Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 3/20 | 0.47 |
| ▸ | LMNA | P02545 | 2/20 | 0.45 |
| ▸ | LDHA | P00338 | 1/20 | 0.40 |
| ▸ | SRR | Q9GZT4 | 1/20 | 0.40 |
| ▸ | HCAR2 | Q8TDS4 | 1/20 | 0.39 |
| ▸ | MAPT | P10636 | 2/20 | 0.39 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.36 |
| ▸ | MMP1 | P03956 | 1/20 | 0.35 |
| ▸ | MMP2 | P08253 | 1/20 | 0.35 |
| ▸ | MMP3 | P08254 | 1/20 | 0.35 |
| ▸ | MMP9 | P14780 | 1/20 | 0.35 |
| ▸ | MMP13 | P45452 | 1/20 | 0.35 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.35 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.34 |
| ▸ | MEN1 | O00255 | 1/20 | 0.34 |
| ▸ | KMT2A | Q03164 | 1/20 | 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 | |
|---|---|---|---|---|
| Benzene SCHEMBL28101101 | 0.95 | TSHR (0.53) | TSHRLMNALDHASRRHCAR2 | |
| Alcohol SCHEMBL28450885 | 0.93 | LMNA (0.45) | TSHRLMNALDHASRRHCAR2 | |
| Butane SCHEMBL452862 | 0.93 | LMNA (0.50) | TSHRLMNALDHASRRHCAR2 | |
| Cyclopropane SCHEMBL29205269 | 0.93 | TSHR (0.42) | TSHRLMNALDHASRRHCAR2 | |
| Acetoacetic Acid SCHEMBL28243853 | 0.86 | MGAM (0.46) | TSHRLMNALDHASRRHCAR2 | |
| SCHEMBL229792 | 0.86 | TSHR (0.50) | TSHRLMNAHCAR2MAPTCYP2D6 | |
| SCHEMBL28727541 | 0.83 | LMNA (0.48) | TSHRLMNAHCAR2MAPTCYP2D6 | |
| SCHEMBL28875912 | 0.83 | LMNA (0.48) | TSHRLMNAHCAR2MAPTCYP2D6 | |
| SCHEMBL18152012 | 0.83 | LMNA (0.48) | TSHRLMNAHCAR2MAPTCYP2D6 | |
| SCHEMBL28315849 | 0.83 | LMNA (0.48) | TSHRLMNAHCAR2MAPTCYP2D6 |
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 570 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118026834-B | Preparation method of planar chiral indene metal complex with phenylindene skeleton, synthesis intermediate and catalytic application | 中山大学 | 2026-05-12 | — | — | CN | claimed |
| CN-119859146-A | Gamma-lactam podophyllotoxin compound and preparation method and application thereof | 河南农业大学 | 2025-04-22 | — | — | CN | claimed |
| CN-116285384-B | Method for preparing trays for carrying leather in tannery by utilizing tannery chrome-containing leather ash | 烟台大学 | 2025-03-25 | — | — | CN | claimed |
| CN-118206540-B | Fluorescent probe for identifying hydrazine and preparation method and application thereof | 渤海大学 | 2025-03-07 | — | — | CN | claimed |
| CN-119080602-A | Preparation method of 7-alkyne-4-oxygen-octanoic acid | 江苏南创化学与生命健康研究院有限公司 | 2024-12-06 | — | — | CN | claimed |
| CN-114573434-B | Chiral bridged cyclic ketone and preparation method thereof | 四川海思科制药有限公司 | 2024-12-06 | — | — | CN | claimed |
| CN-115819222-B | Preparation method of valproic acid | 湖南省湘中制药有限公司 | 2024-11-26 | — | — | CN | claimed |
| CN-118878515-A | Substituted aniline pyrimidine compound and preparation method and application thereof | 河北科技大学 | 2024-11-01 | — | — | CN | claimed |
| CN-118561677-A | Synthesis method of 2-methyl-4-acetyl benzoic acid | 丽珠集团福州福兴医药有限公司 | 2024-08-30 | — | — | CN | claimed |
| CN-118406007-A | Synthesis method of 3- (quinoline-6-yl) propionic acid | 上海毕得医药科技股份有限公司 | 2024-07-30 | — | — | CN | claimed |
| US-7312001-B2 | Non-aqueous electrolytic solution and lithium battery employing the same | SAMSUNG SDI CO., LTD. (KR) | 2007-12-25 | — | — | US | claimed |
| CN-100999473-A | 5-nitro coffeic acid phenylglycollic ester and its preparation and use | UNIV ZHEJIANG TECHNOLOGY (CN) | 2007-07-18 | — | — | CN | claimed |
| CN-1264243-C | Non-aqueous electrolytic solution and lithium battery employing the same | SAMSUNG SDI CO LTD (KR) | 2006-07-12 | — | — | CN | claimed |
| CN-1696221-A | Sunlight controlled coating solution in low radiation, preparation method and application | ZHONGKE NANO TECH ENGINEERING (CN) | 2005-11-16 | — | — | CN | claimed |
| CN-1544409-A | Ferulic acid and ferulate preparation method | 丽珠集团利民制药厂 | 2004-11-10 | — | — | CN | claimed |
| CN-1501541-A | Non-aqueous electrolytic solution and lithium battery employing the same | 三星SDI株式会社 | 2004-06-02 | — | — | CN | claimed |
| US-20040096750-A1 | Non-aqueous electrolytic solution and lithium battery employing the same | SAMSUNG SDI CO., LTD. (KR) | 2004-05-20 | — | — | US | claimed |
| US-6462224-B2 | CYCLIZATION OF MALONIC ACID ESTER, 1,2-DIAHALOETHANE AND ALKALI METAL COARBONATE IN PRESENC EOF PHASE TRANSFER CATALYST | DEGUSSA AG (DE) | 2002-10-08 | — | — | US | claimed |
| US-20010007040-A1 | Process for the preparation of 1,1-cyclopropanedicarboxylic diesters | EVONIK DEGUSSA GMBH (DE) | 2001-07-05 | — | — | US | claimed |
| CN-1161362-A | Method for preparing single component polyurethane adhesive/seal gum | JILIN SCIENCE & TECH DEV IND C (CN) | 1997-10-08 | — | — | CN | 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 (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-20010007040-A1 | Process for the preparation of 1,1-cyclopropanedicarboxylic diesters | ME1, DECR1, MAGT1 | TSHR 4788/4885LMNA 2391/4885LDHA 2293/4885 |
“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.