Predicted protein targets (top 12)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.38 |
| ▸ | LMNA | P02545 | 1/20 | 0.37 |
| ▸ | CA2 | P00918 | 6/20 | 0.35 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.35 |
| ▸ | CA1 | P00915 | 4/20 | 0.34 |
| ▸ | SPHK1 | Q9NYA1 | 1/20 | 0.34 |
| ▸ | TSHR | P16473 | 3/20 | 0.33 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.33 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.32 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.32 |
| ▸ | FDPS | P14324 | 1/20 | 0.32 |
| ▸ | DNM1 | Q05193 | 1/20 | 0.32 |
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 | |
|---|---|---|---|---|
| SCHEMBL20779324 | 0.86 | ALDH1A1 (0.38) | ALDH1A1LMNACA2MAPK1CA1 | |
| SCHEMBL14125822 | 0.85 | ALDH1A1 (0.44) | ALDH1A1LMNACA2MAPK1CA1 | |
| SCHEMBL11832228 | 0.85 | ALDH1A1 (0.44) | ALDH1A1LMNACA2MAPK1CA1 | |
| SCHEMBL14561036 | 0.84 | ALDH1A1 (0.39) | ALDH1A1LMNACA2MAPK1CA1 | |
| SCHEMBL3093612 | 0.83 | ALDH1A1 (0.42) | ALDH1A1LMNACA2MAPK1CA1 | |
| SCHEMBL14125514 | 0.83 | ALDH1A1 (0.42) | ALDH1A1LMNACA2MAPK1CA1 | |
| SCHEMBL18664275 | 0.83 | ALDH1A1 (0.42) | ALDH1A1LMNACA2MAPK1CA1 | |
| Hydrochloric Acid SCHEMBL30528602 | 0.81 | ALDH1A1 (0.41) | ALDH1A1LMNACA2MAPK1CA1 | |
| SCHEMBL2840090 | 0.80 | SPHK1 (0.47) | ALDH1A1LMNACA2CA1SPHK1 | |
| SCHEMBL4258146 | 0.80 | TSHR (0.44) | LMNATSHRTDP1 |
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 17 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20220033335-A1 | METHOD FOR PRODUCING DIVINYL ETHER COMPOUND HAVING ALKYLENE SKELETON | MARUZEN PETROCHEMICAL CO., LTD. (JP) | 2022-02-03 | — | — | US | disclosed |
| US-20220033334-A1 | METHOD FOR PRODUCING DIVINYL ETHER COMPOUND HAVING ALKYLENE SKELETON | MARUZEN PETROCHEMICAL CO., LTD. (JP) | 2022-02-03 | — | — | US | disclosed |
| EP-3889125-A1 | METHOD FOR PRODUCING DIVINYL ETHER COMPOUND HAVING ALKYLENE SKELETON | Maruzen Petrochemical Co., Ltd. (JP) | 2021-10-06 | — | — | EP | disclosed |
| EP-3889126-A1 | METHOD FOR PRODUCING DIVINYL ETHER COMPOUND HAVING ALKYLENE SKELETON | Maruzen Petrochemical Co., Ltd. (JP) | 2021-10-06 | — | — | EP | disclosed |
| CN-113166016-A | Method for producing divinyl ether compound having alkylene skeleton | 丸善石油化学株式会社 | 2021-07-23 | — | — | CN | disclosed |
| CN-113166015-A | Method for producing divinyl ether compound having alkylene skeleton | 丸善石油化学株式会社 | 2021-07-23 | — | — | CN | disclosed |
| CN-101023111-B | Modified phenol novolac resin and application thereof | INDSPEC CHEMICAL CORP | 2010-09-29 | — | — | CN | disclosed |
| US-7498371-B2 | Obtained by reacting resorcinol, 2,4-pentanediol, and aldehyde in the presence of an acid catalyst ; relatively low level of free resorcinol; low fuming, lower Mooney viscosity (better processing), better dynamic stiffness properties; used as a methylene acceptor in a vulcanizable rubber; reinforcement | SUMITOMO CHEMICAL CO., LTD. (JP) | 2009-03-03 | — | — | US | disclosed |
| CN-101023111-A | Modified phenol novolac resin and application thereof | INDSPEC CHEMICAL CORP (US) | 2007-08-22 | — | — | CN | disclosed |
| EP-1812487-A2 | MODIFIED PHENOLIC NOVOLAK RESINS AND APPLICATIONS THEREOF | INDSPEC CHEMICAL CORPORATION (US) | 2007-08-01 | — | — | EP | disclosed |
| EP-1618157-B1 | USE OF POLYANHYDRIDES IN ANTIFOULING PAINT AND ANTIFOULING PAINT CONTAINING POLYANHYDRIDES | JOTUN AS (NO) | 2007-03-14 | — | — | EP | disclosed |
| WO-2006036760-A2 | MODIFIED PHENOLIC NOVOLAK RESINS AND APPLICATIONS THEREOF | INDSPEC CHEMICAL CORPORATION (US) | 2006-04-06 | — | — | WO | disclosed |
| US-20060069191-A1 | Modified phenolic novolak resins and applications thereof | INDSPEC CHEMICAL CORPORATION (US) | 2006-03-30 | — | — | US | disclosed |
| EP-1618157-A1 | POLYANHYDRIDES, PROCESS FOR THE PREPARATION, USE IN ANTIFOULING PAINT AND ANTIFOULING PAINT CONTAINING POLYANHYDRIDES | Jotun AS (NO) | 2006-01-25 | — | — | EP | disclosed |
| WO-2004096927-A1 | POLYANHYDRIDES, PROCESS FOR THE PREPARATION, USE IN ANTIFOULING PAINT AND ANTIFOULING PAINT CONTAINING POLYANHYDRIDES | JOTUN AS (NO) | 2004-11-11 | — | — | WO | disclosed |
| US-6242514-B1 | CYCLIC PHOSPHATE OR PHOSPHONATE; HEAT AND OXIDATION STABILIZER ESPECIALLY FOR OLEFIN POLYMERS AND ENGINEERING THERMOPLASTICS | SUMITOMO CHEMICAL COMPANY, LTD. (JP) | 2001-06-05 | — | — | US | disclosed |
| US-4557913-A | Borax recovery using sodium metaborate and boric acid intermediates | KERR-MCGEE CHEMICAL CORPORATION (US) | 1985-12-10 | — | — | 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-20220033334-A1 | METHOD FOR PRODUCING DIVINYL ETHER COMPOUND HAVING ALKYLENE SKELETON | DECR2, KAT8, DECR1 | ALDH1A1 2263/4885LMNA 215/4885CA2 852/4885 |
| US-20220033335-A1 | METHOD FOR PRODUCING DIVINYL ETHER COMPOUND HAVING ALKYLENE SKELETON | DECR2, DECR1, ACMSD | ALDH1A1 1072/4885LMNA 657/4885CA2 303/4885 |
“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.