US2008214670A1PendingUtilityA1
Therapeutic Malonic Acid/Acetic Acid C60 Tri-Adducts of Buckminsterfullerene and Methods Related Thereto
Est. expiryFeb 23, 2022(expired)· nominal 20-yr term from priority
A61P 39/06A61P 43/00A61P 25/00A61P 3/02B82Y 40/00B82Y 30/00C01B 32/156C07C 61/39A61K 31/19C07C 69/753C01B 32/15C07C 2604/00
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Claims
Abstract
Disclosed and claimed herein are e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene of the general formula C 60 R 3 , wherein each R is independently selected from groups of the formula —CR 1 R 2 wherein each R 1 and R 2 is independently selected from the group consisting of —H and —COOH, provided, however, that at least one of the R 1 's and R 2 's is a hydrogen. Processes for preparing and uses of the same for treating neuronal injury and for life-extension are also disclosed and claimed herein.
Claims
exact text as granted — not AI-modified1 .- 21 . (canceled)
22 . A process for extending the lifespan of a mammalian cell comprising administering to a mammal a composition comprising an e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene of the formula C 60 (R) 3 represented by the following structure:
wherein each R is independently selected from the group consisting of moieties of the formula ═CR 1 R 2 , wherein each R 1 and R 2 of said ═CR 1 R 2 moiety is independently selected from the group consisting of —H and —COOH, provided, however, that at least one R 1 or R 2 of at least one of said ═CR 1 R 2 moieties is a hydrogen, and wherein the C in each of said ═CR 1 R 2 moieties is bonded directly to two adjacent carbons of the C 60 moiety.
23 . The process of claim 22 wherein said e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene is selected from the group consisting of C 60 (C(COOH) 2 ) 2 (CHCOOH), C 60 (C(COOH) 2 )(CHCOOH) 2 , and C 60 (CHCOOH 3 .
24 . The process of claim 22 wherein said composition comprises said e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene, its pharmaceutically acceptable salts and pharmaceutically accepted esters, and a pharmaceutically acceptable carrier, present in said composition in a therapeutically effective amount.
25 . The process of claim 24 wherein said e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene is administered intravenously, intramuscularly, subcutaneously or orally.
26 . The process of claim 25 wherein said e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene is administered intravenously, intramuscularly or subcutaneously in an amount of at least 0.1 mg/kg.
27 . The process of claim 26 wherein said e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene is administered intravenously, intramuscularly or subcutaneously in an amount of about 3 mg/kg.
28 . The process of claim 25 wherein said e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene is administered orally in an amount of at least 0.1 mg/kg.
29 . The process of claim 25 wherein said e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene is administered orally in an amount of about 15 mg/kg.
30 . The process of claim 25 wherein said e,e,e malonic acid/acetic acid tri-adduct of buckminsterfullerene is administered daily.
31 . (canceled)
32 . The process of claim 1 wherein said mammal is a human.
33 . The process of claim 1 wherein said mammal is a companion animal.
34 .- 69 . (canceled)Join the waitlist — get patent alerts
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