substituted alkyl, carbocyclyl, substituted carbocyclyl; heterocyclyl, substituted heterocyclyl, heteroalkyl, or substituted heteroalkyl.
26. The ingestible composition of claim 1 , wherein the compound is selected from the groups consisting of
or a tautomer, and/or salt thereof.
27. A ingestible composition comprising a compound is selected from the group consisting of
or a tautomer, and/or salt thereof; and
an ingestibly acceptable excipient.