Process for synthesizing 2-bromolysergic acid diethylamide via controlled hydrolysis of bromocriptine
US-2024287057-A1 · Aug 29, 2024 · US
US2024226126A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024226126-A1 |
| Application number | US-202218568162-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 15, 2022 |
| Priority date | Jun 16, 2021 |
| Publication date | Jul 11, 2024 |
| Grant date | — |
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Methods of treatment for psoriasis, and compositions for use in such methods are provided, utilizing repositioned drugs identified as anti-psoriasis agents.
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1 . A method of treating psoriasis in a subject, the method comprising: administering to the subject an effective dose of a compound of Table 1 for duration and periodicity sufficient to reduce the symptoms of psoriasis. 2 . The method of claim 1 , wherein the anti-psoriasis agent is selected from quinostatin or a derivative thereof; bromocriptine or a derivative thereof; trifluoperazine or a derivative thereof; sirolimus or a derivative thereof; 0297417-0002B or a derivative thereof; 0198306-0000, PD-198306 or a derivative thereof; PHA-00665752 or a derivative thereof; PNU-0230031 [267429-39-0] or a derivative thereof; AG-012559 [369370-06-9] or a derivative thereof; etoposide or a derivative thereof; or ethacrynic acid or a derivative thereof. 3 - 12 . (canceled) 13 . The method of claim 2 , wherein the administration is systemic. 14 . The method of claim 2 , wherein the administration is topical. 15 . The method of claim 2 , wherein dose is administered to the subject upon a flare of psoriasis. 16 . The method of claim 2 , wherein the psoriasis is chronic psoriasis. 17 . The method of claim 2 , wherein the psoriasis is plaque psoriasis. 18 . A composition in a unit dose formulation of an anti-psoriasis agent of Table 1, suitable for use in the methods of claim 2 . 19 . The composition of claim 18 , wherein the anti-psoriasis agent is quinostatin or a derivative thereof. 20 . The composition of claim 18 , wherein the anti-psoriasis agent is bromocriptine or a derivative thereof. 21 . The composition of claim 18 , wherein the anti-psoriasis agent is trifluoperazine or a derivative thereof. 22 . The composition of claim 18 , wherein the anti-psoriasis agent is sirolimus or a derivative thereof. 23 . The composition of claim 18 , wherein the anti-psoriasis agent is 0297417-0002B or a derivative thereof. 24 . The composition of claim 18 , wherein the anti-psoriasis agent is 0198306-0000, PD-198306 or a derivative thereof. 25 . The composition of claim 18 , wherein the anti-psoriasis agent is PHA-00665752 or a derivative thereof. 26 . The composition of claim 18 , wherein the anti-psoriasis agent is PNU-0230031 [267429-39-0] or a derivative thereof. 27 . The composition of claim 18 , wherein the anti-psoriasis agent is AG-012559 [369370-06-9] or a derivative thereof. 28 . The composition of claim 18 , wherein the anti-psoriasis agent is etoposide or a derivative thereof. 29 . The composition of claim 18 , wherein the anti-psoriasis agent is ethacrynic acid or a derivative thereof. 30 . The composition of claim 18 , wherein the anti-psoriasis agent is the sole active agent. 31 . The composition of claim 18 , further comprising a second therapeutic agent for treatment of psoriasis. 32 - 33 . (canceled)
ortho- or peri-condensed with carbocyclic ring systems, e.g. phenothiazine, chlorpromazine, piroxicam · CPC title
ortho- or peri-condensed with heterocyclic rings · CPC title
Ergoline derivatives, e.g. lysergic acid, ergotamine · CPC title
containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole (nicotine A61K31/465) · CPC title
the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin · CPC title
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