Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | KDM4E | B2RXH2 | 4/20 | 0.66 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.55 |
| ▸ | AKR1C4 | P17516 | 1/20 | 0.47 |
| ▸ | AKR1C3 | P42330 | 1/20 | 0.47 |
| ▸ | AKR1C2 | P52895 | 1/20 | 0.47 |
| ▸ | AKR1C1 | Q04828 | 1/20 | 0.47 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.44 |
| ▸ | TP53 | P04637 | 1/20 | 0.44 |
| ▸ | NOTUM | Q6P988 | 1/20 | 0.43 |
| ▸ | MYC | P01106 | 3/20 | 0.43 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.43 |
| ▸ | HPGD | P15428 | 1/20 | 0.43 |
| ▸ | GABRP | O00591 | 1/20 | 0.43 |
| ▸ | GABRD | O14764 | 1/20 | 0.43 |
| ▸ | GABRA1 | P14867 | 1/20 | 0.43 |
| ▸ | GABRB1 | P18505 | 1/20 | 0.43 |
| ▸ | GABRG2 | P18507 | 1/20 | 0.43 |
| ▸ | GABRB3 | P28472 | 1/20 | 0.43 |
| ▸ | GABRA5 | P31644 | 1/20 | 0.43 |
| ▸ | GABRA3 | P34903 | 1/20 | 0.43 |
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 | |
|---|---|---|---|---|
| SCHEMBL29917566 | 1.00 | KDM4E (0.66) | KDM4ECYP3A4AKR1C4AKR1C3AKR1C2 | |
| Hydrochloric Acid SCHEMBL29208275 | 0.98 | KDM4E (0.63) | KDM4ECYP3A4AKR1C4AKR1C3AKR1C2 | |
| SCHEMBL28704965 | 0.85 | CYP3A4 (0.65) | KDM4ECYP3A4AKR1C4AKR1C3AKR1C2 | |
| SCHEMBL14234313 | 0.84 | KDM4E (0.46) | KDM4ECYP3A4AKR1C4AKR1C3AKR1C2 | |
| SCHEMBL29373932 | 0.84 | KDM4E (0.46) | KDM4ECYP3A4ALDH1A1HPGDSMN1; SMN2 | |
| SCHEMBL19646057 | 0.84 | KDM4E (0.46) | KDM4ECYP3A4ALDH1A1HPGDSMN1; SMN2 | |
| SCHEMBL26603550 | 0.84 | KDM4E (0.46) | KDM4ECYP3A4ALDH1A1HPGDKMT2A | |
| SCHEMBL27868371 | 0.80 | CYP3A4 (0.55) | KDM4ECYP3A4AKR1C4AKR1C3AKR1C2 | |
| SCHEMBL25262460 | 0.79 | KDM4E (0.42) | KDM4ECYP3A4AKR1C4AKR1C3AKR1C2 | |
| SCHEMBL384330 | 0.79 | KDM4E (0.42) | KDM4ECYP3A4ALDH1A1CYP1A1CYP1A2 |
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 637 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116730859-B | Preparation method of 2-amino-5-chloro-N, 3-dimethylbenzamide | 青岛科技大学 | 2025-06-13 | — | — | CN | claimed |
| EP-3902792-B1 | PROCESS FOR PREPARATION OF ANTHRANILAMIDES | UPL LTD (IN) | 2025-05-21 | — | — | EP | claimed |
| CN-119500077-A | Preparation method and application of efficient desulfurizing agent | 江苏德隆环保工程有限公司 | 2025-02-25 | — | — | CN | claimed |
| CN-119431170-A | Method for producing 2-amino-5-chloro-3-methylbenzoic acid by reaction crystallization | 宁波诺丁汉大学 | 2025-02-14 | — | — | CN | claimed |
| CN-119143618-A | Preparation method of 2-amino-3-methyl-5-chlorobenzoic acid | 湖北泰盛化工有限公司 | 2024-12-17 | — | — | CN | claimed |
| CN-115611763-B | O-aminobenzoyl Process for producing amine derivative | 山东友道化学有限公司 | 2024-12-13 | — | — | CN | claimed |
| CN-119059923-A | Scandium catalytic synthesis process of 2-amino-5-chloro-3-methylbenzoic acid | 南京工业大学 | 2024-12-03 | — | — | CN | claimed |
| CN-118771987-A | Preparation method of 2-nitro-3-methyl-5-chlorobenzoic acid | 帕潘纳(北京)科技有限公司 | 2024-10-15 | — | — | CN | claimed |
| CN-115745959-B | Industrial production method of chlorantraniliprole | 山东友道化学有限公司 | 2024-06-21 | — | — | CN | claimed |
| CN-115772090-B | Synthesis method of chlorantraniliprole key intermediate | 九江善水科技股份有限公司 | 2024-06-07 | — | — | CN | claimed |
| CN-111517975-A | Preparation method of 2-amino-5-chloro-N, 3-dimethylbenzamide | 江苏七洲绿色化工股份有限公司 | 2020-08-11 | — | — | CN | claimed |
| CN-110615780-A | Preparation method of chlorantraniliprole | 南通雅本化学有限公司 | 2019-12-27 | — | — | CN | claimed |
| CN-104031026-A | O-formylamino benzamide derivatives containing N-cyano sulfone(sulfur)imine, preparation method thereof and uses thereof | UNIV NANKAI | 2014-09-10 | — | — | CN | claimed |
| EP-1903030-B1 | Method for catalytic manufacture of aromatic or heteroaromatic nitriles | SALTIGO GMBH (DE) | 2014-06-04 | — | — | EP | claimed |
| CN-103058993-B | Chlorantraniliprole preparation method | UNIV HENAN NORMAL | 2014-06-04 | — | — | CN | claimed |
| CN-103172613-A | O-formamido benzamide derivative containing N-cyano sulfone (sulfur) imine and preparation method and application thereof | UNIV NANKAI | 2013-06-26 | — | — | CN | claimed |
| CN-103058993-A | Chlorantraniliprole preparation method | UNIV HENAN NORMAL | 2013-04-24 | — | — | CN | claimed |
| US-7592452-B2 | Process for catalytically preparing aromatic or heteroaromatic nitriles | SALTIGOGMBH (DE) | 2009-09-22 | — | — | US | claimed |
| US-20090062541-A1 | Process for catalytically preparing aromatic or heteroaromatic nitriles | SALTIGO GMBH (DE) | 2009-03-05 | — | — | US | claimed |
| EP-1903030-A1 | Method for catalytic manufacture of aromatic or heteroaromatic nitriles | Saltigo GmbH (DE) | 2008-03-26 | — | — | 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 (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-20090062541-A1 | Process for catalytically preparing aromatic or heteroaromatic nitriles | AHR, PAH, AOC3 | KDM4E 612/4885CYP3A4 12/4885AKR1C4 117/4885 |
“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.