Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | L3MBTL1 | Q9Y468 | 3/20 | 1.00 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 1.00 |
| ▸ | MEN1 | O00255 | 3/20 | 0.48 |
| ▸ | KMT2A | Q03164 | 3/20 | 0.48 |
| ▸ | KDM4E | B2RXH2 | 3/20 | 0.46 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.46 |
| ▸ | CA2 | P00918 | 3/20 | 0.45 |
| ▸ | CA4 | P22748 | 2/20 | 0.45 |
| ▸ | CA5A | P35218 | 2/20 | 0.45 |
| ▸ | CA12 | O43570 | 1/20 | 0.45 |
| ▸ | CA1 | P00915 | 1/20 | 0.45 |
| ▸ | CA7 | P43166 | 1/20 | 0.45 |
| ▸ | CA9 | Q16790 | 1/20 | 0.45 |
| ▸ | CA5B | Q9Y2D0 | 1/20 | 0.45 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.41 |
| ▸ | POLB | P06746 | 1/20 | 0.40 |
| ▸ | TSHR | P16473 | 2/20 | 0.39 |
| ▸ | ESR1 | P03372 | 1/20 | 0.39 |
| ▸ | GAA | P10253 | 1/20 | 0.38 |
| ▸ | PKM | P14618 | 1/20 | 0.38 |
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 | |
|---|---|---|---|---|
| SCHEMBL16045841 | 0.86 | ALDH1A1 (0.76) | L3MBTL1ALDH1A1MEN1KMT2AKDM4E | |
| SCHEMBL16046722 | 0.83 | ALDH1A1 (0.70) | L3MBTL1ALDH1A1MEN1KMT2AKDM4E | |
| SCHEMBL5100861 | 0.83 | ALDH1A1 (0.70) | L3MBTL1ALDH1A1MEN1KMT2AKDM4E | |
| SCHEMBL4193997 | 0.82 | L3MBTL1 (0.69) | L3MBTL1ALDH1A1MEN1KMT2AKDM4E | |
| SCHEMBL16046799 | 0.81 | L3MBTL1 (0.68) | L3MBTL1ALDH1A1MEN1KMT2AKDM4E | |
| SCHEMBL16044582 | 0.81 | ALDH1A1 (0.68) | L3MBTL1ALDH1A1MEN1KMT2ACA2 | |
| SCHEMBL16048053 | 0.81 | ALDH1A1 (0.68) | L3MBTL1ALDH1A1MEN1KMT2ACA2 | |
| SCHEMBL5100872 | 0.81 | L3MBTL1 (0.68) | L3MBTL1ALDH1A1MEN1KMT2AKDM4E | |
| SCHEMBL11245675 | 0.79 | ALDH1A1 (0.66) | L3MBTL1ALDH1A1MEN1KMT2AKDM4E | |
| SCHEMBL16045713 | 0.79 | ALDH1A1 (0.66) | L3MBTL1ALDH1A1MEN1KMT2AKDM4E |
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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-8633127-B2 | Selective hydrogenation catalyst and methods of making and using same | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2014-01-21 | — | — | US | claimed |
| CN-114787124-B | Method for preparing acrylonitrile dimer | 株式会社LG化学 | 2024-05-24 | — | — | CN | disclosed |
| WO-2023172880-A2 | PCNA INHIBITORS AND USES THEREOF | CITY OF HOPE (US) | 2023-09-14 | — | — | WO | disclosed |
| CN-113372383-B | Preparation method of organic phosphate compound | 中南大学 | 2022-08-02 | — | — | CN | disclosed |
| CN-113372383-A | Preparation method of organic phosphate compound | 中南大学 | 2021-09-10 | — | — | CN | disclosed |
| EP-3144064-B1 | SELECTIVE HYDROGENATION CATALYST AND METHODS OF MAKING AND USING SAME | CHEVRON PHILLIPS CHEMICAL CO LP (US) | 2021-07-28 | — | — | EP | disclosed |
| CN-106749396-B | Method for preparing organic phosphonate compound by efficiently esterifying compound containing P (O) -OH and alcohol | 湖南理工学院 | 2020-12-15 | — | — | CN | disclosed |
| CN-107082788-B | The synthetic method that one kind is efficiently esterified with imines catalysis P (O)-OH class compound and alcohol | 湖南理工学院 | 2019-05-28 | — | — | CN | disclosed |
| EP-3377596-A1 | SELECTIVE HYDROGENATION USING A FLOW INDEX | Chevron Phillips Chemical Company LP (US) | 2018-09-26 | — | — | EP | disclosed |
| CN-108291157-A | Selective hydrogenation using flow index | 切弗朗菲利浦化学公司 | 2018-07-17 | — | — | CN | disclosed |
| US-9012348-B2 | Selective hydrogenation catalyst and methods of making and using same | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2015-04-21 | — | — | US | disclosed |
| CN-103980306-A | Preparation method for hypophosphorous acid / phosphorous acid/ phosphate compounds by adopting P(O)-OH-contained compounds | UNIV HUNAN | 2014-08-13 | — | — | CN | disclosed |
| US-20140107383-A1 | Selective Hydrogenation Catalyst and Methods of Making and Using Same | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2014-04-17 | — | — | US | disclosed |
| US-8633127-B2 | Selective hydrogenation catalyst and methods of making and using same | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2014-01-21 | — | — | US | disclosed |
| CN-102341175-A | Selective hydrogenation catalyst and methods of making and using same | CHEVRON PHILLIPS CHEMICAL CO | 2012-02-01 | — | — | CN | disclosed |
| EP-2403642-A2 | SELECTIVE HYDROGENATION CATALYST AND METHODS OF MAKING AND USING SAME | Chevron Phillips Chemical Company LP (US) | 2012-01-11 | — | — | EP | disclosed |
| WO-2010101736-A2 | SELECTIVE HYDROGENATION CATALYST AND METHODS OF MAKING AND USING SAME | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2010-09-10 | — | — | WO | disclosed |
| US-20100228065-A1 | Selective Hydrogenation Catalyst and Methods of Making and Using Same | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2010-09-09 | — | — | US | disclosed |
| CN-1554680-A | In mold addition polymerization composition of norbornene-type monomers and its crosslinking addition polymer | ס�ѵ�ľ��ʽ���� | 2004-12-15 | — | — | CN | disclosed |
| CN-1333788-A | In-mold addition polymerization of norbornene-type monomers using group 10 metal complexes | GOODRICH CO B F (US) | 2002-01-30 | — | — | CN | disclosed |