Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | KMT2A | Q03164 | 5/20 | 0.77 |
| ▸ | HTR1A | P08908 | 1/20 | 0.61 |
| ▸ | LMNA | P02545 | 4/20 | 0.59 |
| ▸ | MAPT | P10636 | 3/20 | 0.59 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.59 |
| ▸ | HDAC3 | O15379 | 2/20 | 0.59 |
| ▸ | HDAC4 | P56524 | 2/20 | 0.59 |
| ▸ | HDAC1 | Q13547 | 2/20 | 0.59 |
| ▸ | HDAC2 | Q92769 | 2/20 | 0.59 |
| ▸ | HDAC8 | Q9BY41 | 2/20 | 0.59 |
| ▸ | HDAC6 | Q9UBN7 | 2/20 | 0.59 |
| ▸ | PLIN1 | O60240 | 2/20 | 0.59 |
| ▸ | RECQL | P46063 | 2/20 | 0.59 |
| ▸ | PLIN5 | Q00G26 | 2/20 | 0.59 |
| ▸ | ABHD5 | Q8WTS1 | 2/20 | 0.59 |
| ▸ | TNKS | O95271 | 1/20 | 0.59 |
| ▸ | HCAR2 | Q8TDS4 | 1/20 | 0.59 |
| ▸ | HDAC7 | Q8WUI4 | 1/20 | 0.59 |
| ▸ | HDAC10 | Q969S8 | 1/20 | 0.59 |
| ▸ | HDAC11 | Q96DB2 | 1/20 | 0.59 |
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 | |
|---|---|---|---|---|
| Phenyl Cinnamate SCHEMBL1055160 | 1.00 | KMT2A (0.77) | KMT2AHTR1ALMNAMAPTSMN1; SMN2 | |
| SCHEMBL16982630 | 0.96 | KMT2A (0.83) | KMT2AHTR1ALMNAMAPTSMN1; SMN2 | |
| Phenyl Cinnamate SCHEMBL27584041 | 0.93 | KMT2A (0.68) | KMT2AHTR1ALMNAMAPTSMN1; SMN2 | |
| SCHEMBL13978652 | 0.90 | KMT2A (0.69) | KMT2AHTR1ALMNAMAPTSMN1; SMN2 | |
| SCHEMBL17802341 | 0.89 | KMT2A (0.68) | KMT2AHTR1ALMNAHDAC2ALDH1A1 | |
| SCHEMBL14634510 | 0.89 | KMT2A (0.68) | KMT2AHTR1AMAPTHCAR2CYP2D6 | |
| SCHEMBL14634502 | 0.89 | KMT2A (0.73) | KMT2AHTR1ALMNAMAPTSMN1; SMN2 | |
| SCHEMBL31453510 | 0.89 | KMT2A (0.73) | KMT2AHTR1ALMNAMAPTSMN1; SMN2 | |
| SCHEMBL14634511 | 0.89 | KMT2A (0.68) | KMT2AHTR1AMAPTHCAR2CYP2D6 | |
| SCHEMBL15908399 | 0.89 | KMT2A (0.68) | KMT2AHTR1ALMNAHDAC2ALDH1A1 |
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 194 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122011640-A | Intermediate film for dimming glass and application thereof | 浙江精一新材料科技有限公司 | 2026-05-12 | — | — | CN | claimed |
| CN-116023202-A | Synthetic method of alpha-chlorarone derivative | 西南大学 | 2023-04-28 | — | — | CN | claimed |
| US-20220234987-A1 | STYRYL CARBOXYLATE DERIVATIVES | Renovel Innovations, Inc. | 2022-07-28 | — | — | US | claimed |
| CN-109004051-A | A kind of solar battery back film | 苏州中来光伏新材股份有限公司 | 2018-12-14 | — | — | CN | claimed |
| EP-3149135-A2 | PERFUME COMPOSITIONS | Givaudan S.A. (CH) | 2017-04-05 | — | — | EP | claimed |
| US-20170073614-A1 | Perfume Compositions | GIVAUDAN SA (CH) | 2017-03-16 | — | — | US | claimed |
| WO-2015181257-A2 | PERFUME COMPOSITIONS | GIVAUDAN SA (CH) | 2015-12-03 | — | — | WO | claimed |
| US-20100234467-A1 | METHODS FOR IMPROVING BIOAVAILABILITY OF A RENIN INHIBITOR | OTTINGER ISABEL | 2010-09-16 | — | — | US | claimed |
| US-20100034766-A1 | Malodor Counteracting Compositions | GIVAUDAN SA (CH) | 2010-02-11 | — | — | US | claimed |
| US-20100021413-A1 | Malodor Counteracting Compositions | GIVAUDAN SA (CH) | 2010-01-28 | — | — | US | claimed |
| EP-2086594-A1 | MALODOR COUNTERACTING COMPOSITIONS | Givaudan SA (CH) | 2009-08-12 | — | — | EP | claimed |
| EP-2079487-A1 | MALODOR COUNTERACTING COMPOSITIONS | Givaudan SA (CH) | 2009-07-22 | — | — | EP | claimed |
| CN-101356173-A | Novel pyridopyrazines and their use as modulators of kinases | AETERNA ZENTARIS GMBH (DE) | 2009-01-28 | — | — | CN | claimed |
| EP-1927350-A1 | Methods for improving bioavailability of a renin inhibitor | Novartis AG (CH) | 2008-06-04 | — | — | EP | claimed |
| WO-2008062066-A1 | METHODS FOR IMPROVING BIOAVAILABILITY OF A RENIN INHIBITOR | NOVARTIS AG (CH) | 2008-05-29 | — | — | WO | claimed |
| WO-2008055372-A1 | MALODOR COUNTERACTING COMPOSITIONS | GIVAUDAN SA (CH) | 2008-05-15 | — | — | WO | claimed |
| WO-2008049257-A1 | MALODOR COUNTERACTING COMPOSITIONS | GIVAUDAN SA (CH) | 2008-05-02 | — | — | WO | claimed |
| US-20070149484-A1 | NOVEL PYRIDOPYRAZINES AND THEIR USE AS MODULATORS OF KINASES | ZENTARIS GMBH (DE) | 2007-06-28 | — | — | US | claimed |
| EP-0430023-A1 | Process for the preparation of substituted phenylcinnamates | BASF Corporation (US) | 1991-06-05 | — | — | EP | claimed |
| EP-0320954-A2 | Transparent resin and transparent resin products | NIPPON OIL AND FATS COMPANY, LIMITED (JP) | 1989-06-21 | — | — | EP | 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 (4 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-20100034766-A1 | Malodor Counteracting Compositions | MTNR1A, MTNR1B, MC4R | KMT2A 3591/4885HTR1A 1102/4885LMNA 4312/4885 |
| US-20070149484-A1 | NOVEL PYRIDOPYRAZINES AND THEIR USE AS MODULATORS OF KINASES | MAP4K2, MAP3K15, MAP3K5 | KMT2A 1329/4885HTR1A 1754/4885LMNA 2535/4885 |
| US-20220234987-A1 | STYRYL CARBOXYLATE DERIVATIVES | ACACB, ACACA, FABP7 | KMT2A 1056/4885HTR1A 2749/4885LMNA 4061/4885 |
| US-20100234467-A1 | METHODS FOR IMPROVING BIOAVAILABILITY OF A RENIN INHIBITOR | REN, ACE, AGTR1 | KMT2A 3919/4885HTR1A 1183/4885LMNA 1104/4885 |
“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.