US2011038853A1PendingUtilityA1
Use of Kif13A and AP-1 Inhibitors for Inhibiting Melanogenesis
Est. expiryApr 22, 2028(~1.7 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 29/00A61K 2800/782C12N 15/1137C12N 15/113C12N 2310/14A61P 17/00A61P 17/16A61P 17/18A61K 31/7105A61K 31/7088A61Q 19/02A61K 8/606
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Claims
Abstract
The present invention relates to novel pharmaceutical or cosmetic compositions comprising at least one inhibitor of a sub-unit of AP-1 adaptor complex, of a kinesin interacting with AP-1, in particular Kif13A, or of the interaction between a sub-unit of AP-1 adaptor complex and said kinesin, as well as the use of same to manufacture a drug intended for the treatment of pigmentary disorders and as a depigmentation agent.
Claims
exact text as granted — not AI-modified1 - 16 . (canceled)
17 . A pharmaceutical or cosmetic composition comprising at least one kinesin Kif13A inhibitor, an inhibitor of a sub-unit of AP-1 adaptor complex, and/or an inhibitor of the interaction between a sub-unit of AP-1 adaptor complex or the AP-1 complex and kinesin Kif13A.
18 . The composition of claim 17 , wherein said inhibitor is a kinesin Kif13A inhibitor.
19 . The composition of claim 17 , wherein said inhibitor is an inhibitor of a sub-unit of AP-1 adaptor complex.
20 . The composition of claim 17 , wherein said inhibitor is an inhibitor of the interaction between a sub-unit of AP-1 adaptor complex or the AP-1 complex and kinesin Kif13A.
21 . The composition of claim 17 , wherein said inhibitor is a small molecule, an aptamer, an antibody, a nucleic acid or a dominant negative peptide.
22 . The composition of claim 21 , wherein said inhibitor is an aptamer, an antibody, a nucleic acid or a dominant negative peptide.
23 . The composition of claim 17 , wherein said inhibitor is a nucleic acid comprising a sequence able to hybridize specifically with a gene or mRNA coding for a sub-unit of AP-1 adaptor complex or for kinesin Kif13A and to decrease or suppress the expression of said protein.
24 . The composition of claim 23 , wherein said nucleic acid is an antisense oligonucleotide or a iRNA.
25 . The composition of claim 23 , wherein said nucleic acid is a siRNA.
26 . The composition of claim 23 , wherein said nucleic acid has a sequence of 15 to 50 nucleotides.
27 . The composition of claim 23 , wherein said nucleic acid has a sequence of 15 to 30 nucleotides.
28 . The composition of claim 23 , wherein said nucleic acid comprises a sequence selected from the group consisting of SEQ ID NO: 1, 2, 3, 4, 5, 6, 11, 2, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23 and 24.
29 . The composition of claim 17 , wherein said composition further comprises one or more active substances selected from the group consisting of ellagic acid; arbutin; resorcinol; vitamin C; pantothenate; kojic acid; placental extracts; molecules interfering directly or indirectly with melanotropin (MSH), its receptor or adrenocorticotropic hormone (ACTH); polyols; vitamins; keratolytic and/or exfoliating agents; alpha-hydroxy acids; ascorbic acid; retinoic acid; retinaldehyde; retinol; palmitate, propionate; acetate; anti-glycation and/or antioxidant agents; anti-inflammatory agents; soothing agents and mixtures thereof; chemical or physical sun filters; deoxyribonucleic acids; and ribonucleic acids.
30 . The composition of claim 29 , wherein said anti-glyation and/or antioxidant agents are tocopherol, thiotaurine, hypotaurine, aminoguanidine, thiamin pyrophosphate, pyridoxamine, lysine, histidine, arginine, phenylalanine, pyridoxine or adenosine triphosphate.
31 . The composition of claim 17 , wherein said composition is a cosmetic composition.
32 . The composition of claim 17 , wherein said composition is a pharmaceutical composition.
33 . A method for treating or preventing a pigmentary disorder in a subject comprising applying to the skin of the subject a pharmaceutical composition of claim 17 .
34 . The method of claim 33 , wherein the pigmentary disorder is hyperpigmentation.Join the waitlist — get patent alerts
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