Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | NPC1 | O15118 | 4/20 | 0.59 |
| ▸ | SMN1; SMN2 | Q16637 | 3/20 | 0.59 |
| ▸ | L3MBTL1 | Q9Y468 | 3/20 | 0.59 |
| ▸ | RAB9A | P51151 | 3/20 | 0.59 |
| ▸ | PKM | P14618 | 2/20 | 0.59 |
| ▸ | MITF | O75030 | 1/20 | 0.59 |
| ▸ | GAA | P10253 | 1/20 | 0.59 |
| ▸ | KDM4E | B2RXH2 | 6/20 | 0.56 |
| ▸ | LMNA | P02545 | 3/20 | 0.56 |
| ▸ | CYP1A2 | P05177 | 3/20 | 0.56 |
| ▸ | CCR1 | P32246 | 2/20 | 0.56 |
| ▸ | CCR5 | P51681 | 2/20 | 0.56 |
| ▸ | CCR8 | P51685 | 2/20 | 0.56 |
| ▸ | POLB | P06746 | 1/20 | 0.56 |
| ▸ | METAP1 | P53582 | 1/20 | 0.56 |
| ▸ | BLM | P54132 | 1/20 | 0.56 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.56 |
| ▸ | DOHH | Q9BU89 | 1/20 | 0.56 |
| ▸ | P4HTM | Q9NXG6 | 1/20 | 0.56 |
| ▸ | TGFBR1 | P36897 | 1/20 | 0.53 |
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 | |
|---|---|---|---|---|
| SCHEMBL30229669 | 1.00 | NPC1 (0.59) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| SCHEMBL30427456 | 1.00 | NPC1 (0.59) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| SCHEMBL3714209 | 0.98 | NPC1 (0.57) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| SCHEMBL21742496 | 0.91 | NPC1 (0.56) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| Acetamide SCHEMBL5077465 | 0.87 | NPC1 (0.49) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| SCHEMBL28963427 | 0.87 | KDM4E (0.52) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| SCHEMBL12731340 | 0.86 | KDM4E (0.67) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| SCHEMBL17532979 | 0.86 | TGFBR1 (0.57) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| SCHEMBL13834140 | 0.86 | TGFBR1 (0.53) | NPC1SMN1; SMN2L3MBTL1RAB9APKM | |
| SCHEMBL16526771 | 0.86 | TGFBR1 (0.50) | NPC1SMN1; SMN2L3MBTL1RAB9APKM |
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 983 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118813261-A | Silicon nitride etching solution suitable for deep trench etching | 湖北兴福电子材料股份有限公司 | 2024-10-22 | — | — | CN | claimed |
| CN-117003199-A | Dehydrogenation method and hydrogen production system using same | 现代自动车株式会社 | 2023-11-07 | — | — | CN | claimed |
| US-20230348266-A1 | DEHYDROGENATION METHOD AND HYDROGEN PRODUCTION SYSTEM USING THE SAME | HYUNDAI MOTOR COMPANY (KR) | 2023-11-02 | — | — | US | claimed |
| CN-115584142-B | Cyanine dye with red luminous ring structure and synthesis method thereof | 三峡大学 | 2023-07-11 | — | — | CN | claimed |
| CN-115989190-A | Liquid formulations for hydrogen storage | 阿科玛法国公司 | 2023-04-18 | — | — | CN | claimed |
| CN-115835916-A | Purification of aromatic liquids | 阿科玛法国公司 | 2023-03-21 | — | — | CN | claimed |
| CN-115768717-A | Process for improving the quality of organic liquids with hydrogen | 阿科玛法国公司 | 2023-03-07 | — | — | CN | claimed |
| CN-115715272-A | Liquid formulations for hydrogen storage | 阿科玛法国公司 | 2023-02-24 | — | — | CN | claimed |
| CN-109148796-B | Acid scavenging functional diaphragm for lithium ion electrochemical cell functional performance | 通用汽车环球科技运作有限责任公司 | 2022-01-25 | — | — | CN | claimed |
| EP-2278637-B2 | Complexes of form L2MX | UNIV PRINCETON (US) | 2021-06-09 | — | — | EP | claimed |
| CN-1413426-A | Complexes in the form of phosphorescent dopants L2MX as organic light-emitting devices | UNIV PRINCETON (US) | 2003-04-23 | — | — | CN | claimed |
| EP-1252803-A4 | COMPLEXES OF FORM L 2?MX AS PHOSPHORESCENT DOPANTS FOR ORGANIC LEDS | UNIV PRINCETON (US) | 2003-04-16 | — | — | EP | claimed |
| US-20030017361-A1 | Organometallic complexes as phosphorescent emitters in organic LEDs | THOMPSON MARK E (US) | 2003-01-23 | — | — | US | claimed |
| EP-1252803-A1 | COMPLEXES OF FORM L 2?MX AS PHOSPHORESCENT DOPANTS FOR ORGANIC LEDS | THE TRUSTEES OF PRINCETON UNIVERSITY (US) | 2002-10-30 | — | — | EP | claimed |
| US-20020034656-A1 | Organometallic complexes as phosphorescent emitters in organic LEDs | THE UNIVERSITY OF SOUTHERN CALIFORNIA | 2002-03-21 | — | — | US | claimed |
| US-6337305-B1 | HERBICIDES FOR AGRICULTURE | BASF AKTIENGESELLSCHAFT (DE) | 2002-01-08 | — | — | US | claimed |
| WO-2001041512-A1 | COMPLEXES OF FORM L2MX AS PHOSPHORESCENT DOPANTS FOR ORGANIC LEDS | THE TRUSTEES OF PRINCETON UNIVERSITY (US) | 2001-06-07 | — | — | WO | claimed |
| WO-1998033786-A1 | ACCELERATED CATALYSIS OF OLEFINIC EPOXIDATIONS | THE SCRIPPS RESEARCH INSTITUTE (US) | 1998-08-06 | — | — | WO | claimed |
| US-5763645-A | ADSORPTION, CONCENTRATION, DESORPTION, ELUENT RECOVERY | DAICEL CHEMICAL INDUSTRIES, LTD. (JP) | 1998-06-09 | — | — | US | claimed |
| US-5498752-A | Process for recovering optical isomers and solvent, process for using solvent by circulation and process for reusing optical isomers in optical resolution | DAICEL CHEMICAL INDUSTRIES, LTD. (JP) | 1996-03-12 | — | — | US | claimed |