PSMA ligands and uses thereof
US-9889199-B2 · Feb 13, 2018 · US
US10363313B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10363313-B2 |
| Application number | US-201815895855-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 13, 2018 |
| Priority date | Feb 15, 2013 |
| Publication date | Jul 30, 2019 |
| Grant date | Jul 30, 2019 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Compounds that are PSMA ligands, pharmaceutical compositions comprising these compounds, methods for treating and detecting cancers in a subject, methods for identifying cancer cells in a sample are described herein.
Opening claim text (preview).
Having described the invention, we claim: 1. A method of treating cancer in a subject in need thereof, the method comprising: administering to the subject a therapeutically effective amount of a compound having the following formula (I): wherein: n and n 1 are each independently 1, 2, 3, or 4; L comprises at least one ring selected from the group consisting of an optionally substituted 4 to 7 membered nonaromatic heterocyclic ring and an optionally substituted C4-C7 cycloalkyl ring; B comprises at least one glutamic acid residue; and Y is a H of B or includes at least one of a detectable moiety, therapeutic agent, or a theranostic agent that is directly or indirectly linked to B. 2. The method of claim 1 , wherein Y is selected from the group consisting of an imaging agent, anticancer agent, or combination thereof. 3. The method of claim 1 , wherein B has the following formula: wherein m is 1, 2, 3, or 4, X 1 is an amino acid, and Y 1 is a H of X 1 or includes at least one of an amino acid, peptide, detectable moiety, therapeutic agent, or theranostic agent that is directly or indirectly linked to X 1 . 4. The method of claim 1 , the compound having the general formula: wherein m, n, and n 1 is 1, 2, 3, or 4; n and n 1 are each independently 1, 2, 3, or 4; and Y 2 is a H or includes at least one of an amino acid, peptide, detectable moiety, therapeutic agent, or theranostic agent. 5. The method of claim 1 , wherein Y is a (PEGylated) nanoparticle that is directly or indirectly linked to B, and at least one anti-cancer agent coupled to the surface of the nanoparticle. 6. The method of claim 5 , wherein the anti-cancer agent comprising Phthalocyanine 4. 7. The method of claim 1 , wherein the compound has the following formula: 8. The method of claim 1 , wherein the compound has the following formula: 9. The method of claim 1 , wherein the compound has the following formula:
Antineoplastic agents · CPC title
Small organic molecules (oligomers, polymers, dendrimers A61K49/0054) · CPC title
PDT with porphyrins having exactly 20 ring atoms, i.e. based on the non-expanded tetrapyrrolic ring system, e.g. bacteriochlorin, chlorin-e6, or phthalocyanines · CPC title
Photodynamic therapy, i.e. excitation of an agent · CPC title
Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.