Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SRC | P12931 | 1/20 | 0.58 |
| ▸ | MAPT | P10636 | 3/20 | 0.53 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.53 |
| ▸ | ALOX15 | P16050 | 2/20 | 0.53 |
| ▸ | SLC22A12 | Q96S37 | 1/20 | 0.51 |
| ▸ | PTGS2 | P35354 | 5/20 | 0.50 |
| ▸ | MEN1 | O00255 | 2/20 | 0.50 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.50 |
| ▸ | NPC1 | O15118 | 1/20 | 0.49 |
| ▸ | RAB9A | P51151 | 1/20 | 0.49 |
| ▸ | TAAR1 | Q96RJ0 | 1/20 | 0.48 |
| ▸ | TSHR | P16473 | 2/20 | 0.47 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.45 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.45 |
| ▸ | GAA | P10253 | 1/20 | 0.45 |
| ▸ | HPGD | P15428 | 1/20 | 0.45 |
| ▸ | ABCB11 | O95342 | 1/20 | 0.44 |
| ▸ | PTGS1 | P23219 | 1/20 | 0.44 |
| ▸ | PPARG | P37231 | 1/20 | 0.44 |
| ▸ | NR1I3 | Q14994 | 1/20 | 0.44 |
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 | |
|---|---|---|---|---|
| SCHEMBL29375293 | 1.00 | SRC (0.58) | SRCMAPTSMN1; SMN2ALOX15SLC22A12 | |
| SCHEMBL28007584 | 0.98 | SRC (0.56) | SRCMAPTSMN1; SMN2ALOX15SLC22A12 | |
| Hydrochloric Acid SCHEMBL2531969 | 0.98 | SRC (0.56) | SRCMAPTSMN1; SMN2ALOX15SLC22A12 | |
| SCHEMBL12258207 | 0.85 | SRC (0.65) | SRCMAPTSMN1; SMN2ALOX15SLC22A12 | |
| SCHEMBL19512763 | 0.85 | RXRA (0.49) | SRCMAPTSMN1; SMN2ALOX15SLC22A12 | |
| SCHEMBL9969945 | 0.83 | TAAR1 (0.48) | SRCSLC22A12MEN1KMT2ANPC1 | |
| SCHEMBL1257788 | 0.83 | SRC (0.62) | SRCMAPTSMN1; SMN2ALOX15PTGS2 | |
| SCHEMBL1259688 | 0.83 | TAAR1 (0.48) | SRCSLC22A12MEN1KMT2ANPC1 | |
| SCHEMBL15780476 | 0.83 | SRC (0.62) | SRCMAPTSMN1; SMN2ALOX15SLC22A12 | |
| SCHEMBL37438 | 0.82 | TAAR1 (0.47) | SRCSMN1; SMN2SLC22A12PTGS2MEN1 |
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 304 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117886737-A | Spiroteine framework compound and preparation method and application thereof | 安徽农业大学 | 2024-04-16 | — | — | CN | claimed |
| CN-115872849-A | Method for preparing 2, 5-dimethylphenylacetic acid | 阜新睿光氟化学有限公司 | 2023-03-31 | — | — | CN | claimed |
| CN-114790136-A | Preparation method and application of active trivalent organic chromium compound | 中国石油天然气股份有限公司 | 2022-07-26 | — | — | CN | claimed |
| CN-110305010-B | Preparation method of 2, 5-dimethylphenylacetic acid | 江苏中旗科技股份有限公司 | 2022-05-13 | — | — | CN | claimed |
| CN-113603968-A | Toughening modified PP plastic particle | 安徽成龙塑业科技有限公司 | 2021-11-05 | — | — | CN | claimed |
| CN-111072470-A | Method for preparing 2, 5-dimethyl phenylacetyl chloride | 大连奇凯医药科技有限公司 | 2020-04-28 | — | — | CN | claimed |
| CN-107250102-B | Method for producing benzidine from azobenzene by ruthenium catalysis | 拜耳作物科学股份公司 | 2020-04-24 | — | — | CN | claimed |
| CN-110357774-A | A method of 2,5- dimethyl phenyl acetic acid is prepared by raw material of 2,5- dimethyl halobenzene | 江苏中旗科技股份有限公司 | 2019-10-22 | — | — | CN | claimed |
| CN-110305009-A | A method of 2,5- dimethyl phenyl acetic acid is synthesized by 2,5- dimethylbenzyl halogen | 江苏中旗科技股份有限公司 | 2019-10-08 | — | — | CN | claimed |
| CN-110305010-A | Preparation method of 2, 5-dimethylphenylacetic acid | 江苏中旗科技股份有限公司 | 2019-10-08 | — | — | CN | claimed |
| US-8664424-B2 | Method for preparing 2,5-dimethylphenylacetic acid | LIANHE CHEMICAL TECHNOLOGY CO., LTD (CN) | 2014-03-04 | — | — | US | claimed |
| EP-2562152-A1 | A METHOD FOR PREPARING 2,5-DIMETHYLPHENYLACETIC ACID | Lianhe Chemical Technology Co., Ltd. (CN) | 2013-02-27 | — | — | EP | claimed |
| US-20130046108-A1 | METHOD FOR PREPARING 2,5-DIMETHYLPHENYLACETIC ACID | JIANGSU LIANHE CHEMICAL TECHNOLOGY CO., LTD. (CN) | 2013-02-21 | — | — | US | claimed |
| JP-4668212-B2 | — | — | 2011-04-13 | — | — | JP | claimed |
| EP-1713755-B1 | METHOD FOR PRODUCING 2,5-DIMETHYLPHENYL ACETIC ACID | BAYER CROPSCIENCE AG (DE) | 2010-01-13 | — | — | EP | claimed |
| US-7579500-B2 | Method for producing 2,5-dimethylphenyl acetic acid | ARCHER-DANIELS-MIDLAND COMPANY (US) | 2009-08-25 | — | — | US | claimed |
| US-20080234501-A1 | Method for Producing 2,5-Dimethylphenyl Acetic Acid | BAYER CROPSCIENCE AG (DE) | 2008-09-25 | — | — | US | claimed |
| JP-2007522139-A | — | — | 2007-08-09 | — | — | JP | claimed |
| EP-1713755-A1 | METHOD FOR PRODUCING 2,5-DIMETHYLPHENYL ACETIC ACID | Bayer CropScience Aktiengesellschaft (DE) | 2006-10-25 | — | — | EP | claimed |
| WO-2005075401-A1 | METHOD FOR PRODUCING 2,5-DIMETHYLPHENYL ACETIC ACID | BAYER CROPSCIENCE AKTIENGESELLSCHAFT (DE) | 2005-08-18 | — | — | WO | 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-20130046108-A1 | METHOD FOR PREPARING 2,5-DIMETHYLPHENYLACETIC ACID | DDC, DDT, HPD | SRC 2096/4885MAPT 1888/4885SMN1; SMN2 4491/4885 |
| US-20080234501-A1 | Method for Producing 2,5-Dimethylphenyl Acetic Acid | DDC, HACL2, DDT | SRC 3019/4885MAPT 3918/4885SMN1; SMN2 4846/4885 |
“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.