Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ACHE | P22303 | 1/20 | 0.54 |
| ▸ | HCAR2 | Q8TDS4 | 2/20 | 0.43 |
| ▸ | LDHA | P00338 | 1/20 | 0.38 |
| ▸ | LDHB | P07195 | 1/20 | 0.38 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.36 |
| ▸ | LMNA | P02545 | 2/20 | 0.36 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.36 |
| ▸ | OR51E2 | Q9H255 | 1/20 | 0.36 |
| ▸ | F7 | P08709 | 1/20 | 0.35 |
| ▸ | F3 | P13726 | 1/20 | 0.35 |
| ▸ | SARM1 | Q6SZW1 | 1/20 | 0.35 |
| ▸ | SIRT2 | Q8IXJ6 | 1/20 | 0.35 |
| ▸ | SIRT6 | Q8N6T7 | 1/20 | 0.35 |
| ▸ | SIRT1 | Q96EB6 | 1/20 | 0.35 |
| ▸ | SIRT3 | Q9NTG7 | 1/20 | 0.35 |
| ▸ | SIRT5 | Q9NXA8 | 1/20 | 0.35 |
| ▸ | SIRT4 | Q9Y6E7 | 1/20 | 0.35 |
| ▸ | BLM | P54132 | 2/20 | 0.32 |
| ▸ | PMP22 | Q01453 | 2/20 | 0.32 |
| ▸ | TSHR | P16473 | 2/20 | 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 | |
|---|---|---|---|---|
| Carbamic Acid SCHEMBL7251118 | 1.00 | ACHE (0.54) | ACHEHCAR2LDHALDHBTDP1 | |
| Carbamic Acid SCHEMBL8573342 | 1.00 | ACHE (0.54) | ACHEHCAR2LDHALDHBTDP1 | |
| Carbamic Acid SCHEMBL782968 | 1.00 | ACHE (0.54) | ACHEHCAR2LDHALDHBTDP1 | |
| Urea SCHEMBL2538456 | 0.88 | LMNA (0.50) | ACHEHCAR2LDHALDHBTDP1 | |
| Urea SCHEMBL5146646 | 0.88 | LMNA (0.50) | ACHEHCAR2LDHALDHBTDP1 | |
| Bicarbonate SCHEMBL27606044 | 0.84 | HCAR2 (0.47) | HCAR2NAPRTBCAT2 | |
| Bicarbonate SCHEMBL3158090 | 0.84 | HCAR2 (0.47) | HCAR2NAPRTBCAT2 | |
| Pyrimidine SCHEMBL28643613 | 0.83 | F7 (0.46) | ACHEHCAR2TDP1ALDH1A1F7 | |
| Pyrimidine SCHEMBL1150634 | 0.83 | F7 (0.46) | ACHEHCAR2TDP1ALDH1A1F7 | |
| Pyrimidine SCHEMBL27627207 | 0.81 | F7 (0.44) | ACHEHCAR2TDP1ALDH1A1F7 |
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 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2044035-A1 | PROCESS FOR THE COVALENT COUPLING OF TWO MOLECULES BY MEANS OF A DIELS-ALDER REACTION WITH INVERSE ELECTRON REQUIREMENT | Deutsches Krebsforschungszentrum, Stiftung des öffentlichen Rechts (DE) | 2009-04-08 | — | — | EP | claimed |
| WO-2007144200-A1 | PROCESS FOR THE COVALENT COUPLING OF TWO MOLECULES BY MEANS OF A DIELS-ALDER REACTION WITH INVERSE ELECTRON REQUIREMENT | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts (DE) | 2007-12-21 | — | — | WO | claimed |
| EP-1867638-A1 | Procedure for the Conection of two Molecules via Diels-Alder Reactions with Inverse Electron Demand | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts (DE) | 2007-12-19 | — | — | EP | claimed |
| EP-0604922-B1 | Durable compositions and use of same | CYTEC TECH CORP (US) | 2004-11-17 | — | — | EP | claimed |
| EP-0604922-A1 | Durable compositions and use of same | CYTEC TECHNOLOGY CORP. (US) | 1994-07-06 | — | — | EP | claimed |
| EP-2044035-A1 | PROCESS FOR THE COVALENT COUPLING OF TWO MOLECULES BY MEANS OF A DIELS-ALDER REACTION WITH INVERSE ELECTRON REQUIREMENT | Deutsches Krebsforschungszentrum, Stiftung des öffentlichen Rechts (DE) | 2009-04-08 | — | — | EP | disclosed |
| WO-2007144200-A1 | PROCESS FOR THE COVALENT COUPLING OF TWO MOLECULES BY MEANS OF A DIELS-ALDER REACTION WITH INVERSE ELECTRON REQUIREMENT | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts (DE) | 2007-12-21 | — | — | WO | disclosed |
| EP-1737834-B1 | METHOD FOR PRODUCING 1,3,5-TRIAZINE CARBAMATES AND UREAS | BASF AG (DE) | 2007-10-03 | — | — | EP | disclosed |
| EP-0604922-B1 | Durable compositions and use of same | CYTEC TECH CORP (US) | 2004-11-17 | — | — | EP | disclosed |
| EP-0930303-B1 | A process for preparing isocyanate compounds from haloaminotriazines and acid halides | CYTEC TECH CORP (US) | 2004-02-04 | — | — | EP | disclosed |
| EP-0933371-B1 | N-halo acid amides | CYTEC TECH CORP (US) | 2003-04-09 | — | — | EP | disclosed |
| EP-0565774-B1 | Process for preparing amide derivatives from halominotriazines and acid halides | CYTEC TECH CORP (US) | 2001-03-28 | — | — | EP | disclosed |
| US-5574103-A | ETCH RESISTANCE, NO FORMALDEHYDE | CYTEC TECHNOLOGY CORP. (US) | 1996-11-12 | — | — | US | disclosed |
| US-5574103-A | ETCH RESISTANCE, NO FORMALDEHYDE | CYTEC TECHNOLOGY CORP. (US) | 1996-11-12 | — | — | US | disclosed |
| US-5571915-A | Process for preparing amide derivatives from haloaminotriazines and acid halides | CYTEC TECHNOLOGY CORP. (US) | 1996-11-05 | — | — | US | disclosed |
| US-5405959-A | Haloaminotraizines and acid halides | CYTEC TECHNOLOGY CORP. (US) | 1995-04-11 | — | — | US | disclosed |
| EP-0604922-A1 | Durable compositions and use of same | CYTEC TECHNOLOGY CORP. (US) | 1994-07-06 | — | — | EP | disclosed |
| US-5288865-A | Process for preparing amide derivatives from haloaminotriazines and acid halides | AMERICAN CYANAMID COMPANY (US) | 1994-02-22 | — | — | US | disclosed |
| EP-0565774-A2 | Process for preparing amide derivatives from halominotriazines and acid halides | CYTEC TECHNOLOGY CORP. (US) | 1993-10-20 | — | — | EP | disclosed |
| EP-0541966-A2 | Process for preparing amide derivatives from halomines and acid halides | AMERICAN CYANAMID COMPANY (US) | 1993-05-19 | — | — | EP | disclosed |