(12) United States Patent (10) Patent No.: US 9,302,982 B2 Christian (45) Date of Patent: *Apr

(12) United States Patent (10) Patent No.: US 9,302,982 B2 Christian (45) Date of Patent: *Apr

US009302982B2 (12) United States Patent (10) Patent No.: US 9,302,982 B2 Christian (45) Date of Patent: *Apr. 5, 2016 (54) PHARMACEUTICAL DOPAMINE 6,339,064 B1 1/2002 McDevitt et al. GIYCOCONJUGATECOMPOSITIONS AND 355 R. 393 Eas 51462 METHODS OF THEIR PREPARATION AND 8,352.752 B2 8/2012 Christian ........................ 514.42 USE 9,023,818 B2 5/2015 Christian 2006/0189547 A1 8, 2006 Christian (75) Inventor: Samuel T. Christian, Alabaster, AL (US) FOREIGN PATENT DOCUMENTS (73) Assignee: GLYCON LLC, Riverside, AL (US) WO 9728174 8, 1997 WO 9905089 2, 1999 (*) Notice: Subject to any disclaimer, the term of this WO O197244 12/2001 patent is extended or adjusted under 35 OTHER PUBLICATIONS U.S.C. 154(b) by 255 days. This patent is Subject to a terminal dis- Thomas et al., “Parkinson's Disease” Human Molecular Genetics claimer. (2007) vol. 16 reviss 2, pp. R183-R194.* Rao et al., “Parkinson's Disease:Diagnosis and Treatment” American Family Physician (2006) vol. 74 No. 2 pp. 2046-2054.* (21) Appl. No.: 13/551,131 “Remington: The Science and Practice of Pharmacy, 20' edition”, (22) Filed: Jul. 17, 2012 iamsEdited A by Wii Alfonso M. pp.R. Gennaro,218, publishedity. 2000 by Lippincott PP Will O O Czarnocki et al., "Enantioselective Synthesis of (R)-(-) Laudanosine (65) Prior Publication Data and (R)-(-) Glaucine from E. Acid', E.A. Asym US 2013/0203855A1 Aug. 8, 2013 metry, vol. 7, No. 9, Sep. 1996, pp. 2711-2720. Doherty, “The Synthesis of Glyconyl Peptides”,Journal of Biologi Related U.S. Application Data cal Chemistry, vol. 201(2), May 1953, pp. 857-866. Fernandez et al., “Synthesis and biological studies of glycosyl (63) Continuation-in-part of application No. 1 1/965,444, dopamine deriviatives”. Carbohyd. Res. vol. 327, 2000, pp. 353-365. filed on Dec. 27, 2007, now Pat. No. 8,252,752, which Glinsky et al., “Inhibition of colony formation in agarose of meta is a continuation of application No. 10/625,645, filed static human breast carcinoma and melanoma cells by Synthetic on Jul. 22, 2003, now Pat. No. 7,345,031, application glycoamine analogs”. Clin. Exp. Metastasis, vol. 14(3), May 1996, No. 13/551,131, which is a continuation-in-part of pp. 253-267. application No. 12/913,543, filed on Oct. 27, 2010, Haavik et al., "Tyrosine hydroxylase and Parkinson's disease'. now Pat. No. 9.023.818, which is a continuation of Molecular Neurobiology, vol. 16, No. 3, Jun. 1998, pp. 285-309. application No. 1 1/343 266 filed on Jan. 30, 2006 Jakaset al. “Synthesis and 13C NMR investigation of novel Amadori now abandoned,s which is a continuation of application opioidcompounds peptide, (1-amino leucine—enkephalin'. -1-deoxy-D-fructose J. Chem. derivatives) Soc., Perkin related Trans. to the No. 09/547.501, filed on Apr. 12, 2000, now vol. 2, DOI 10.1039/P29960000789, 1996, pp. 789-794. abandoned. Jiang et al., “Dopaminergic properties and experimental anti Parkinsonian effects . Clin. Neuropharmacol vol. 27, No. 2, (51) Int. Cl. 2004, 63-73. A6 IK3I/7008 (2006.01) Knoerzer et al., “Dopaminergic Benzoaphenanthridines: Resolu A 6LX3L/7032 (2006.01) tion and Pharmacological Evaluation of the Enantiomers of C7H5/04 (2006.01) Dihydrexidine, the Full Efficacy D1 Dopamine Receptor Agonist'. C7H 5/18 (2006.01) Journal of Medicinal Chemistry, vol. 37 No. 15, Jul. 1994, pp. 2453 C07C 235/08 (2006.01) iRoberto et al., “Giycoconjugates of amines: alkylation of pri A6 IK 47/48 (2006.01) marv and second amines Russ. Chem. Bull vol 47. No. 6 iss. A6 IK3I/704 (2006.01) s: Hisplay v w w K-1 - w C07H 17/00 (2006.01) Likhoshersfov et al., “Synthesis of N-chloroacetyi-B- (52) U.S. Cl. glycopyranosylamines, derivatives of monosaccharides and CPC ............. C07C 235/08 (2013.01); A61 K3I/704 lactose.”. Russ. Chern. B1 vol: 45, 1996, pp. 1760-1763. (2013.01); A61K47/48092 (2013.01); C07H Maher et al., “Substrate specificity and kinetic parameters of 5/04 (2013.01); C07H 1700 (2013.01) GLUT3". Biochem. J. vol.315, 1996, pp. 827-831. (58) Field of Classification Search (Continued) CPC. C07H 15/2013; C07H5/06; A61K31/7032: A61K 3.1 F7008 See application file for complete search history. Primary Examiner — Eric Olson (74) Attorney, Agent, or Firm — Kilpatrick Townsend & (56) References Cited Stockton LLP U.S. PATENT DOCUMENTS (57) ABSTRACT 3,929,813 A 12/1975 Higuchi 3,962.447 A 6/1976 Higuchi et al. Hydrophilic transportable N-linked glycosyl dopaminergic 4,032,676 A 6, 1977 Heins et al. prodrug compounds and methods of their use. 4,190,672 A 2, 1980 Fahn 5,380,837 A 1/1995 Nakada et al. 5,639,737 A 6, 1997 Rubin 9 Claims, 22 Drawing Sheets U.S. Patent Apr. 5, 2016 Sheet 1 of 22 US 9,302,982 B2 360- P=0.6349 340 320 500 280 260 240 220 200 180 160 140 120 P=0.0066 100 80 60 40 20 Z Before(n=2 2 ) AfterNoC ( r 6) AfterMPTP(n=18) FG 1 U.S. Patent Apr. 5, 2016 Sheet 3 of 22 US 9,302,982 B2 O Before IPX-750 IPX-750 St week 700 IPX-750 2nd week ZIPX-750 3rd week NY IPX-750 4th week as 500 3. , N soto 3.WN NN i 200 WN NZN % SNN Z 3.3 t SN WN | 2NZN3N t NZN MPTP+NoCI(n=6) MPTP-IPX-750 MPTP-IPX-750 (20mg/kg)(n=6) (80mg/kg)(n=6) Roto-Rod test for different time of IPX-750 treatment FIG.3 U.S. Patent Apr. 5, 2016 US 9,302,982 B2 700 O After MPP After treotment of IPX-750 600 WOsh-Out 1st Week ZZ Wosh-out 2nd week 500 ? 500 200 100 <> N N` MPTP+PX-750 MPTP+IPX-750 (20mg/kg)(n=6) (80mg/kg)(n=6) FIG.4 U.S. Patent Apr. 5, 2016 Sheet 5 of 22 US 9,302,982 B2 6-OHDA+ 6-OHDA+ 6-OHDA 6-OHDA+ Apomorphine 0.9% NgC PX-750 IPX-750 (80mg/kg) (200mg/kg) Acute effects of IPX-750 FIG.5 U.S. Patent Apr. 5, 2016 Sheet 6 of 22 US 9,302,982 B2 is NZNZ W 2 N N r" as cry co - to r- in CN " . any led Sapko u000 U.S. Patent Apr. 5, 2016 Sheet 7 of 22 US 9,302,982 B2 is is is 55 E E2 E . ÉS 33 3 SSS3 -s a N. N. N. N. x:it a is s 33s is a g a set is is is is is ww. SS is a a r sSS s SSSSSSSSSSSSSSSSSSS SXSS s s XXX RSSSSSSSSSSSSSSSSSSS Xs deRys SS SSSSs SSSSSSSSSSS N sExx s XXXXXXSSSS s : wa + HE Š& eaw –2aÉs • 2 - al a &YsS E . &Si; s SES ZZZZZZZZZZZZZZZ N S. 2 S se S S S S 3 g S S S se c was saw was was views (SPU003S) au PO1-Dog U.S. Patent Apr. 5, 2016 Sheet 8 of 22 US 9,302,982 B2 OThe lost treatment 120 1st week wash-out 2nd week wosh-out 3rd week WOsh-out OO 80 k (spu008S)ºupou-0308 60 40 O N N```` Hetero HetN Ø>s oC (PX-750 20mg/kg) RotO-rod T t with IPX-750 (20mg/kg)/0.9% NoC in heterozygous/WT Mice FIG.8 U.S. Patent Apr. 5, 2016 Sheet 9 of 22 US 9,302,982 B2 U.S. Patent Apr. 5, 2016 Sheet 12 of 22 US 9,302,982 B2 |Gipons]fra U.S. Patent Apr. 5, 2016 Sheet 13 of 22 US 9,302,982 B2 Spl Cenotoxic Compounds. Spl cnd GLUT1 mRNA e.g. eioposide, cisplotin, -radiation decrease after myogenesis Myobicsts-kiyotubes Differentition Repressor re cities Sp1 Repressor. FO Cell cycle plO7 RelA of NFy -27Rip to -J.3%ip Housekeeping - Eoholicer-fi) -ette to -2dio is -33bp to -99bp Growth Factors e.g. insulin, Serum, PDGF, Oncogene products IkB Phosphorylation (inhibitory subunit of NFkB) Doponine-induced Apoptosis Inlommctory Cytokines c.g. IL-1, THF-, a FN- 7 FIG. 1 OA U.S. Patent Apr. 5, 2016 Sheet 14 of 22 US 9,302,982 B2 yPTP Insecticides: e.g., -- Rolenone, 02/03 Agonists pyrethroids, Alpha-Synuclein chlorpyrifos, + permethrin Growth foctors e.g. Scrum, PDCF, l C2/03 Receptor Activotion Oncogene products Kurr1 mRNA Down-Regulation and Blocks Nurri Nuclear Trorislocation ove CLU RNA f +16.7Kbp to +1.8Kbp Enhancer-2E2) in intron 2 Guti ni 3 tip at 2.18%ip to 24Kip 80kDo cylosolic protein tronscribed from 3'UTR of CLUI in recction to hypoxic C or tumorigenesis, i.e., an pge \ mRNA stabilizer protein P53, HPTF Targeted Endonucleose Stabilized Sensitive it rRNA Ubiquinotor WHL Pro PI3K/AKT Gut frMA Closes, Signaling ProteoSome Clucose Degradation deprivation Hific A inctive Hypoxie: Ferroprotein Sensor Co2t Fe2+ chelotion OH-pyridinones Growth Fociors: e.g. insulin, IGF-1 FIG. 1 OB U.S. Patent Apr. 5, 2016 Sheet 15 of 22 US 9,302,982 B2 jossaJdeu-c) U.S. Patent Apr. 5, 2016 Sheet 16 of 22 US 9,302,982 B2 (01-6'0E005) uchopp1783 OXd10/pub(01-6(9.3935) |dS U.S. Patent Apr. 5, 2016 Sheet 18 of 22 US 9,302,982 B2 U.S. Patent Apr. 5, 2016 Sheet 19 of 22 US 9,302,982 B2 |-5H$ &### U.S. Patent Apr. 5, 2016 Sheet 20 of 22 US 9,302,982 B2 udsoqd-90 U.S. Patent US 9,302,982 B2 30 U.S.

View Full Text

Details

  • File Type
    pdf
  • Upload Time
    -
  • Content Languages
    English
  • Upload User
    Anonymous/Not logged-in
  • File Pages
    54 Page
  • File Size
    -

Download

Channel Download Status
Express Download Enable

Copyright

We respect the copyrights and intellectual property rights of all users. All uploaded documents are either original works of the uploader or authorized works of the rightful owners.

  • Not to be reproduced or distributed without explicit permission.
  • Not used for commercial purposes outside of approved use cases.
  • Not used to infringe on the rights of the original creators.
  • If you believe any content infringes your copyright, please contact us immediately.

Support

For help with questions, suggestions, or problems, please contact us