SCHEMBL425264

SCHEMBL425264

CN(C)C(=O)CCO

nearest known ligand 0.00

⚠ 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.

Compoundsimilaritytop predictedshared 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) —
SCHEMBL16945134 0.78 ALDH1A1 (0.58) —
SCHEMBL9432308 0.78 ALDH1A1 (0.58) —
SCHEMBL9162783 0.78 ALDH1A1 (0.58) —
SCHEMBL9353528 0.78 ALDH1A1 (0.58) —
SCHEMBL9162411 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.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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