Predicted protein targets (top 2)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | STAT3 | P40763 | 1/20 | 0.50 |
| ▸ | STAT1 | P42224 | 1/20 | 0.50 |
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 | |
|---|---|---|---|---|
| SCHEMBL5062037 | 0.97 | STAT3 (0.53) | STAT3STAT1 | |
| SCHEMBL224519 | 0.95 | STAT3 (0.48) | STAT3STAT1 | |
| SCHEMBL8831500 | 0.93 | STAT3 (0.50) | STAT3STAT1 | |
| SCHEMBL4168760 | 0.88 | STAT3 (0.44) | STAT3STAT1 | |
| Phosphoric Acid SCHEMBL30944426 | 0.88 | STAT3 (0.46) | STAT3STAT1 | |
| SCHEMBL722603 | 0.83 | STAT3 (0.50) | STAT3STAT1 | |
| SCHEMBL51570 | 0.82 | STAT3 (0.59) | STAT3STAT1 | |
| SCHEMBL6479855 | 0.82 | STAT3 (0.49) | STAT3STAT1 | |
| SCHEMBL38329 | 0.82 | STAT3 (0.49) | STAT3STAT1 | |
| SCHEMBL9866324 | 0.82 | STAT3 (0.49) | STAT3STAT1 |
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 58 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-113024583-A | Preparation and application of compound containing biporphyrin | 中南大学 | 2021-06-25 | — | — | CN | claimed |
| CN-118852182-A | Porphyrin-like chrysin conjugate and synthetic method and application thereof | 中南大学 | 2024-10-29 | — | — | CN | disclosed |
| CN-118184679-A | Photothermal agent and preparation method thereof, photothermal nanoparticle and preparation method thereof, insulating material and self-repairing method of insulating material | 中国石油天然气股份有限公司 | 2024-06-14 | — | — | CN | disclosed |
| CN-116813626-A | Chiral porphyrin ligand and preparation method thereof, chiral metalloporphyrin complex and application thereof | 南方科技大学 | 2023-09-29 | — | — | CN | disclosed |
| CN-114907571-B | Preparation and application of Eu metal-organic framework material based on difunctional pyridine carboxylic acid porphyrin ligand | 北京工业大学 | 2023-09-12 | — | — | CN | disclosed |
| CN-113698579-B | Porphyrin conjugated microporous polymer and its synthesis method and application | 西北民族大学 | 2023-09-01 | — | — | CN | disclosed |
| CN-114854033-B | Preparation and application of Eu metal-organic framework material based on non-planar porphyrin ligand | 北京工业大学 | 2023-09-01 | — | — | CN | disclosed |
| CN-114621453-B | Preparation and application of zirconium metal organic framework material of difunctional pyridine carboxylic acid porphyrin ligand | 北京工业大学 | 2023-06-30 | — | — | CN | disclosed |
| US-11495368-B2 | Hydrophobic, conductive organic materials for metallic surfaces | INTERNATIONAL BUSINESS MACHINES CORPORATION (US) | 2022-11-08 | — | — | US | disclosed |
| CN-114907571-A | Preparation and application of Eu metal-organic framework material based on bifunctional pyridine carboxylic acid porphyrin ligand | 北京工业大学 | 2022-08-16 | — | — | CN | disclosed |
| US-20050124596-A1 | Chiral porphyrins, chiral metalloporphyrins, and methods for synthesis of the same | UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION | 2005-06-09 | — | — | US | disclosed |
| WO-2004109768-A2 | METHODS AND INTERMEDIATES FOR THE SYNTHESIS OF DIPYRRIN-SUBSTITUTED PORPHYRINIC MACROCYCLES | NORTH CAROLINA STATE UNIVERSITY (US) | 2004-12-16 | — | — | WO | disclosed |
| US-20040254383-A1 | Reacting a dipyrromethane with an oxidant and a metal salt to produce the bis(dipyrrinato)metal complex; for making molecular memory devices, solar cells and light harvesting arrays | UNITED STATE DEPARTMENT OF ENERGY | 2004-12-16 | — | — | US | disclosed |
| US-20030236400-A1 | Heteroatom-substituted porphyrins and methods for synthesis of same | UNIVERSITY OF TENNESSEE RESEARCH CORPORATION | 2003-12-25 | — | — | US | disclosed |
| US-6603070-B2 | Convergent method for the synthesis of light harvesting rods. The rods are oligomers of the formula A1(Ab+1)b, wherein b is at least 1, A1 through Ab+1 are covalently coupled rod segments, and each rod segment A1 through A1+b comprises a | NORTH CAROLINA STATE UNIVERSITY | 2003-08-05 | — | — | US | disclosed |
| US-20030111108-A1 | Convergent synthesis of multiporphyrin light-harvesting rods | UNITED STATES DEPARTMENT OF ENERGY | 2003-06-19 | — | — | US | disclosed |
| US-5663328-A | Haloporphyrins and their preparation and use as catalysts | SUN COMPANY, INC. (R&M) (US) | 1997-09-02 | — | — | US | disclosed |
| EP-0704447-A1 | Reactions catalyzed by haloporphyrins | SUN COMPANY, INC. (R&M) (US) | 1996-04-03 | — | — | EP | disclosed |
| EP-0700915-A1 | Haloporphyrins and their preparation | SUN COMPANY, INC. (R&M) (US) | 1996-03-13 | — | — | EP | disclosed |
| US-5489716-A | Reactions catalyzed by haloporphyrins | SUN COMPANY, INC. (R&M) (US) | 1996-02-06 | — | — | US | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20040254383-A1 | Reacting a dipyrromethane with an oxidant and a metal salt to produce the bis(dipyrrinato)metal complex; for making molecular memory devices, solar cells and light harvesting arrays | PPOX, NCS1, CRY1 | STAT3 750/4885STAT1 2028/4885 |
| US-20030236400-A1 | Heteroatom-substituted porphyrins and methods for synthesis of same | PPOX, HMBS, UROD | STAT3 4156/4885STAT1 3973/4885 |
| US-20050124596-A1 | Chiral porphyrins, chiral metalloporphyrins, and methods for synthesis of the same | PPOX, PPIF, HMBS | STAT3 2986/4885STAT1 3579/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.