IP Library Granted Patent US 10,315,990
Granted Patent B2
US 10,315,990 · App. 15/550,783 · Granted Jun 11, 2019

Isothiocyanate compounds and isothiocyanate XPO1 protein inhibitor drugs thereof

Inventor: Yongliang Yang (Dalian, CN)
Assignee: DRIVINGFORCE THERAPEUTICS
C07C331/24A61K31/26A61K31/428C07C331/22C07D213/71C07D215/36C07D235/28C07D239/74C07D257/04C07D277/76C07D295/096C07D311/14C07C2602/10C07C2603/18C07C2603/24C07C2603/28
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Quick Facts
Patent No.
US 10,315,990
App. No.
15/550,783
Granted
Jun 11, 2019
Kind
B2
Abstract

The present invention provides an isothiocyanate compound and its application. The compound is an aryl-substituted isothiocyanate compound that has a structure of the general formula I. The isothiocyanate compound of the present invention has very good solubility in water, far better inhibitory activity for XPO1 protein than other non-aryl substituted congeneric compounds, little side effects, and good biological safety and bioavailability, and is quite suitable for clinical application. Therefore, the isothiocyanate compound would have tremendous potential market space and economic benefits.

Claims (38)

1. An isothiocyanate compound of formula I:

wherein R is selected from phenyl, a five- to six-membered mononuclear heteroaryl including 1-3 heteroatoms each independently selected from nitrogen, oxygen or sulfur, an eight- to ten-membered dinuclear aryl, an eight- to ten-membered dinuclear heteroaryl including 1-4 heteroatoms each independently selected from nitrogen, oxygen or sulfur, a ten- to fourteen-membered trinuclear aryl, or a ten- to fourteen-membered trinuclear heteroaryl including 1-4 heteroatoms each independently selected from nitrogen, oxygen or sulfur;

wherein R is unsubstituted, or is optionally substituted with one or more independently selected W substituents,

wherein the W substituent is selected from halogen, C 1-4 alkoxy, C 1-4 haloalkyl, a five- to six-membered mononuclear heteroaryl including 1-3 heteroatoms, each independently selected from nitrogen, oxygen or sulfur, a four- to seven-membered heterocycloalkyl, including 1-3 heteroatoms, each independently selected from nitrogen, oxygen or sulfur, or an eight- to ten-membered dinuclear heteroaryl including 1-4 heteroatoms, each independently selected from nitrogen, oxygen or sulfur; and

wherein n is 0, 1 or 2.

2. The isothiocyanate compound according to claim 1 , wherein R is further selected from, benzofuryl, benzopyranyl, benzopyronyl, benzothienyl, benzothiazolyl, benzopyrazolyl, benzoimidazolyl, benzooxazolyl, carbazolyl, cinnolinyl, dibenzofuryl, dibenzothienyl, furyl, indolyl, imidazolyl, isoquinolyl, oxazolyl, quinolyl, quinazolinyl, quinoxalinyl, thienyl, tetrazolyl, thiazolyl, pyranyl, pyronyl, pyridyl, pyridazinyl, pyrazolyl, pyrimidyl, pyrazinyl, phenoxazinyl, phenothiazinyl, phenazinyl, purinyl, or a di- to tri-nuclear group optionally fused from the above mononuclear groups.

3. An isothiocyanate compound according to claim 1 , wherein the compound is one of the following compounds:

(1) (E)-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)benzene

(2) (E)-1-bromo-4-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)benzene

(3) (E)-1-chloro-4-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-2-(trifluoromethyl)benzene

(4) (E)-1-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-3,5-bis(trifluoromethyl)benzene

(5) (E)-1-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-3-methoxy-5-(trifluoromethyl)benzene

(6) (E)-5-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-1,2,3-trimethoxybenzene

(7) (E)-3-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-5-(trifluoromethyl)benzenesulfonamide

(8) (E)-3-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-5-(trifluoromethyl)benzonitrile

(9) (E)-4-(4-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)phenyl)morpholine

(10) (E)-6-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-1,2,3,4-tetrahydronaphthalene

(11) (E)-2-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)naphthalene

(12) (E)-2-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)anthracene

(13) (E)-9-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-1H-phenalene

(14) (E)-2-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-9H-fluorene

(15) (E)-3-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)pyridine

(16) (E)-3-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-5-(trifluoromethyl)pyridine

(17) (E)-6-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)quinoline

(18) (E)-6-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)quinazoline

(19) (E)-6-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-2H-chromen-2-one

(20) (E)-2-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)benzo[d]thiazole

(21) (E)-2-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-5-(trifluoromethyl)benzo[d]thiazole

(22) (E)-2-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-1H-benzo[d]imidazole

(23) (E)-2-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-6-(trifluoromethyl)-1H-benzo[d]imidazole

(24) (E)-2-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-6-methoxy-1H-benzo[d]imidazole

(25) (E)-5-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-1-phenyl-1H-tetrazole

(26) (E)-4-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-1,1′-biphenyl

(27) (E)-1-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)-4-phenoxybenzene

(28) (E)-(4-((4-isothiocyanatobut-1-en-1-yl)sulfinyl)phenyl)(4-methoxyphenyl)sulfane.

4. An XPO1 protein inhibitor drug including an isothiocyanate compound according to claim 3 and a pharmaceutically acceptable carrier.

5. The XPO1 protein inhibitor drug according to claim 4 ,

wherein the pharmaceutically acceptable carrier is an excipient, a filler, an adhesive, a wetter, a disintegrant, a surfactant, a lubricant, a dispersant, a pH regulator, a conservant, a chelating agent, a cosolvent or a stabilizer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 13, 2017
From: YANG, YONGLIANG
To: DRIVINGFORCE THERAPEUTICS CO., LTD.
Reel/Frame 043277/0209 →
Priority Claims (1)
CN 2015 1 0073762 · Feb 12, 2015 · national
Continuity (1)
Related Publication 20180029979A1 · Feb 1, 2018
Cited By (2)
US 12,239,626 US 12,310,939