Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALOX15 | P16050 | 1/20 | 0.44 |
| ▸ | ELANE | P08246 | 1/20 | 0.42 |
| ▸ | ESR1 | P03372 | 2/20 | 0.40 |
| ▸ | HIF1A | Q16665 | 2/20 | 0.40 |
| ▸ | PTGDR2 | Q9Y5Y4 | 1/20 | 0.40 |
| ▸ | KMT2A | Q03164 | 4/20 | 0.40 |
| ▸ | MEN1 | O00255 | 2/20 | 0.40 |
| ▸ | RECQL | P46063 | 2/20 | 0.40 |
| ▸ | ACHE | P22303 | 2/20 | 0.40 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.40 |
| ▸ | THRA | P10827 | 1/20 | 0.39 |
| ▸ | THRB | P10828 | 1/20 | 0.39 |
| ▸ | USP2 | O75604 | 1/20 | 0.39 |
| ▸ | NFE2L2 | Q16236 | 2/20 | 0.39 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.39 |
| ▸ | HPGD | P15428 | 1/20 | 0.39 |
| ▸ | HTT | P42858 | 1/20 | 0.39 |
| ▸ | PLIN1 | O60240 | 1/20 | 0.39 |
| ▸ | LMNA | P02545 | 1/20 | 0.39 |
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 | |
|---|---|---|---|---|
| SCHEMBL766471 | 0.87 | KMT2A (0.48) | ALOX15PTGDR2KMT2AMEN1RECQL | |
| SCHEMBL1200995 | 0.86 | ALDH1A1 (0.55) | ALOX15ELANEESR1HIF1APTGDR2 | |
| SCHEMBL11619491 | 0.85 | NFE2L2 (0.40) | ALOX15ELANEESR1HIF1APTGDR2 | |
| SCHEMBL17417576 | 0.83 | PTGDR2 (0.41) | PTGDR2KMT2AMEN1KDM4EUSP2 | |
| SCHEMBL30634925 | 0.83 | MEN1 (0.40) | PTGDR2KMT2AMEN1KDM4ETHRA | |
| SCHEMBL27573383 | 0.83 | ALOX15 (0.48) | ALOX15PTGDR2KMT2AMEN1KDM4E | |
| SCHEMBL1908275 | 0.83 | KDM4E (0.55) | ALOX15KMT2AMEN1RECQLKDM4E | |
| SCHEMBL1902239 | 0.83 | PTGDR2 (0.40) | PTGDR2KMT2AMEN1KDM4ENFE2L2 | |
| SCHEMBL27562951 | 0.83 | PTGDR2 (0.40) | PTGDR2KMT2AMEN1RECQLKDM4E | |
| SCHEMBL27579253 | 0.82 | KDM4E (0.54) | ALOX15KMT2AMEN1RECQLKDM4E |
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 120 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118271496-A | Isoalkenyl terpolymer containing oxygen polar groups and preparation method thereof | 常州汉韦聚合物有限公司 | 2024-07-02 | — | — | CN | claimed |
| US-4137137-A | Radiation process for the production of graft copolymer to be used for ion-exchange membrane | JAPAN ATOMIC ENERGY RESEARCH INSTITUTE (JP) | 1979-01-30 | — | — | US | claimed |
| CN-118271496-A | Isoalkenyl terpolymer containing oxygen polar groups and preparation method thereof | 常州汉韦聚合物有限公司 | 2024-07-02 | — | — | CN | disclosed |
| CN-117263778-A | Preparation method of styrene series compound for 248nm photoresist | 河北凯诺中星科技有限公司 | 2023-12-22 | — | — | CN | disclosed |
| CN-107207456-B | Latent acids and their use | 巴斯夫欧洲公司 | 2021-05-04 | — | — | CN | disclosed |
| EP-3253735-B1 | LATENT ACIDS AND THEIR USE | BASF SE (DE) | 2021-03-31 | — | — | EP | disclosed |
| US-10593980-B2 | Ionomer resin, and ionomer solution, multilayer body, member, electrochemical element, and electrochemical device that include the same | NITTO DENKO CORPORATION (JP) | 2020-03-17 | — | — | US | disclosed |
| EP-2539316-B1 | LATENT ACIDS AND THEIR USE | BASF SE (DE) | 2019-10-23 | — | — | EP | disclosed |
| CN-108084331-B | A kind of biology base film-forming resin and its photoresist of preparation | 江南大学 | 2019-08-16 | — | — | CN | disclosed |
| US-9994538-B2 | Latent acids and their use | BASF SE (DE) | 2018-06-12 | — | — | US | disclosed |
| US-20180050336-A1 | ANION-EXCHANGE MEMBRANE, AND ELECTROCHEMICAL ELEMENT AND ELECTROCHEMICAL DEVICE HAVING SAME | NITTO DENKO CORPORATION (JP) | 2018-02-22 | — | — | US | disclosed |
| US-6512020-B1 | Photosensitive acid-donors in chemically amplified resist formulations. activated by irradiation with actinic electromagnetic radiation and electron beams. | CIBA SPECIALTY CHEMICALS CORPORATION | 2003-01-28 | — | — | US | disclosed |
| WO-2002098870-A1 | SUBSTITUTED OXIME DERIVATIVES AND THE USE THEREOF AS LATENT ACIDS | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 2002-12-12 | — | — | WO | disclosed |
| WO-2002046507-A2 | ONIUM SALTS AND THE USE THEROF AS LATENT ACIDS | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 2002-06-13 | — | — | WO | disclosed |
| WO-2002025376-A2 | OXIME DERIVATIVES AND THE USE THEREOF AS LATENT ACIDS | CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) | 2002-03-28 | — | — | WO | disclosed |
| US-20010036591-A1 | Iodonium salts as latent acid donors | IGM GROUP B.V. (NL) | 2001-11-01 | — | — | US | disclosed |
| US-6306555-B1 | RADIATION-SENSITIVE COMPOSITION COMPRISING CATIONICALLY OR ACID-CATALYTICALLY POLYMERISABLE OR CROSSLINKABLE COMPOUND OR COMPOUND THAT INCREASES ITS SOLUBILITY IN DEVELOPER UNDER ACTION OF ACID, AND AT LEAST ONE DIARYLIODONIUM SALT | CIBA SPECIALTY CHEMICALS CORP. | 2001-10-23 | — | — | US | disclosed |
| US-6261738-B1 | LATENT CURING CATALYSTS FOR PHOTORESISTS SUCH AS 2,2,2-TRIFLUORO-1-PHENYL-ETHANONE OXIME-O-METHYL SULFONATE | CIBA SPECIALTY CHEMICALS CORPORATION | 2001-07-17 | — | — | US | disclosed |
| US-4137137-A | Radiation process for the production of graft copolymer to be used for ion-exchange membrane | JAPAN ATOMIC ENERGY RESEARCH INSTITUTE (JP) | 1979-01-30 | — | — | US | disclosed |
| US-4129617-A | Fluoro carbon graft copolymer and process for the production thereof | JAPAN ATOMIC ENERGY RESEARCH INSTITUTE (JP) | 1978-12-12 | — | — | US | disclosed |