SCHEMBL1153789

SCHEMBL1153789

COC(CCC=O)OC

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
Alcohol SCHEMBL27389623 0.91 ALDH1A1 (0.36)
SCHEMBL198865 0.84 HIF1A (0.43)
SCHEMBL1367335 0.82 TSHR (0.42)
SCHEMBL1008818 0.80 TSHR (0.46)
SCHEMBL4016773 0.80 TSHR (0.46)
SCHEMBL2494420 0.80 TSHR (0.46)
SCHEMBL3187642 0.79 HIF1A (0.32)
SCHEMBL3187653 0.79 HIF1A (0.32)
SCHEMBL2276292 0.76
SCHEMBL5014072 0.76

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 137 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109912519-A A kind of synthetic method of Su Woleisheng intermediate 成都美域高制药有限公司 2019-06-21 CN claimed
CN-103274984-B A kind of preparation method of 5-methyl-pyrrol-2 Ethyl formate 四川铂瑞生物医药有限公司 2016-08-24 CN claimed
CN-103540312-B Rhodamine fluorescent probe with pseudonucleobase as recognition site, preparation thereof and application thereof in nucleotide image DALIAN UNIVERSITY OF TECHNOLOGY (CN) 2015-11-18 CN claimed
CN-103540312-A Rhodamine fluorescent probe with pseudonucleobase as recognition site, preparation thereof and application thereof in nucleotide image UNIV DALIAN TECH 2014-01-29 CN claimed
CN-103274984-A Preparation method of ethyl 5-methyl-pyrrol-2 formate SICHUAN BERARE BIOLOG MEDICAL CO LTD 2013-09-04 CN claimed
CN-102010311-A Method for synthesizing 4,4-dimethoxy-2-butanone UNIV SOUTHEAST 2011-04-13 CN claimed
CN-1973006-B Single-component system based on co-reactive latex, preparation method and use in the field of formol-free coatings ARKEMA 2010-11-10 CN claimed
EP-1778804-B1 SINGLE-COMPONENT SYSTEM BASED ON CO-REACTIVE LATEX, PREPARATION METHOD AND USE IN THE FIELD OF FORMOL-FREE COATINGS ARKEMA FRANCE (FR) 2010-01-20 EP claimed
US-20080028982-A1 Single-Component System Based On Co-Reactive Latex, Preparation Method And Use In The Field Of Formol-Free Coatings VERGE CHRISTOPHE 2008-02-07 US claimed
CN-1973006-A Single-component system based on co-reactive latex, preparation method and use in the field of formol-free coatings ARKEMA (FR) 2007-05-30 CN claimed
EP-1778804-A1 SINGLE-COMPONENT SYSTEM BASED ON CO-REACTIVE LATEX, PREPARATION METHOD AND USE IN THE FIELD OF FORMOL-FREE COATINGS Arkema France (FR) 2007-05-02 EP claimed
WO-2006010804-A1 SINGLE-COMPONENT SYSTEM BASED ON CO-REACTIVE LATEX, PREPARATION METHOD AND USE IN THE FIELD OF FORMOL-FREE COATINGS ARKEMA FRANCE (FR) 2006-02-02 WO claimed
EP-0318845-B1 METHOD FOR THE PREPARATION OF SUBSTITUTED PYRIDINES BASF Aktiengesellschaft (DE) 1992-09-16 EP claimed
US-4680420-A Process for the producing 2,5-dimethoxytetrahydrofuran and 2,5-diethoxytetrahydrofuran DEGUSSA AKTIENGESELLSCHAFT (DE) 1987-07-14 US claimed
EP-3151920-B1 USE OF INHIBITOR OF APOPTOSIS PROTEIN (IAP) ANTAGONISTS IN HIV THERAPY SANFORD BURNHAM MED RES INST (US) 2025-08-06 EP disclosed
US-20240368159-A1 HPK1 DEGRADERS, COMPOSITIONS COMPRISING THE HPK1 DEGRADER, AND METHODS OF USING THE SAME BIOFRONT LTD (KY) 2024-11-07 US disclosed
EP-4392420-A1 HPK1 DEGRADERS, COMPOSITIONS THEREOF, AND METHODS OF USING THE SAME BIOFRONT LTD (KY) 2024-07-03 EP disclosed
US-4608443-A Method for the preparation of 1,4-butandial DEGUSSA AKTIENGESELLSCHAFT (DE) 1986-08-26 US disclosed
EP-0151241-A1 Process for the preparation of 1,4-butane-dialdehyde Degussa Aktiengesellschaft (DE) 1985-08-14 EP disclosed
US-4044026-A PERFUMES BASF AKTIENGESELLSCHAFT (DT) 1977-08-23 US disclosed