HSP90-TARGETING CONJUGATES AND FORMULATIONS THEREOF
Conjugates of an active agent attached to a targeting moiety, such as an HSP90 binding moiety, via a linker, and particles comprising such conjugates have been designed. Such conjugates and particles can provide improved temporospatial delivery of the active agent, improved biodistribution and penetration in tumor, and/or decreased toxicity. Methods of making the conjugates, the particles, and the formulations thereof are provided. Methods of administering the formulations to a subject in need thereof are provided, for example, to treat or prevent cancer.
1 . A conjugate comprising an active agent coupled, via a linker, to an HSP90 targeting moiety.
2 . The conjugate of claim 1 , wherein the active agent inhibits PI3K activity.
3 . The conjugate of claim 2 , wherein the conjugate inhibits PI3K activity less than the active agent.
4 . The conjugate of claim 2 , wherein the active agent is selected from the group consisting of BAY 80-6946 (Copanlisib), Omipalisib (GSK2126458, GSK458), PF-04691502, PI-103, BGT226 (NVP-BGT226), Apitolisib (GDC-0980, RG7422), Duvelisib (IPI-145, INK1197), AZD8186, Pilaralisib (XL147), PIK-93, Idelalisib (GS-1101), MLN1117, VS-5584, SB2343, GDC-0941, BM120, NVP-BKM120, Buparlisib, AZD8835, XL765 (SAR245409), GS-9820 Acalisib, GSK2636771, AMG-319, IPI-549, Perifosine, Alpelisib, TGR 1202 (RP5264), PX-866, and derivatives/analogs thereof.
5 . The conjugate of claim 1 , wherein the HSP90 targeting moiety is an HSP90 inhibitor.
6 . The conjugate of claim 5 , wherein the HSP90 inhibitor is a small molecule.
7 . The conjugate of claim 6 , wherein the HSP90 inhibitor is selected from the group consisting of Ganetespib, Luminespib (AUY-922, NVP-AUY922), Debio-0932, MPC-3100, or Onalespib (AT-13387), SNX-2112, 17-amino-geldanamycin hydroquinone, PU-H71, AT13387, and derivatives/analogs thereof.
8 . The conjugate of claim 1 , wherein the HSP90 targeting moiety is ganetespib or a derivative thereof.
9 . The conjugate of claim 8 , wherein the HSP90 targeting moiety is selected from the group consisting of TM1, TM2, TM3, TM4, TM5, or TM8.
10 . The conjugate of claim 1 , wherein the HSP90 targeting moiety is Onalespib or a derivative thereof.
11 . The conjugate of claim 10 , wherein the HSP90 targeting moiety is selected from the group consisting of TM6 and TM7.
12 . The conjugate of claim 1 , wherein the linker comprises an ester group, a disulfide group, an amide group, an acylhydrazone group, an ether group, a carbamate group, a carbonate group, or an urea group.
13 . The conjugate of claim 1 , wherein the linker is a cleavable linker.
14 . The conjugate of claim 1 , wherein the conjugate has a molecular weight of less than about 50,000 Da, less than about 40,000 Da, less than about 30,000 Da, less than about 20,000 Da, less than about 15,000 Da, less than about 10,000 Da, less than about 8,000 Da, less than about 5,000 Da, less than about 3,000 Da, less than 2000 Da, less than 1500 Da, less than 1000 Da, or less than 500 Da.
15 . The conjugate of claim 1 , wherein the conjugate comprises copanlisib or its derivative and ganetespib or its derivative.
16 . The conjugate of claim 15 , wherein the conjugate is selected from the group consisting of Conjugate 38, Conjugate 40, Conjugate 39, Conjugate 27, Conjugate 28, Conjugate 29, Conjugate 32, Conjugate 33, Conjugate 34, Conjugate 41, Conjugate 42, Conjugate 44, Conjugate 30, Conjugate 35, Conjugate 37, Conjugate 43, Conjugate 31, and Conjugate 36, or a pharmaceutically acceptable salt thereof.
17 . The conjugate of claim 1 , wherein the conjugate comprises Omipalisib or its derivative and ganetespib or its derivative.
18 . The conjugate of claim 17 , wherein the conjugate is selected from the group consisting of Conjugate 18, Conjugate 22, Conjugate 23, and Conjugate 17.
19 . The conjugate of claim 1 , wherein the conjugate comprises P1-103 or its derivative and ganetespib or its derivative.
20 . The conjugate of claim 19 , wherein the conjugate is selected from the group consisting of Conjugate 24, Conjugate 25, and Conjugate 19, or a pharmaceutically acceptable salt thereof.
21 . The conjugate of claim 1 , wherein the conjugate comprises P1-103 or its derivative and Onalespib or its derivative.
22 . conjugate of claim 21 , wherein the conjugate is selected from the group consisting of Conjugate 20, Conjugate 26, and Conjugate 21, or a pharmaceutically acceptable salt thereof.
23 . The conjugate of claim 1 , further comprising a permeability modulating unit.
24 . The conjugate of claim 1 , further comprising a pharmacokinetic modulating unit.
25 . A pharmaceutical composition comprising the conjugate of claim 1 and at least one pharmaceutically acceptable excipient.
26 . A method of reducing cell proliferation comprising administering a therapeutically effective amount of at least one conjugate of claim 1 to the cell.
27 . The method of claim 26 , wherein the cell is a cancer cell.
28 . The method of claim 27 , wherein the cancer cell is a small-cell lung cancer cell, a non-small-cell lung cancer cell, a sarcoma cell, a pancreatic cancer cell, a breast cancer cell, or a colon cancer cell.
29 . A method of treating cancer of a subject in need thereof, comprising administering a pharmaceutically effective amount of the pharmaceutical composition of claim 25 to said subject.
30 . The method of claim 29 , wherein the cancer is small-cell lung cancer, non-small-cell lung cancer, sarcoma, pancreatic cancer, ovarian cancer, breast cancer, or colon cancer.
31 . The method of claim 29 , wherein the blood glucose level of the subject does not show a significant increase.
32 . The method of claim 29 , wherein the cancer has a PIK3CA mutation.