Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.65 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.65 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.55 |
| ▸ | PTGS2 | P35354 | 2/20 | 0.52 |
| ▸ | PTGS1 | P23219 | 1/20 | 0.52 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.50 |
| ▸ | RAB9A | P51151 | 2/20 | 0.47 |
| ▸ | MAP4K4 | O95819 | 1/20 | 0.46 |
| ▸ | MEN1 | O00255 | 1/20 | 0.44 |
| ▸ | NPC1 | O15118 | 1/20 | 0.44 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.44 |
| ▸ | TSHR | P16473 | 1/20 | 0.44 |
| ▸ | TDO2 | P48775 | 1/20 | 0.44 |
| ▸ | F10 | P00742 | 1/20 | 0.43 |
| ▸ | SLC6A4 | P31645 | 1/20 | 0.43 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.43 |
| ▸ | ADORA2A | P29274 | 2/20 | 0.42 |
| ▸ | ADORA1 | P30542 | 2/20 | 0.42 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.41 |
| ▸ | ALOX15 | P16050 | 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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL28121282 | 0.98 | ALDH1A1 (0.62) | ALDH1A1HSD17B10L3MBTL1PTGS2PTGS1 | |
| SCHEMBL21933890 | 0.91 | ALDH1A1 (0.56) | ALDH1A1HSD17B10L3MBTL1PTGS2PTGS1 | |
| Sulfuric Acid SCHEMBL28874742 | 0.88 | PTGS2 (0.56) | ALDH1A1HSD17B10L3MBTL1PTGS2PTGS1 | |
| Toluene SCHEMBL28789811 | 0.88 | ALDH1A1 (0.57) | ALDH1A1HSD17B10L3MBTL1PTGS2PTGS1 | |
| SCHEMBL6480845 | 0.87 | ALDH1A1 (0.83) | ALDH1A1HSD17B10L3MBTL1RAB9ANPC1 | |
| SCHEMBL31264295 | 0.85 | ALDH1A1 (0.79) | ALDH1A1HSD17B10L3MBTL1RAB9AMEN1 | |
| SCHEMBL13729960 | 0.82 | PTGS2 (0.44) | ALDH1A1HSD17B10L3MBTL1PTGS2PTGS1 | |
| SCHEMBL9862848 | 0.82 | CYP1A2 (0.63) | ALDH1A1HSD17B10L3MBTL1PTGS2PTGS1 | |
| SCHEMBL6350642 | 0.80 | PTGS2 (0.43) | ALDH1A1HSD17B10PTGS2PTGS1CYP1A2 | |
| SCHEMBL599657 | 0.80 | ALDH1A1 (0.71) | ALDH1A1HSD17B10L3MBTL1RAB9AMEN1 |
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 246 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122032423-A | Catalyst for continuous production of 4' -chloro-2-aminobiphenyl, reaction system and process | 厦门嘉氢科技有限公司 | 2026-05-15 | — | — | CN | claimed |
| CN-119977817-A | Green preparation process for synthesizing 4' -chloro-2-aminobiphenyl by micro-channel reactor method | 南京工业大学 | 2025-05-13 | — | — | CN | claimed |
| CN-116640064-B | Synthesis method of 4' -chloro-2-aminobiphenyl | 山东京博农化科技股份有限公司 | 2025-03-04 | — | — | CN | claimed |
| CN-119080689-A | Botrytis cinerea method for synthesizing amine | 浙江新安化工集团股份有限公司 | 2024-12-06 | — | — | CN | claimed |
| CN-117903168-A | Pyrrolo [2,3-d ] thiazole derivatives, and preparation method and application thereof | 南开大学 | 2024-04-19 | — | — | CN | claimed |
| CN-117658903-A | Boscalid hapten, artificial antigen and antibody as well as preparation methods and applications thereof | 北京勤邦科技股份有限公司 | 2024-03-08 | — | — | CN | claimed |
| CN-117589994-A | Test strip for detecting boscalid and application thereof | 北京勤邦科技股份有限公司 | 2024-02-23 | — | — | CN | claimed |
| CN-113880759-B | Preparation method of boscalid | 江苏七洲绿色科技研究院有限公司 | 2023-09-05 | — | — | CN | claimed |
| CN-116640064-A | Synthesis method of 4' -chloro-2-aminobiphenyl | 山东京博农化科技股份有限公司 | 2023-08-25 | — | — | CN | claimed |
| CN-113831280-B | Preparation method of boscalid | 上海埃农生物科技有限公司 | 2023-08-15 | — | — | CN | claimed |
| CN-113831280-A | Preparation method of boscalid | 上海埃农生物科技有限公司 | 2021-12-24 | — | — | CN | claimed |
| EP-3500551-B1 | PROCESS FOR PREPARING SUBSTITUTED BIPHENYLS | BASF SE (DE) | 2021-11-10 | — | — | EP | claimed |
| US-10683256-B2 | Process for preparing substituted biphenyls | BASF SE (DE) | 2020-06-16 | — | — | US | claimed |
| CN-111235194-A | Preparation method of boscalid | 安徽赛乐普制药有限公司 | 2020-06-05 | — | — | CN | claimed |
| CN-111056951-A | Method for preparing 4' -chloro-2-aminobiphenyl | 广东石油化工学院 | 2020-04-24 | — | — | CN | claimed |
| CN-111039796-A | Novel synthesis method of 4' -chloro-2-aminobiphenyl | 德州学院 | 2020-04-21 | — | — | CN | claimed |
| CN-111039860-A | Synthetic method and application of 2-hydroxy-N- (4' -chlorobiphenyl-2-yl) nicotinamide | 河北科技大学 | 2020-04-21 | — | — | CN | claimed |
| US-20190210954-A1 | Process for Preparing Substituted Biphenyls | LIANHE CHEMICAL TECHNOLOGY CO., LTD (CN) | 2019-07-11 | — | — | US | claimed |
| WO-2018024146-A1 | PROCESS FOR PREPARATION OF BOSCALID | JIANGSU ROTAM CHEMISTRY CO., LTD (CN) | 2018-02-08 | — | — | WO | claimed |
| EP-1252140-B1 | PYRROLECARBOXAMIDES AND PYRROLETHIOAMIDES AS FUNGICIDES | SYNGENTA PARTICIPATIONS AG (CH) | 2009-05-13 | — | — | EP | 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 (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-10683256-B2 | Process for preparing substituted biphenyls | PIK3CA, PIK3CB, PIK3CG | ALDH1A1 3096/4885HSD17B10 3163/4885L3MBTL1 4115/4885 |
| US-20190210954-A1 | Process for Preparing Substituted Biphenyls | PIK3CA, PIK3CB, PIK3CG | ALDH1A1 3096/4885HSD17B10 3163/4885L3MBTL1 4115/4885 |
“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.