Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CD274 | Q9NZQ7 | 2/20 | 0.59 |
| ▸ | HTR2C | P28335 | 2/20 | 0.57 |
| ▸ | HTR2A | P28223 | 1/20 | 0.57 |
| ▸ | HTR2B | P41595 | 1/20 | 0.57 |
| ▸ | KCNH2 | Q12809 | 1/20 | 0.57 |
| ▸ | RYR2 | Q92736 | 1/20 | 0.57 |
| ▸ | ASIC3 | Q9UHC3 | 1/20 | 0.55 |
| ▸ | DRD2 | P14416 | 2/20 | 0.51 |
| ▸ | DRD3 | P35462 | 2/20 | 0.51 |
| ▸ | HRH3 | Q9Y5N1 | 1/20 | 0.50 |
| ▸ | DRD1 | P21728 | 1/20 | 0.50 |
| ▸ | DRD5 | P21918 | 1/20 | 0.50 |
| ▸ | ADRA2A | P08913 | 1/20 | 0.49 |
| ▸ | ADRA2B | P18089 | 1/20 | 0.49 |
| ▸ | ADRA2C | P18825 | 1/20 | 0.49 |
| ▸ | HTR7 | P34969 | 1/20 | 0.49 |
| ▸ | NISCH | Q9Y2I1 | 1/20 | 0.49 |
| ▸ | LMNA | P02545 | 1/20 | 0.49 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.49 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.49 |
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 | |
|---|---|---|---|---|
| SCHEMBL8467911 | 1.00 | CD274 (0.59) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| Hydrochloric Acid SCHEMBL587493 | 0.98 | CD274 (0.58) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| SCHEMBL29558442 | 0.93 | HTR2C (0.57) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| SCHEMBL746109 | 0.93 | HTR2C (0.57) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| Hydrochloric Acid SCHEMBL1124555 | 0.91 | HTR2C (0.55) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| Hydrochloric Acid SCHEMBL31062521 | 0.91 | HTR2C (0.55) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| Oxalic Acid SCHEMBL7199943 | 0.91 | CD274 (0.52) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| SCHEMBL29758918 | 0.89 | KCNH2 (0.54) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| SCHEMBL4859823 | 0.89 | KCNH2 (0.54) | CD274HTR2CHTR2AHTR2BKCNH2 | |
| Bromide SCHEMBL19644475 | 0.89 | CD274 (0.51) | CD274HTR2CHTR2AHTR2BKCNH2 |
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 482 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12294088-B2 | Secondary Li ion battery and Li capacitor electrode compositions | HENKEL AG & CO. KGAA (DE) | 2025-05-06 | — | — | US | claimed |
| EP-3555939-B1 | IMPROVED SECONDARY LI ION BATTERY AND LI CAPACITOR ELECTRODE COMPOSITIONS | HENKEL AG & CO KGAA (DE) | 2025-02-05 | — | — | EP | claimed |
| US-11791468-B2 | Secondary Li ion battery and Li capacitor electrode compositions | HENKEL AG & CO. KGAA (DE) | 2023-10-17 | — | — | US | claimed |
| US-20230307657-A1 | SECONDARY Li ION BATTERY AND Li CAPACITOR ELECTRODE COMPOSITIONS | HENKEL AG & CO. KGAA (DE) | 2023-09-28 | — | — | US | claimed |
| CN-110050365-B | Improved secondary lithium ion battery and lithium capacitor electrode compositions | 汉高股份有限及两合公司 | 2023-04-28 | — | — | CN | claimed |
| CN-111621805-B | Method for preparing 3, 4-dihydroisoquinoline by electrocatalytic selective dehydrogenation | 天津大学 | 2022-02-18 | — | — | CN | claimed |
| CN-110294758-B | 2-substituted 5, 6-dihydropyrazolo [5, 1-alpha ] isoquinoline, derivatives and synthesis method thereof | 湘潭大学 | 2021-10-22 | — | — | CN | claimed |
| CN-109293569-B | Method for preparing formamide derivative through amine transfer reaction without participation of catalyst | 湘潭大学 | 2021-08-06 | — | — | CN | claimed |
| CN-109943861-B | Method for synthesizing alpha-phosphoramidate by electrochemical oxidation | 南京大学 | 2020-11-27 | — | — | CN | claimed |
| CN-111621805-A | Method for preparing 3, 4-dihydroisoquinoline by electrocatalytic selective dehydrogenation | 天津大学 | 2020-09-04 | — | — | CN | claimed |
| US-20040019083-A1 | Asymmetric synthesis of (S,S,R)-(-)-actinonin and its analogs and uses therefor | SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH | 2004-01-29 | — | — | US | claimed |
| US-6562836-B1 | Islet amyloid polypeptide (IAPP) is known to be capable of forming fibrils which are deposited in the pancreas of patients wtih type II diabetes | QUEEN'S UNIVERSITY OF KINGSTON (CA) | 2003-05-13 | — | — | US | claimed |
| US-20020198156-A1 | Asymmetric synthesis of (S,S,R)-(-)-actinonin and its analogs and uses therefor | SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH | 2002-12-26 | — | — | US | claimed |
| EP-1025165-A4 | PROCESS AND COMPOSITIONS CONTAINING POLYPHENOL COPOLYMERS | HENKEL CORP (US) | 2001-06-13 | — | — | EP | claimed |
| EP-1025165-A1 | PROCESS AND COMPOSITIONS CONTAINING POLYPHENOL COPOLYMERS | HENKEL CORPORATION (US) | 2000-08-09 | — | — | EP | claimed |
| WO-1999016827-A1 | PROCESS AND COMPOSITIONS CONTAINING POLYPHENOL COPOLYMERS | HENKEL CORPORATION (US) | 1999-04-08 | — | — | WO | claimed |
| US-5891952-A | FREE OF ORGANIC SOLVENTS; REACTION PRODUCTS OF A PHENOLIC POLYMER SUCH AS POLYVINYLPHENOL, A BASE, AN AMINE, AN ALDEHYDE OF KETONE OR MIXTURE; USE AS SURFACE COATINGS | HENKEL CORPORATION (US) | 1999-04-06 | — | — | US | claimed |
| EP-0461113-A1 | TANNIN MANNICH ADDUCTS FOR IMPROVING CORROSION RESISTANCE OF METALS | HENKEL CORPORATION (US) | 1991-12-18 | — | — | EP | claimed |
| US-4944812-A | Tannin mannich adducts for improving corrosion resistance of metals | HENKEL CORPORATION (US) | 1990-07-31 | — | — | US | claimed |
| WO-1990005794-A1 | TANNIN MANNICH ADDUCTS FOR IMPROVING CORROSION RESISTANCE OF METALS | HENKEL CORPORATION (US) | 1990-05-31 | — | — | WO | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (2 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-20020198156-A1 | Asymmetric synthesis of (S,S,R)-(-)-actinonin and its analogs and uses therefor | HASPIN, CYTH2, ACTR3 | CD274 3951/4885HTR2C 168/4885HTR2A 1149/4885 |
| US-20040019083-A1 | Asymmetric synthesis of (S,S,R)-(-)-actinonin and its analogs and uses therefor | HASPIN, CYTH2, CYTH3 | CD274 3926/4885HTR2C 157/4885HTR2A 1114/4885 |
“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.