Predicted protein targets (top 13)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | GAA | P10253 | 10/20 | 0.60 |
| ▸ | AHR | P35869 | 1/20 | 0.59 |
| ▸ | PKM | P14618 | 2/20 | 0.53 |
| ▸ | SMYD3 | Q9H7B4 | 1/20 | 0.53 |
| ▸ | IDO1 | P14902 | 1/20 | 0.53 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.53 |
| ▸ | MAPT | P10636 | 1/20 | 0.53 |
| ▸ | MEN1 | O00255 | 1/20 | 0.51 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.51 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.51 |
| ▸ | PGR | P06401 | 1/20 | 0.49 |
| ▸ | PDE3B | Q13370 | 1/20 | 0.49 |
| ▸ | PDE3A | Q14432 | 1/20 | 0.49 |
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 | |
|---|---|---|---|---|
| SCHEMBL2586707 | 0.85 | PKM (0.60) | PKMIDO1 | |
| SCHEMBL30114411 | 0.85 | PKM (0.60) | PKMIDO1 | |
| SCHEMBL689168 | 0.83 | GAA (0.60) | GAAAHRPKMSMYD3IDO1 | |
| SCHEMBL10293161 | 0.83 | GAA (0.60) | GAAAHRPKMSMYD3IDO1 | |
| SCHEMBL1556955 | 0.83 | GAA (0.60) | GAAAHRPKMSMYD3IDO1 | |
| SCHEMBL2203244 | 0.83 | GAA (0.64) | GAAAHRPKMSMYD3IDO1 | |
| SCHEMBL22400700 | 0.82 | PKM (0.56) | PKMIDO1MAPT | |
| SCHEMBL17231399 | 0.81 | GAA (0.41) | GAAAHRPKMSMYD3IDO1 | |
| Hydrochloric Acid SCHEMBL28865546 | 0.81 | GAA (0.62) | GAAAHRPKMSMYD3IDO1 | |
| SCHEMBL6602558 | 0.80 | GAA (0.57) | GAAAHRPKMSMYD3IDO1 |
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 295 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-110669088-B | N- (2-ethylamine) benzenesulfonylamino cordycepin derivative and preparation method and application thereof | 成都阿奇生物医药科技有限公司 | 2023-03-28 | — | — | CN | claimed |
| WO-2021260722-A1 | DESIGN, SYNTHESIS OF NOVEL OXYINDOLE INHIBITORS OF DENV RNA DEPENDENT RNA POLYMERASE | TRANSLATIONAL HEALTH SCIENCE AND TECHNOLOGY INSTITUTE (IN) | 2021-12-30 | — | — | WO | claimed |
| CN-110669088-A | N- (2-ethylamine) benzenesulfonylamino cordycepin derivative and preparation method and application thereof | 成都阿奇生物医药科技有限公司 | 2020-01-10 | — | — | CN | claimed |
| US-12559455-B2 | Compound as a UBR box domain ligand | AUTOTAC INC. (KR) | 2026-02-24 | — | — | US | disclosed |
| US-12428394-B2 | 2,4-disubstituted pyrimidine derivative, preparation method therefor and use thereof | CHENGDU ZENITAR BIOMEDICAL TECHNOLOGY CO., LTD. (CN) | 2025-09-30 | — | — | US | disclosed |
| CN-118955475-A | Compound for inhibiting tumor cells and application thereof | 中国人民解放军军事科学院军事医学研究院 | 2024-11-15 | — | — | CN | disclosed |
| EP-3985000-B1 | 2,4-DISUBSTITUTED PYRIMIDINE DERIVATIVE, PREPARATION METHOD FOR SAME, AND USES THEREOF | CHENGDU ZENITAR BIOMEDICAL TECH CO LTD (CN) | 2024-09-25 | — | — | EP | disclosed |
| WO-2024120519-A1 | TEAD INHIBITOR, PREPARATION METHOD THEREFOR. AND MEDICAL USE THEREOF | 捷思英达控股有限公司 | 2024-06-13 | — | — | WO | disclosed |
| CN-114423750-B | 2, 4-Disubstituted pyrimidine derivative, preparation method and application thereof | 成都赜灵生物医药科技有限公司 | 2024-04-19 | — | — | CN | disclosed |
| CN-114181199-B | 2, 4-disubstituted pyrimidine derivative, preparation method and application thereof | 成都赜灵生物医药科技有限公司 | 2023-09-26 | — | — | CN | disclosed |
| US-20230174470-A1 | COMPOUND AS A UBR BOX DOMAIN LIGAND | AUTOTAC INC. (KR) | 2023-06-08 | — | — | US | disclosed |
| US-6051593-A | USEFUL IN THE PREVENTION AND TREATMENT OF PROTEIN TYROSINE KINASE RELATED CELLULAR DISORDERS SUCH AS CANCER | SUGEN, INC. (US) | 2000-04-18 | — | — | US | disclosed |
| EP-0984930-A1 | 2-INDOLINONE DERIVATIVES AS MODULATORS OF PROTEIN KINASE ACTIVITY | Sugen, Inc. (US) | 2000-03-15 | — | — | EP | disclosed |
| WO-2000008202-A2 | 3-METHYLIDENYL-2-INDOLINONE MODULATORS OF PROTEIN KINASE | SUGEN, INC. (US) | 2000-02-17 | — | — | WO | disclosed |
| WO-1999061422-A1 | PYRROLE SUBSTITUTED 2-INDOLINONE PROTEIN KINASE INHIBITORS | SUGEN, INC. (US) | 1999-12-02 | — | — | WO | disclosed |
| WO-1999048868-A2 | HETEROCYCLIC CLASSES OF COMPOUNDS FOR THE MODULATING TYROSINE PROTEIN KINASE | SUGEN, INC. (US) | 1999-09-30 | — | — | WO | disclosed |
| EP-0912557-A1 | OXINDOLE DERIVATIVES | ZENECA LIMITED (GB) | 1999-05-06 | — | — | EP | disclosed |
| WO-1998050356-A1 | 2-INDOLINONE DERIVATIVES AS MODULATORS OF PROTEIN KINASE ACTIVITY | SUGEN, INC. (US) | 1998-11-12 | — | — | WO | disclosed |
| WO-1998007742-A1 | SULFONAMIDES | ZENECA LIMITED (GB) | 1998-02-26 | — | — | WO | disclosed |
| WO-1997042187-A1 | OXINDOLE DERIVATIVES | ZENECA LIMITED (GB) | 1997-11-13 | — | — | 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 (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-20230174470-A1 | COMPOUND AS A UBR BOX DOMAIN LIGAND | UBR4, UBQLN2, UBTF | GAA 996/4885AHR 347/4885PKM 3496/4885 |
| US-12559455-B2 | Compound as a UBR box domain ligand | UBR4, UBTF, UBQLN1 | GAA 1736/4885AHR 258/4885PKM 4352/4885 |
| US-12428394-B2 | 2,4-disubstituted pyrimidine derivative, preparation method therefor and use thereof | JAK2, FLT3, JAK1 | GAA 3635/4885AHR 957/4885PKM 2617/4885 |
“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.