Predicted protein targets (top 11)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SLC29A1 | Q99808 | 4/20 | 0.51 |
| ▸ | CRHR1 | P34998 | 1/20 | 0.46 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.41 |
| ▸ | DNM2 | P50570 | 7/20 | 0.40 |
| ▸ | KCNH3 | Q9ULD8 | 1/20 | 0.39 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.39 |
| ▸ | TP53 | P04637 | 1/20 | 0.38 |
| ▸ | CA1 | P00915 | 2/20 | 0.38 |
| ▸ | CA2 | P00918 | 2/20 | 0.38 |
| ▸ | CA9 | Q16790 | 2/20 | 0.38 |
| ▸ | MAPT | P10636 | 1/20 | 0.38 |
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 | |
|---|---|---|---|---|
| SCHEMBL6716597 | 0.98 | SLC29A1 (0.50) | SLC29A1CRHR1SMN1; SMN2DNM2KCNH3 | |
| SCHEMBL6641031 | 0.96 | SLC29A1 (0.51) | SLC29A1CRHR1SMN1; SMN2DNM2KCNH3 | |
| SCHEMBL7776204 | 0.91 | SLC29A1 (0.50) | SLC29A1CRHR1SMN1; SMN2DNM2KCNH3 | |
| SCHEMBL7774646 | 0.91 | SLC29A1 (0.50) | SLC29A1CRHR1SMN1; SMN2DNM2KCNH3 | |
| SCHEMBL2370354 | 0.89 | SLC29A1 (0.49) | SLC29A1CRHR1SMN1; SMN2KMT2AMAPT | |
| SCHEMBL11798265 | 0.86 | SLC29A1 (0.43) | SLC29A1CRHR1SMN1; SMN2DNM2KCNH3 | |
| SCHEMBL21427481 | 0.86 | SLC29A1 (0.47) | SLC29A1CRHR1SMN1; SMN2DNM2KCNH3 | |
| SCHEMBL12109988 | 0.84 | CRHR1 (0.59) | SLC29A1CRHR1SMN1; SMN2DNM2 | |
| SCHEMBL20740706 | 0.83 | SLC29A1 (0.39) | SLC29A1CRHR1SMN1; SMN2DNM2KCNH3 | |
| SCHEMBL7535691 | 0.83 | TP53 (0.46) | SLC29A1SMN1; SMN2DNM2KCNH3KMT2A |
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 11 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20040200993-A1 | Reactive liquid polymer crosslinking agent and process for preparation | LCB WORLDWIDE, INC. | 2004-10-14 | — | — | US | disclosed |
| US-20030168629-A1 | Reactive liquid polymer crosslinking agent and process for preparation | LCB WORLDWIDE, INC. | 2003-09-11 | — | — | US | disclosed |
| WO-2003050094-A1 | REACTIVE LIQUID POLYMER CROSSLINKING AGENT AND PROCESS FOR PREPARATION | LCB WORLDWIDE INC. (US) | 2003-06-19 | — | — | WO | disclosed |
| EP-0711760-B1 | METHOD OF ALKYLATING TRIAZINE DERIVATIVE | NISSAN CHEMICAL IND LTD (JP) | 2002-05-15 | — | — | EP | disclosed |
| EP-0882720-B1 | METHODS FOR MODIFYING 1,3,5-TRIAZINE DERIVATIVES | NISSAN CHEMICAL IND LTD (JP) | 2001-08-22 | — | — | EP | disclosed |
| US-6130332-A | USING A GROUP 8 METAL CATALYST AND ALDEHYDES OR KETONE | NISSAN CHEMICAL INDUSTRIES, LTD. (JP) | 2000-10-10 | — | — | US | disclosed |
| US-6127538-A | HYDROXYALKYLATION OF A TRIAMINO TRIAZINE DERIVATIVE HAVING AT LEAST ONE REACTIVE NITROGEN BY REACTING WHILE HEATING WITH AN ALKANEDIOL OR ITS ADDUCT IN THE PRESENCE OF HYDROGEN AND A METAL CATALYST; BY-PRODUCT INHIBITION | NISSAN CHEMICAL INDUSTRIES, LTD. (JP) | 2000-10-03 | — | — | US | disclosed |
| EP-0882720-A1 | METHODS FOR MODIFYING 1,3,5-TRIAZINE DERIVATIVES | NISSAN CHEMICAL INDUSTRIES, LIMITED (JP) | 1998-12-09 | — | — | EP | disclosed |
| US-5792867-A | Method of alkylating of triazine derivatives | NISSAN CHEMICAL INDUSTRIES, LTD. (JP) | 1998-08-11 | — | — | US | disclosed |
| EP-0760369-A1 | PROCESS FOR ALKYLATING TRIAZINE DERIVATIVE | NISSAN CHEMICAL INDUSTRIES, LIMITED (JP) | 1997-03-05 | — | — | EP | disclosed |
| EP-0711760-A1 | METHOD OF ALKYLATING TRIAZINE DERIVATIVE | NISSAN CHEMICAL INDUSTRIES, LIMITED (JP) | 1996-05-15 | — | — | EP | disclosed |