Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 4/20 | 0.61 |
| ▸ | GAA | P10253 | 2/20 | 0.61 |
| ▸ | GLA | P06280 | 1/20 | 0.61 |
| ▸ | POLB | P06746 | 1/20 | 0.61 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.52 |
| ▸ | CASP1 | P29466 | 4/20 | 0.50 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.46 |
| ▸ | NR1H2 | P55055 | 1/20 | 0.44 |
| ▸ | KIF11 | P52732 | 1/20 | 0.42 |
| ▸ | PDE10A | Q9Y233 | 1/20 | 0.41 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.41 |
| ▸ | LMNA | P02545 | 1/20 | 0.41 |
| ▸ | MAPT | P10636 | 1/20 | 0.41 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.41 |
| ▸ | AR | P10275 | 2/20 | 0.41 |
| ▸ | MEN1 | O00255 | 1/20 | 0.41 |
| ▸ | SRC | P12931 | 1/20 | 0.41 |
| ▸ | HPGD | P15428 | 1/20 | 0.41 |
| ▸ | CASP7 | P55210 | 1/20 | 0.41 |
| ▸ | KMT2A | Q03164 | 1/20 | 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 | |
|---|---|---|---|---|
| SCHEMBL29766284 | 1.00 | TSHR (0.61) | TSHRGAAGLAPOLBALDH1A1 | |
| SCHEMBL20971955 | 0.85 | TSHR (0.55) | TSHRGAAGLAPOLBALDH1A1 | |
| SCHEMBL12024599 | 0.84 | ALDH1A1 (0.50) | TSHRGAAGLAPOLBALDH1A1 | |
| Tert-Butyl Formate SCHEMBL28075418 | 0.84 | TSHR (0.46) | TSHRGAAGLAPOLBALDH1A1 | |
| SCHEMBL2059016 | 0.82 | TSHR (0.56) | TSHRGAAGLAPOLBALDH1A1 | |
| SCHEMBL30750882 | 0.82 | TSHR (0.56) | TSHRGAAGLAPOLBALDH1A1 | |
| SCHEMBL10021502 | 0.79 | GAA (0.77) | TSHRGAAGLAPOLBALDH1A1 | |
| SCHEMBL14070070 | 0.79 | ALDH1A1 (0.54) | TSHRGAAGLAPOLBALDH1A1 | |
| SCHEMBL827884 | 0.78 | TSHR (0.70) | TSHRGAAGLAPOLBALDH1A1 | |
| SCHEMBL29420085 | 0.78 | TSHR (0.70) | TSHRGAAGLAPOLBALDH1A1 |
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 750 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120157609-A | Polynorbornene imide film and preparation method and application thereof | 哈尔滨理工大学 | 2025-06-17 | — | — | CN | claimed |
| EP-4479546-A2 | PROCESSES FOR PREPARATION OF AVACOPAN AND INTERMEDIATES THEREOF | Teva Pharmaceuticals International GmbH (CH) | 2024-12-25 | — | — | EP | claimed |
| CN-113957106-B | Avacopan and preparation method of intermediate thereof | 暨明医药科技(苏州)有限公司 | 2024-04-19 | — | — | CN | claimed |
| US-11845729-B2 | Processes and intermediates in the preparation of C5aR antagonists | CHEMOCENTRYX, INC. (US) | 2023-12-19 | — | — | US | claimed |
| WO-2023158722-A2 | PROCESSES FOR PREPARATION OF AVACOPAN AND INTERMEDIATES THEREOF | TEVA PHARMACEUTICALS INTERNATIONAL GMBH (CH) | 2023-08-24 | — | — | WO | claimed |
| US-20230008966-A1 | PROCESSES AND INTERMEDIATES IN THE PREPARATION OF C5aR ANTAGONISTS | CHEMOCENTRYX, INC. | 2023-01-12 | — | — | US | claimed |
| EP-3682879-B1 | PROCESSES AND INTERMEDIATES IN THE PREPARATION OF C5AR ANTAGONISTS | CHEMOCENTRYX INC (US) | 2022-08-03 | — | — | EP | claimed |
| CN-113957106-A | Preparation method of Avacopan and intermediate thereof | 暨明医药科技(苏州)有限公司 | 2022-01-21 | — | — | CN | claimed |
| CN-111606923-B | Synthesis method of racemic clopidogrel | 武汉理工大学 | 2021-08-24 | — | — | CN | claimed |
| CN-113121415-A | Processes and intermediates for preparing C5aR antagonists | 凯莫森特里克斯股份有限公司 | 2021-07-16 | — | — | CN | claimed |
| US-20090030009-A1 | Heterobicyclic Carboxamides as Inhibitors for Kinases | NOVARTIS AG (CH) | 2009-01-29 | — | — | US | claimed |
| EP-1996558-A1 | HETEROBICYCLIC CARBOXAMIDES AS INHIBITORS FOR KINASES | Novartis AG (CH) | 2008-12-03 | — | — | EP | claimed |
| EP-1996578-A1 | HETEROBICYCLIC CARBOXAMIDES AS INHIBITORS FOR KINASES | Novartis AG (CH) | 2008-12-03 | — | — | EP | claimed |
| WO-2008009487-A1 | HETEROBICYCLIC CARBOXAMIDES AS INHIBITORS FOR KINASES | NOVARTIS AG (CH) | 2008-01-24 | — | — | WO | claimed |
| WO-2007104538-A1 | HETEROBICYCLIC CARBOXAMIDES AS INHIBITORS FOR KINASES | NOVARTIS AG (CH) | 2007-09-20 | — | — | WO | claimed |
| JP-2007523865-A | — | — | 2007-08-23 | — | — | JP | claimed |
| US-7129235-B2 | Amides useful for treating pain | ABBOTT LABORATORIES (US) | 2006-10-31 | — | — | US | claimed |
| EP-1646621-A2 | NOVEL AZAHETEROCYCLIC AMIDES USEFUL FOR TREATING PAIN | Abbott Laboratories (US) | 2006-04-19 | — | — | EP | claimed |
| US-20050080095-A1 | administering a therapeuitcally effective amount of 3'-(trifluoromethyl)-N-{4-[(trifluoromethyl)sulfonyl]phenyl}-3,6-dihydro-2H-1,2'-bipyridine-4-carboxamide; antagonists of vanilloid receptor subtype I | ABBVIE INC. | 2005-04-14 | — | — | US | claimed |
| WO-2005007642-A2 | NOVEL AZAHETEROCYCLIC AMIDES USEFUL FOR TREATING PAIN | ABBOTT LABORATORIES (US) | 2005-01-27 | — | — | WO | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (4 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-20090030009-A1 | Heterobicyclic Carboxamides as Inhibitors for Kinases | PHKG1, MAP3K20, CDK2 | TSHR 3579/4885GAA 1247/4885GLA 4100/4885 |
| US-11845729-B2 | Processes and intermediates in the preparation of C5aR antagonists | C5AR1, C5AR2, C3AR1 | TSHR 192/4885GAA 4738/4885GLA 2778/4885 |
| US-20230008966-A1 | PROCESSES AND INTERMEDIATES IN THE PREPARATION OF C5aR ANTAGONISTS | C5AR1, C5AR2, C3AR1 | TSHR 192/4885GAA 4738/4885GLA 2778/4885 |
| US-20050080095-A1 | administering a therapeuitcally effective amount of 3'-(trifluoromethyl)-N-{4-[(trifluoromethyl)sulfonyl]phenyl}-3,6-dihydro-2H-1,2'-bipyridine-4-carboxamide; antagonists of vanilloid receptor subtype I | TRPV1, OPRL1, TRPV6 | TSHR 397/4885GAA 2594/4885GLA 3881/4885 |
“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.