Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.75 |
| ▸ | HDAC3 | O15379 | 2/20 | 0.69 |
| ▸ | HDAC1 | Q13547 | 2/20 | 0.69 |
| ▸ | HDAC2 | Q92769 | 2/20 | 0.69 |
| ▸ | HDAC10 | Q969S8 | 2/20 | 0.69 |
| ▸ | HDAC11 | Q96DB2 | 2/20 | 0.69 |
| ▸ | HDAC8 | Q9BY41 | 2/20 | 0.69 |
| ▸ | HDAC6 | Q9UBN7 | 2/20 | 0.69 |
| ▸ | NCOR2 | Q9Y618 | 1/20 | 0.69 |
| ▸ | GNAI3 | P08754 | 1/20 | 0.69 |
| ▸ | GNAO1 | P09471 | 1/20 | 0.69 |
| ▸ | GNAI1 | P63096 | 1/20 | 0.69 |
| ▸ | EPHX1 | P07099 | 9/20 | 0.61 |
| ▸ | EPHX2 | P34913 | 2/20 | 0.61 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.58 |
| ▸ | TRPV1 | Q8NER1 | 2/20 | 0.57 |
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 | |
|---|---|---|---|---|
| SCHEMBL14520558 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| SCHEMBL12196021 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| SCHEMBL28519164 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| SCHEMBL5002618 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| Hexadecanoic Acid Cyclohexylamide SCHEMBL1456860 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| SCHEMBL30590541 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| SCHEMBL11080983 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| SCHEMBL21443012 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| SCHEMBL21442874 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 | |
| SCHEMBL27622463 | 1.00 | SMN1; SMN2 (0.75) | SMN1; SMN2HDAC3HDAC1HDAC2HDAC10 |
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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| JP-59002886-A | — | — | None | — | — | JP | disclosed |
| CN-112358415-A | Gel factor for curing organic waste liquid at normal temperature and preparation method thereof | 中北大学 | 2021-02-12 | — | — | CN | disclosed |
| EP-1592418-B1 | USE OF ENDOCANNABINOID-LIKE COMPOUNDS FOR TREATING CNS DEGENERATIVE DISORDERS | RES & INNOVATION S P A (IT) | 2017-09-06 | — | — | EP | disclosed |
| US-20130190502-A1 | ACYLATION REACTION OF HYDROXYL GROUP | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2013-07-25 | — | — | US | disclosed |
| US-8431709-B2 | Acylation reaction of hydroxyl group | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2013-04-30 | — | — | US | disclosed |
| EP-1900365-B9 | Endocannabinoid-like compounds and their use for treating dermatitis | RES & INNOVATION S P A (IT) | 2012-01-18 | — | — | EP | disclosed |
| EP-1900365-B1 | Endocannabinoid-like compounds and their use for treating dermatitis | RES & INNOVATION S P A (IT) | 2011-03-30 | — | — | EP | disclosed |
| US-20100249422-A1 | ACYLATION REACTION OF HYDROXYL GROUP | TAKASAGO INTERNATIONAL CORPORATION (JP) | 2010-09-30 | — | — | US | disclosed |
| EP-1900365-A2 | New endocannabinoid-like compounds and their use | RESEARCH & INNOVATION SOC. COOP. A R.L. (IT) | 2008-03-19 | — | — | EP | disclosed |
| EP-1592418-A2 | USE IN THERAPY OF ENDOCANNABINOID-LIKE COMPOUNDS | Research & Innovation Soc. Coop. A R.L. (IT) | 2005-11-09 | — | — | EP | disclosed |
| US-4587537-A | WAX, A TEREPHTHALATE, BENZYL P-HYDROXYBENZOATE DEVELOPER | MITSUBISHI PAPER MILLS, LTD. (JP) | 1986-05-06 | — | — | US | disclosed |
| US-4575734-A | LEVCO DYES | RICOH COMPANY, LTD. (JP) | 1986-03-11 | — | — | US | disclosed |
| US-4562448-A | Heat-sensitive transfer medium | RICOH CO., LTD. (JP) | 1985-12-31 | — | — | US | disclosed |
| US-4547788-A | SHEET HAVING LAYER CONTAINING LEVCO DYE; ACCEPTOR SHEET CONTAININGCOLORING AGENT; POROUS FILLER | RICOH COMPANY, LTD. (JP) | 1985-10-15 | — | — | US | disclosed |
| US-4538164-A | LEUCO DYE, HYDROXYPHENOLIC ETHER DEVELOPER, OIL ABSORBING FILLER | RICOH CO., LTD. (JP) | 1985-08-27 | — | — | US | disclosed |
| US-4500896-A | Heat-sensitive recording medium affording patterns with different colors | RICOH COMPANY, LTD. (JP) | 1985-02-19 | — | — | US | disclosed |
| US-4462926-A | CYCLOHEXYL AMIDES OF FATTY ACIDS AND POLYESTERAMIDES | BAYER AKTIENGESELLSCHAFT (DE) | 1984-07-31 | — | — | US | disclosed |
| JP-S592886-A | DIAZO-BASED HEAT-SENSITIVE RECORDING MATERIAL | RICOH CO LTD | 1984-01-09 | — | — | JP | disclosed |
| US-4352860-A | Thermosensitive recording material | RICOH COMPANY, LTD. (JP) | 1982-10-05 | — | — | US | disclosed |
| US-3989677-A | STEAM, WATER | BAYER AKTIENGESELLSCHAFT (DT) | 1976-11-02 | — | — | 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 (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-20130190502-A1 | ACYLATION REACTION OF HYDROXYL GROUP | ADH5, ADH1A, ACADM | SMN1; SMN2 4601/4885HDAC3 243/4885HDAC1 229/4885 |
| US-20100249422-A1 | ACYLATION REACTION OF HYDROXYL GROUP | ADH5, ADH1A, ACADM | SMN1; SMN2 4601/4885HDAC3 243/4885HDAC1 229/4885 |
“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.