Predicted protein targets (top 15)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MMP8 | P22894 | 1/20 | 0.51 |
| ▸ | PIN1 | Q13526 | 1/20 | 0.47 |
| ▸ | MEN1 | O00255 | 1/20 | 0.46 |
| ▸ | NPC1 | O15118 | 1/20 | 0.46 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.46 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.46 |
| ▸ | TSHR | P16473 | 1/20 | 0.44 |
| ▸ | POLB | P06746 | 1/20 | 0.44 |
| ▸ | DPP4 | P27487 | 2/20 | 0.43 |
| ▸ | GAA | P10253 | 1/20 | 0.43 |
| ▸ | METAP2 | P50579 | 1/20 | 0.43 |
| ▸ | CA12 | O43570 | 1/20 | 0.43 |
| ▸ | CA1 | P00915 | 1/20 | 0.43 |
| ▸ | CA2 | P00918 | 1/20 | 0.43 |
| ▸ | CA9 | Q16790 | 1/20 | 0.43 |
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 | |
|---|---|---|---|---|
| SCHEMBL4884767 | 1.00 | MMP8 (0.51) | MMP8PIN1MEN1NPC1KMT2A | |
| SCHEMBL4881723 | 1.00 | MMP8 (0.51) | MMP8PIN1MEN1NPC1KMT2A | |
| SCHEMBL4881722 | 1.00 | MMP8 (0.51) | MMP8PIN1MEN1NPC1KMT2A | |
| Hydrochloric Acid SCHEMBL4881666 | 0.98 | PIN1 (0.50) | MMP8PIN1MEN1NPC1KMT2A | |
| SCHEMBL4450071 | 0.86 | ALDH1A1 (0.45) | MEN1KMT2ASMN1; SMN2TSHR | |
| SCHEMBL5652736 | 0.84 | MMP8 (0.47) | MMP8PIN1MEN1NPC1KMT2A | |
| SCHEMBL16746620 | 0.84 | NPC1 (0.50) | NPC1SMN1; SMN2TSHRPOLB | |
| SCHEMBL5651686 | 0.84 | MMP8 (0.47) | MMP8PIN1MEN1NPC1KMT2A | |
| SCHEMBL27813870 | 0.83 | MMP8 (0.51) | MMP8PIN1MEN1NPC1KMT2A | |
| SCHEMBL23342965 | 0.82 | MMP8 (0.54) | MMP8PIN1MEN1NPC1KMT2A |
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 49 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0837846-B1 | C-2' HYDROXYL-BENZYL PROTECTED, N-CARBAMATE PROTECTED (2R,3S)-3-PHENYLISOSERINE AND PRODUCTION PROCESS THEREFOR | NAPRO BIOTHERAPEUTICS INC (US) | 2001-11-07 | — | — | EP | claimed |
| EP-0837846-A4 | C-2' HYDROXYL-BENZYL PROTECTED, N-CARBAMATE PROTECTED (2R,3S)-3-PHENYLISOSERINE AND PRODUCTION PROCESS THEREFOR | NAPRO BIOTHERAPEUTICS INC (US) | 1998-10-07 | — | — | EP | claimed |
| EP-0837846-A1 | C-2' HYDROXYL-BENZYL PROTECTED, N-CARBAMATE PROTECTED (2R,3S)-3-PHENYLISOSERINE AND PRODUCTION PROCESS THEREFOR | NAPRO BIOTHERAPEUTICS, INC. (US) | 1998-04-29 | — | — | EP | claimed |
| WO-1996040624-A1 | C-2' HYDROXYL-BENZYL PROTECTED, N-CARBAMATE PROTECTED (2R,3S)-3-PHENYLISOSERINE AND PRODUCTION PROCESS THEREFOR | NAPRO BIOTHERAPEUTICS, INC. (US) | 1996-12-19 | — | — | WO | claimed |
| EP-0935596-B1 | METHOD FOR PACLITAXEL SYNTHESIS | NAPRO BIOTHERAPEUTICS INC (US) | 2005-02-02 | — | — | EP | disclosed |
| EP-1497374-A1 | FILLER REINFORCED POLYETHER IMIDE RESIN COMPOSITION AND MOLDED ARTICLE THEREOF | GENERAL ELECTRIC COMPANY (US) | 2005-01-19 | — | — | EP | disclosed |
| EP-1082316-B1 | METHODS AND USEFUL INTERMEDIATES FOR PACLITAXEL SYNTHESIS FROM C-7, C-10 DI-CBZ BACCATIN III | NAPRO BIOTHERAPEUTICS INC (US) | 2004-06-23 | — | — | EP | disclosed |
| EP-1412319-A1 | CHIRAL RESOLUTION METHOD FOR PRODUCING COMPOUNDS USEFUL IN THE SYNTHESIS OF TAXANES | NAPRO BIOTHERAPEUTICS, INC. (US) | 2004-04-28 | — | — | EP | disclosed |
| WO-2004014995-A1 | RESIN COMPOSITION FOR WIRE AND CABLE COVERINGS | GENERAL ELECTRIC COMPANY (US) | 2004-02-19 | — | — | WO | disclosed |
| US-6653501-B2 | Using chromatographic process for separating a target chiral compound from its enantiomer in a racemic mixtures; purification | NAPRO BIOTHERAPEUTICS, INC. | 2003-11-25 | — | — | US | disclosed |
| WO-2003087226-A1 | FILLER REINFORCED POLYETHER IMIDE RESIN COMPOSITION AND MOLDED ARTICLE THEREOF | GENERAL ELECTRIC COMPAMY (US) | 2003-10-23 | — | — | WO | disclosed |
| EP-0847393-B1 | PACLITAXEL SYNTHESIS FROM PRECURSOR COMPOUNDS AND METHODS OF PRODUCING THE SAME | NAPRO BIOTHERAPEUTICS INC (US) | 2003-10-01 | — | — | EP | disclosed |
| US-5688977-A | Method for docetaxel synthesis | NAPRO BIOTHERAPEUTICS, INC. (US) | 1997-11-18 | — | — | US | disclosed |
| US-5684175-A | C-2' hydroxyl-benzyl protected, N-carbamate protected (2R, 3S)- 3-phenylisoserine and production process therefor | NAPRO BIOTHERAPEUTICS, INC. (US) | 1997-11-04 | — | — | US | disclosed |
| US-5675025-A | Paclitaxel synthesis from precursor compounds and methods of producing the same | NAPRO BIOTHERAPEUTICS, INC. (US) | 1997-10-07 | — | — | US | disclosed |
| WO-1997034866-A1 | METHOD FOR DOCETAXEL SYNTHESIS | NAPRO BIOTHERAPEUTICS, INC. (US) | 1997-09-25 | — | — | WO | disclosed |
| WO-1997031911-A1 | INTERMEDIATE FOR USE IN DOCETAXEL SYNTHESIS AND PRODUCTION METHOD THEREFOR | NAPRO BIOTHERAPEUTICS, INC. (US) | 1997-09-04 | — | — | WO | disclosed |
| WO-1996040667-A1 | PACLITAXEL SYNTHESIS FROM PRECURSOR COMPOUNDS AND METHODS OF PRODUCING THE SAME | NAPRO BIOTHERAPEUTICS, INC. (US) | 1996-12-19 | — | — | WO | disclosed |
| WO-1996040666-A1 | PACLITAXEL SYNTHESIS FROM PRECURSOR COMPOUNDS AND METHODS OF PRODUCING THE SAME | NAPRO BIOTHERAPEUTICS, INC. (US) | 1996-12-19 | — | — | WO | disclosed |
| WO-1996040624-A1 | C-2' HYDROXYL-BENZYL PROTECTED, N-CARBAMATE PROTECTED (2R,3S)-3-PHENYLISOSERINE AND PRODUCTION PROCESS THEREFOR | NAPRO BIOTHERAPEUTICS, INC. (US) | 1996-12-19 | — | — | WO | disclosed |