Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ENPP2 | Q13822 | 5/20 | 1.00 |
| ▸ | CA1 | P00915 | 2/20 | 0.61 |
| ▸ | CA2 | P00918 | 2/20 | 0.61 |
| ▸ | ACHE | P22303 | 1/20 | 0.50 |
| ▸ | NLRP3 | Q96P20 | 1/20 | 0.49 |
| ▸ | CES2 | O00748 | 1/20 | 0.48 |
| ▸ | CES1 | P23141 | 1/20 | 0.48 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.48 |
| ▸ | CA7 | P43166 | 1/20 | 0.48 |
| ▸ | CA9 | Q16790 | 1/20 | 0.48 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.48 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.48 |
| ▸ | CA4 | P22748 | 1/20 | 0.48 |
| ▸ | MGLL | Q99685 | 1/20 | 0.47 |
| ▸ | TUBB4A | P04350 | 1/20 | 0.46 |
| ▸ | TUBB | P07437 | 1/20 | 0.46 |
| ▸ | TUBA3C | P0DPH7 | 1/20 | 0.46 |
| ▸ | TUBA1B | P68363 | 1/20 | 0.46 |
| ▸ | TUBA4A | P68366 | 1/20 | 0.46 |
| ▸ | TUBB4B | P68371 | 1/20 | 0.46 |
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 | |
|---|---|---|---|---|
| SCHEMBL7344145 | 1.00 | ENPP2 (1.00) | ENPP2CA1CA2ACHENLRP3 | |
| Methyl Alcohol SCHEMBL28712606 | 0.98 | ENPP2 (0.96) | ENPP2CA1CA2ACHENLRP3 | |
| SCHEMBL28060965 | 0.92 | ENPP2 (0.85) | ENPP2CA1CA2ACHENLRP3 | |
| Acetonitrile SCHEMBL28133848 | 0.91 | ENPP2 (0.82) | ENPP2CA1CA2ACHENLRP3 | |
| SCHEMBL4974692 | 0.89 | ENPP2 (0.79) | ENPP2CA1CA2ACHENLRP3 | |
| Bicarbonate SCHEMBL28687639 | 0.89 | ENPP2 (0.79) | ENPP2CA1CA2ACHENLRP3 | |
| SCHEMBL26693037 | 0.86 | ENPP2 (0.74) | ENPP2CA1CA2ACHENLRP3 | |
| SCHEMBL30693949 | 0.86 | ENPP2 (0.75) | ENPP2CA1CA2NLRP3ALDH1A1 | |
| SCHEMBL28948432 | 0.85 | ENPP2 (0.73) | ENPP2CA1CA2ACHENLRP3 | |
| SCHEMBL30219783 | 0.85 | ENPP2 (0.73) | ENPP2CA1CA2ACHENLRP3 |
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
Appears in 6853 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122036736-A | Pyrrolo [2,3-d ] pyrimidine derivative, synthetic method and application | 云南大学 | 2026-05-15 | — | — | CN | claimed |
| WO-2025215126-A1 | SYNTHESIS OF VIDOFLUDIMUS AND ITS CALCIUM SALT | IMMUNIC AG (DE) | 2025-10-16 | — | — | WO | claimed |
| US-20250194617-A1 | Materials and Methods for Extending Shelf-Life of Foods | JP LABORATORIES, INC. | 2025-06-19 | — | — | US | claimed |
| US-20250169514-A1 | Materials and Methods for Extending Shelf-Life of Foods | JP LABORATORIES, INC. | 2025-05-29 | — | — | US | claimed |
| CN-115850346-B | Pinene pyridazine tetradentate platinum (II) and palladium (II) complex based on intramolecular hydrogen bond and preparation method and application thereof | 南京邮电大学 | 2025-05-16 | — | — | CN | claimed |
| CN-119799320-A | Organic narrow-band afterglow material based on halation benzene derivative and preparation and application methods thereof | 中国科学院上海有机化学研究所 | 2025-04-11 | — | — | CN | claimed |
| CN-119264060-A | 6-Morpholine-N, 2-diphenyl pyrimidine-4-carboxamide compound and preparation method and application thereof | 浙江科技大学 | 2025-01-07 | — | — | CN | claimed |
| CN-118344378-A | Beta-axis chiral porphyrin compound and preparation method thereof through Suzuki coupling reaction | 同济大学 | 2024-07-16 | — | — | CN | claimed |
| CN-118344321-A | Gamma-pyrone derivative and synthetic method and application thereof | 武汉轻工大学 | 2024-07-16 | — | — | CN | claimed |
| CN-117886736-A | 2-indolyl-3-imine indoline derivative, preparation method and application thereof | 苏州昊帆生物股份有限公司 | 2024-04-16 | — | — | CN | claimed |
| CN-101050157-A | Method for preparing compound in biphenyl class | UNIV DALIAN TECH (CN) | 2007-10-10 | — | — | CN | claimed |
| EP-1799677-A1 | OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS | Ranbaxy Laboratories Limited (IN) | 2007-06-27 | — | — | EP | claimed |
| WO-2006038100-A1 | OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS | RANBAXY LABORATORIES LIMITED (IN) | 2006-04-13 | — | — | WO | claimed |
| US-6908505-B2 | Thermochromic compositions of color formers and lewis acids | SPECTRA SYSTEMS CORPORATION (US) | 2005-06-21 | — | — | US | claimed |
| US-6800784-B1 | REACTING AROMATIC COMPOUND CARRYING AT LEAST ONE AMINO GROUP AND LEAVING GROUP WITH ARYLBORONIC ACID OR DERIVATIVE THEREOF, IN AQUEOUS MEDIUM, AND IN PRESENCE OF EFFECTIVE QUANTITY OF PALLADIUM CATALYST | RHODIA CHIMIE (FR) | 2004-10-05 | — | — | US | claimed |
| US-20040119057-A1 | Thermochromic compositions of color formers and lewis acids | SPECTRA SYSTEMS CORPORATION | 2004-06-24 | — | — | US | claimed |
| US-20030211138-A1 | Temperature control system for cutaneous photodynamic therapy | SPECTRA SYSTEMS CORPORATION | 2003-11-13 | — | — | US | claimed |
| WO-2003070315-A2 | TEMPERATURE CONTROL SYSTEM FOR CUTANEOUS PHOTODYNAMIC THERAPY | SPECTRA SYSTEMS CORPORATION (US) | 2003-08-28 | — | — | WO | claimed |
| US-6590100-B2 | Reacting an aromatic compound bearing a leaving group and an arylboronic acid and/or its derivatives in the presence of a base and an effective amount of a nickel catalyst | RHODIA CHIMIE (FR) | 2003-07-08 | — | — | US | claimed |
| US-20020173652-A1 | Process for preparing a polyaromatic compound | SHASUN PHARMA SOLUTIONS, INC. | 2002-11-21 | — | — | US | claimed |