SCHEMBL4926419

SCHEMBL4926419

C=C=C1CC=CC=C1O

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
SCHEMBL2138122 0.82
SCHEMBL149795 0.69
SCHEMBL205153 0.64
SCHEMBL19030878 0.64
SCHEMBL345406 0.64
SCHEMBL27942986 0.62
SCHEMBL3287943 0.62
SCHEMBL1068225 0.62
SCHEMBL208011 0.62
SCHEMBL8154032 0.61

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3107944-B1 UV-CROSSLINKABLE POLYMER COMPOSITION TESA SE (DE) 2018-01-31 EP claimed
US-9951162-B2 UV-crosslinkable polymer composition TESA SE (DE) 2018-04-24 US disclosed
US-9951162-B2 UV-crosslinkable polymer composition TESA SE (DE) 2018-04-24 US disclosed
US-20170166671-A1 UV-CROSSLINKABLE POLYMER COMPOSITION TESA SE (DE) 2017-06-15 US disclosed
US-20170166671-A1 UV-CROSSLINKABLE POLYMER COMPOSITION TESA SE (DE) 2017-06-15 US disclosed
EP-3107944-A1 UV-CROSSLINKABLE POLYMER COMPOSITION tesa SE (DE) 2016-12-28 EP disclosed
EP-3107944-A1 UV-CROSSLINKABLE POLYMER COMPOSITION tesa SE (DE) 2016-12-28 EP disclosed
CN-106029718-A UV-crosslinkable polymer composition 德莎欧洲公司 2016-10-12 CN disclosed
WO-2015124593-A1 UV-CROSSLINKABLE POLYMER COMPOSITION TESA SE (DE) 2015-08-27 WO disclosed
WO-2015124593-A1 UV-CROSSLINKABLE POLYMER COMPOSITION TESA SE (DE) 2015-08-27 WO disclosed
US-8242162-B2 Sensor group attachec to imide of aromatictetracarboxylic dianhydride; aromatic core may be anthracene, phenanthrene, perylene, or benzo[e]pyrene; sensor groups include crown ethers, aryl amines, porphyrins, and phenylboronic acid; detecting nitroaromatic explosives and chemical warfare agents OHIO AEROSPACE INSTITUTE (US) 2012-08-14 US disclosed
US-20080242870-A1 FLUORESCENT AROMATIC SENSORS AND THEIR METHODS OF USE OHIO AEROSPACE INSTITUTE (US) 2008-10-02 US disclosed
EP-1501830-A1 7-ARYL-3,9-DIAZABICYCLO[3.3.1]NON-6-ENE DERIVATIVES AND THEIR USE AS RENIN INHIBITORS IN THE TREATMENT OF HYPERTENSION, CARDIOVASCULAR OR RENAL DISEASES Actelion Pharmaceuticals Ltd. (CH) 2005-02-02 EP disclosed
WO-2003093267-A1 7-ARYL-3,9-DIAZABICYCLO(3.3.1)NON-6-ENE DERIVATIVES AND THEIR USE AS RENIN INHIBITORS IN THE TREATMENT OF HYPERTENSION, CARDIOVASCULAR OR RENAL DISEASES ACTELION PHARMACEUTICALS LTD (CH) 2003-11-13 WO disclosed