IP Library Granted Patent US 9,604,913
Granted Patent B2
US 9,604,913 · App. 14/519,408 · Granted Mar 28, 2017

Crystalline diacylhydrazine and the use thereof

Inventors: Robert E. Hormann (Elkins Park, PA); Inna Shulman (Langhorne, PA); Eva Rödel (Basel, CH); Rolf Hilfiker (Allschwil, CH); Susan M. De Paul (Zürich, CH)
Assignee: Intrexon Corporation
C07C243/38A01N37/28A01N37/40A61K31/166C07B2200/07C07B2200/13C12N2710/10341C12N2830/002Y10T428/2982
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Quick Facts
Patent No.
US 9,604,913
App. No.
14/519,408
Granted
Mar 28, 2017
Kind
B2
Abstract

The present disclosure provides crystalline polymorphic and amorphous forms of (R)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-N′-(2-ethyl-3-methoxy-benzoyl)-hydrazide (Compound 1) or (S)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-N′-(2-ethyl-3-methoxy-benzoyl)-hydrazide (Compound 2). The present disclosure further provides compositions comprising crystalline polymorphic and amorphous forms of Compound 1 or Compound 2 and an excipient, methods of making crystalline polymorphic or amorphous forms of Compound 1 or Compound 2, and methods of using crystalline polymorphic or amorphous forms of Compound 1 or Compound 2 to regulate gene expression in a cell or in a subject.

Claims (9)

1. Crystalline (R)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-N′-(2-ethyl-3-methoxy-benzoyl)-hydrazide hydrate Form IV,

characterized as having a powder x-ray diffraction pattern with peaks at 6.83, 10.31, 11.30, 12.18, 12.98, 13.69, 15.11, 16.23, 17.60, 17.99, 20.70, 21.15, 21.68, 22.71, 23.79, and 24.86 degrees 2Θ.

2. The (R)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-N′-(2-ethyl-3-methoxy-benzoyl)-hydrazide hydrate Form IV of claim 1 having an average particle size distribution of about 10 μm or less.

3. A composition comprising the (R)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-N′-(2-ethyl-3-methoxy-benzoyl)-hydrazide hydrate Form IV of claim 1 and one or more excipients.

4. The composition of claim 3 , wherein said one or more excipients comprise one or more pharmaceutically acceptable excipients.

5. The composition of claim 4 , wherein said one or more pharmaceutically acceptable excipients comprise Miglyol 812, phospholipon 90G, or tocopheryl polyethylene glycol 1000 succinate, or a mixture thereof.

6. A method of making a composition, the method comprising admixing the (R)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-N′-(2-ethyl-3-methoxy-benzoyl)-hydrazide hydrate Form IV of claim 1 and an excipient.

7. A kit comprising the (R)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-N′-(2-ethyl-3-methoxy-benzoyl)-hydrazide hydrate Form IV of claim 1 .

8. The crystalline (R)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-N′-(2-ethyl-3-methoxy-benzoyl)-hydrazide hydrate Form IV of claim 2 having an average particle size distribution of about 1 μm or less.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 17, 2017
From: HORMANN, ROBERT E.; SHULMAN, INNA; RODEL, EVA; HILFIKER, ROLF; DE PAUL, SUSAN M.
To: INTREXON CORPORATION
Reel/Frame 042026/0814 →
Continuity (3)
Division 13606444 · Sep 7, 2012
Provisional Application 61532368 · Sep 8, 2011
Related Publication 20150045441A1 · Feb 12, 2015