Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CYP2A6 | P11509 | 7/20 | 0.94 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.54 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.54 |
| ▸ | MEN1 | O00255 | 1/20 | 0.54 |
| ▸ | MAPT | P10636 | 1/20 | 0.54 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.54 |
| ▸ | CYP1A2 | P05177 | 5/20 | 0.46 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.46 |
| ▸ | HTT | P42858 | 1/20 | 0.46 |
| ▸ | CA1 | P00915 | 2/20 | 0.46 |
| ▸ | CA2 | P00918 | 2/20 | 0.46 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.46 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.46 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.46 |
| ▸ | CA7 | P43166 | 1/20 | 0.46 |
| ▸ | CA9 | Q16790 | 1/20 | 0.46 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.44 |
| ▸ | CYP11B1 | P15538 | 1/20 | 0.44 |
| ▸ | CYP11B2 | P19099 | 1/20 | 0.44 |
| ▸ | PTPN1 | P18031 | 2/20 | 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 | |
|---|---|---|---|---|
| SCHEMBL154221 | 0.97 | CYP2A6 (1.00) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| SCHEMBL29485684 | 0.97 | CYP2A6 (1.00) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| SCHEMBL29002798 | 0.94 | CYP2A6 (0.94) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| Benzene SCHEMBL27861653 | 0.94 | CYP2A6 (0.94) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| SCHEMBL22909955 | 0.94 | CYP2A6 (0.94) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| Methyl Alcohol SCHEMBL28320856 | 0.90 | CYP2A6 (0.85) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| Formaldehyde SCHEMBL28823619 | 0.90 | CYP2A6 (0.85) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| SCHEMBL17849081 | 0.89 | CYP2A6 (0.84) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| SCHEMBL29681779 | 0.89 | CYP2A6 (0.84) | CYP2A6ALDH1A1KDM4EMEN1MAPT | |
| SCHEMBL1304424 | 0.89 | CYP2A6 (0.84) | CYP2A6ALDH1A1KDM4EMEN1MAPT |
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 107 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116768733-B | Aryl cyclic ammonium salt arylation and silicon-based method | 中国科学技术大学 | 2025-05-23 | — | — | CN | claimed |
| CN-119859156-A | Boron-nitrogen organic compound, preparation method and application thereof, composition and photoelectric device | 广东聚华印刷显示技术有限公司 | 2025-04-22 | — | — | CN | claimed |
| CN-118908996-A | A composition containing C (sp2) P bond or C (sp)3) Process for preparing organic phosphine compound of-P bond | 烟台大学 | 2024-11-08 | — | — | CN | claimed |
| CN-116768733-A | Aryl cyclic ammonium salt arylation and silicon-based method | 中国科学技术大学 | 2023-09-19 | — | — | CN | claimed |
| WO-2023124996-A1 | SULFUR-CONTAINING CHIRAL BRIDGED METALLOECENE COMPOUND, PREPARATION THEREOF, AND APPLICATION | 中国石油天然气股份有限公司 | 2023-07-06 | — | — | WO | claimed |
| CN-108409764-B | Organic photosensitizer capable of forming C-X bond by concerted catalysis with metallic nickel and synthetic method thereof | 陕西师范大学 | 2020-07-28 | — | — | CN | claimed |
| CN-110759945-A | Preparation method of phosphine chiral center sodium salt | 南京理工大学 | 2020-02-07 | — | — | CN | claimed |
| CN-100548950-C | Process for preparing esters and ethers of probucol and derivatives thereof | ATHEROGENICS INC (US) | 2009-10-14 | — | — | CN | claimed |
| CN-1759084-A | Process for preparing esters and ethers of probucol and derivatives thereof | ATHEROGENICS INC (US) | 2006-04-12 | — | — | CN | claimed |
| CN-118908996-A | A composition containing C (sp2) P bond or C (sp)3) Process for preparing organic phosphine compound of-P bond | 烟台大学 | 2024-11-08 | — | — | CN | disclosed |
| CN-117230123-A | Method for biosynthesis of 2- (naphthalene-2-yl) ethanol by using saccharomyces cerevisiae | 江南大学 | 2023-12-15 | — | — | CN | disclosed |
| CN-116410238-A | Sulfur-containing chiral bridged metallocene compound, and preparation and application thereof | 中国石油天然气股份有限公司 | 2023-07-11 | — | — | CN | disclosed |
| WO-2023124996-A1 | SULFUR-CONTAINING CHIRAL BRIDGED METALLOECENE COMPOUND, PREPARATION THEREOF, AND APPLICATION | 中国石油天然气股份有限公司 | 2023-07-06 | — | — | WO | disclosed |
| CN-108373416-B | Method for synthesizing diarylamine by photo/nickel concerted catalysis | 陕西师范大学 | 2020-11-17 | — | — | CN | disclosed |
| EP-0722448-A1 | O-ARYL, O-ALKYL, O-ALKENYL AND O-ALKYNYL-MACROLIDES HAVING IMMUNOSUPPRESSIVE ACTIVITY | MERCK & CO. INC. (US) | 1996-07-24 | — | — | EP | disclosed |
| US-5532248-A | O-aryl,O-alkyl, and O-alkenyl-macrolides having immunosuppressive activity | MERCK CO., INC. (US) | 1996-07-02 | — | — | US | disclosed |
| WO-1995009857-A1 | O-ARYL, O-ALKYL, O-ALKENYL AND O-ALKYNYL-MACROLIDES HAVING IMMUNOSUPPRESSIVE ACTIVITY | MERCK & CO., INC. (US) | 1995-04-13 | — | — | WO | disclosed |
| CN-1082035-A | The inhibitors of hiv protease that is used for the treatment of AIDS | LILLY CO ELI (US) | 1994-02-16 | — | — | CN | disclosed |
| EP-0558321-A1 | Antivirally active N-cycloalkyl alkanol compounds | SANWA KAGAKU KENKYUSHO CO., LTD. (JP) | 1993-09-01 | — | — | EP | disclosed |
| US-4048330-A | Compositions containing 2-(6'-substituted-2'-naphthyl)acetic acid esters used for treating inflammation, pain or pyrexia | SYNTEX CORPORATION (US) | 1977-09-13 | — | — | US | disclosed |