Claims for Patent: 9,522,876

Summary for Patent: 9,522,876

Title:	Cytotoxic and anti-mitotic compounds, and methods of using the same
Abstract:	Compounds having cytotoxic and/or anti-mitotic activity are disclosed. The compounds have the following structure (I): ##STR00001## including stereoisomers, pharmaceutically acceptable salts and prodrugs thereof, wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4 and R.sub.5 are as defined herein. Methods associated with preparation and use of such compounds, as well as pharmaceutical compositions comprising such compounds, are also disclosed. Also disclosed are compositions having the structure: (T)-(L)-(D), wherein (T) is a targeting moiety, (L) is an optional linker, and (D) is a compound having structure (I).
Inventor(s):	Winters; Geoffrey C. (Vancouver, CA), Mandel; Alexander L. (Vancouver, CA), Hedberg; Bradley J. (Vancouver, CA), Babcook; John (Vancouver, CA), Rich; James R. (Vancouver, CA), Hsieh; Tom Han Hsiao (Vancouver, CA), Bourque; Elyse Marie Josee (Blaine, WA)
Assignee:	ZYMEWORKS INC. (Vancouver, BC, unknown)
Application Number:	14/213,504
Patent Claims:	1. A compound having the following structure (I): ##STR00178## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof, wherein: R.sub.1 is selected from the group consisting of optionally substituted alkyl, optionally substituted alkylamino, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heterocyclyl and optionally substituted heteroaryl; R.sub.2 is selected from the group consisting of optionally substituted alkyl, optionally substituted alkylamino, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heterocyclyl and optionally substituted heteroaryl; R.sub.3 is selected from the group consisting of H and C.sub.1-6alkyl; R.sub.4 is selected from the group consisting of H and C.sub.1-6alkyl; and R.sub.5 is selected from the group consisting of C.sub.1-6alkyl and --SH. 2. The compound according to claim 1, wherein each optionally substituted alkyl, optionally substituted alkylamino, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heterocyclyl and optionally substituted heteroaryl is, independently, optionally substituted with .dbd.O, .dbd.S, --OH, --OR.sub.6, --O.sub.2CR.sub.6, --SH, --SR.sub.6, --SOCR.sub.6, --NH.sub.2, --N.sub.3, --NHR.sub.6, --N(R.sub.6).sub.2, --NHCOR.sub.6, --NR.sub.6COR.sub.6, --I, --Br, --Cl, --F, --CN, --CO.sub.2H, --CO.sub.2R.sub.6, --CHO, --COR.sub.6, --CONH.sub.2, --CONHR.sub.6, --CON(R.sub.6).sub.2, --COSH, --COSR.sub.6, --NO.sub.2, --SO.sub.3H, --SOR.sub.6 or --SO.sub.2R.sub.6, wherein each R.sub.6 is, independently, alkyl optionally substituted with halogen, --OH or --SH. 3. The compound according to claim 1, wherein each optionally substituted aryl and optionally substituted heteroaryl is, independently, selected from the group consisting of optionally substituted phenyl, optionally substituted naphthyl, optionally substituted anthracyl, optionally substituted phenanthryl, optionally substituted furyl, optionally substituted pyrrolyl, optionally substituted thiophenyl, optionally substituted benzofuryl, optionally substituted benzothiophenyl, optionally substituted quinolinyl, optionally substituted isoquinolinyl, optionally substituted imidazolyl, optionally substituted thiazolyl, optionally substituted oxazolyl, and optionally substituted pyridinyl. 4. The compound according to claim 1, wherein R.sub.2 is selected from one of the following structures (III), (IV), (V), (VI): ##STR00179## wherein: Q is CR.sub.7 or N; Z is C(R.sub.7).sub.2, NR.sub.7, S, or O; wherein in structure (VI), one instance of Z is CR.sub.7 or N, and the other instance is C(R.sub.7).sub.2, NR.sub.7, S, or O; each R.sub.7 is, independently, selected from the group consisting of H, --OH, --OR.sub.6, --O.sub.2CR.sub.6, --SH, --SR.sub.6, --SOCR.sub.6, --NH.sub.2, --N.sub.3, --NHR.sub.6, --N(R.sub.6).sub.2, --NHCOR.sub.6, --NR.sub.6COR.sub.6, --I, --Br, --Cl, --F, --CN, --CO.sub.2H, --CO.sub.2R.sub.6, --CHO, --COR.sub.6, --CONH.sub.2, --CONHR.sub.6, --CON(R.sub.6).sub.2, --COSH, --COSR.sub.6, --NO.sub.2, --SO.sub.3H, --SOR.sub.6 or --SO.sub.2R.sub.6, wherein each R.sub.6 is, independently, alkyl optionally substituted with halogen, --OH or --SH. 5. The compound according to claim 4, wherein R.sub.2 is selected from the group consisting of: ##STR00180## ##STR00181## 6. The compound according to claim 5 wherein R.sub.2 is: ##STR00182## 7. The compound according to claim 1, wherein R.sub.3, R.sub.4 and R.sub.5 are each methyl. 8. The compound according to claim 1, wherein R.sub.3 is H, R.sub.4 is methyl, and R.sub.5 is methyl. 9. The compound according to claim 1, which is (S,E)-N-(benzylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimethyl-2-((S)-3-me- thyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide, having the following structure: ##STR00183## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 10. The compound according to claim 1, which is (S,E)-2,5-dimethyl-N-(4-(2,2,2-trifluoroacetamido)phenylsulfonyl)-4-((S)-- -N,3,3-trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butana- mido)hex-2-enamide, having the following structure: ##STR00184## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 11. The compound according to claim 1, which is (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimethyl-2-((- S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide, having the following structure: ##STR00185## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 12. The compound according to claim 1, which is (S,E)-4-((S)-2-((S)-3-(4-(aminomethyl)phenyl)-3-methyl-2-(methylamino)but- anamido)-N,3,3-trimethylbutanamido)-N-(benzylsulfonyl)-2,5-dimethylhex-2-e- namide, having the following structure: ##STR00186## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 13. The compound according to claim 1, which is (S,E)-N-(3-aminophenylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimethyl-2-((- S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide, having the following structure: ##STR00187## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 14. The compound according to claim 1, which is (S,E)-N-(4-(1-aminocyclopropyl)benzylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3- -trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)h- ex-2-enamide, having the following structure: ##STR00188## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 15. The compound according to claim 1, which is (S,E)-N-(4-(1-aminocyclopropyl)phenylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3- -trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)h- ex-2-enamide, having the following structure: ##STR00189## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 16. The compound according to claim 1, which is (S,E)-N-(4-(aminomethyl)benzylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimet- hyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-en- amide, having the following structure: ##STR00190## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 17. The compound according to claim 1, which is (S,E)-N-(4-(aminomethyl)phenylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimet- hyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-en- amide, having the following structure: ##STR00191## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof. 18. A method of inhibiting tumor growth in a mammal, comprising administering to a mammal in need thereof an effective amount of the compound of any one of claims 1-8 and 9-17. 19. A pharmaceutical composition comprising the compound of any one of claims 1-8 and 9-17, or a stereoisomer, pharmaceutically acceptable salt or prodrug thereof, and a pharmaceutically acceptable carrier, diluent or excipient. 20. A method of inhibiting tumor growth in a mammal, comprising administering to a mammal in need thereof an effective amount of the pharmaceutical composition of claim 19. 21. A composition having the following structure: (T)-(L)-(D) (II) wherein (T) is a targeting moiety, (L) is an optional linker, and (D) is a compound having the following structure (I): ##STR00192## or a stereoisomer, prodrug or pharmaceutically acceptable salt thereof, wherein: R.sub.1 is selected from the group consisting of optionally substituted alkyl, optionally substituted alkylamino, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heterocyclyl and optionally substituted heteroaryl; R.sub.2 is selected from the group consisting of optionally substituted alkyl, optionally substituted alkylamino, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heterocyclyl and optionally substituted heteroaryl; R.sub.3 is selected from the group consisting of H and C.sub.1-6alkyl; R.sub.4 is selected from the group consisting of H and C.sub.1-6alkyl; and R.sub.5 is selected from the group consisting of C.sub.1-6alkyl and --SH. 22. The composition according to claim 21, wherein each optionally substituted alkyl, optionally substituted alkylamino, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heterocyclyl and optionally substituted heteroaryl is, independently, optionally substituted with .dbd.O, .dbd.S, --OH, --OR.sub.6, --O.sub.2CR.sub.6, --SH, --SR.sub.6, --SOCR.sub.6, --NH.sub.2, --N.sub.3, --NHR.sub.6, --N(R.sub.6).sub.2, --NHCOR.sub.6, --NR.sub.6COR.sub.6, --I, --Br, --Cl, --F, --CN, --CO.sub.2H, --CO.sub.2R.sub.6, --CHO, --COR.sub.6, --CONH.sub.2, --CONHR.sub.6, --CON(R.sub.6).sub.2, --COSH, --COSR.sub.6, --NO.sub.2, --SO.sub.3H, --SOR.sub.6 or --SO.sub.2R.sub.6, wherein each R.sub.6 is, independently, alkyl optionally substituted with halogen, --OH or --SH. 23. The composition according to claim 21, wherein each optionally substituted aryl and optionally substituted heteroaryl is, independently, selected from the group consisting of optionally substituted phenyl, optionally substituted naphthyl, optionally substituted anthracyl, optionally substituted phenanthryl, optionally substituted furyl, optionally substituted pyrrolyl, optionally substituted thiophenyl, optionally substituted benzofuryl, optionally substituted benzothiophenyl, optionally substituted quinolinyl, optionally substituted isoquinolinyl, optionally substituted imidazolyl, optionally substituted thiazolyl, optionally substituted oxazolyl, and optionally substituted pyridinyl. 24. The composition according to claim 21, wherein R.sub.2 is selected from one of the following structures (III), (IV), (V), (VI): ##STR00193## wherein: Q is CR.sub.7 or N; Z is C(R.sub.7).sub.2, NR.sub.7, S, or O; wherein in structure (VI), one instance of Z is CR.sub.7 or N, and the other instance is C(R.sub.7).sub.2, NR.sub.7, S, or O; each R.sub.7 is, independently, selected from the group consisting of H, --OH, --OR.sub.6, --O.sub.2CR.sub.6, --SH, --SR.sub.6, --SOCR.sub.6, --NH.sub.2, --N.sub.3, --NHR.sub.6, --N(R.sub.6).sub.2, --NHCOR.sub.6, --NR.sub.6COR.sub.6, --I, --Br, --Cl, --F, --CN, --CO.sub.2H, --CO.sub.2R.sub.6, --CHO, --COR.sub.6, --CONH.sub.2, --CONHR.sub.6, --CON(R.sub.6).sub.2, --COSH, --COSR.sub.6, --NO.sub.2, --SO.sub.3H, --SOR.sub.6 or --SO.sub.2R.sub.6, wherein each R.sub.6 is, independently, alkyl optionally substituted with halogen, --OH or --SH. 25. The composition according to claim 24, wherein R.sub.2 is selected from the group consisting of: ##STR00194## ##STR00195## 26. The composition according to claim 25 wherein R.sub.2 is: ##STR00196## 27. The composition according to claim 21, wherein R.sub.3, R.sub.4 and R.sub.5 are each methyl. 28. The composition according to claim 21, wherein R.sub.3 is H, R.sub.4 is methyl, and R.sub.5 is methyl. 29. The composition according to claim 21, wherein (D) is (S,E)-N-(benzylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimethyl-2-((S)-3-me- thyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide, having the following structure: ##STR00197## 30. The composition according to claim 21, wherein (D) is (S,E)-N-(4-aminophenylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimethyl-2-((- S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide, having the following structure: ##STR00198## 31. The composition according to claim 21, wherein (D) is (S,E)-4-((S)-2-((S)-3-(4-(aminomethyl)phenyl)-3-methyl-2-(methylamino)but- anamido)-N,3,3-trimethylbutanamido)-N-(benzylsulfonyl)-2,5-dimethylhex-2-e- namide, having the following structure: ##STR00199## 32. The composition according to claim 21, wherein (D) is (S,E)-N-(3-aminophenylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimethyl-2-((- S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-enamide, having the following structure: ##STR00200## 33. The composition according to claim 21, wherein (D) is (S,E)-N-(4-(1-aminocyclopropyl)benzylsulfonyl)-2,5-dimethyl-44(S)--N,3,3-- trimethyl-24(S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex- -2-enamide, having the following structure: ##STR00201## 34. The composition according to claim 21, wherein (D) is (S,E)-N-(4-(1-aminocyclopropyl)phenylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3- -trimethyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)h- ex-2-enamide, having the following structure: ##STR00202## 35. The composition according to claim 21, wherein (D) is (S,E)-N-(4-(aminomethyl)benzylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimet- hyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-en- amide, having the following structure: ##STR00203## 36. The composition according to claim 21, wherein (D) is (S,E)-N-(4-(aminomethyl)phenylsulfonyl)-2,5-dimethyl-4-((S)--N,3,3-trimet- hyl-2-((S)-3-methyl-2-(methylamino)-3-phenylbutanamido)butanamido)hex-2-en- amide, having the following structure: ##STR00204## 37. The composition according to claim 21, wherein (L-D) is MC-VC-PABC-77, having the following structure: ##STR00205## 38. The composition according to claim 21, wherein (L-D) is 4-((R)-2-((R)-2-(6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanamido)-3-me- thylbutanamido)-5-ureidopentanamido)benzyl 4-(N--((S,E)-2,5-dimethyl-4-((S)--N,3,3-trimethyl-2-((S)-3-methyl-2-(meth- ylamino)-3-phenylbutanamido)butanamido)hex-2-enoyl)sulfamoyl)benzylcarbama- te (MC-VC-PABC-85), having the following structure: ##STR00206## 39. The composition according to claim 21, wherein (L-D) is MC-VC-PABC-41, having the following structure: ##STR00207## 40. The composition according to claim 21, wherein (L-D) is MC-VC-PABC-58, having the following structure: ##STR00208## 41. The composition according to claim 21, wherein (L-D) is MC-VC-PABC-63, having the following structure: ##STR00209## 42. The composition according to claim 21, wherein (T-L-D) is mAb-MC-VC-PABC-58, having the following structure: ##STR00210## wherein mAb is trastuzumab. 43. The composition according to claim 21, wherein (T-L-D) is mAb-MC-VC-PABC-63, having the following structure: ##STR00211## wherein mAb is trastuzumab. 44. A method of killing cancer cells in a mammal, comprising administering to a mammal in need thereof an effective amount of the composition of any one of claims 21-43. 45. A method of inhibiting tumor growth in a mammal, comprising administering to a mammal in need thereof an effective amount of the composition of any one of claims 21-43. 46. A pharmaceutical composition, comprising the composition of any one of claims 21-43, or a stereoisomer, pharmaceutically acceptable salt or prodrug thereof, and a pharmaceutically acceptable carrier, diluent or excipient. 47. A method of inhibiting tumor growth in a mammal, comprising administering to a mammal in need thereof an effective amount of the pharmaceutical composition of claim 46. 48. A method of killing cancer cells in a mammal, comprising administering to a mammal in need thereof an effective amount of the pharmaceutical composition of claim 46.

Details for Patent 9,522,876

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	09/25/1998		2033-03-15
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	02/10/2017		2033-03-15
Genentech, Inc.	HERCEPTIN HYLECTA	trastuzumab and hyaluronidase-oysk	Injection	761106	02/28/2019		2033-03-15