US2017283464A1PendingUtilityA1
Crystalline And Amorphous Forms Of A Beta-Arrestin Effector
Est. expiryFeb 7, 2034(~7.6 yrs left)· nominal 20-yr term from priority
Inventors:Ritesh SanghviGregory AlcornGraham Richard LawtonMeiki YuMatthew RonsheimJiaher TianShao Hong ZhouYuriy B. Kalyan
A61P 9/00A61P 43/00A61P 9/12A61P 9/04C07K 7/64A61K 38/12A61P 13/12A61K 38/00C07K 7/06
38
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present disclosure provides novel crystalline forms of a compound that acts as a β-arrestin effector, processes for preparing novel crystalline and amorphous forms of a compound that acts as a β-arrestin effector and uses thereof.
Claims
exact text as granted — not AI-modified1 - 42 . (canceled)
43 . A process for preparing a crystalline form of a peptide having a sequence of SEQ. ID. NO.1, comprising crystallizing SEQ. ID. NO. 1 to form a crystalline form of a peptide having a sequence of SEQ. ID. NO. 1.
44 . The process of claim 43 , wherein the crystallizing comprises dissolving peptide in an aqueous solution and crystallizing the peptide to form the crystalline form therefrom.
45 . The process of claim 44 , wherein the aqueous solution is deionized water.
46 . The process of claim 44 , wherein the aqueous solution consists of deionized water.
47 . The process of claim 44 , wherein the process further comprises precipitating the peptide after dissolving the peptide in the aqueous solution.
48 . The process of claim 47 , wherein the precipitating comprises heating the aqueous solution and cooling the aqueous solution to ambient temperature to precipitate the peptide in the crystalline form.
49 . The process of claim 48 , wherein the process further comprises cooling the aqueous solution to a temperature of about 0 to about 5° C. to precipitate the peptide in the crystalline form.
50 . The process of claim 43 , further comprising lyophilizing the crystalline form.
51 . A pharmaceutical composition comprising a crystalline form of a peptide having a sequence of SEQ. ID. NO.1.
52 . A method of treating a cardiovascular or a cardiorenal disorder comprising administering to a patient in need thereof the pharmaceutical composition of claim 51 .
53 . A crystalline form of a peptide having a sequence of SEQ. ID. NO. 1.
54 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising a peak at about 18.5±0.5 degrees 2θ.
55 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising a peak at about 10.1±0.5 degrees 2θ.
56 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising a peak at about 8.2±0.5 degrees 2θ.
57 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising a peak at about 20.2±0.5 degrees 2θ.
58 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising a peak at about 24.4±0.5 degrees 2θ.
59 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising peaks at about 18.5, and at about 10.1±0.5 degrees 2θ.
60 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising peaks at about 10.1, and at about 8.2±0.5 degrees 2θ.
61 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising peaks at about 8.2, and at about 20.2±0.5 degrees 2θ.
62 . The crystalline form of claim 53 , characterized by an X-ray powder diffraction pattern comprising peaks at about 20.2, and at about 10.1±0.5 degrees 2θ.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.