Predicted protein targets (top 8)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ACE2 | Q9BYF1 | 1/20 | 0.50 |
| ▸ | FDPS | P14324 | 4/20 | 0.45 |
| ▸ | SPHK1 | Q9NYA1 | 1/20 | 0.45 |
| ▸ | LMNA | P02545 | 1/20 | 0.44 |
| ▸ | OPRM1 | P35372 | 1/20 | 0.42 |
| ▸ | GPR84 | Q9NQS5 | 6/20 | 0.42 |
| ▸ | LAP3 | P28838 | 1/20 | 0.42 |
| ▸ | SMPD1 | P17405 | 3/20 | 0.41 |
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 | |
|---|---|---|---|---|
| SCHEMBL28277613 | 1.00 | ACE2 (0.50) | ACE2FDPSSPHK1LMNAOPRM1 | |
| SCHEMBL28277594 | 1.00 | ACE2 (0.50) | ACE2FDPSSPHK1LMNAOPRM1 | |
| SCHEMBL28154759 | 1.00 | ACE2 (0.50) | ACE2FDPSSPHK1LMNAOPRM1 | |
| SCHEMBL5683923 | 0.98 | ACE2 (0.47) | ACE2FDPSSPHK1LMNAOPRM1 | |
| SCHEMBL7434805 | 0.90 | FDPS (0.41) | ACE2FDPSSPHK1OPRM1 | |
| SCHEMBL13176543 | 0.82 | ACE2 (0.57) | ACE2FDPSGPR84 | |
| SCHEMBL17104323 | 0.82 | ACE2 (0.57) | ACE2FDPSGPR84 | |
| SCHEMBL1783969 | 0.82 | ACE2 (0.57) | ACE2FDPSGPR84 | |
| SCHEMBL22806886 | 0.82 | ACE2 (0.47) | ACE2FDPSSPHK1LMNAOPRM1 | |
| SCHEMBL2004971 | 0.82 | ACE2 (0.47) | ACE2FDPSSPHK1LMNAOPRM1 |
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 20 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-106893581-B | Organic electroluminescent compounds, organic electroluminescence device and its application | 南京高光半导体材料有限公司 | 2019-11-05 | — | — | CN | disclosed |
| CN-106892914-B | Organic electroluminescent compounds, organic electroluminescence device and its application | 南京高光半导体材料有限公司 | 2019-02-01 | — | — | CN | disclosed |
| CN-108101922-A | Organic electroluminescent compounds, organic electroluminescence device and its application | 南京高光半导体材料有限公司 | 2018-06-01 | — | — | CN | disclosed |
| CN-106893581-A | Organic electroluminescent compounds, organic electroluminescence device and its application | 南京高光半导体材料有限公司 | 2017-06-27 | — | — | CN | disclosed |
| CN-106892914-A | Organic electroluminescent compounds, organic electroluminescence device and its application | 南京高光半导体材料有限公司 | 2017-06-27 | — | — | CN | disclosed |
| CN-106866498-A | Organic compound, organic electroluminescence device and its application | 南京高光半导体材料有限公司 | 2017-06-20 | — | — | CN | disclosed |
| CN-101970448-B | Electroluminescent metal complexes with dibenzo [ f, h ] quinoxalines | BASF SE (DE) | 2016-05-11 | — | — | CN | disclosed |
| WO-2015094754-A1 | HETEROGENEOUS ADVANCED EPOXY RESIN | DOW GLOBAL TECHNOLOGIES LLC (US) | 2015-06-25 | — | — | WO | disclosed |
| EP-1291345-B1 | Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors | WARNER LAMBERT CO (US) | 2005-11-30 | — | — | EP | disclosed |
| US-6924276-B2 | Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors | WARNER-LAMBERT COMPANY (US) | 2005-08-02 | — | — | US | disclosed |
| US-20040039208-A1 | Process for making n-aryl-anthranilic acids and their derivatives | CHEN MICHAEL HUAI GU (US) | 2004-02-26 | — | — | US | disclosed |
| CN-1458921-A | Process for making N-aryl-anthranilic acid and their derivatives | WARNER LAMBERT CO (US) | 2003-11-26 | — | — | CN | disclosed |
| US-20030099632-A1 | Method for preparing a purified matrix metalloproteinase | MUELLER WILLIAM THOMAS (US) | 2003-05-29 | — | — | US | disclosed |
| EP-1313694-A1 | PROCESS FOR MAKING N-ARYL-ANTHRANILIC ACIDS AND THEIR DERIVATIVES | WARNER-LAMBERT COMPANY (US) | 2003-05-28 | — | — | EP | disclosed |
| US-20030087924-A1 | Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors | SORENSON RODERICK JOSEPH (US) | 2003-05-08 | — | — | US | disclosed |
| WO-2003033018-A1 | METHOD FOR PREPARING PURIFIED MATRIX METALLOPROTEINASE | WARNER-LAMBERT COMPANY LLC (US) | 2003-04-24 | — | — | WO | disclosed |
| EP-1304373-A2 | Method for preparing a purified matrix metalloproteinase | WARNER-LAMBERT COMPANY (US) | 2003-04-23 | — | — | EP | disclosed |
| EP-1291345-A1 | Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors | WARNER-LAMBERT COMPANY (US) | 2003-03-12 | — | — | EP | disclosed |
| WO-2002018319-A1 | PROCESS FOR MAKING N-ARYL-ANTHRANILIC ACIDS AND THEIR DERIVATIVES | WARNER-LAMBERT COMPANY LLC (US) | 2002-03-07 | — | — | WO | disclosed |
| US-4935426-A | FUNGICIDES | BASF AKTIENGESELLSCHAFT (DE) | 1990-06-19 | — | — | US | 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 (3 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-20040039208-A1 | Process for making n-aryl-anthranilic acids and their derivatives | AADAC, AHR, AADAT | ACE2 1339/4885FDPS 250/4885SPHK1 4468/4885 |
| US-20030099632-A1 | Method for preparing a purified matrix metalloproteinase | MMP3, MMP25, MMP7 | ACE2 281/4885FDPS 3318/4885SPHK1 3320/4885 |
| US-20030087924-A1 | Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors | MMP13, MMP3, MMP9 | ACE2 91/4885FDPS 3058/4885SPHK1 2383/4885 |
“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.