Predicted protein targets (top 19)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SMYD2 | Q9NRG4 | 3/20 | 0.41 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.35 |
| ▸ | TOP2A | P11388 | 1/20 | 0.35 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.35 |
| ▸ | HTT | P42858 | 1/20 | 0.35 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.35 |
| ▸ | PSEN1 | P49768 | 1/20 | 0.33 |
| ▸ | PSEN2 | P49810 | 1/20 | 0.33 |
| ▸ | APH1B | Q8WW43 | 1/20 | 0.33 |
| ▸ | NCSTN | Q92542 | 1/20 | 0.33 |
| ▸ | APH1A | Q96BI3 | 1/20 | 0.33 |
| ▸ | PSENEN | Q9NZ42 | 1/20 | 0.33 |
| ▸ | CA2 | P00918 | 1/20 | 0.33 |
| ▸ | GRM5 | P41594 | 2/20 | 0.33 |
| ▸ | GRM1 | Q13255 | 1/20 | 0.33 |
| ▸ | BACE1 | P56817 | 1/20 | 0.32 |
| ▸ | GRM2 | Q14416 | 1/20 | 0.31 |
| ▸ | CA1 | P00915 | 1/20 | 0.30 |
| ▸ | CA9 | Q16790 | 1/20 | 0.30 |
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 | |
|---|---|---|---|---|
| SCHEMBL9128317 | 1.00 | SMYD2 (0.41) | SMYD2CYP1A2TOP2ACYP3A4HTT | |
| SCHEMBL1740050 | 1.00 | SMYD2 (0.41) | SMYD2CYP1A2TOP2ACYP3A4HTT | |
| SCHEMBL1117861 | 0.92 | SMYD2 (0.40) | SMYD2TOP2ACYP3A4HTTSMN1; SMN2 | |
| SCHEMBL52552 | 0.82 | SMYD2 (0.40) | SMYD2CYP3A4HTTSMN1; SMN2PSEN1 | |
| SCHEMBL29946810 | 0.82 | SMYD2 (0.40) | SMYD2CYP3A4HTTSMN1; SMN2PSEN1 | |
| SCHEMBL18026905 | 0.82 | SMYD2 (0.40) | SMYD2CYP3A4HTTSMN1; SMN2PSEN1 | |
| SCHEMBL9274167 | 0.81 | TOP2A (0.40) | SMYD2TOP2A | |
| SCHEMBL9266676 | 0.81 | TOP2A (0.40) | SMYD2TOP2A | |
| SCHEMBL28346561 | 0.79 | SMYD2 (0.40) | SMYD2CYP3A4HTTSMN1; SMN2PSEN1 | |
| SCHEMBL6412838 | 0.79 | SMYD2 (0.41) | SMYD2TOP2ACYP3A4HTTSMN1; SMN2 |
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 112 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250122223-A1 | HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS | ALMAC DISCOVERY LIMITED (GB) | 2025-04-17 | — | — | US | disclosed |
| EP-4466072-A1 | HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS | Almac Discovery Limited (GB) | 2024-11-27 | — | — | EP | disclosed |
| CN-118946566-A | Heterocyclic compounds as ubiquitin-specific protease 7 inhibitors | 阿尔麦克探索有限公司 | 2024-11-12 | — | — | CN | disclosed |
| CN-117881402-A | Nucleotide and nucleoside therapeutic compositions, combinations, and uses related thereto | 埃默里大学 | 2024-04-12 | — | — | CN | disclosed |
| WO-2023139241-A1 | HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS | ALMAC DISCOVERY LIMITED (GB) | 2023-07-27 | — | — | WO | disclosed |
| EP-4001283-A1 | SUBSTITUTED AMINOTHIAZOLOPYRIMIDINEDIONE DERIVATIVES FOR THE TREATMENT AND PROPHYLAXIS OF VIRUS INFECTION | F. Hoffmann-La Roche AG (CH) | 2022-05-25 | — | — | EP | disclosed |
| US-11180525-B2 | Process for making 3-substituted 5-amino-6H-thiazolo[4,5-d]pyrimidine-2, 7-dione compounds useful for the treatment of virus infection | HOFFMANN-LA ROCHE, INC. (US) | 2021-11-23 | — | — | US | disclosed |
| EP-3294746-B1 | SUBSTITUTED AMINOTHIAZOLOPYRIMIDINEDIONE DERIVATIVES FOR THE TREATMENT AND PROPHYLAXIS OF VIRUS INFECTION | HOFFMANN LA ROCHE (CH) | 2021-10-06 | — | — | EP | disclosed |
| CN-107445980-B | 3-substituted 5-amino-6H-thiazolo [4,5-d ] pyrimidine-2, 7-dione compounds | 豪夫迈·罗氏有限公司 | 2021-04-20 | — | — | CN | disclosed |
| CN-107592864-B | Novel substituted aminothiazolopyrimidinediones for the treatment and prevention of viral infections | 豪夫迈·罗氏有限公司 | 2021-04-16 | — | — | CN | disclosed |
| EP-1058686-A1 | 2'-FLUORONUCLEOSIDES | EMORY UNIVERSITY (US) | 2000-12-13 | — | — | EP | disclosed |
| US-6121431-A | VIRICIDES AGAINST HUMAN IMMUNODEFICIENCY VIRUS AND HEPATITIS B VIRUS | MEDIVIR AB (SE) | 2000-09-19 | — | — | US | disclosed |
| US-5952500-A | VIRICIDES CAN BE USED IN THERAPEUTIC AND PROPHYLACTIC TREATMENT OF THE ACQUIRED IMMUNE DEFICIENCY SYNDROME (AIDS), INFECTIONS OF HUMAN IMMUNE DEFICIENCY VIRUSES, HEPATITIS B VIRUS, HERPES VIRUSES AND CANCER | MEDIVIR AB (SE) | 1999-09-14 | — | — | US | disclosed |
| WO-1999043691-A1 | 2'-FLUORONUCLEOSIDES | EMORY UNIVERSITY (US) | 1999-09-02 | — | — | WO | disclosed |
| US-5747473-A | L-nucleoside analogues and pharmaceutical compositions | MEDIVIR AB (SE) | 1998-05-05 | — | — | US | disclosed |
| US-5576429-A | HUMAN T-CELL LEUKEMIA/LYMPHOMA VIRICIDE; ANTITUMOR AGENT | MEDIVIR AB (SE) | 1996-11-19 | — | — | US | disclosed |
| US-5473063-A | Reacting 2,3-epoxy-butanediol/1,4-/(having protected hydroxyl groups) with an alpha allylic nucleophile yields 2-hydroxy-3-allyl-1,4-butanediol, then oxidatively cleaving the double bond, cyclization, halogenation, acetylation or oxyalkylation | MEDIVIR AB (SE) | 1995-12-05 | — | — | US | disclosed |
| US-5440040-A | Drug for Aids therapy; viricides | MEDIVIR AB (SE) | 1995-08-08 | — | — | US | disclosed |
| US-5175267-A | Stereoselective glycosylation of hetercyclic bases | UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) | 1992-12-29 | — | — | US | disclosed |
| WO-1989012061-A1 | PYRIMIDINE NUCLEOSIDES AND INTERMEDIATES | MEDIVIR AB (SE) | 1989-12-14 | — | — | 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 (2 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-11180525-B2 | Process for making 3-substituted 5-amino-6H-thiazolo[4,5-d]pyrimidine-2, 7-dione compounds useful for the treatment of virus infection | DHPS, TYMS, DPYD | SMYD2 3563/4885CYP1A2 309/4885TOP2A 1473/4885 |
| US-20250122223-A1 | HETEROCYCLIC COMPOUNDS AS UBIQUITIN SPECIFIC PROTEASE 7 INHIBITORS | USP7, UBA7, SENP7 | SMYD2 3468/4885CYP1A2 1425/4885TOP2A 2421/4885 |
“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.