Certain chemical entities, compositions, and methods

US2020102344A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2020102344-A1
Application numberUS-201916595749-A
CountryUS
Kind codeA1
Filing dateOct 8, 2019
Priority dateApr 29, 2012
Publication dateApr 2, 2020
Grant date

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  1. Title

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  5. First independent claim

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Abstract

Official abstract text for this publication.

Chemical entities that are novel compounds, pharmaceutical compositions and methods of treatment of cancer are described.

First claim

Opening claim text (preview).

1 .- 58 . (canceled) 59 . A compound selected from the group consisting of: N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)morpholine-4-carboxamide; N-((3R,5R,8R,95,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)piperazine-1-carboxamide; N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)piperazine-1-carboxamide; N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)pyrrolidine-1-carboxamide; 1-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)-3-(2-hydroxyethyl)urea; 1-(2-aminoethyl)-3-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)urea; 2-amino-N-((3R,5R,8R,95,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)acetamide; 2-amino-N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)acetamide; (S)—N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)pyrrolidine-2-carboxamide; 5-((5R,8R,95,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-3-(piperazin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2H-pyran-2-one; N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)methanesulfonamide; methyl ((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)carbamate; methyl ((5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)(methyl)carbamate; (R)-2-amino-N-((3S,5R,8R,95,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)-3-methylbutanamide; (R)-2-amino-N-((3S,5R,8R,95,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)propanamide; N-((5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)morpholine-4-carboxamide; and (2R)—N-((5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)pyrrolidine-2-carboxamide; or a pharmaceutically acceptable salt thereof. 60 . The compound of claim 59 , wherein the compound is: N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)morpholine-4-carboxamide, or a pharmaceutically acceptable salt thereof. 61 . The compound of claim 59 , wherein the compound is: N-((3R,5R,8R,95,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)piperazine-1-carboxamide, or a pharmaceutically acceptable salt thereof. 62 . The compound of claim 59 , wherein the compound is: N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)piperazine-1-carboxamide, or a pharmaceutically acceptable salt thereof. 63 . The compound of claim 59 , wherein the compound is: N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)pyrrolidine-1-carboxamide, or a pharmaceutically acceptable salt thereof. 64 . The compound of claim 59 , wherein the compound is: 1-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)-3-(2-hydroxyethyl)urea, or a pharmaceutically acceptable salt thereof. 65 . The compound of claim 59 , wherein the compound is: 1-(2-aminoethyl)-3-((3S,5R,8R,9 S, 10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)urea, or a pharmaceutically acceptable salt thereof. 66 . The compound of claim 59 , wherein the compound is: 2-amino-N-((3R,5R,8R,95,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)acetamide, or a pharmaceutically acceptable salt thereof. 67 . The compound of claim 59 , wherein the compound is: 2-amino-N-((3S,5R,8R,9 S, 10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)acetamide, or a pharmaceutically acceptable salt thereof. 68 . The compound of claim 59 , wherein the compound is: (S)—N-((3S,5R,8R,9 S, 10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta [a]phenanthren-3-yl)pyrrolidine-2-carboxamide, or a pharmaceutically acceptable salt thereof. 69 . The compound of claim 59 , wherein the compound is: 5-((5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-3-(piperazin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)-2H-pyran-2-one, or a pharmaceutically acceptable salt thereof. 70 . The compound of claim 59 , wherein the compound is: N-((3 S, 5R, 8R,9 S, 10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)methanesulfonamide, or a pharmaceutically acceptable salt thereof. 71 . The compound of claim 59 , wherein the compound is: methyl ((3S,5R,8R,9 S, 10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)carbamate, or a pharmaceutically acceptable salt thereof. 72 . The compound of claim 59 , wherein the compound is: methyl ((5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)(methyl)carbamate, or a pharmaceutically acceptable salt thereof. 73 . The compound of claim 59 , wherein the compound is: (R)-2-amino-N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)-3-methylbutanamide, or a pharmaceutically acceptable salt thereof. 74 . The compound of claim 59 , wherein the compound is: (R)-2-amino-N-((3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)propanamide, or a pharmaceutically acceptable salt thereof. 75 . The compound of claim 59 , wherein the compound is: N-((5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)morpholine-4-carboxamide, or a pharmaceutically acceptable salt thereof. 76 . The compound of claim 59 , wherein the compound is: (2R)—N-((5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-10,13-dimethyl-17-(2-oxo-2H-pyran-5-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-3-yl)pyrrolidine-2-carboxamide, or a pharmaceutically acceptable salt thereof. 77 . A pharmaceutical composition comprising a pharmaceutically acceptable carrier and the compound or pharmaceutically acceptable salt of claim 59 . 78 . A method of ameliorating symptoms or slowing progression of lung cancer in a subject, the method comprising administering to the subject in need thereof a therapeutically effective amount of the compound or ph

Assignees

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Classifications

  • Unsubstituted amino radicals · CPC title

  • not condensed · CPC title

  • the nitrogen atom being directly linked to the cyclopenta(a)hydro phenanthrene skeleton · CPC title

  • at position 14(15) · CPC title

  • Antineoplastic agents · CPC title

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What does patent US2020102344A1 cover?
Chemical entities that are novel compounds, pharmaceutical compositions and methods of treatment of cancer are described.
Who is the assignee on this patent?
Neupharma Inc
What technology area does this patent fall under?
Primary CPC classification C07J41/0011. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Apr 02 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).