NZ725603B2 - Pladienolide pyridine compounds and methods of use - Google Patents

Pladienolide pyridine compounds and methods of use Download PDF

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Publication number
NZ725603B2
NZ725603B2 NZ725603A NZ72560315A NZ725603B2 NZ 725603 B2 NZ725603 B2 NZ 725603B2 NZ 725603 A NZ725603 A NZ 725603A NZ 72560315 A NZ72560315 A NZ 72560315A NZ 725603 B2 NZ725603 B2 NZ 725603B2
Authority
NZ
New Zealand
Prior art keywords
compound
treatment
use according
medicament
cancer
Prior art date
Application number
NZ725603A
Other versions
NZ725603A (en
Inventor
Kenzo Arai
Silvia Buonamici
Betty Chan
Nicholas C Gearhart
Baudouin Gerard
Sonobe Regina Kanada
Gregg F Keaney
Kazunobu Kira
Yoshihiko Kotake
Kian Huat Lim
Original Assignee
Eisai R&D Management Co Ltd
Filing date
Publication date
Application filed by Eisai R&D Management Co Ltd filed Critical Eisai R&D Management Co Ltd
Priority to NZ764190A priority Critical patent/NZ764190B2/en
Priority claimed from PCT/US2015/030464 external-priority patent/WO2015175594A1/en
Publication of NZ725603A publication Critical patent/NZ725603A/en
Publication of NZ725603B2 publication Critical patent/NZ725603B2/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Abstract

The present invention provides novel pladienolide pyridine compounds, pharmaceutical compositions containing such compounds, and methods for using the compounds as therapeutic agents. These compounds may be useful in the treatment of cancer, particularly cancers in which agents that target the spliceosome and mutations therein are known to be useful.

Claims (29)

We claim:
1. A compound selected from a nd of formula 1: a compound of formula 2: a compound of formula 3: N O OH 3 , a compound of formula 4: and pharmaceutically acceptable salts thereof.
2. The compound according to claim 1 selected from a nd of formula 1: and pharmaceutically acceptable salts thereof.
3. The compound according to claim 1 selected from a compound of formula 2: N O OH , and pharmaceutically acceptable salts thereof.
4. The compound ing to claim 1 selected from a compound of formula 3: N O OH 3 , and pharmaceutically acceptable salts thereof.
5. The compound according to claim 1 selected from a compound of formula 4: and pharmaceutically acceptable salts thereof.
6. The compound according to any one of claims 1-5, wherein said compound comprises greater than about 80% by weight of one stereoisomer of the nd and less than about 20% by weight of the other stereoisomers of the compound, or a pharmaceutically acceptable salt thereof.
7. The compound according to any one of claims 1-5, wherein said compound comprises r than about 97% by weight of one stereoisomer of the compound and less than about 3% by weight of the other stereoisomers of the compound, or a pharmaceutically acceptable salt
8. A pharmaceutical composition comprising the compound or pharmaceutically acceptable salt thereof according to any one of claims 1-7.
9. The pharmaceutical composition according to claim 8, wherein said composition is formulated for intravenous, oral, subcutaneous, or intramuscular administration.
10. The pharmaceutical composition according to claim 9, wherein said composition is formulated for oral administration.
11. Use of the compound or pharmaceutically acceptable salt thereof according to any one of claims 1-7 in the manufacture of a medicament for the therapeutic treatment of myelodysplastic syndrome, chronic cytic leukemia, acute blastic leukemia, chronic myelomonocytic ia, acute d leukemia, colon cancer, pancreatic cancer, endometrial , ovarian , breast cancer, uveal melanoma, c cancer, cholangiocarcinoma, or lung cancer.
12. The use according to claim 11, wherein said medicament is for the treatment of acute myeloid leukemia.
13. The use according to claim 11, wherein said medicament is for the treatment of myelodysplastic syndrome.
14. The use according to claim 11, wherein said medicament is for the treatment of chronic lymphocytic leukemia.
15. The use according to claim 11, wherein said medicament is for the treatment of acute lymphoblastic leukemia.
16. The use according to claim 11, wherein said medicament is for the treatment of chronic myelomonocytic leukemia.
17. The use according to claim 11, n said medicament is for the treatment of colon cancer.
18. The use according to claim 11, wherein said medicament is for the treatment of pancreatic cancer.
19. The use according to claim 11, wherein said medicament is for the treatment of endometrial cancer.
20. The use according to claim 11, n said medicament is for the treatment of ovarian cancer.
21. The use according to claim 11, wherein said medicament is for the treatment of breast
22. The use according to claim 11, wherein said ment is for the treatment of uveal melanoma.
23. The use according to claim 11, wherein said ment is for the treatment of gastric cancer.
24. The use according to claim 11, wherein said medicament is for the treatment of cholangiocarcinoma.
25. The use according to claim 11, wherein said medicament is for the treatment of lung cancer.
26. The use according to claim 11, wherein said myelodysplastic syndrome, chronic lymphocytic leukemia, acute lymphoblastic leukemia, chronic myelomonocytic leukemia, acute myeloid leukemia, colon cancer, pancreatic cancer, endometrial cancer, ovarian cancer, breast cancer, uveal ma, gastric cancer, giocarcinoma, or lung cancer, is positive for one or more mutations in a spliceosome gene or protein.
27. The use according to claim 26, wherein said spliceosome gene or protein is selected from splicing factor 3B subunit 1 (SF3B1), U2 small nuclear RNA auxiliary factor 1 (U2AF1), serine/arginine-rich splicing factor 2 (SRSF2), zinc finger (CCCH type) RNA-binding motif and serine/arginine rich 2 (ZRSR2), pre-mRNA-processing-splicing factor 8 (PRPF8), U2 small nuclear RNA auxiliary factor 2 ), splicing factor 1 (SF1), splicing factor 3a subunit 1 (SF3A1), PRP40 pre-mRNA processing factor 40 g B (PRPF40B), RNA binding motif n 10 (RBM10), poly(rC) binding protein 1 (PCBP1), crooked neck pre-mRNA splicing factor 1 (CRNKL1), DEAH (Asp-Glu-Ala-His) box helicase 9 (DHX9), peptidyl-prolyl cis-trans isomerase-like 2 (PPIL2), RNA binding motif protein 22 (RBM22), small r ribonucleoprotein Sm D3 (SNRPD3), probable ATP-dependent RNA helicase DDX5 (DDX5), pre-mRNA-splicing factor ATP-dependent RNA se DHX15 (DHX15), and polyadenylatebinding protein 1 (PABPC1).
28. The use according to claim 27, wherein said spliceosome gene or protein is splicing factor 3B subunit 1.
29. The compound according to claim 1, substantially as herein described with nce to any one of the examples and/or
NZ725603A 2015-05-13 Pladienolide pyridine compounds and methods of use NZ725603B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
NZ764190A NZ764190B2 (en) 2015-05-13 Pladienolide pyridine compounds and methods of use

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201461993423P 2014-05-15 2014-05-15
PCT/US2015/030464 WO2015175594A1 (en) 2014-05-15 2015-05-13 Pladienolide pyridine compounds and methods of use

Publications (2)

Publication Number Publication Date
NZ725603A NZ725603A (en) 2023-11-24
NZ725603B2 true NZ725603B2 (en) 2024-02-27

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