Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NR4A2 | P43354 | 2/20 | 0.73 |
| ▸ | CYP2A6 | P11509 | 4/20 | 0.68 |
| ▸ | CYP1A2 | P05177 | 3/20 | 0.68 |
| ▸ | TSHR | P16473 | 4/20 | 0.52 |
| ▸ | CYP3A4 | P08684 | 3/20 | 0.52 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.52 |
| ▸ | HPGD | P15428 | 2/20 | 0.52 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.52 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.52 |
| ▸ | IDO1 | P14902 | 2/20 | 0.52 |
| ▸ | EP300 | Q09472 | 2/20 | 0.52 |
| ▸ | KAT8 | Q9H7Z6 | 2/20 | 0.52 |
| ▸ | HDAC3 | O15379 | 1/20 | 0.52 |
| ▸ | KAT2B | Q92831 | 1/20 | 0.52 |
| ▸ | NCOR2 | Q9Y618 | 1/20 | 0.52 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.48 |
| ▸ | ATM | Q13315 | 1/20 | 0.48 |
| ▸ | CHEK1 | O14757 | 1/20 | 0.46 |
| ▸ | NEK2 | P51955 | 1/20 | 0.46 |
| ▸ | LIMK1 | P53667 | 1/20 | 0.46 |
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 | |
|---|---|---|---|---|
| SCHEMBL31499475 | 1.00 | NR4A2 (0.73) | NR4A2CYP2A6CYP1A2TSHRCYP3A4 | |
| SCHEMBL29418802 | 0.84 | NR4A2 (1.00) | NR4A2CYP2A6CYP1A2TSHRCYP3A4 | |
| SCHEMBL3183644 | 0.84 | NR4A2 (1.00) | NR4A2CYP2A6CYP1A2TSHRCYP3A4 | |
| SCHEMBL29404342 | 0.83 | ALDH1A1 (0.73) | NR4A2TSHRCYP3A4ALDH1A1HPGD | |
| SCHEMBL2473555 | 0.83 | CYP2A6 (1.00) | NR4A2CYP2A6CYP1A2TSHRALDH1A1 | |
| SCHEMBL201893 | 0.83 | ALDH1A1 (0.73) | NR4A2TSHRCYP3A4ALDH1A1HPGD | |
| SCHEMBL29494605 | 0.83 | CYP2A6 (1.00) | NR4A2CYP2A6CYP1A2TSHRALDH1A1 | |
| Hydrochloric Acid SCHEMBL7191297 | 0.80 | CYP3A4 (0.69) | NR4A2TSHRCYP3A4ALDH1A1HPGD | |
| SCHEMBL21854609 | 0.77 | ALDH1A1 (0.87) | NR4A2TSHRCYP3A4ALDH1A1HPGD | |
| SCHEMBL9404198 | 0.75 | NR4A2 (0.60) | NR4A2CYP2A6CYP1A2TSHRCYP3A4 |
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 356 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119510639-A | Method for detecting 2 chloronaphthylamines in drinking water by gas chromatography-mass spectrometry | 苏州见远检测技术有限公司 | 2025-02-25 | — | — | CN | claimed |
| CN-119059874-A | Synthesis method of 3-bromo-1-chloronaphthalene | 棓诺(苏州)新材料有限公司 | 2024-12-03 | — | — | CN | claimed |
| CN-115368292-A | Benzoindole compound and synthetic method thereof | 陕西科技大学 | 2022-11-22 | — | — | CN | claimed |
| EP-1773768-A4 | PYRROLE DERIVATIVES AS PHARMACEUTICAL AGENTS | EXELIXIS INC (US) | 2008-08-06 | — | — | EP | claimed |
| EP-1773768-A2 | PYRROLE DERIVATIVES AS PHARMACEUTICAL AGENTS | Exelixis, Inc. (US) | 2007-04-18 | — | — | EP | claimed |
| WO-2006012642-A2 | PYRROLE DERIVATIVES AS PHARMACEUTICAL AGENTS | EXELIXIS, INC. (US) | 2006-02-02 | — | — | WO | claimed |
| JP-2002544186-A | — | — | 2002-12-24 | — | — | JP | claimed |
| US-6417195-B1 | LIBRARIES AND COMBINATORIAL CHEMISTRY | LION BIOSCIENCE AG (DE) | 2002-07-09 | — | — | US | claimed |
| EP-1178953-A1 | AROMATIC AMIDES | WARNER-LAMBERT COMPANY (US) | 2002-02-13 | — | — | EP | claimed |
| WO-2000068184-A1 | AROMATIC AMIDES | WARNER-LAMBERT COMPANY (US) | 2000-11-16 | — | — | WO | claimed |
| US-5916899-A | SOLID PHASE SYNTHESIS, REACTING PROTECTED AMINO ACID WITH SOLID SUPPORT; FORMING IMINE BY REACTION WITH ALDEHYDE, CYCLIZATION WITH ANHYDRIDE, CLEAVAGE AND DEPROTECTION. | TREGA BIOSCIENCES, INC. (US) | 1999-06-29 | — | — | US | claimed |
| US-5874443-A | BIOSYNTHESIS | TREGA BIOSCIENCES, INC. (US) | 1999-02-23 | — | — | US | claimed |
| US-5663030-A | A PHENYL OR NORBORNANE DERIVATIVE AS AN ADDITIVE TO REDUCE HEAT AND ENERGY REQUIRED TO FUSE THE TONER AND TO REDUCE JAMMING OF THE EQUIPMENT | XEROX CORPORATION (US) | 1997-09-02 | — | — | US | claimed |
| US-20260062412-A1 | NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY | CHUGAI PHARMACEUTICAL CO LTD (JP) | 2026-03-05 | — | — | US | disclosed |
| EP-4647424-A1 | NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2025-11-12 | — | — | EP | disclosed |
| CN-119510639-A | Method for detecting 2 chloronaphthylamines in drinking water by gas chromatography-mass spectrometry | 苏州见远检测技术有限公司 | 2025-02-25 | — | — | CN | disclosed |
| EP-0102680-B1 | SUBSTITUTED N-(2,4-DINITRO-6-(TRIFLUOROMETHYL)PHENYL)-NAPHTHALENAMINE DERIVATIVES | ELI LILLY AND COMPANY (US) | 1986-03-05 | — | — | EP | disclosed |
| EP-0102680-A1 | Substituted N-(2,4-dinitro-6-(trifluoromethyl)phenyl)-naphthalenamine derivatives | ELI LILLY AND COMPANY (US) | 1984-03-14 | — | — | EP | disclosed |
| US-4423065-A | MITICIDES, PARASITICIDES | ELI LILLY AND COMPANY (US) | 1983-12-27 | — | — | US | disclosed |
| US-3931340-A | Chlorination of aromatic compounds | ASAHI DENKA KOGYO K.K. (JA) | 1976-01-06 | — | — | 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-20260062412-A1 | NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY | MYT1, NTMT1, MYL6 | NR4A2 2643/4885CYP2A6 2185/4885CYP1A2 3172/4885 |
“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.