Claims for Patent: 9,090,640

Summary for Patent: 9,090,640

Title:	Targeted delivery and prodrug designs for platinum-acridine anti-cancer compounds and methods thereof
Abstract:	Acridine containing cisplatin compounds have been disclosed that show greater efficacy against cancer than other cisplatin compounds. Methods of delivery of those more effective cisplatin compounds to the nucleus in cancer cells is disclosed using one or more amino acids, one or more sugars, one or more polymeric ethers, C.sub.1-6alkylene-phenyl-NH--C(O)--R.sub.15, folic acid, .alpha..sub.v.beta..sub.3 integrin RGD binding peptide, tamoxifen, endoxifen, epidermal growth factor receptor, antibody conjugates, kinase inhibitors, diazoles, triazoles, oxazoles, erlotinib, and/or mixtures thereof; wherein R.sub.15 is a peptide.
Inventor(s):	Bierbach; Ulrich (Winston-Salem, NC), Ding; Song (Winston-Salem, NC)
Assignee:
Application Number:	14/241,900
Patent Claims:	1. A compound of Formula I: ##STR00065## wherein X is halo, OC(O)R.sub.9, nitrate or sulfate; R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which they are attached, R.sub.1 and R.sub.2 form the ring --NH.sub.2--(CH.sub.2).sub.v--NH.sub.2-- wherein v is 1, 2, 3, or 4 or R.sub.1 and R.sub.2 together can be any of the following groups a-h; ##STR00066## wherein A is H, --CH.sub.3, --OCH.sub.3, --CF.sub.3 or NO.sub.2; R.sub.3 is --N(R.sub.6)--; wherein R.sub.6 is hydrogen or C.sub.1-C.sub.6alkyl; R.sub.4 is independently an amino, a nitro, --NHC(O)(R.sub.10), --NHC(O)O(R.sub.10), --C(O)NHR.sub.10, --OC(O)NHR.sub.10, or halo; R.sub.10 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, or adamantyl; q is 0, 1, or 2; R.sub.5 is a direct bond, --NH-- or C.sub.1-C.sub.6alkylene; or R.sub.5 and X together with the atoms to which they are attached form a 6- or 7-membered ring, wherein said 6- or 7-membered ring contains a linking group --C(O)O-- or --OC(O)--; R.sub.7 is hydrogen, methyl, or --C(O)O--R.sub.8; wherein R.sub.8 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, adamantyl, a natural or unnatural amino acid or a peptide; R.sub.9 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, adamantyl, a natural or unnatural amino acid or a peptide; either or both of R.sub.11 and R.sub.12 contain a reactive group on to which a linker and/or one or more of compound W can be added; and if only one of R.sub.11 and R.sub.12 contains a reactive group, then the other of R.sub.11 and R.sub.12 is hydrogen; compound W is one or more amino acids, one or more sugars, polymeric ethers, C.sub.1-6alkylene-phenyl-NH--C(O)--R.sub.15, folic acid, .alpha..sub.v.beta..sub.3 integrin RGD binding peptide, tamoxifen, endoxifen, EGFR (epidermal growth factor receptor) antibody conjugates, kinase inhibitors, diazoles, triazoles, oxazoles, erlotinib, and mixtures thereof; wherein R.sub.15 is a peptide; Y is C.sub.1-C.sub.6alkyl; and Z is one or more counterions sufficient to balance the charge of the compound. 2. The compound of claim 1, wherein R.sub.11 and R.sub.12 are --OH, --N.sub.3, --COOH, --CONH.sub.2, --CH.dbd.CH.sub.2, --C.ident.CH, --(CH.sub.2).sub.1-6--OH, --(CH.sub.2).sub.1-6--N.sub.3, --(CH.sub.2).sub.1-6--COOH, or --(CH.sub.2).sub.1-6--CH.dbd.CH.sub.2, or --(CH.sub.2).sub.1-6--C.ident.CH. 3. The compound of claim 1, wherein R.sub.11 and R.sub.12 combined with the linker and compound W are --NH--R.sub.13, ##STR00067## --O--R.sub.13, --CH.dbd.CH--R.sub.13, --C.ident.C--R.sub.13, --N.sub.3, --COOH, --COOR.sub.14, --C(O)NH--R.sub.13, --NHC(O)--R.sub.13, --OC(O)NH--R.sub.13, --OC(O)O--R.sub.13, --(CH.sub.2).sub.1-6--NH--R.sub.13, ##STR00068## --(CH.sub.2).sub.1-6--O--R.sub.13, --(CH.sub.2).sub.1-6--N.sub.3, --(CH.sub.2).sub.1-6--COOH, --(CH.sub.2).sub.1-6--COOR.sub.14 or --(CH.sub.2).sub.1-6--CH.dbd.CH--R.sub.13; wherein R.sub.13 and R.sub.14 are independently selected from the group consisting of one or more amino acids, one or more sugars, polymeric ethers, C.sub.1-6alkylene-phenyl-NH--C(O)--R.sub.15, folic acid, .alpha..sub.v.beta..sub.3 integrin RGD binding peptide, tamoxifen, endoxifen, EGFR (epidermal growth factor receptor) antibody conjugates, kinase inhibitors, diazoles, triazoles, oxazoles, erlotinib, and mixtures thereof; wherein R.sub.15 is a peptide. 4. The compound of claim 1, wherein R.sub.6 is hydrogen or methyl and R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which they are attached, R.sub.1 and R.sub.2 form the ring --NH.sub.2--(CH.sub.2).sub.v--NH.sub.2--wherein v is 2 or 3. 5. The compound of claim 4, wherein Y is --CH.sub.2--. 6. The compound of claim 5, wherein R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which R.sub.1 and R.sub.2 are attached are --NH.sub.2--CH.sub.2--NH.sub.2--. 7. The compound of claim 6, wherein the one or more counter ions of Z comprise NO.sub.3. 8. The compound of claim 7, wherein R.sub.5 is --NH-- or --CH.sub.2--. 9. The compound of claim 8, wherein R.sub.6 is hydrogen. 10. The compound of claim 9, wherein the compound is Example 1 ##STR00069## 11. The compound of claim 7, wherein the compound is Example 2: ##STR00070## 12. A method of treating cancer comprising administering to a subject in need thereof an effective amount of the compound of Formula I: ##STR00071## wherein X is halo, OC(O)R.sub.9, nitrate or sulfate; R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which they are attached, R.sub.1 and R.sub.2 form the ring --NH.sub.2--(CH.sub.2).sub.v--NH.sub.2-- wherein v is 1, 2, 3, or 4 or R.sub.1 and R.sub.2 together can be any of the following groups a-h; ##STR00072## wherein A is H, --CH.sub.3, --OCH.sub.3, CF.sub.3 or NO.sub.2; R.sub.3 is --N(R.sub.6)--; wherein R.sub.6 is hydrogen or C.sub.1-C.sub.6alkyl; R.sub.4 is independently an amino, a nitro, --NHC(O)(R.sub.10), --NHC(O)O(R.sub.10), --C(O)NHR.sub.10, --OC(O)NHR.sub.10, or halo; R.sub.10 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, or adamantyl; q is 0, 1, or 2; R.sub.5 is a direct bond, --NH-- or C.sub.1-C.sub.6alkylene; or R.sub.5 and X together with the atoms to which they are attached form a 6- or 7-membered ring, wherein said 6- or 7-membered ring contains a linking group --C(O)O-- or --OC(O)--; R.sub.7 is hydrogen, methyl, or --C(O)O--R.sub.8; wherein R.sub.8 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, adamantyl, a natural or unnatural amino acid or a peptide; R.sub.9 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, adamantyl, a natural or unnatural amino acid or a peptide; either or both of R.sub.11 and R.sub.12 contain a reactive group on to which a linker and/or one or more of compound W can be added; and if only one of R.sub.11 and R.sub.12 contains a reactive group, then the other of R.sub.11 and R.sub.12 is hydrogen; compound W is one or more amino acids, one or more sugars, polymeric ethers, C.sub.1-6alkylene-phenyl-NH--C(O)--R.sub.15, folic acid, .alpha..sub.v.beta..sub.3 integrin RGD binding peptide, tamoxifen, endoxifen, EGFR (epidermal growth factor receptor) antibody conjugates, kinase inhibitors, diazoles, triazoles, oxazoles, erlotinib, and mixtures thereof; wherein R.sub.15 is a peptide; Y is C.sub.1-C.sub.6alkyl; and Z is one or more counterions sufficient to balance the charge of the compound. 13. The method of claim 12, wherein the cancer is selected from the group consisting of lung cancer, testicular cancers, ovarian carcinomas, head and neck cancers, leukemias and lymphomas. 14. The method of claim 13, wherein R.sub.6 is hydrogen or methyl and R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which they are attached, R.sub.1 and R.sub.2 form the ring --NH.sub.2--(CH.sub.2).sub.v--NH.sub.2--wherein v is 2 or 3. 15. The method of claim 14, wherein Y is --CH.sub.2--. 16. The method of claim 15, wherein R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which R.sub.1 and R.sub.2 are attached are --NH.sub.2--CH.sub.2--CH.sub.2--NH.sub.2--. 17. The method of claim 16, wherein the one or more counter ions of Z comprise NO.sub.3. 18. The method of claim 17, wherein R.sub.5 is --NH-- or --CH.sub.2--. 19. The method of claim 18, wherein R.sub.6 is hydrogen. 20. A pharmaceutical composition comprising the compound of Formula 1: ##STR00073## wherein X is halo, OC(O)R.sub.9, nitrate or sulfate; R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which they are attached, R.sub.1 and R.sub.2 form the ring --NH.sub.2--(CH.sub.2).sub.v--NH.sub.2-- wherein v is 1, 2, 3, or 4 or R.sub.1 and R.sub.2 together can be any of the following groups a-h; ##STR00074## wherein A is H, --CH.sub.3, --OCH.sub.3, CF.sub.3 or NO.sub.2; R.sub.3 is --N(R.sub.6)--; wherein R.sub.6 is hydrogen or C.sub.1-C.sub.6alkyl; R.sub.4 is independently an amino, a nitro, --NHC(O)(R.sub.10), --NHC(O)O(R.sub.10), --C(O)NHR.sub.10, --OC(O)NHR.sub.10, or halo; R.sub.10 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, or adamantyl; q is 0, 1, or 2; R.sub.5 is a direct bond, --NH-- or C.sub.1-C.sub.6alkylene; or R.sub.5 and X together with the atoms to which they are attached form a 6- or 7-membered ring, wherein said 6- or 7-membered ring contains a linking group --C(O)O-- or --OC(O)--; R.sub.7 is hydrogen, methyl, or --C(O)O--R.sub.8; wherein R.sub.8 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, adamantyl, a natural or unnatural amino acid or a peptide; R.sub.9 is hydrogen, C.sub.1-6 alkyl, phenyl, naphthyl, C.sub.3-6 cycloalkyl, norbornyl, adamantyl, a natural or unnatural amino acid or a peptide; either or both of R.sub.11 and R.sub.12 contain a reactive group on to which a linker and/or one or more of compound W can be added; and if only one of R.sub.11 and R.sub.12 contains a reactive group, then the other of R.sub.11 and R.sub.12 is hydrogen; compound W is one or more amino acids, one or more sugars, polymeric ethers, C.sub.1-6alkylene-phenyl-NH--C(O)--R.sub.15, folic acid, .alpha..sub.v.beta..sub.3 integrin RGD binding peptide, tamoxifen, endoxifen, EGFR (epidermal growth factor receptor) antibody conjugates, kinase inhibitors, diazoles, triazoles, oxazoles, erlotinib, and mixtures thereof; wherein R.sub.15 is a peptide; Y is C.sub.1-C.sub.6alkyl; and Z is one or more counterions sufficient to balance the charge of the compound; and a pharmaceutically acceptable diluent, carrier, or excipient. 21. The pharmaceutical composition of claim 20, wherein Y is --CH.sub.2--, wherein R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which R.sub.1 and R.sub.2 are attached are --NH.sub.2--CH.sub.2--CH.sub.2--NH.sub.2--, and wherein the one or more counter ions of Z comprise NO.sub.3. 22. The pharmaceutical composition of claim 21, wherein R.sub.5 is --NH-- or --CH.sub.2--, wherein R.sub.6 is hydrogen or methyl and R.sub.1 and R.sub.2 are amino groups or together with the platinum atom to which they are attached, R.sub.1 and R.sub.2 form the ring --NH.sub.2--(CH.sub.2).sub.v--NH.sub.2-- wherein v is 2 or 3. 23. The pharmaceutical composition of claim 20, further comprising one or more compounds selected from the group consisting of HERCEPTIN.TM. (trastuzumab), RITUXAN.TM. (rituximab), ZEVALIN.TM. (ibritumomab tiuxetan), LYMPHOCIDE.TM. (epratuzumab), GLEEVAC.TM., BEXXAR.TM. (iodine 131 tositumomab), ERBITUX.TM. (IMC-C225), KDR inhibitory agents, AVASTIN.TM., VEGF-TRAP.TM., ABX-EGF (panitumumab), IRESSA.TM. (gefitinib), TARCEVA.TM. (erlotinib), Campath, IL-8, B-FGF, Tek antagonists, anti-TWEAK agents, anti-PDGF-BB antagonists, SD-7784, cilengitide; pegaptanib octasodium; Alphastatin, M-PGA; ilomastat, emaxanib, vatalanib, 2-methoxyestradiol, TLC ELL-12, anecortave acetate, alpha-D148 Mab, CEP-7055, anti-Vn Mab, DAC:antiangiogenic, Angiocidin, KM-2550, SU-0879, CGP-79787, YIGSR-Stealth, fibrinogen-E fragment, TBC-1635; SC-236, ABT-567, Metastatin, maspin, ER-68203-00, Benefin, Tz-93, TAN-1120, FR-111142, platelet factor 4, vascular endothelial growth factor antagonist, bevacizumab (pINN), XL 784, XL 647, MAb, alpha5beta3 integrin, enzastaurin hydrochloride (USAN), CEP 7055, BC 1, VEGF antagonist, rBPI 21 and BPI-derived antiangiogenic, PI 88, cilengitide (pINN), cetuximab (INN), AVE 8062, AS 1404, SG 292, Endostatin, ATN 161, ANGIOSTATIN, ZD 6474, ZD 6126, PPI 2458, AZD 9935, AZD 2171, vatalanib (pINN), pegaptanib (Pinn), xanthorrhizol, SPV5.2, SDX 103, PX 478, METASTATIN, troponin I, SU 6668, OXI 4503, o-guanidines, motuporamine C, CDP 791, atiprimod (pINN), E 7820, CYC 381, AE 941, urokinase plasminogen activator inhibitor, oglufanide (pINN), HIF-1alfa inhibitors, CEP 5214, BAY RES 2622; Angiocidin, A6, KR 31372, GW 2286, EHT 0101, CP 868596, CP 564959, CP 547632, compound 786034 from GlaxoSmithKline, KRN 633, anginex, ABT 510, AAL 993, VEGI, tumor necrosis factor-alpha inhibitors, SU 11248, ABT 518, YH16, S-3APG, KDR, GEB 116, CS 706, combretastatin A4 prodrugs, chondroitinase AC, BAY RES 2690, AGM 1470, AG 13925, Tetrathiomolybdate, GCS 100, CV 247, CKD 732, irsogladine (INN), RG 13577, WX 360, squalamine (pIN), RPI 4610, heparanase inhibitors, KL 3106, Honokiol, ZK CDK, ZK Angio, ZK 229561, XMP 300, VGA 1102, Vasostatin, Flk-1, TZ 93, TumStatin, truncated soluble FLT 1 Tie-2 ligands and thrombospondin 1 inhibitor. 24. A system of delivering a compound of formula I as claimed in claim 1 to a patient in need thereof, wherein said system employs directly or indirectly binding said compound of formula I to one or more members selected from the group consisting of one or more amino acids, one or more sugars, one or more polymeric ethers, C.sub.1-6alkylene-phenyl-NH--C(O)--R.sub.15, folic acid, .alpha..sub.v.beta..sub.3 integrin RGD binding peptide, tamoxifen, endoxifen, EGFR (epidermal growth factor receptor) antibody conjugates, kinase inhibitors, diazoles, triazoles, oxazoles, erlotinib, and mixtures thereof; wherein R.sub.15 is a peptide.

Details for Patent 9,090,640

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Microbix Biosystems Inc.	KINLYTIC	urokinase	For Injection	021846	01/16/1978		2031-09-02
Genentech, Inc.	RITUXAN	rituximab	Injection	103705	11/26/1997		2031-09-02
Idec Pharmaceuticals Corp.	RITUXAN	rituximab	Injection	103737	02/19/2002		2031-09-02
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	09/25/1998		2031-09-02
Genentech, Inc.	HERCEPTIN	trastuzumab	For Injection	103792	02/10/2017		2031-09-02
Genzyme Corporation	CAMPATH	alemtuzumab	Injection	103948	05/07/2001		2031-09-02
Genzyme Corporation	LEMTRADA	alemtuzumab	Injection	103948	11/14/2014		2031-09-02