⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| SCHEMBL11314685 | 0.98 | — | — | |
| SCHEMBL28677253 | 0.88 | ALDH1A1 (0.32) | — | |
| SCHEMBL27513464 | 0.86 | — | — | |
| SCHEMBL28963744 | 0.86 | — | — | |
| SCHEMBL28107586 | 0.86 | — | — | |
| SCHEMBL8846964 | 0.86 | — | — | |
| SCHEMBL9591258 | 0.86 | TSHR (0.35) | — | |
| SCHEMBL27957510 | 0.84 | — | — | |
| SCHEMBL28049799 | 0.84 | SENP1 (0.30) | — | |
| SCHEMBL5013694 | 0.84 | — | — |
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 88 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119454945-A | Ultrasonic activated carrier-free nano-drug and preparation method and application thereof | 浙江大学 | 2025-02-18 | — | — | CN | claimed |
| CN-104897733-B | A kind of nitrogen dioxide gas sensor based on p-aminophenyl substitution porphyrin aggregate material | 济南大学 | 2017-12-15 | — | — | CN | claimed |
| CN-104865292-B | A kind of nitrogen dioxide gas sensor based on o-aminophenyl substitution porphyrin nano material | 济南大学 | 2017-12-15 | — | — | CN | claimed |
| CN-107219280-A | A kind of Metalloporphyrins gas sensor element and its preparation method and application | 济南大学 | 2017-09-29 | — | — | CN | claimed |
| CN-103487416-A | Fluorescent sensor for detecting zinc ions based on asymmetrical porphyrin fluorescence ratio | UNIV NORTH CHINA | 2014-01-01 | — | — | CN | claimed |
| US-6825343-B2 | REFLUXING TETRACYANOETHYLENE OXIDE WITH TETRAPHENYLPORPHYRIN TO FORM (5,10,15,20-TETRAPHENYL-2,3-(3'-DICYANO)CYCLOPROPANO -2,3-CHLORIN); MACROMOLECULE INTERMEDIATES USED AS CHELATE COMPOUNDS; PHOTOSENSITIVITY | UNIVERSITY OF BRITISH COLUMBIA (CA) | 2004-11-30 | — | — | US | claimed |
| US-20040019201-A1 | 1,3-Dipolar cycloadditions to polypyrrolic macrocycles | MACALPINE JILL KIRSTEN (US) | 2004-01-29 | — | — | US | claimed |
| US-6620929-B1 | Condensing tetracyanoethylene oxide with porphyrins to form macromolecules such as 5,10,15,20-tetraphenyl-2,3-(3'-dicyano) cyclopropano-2,3-chlorin, used for photodynamic therapy; cyclization | UNIVERSITY OF BRITISH COLUMBIA (CA) | 2003-09-16 | — | — | US | claimed |
| CN-119219645-B | Preparation method of substituted diphenyl porphyrin-2-formaldehyde | 湖南科技大学 | 2026-05-19 | — | — | CN | disclosed |
| CN-119899348-B | Preparation method of novel photoelectric catalyst of covalent organic framework and photoelectric catalyst thereof | 广东药科大学 | 2025-09-30 | — | — | CN | disclosed |
| WO-2025089411-A1 | COMPOSITION, PREPARATION METHOD FOR COMPOSITION, AND PHOTOELECTRIC CONVERSION ELEMENT | キヤノン株式会社 | 2025-05-01 | — | — | WO | disclosed |
| WO-2025089409-A1 | PHOTOELECTRIC CONVERSION ELEMENT, PHOTOELECTRIC CONVERSION DEVICE, MOBILE BODY, AND BUILDING MATERIAL | キヤノン株式会社 | 2025-05-01 | — | — | WO | disclosed |
| WO-2025089384-A1 | PHOTOELECTRIC CONVERSION ELEMENT AND PHOTOELECTRIC CONVERSION DEVICE | キヤノン株式会社 | 2025-05-01 | — | — | WO | disclosed |
| CN-119899348-A | Preparation method of novel photoelectric catalyst of covalent organic framework and photoelectric catalyst thereof | 广东药科大学 | 2025-04-29 | — | — | CN | disclosed |
| WO-1999020081-A2 | HIGHLY TRANSPARENT NON-METALLIC CATHODES | THE TRUSTEES OF PRINCETON UNIVERSITY (US) | 1999-04-22 | — | — | WO | disclosed |
| US-5760217-A | Porphyrins and their synthesis from dipyrromethanes and aldehydes | SUN COMPANY, INC. (US) | 1998-06-02 | — | — | US | disclosed |
| US-5723677-A | Method for hydroperoxide decomposition using novel porphyrins synthesized from dipyrromethanes and aldehydes | SUN COMPANY, INC. (R&M) (US) | 1998-03-03 | — | — | US | disclosed |
| US-5571908-A | Porphyrins | SUN COMPANY, INC. (R&M) (US) | 1996-11-05 | — | — | US | disclosed |
| EP-0665056-A2 | Method for oxidizing alkanes using halocarbyl-substituted porphyrins synthesized from meso-halocarbyl-dipyrromethanes and aldehydes | SUN COMPANY, INC. (R&M) (US) | 1995-08-02 | — | — | EP | disclosed |
| EP-0665230-A2 | Halocarbyl-substituted porphyrins and their synthesis from meso-halocarbyl-dipyrromethanes and aldehydes | SUN COMPANY, INC. (R&M) (US) | 1995-08-02 | — | — | EP | disclosed |