⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| Methyl Alcohol SCHEMBL1169280 | 0.97 | ALDH1A1 (0.52) | — | |
| SCHEMBL1191256 | 0.83 | ALDH1A1 (0.63) | — | |
| SCHEMBL96642 | 0.82 | — | — | |
| SCHEMBL1049266 | 0.80 | ALDH1A1 (0.61) | — | |
| Tradecamide SCHEMBL9157947 | 0.78 | ALDH1A1 (0.58) | — | |
| SCHEMBL9162411 | 0.78 | ALDH1A1 (0.58) | — | |
| SCHEMBL9432308 | 0.78 | ALDH1A1 (0.58) | — | |
| SCHEMBL9162783 | 0.78 | ALDH1A1 (0.58) | — | |
| SCHEMBL9353528 | 0.78 | ALDH1A1 (0.58) | — | |
| SCHEMBL9353551 | 0.78 | ALDH1A1 (0.58) | — |
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 449 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2024141444-A1 | NEW BENZIMIDAZOLE DERIVATIVES | F. HOFFMANN-LA ROCHE AG (CH) | 2024-07-04 | — | — | WO | claimed |
| CN-117964512-B | Synthesis method of N, N-dimethyl-3-methoxy propionamide | 山东惟普控股有限公司 | 2024-06-04 | — | — | CN | claimed |
| CN-117964512-A | Synthesis method of N, N-dimethyl-3-methoxy propionamide | 山东惟普控股有限公司 | 2024-05-03 | — | — | CN | claimed |
| CN-113710664-B | JAK1 selective kinase inhibitors | 迪哲(江苏)医药股份有限公司 | 2024-01-26 | — | — | CN | claimed |
| CN-113710664-A | JAK1 selective kinase inhibitors | 迪哲(江苏)医药股份有限公司 | 2021-11-26 | — | — | CN | claimed |
| CN-110540540-B | Method for preparing dihydro [1, 2, 4] triazolo [1, 5-a ] pyrimidine derivatives through catalysis | 马鞍山市泰博化工科技有限公司 | 2021-02-02 | — | — | CN | claimed |
| CN-110028518-B | Method for preparing medical intermediate pyrano [2, 3-d ] pyrimidone derivative through catalysis | 马鞍山市泰博化工科技有限公司 | 2020-07-14 | — | — | CN | claimed |
| CN-110540540-A | method for preparing dihydro [1, 2, 4] triazolo [1, 5-a ] pyrimidine derivatives through catalysis | MAANSHAN TAIBO CHEMICAL TECH CO LTD | 2019-12-06 | — | — | CN | claimed |
| CN-107129435-B | A method of preparing 2-amino-2-methyl-1-propanol | 万华化学集团股份有限公司 | 2019-07-23 | — | — | CN | claimed |
| CN-105837568-A | Fluorenyl-[beta]-carboline compound, application thereof as organic light-emitting material and aggregation-induced emission enhancement material, and preparation method of the compound | 中国广州分析测试中心 | 2016-08-10 | — | — | CN | claimed |
| US-20060089262-A1 | Substituted (thioxo)carbonylamino phenyl uraciles | BAYER CROPSCIENCE AG (DE) | 2006-04-27 | — | — | US | claimed |
| US-6992044-B1 | Substituted phenyluracils | BAYER CROPSCIENCE AG (DE) | 2006-01-31 | — | — | US | claimed |
| WO-2005026150-A1 | QUINAZOLINE DERIVATIVES AS TYROSINE KINASE INHIBITORS | ASTRAZENECA AB (SE) | 2005-03-24 | — | — | WO | claimed |
| EP-1503994-A1 | SUBSTITUTED (THIOXO)CARBONYLAMINO PHENYL URACILES | Bayer CropScience AG (DE) | 2005-02-09 | — | — | EP | claimed |
| EP-1383779-B1 | A PROCESS FOR MANUFACTURE OF FOSINOPRIL SODIUM | LUPIN LAB LTD (IN) | 2004-10-13 | — | — | EP | claimed |
| WO-2003093244-A1 | SUBSTITUTED (THIOXO)CARBONYLAMINO PHENYL URACILES | BAYER CROPSCIENCE AG (DE) | 2003-11-13 | — | — | WO | claimed |
| EP-1272478-A1 | SUBSTITUTED PHENYLURACILS | Bayer Aktiengesellschaft (DE) | 2003-01-08 | — | — | EP | claimed |
| WO-2001077084-A1 | SUBSTITUTED PHENYLURACILS | BAYER CROPSCIENCE AG (DE) | 2001-10-18 | — | — | WO | claimed |
| EP-0832082-A1 | N-HETEROARYL-PYRIDINESULFONAMIDE DERIVATIVES AND THEIR USE AS ENDOTHELIN ANTAGONISTS | ZENECA LIMITED (GB) | 1998-04-01 | — | — | EP | claimed |
| WO-1996040681-A1 | N-HETEROARYL-PYRIDINESULFONAMIDE DERIVATIVES AND THEIR USE AS ENDOTHELIN ANTAGONISTS | ZENECA LIMITED (GB) | 1996-12-19 | — | — | WO | claimed |