Predicted protein targets (top 19)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CYP19A1 | P11511 | 4/20 | 0.53 |
| ▸ | TSHR | P16473 | 3/20 | 0.48 |
| ▸ | NAPRT | Q6XQN6 | 1/20 | 0.45 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.45 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.42 |
| ▸ | KIF11 | P52732 | 1/20 | 0.41 |
| ▸ | NOTUM | Q6P988 | 1/20 | 0.40 |
| ▸ | CYP1A2 | P05177 | 2/20 | 0.39 |
| ▸ | CYP11B1 | P15538 | 1/20 | 0.38 |
| ▸ | CYP11B2 | P19099 | 1/20 | 0.38 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.37 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.37 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.37 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.37 |
| ▸ | KCNA5 | P22460 | 1/20 | 0.37 |
| ▸ | KCNN4 | O15554 | 1/20 | 0.36 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.36 |
| ▸ | SLC6A4 | P31645 | 1/20 | 0.36 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.36 |
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 | |
|---|---|---|---|---|
| SCHEMBL5309862 | 0.92 | CYP19A1 (0.50) | CYP19A1TSHRALDH1A1KIF11NOTUM | |
| Hydrochloric Acid SCHEMBL3572356 | 0.90 | CYP19A1 (0.48) | CYP19A1TSHRALDH1A1KIF11NOTUM | |
| Pyridine SCHEMBL28116441 | 0.85 | TSHR (0.70) | CYP19A1TSHRNAPRTTDP1ALDH1A1 | |
| SCHEMBL14432852 | 0.84 | CYP19A1 (0.75) | CYP19A1CYP1A2CYP3A4CYP2C9CYP2C19 | |
| Chlorotriphenylmethane SCHEMBL461 | 0.84 | TSHR (0.65) | CYP19A1TSHRALDH1A1CYP1A2CYP3A4 | |
| Chlorotriphenylmethane SCHEMBL16781670 | 0.84 | TSHR (0.65) | CYP19A1TSHRALDH1A1CYP1A2CYP3A4 | |
| Pyridine SCHEMBL2907844 | 0.83 | AHR (0.47) | CYP19A1KIF11CYP1A2CYP3A4CYP2C9 | |
| Chlorotriphenylmethane SCHEMBL7246540 | 0.81 | TSHR (0.61) | CYP19A1TSHRALDH1A1CYP1A2CYP3A4 | |
| Chlorotriphenylmethane SCHEMBL7567317 | 0.81 | TSHR (0.61) | CYP19A1TSHRALDH1A1CYP1A2CYP3A4 | |
| Chlorotriphenylmethane SCHEMBL11237663 | 0.81 | TSHR (0.61) | CYP19A1TSHRALDH1A1CYP1A2CYP3A4 |
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 16 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108779138-A | Design and synthesis of nucleotides based on novel disulfide linkers for use as reversible terminators for DNA sequencing by synthesis | 哥伦比亚大学董事会 | 2018-11-09 | — | — | CN | disclosed |
| CN-102702260-A | Methods of reducing nephrotoxicity in subjects administered with nucleoside | CHIMERIX INC | 2012-10-03 | — | — | CN | disclosed |
| EP-2170917-A2 | N-SUBSTITUTED-AMINOMETHYLENE BRIDGED BICYCLIC NUCLEIC ACID ANALOGS | Isis Pharmaceuticals, Inc. (US) | 2010-04-07 | — | — | EP | disclosed |
| CN-101678122-A | Methods of reducing nephrotoxicity in recipients of nucleoside administration | CHIMERIX INC | 2010-03-24 | — | — | CN | disclosed |
| WO-2008150729-A2 | N-SUBSTITUTED-AMINOMETHYLENE BRIDGED BICYCLIC NUCLEIC ACID ANALOGS | ISIS PHARMACEUTICALS, INC. (US) | 2008-12-11 | — | — | WO | disclosed |
| EP-0686160-A4 | SOLUTION AND SOLID-PHASE FORMATION OF GLYCOSIDIC LINKAGES | UNIV PRINCETON (US) | 2003-03-12 | — | — | EP | disclosed |
| US-6194393-B1 | A GLYCOSIDE CONTAINING AN ANOMERIC SULFOXIDE AND NUCLEOPHILIC FUNCTIONAL GROUPS AND HAVING POTENTIAL GLYCOSYL ACCEPTING/DONATING CHARACTERISTICS AND AN ACTIVATING AGENT; RAPID CONSTRUCTION OLIGOSACCHARIDES; GLYCOSYLATION; LIBRARY | THE TRUSTEES OF PRINCETON UNIVERSITY | 2001-02-27 | — | — | US | disclosed |
| US-5861492-A | LIBRARIES OF SULFOXIDE-SUBSTITUTED GLYCOSIDES WHICH CAN BIND TO OTHER GLYCOSIDES, STEROIDS, AMINO ACIDS, PEPTIDES, LIPIDS OR POLYCYCLIC AROMATIC COMPOUNDS; FOR RAPID, EFFICIENT, SELECTIVE, MULTIPLE GLYCOSYLATION REACTIONS IN ONE STEP | THE TRUSTEES OF PRINCETON UNIVERSITY (US) | 1999-01-19 | — | — | US | disclosed |
| US-5792839-A | REACTING GLCOSYL DONOR HAVING ANOMERIC SULFOXIDE GROUP AND GLYCOSYL ACCEPTOR AT LOW TEMPERATURE | TRUSTEES OF PRINCETON UNIVERSITY (US) | 1998-08-11 | — | — | US | disclosed |
| CN-1181078-A | Non-nucleosidic coumarin derivatives as polynucleotide -cross -linking agents | NAXCOR (US) | 1998-05-06 | — | — | CN | disclosed |
| US-5700916-A | INTERMEDIATES FOR FORMING OLIGOSACCHARIDES, INCLUDING 4-HYDROXYTHIOPHENYL-/2-AZIDO-2-DEOXYGLUCO/PYRANOSIDE | TRUSTEES OF PRINCETON UNIVERSITY (US) | 1997-12-23 | — | — | US | disclosed |
| US-5639866-A | EXPOSING GLYCOSYL ACCEPTOR BOUND TO SOLID SUPPORT TO GLYCOSIDE HAVING ACTIVATED ANOMERIC SULFOXIDE GROUP, FORMING GLYCOSIDIC BOND | PRINCETON UNIVERSITY (US) | 1997-06-17 | — | — | US | disclosed |
| US-5635612-A | Method of forming multiple glycosidic linkages in a single step | THE TRUSTEES OF PRINCETON UNIVERSITY (US) | 1997-06-03 | — | — | US | disclosed |
| EP-0686160-A1 | SOLUTION AND SOLID-PHASE FORMATION OF GLYCOSIDIC LINKAGES | THE TRUSTEES OF PRINCETON UNIVERSITY (US) | 1995-12-13 | — | — | EP | disclosed |
| WO-1994019360-A1 | SOLUTION AND SOLID-PHASE FORMATION OF GLYCOSIDIC LINKAGES | THE TRUSTEES OF PRINCETON UNIVERSITY (US) | 1994-09-01 | — | — | WO | disclosed |
| CN-1009931-B | The method for preparing glycerol ether phosphatides | HOFFMANN LA ROCHE (CH) | 1990-10-10 | — | — | CN | disclosed |