Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LIPG | Q9Y5X9 | 1/20 | 0.45 |
| ▸ | ALOX5 | P09917 | 1/20 | 0.44 |
| ▸ | PTGS2 | P35354 | 1/20 | 0.44 |
| ▸ | TYR | P14679 | 1/20 | 0.42 |
| ▸ | BID | P55957 | 3/20 | 0.42 |
| ▸ | MCL1 | Q07820 | 3/20 | 0.42 |
| ▸ | BCL2L1 | Q07817 | 2/20 | 0.42 |
| ▸ | BAK1 | Q16611 | 2/20 | 0.42 |
| ▸ | KAT8 | Q9H7Z6 | 2/20 | 0.42 |
| ▸ | PPARG | P37231 | 1/20 | 0.42 |
| ▸ | PPARA | Q07869 | 1/20 | 0.42 |
| ▸ | EP300 | Q09472 | 1/20 | 0.42 |
| ▸ | KAT2A | Q92830 | 1/20 | 0.42 |
| ▸ | KAT2B | Q92831 | 1/20 | 0.42 |
| ▸ | KAT5 | Q92993 | 1/20 | 0.42 |
| ▸ | SAE1 | Q9UBE0 | 1/20 | 0.42 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.42 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.42 |
| ▸ | CYP2C9 | P11712 | 1/20 | 0.42 |
| ▸ | KCNH2 | Q12809 | 2/20 | 0.40 |
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 | |
|---|---|---|---|---|
| Ammonia Solution, Strong SCHEMBL9810933 | 0.98 | LIPG (0.44) | LIPGALOX5PTGS2TYRBID | |
| Water SCHEMBL27341058 | 0.98 | LIPG (0.44) | LIPGALOX5PTGS2TYRBID | |
| SCHEMBL28355115 | 0.95 | LIPG (0.42) | LIPGALOX5PTGS2TYRBID | |
| SCHEMBL5425023 | 0.93 | LIPG (0.55) | LIPGALOX5PTGS2TYRBID | |
| SCHEMBL28335821 | 0.93 | LIPG (0.55) | LIPGALOX5PTGS2TYRBID | |
| SCHEMBL10918220 | 0.93 | LIPG (0.41) | LIPGALOX5PTGS2TYRBID | |
| SCHEMBL861958 | 0.93 | LIPG (0.53) | LIPGALOX5PTGS2TYRBID | |
| SCHEMBL5421151 | 0.91 | LIPG (0.57) | LIPGALOX5PTGS2TYRBID | |
| SCHEMBL11341318 | 0.91 | LIPG (0.57) | LIPGALOX5PTGS2TYRBID | |
| SCHEMBL5675055 | 0.91 | LIPG (0.57) | LIPGALOX5PTGS2TYRBID |
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 270 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-107306972-A | Thymol and combinations thereof | 中国农业科学院植物保护研究所 | 2017-11-03 | — | — | CN | claimed |
| CN-107094775-A | A kind of composition for preventing and treating agricultural disease and the spiral shell that goes out | 中国农业科学院植物保护研究所 | 2017-08-29 | — | — | CN | claimed |
| CN-105016961-B | Organo-tin compound cycle applications Stille is synthesized the method for biphenyl | 齐齐哈尔大学 | 2016-08-31 | — | — | CN | claimed |
| CN-1290974-A | Nonaqueous electrolyte solution and lithium secondary battery using same | UBE INDUSTRIES (JP) | 2001-04-11 | — | — | CN | claimed |
| US-5475108-A | Camptothecin intermediates and method of making camptothecin and comptothecin analogs | NORTH CAROLINA STATE UNIVERSITY (US) | 1995-12-12 | — | — | US | claimed |
| EP-0395360-B1 | Process for production of sec-butylbenzene | SUMITOMO CHEMICAL CO (JP) | 1994-03-16 | — | — | EP | claimed |
| US-5059736-A | Butylating benzene using liquid aluminum chloride catalyst; decreased isobutylene formation; chemical intermediate | SUMITOMO CHEMICAL CO., LTD. (JP) | 1991-10-22 | — | — | US | claimed |
| EP-0395360-A1 | Process for production of sec-butylbenzene | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1990-10-31 | — | — | EP | claimed |
| JP-3047139-A | — | — | None | — | — | JP | disclosed |
| US-12343406-B2 | Immunoreactant carrier | LEMONEX INC. (KR) | 2025-07-01 | — | — | US | disclosed |
| EP-3659585-B1 | COMPOSITION FOR DELIVERING PHYSIOLOGICALLY ACTIVE INGREDIENTS INTO BLOOD VESSEL | LEMONEX INC (KR) | 2025-06-25 | — | — | EP | disclosed |
| CN-119564881-A | Physiologically active substance carrier | 雷莫内克斯生物制药有限公司 | 2025-03-07 | — | — | CN | disclosed |
| US-12234458-B2 | Composition for inhibiting CTGF expression | LEMONEX INC. (KR) | 2025-02-25 | — | — | US | disclosed |
| US-20250032414-A1 | PHYSIOLOGICALLY ACTIVE SUBSTANCE CARRIER | LEMONEX INC. (KR) | 2025-01-30 | — | — | US | disclosed |
| EP-0356247-A1 | Analgesic carboxylic acid amide derivatives | Sankyo Company Limited (JP) | 1990-02-28 | — | — | EP | disclosed |
| US-4434246-A | Process for preparing ethylene glycol and lower monohydric alcohols from syngas using a novel catalyst system | TEXACO INC. (US) | 1984-02-28 | — | — | US | disclosed |
| US-4297508-A | BY REACTING CARBON DIOXIDE WITH B-NAPHTHOL, AN ALKALI METAL SALT OF B-NAPHTHOL, AND AN ALKYLBENZENE | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1981-10-27 | — | — | US | disclosed |
| EP-0005310-A1 | Process for preparing dialkylphosphorochloridothioates, the use of the so prepared compounds as intermediates, and the use of some of the final products as insecticides | ETHYL CORPORATION (US) | 1979-11-14 | — | — | EP | disclosed |
| US-4159289-A | FROM PHOSPHORUS PENTASULFIDE AND AN ALKANOL WITH SUBSEQUENT CHLORINATION, DISTILLATION, SOLUBILIZING SULFUR BY-PRODUCT USING HYDROCARBON | ETHYL CORPORATION (US) | 1979-06-26 | — | — | US | disclosed |
| US-4005156-A | Novel flame retardant compositions of matter | UNIVERSAL OIL PRODUCTS COMPANY (US) | 1977-01-25 | — | — | US | disclosed |