Predicted protein targets (top 12)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | PSIP1 | O75475 | 1/20 | 0.44 |
| ▸ | HSD11B1 | P28845 | 4/20 | 0.43 |
| ▸ | CES2 | O00748 | 1/20 | 0.42 |
| ▸ | CES1 | P23141 | 1/20 | 0.42 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.40 |
| ▸ | HPGD | P15428 | 1/20 | 0.40 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.40 |
| ▸ | MEN1 | O00255 | 1/20 | 0.39 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.39 |
| ▸ | NPC1 | O15118 | 1/20 | 0.39 |
| ▸ | RAB9A | P51151 | 1/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.39 |
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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL6170808 | 0.98 | PSIP1 (0.42) | PSIP1HSD11B1CES2CES1SMN1; SMN2 | |
| SCHEMBL6751980 | 0.98 | PSIP1 (0.42) | PSIP1HSD11B1CES2CES1SMN1; SMN2 | |
| SCHEMBL6683340 | 0.90 | MEN1 (0.49) | PSIP1HSD11B1CES2CES1HPGD | |
| SCHEMBL8542959 | 0.88 | MEN1 (0.50) | CES2CES1MEN1KMT2A | |
| SCHEMBL9712116 | 0.87 | MEN1 (0.49) | CES2CES1MEN1KMT2A | |
| SCHEMBL3032957 | 0.87 | MEN1 (0.49) | CES2CES1MEN1KMT2A | |
| SCHEMBL11057714 | 0.87 | MEN1 (0.49) | CES2CES1MEN1KMT2A | |
| SCHEMBL7290861 | 0.87 | MEN1 (0.49) | CES2CES1MEN1KMT2A | |
| SCHEMBL3030933 | 0.87 | MEN1 (0.49) | CES2CES1MEN1KMT2A | |
| SCHEMBL27799463 | 0.87 | MEN1 (0.49) | CES2CES1MEN1KMT2A |
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 42 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117355153-A | Method for passivating perovskite solar cell by using phenylsulfone micromolecules | 浙江工业大学 | 2024-01-05 | — | — | CN | claimed |
| EP-1534693-A2 | 1, 3-DIAMINO-2-HYDROXYPROPANE PRODRUG DERIVATIVES | Elan Pharmaceuticals, Inc. (US) | 2005-06-01 | — | — | EP | claimed |
| WO-2004022523-A2 | 1, 3-DIAMINO-2-HYDROXYPROPANE PRODRUG DERIVATIVES | ELAN PHARMACEUTICALS, INC. (US) | 2004-03-18 | — | — | WO | claimed |
| CN-120004823-A | Sensitizer DPN and synthesis method thereof | 南京理工大学 | 2025-05-16 | — | — | CN | disclosed |
| CN-120004823-A | Sensitizer DPN and synthesis method thereof | 南京理工大学 | 2025-05-16 | — | — | CN | disclosed |
| CN-117355153-A | Method for passivating perovskite solar cell by using phenylsulfone micromolecules | 浙江工业大学 | 2024-01-05 | — | — | CN | disclosed |
| CN-116217426-A | Method for synthesizing S-fluorobutyramide from (R) -2-sulfonyl butyrate alkyl ester | 山东省农药科学研究院 | 2023-06-06 | — | — | CN | disclosed |
| CN-111116556-B | Preparation method of (R) -2- [ (4-chlorphenyl) (4-piperidinyloxy) methyl ] pyridine | 北京鑫开元医药科技有限公司 | 2021-11-02 | — | — | CN | disclosed |
| CN-111116556-A | Preparation method of (R) -2- [ (4-chlorphenyl) (4-piperidinyloxy) methyl ] pyridine | 北京鑫开元医药科技有限公司 | 2020-05-08 | — | — | CN | disclosed |
| CN-108299363-B | A kind of synthetic method of 3- benzene sulfonyl class coumarin kind compound | 青岛农业大学 | 2019-10-08 | — | — | CN | disclosed |
| CN-108299363-A | A kind of synthetic method of 3- benzene sulfonyls class coumarin kind compound | 青岛农业大学 | 2018-07-20 | — | — | CN | disclosed |
| EP-1888009-A1 | METHOD FOR PHOTOSTABILIZING A DIBENZOYLMETHANE DERIVATIVE USING A MEROCYANINE SULPHONE DERIVATIVE; PHOTOPROTECTIVE COSMETIC COMPOSITIONS CONTAINING SAID COMBINATION | L'Oréal (FR) | 2008-02-20 | — | — | EP | disclosed |
| CN-101023128-A | Stabilization of organic materials | CIBA SC HOLDING AG (CH) | 2007-08-22 | — | — | CN | disclosed |
| WO-2006125676-A1 | METHOD FOR PHOTOSTABILIZING A DIBENZOYLMETHANE DERIVATIVE USING A MEROCYANINE SULPHONE DERIVATIVE; PHOTOPROTECTIVE COSMETIC COMPOSITIONS CONTAINING SAID COMBINATION | L'OREAL (FR) | 2006-11-30 | — | — | WO | disclosed |
| EP-0438994-B1 | Process for preparing sulfonyl acids | MONSANTO CO (US) | 1995-04-19 | — | — | EP | disclosed |
| EP-0438994-A1 | Process for preparing sulfonyl acids | Monsanto Company (US) | 1991-07-31 | — | — | EP | disclosed |
| US-4966731-A | Process for preparing sulfonyl acids | MONSANTO COMPANY (US) | 1990-10-30 | — | — | US | disclosed |
| US-4705737-A | Heat developable photographic materials | FUJI PHOTO FILM CO., LTD. (JP) | 1987-11-10 | — | — | US | disclosed |
| EP-0120403-B1 | HEAT DEVELOPABLE COLOR PHOTOGRAPHIC MATERIALS | FUJI PHOTO FILM CO., LTD. (JP) | 1987-06-10 | — | — | EP | disclosed |
| EP-0120403-A2 | Heat developable color photographic materials | FUJI PHOTO FILM CO., LTD. (JP) | 1984-10-03 | — | — | EP | disclosed |