Predicted protein targets (top 14)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 1/20 | 0.60 |
| ▸ | CXCR3 | P49682 | 1/20 | 0.42 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.42 |
| ▸ | IGF1R | P08069 | 8/20 | 0.41 |
| ▸ | PGR | P06401 | 1/20 | 0.41 |
| ▸ | HMOX1 | P09601 | 1/20 | 0.41 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.41 |
| ▸ | SLC6A4 | P31645 | 1/20 | 0.41 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.41 |
| ▸ | MEN1 | O00255 | 1/20 | 0.40 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.40 |
| ▸ | GAA | P10253 | 1/20 | 0.40 |
| ▸ | SLC18A3 | Q16572 | 1/20 | 0.39 |
| ▸ | HTR2A | P28223 | 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 | |
|---|---|---|---|---|
| SCHEMBL16479573 | 1.00 | LMNA (0.60) | LMNACXCR3CYP1A2IGF1RPGR | |
| SCHEMBL1607138 | 0.87 | LMNA (0.75) | LMNACYP1A2PGRSLC6A2SLC6A3 | |
| SCHEMBL20639920 | 0.84 | IGF1R (0.61) | LMNAIGF1RMEN1KMT2A | |
| SCHEMBL6111588 | 0.82 | KMT2A (0.41) | LMNACXCR3CYP1A2IGF1RHMOX1 | |
| SCHEMBL8077200 | 0.81 | IGF1R (0.41) | LMNACXCR3CYP1A2IGF1RHMOX1 | |
| SCHEMBL6686061 | 0.80 | KDM4E (0.42) | LMNACXCR3CYP1A2IGF1RHMOX1 | |
| SCHEMBL241160 | 0.80 | IGF1R (0.43) | CXCR3CYP1A2IGF1RHMOX1MEN1 | |
| SCHEMBL1986354 | 0.80 | IGF1R (0.43) | CXCR3CYP1A2IGF1RHMOX1MEN1 | |
| SCHEMBL2368070 | 0.80 | IGF1R (0.43) | CXCR3CYP1A2IGF1RHMOX1MEN1 | |
| SCHEMBL29861210 | 0.80 | LMNA (0.65) | LMNACYP1A2PGRSLC6A2SLC6A3 |
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 48 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116574033-A | Phenylalanine derivative containing alkynyl and benzophenone groups and synthesis method | 中国人民解放军军事科学院防化研究院 | 2023-08-11 | — | — | CN | claimed |
| CN-115074138-B | Liquid crystal composition and liquid crystal display device | 达兴材料股份有限公司 | 2024-11-19 | — | — | CN | disclosed |
| CN-118955244-A | Method for preparing primary alcohol by homogeneously catalyzing and reducing carboxylic acid derivative by using N-heterocyclic carbene copper complex | 延安大学 | 2024-11-15 | — | — | CN | disclosed |
| CN-118598898-A | Synthetic method of non-natural alpha-amino acid derivative | 华中科技大学 | 2024-09-06 | — | — | CN | disclosed |
| CN-118344244-A | Preparation method of deuterated compound based on alkyl alcohol | 大连理工大学 | 2024-07-16 | — | — | CN | disclosed |
| WO-2024067560-A1 | SULFONAMIDE COMPOUND AND MEDICAL USE THEREOF | 中国药科大学 | 2024-04-04 | — | — | WO | disclosed |
| CN-117682973-A | Sulfonamide compound and medical application thereof | 中国药科大学 | 2024-03-12 | — | — | CN | disclosed |
| CN-117682967-A | Inhibitor for targeting c-Myc and application thereof | 四川大学 | 2024-03-12 | — | — | CN | disclosed |
| CN-115215762-B | Method for synthesizing aliphatic nitrile from alcohol | 陕西师范大学 | 2024-02-02 | — | — | CN | disclosed |
| CN-115066423-B | PD-L1 antagonist compounds | 厦门宝太生物科技股份有限公司 | 2024-02-02 | — | — | CN | disclosed |
| WO-2009128559-A1 | [1]BENZOTHIENO[3,2-B][1]BENZOTHIOPHENE COMPOUND AND METHOD FOR PRODUCING THE SAME, AND ORGANIC ELECTRONIC DEVICE USING THE SAME | RICOH COMPANY, LTD. (JP) | 2009-10-22 | — | — | WO | disclosed |
| US-7534547-B2 | Optically active compound and photosensitive resin composition | OSAKA GAS COMPANY LIMITED (JP) | 2009-05-19 | — | — | US | disclosed |
| EP-0985649-B1 | Method for producing an aromatic compound having an alkyl group with at least three carbon atoms | TORAY INDUSTRIES (JP) | 2004-11-24 | — | — | EP | disclosed |
| US-6462248-B1 | THROUGH CONVERSION, ISOMERIZATION AND/OR ADSORPTIVE SEPARATION OF AROMATIC COMPOUNDS | TORAY INDUSTRIES, INC. (JP) | 2002-10-08 | — | — | US | disclosed |
| EP-1107944-A1 | AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA 3 ADRENERGIC AGONISTS | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 2001-06-20 | — | — | EP | disclosed |
| EP-0985649-A2 | Method for producing an aromatic compound having an alkyl group with at least three carbon atoms | TORAY INDUSTRIES, INC. (JP) | 2000-03-15 | — | — | EP | disclosed |
| WO-2000012462-A1 | AMINOALCOHOL DERIVATIVES AND THEIR USE AS BETA 3 ADRENERGIC AGONISTS | FUJISAWA PHARMACEUTICAL CO., LTD. (JP) | 2000-03-09 | — | — | WO | disclosed |
| EP-0354655-B1 | 1-PHENYL-1-PROPANOL DERIVATIVES | CHISSO CORPORATION (JP) | 1993-04-07 | — | — | EP | disclosed |
| US-5076947-A | Optically active; free from temperature dependence | CHISSO CORPORATION (JP) | 1991-12-31 | — | — | US | disclosed |
| EP-0354655-A2 | 1-Phenyl-1-propanol derivatives | CHISSO CORPORATION (JP) | 1990-02-14 | — | — | EP | disclosed |