Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ESR1 | P03372 | 2/20 | 0.39 |
| ▸ | NR5A1 | Q13285 | 1/20 | 0.38 |
| ▸ | HDAC3 | O15379 | 1/20 | 0.36 |
| ▸ | HDAC1 | Q13547 | 1/20 | 0.36 |
| ▸ | HDAC2 | Q92769 | 1/20 | 0.36 |
| ▸ | HRH3 | Q9Y5N1 | 1/20 | 0.35 |
| ▸ | TSHR | P16473 | 2/20 | 0.34 |
| ▸ | TP53 | P04637 | 1/20 | 0.34 |
| ▸ | S1PR1 | P21453 | 2/20 | 0.34 |
| ▸ | FAAH | O00519 | 1/20 | 0.34 |
| ▸ | MGLL | Q99685 | 1/20 | 0.34 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.34 |
| ▸ | RECQL | P46063 | 1/20 | 0.34 |
| ▸ | S1PR4 | O95977 | 1/20 | 0.34 |
| ▸ | S1PR3 | Q99500 | 1/20 | 0.34 |
| ▸ | S1PR5 | Q9H228 | 1/20 | 0.34 |
| ▸ | VDR | P11473 | 1/20 | 0.33 |
| ▸ | PLA2G4B | P0C869 | 1/20 | 0.33 |
| ▸ | MEN1 | O00255 | 1/20 | 0.33 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.33 |
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 | |
|---|---|---|---|---|
| SCHEMBL27822526 | 1.00 | ESR1 (0.39) | ESR1NR5A1HDAC3HDAC1HDAC2 | |
| SCHEMBL11412994 | 1.00 | ESR1 (0.39) | ESR1NR5A1HDAC3HDAC1HDAC2 | |
| SCHEMBL1092732 | 0.93 | ESR1 (0.36) | ESR1HDAC3HDAC1HDAC2HRH3 | |
| SCHEMBL10745707 | 0.88 | HRH3 (0.40) | HRH3 | |
| SCHEMBL5145880 | 0.86 | CNR2 (0.44) | ESR1 | |
| SCHEMBL5145878 | 0.85 | CYP3A4 (0.40) | ESR1NR5A1HRH3TSHRTP53 | |
| SCHEMBL8469758 | 0.81 | CNR2 (0.42) | ESR1 | |
| SCHEMBL2783422 | 0.81 | EPHX2 (0.35) | ESR1TSHRKDM4EALDH1A1SMN1; SMN2 | |
| SCHEMBL5116391 | 0.81 | HRH3 (0.41) | HRH3MAPT | |
| SCHEMBL21268265 | 0.79 | PTGDR2 (0.38) | ESR1FAAHMEN1ALDH1A1MAPT |
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 61 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1683782-B1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2012-03-14 | — | — | EP | claimed |
| EP-1683783-B1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2012-03-14 | — | — | EP | claimed |
| EP-1120402-B1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2008-06-25 | — | — | EP | claimed |
| CN-1310924-C | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2007-04-18 | — | — | CN | claimed |
| EP-1683782-A2 | Chiral copper complex and production processes thereof and using the same | Sumitomo Chemical Company, Limited (JP) | 2006-07-26 | — | — | EP | claimed |
| EP-1683783-A2 | Chiral copper complex and production processes thereof and using the same | Sumitomo Chemical Company, Limited (JP) | 2006-07-26 | — | — | EP | claimed |
| US-7009079-B2 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2006-03-07 | — | — | US | claimed |
| CN-1616465-A | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2005-05-18 | — | — | CN | claimed |
| US-20050090684-A1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO., LTD. | 2005-04-28 | — | — | US | claimed |
| US-6670500-B2 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2003-12-30 | — | — | US | claimed |
| US-20020004618-A1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2002-01-10 | — | — | US | claimed |
| CN-1313277-A | Chiral copper complex, preparation method and application thereof | SUMITOMO CHEMICAL CO (JP) | 2001-09-19 | — | — | CN | claimed |
| EP-1120402-A2 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2001-08-01 | — | — | EP | claimed |
| EP-0128012-B1 | NOVEL CHIRAL COPPER COMPLEX AND ASYMMETRIC SYNTHESIS OF CYCLOPROPANECARBOXYLATE DERIVATIVES USING SAID COMPLEX AS CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1986-11-20 | — | — | EP | claimed |
| US-4552972-A | Chiral copper complex | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1985-11-12 | — | — | US | claimed |
| EP-0128012-A2 | Novel chiral copper complex and asymmetric synthesis of cyclopropanecarboxylate derivatives using said complex as catalyst | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1984-12-12 | — | — | EP | claimed |
| US-4197408-A | COPPER COMPLEX CATALYST, 2,5-DIMETHYL-2,4-HEXADIEN) REACTED WITH DIAZOACETATE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1980-04-08 | — | — | US | claimed |
| US-4029690-A | WITH 2,5-DIMETHYL-2,4-HEXADIENE AND AN ALKYL DIAZOACETATE WITH A COPPER COMPLEX CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | US | claimed |
| US-4029683-A | WITH A SCHIFF BASE, CHRYSANTHEMATE SYNTHESIS CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | US | claimed |
| CN-101528673-B | Method for producing asymmetric copper complex crystal | SUMITOMO CO LTD | 2012-08-01 | — | — | CN | disclosed |
| US-8153830-B2 | Production method of asymmetric copper complex crystal | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2012-04-10 | — | — | US | disclosed |
| EP-1683782-B1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2012-03-14 | — | — | EP | disclosed |
| EP-1683783-B1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2012-03-14 | — | — | EP | disclosed |
| CN-101945590-A | The deoxygenation mixture | BASF SE | 2011-01-12 | — | — | CN | disclosed |
| US-20100094036-A1 | PRODUCTION METHOD OF ASYMMETRIC COPPER COMPLEX CRYSTAL | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2010-04-15 | — | — | US | disclosed |
| CN-101528673-A | Method for producing asymmetric copper complex crystal | SUMITOMO CHEMICAL CO (JP) | 2009-09-09 | — | — | CN | disclosed |
| EP-2078710-A1 | METHOD FOR PRODUCING ASYMMETRIC COPPER COMPLEX CRYSTAL | Sumitomo Chemical Company, Limited (JP) | 2009-07-15 | — | — | EP | disclosed |
| EP-1120402-B1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2008-06-25 | — | — | EP | disclosed |
| CN-1310924-C | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2007-04-18 | — | — | CN | disclosed |
| CN-1309723-C | Method for producing optically active salicylaldimine copper complex | SUMITOMO CHEMICAL CO (JP) | 2007-04-11 | — | — | CN | disclosed |
| EP-1683782-A2 | Chiral copper complex and production processes thereof and using the same | Sumitomo Chemical Company, Limited (JP) | 2006-07-26 | — | — | EP | disclosed |
| EP-1683783-A2 | Chiral copper complex and production processes thereof and using the same | Sumitomo Chemical Company, Limited (JP) | 2006-07-26 | — | — | EP | disclosed |
| CN-1246299-C | Chiral copper complex, preparation method and application thereof | SUMITOMO CHEMICAL CO (JP) | 2006-03-22 | — | — | CN | disclosed |
| US-7009079-B2 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2006-03-07 | — | — | US | disclosed |
| CN-1616465-A | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO (JP) | 2005-05-18 | — | — | CN | disclosed |
| US-20050090684-A1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL CO., LTD. | 2005-04-28 | — | — | US | disclosed |
| US-6852871-B2 | Method for producing optically active salicylaldimine copper complex | SUMITOMO CHEMICAL COMPANY LIMITED (JP) | 2005-02-08 | — | — | US | disclosed |
| CN-1467211-A | Method for producing optically active salicylaldimine copper complex | ס�ѻ�ѧ��ҵ��ʽ���� | 2004-01-14 | — | — | CN | disclosed |
| US-6670500-B2 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2003-12-30 | — | — | US | disclosed |
| US-20030233003-A1 | Method for producing optically active salicylaldimine copper complex | SUMITOMO CHEMICAL COMPANY, LIMITED | 2003-12-18 | — | — | US | disclosed |
| EP-1371631-A1 | Method for producing optically active salicylaldimine copper complex | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2003-12-17 | — | — | EP | disclosed |
| US-6469198-B2 | OBTAINED BY CONTACTING N-SALICYLIDENEAMINOALCOHOL WITH MONO OR DIVALENT COPPER COMPOUND; FORMATION OF OPTICALLY ACTIVE CYCLOPROPANE-CARBOXYLIC ESTER FROM PROCHIRAL OLEFIN AND DIAZOACETIC ACID ESTER | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2002-10-22 | — | — | US | disclosed |
| US-20020004618-A1 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2002-01-10 | — | — | US | disclosed |
| US-20010037036-A1 | Chiral copper complex catalyst composition and asymmetric production process using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2001-11-01 | — | — | US | disclosed |
| CN-1313277-A | Chiral copper complex, preparation method and application thereof | SUMITOMO CHEMICAL CO (JP) | 2001-09-19 | — | — | CN | disclosed |
| EP-1120401-A2 | Chiral copper complex catalyst composition and asymmetric production process using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2001-08-01 | — | — | EP | disclosed |
| EP-1120402-A2 | Chiral copper complex and production processes thereof and using the same | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 2001-08-01 | — | — | EP | disclosed |
| EP-0128012-B1 | NOVEL CHIRAL COPPER COMPLEX AND ASYMMETRIC SYNTHESIS OF CYCLOPROPANECARBOXYLATE DERIVATIVES USING SAID COMPLEX AS CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1986-11-20 | — | — | EP | disclosed |
| US-4603218-A | Asymmetric synthesis of cyclopropanecarboxylate derivatives using chiral copper complex as catalyst | SUMITOMO CHEMICAL CO., LTD. (JP) | 1986-07-29 | — | — | US | disclosed |
| US-4552972-A | Chiral copper complex | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1985-11-12 | — | — | US | disclosed |
| EP-0128012-A2 | Novel chiral copper complex and asymmetric synthesis of cyclopropanecarboxylate derivatives using said complex as catalyst | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1984-12-12 | — | — | EP | disclosed |
| EP-0022608-B1 | PROCESS FOR THE PREPARATION OF CYCLOPROPANE CARBOXYLIC ACID ESTERS | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1983-07-06 | — | — | EP | disclosed |
| US-4344894-A | TRANSITION METAL COMPLEX OF SCHIFF BASES AS CATALYSTS | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1982-08-17 | — | — | US | disclosed |
| US-4343935-A | CATALYSTS FOR CYCLOPROPANIZATION OF OLEFINS BY DIAZOACETATES | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1982-08-10 | — | — | US | disclosed |
| US-4288387-A | REACTION OF A HALOGENOPENTENE OR HEXENE WITH A DIAZOACETIC ESTER IN THE PRESENCE OF CATALYST WHICH IS METALLIC COPPER, A COPPER SALT, A RHODIUM SALT, OR A TRANSITION METAL COMPLEX OF A CHIRAL SCHIFF BASE | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1981-09-08 | — | — | US | disclosed |
| EP-0024795-A1 | Chiral compounds and process for their preparation | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1981-03-11 | — | — | EP | disclosed |
| EP-0023075-A1 | Process for the preparation of cyclopropane carboxylic acid esters | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1981-01-28 | — | — | EP | disclosed |
| EP-0022608-A1 | Process for the preparation of cyclopropane carboxylic acid esters | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1981-01-21 | — | — | EP | disclosed |
| US-4197408-A | COPPER COMPLEX CATALYST, 2,5-DIMETHYL-2,4-HEXADIEN) REACTED WITH DIAZOACETATE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1980-04-08 | — | — | US | disclosed |
| US-4029690-A | WITH 2,5-DIMETHYL-2,4-HEXADIENE AND AN ALKYL DIAZOACETATE WITH A COPPER COMPLEX CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | US | disclosed |
| US-4029690-A | WITH 2,5-DIMETHYL-2,4-HEXADIENE AND AN ALKYL DIAZOACETATE WITH A COPPER COMPLEX CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | US | disclosed |
| US-4029683-A | WITH A SCHIFF BASE, CHRYSANTHEMATE SYNTHESIS CATALYST | SUMITOMO CHEMICAL COMPANY, LIMITED (JA) | 1977-06-14 | — | — | 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 (5 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-20030233003-A1 | Method for producing optically active salicylaldimine copper complex | ADH1A, ALDH3A1, ADH1C | ESR1 2927/4885NR5A1 553/4885HDAC3 4650/4885 |
| US-20050090684-A1 | Chiral copper complex and production processes thereof and using the same | SOD1, CYP1A1, NFXL1 | ESR1 633/4885NR5A1 831/4885HDAC3 4050/4885 |
| US-20010037036-A1 | Chiral copper complex catalyst composition and asymmetric production process using the same | AP1M1, UBA3, AP1S1 | ESR1 2902/4885NR5A1 847/4885HDAC3 4585/4885 |
| US-20100094036-A1 | PRODUCTION METHOD OF ASYMMETRIC COPPER COMPLEX CRYSTAL | ADH1A, ADH1C, ALDH3A1 | ESR1 3734/4885NR5A1 1429/4885HDAC3 4515/4885 |
| US-20020004618-A1 | Chiral copper complex and production processes thereof and using the same | SOD1, XDH, NFXL1 | ESR1 1529/4885NR5A1 448/4885HDAC3 4014/4885 |
“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.