Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ABL1 | P00519 | 16/20 | 0.82 |
| ▸ | PDGFRA | P16234 | 14/20 | 0.82 |
| ▸ | BCR | P11274 | 9/20 | 0.82 |
| ▸ | PDGFRB | P09619 | 9/20 | 0.82 |
| ▸ | PRKCA | P17252 | 2/20 | 0.82 |
| ▸ | EGFR | P00533 | 1/20 | 0.82 |
| ▸ | KIT | P10721 | 6/20 | 0.74 |
| ▸ | LCK | P06239 | 2/20 | 0.72 |
| ▸ | LYN | P07948 | 2/20 | 0.72 |
| ▸ | FLT3 | P36888 | 2/20 | 0.72 |
| ▸ | DDR2 | Q16832 | 2/20 | 0.72 |
| ▸ | PRKD3 | O94806 | 1/20 | 0.68 |
| ▸ | PRKCG | P05129 | 1/20 | 0.68 |
| ▸ | PRKCB | P05771 | 1/20 | 0.68 |
| ▸ | SRC | P12931 | 1/20 | 0.68 |
| ▸ | PRKCH | P24723 | 1/20 | 0.68 |
| ▸ | PRKCI | P41743 | 1/20 | 0.68 |
| ▸ | PRKCE | Q02156 | 1/20 | 0.68 |
| ▸ | PRKCQ | Q04759 | 1/20 | 0.68 |
| ▸ | PRKCZ | Q05513 | 1/20 | 0.68 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
Similar compounds — the chemically nearest patent molecules
Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL1654172 | 0.95 | PDGFRA (0.79) | ABL1PDGFRABCRPDGFRBPRKCA | |
| SCHEMBL1927373 | 0.92 | ABL1 (0.82) | ABL1PDGFRABCRPDGFRBPRKCA | |
| Ethyl Acetate SCHEMBL3904872 | 0.92 | PDGFRA (0.71) | ABL1PDGFRABCRPDGFRBPRKCA | |
| SCHEMBL1927376 | 0.92 | PDGFRA (0.79) | ABL1PDGFRABCRPDGFRBPRKCA | |
| SCHEMBL1656154 | 0.92 | PDGFRA (0.90) | ABL1PDGFRABCRPDGFRBPRKCA | |
| SCHEMBL9782 | 0.90 | PDGFRA (1.00) | ABL1PDGFRABCRPDGFRBPRKCA | |
| SCHEMBL29498750 | 0.90 | PDGFRA (1.00) | ABL1PDGFRABCRPDGFRBPRKCA | |
| SCHEMBL1929404 | 0.90 | ABL1 (0.80) | ABL1PDGFRABCRPDGFRBPRKCA | |
| Methane SCHEMBL5972158 | 0.89 | PDGFRA (0.98) | ABL1PDGFRABCRPDGFRBPRKCA | |
| SCHEMBL11927817 | 0.89 | PDGFRA (0.92) | ABL1PDGFRABCRPDGFRBPRKCA |
Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.
Patent provenance — the patents this molecule appears in, and who filed them
Claimed or disclosed in 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20070129389-A1 | Use of pyridinyl-pyrimidinylamino-benzamide derivatives for the treatment of amyloid related disorders | NOVARTIS AG (CH) | 2007-06-07 | — | — | US | claimed |
| WO-2005039586-A1 | USE OF PYRIDINYL-PYRIMIDINYLAMINO-BENZAMIDE DERIVATIVES FOR THE TREATMENT OF AMYLOID RELATED DISORDERS | NOVARTIS AG (CH) | 2005-05-06 | — | — | WO | claimed |
| US-20200368267-A1 | PROPHYLACTIC AND/OR THERAPEUTIC AGENT FOR AMYOTROPHIC LATERAL SCLEROSIS | KYOTO UNIVERSITY (JP) | 2020-11-26 | — | — | US | disclosed |
| EP-2606890-A1 | Combinations comprising BCR-ABL/C-KIT/PDGF-R TK inhibitors for treating cancer | Novartis AG (CH) | 2013-06-26 | — | — | EP | disclosed |
| US-20120252811-A1 | COMBINATIONS OF THERAPEUTIC AGENTS FOR TREATING CANCER | BURKE GREGORY PETER (US) | 2012-10-04 | — | — | US | disclosed |
| EP-2368889-A1 | Inhibitors of tyrosine kinases | Novartis AG (CH) | 2011-09-28 | — | — | EP | disclosed |
| US-20110218187-A1 | INHIBITORS OF TYROSINE KINASES | BREITENSTEIN WERNER | 2011-09-08 | — | — | US | disclosed |
| EP-2357182-A1 | Inhibitors of tyrosine kinases | Novartis AG (CH) | 2011-08-17 | — | — | EP | disclosed |
| US-7956053-B2 | Inhibitors of tyrosine kinases | NOVARTIS AG (CH) | 2011-06-07 | — | — | US | disclosed |
| EP-2314297-A1 | Combinations comprising bcr-abl/c-kit/pdgf-r tk inhibitors for treating cancer | Novartis AG (CH) | 2011-04-27 | — | — | EP | disclosed |
| US-7687512-B2 | 4-Methyl-N-[3-(4-methyl-imidazol-1-yl)-5-trifluoromethyl-phenyl]-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-benzamide; for neurodegenerative diseases like Alzheimer's disease, Down's Syndrome, memory and cognitive impairment, dementia, amyloid neuropathies, brain inflammation, nerve and brain trauma | NOVARTIS AG (CH) | 2010-03-30 | — | — | US | disclosed |
| WO-2007115289-A2 | COMBINATIONS COMPRISING BCR-ABL/C-KIT/PDGF-R TK INHIBITORS FOR TREATING CANCER | NOVARTIS AG (CH) | 2007-10-11 | — | — | WO | disclosed |
| CN-101045727-A | Inhibitors of tyrosine kinases | NOVARTIS AG (CH) | 2007-10-03 | — | — | CN | disclosed |
| CN-1324022-C | Tyrosine kinase inhibitors | NOVARTIS AG (CH) | 2007-07-04 | — | — | CN | disclosed |
| US-20070129389-A1 | Use of pyridinyl-pyrimidinylamino-benzamide derivatives for the treatment of amyloid related disorders | NOVARTIS AG (CH) | 2007-06-07 | — | — | US | disclosed |
| US-7169791-B2 | Inhibitors of tyrosine kinases | NOVARTIS AG (CH) | 2007-01-30 | — | — | US | disclosed |
| US-20060167015-A1 | 4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-N-[5-(4-methyl-1H-imidazol1yl)-3-(trifluoromethyl)phenyl]benzamide or an N-oxide or salts; anticarcinogenic agent (leukaemia) | NOVARTIS AG (CH) | 2006-07-27 | — | — | US | disclosed |
| CN-1675195-A | Tyrosine kinase inhibitors | NOVARTIS AG (CH) | 2005-09-28 | — | — | CN | disclosed |
| EP-1532138-A1 | INHIBITORS OF TYROSINE KINASES | Novartis AG (CH) | 2005-05-25 | — | — | EP | disclosed |
| WO-2004005281-A1 | INHIBITORS OF TYROSINE KINASES | NOVARTIS AG (CH) | 2004-01-15 | — | — | WO | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20110218187-A1 | INHIBITORS OF TYROSINE KINASES | ABL1, BTK, FLT3 | ABL1 1/4885PDGFRA 382/4885BCR 28/4885 |
| US-20120252811-A1 | COMBINATIONS OF THERAPEUTIC AGENTS FOR TREATING CANCER | KIT, ABL1, PDGFRB | ABL1 2/4885PDGFRA 4/4885BCR 8/4885 |
| US-20070129389-A1 | Use of pyridinyl-pyrimidinylamino-benzamide derivatives for the treatment of amyloid related disorders | TIE1, ABL2, FYN | ABL1 19/4885PDGFRA 5/4885BCR 62/4885 |
| US-20200368267-A1 | PROPHYLACTIC AND/OR THERAPEUTIC AGENT FOR AMYOTROPHIC LATERAL SCLEROSIS | SMN1; SMN2, SOD1, CAPNS1 | ABL1 228/4885PDGFRA 545/4885BCR 1806/4885 |
| US-20060167015-A1 | 4-Methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-N-[5-(4-methyl-1H-imidazol1yl)-3-(trifluoromethyl)phenyl]benzamide or an N-oxide or salts; anticarcinogenic agent (leukaemia) | ABL1, CDK2, CDKN1A | ABL1 1/4885PDGFRA 440/4885BCR 181/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.