SCHEMBL325503

SCHEMBL325503

O=C(O)C1=CC1

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
SCHEMBL1353356 0.97 TSHR (0.42) —
SCHEMBL1046193 0.78 — —
SCHEMBL25404850 0.76 — —
SCHEMBL22290 0.73 — —
SCHEMBL17503288 0.73 — —
SCHEMBL11498473 0.72 TSHR (0.45) —
SCHEMBL18733146 0.72 ABAT (0.40) —
SCHEMBL1286825 0.72 TSHR (0.40) —
SCHEMBL11674817 0.71 TSHR (0.50) —
SCHEMBL11674811 0.71 TSHR (0.50) —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110938201-B Comb-shaped bio-based polycarbonate phase-change material and preparation method thereof 河北工业大学 2022-02-08 — — CN claimed
CN-110938201-A Comb-shaped bio-based polycarbonate phase-change material and preparation method thereof 河北工业大学 2020-03-31 — — CN claimed
EP-2699606-B1 POLYMERS FUNCTIONALIZED WITH A CARBOXYLIC OR THIOCARBOXYLIC ESTER CONTAINING A SILYLATED AMINO GROUP BRIDGESTONE CORP (JP) 2016-09-28 — — EP claimed
WO-2016119848-A1 METHOD FOR THE PREPARATION OF CYCLOALIPHATIC EPOXY RESINS HENKEL AG & CO. KGAA (DE) 2016-08-04 — — WO claimed
EP-2699606-A2 POLYMERS FUNCTIONALIZED WITH A CARBOXYLIC OR THIOCARBOXYLIC ESTER CONTAINING A SILYLATED AMINO GROUP Bridgestone Corporation (JP) 2014-02-26 — — EP claimed
EP-2483317-B1 FUNCTIONALIZED POLYMERS AND METHODS FOR THEIR MANUFACTURE BRIDGESTONE CORP (JP) 2014-02-26 — — EP claimed
US-20140018500-A1 Polymers Functionalized With A Carboxylic Or Thiocarboxylic Ester Containing A Silylated Amino Group BRIDGESTONE CORPORATION (JP) 2014-01-16 — — US claimed
WO-2012135451-A2 POLYMERS FUNCTIONALIZED WITH A CARBOXYLIC OR THIOCARBOXYLIC ESTER CONTAINING A SILYLATED AMINO GROUP BRIDGESTONE CORPORATION (JP) 2012-10-04 — — WO claimed
EP-2483317-A1 FUNCTIONALIZED POLYMERS AND METHODS FOR THEIR MANUFACTURE Bridgestone Corporation (JP) 2012-08-08 — — EP claimed
US-20120184677-A1 FUNCTIONALIZED POLYMERS AND METHODS FOR THEIR MANUFACTURE BRIDGESTONE CORPORATION (JP) 2012-07-19 — — US claimed
WO-2011041534-A1 FUNCTIONALIZED POLYMERS AND METHODS FOR THEIR MANUFACTURE BRIDGESTONE CORPORATION (JP) 2011-04-07 — — WO claimed
US-20110077325-A1 FUNCTIONALIZED POLYMERS AND METHODS FOR THEIR MANUFACTURE BRIDGESTONE CORPORATION (JP) 2011-03-31 — — US claimed
US-4299973-A Alkyl 3,3-dimethyl-2-(2-hydroxy-2-methyl-propyl)-1-cyclopropene-1-carboxylates ROUSSEL UCLAF (FR) 1981-11-10 — — US claimed
JP-1247036-A — — None — — JP disclosed
JP-8073400-A — — None — — JP disclosed
US-12516139-B2 Resin composition, resin sheet, multilayer printed wiring board, and semiconductor device MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2026-01-06 — — US disclosed
US-4410721-A Process for the preparation of cyclopropene intermediates ROUSSEL UCLAF (FR) 1983-10-18 — — US disclosed
US-4299973-A Alkyl 3,3-dimethyl-2-(2-hydroxy-2-methyl-propyl)-1-cyclopropene-1-carboxylates ROUSSEL UCLAF (FR) 1981-11-10 — — US disclosed
US-4299973-A Alkyl 3,3-dimethyl-2-(2-hydroxy-2-methyl-propyl)-1-cyclopropene-1-carboxylates ROUSSEL UCLAF (FR) 1981-11-10 — — US disclosed
US-4031239-A Cyclopropanecarboxylates for systemic control of ectoparasites AMERICAN CYANAMID COMPANY (US) 1977-06-21 — — US disclosed
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