IP Library Granted Patent US 12,098,120
Granted Patent B2
US 12,098,120 · App. 17/820,861 · Granted Sep 24, 2024

Patent

Inventor: Patrick Foley (New Haven, CT)
Assignee: P2 SCIENCE, INC.
C07C35/06C07C13/10C07C13/18C07C35/14C07C49/297C07C49/303C07C49/537C07C49/703C07C2601/08C07C2601/10C07C2601/14C07C2601/16
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Quick Facts
Patent No.
US 12,098,120
App. No.
17/820,861
Granted
Sep 24, 2024
Kind
B2
Abstract

The present disclosure is directed to novel derivatives of naturally occurring humulones and lupulones, methods of making them, compositions comprising them, and methods for using them.

Claims (41)

1. A composition comprising a compound which is a hydrogenated derivative of a humulone, lupulone or isohumulone, comprising the compound in admixture with one or more pharmaceutically acceptable, cosmetically acceptable, or industrially acceptable excipients or carriers selected from solvents, oils, surfactants, emollients, diluents, glidants, abrasives, humectants, polymers, plasticizers, catalysts, antioxidants, coloring agents, flavoring agents, fragrance agents, antiperspirant agents, antibacterial agents, antifungal agents, hydrocarbons, stabilizers, and viscosity controlling agents.

2. The composition of claim 1 , wherein the compound is a hydrogenated derivative of humulone, cohumulone, or adhumulone.

3. The composition of claim 1 , wherein the compound is a hydrogenated derivative of lupulone, colupulone, or adlupulone.

4. A compound which has a structure selected from the following:

wherein:

R 1 , R 2 , R 3 , R 4 , and R 5 , are each independently selected from H, C 1-21 alkyl, —C(O)—C 1-21 alkyl, C 2-21 alkenyl, —C(O)—C 2-21 alkenyl, C 3-7 cycloalkyl, —C(O)—C 3-7 cycloalkyl, C 1-6 haloalkyl, —C(O)—C 1-6 haloalkyl, (CH 2 CH 2 O)nCH 2 CH 2 OH, (CH 2 CH(CH 3 )O)nCH 2 CH(CH 3 )OH, C 1-21 alkyl-OH, —C(O)—C 1-21 alkyl-OH, C 1-21 alkyl-C(O)—OC 1-6 alkyl, C(O)—C 1-21 alkyl-C(O)—OC 1-6 alkyl, C 1-21 alkyl-COOH, —C(O)—C 1-21 alkyl-COOH, —P(O)(OC 1-21 alkyl)(OC 1-21 alkyl), —SO 2 OC 1-21 alkyl, —SO 2 C 1-21 alkyl, C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH) 2 , —C(O)—C 1-21 alkyl-P(O)(OH) 2 , C 1-21 alkyl-SO 2 OC 1-6 alkyl), —C(O)—C 1-21 alkyl-SO 20 C 1-6 alkyl, C 1-21 alkyl-SO 3 H, and —C(O)—C 1-21 alkyl-SO 3 H; or any of R 1 , R 2 , R 3 , or R 4 , is absent; and wherein each n is independently an integer selected from 0 to 20.

5. The composition according to claim 1 , wherein the compound has a structure selected from:

wherein each R is independently H or OH, R 1 , R 2 , R 3 , R 4 , and R 5 , are each independently selected from H, C 1-21 alkyl, —C(O)—C 1-21 alkyl, C 2-21 alkenyl, —C(O)—C 2-21 alkenyl, C 3-7 cycloalkyl,—C(O)—C 3-7 cycloalkyl, C 1-6 haloalkyl,-C(O)—C 1-6 haloalkyl, (CH 2 CH 20 )nCH 2 CH 2 OH, (CH 2 CH(CH 3 )O)nCH 2 CH(CH 3 )OH, C 1-21 alkyl-OH, —C(O)—C 1-21 alkyl-OH, C 1-21 alkyl—C(O)—OC 1-6 alkyl, C(O)—C 1-21 alkyl—C(O)—OC 1-6 alkyl, C 1-21 alkyl-COOH, —C(O)—C 1-21 alkyl-COOH, —P(O)(OC 1-21 alkyl)(OC 1-21 alkyl), —SO 20 C 1-21 alkyl,-SO 2 C 1-21 alkyl, C 1-21 alkyl —P(O)(OC 1-6 alkyl)(OC 1-6 alkyl),-C(O)-C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), C 1-21 alkyl —P(O)(OH)(OC 1-6 alkyl),-C(O)-C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH) 2, —C(O)—C 1-21 alkyl-P(O)(OH) 2, C 1-21 alkyl—SO 20 C 1-6 alkyl), —C(O)—C 1-21 alkyl-SO 2 OC 1-6 alkyl, C 1-21 alkyl—SO 3 H, and—C(O)—C 1-21 alkyl-SO 3 H; or any of R 1, R 2, R 3, or R 4, is absent; and

wherein each n is independently an integer selected from 0 to 20;

wherein each is either a single bond or a double bond, and wherein each is either a single bond or is absent; and

provided that the bonds and are selected such that all carbon atoms and oxygen atoms to which these bonds are attached have a total of four attached bonds inclusive of single and double bonds.

6. The composition according to claim 1 , wherein the compound has a structure selected from:

wherein R 1 , R 2 , R 3 , R 4 , and R 5 , are each independently selected from H, C 1-21 alkyl, —C(O)—C 1-21 alkyl, C 2-21 alkenyl, —C(O)—C 2-21 alkenyl, C 3-7 cycloalkyl, —C(O)—C 3-7 cycloalkyl, C 1-6 haloalkyl, —C(O)—C 1-6 haloalkyl, (CH 2 CH 2 O)nCH 2 CH 2 OH, (CH 2 CH(CH 3 )O)nCH 2 CH(CH 3 )OH, C 1-21 alkyl-OH, —C(O)—C 1-21 alkyl-OH, C 1-21 alkyl-C(O)—OC 1-6 alkyl, C(O)—C 1-21 alkyl-C(O)—OC 1-6 alkyl, C 1-21 alkyl-COOH, —C(O)—C 1-21 alkyl-COOH, —P(O)(OC 1-21 alkyl)(OC 1-21 alkyl), —SO 2 OC 1-21 alkyl, —SO 2 C 1-21 alkyl, C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH) 2 , —C(O)—C 1-21 alkyl-P(O)(OH) 2 , C 1-21 alkyl-SO 2 OC 1-6 alkyl), —C(O)—C 1-21 alkyl-SO 20 C 1-6 alkyl, C 1-21 alkyl-SO 3 H, and —C(O)—C 1-21 alkyl-SO 3 H; or any of R 1 , R 2 , R 3 , or R 4 , is absent; and

wherein each n is independently an integer selected from 0 to 20.

wherein each is either a single bond or a double bond, and wherein each is either a single bond or is absent; and

provided that the bonds and are selected such that all carbon atoms and oxygen atoms to which these bonds are attached have a total of four attached bonds inclusive of single and double bonds.

7. The compound of claim 4 , wherein the compound has a structure selected from:

wherein R 1 , R 2 , R 3 , R 4 , and R 5 are each independently selected from H, C 1-21 alkyl, —C(O)—C 1-21 alkyl, C 2-21 alkenyl, —C(O)-C 2-21 alkenyl, C 3-7 cycloalkyl, —C(O)—C 3-7 cycloalkyl, C 1-6 haloalkyl, —C(O)—C 1-6 haloalkyl, (CH 2 CH 2 O)nCH 2 CH 2 OH, (CH 2 CH(CH 3 )O)nCH 2 CH(CH 3 )OH, C 1-21 alkyl-OH, —C(O)—C 1-21 alkyl-OH, C 1-21 alkyl-C(O)—OC 1-6 alkyl, C(O)—C 1-21 alkyl-C(O)—OC 1-6 alkyl, C 1-21 alkyl-COOH, —C(O)—C 1-21 alkyl-COOH, —P(O)(OC 1-21 alkyl)(OC 1-21 alkyl), —SO 2 OC 1-21 alkyl, —SO 2 C 1-21 alkyl, C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH) 2, —C(O)—C 1-21 alkyl-P(O)(OH) 2, C 1-21 alkyl-SO 20 C 1-6 alkyl), —C(O)—C 1-21 alkyl-SO 2 OC 1-6 alkyl, C 1-21 alkyl-SO 3 H, and —C(O)—C 1-21 alkyl-SO 3 H; or any of R 1, R 2, R 3, or R 4, is absent; and wherein each n is independently an integer selected from 0 to 20.

8. The compound of claim 4 , wherein the compound has a structure selected from:

wherein R 1 , R 2 , R 3 , R 4 , and R 5 are each independently selected from H, C 1-21 alkyl, —C(O)—C 1-21 alkyl, C 2-21 alkenyl, —C(O)—C 2 - 21 alkenyl, C 3-7 cycloalkyl, —C(O)—C 3-7 cycloalkyl, C 1-6 haloalkyl, —C(O)—C 1-6 haloalkyl, (CH 2 CH 2 O)nCH 2 CH 2 OH, (CH 2 CH(CH 3 )O)nCH 2 CH(CH 3 )OH, C 1-21 alkyl-OH, —C(O)—C 1-21 alkyl-OH, C 1-21 alkyl-C(O)—OC 1-6 alkyl, C(O)—C 1-21 alkyl-C(O)—OC 1-6 alkyl, C 1-21 alkyl-COOH, —C(O)—C 1-21 alkyl-COOH, —P(O)(OC 1-21 alkyl)(OC 1-21 alkyl), —SO 2 OC 1-21 alkyl, —SO 2 C 1-21 alkyl, C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH) 2, —C(O)—C 1-21 alkyl-P(O)(OH) 2, C 1-21 alkyl-SO 20 C 1-6 alkyl), —C(O)—C 1-21 alkyl-SO 2 OC 1-6 alkyl, C 1-21 alkyl-SO 3 H, and —C(O)—C 1-21 alkyl-SO 3 H; or any of R 1, R 2, R 3, or R 4, is absent; and wherein each n is independently an integer selected from 0 to 20.

9. The compound of claim 4 , wherein the compound has a structure selected from:

wherein R 1 , R 2 , R 3 , R 4 , and R 5 are each independently selected from H, C 1-21 alkyl, —C(O)—C 1-21 alkyl, C 2-21 alkenyl, —C(O)-C 2-21 alkenyl, C 3-7 cycloalkyl, —C(O)—C 3-7 cycloalkyl, C 1-6 haloalkyl, —C(O)—C 1-6 haloalkyl, (CH 2 CH 2 O)nCH 2 CH 2 OH, (CH 2 CH(CH 3 )O)nCH 2 CH(CH 3 )OH, C 1-21 alkyl-OH, —C(O)—C 1-21 alkyl-OH, C 1-21 alkyl-C(O)—OC 1-6 alkyl, C(O)—C 1-21 alkyl-C(O)—OC 1-6 alkyl, C 1-21 alkyl-COOH, —C(O)—C 1-21 alkyl-COOH, —P(O)(OC 1-21 alkyl)(OC 1-21 alkyl), —SO 2 OC 1-21 alkyl, —SO 2 C 1-21 alkyl, C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OC 1-6 alkyl)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), —C(O)—C 1-21 alkyl-P(O)(OH)(OC 1-6 alkyl), C 1-21 alkyl-P(O)(OH) 2, —C(O)—C 1-21 alkyl-P(O)(OH) 2, C 1-21 alkyl-SO 20 C 1-6 alkyl), —C(O)—C 1-21 alkyl-SO 2 OC 1-6 alkyl, C 1-21 alkyl-SO 3 H, and —C(O)—C 1-21 alkyl-SO 3 H; or any of R 1, R 2, R 3, or R 4, is absent; and wherein each n is independently an integer selected from 0 to 20.

10. The compound according to claim 4 , wherein each group R is H; and wherein:

a. R 1 , R 2 , and R 5 are each H, and R 3 and R 4 are absent, or

b. R 2 and R 3 are each H, and R 1 , R 4 , and R 5 are absent, or

c. R 1 , R 2 , R 5 and R 3 are each H; or

d. R 1 , R 2 , R 3 , R 4 , and R 5 are each H.

11. The compound of claim 4 , wherein the compound has a structure selected from:

12. The compound of claim 4 , wherein the compound has a structure selected from:

13. The compound of claim 4 , wherein the compound has a structure selected from:

14. The compound of claim 4 , wherein the compound is selected from:

15. The compound of claim 4 , wherein the compound has a structure selected from:

antiperspirant agents, antibacterial agents, antifungal agents, hydrocarbons, stabilizers, and viscosity controlling agents.

16. An emollient, solubilizer, anti-frizz agent, lubricant, carrier, conditioner, surfactant, adjuvant, dispersant, emulsifier, fuel, paraffin, candle, or precursor of a polymer, film-former, resin, or composite, comprising or consisting of a compound which is a hydrogenated derivative of a humulone, lupulone or isohumulone.

17. A composition comprising a compound according to claim 4 , in admixture with one or more pharmaceutically acceptable, cosmetically acceptable, or industrially acceptable excipients or carriers, for example, selected from solvents, oils, surfactants, emollients, diluents, glidants, abrasives, humectants, polymers, plasticizers, catalysts, antioxidants, coloring agents, flavoring agents, fragrance agents,

wherein R 1 , R 2 , R 3 , R 4 , and R 5 are each as defined in claim 4 .

18. An emollient, solubilizer, anti-frizz agent, lubricant, carrier, conditioner, surfactant, adjuvant, dispersant, emulsifier, fuel, paraffin, candle, or precursor of a polymer, film-former, resin, or composite, comprising or consisting of a compound according to claim 4 .

19. The composition according to claim 1 , wherein the composition is a cosmetic composition, sunscreen composition, plastic composition, lubricant composition, personal care composition, cleaning composition, or air freshener.

20. The composition according to claim 19 , wherein the composition is a soap, skin cream or lotion, balm, shampoo, body wash, hydrating cream, deodorant, antiperspirant, after-shave lotion, cologne, perfume, other hair care or skin care product, surface cleaner, metal cleaner, wood cleaner, glass cleaner, body cleaner, dish-washing detergent, or laundry detergent.

21. The composition according to claim 17 , wherein the composition is a cosmetic composition, sunscreen composition, plastic composition, lubricant composition, personal care composition, cleaning composition, or air freshener.

22. The composition according to claim 21 , wherein the composition is a soap, skin cream or lotion, balm, shampoo, body wash, hydrating cream, deodorant, antiperspirant, after-shave lotion, cologne, perfume, other hair care or skin care product, surface cleaner, metal cleaner, wood cleaner, glass cleaner, body cleaner, dish-washing detergent, or laundry detergent.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 6, 2023
From: FOLEY, PATRICK
To: P2 SCIENCE, INC.
Reel/Frame 063245/0302 →
RELEASE OF SECURITY INTEREST Recorded Feb 6, 2023
From: HG VENTURES LLC
To: P2 SCIENCE, INC.
Reel/Frame 062650/0301 →
SECURITY INTEREST Recorded Dec 3, 2022
From: P2 SCIENCE, INC.
To: HG VENTURES LLC
Reel/Frame 062050/0152 →
Continuity (2)
Provisional Application 63234294 · Aug 18, 2021
Related Publication 20230138884A1 · May 4, 2023