Predicted protein targets (top 11)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA2 | P00918 | 16/20 | 0.50 |
| ▸ | CA1 | P00915 | 15/20 | 0.48 |
| ▸ | MMP1 | P03956 | 5/20 | 0.48 |
| ▸ | MMP2 | P08253 | 5/20 | 0.48 |
| ▸ | MMP9 | P14780 | 5/20 | 0.48 |
| ▸ | MMP8 | P22894 | 5/20 | 0.48 |
| ▸ | MMP13 | P45452 | 5/20 | 0.48 |
| ▸ | F2 | P00734 | 4/20 | 0.43 |
| ▸ | PRSS1 | P07477 | 4/20 | 0.43 |
| ▸ | PRSS2 | P07478 | 4/20 | 0.43 |
| ▸ | PRSS3 | P35030 | 4/20 | 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 | |
|---|---|---|---|---|
| SCHEMBL22818194 | 0.97 | CA2 (0.54) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL2135574 | 0.97 | CA2 (0.54) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL1551243 | 0.97 | CA2 (0.54) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL17185508 | 0.97 | CA2 (0.54) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL1146134 | 0.97 | CA2 (0.54) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL3685584 | 0.97 | CA2 (0.54) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL1395645 | 0.91 | CA2 (0.40) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL1455645 | 0.91 | CA2 (0.38) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL2493205 | 0.84 | CA2 (0.32) | CA2CA1MMP1MMP2MMP9 | |
| SCHEMBL17185504 | 0.83 | CA2 (0.36) | CA2CA1MMP1MMP2MMP9 |
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 278 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122036566-A | Preparation method of perfluoro-butyl sulfonamide | 福建邦孚新材料有限公司 | 2026-05-15 | — | — | CN | claimed |
| CN-119874568-A | Synthesis method of perfluoro butyl sulfonyl fluoride | 福建三农新材料有限责任公司 | 2025-04-25 | — | — | CN | claimed |
| US-12258343-B2 | Method for preparing 2-[(3R)-3-methylmorpholin-4-yl]-4-[1-methyl-1H-pyrazol-5-yl)-8-(1H-pyrazol-5-yl)-1,7-naphthyridine | BAYER AKTIENGESELLSCHAFT (DE) | 2025-03-25 | — | — | US | claimed |
| CN-117624583-A | Preparation method of Z-type perfluoropolyether anti-fingerprint agent | 禾信天成科技(天津)有限公司 | 2024-03-01 | — | — | CN | claimed |
| EP-3841101-B1 | METHOD FOR PREPARING 2-[(3R)-3-METHYLMORPHOLIN-4-YL]-4-[1-METHYL-1H-PYRAZOL-5-YL)-8-(1H-PYRAZOL-5-YL)-1,7-NAPHTHYRIDINE | BAYER AG (DE) | 2023-05-03 | — | — | EP | claimed |
| CN-110028693-B | Preparation method of odor-resistant adsorption pipeline | 杭州气味王国科技有限公司 | 2022-10-28 | — | — | CN | claimed |
| US-20210253573-A1 | METHOD FOR PREPARING 2-[(3R)-3-METHYLMORPHOLIN-4-YL]-4-[1-METHYL-1H-PYRAZOL-5-YL)-8-(1H-PYRAZOL-5-YL)-1,7-NAPHTHYRIDINE | BAYER AKTIENGESELLSCHAFT (DE) | 2021-08-19 | — | — | US | claimed |
| EP-3841101-A1 | METHOD FOR PREPARING 2-[(3R)-3-METHYLMORPHOLIN-4-YL]-4-[1-METHYL-1H-PYRAZOL-5-YL)-8-(1H-PYRAZOL-5-YL)-1,7-NAPHTHYRIDINE | Bayer Aktiengesellschaft (DE) | 2021-06-30 | — | — | EP | claimed |
| CN-106458903-B | Method for producing heteroaromatic sulfonamide compound | 宇部兴产株式会社 | 2021-02-05 | — | — | CN | claimed |
| WO-2020039025-A1 | METHOD FOR PREPARING 2-[(3R)-3-METHYLMORPHOLIN-4-YL]-4-[1-METHYL-1H-PYRAZOL-5-YL)-8-(1H-PYRAZOL-5-YL)-1,7-NAPHTHYRIDINE | BAYER AKTIENGESELLSCHAFT (DE) | 2020-02-27 | — | — | WO | claimed |
| EP-1163250-B1 | IMPROVED SYNTHESIS OF ¬2.2.1|BICYCLO NUCLEOSIDES | EXIQON AS (DK) | 2006-07-12 | — | — | EP | claimed |
| CN-1648127-A | Imide sulfo N-hydroxy maleopimarate as light acid producing agent and its synthetic method | UNIV BEIJING NORMAL (CN) | 2005-08-03 | — | — | CN | claimed |
| US-6734291-B2 | SULFONYLATION OF A DI(HYDROXYMETHANE)FURO(2,3-D)1,3-DIOXOLE DERIVATIVE WITH A SULFONYL HALIDE | EXIQON A/S (DK) | 2004-05-11 | — | — | US | claimed |
| US-6639059-B1 | Novel synthesis strategy comprising novel key intermediate, (2.2.1)bicyclo nucleosides are produced at least two steps shorter than any previously known strategy; 3-O-aryl-4-C-hydroxymethyl-1,2-O-isopropylidene-alpha-D-ribofuranose | EXIQON A/S (DK) | 2003-10-28 | — | — | US | claimed |
| US-6599922-B2 | Process for the preparation of 2,5-bis-(2,2,2-trifluoroethoxy)-N-(2-piperidylmethyl)-benzamide (FLECAINIDE) | A.M.S.A. ANONIMA MATERIE SINTETICHE E AFFINI S.P.A. (IT) | 2003-07-29 | — | — | US | claimed |
| US-20030092905-A1 | Synthesis of [2.2.1]bicyclo nucleosides | EXIQON A/S | 2003-05-15 | — | — | US | claimed |
| US-20030032835-A1 | Antiarrhythmia agents | A.M.S.A. ANONIMA MATERIE SINTETICHE E AFFINI S.P.A (IT) | 2003-02-13 | — | — | US | claimed |
| EP-1283201-A1 | Process for the preparation of 2,5-bis-(2,2,2-trifluoroethoxy)-n-(2-piperidyl-methyl)-benzamide (flecanide) | A.M.S.A. ANONIMA MATERIE SINTETICHE E AFFINI S.p.A. (IT) | 2003-02-12 | — | — | EP | claimed |
| EP-1163250-A2 | IMPROVED SYNTHESIS OF [2.2.1]BICYCLO NUCLEOSIDES | Exiqon A/S (DK) | 2001-12-19 | — | — | EP | claimed |
| WO-2000056746-A2 | IMPROVED SYNTHESIS OF [2.2.1]BICYCLO NUCLEOSIDES | EXIQON A/S (US) | 2000-09-28 | — | — | 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 (3 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-12258343-B2 | Method for preparing 2-[(3R)-3-methylmorpholin-4-yl]-4-[1-methyl-1H-pyrazol-5-yl)-8-(1H-pyrazol-5-yl)-1,7-naphthyridine | CYP1B1, CYP4B1, CYP1A1 | CA2 4874/4885CA1 4881/4885MMP1 4343/4885 |
| US-20030092905-A1 | Synthesis of [2.2.1]bicyclo nucleosides | NSUN2, RNGTT, RNMT | CA2 3694/4885CA1 3530/4885MMP1 4741/4885 |
| US-20210253573-A1 | METHOD FOR PREPARING 2-[(3R)-3-METHYLMORPHOLIN-4-YL]-4-[1-METHYL-1H-PYRAZOL-5-YL)-8-(1H-PYRAZOL-5-YL)-1,7-NAPHTHYRIDINE | CYP1B1, CYP4B1, CYP1A1 | CA2 4874/4885CA1 4881/4885MMP1 4343/4885 |
“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.