Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SMN1; SMN2 | Q16637 | 5/20 | 0.77 |
| ▸ | KMT2A | Q03164 | 4/20 | 0.77 |
| ▸ | PKM | P14618 | 1/20 | 0.77 |
| ▸ | SAE1 | Q9UBE0 | 1/20 | 0.74 |
| ▸ | UBA2 | Q9UBT2 | 1/20 | 0.74 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.74 |
| ▸ | NPC1 | O15118 | 5/20 | 0.70 |
| ▸ | RAB9A | P51151 | 5/20 | 0.70 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.68 |
| ▸ | GBA1 | P04062 | 1/20 | 0.68 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.68 |
| ▸ | MEN1 | O00255 | 3/20 | 0.67 |
| ▸ | RXFP1 | Q9HBX9 | 1/20 | 0.67 |
| ▸ | MAPT | P10636 | 2/20 | 0.66 |
| ▸ | CASP3 | P42574 | 1/20 | 0.66 |
| ▸ | SENP7 | Q9BQF6 | 1/20 | 0.66 |
| ▸ | SENP6 | Q9GZR1 | 1/20 | 0.66 |
| ▸ | GAA | P10253 | 1/20 | 0.64 |
| ▸ | CNR1 | P21554 | 1/20 | 0.63 |
| ▸ | LMNA | P02545 | 1/20 | 0.62 |
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 | |
|---|---|---|---|---|
| SCHEMBL29703055 | 1.00 | SMN1; SMN2 (0.77) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL259602 | 0.94 | SMN1; SMN2 (0.75) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL31054278 | 0.94 | SMN1; SMN2 (0.75) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL5852140 | 0.92 | SAE1 (0.76) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL2632867 | 0.90 | SAE1 (0.68) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL16500681 | 0.89 | KMT2A (0.79) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL709095 | 0.89 | DDX3X (0.79) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL22588905 | 0.89 | SAE1 (0.71) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL29555903 | 0.89 | RAB9A (0.69) | SMN1; SMN2KMT2APKMSAE1UBA2 | |
| SCHEMBL9036479 | 0.88 | HSD17B10 (0.65) | SMN1; SMN2KMT2APKMSAE1UBA2 |
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 71 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20080227999-A1 | Heterogeneous Supported Catalytic Carbamate Process | MOLZAHN DAVID C | 2008-09-18 | — | — | US | claimed |
| EP-1943214-A2 | HETEROGENEOUS SUPPORTED CATALYTIC CARBAMATE PROCESS | Dow Gloval Technologies Inc. (US) | 2008-07-16 | — | — | EP | claimed |
| WO-2007015852-A2 | HETEROGENEOUS SUPPORTED CATALYTIC CARBAMATE PROCESS | DOW GLOBAL TECHNOLOGIES INC. (US) | 2007-02-08 | — | — | WO | claimed |
| JP-60255849-A | — | — | None | — | — | JP | disclosed |
| CN-221621330-U | Welding fixture with clamping and calibrating mechanism | 金威德智能装备(江苏)有限公司 | 2024-08-30 | — | — | CN | disclosed |
| WO-2023176554-A1 | COGNITIVE-FUNCTION-IMPROVING AGENT | 国立大学法人東北大学 | 2023-09-21 | — | — | WO | disclosed |
| CN-219348740-U | Flexible multifunctional sensing network | 华东理工大学 | 2023-07-14 | — | — | CN | disclosed |
| CN-114605408-B | 5-hydroxy-1, 3-disubstituted phenylpyrido [2,3-d ] pyrimidine compound and preparation method and application thereof | 沈阳药科大学 | 2023-06-16 | — | — | CN | disclosed |
| WO-2023102209-A1 | CLAUDIN INHIBITORS AND METHODS OF USE THEREOF | THE UNIVERSITY OF CHICAGO (US) | 2023-06-08 | — | — | WO | disclosed |
| CN-115684355-A | Flexible multifunctional sensing network and manufacturing method thereof | 华东理工大学 | 2023-02-03 | — | — | CN | disclosed |
| CN-114605408-A | 5-hydroxy-1, 3-disubstituted phenyl pyrido [2,3-d ] pyrimidine compound and preparation method and application thereof | 沈阳药科大学 | 2022-06-10 | — | — | CN | disclosed |
| US-4621149-A | PLATINUM GROUP METAL HALOGEN OR HALOGEN COMPOUND | ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) | 1986-11-04 | — | — | US | disclosed |
| US-4567287-A | Preparation of carbamates from organic carbonates and aromatic ureas | THE UPJOHN CO. (US) | 1986-01-28 | — | — | US | disclosed |
| JP-S60255849-A | POLYPHENYLENE ETHER COMPOSITION HAVING IMPROVED MOLDABILITY | MITSUBISHI PETROCHEM CO LTD | 1985-12-17 | — | — | JP | disclosed |
| EP-0142670-A2 | A process for the preparation of known herbicidally active phenyl carbamates | BEROL NOBEL (SUISSE) S.A. (CH) | 1985-05-29 | — | — | EP | disclosed |
| US-4480110-A | FROM SUBSTITUTED UREAS AND ALCOHOL | BAYER AKTIENGESELLSCHAFT (DE) | 1984-10-30 | — | — | US | disclosed |
| US-4430505-A | UREA, PRIMARY AMINES, ALCOHOLS | BAYER AKTIENGESELLSCHAFT (DE) | 1984-02-07 | — | — | US | disclosed |
| EP-0083096-A2 | Production of urethane compounds | Asahi Kasei Kogyo Kabushiki Kaisha (JP) | 1983-07-06 | — | — | EP | disclosed |
| US-4381404-A | Process for the production of N,O-disubstituted urethanes and use thereof as starting materials for the production of organic isocyanates | BAYER AKTIENGESELLSCHAFT (DE) | 1983-04-26 | — | — | US | disclosed |
| US-4084056-A | FROM AN AROMATIC AMIDE AND A GROUP IA OR IIA HYPOCHLORITE WITH A CARBAMATE SUBSTITUTED PHENOL | AB BOFORS (SW) | 1978-04-11 | — | — | 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-20080227999-A1 | Heterogeneous Supported Catalytic Carbamate Process | CPS1, CAT, CA7 | SMN1; SMN2 3171/4885KMT2A 427/4885PKM 1790/4885 |
“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.