Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | PNMT | P11086 | 1/20 | 0.58 |
| ▸ | HTR2B | P41595 | 3/20 | 0.48 |
| ▸ | HTR7 | P34969 | 2/20 | 0.48 |
| ▸ | NPC1 | O15118 | 2/20 | 0.44 |
| ▸ | RAB9A | P51151 | 2/20 | 0.44 |
| ▸ | DRD2 | P14416 | 3/20 | 0.40 |
| ▸ | DRD4 | P21917 | 2/20 | 0.40 |
| ▸ | DRD3 | P35462 | 2/20 | 0.40 |
| ▸ | ADRA1D | P25100 | 1/20 | 0.40 |
| ▸ | HTR2A | P28223 | 1/20 | 0.40 |
| ▸ | HTR2C | P28335 | 1/20 | 0.40 |
| ▸ | ADRA1A | P35348 | 1/20 | 0.40 |
| ▸ | ADRA1B | P35368 | 1/20 | 0.40 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.36 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.36 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.36 |
| ▸ | MEN1 | O00255 | 1/20 | 0.36 |
| ▸ | MAPT | P10636 | 1/20 | 0.36 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.36 |
| ▸ | GABRP | O00591 | 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 | |
|---|---|---|---|---|
| SCHEMBL29892750 | 1.00 | PNMT (0.58) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL17456835 | 0.89 | PNMT (0.52) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL4816545 | 0.88 | PNMT (0.54) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL1830397 | 0.88 | PNMT (0.57) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL1830400 | 0.87 | PNMT (0.55) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL8671794 | 0.87 | PNMT (0.55) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL7036967 | 0.86 | PNMT (0.55) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL8473291 | 0.85 | PNMT (0.54) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL896998 | 0.85 | PNMT (0.54) | PNMTHTR2BHTR7NPC1RAB9A | |
| SCHEMBL6502789 | 0.85 | PNMT (0.54) | PNMTHTR2BHTR7NPC1RAB9A |
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 859 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122011253-A | Sieber resin and preparation method and application thereof | 江苏海普功能材料有限公司 | 2026-05-12 | — | — | CN | claimed |
| CN-118271502-A | Preparation method of dormant low molecular weight amino-terminated fluorine-containing polymer | 沈阳化工大学 | 2024-07-02 | — | — | CN | claimed |
| CN-115650827-B | Preparation method, intermediate compound and synthesis method for anthracycline derivatives | 戊言医药科技（上海）有限公司 | 2024-03-15 | — | — | CN | claimed |
| CN-116947919-A | Fmoc-benzhydrylamine derivatives for synthesis of carbon-terminal amidated polypeptides and method for preparing same | 山西医科大学 | 2023-10-27 | — | — | CN | claimed |
| CN-115650827-A | Preparation method, intermediate compound and synthesis method for anthracycline derivatives | 戊言医药科技（上海）有限公司 | 2023-01-31 | — | — | CN | claimed |
| CN-115651043-A | Preparation method of anthracycline derivative | 戊言医药科技（上海）有限公司 | 2023-01-31 | — | — | CN | claimed |
| CN-114853822-A | Oligonucleotide-disulfide and synthetic method thereof | 康龙化成(宁波)科技发展有限公司 | 2022-08-05 | — | — | CN | claimed |
| CN-114057713-A | Method for synthesizing (R) -salmeterol intermediate | 广东莱佛士制药技术有限公司 | 2022-02-18 | — | — | CN | claimed |
| CN-108070009-B | Method for preparing DNA coding compound library and initial fragment compound and prepared DNA coding compound | 上海药明康德新药开发有限公司 | 2021-04-13 | — | — | CN | claimed |
| CN-112062693-A | Synthetic method of 2- (9H-fluorene-9-methoxycarbonylamino) -3-methyl-2-butenoic acid | 上海吉奉生物科技有限公司 | 2020-12-11 | — | — | CN | claimed |
| WO-1999002532-A2 | PARTIALLY HYDROGENATED POLYCYCLIC COMPOUNDS | NOVARTIS AG (CH) | 1999-01-21 | — | — | WO | claimed |
| US-5859190-A | SOLID PHASE SYNTHESIS TO FORM A PROTECTED DIPEPTIDE FOLLOWED BY REACTING WITH 1,1'-THIOCARBONYLDIIMIDAZOLE TO EFFECT RING FORMATION; EFFICIENCY; ANTICONVULSANT,-ARRHYTHMIC AND DIABETIC AGENTS; HERBICIDES AND FUNGICIDES | TREGA BIOSCIENCES, INC. (US) | 1999-01-12 | — | — | US | claimed |
| WO-1998033776-A1 | COMBINATORIAL LIBRARIES OF HYDANTOIN AND THIOHYDANTOIN DERIVATIVES, METHODS OF MAKING THE LIBRARIES AND COMPOUNDS THEREIN | TREGA BIOSCIENCES, INC. (US) | 1998-08-06 | — | — | WO | claimed |
| US-5684128-A | DEHYDRATION, REDUCTION AND ETHERIFICATION THEN DEACYLATION TO FORM AMINO GROUPS ON CYCLIC OLIGOPEPTIDES | MERCK & CO., INC. (US) | 1997-11-04 | — | — | US | claimed |
| EP-0261283-B2 | Amino-derivatized phosphite and phosphate linking agents, phosphoramidite precursors and useful conjugates thereof | APPLIED BIOSYSTEMS (US) | 1995-04-19 | — | — | EP | claimed |
| US-5258538-A | 2,3-disubstituted-1,3,2-oxazaphosphacycloalkanes as nucleic acid linking agents | APPLIED BIOSYSTEMS, INC. (US) | 1993-11-02 | — | — | US | claimed |
| US-5212304-A | Amino-derivatized phosphoramidite linking agents | APPLIED BIOSYSTEMS, INC. (US) | 1993-05-18 | — | — | US | claimed |
| US-4757141-A | Amino-derivatized phosphite and phosphate linking agents, phosphoramidite precursors, and useful conjugates thereof | APPLIED BIOSYSTEMS, INCORPORATED (US) | 1988-07-12 | — | — | US | claimed |
| EP-0261283-A1 | Amino-derivatized phosphite and phosphate linking agents, phosphoramidite precursors and useful conjugates thereof | APPLIED BIOSYSTEMS, INC. (US) | 1988-03-30 | — | — | EP | claimed |
| WO-1988002004-A1 | AMINO-DERIVATIZED PHOSPHITE AND PHOSPHATE LINKING AGENTS, PHOSPHORAMIDITE PRECURSORS, AND USEFUL CONJUGATES | APPLIED BIOSYSTEMS, INC. (US) | 1988-03-24 | — | — | WO | claimed |