Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | KDM4E | B2RXH2 | 7/20 | 0.38 |
| ▸ | LMNA | P02545 | 5/20 | 0.38 |
| ▸ | POLB | P06746 | 3/20 | 0.38 |
| ▸ | CCR1 | P32246 | 2/20 | 0.38 |
| ▸ | CCR5 | P51681 | 2/20 | 0.38 |
| ▸ | CCR8 | P51685 | 2/20 | 0.38 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.38 |
| ▸ | METAP1 | P53582 | 1/20 | 0.38 |
| ▸ | BLM | P54132 | 1/20 | 0.38 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.38 |
| ▸ | DOHH | Q9BU89 | 1/20 | 0.38 |
| ▸ | P4HTM | Q9NXG6 | 1/20 | 0.38 |
| ▸ | TDP1 | Q9NUW8 | 4/20 | 0.36 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.36 |
| ▸ | TP53 | P04637 | 4/20 | 0.34 |
| ▸ | SMN1; SMN2 | Q16637 | 4/20 | 0.34 |
| ▸ | HTT | P42858 | 4/20 | 0.34 |
| ▸ | L3MBTL1 | Q9Y468 | 4/20 | 0.34 |
| ▸ | NPC1 | O15118 | 3/20 | 0.34 |
| ▸ | RAB9A | P51151 | 3/20 | 0.34 |
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 | |
|---|---|---|---|---|
| SCHEMBL28149886 | 0.98 | KDM4E (0.37) | KDM4ELMNAPOLBCCR1CCR5 | |
| SCHEMBL9132752 | 0.98 | KDM4E (0.37) | KDM4ELMNAPOLBCCR1CCR5 | |
| Dipyridyl SCHEMBL29259897 | 0.98 | KDM4E (0.41) | KDM4ELMNAPOLBCCR1CCR5 | |
| SCHEMBL27609141 | 0.88 | NPSR1 (0.37) | KDM4ELMNAPOLBHIF1ATDP1 | |
| SCHEMBL435396 | 0.80 | KDM4E (0.42) | KDM4ELMNAPOLBCCR1CCR5 | |
| Hydrochloric Acid SCHEMBL38657196 | 0.78 | KDM4E (0.41) | KDM4ELMNAPOLBCCR1CCR5 | |
| SCHEMBL28575256 | 0.78 | KDM4E (0.41) | KDM4ELMNAPOLBCCR1CCR5 | |
| SCHEMBL28452296 | 0.77 | KDM4E (0.39) | KDM4ELMNAPOLBCCR1CCR5 | |
| SCHEMBL1311501 | 0.77 | KDM4E (0.39) | KDM4ELMNAPOLBCCR1CCR5 | |
| SCHEMBL7589592 | 0.76 | KDM4E (0.42) | KDM4ELMNAPOLBCCR1CCR5 |
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 39 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117902966-B | Synthesis method of aromatic aldehyde | 中南大学 | 2026-05-12 | — | — | CN | claimed |
| CN-118908819-B | Preparation method of organic ketone compound under synergistic catalysis of light and metal | 延安大学 | 2025-04-18 | — | — | CN | claimed |
| CN-118908819-A | Preparation method of organic ketone compound under synergistic catalysis of light and metal | 延安大学 | 2024-11-08 | — | — | CN | claimed |
| CN-118047735-A | Preparation method of pramoxine | 中国人民解放军空军军医大学 | 2024-05-17 | — | — | CN | claimed |
| CN-117902966-A | Synthesis method of aromatic aldehyde | 中南大学 | 2024-04-19 | — | — | CN | claimed |
| CN-116589501-A | Oxygen-bridged binuclear tungsten complex and preparation method and application thereof | 江苏科技大学 | 2023-08-15 | — | — | CN | claimed |
| CN-116041198-A | Method for synthesizing amide derivative by vanadium catalysis | 陕西师范大学 | 2023-05-02 | — | — | CN | claimed |
| CN-114890856-A | Method for synthesizing 2,2' -biphenyl-1-carboxylic acid derivative | 华南理工大学 | 2022-08-12 | — | — | CN | claimed |
| CN-112250879-B | Method for synthesizing ginkgo leaf polyprenol metal complex with light-operated activity | 中国林业科学研究院林产化学工业研究所 | 2022-06-28 | — | — | CN | claimed |
| CN-112250879-A | Method for synthesizing ginkgo leaf polyprenol metal complex with light-operated activity | 中国林业科学研究院林产化学工业研究所 | 2021-01-22 | — | — | CN | claimed |
| CN-106748834-A | A kind of method that the bipyridyl of 4,4 dimethoxy 2,2 silver catalytic hydrogenation aromatic nitro compound synthesizes arylamine | 陕西师范大学 | 2017-05-31 | — | — | CN | claimed |
| CN-122079757-A | 1, 2-Diacyl benzene compound and synthesis method and application thereof | — | 2026-05-26 | — | — | CN | disclosed |
| US-20260132143-A1 | HETEROCYCLIC INHIBITORS OF KRAS G12C MUTANT PROTEINS AND USES THEREOF | AMGEN INC. (US) | 2026-05-14 | — | — | US | disclosed |
| CN-117902966-B | Synthesis method of aromatic aldehyde | 中南大学 | 2026-05-12 | — | — | CN | disclosed |
| CN-118908819-B | Preparation method of organic ketone compound under synergistic catalysis of light and metal | 延安大学 | 2025-04-18 | — | — | CN | disclosed |
| US-8268163-B2 | Small volume in vitro analyte sensor and methods of making | ABBOTT DIABETES CARE INC. (US) | 2012-09-18 | — | — | US | disclosed |
| US-8262996-B2 | Small volume in vitro sensor and methods of making | ABBOTT DIABETES CARE INC. (US) | 2012-09-11 | — | — | US | disclosed |
| US-8083924-B2 | Small volume in vitro analyte sensor and methods of making | ABBOTT DIABETES CARE INC. (US) | 2011-12-27 | — | — | US | disclosed |
| US-20110275780-A1 | METHOD FOR PRODUCING CONJUGATED AROMATIC COMPOUND | SUMITOMO CHEMCIAL COMPANY LIMITED | 2011-11-10 | — | — | US | disclosed |
| US-6461496-B1 | BLOOD GLUCOSE | THERASENSE, INC. | 2002-10-08 | — | — | 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 (1 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-20260132143-A1 | HETEROCYCLIC INHIBITORS OF KRAS G12C MUTANT PROTEINS AND USES THEREOF | KRAS, NRAS, HRAS | KDM4E 4400/4885LMNA 1584/4885POLB 2718/4885 |
“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.