Predicted protein targets (top 2)
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 | |
|---|---|---|---|---|
| SCHEMBL995929 | 0.79 | — | — | |
| SCHEMBL28094980 | 0.79 | LMNA (0.48) | LMNATHRB | |
| SCHEMBL23781949 | 0.79 | TSHR (0.34) | — | |
| SCHEMBL7563360 | 0.77 | DNM1 (0.37) | — | |
| SCHEMBL8731775 | 0.76 | — | — | |
| SCHEMBL10755396 | 0.76 | LMNA (0.50) | LMNATHRB | |
| SCHEMBL27064 | 0.76 | LMNA (0.73) | LMNATHRB | |
| SCHEMBL292251 | 0.74 | LMNA (0.48) | LMNATHRB | |
| SCHEMBL7536215 | 0.74 | — | — | |
| Butadiene SCHEMBL625826 | 0.74 | LMNA (0.71) | LMNATHRB |
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 16 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12612352-B2 | Process for preparing perfuming intermediate | FIRMENICH SA (CH) | 2026-04-28 | — | — | US | disclosed |
| EP-4069667-A1 | PROCESS FOR PREPARING PERFUMING INTERMEDIATE | Firmenich SA (CH) | 2022-10-12 | — | — | EP | disclosed |
| CN-115003649-A | Process for the preparation of perfuming intermediates | 弗门尼舍有限公司 | 2022-09-02 | — | — | CN | disclosed |
| WO-2008003737-A1 | METHOD FOR PRODUCING 3,3'-DIHYDROXYISORENIERATINE AND NOVEL INTERMEDIATE PRODUCTS THEREFOR | BASF SE (DE) | 2008-01-10 | — | — | WO | disclosed |
| US-6476240-B2 | POLYMERS DERIVED FROM AN UNSATURATED FUSED CYCLIC HYDROCARBON (SUCH AS PERHYDRO-2,3-DIDEHYDRO-1,4:5,8-DIMETHANONAPHTHALENE) JOINED BY A LINKER TO AN ESTER GROUP HAVING ONE OR TWO PROTECTED HYDROXYLS; USE AS PHOTORESIST | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2002-11-05 | — | — | US | disclosed |
| US-20020042531-A1 | Polymers derived from an unsaturated fused cyclic hydrocarbon (such as perhydro-2,3-didehydro-1,4:5,8-dimethanonaphthalene) joined by a linker to an ester group having one or two protected hydroxyls; use as photoresist | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2002-04-11 | — | — | US | disclosed |
| US-6335143-B1 | Resist composition containing specific cross-linking agent | WAKO PURE CHEMICAL INDUSTRIES LTD. (JP) | 2002-01-01 | — | — | US | disclosed |
| US-6331602-B1 | Monomer and a polymer obtained therefrom | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2001-12-18 | — | — | US | disclosed |
| EP-0875496-B1 | Acrylic or methacrylic acid derivatives and polymers obtained therefrom | WAKO PURE CHEM IND LTD (JP) | 2001-11-07 | — | — | EP | disclosed |
| US-6160068-A | Monomer and a polymer obtained therefrom | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2000-12-12 | — | — | US | disclosed |
| US-6143472-A | Resist composition and a method for formation of a pattern using the composition | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 2000-11-07 | — | — | US | disclosed |
| EP-0918048-A1 | A novel monomer and a polymer obtained therefrom | Wako Pure Chemical Industries, Ltd. (JP) | 1999-05-26 | — | — | EP | disclosed |
| US-5856521-A | Acrylic or methacrylic acid derivatives and polymers obtained therefrom | WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) | 1999-01-05 | — | — | US | disclosed |
| EP-0887706-A1 | Resist composition containing specific cross-linking agent | WAKO PURE CHEMICAL INDUSTRIES, LTD (JP) | 1998-12-30 | — | — | EP | disclosed |
| EP-0875789-A1 | Resist composition and its use for forming pattern | WAKO PURE CHEMICAL INDUSTRIES LTD (JP) | 1998-11-04 | — | — | EP | disclosed |
| EP-0875496-A1 | Acrylic or methacrylic acid derivatives and polymers obtained therefrom | WAKO PURE CHEMICAL INDUSTRIES LTD (JP) | 1998-11-04 | — | — | EP | 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 (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-20020042531-A1 | Polymers derived from an unsaturated fused cyclic hydrocarbon (such as perhydro-2,3-didehydro-1,4:5,8-dimethanonaphthalene) joined by a linker to an ester group having one or two protected hydroxyls; use as photoresist | AHR, DHCR24, FPR1 | LMNA 1686/4885THRB 4410/4885 |
| US-12612352-B2 | Process for preparing perfuming intermediate | CBR1, CYP2E1, CBR3 | LMNA 897/4885THRB 3674/4885 |
“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.