SCHEMBL2540652

SCHEMBL2540652

N[CH]Oc1ccccc1

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
SCHEMBL2818333 0.75 LTA4H (0.50)
SCHEMBL2818335 0.75 LTA4H (0.50)
SCHEMBL6606014 0.75 LTA4H (0.50)
SCHEMBL16782647 0.75 LTA4H (0.50)
SCHEMBL29940586 0.74 LTA4H (0.43)
SCHEMBL28369275 0.73 LTA4H (0.47)
SCHEMBL10637539 0.72 MEN1 (0.50)
Formic Acid Phenyl Ester SCHEMBL2662 0.71
SCHEMBL11541783 0.71 LTA4H (0.45)
SCHEMBL35471 0.71

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-1031788-A None JP disclosed
CN-102812099-B Liquid adhesive for electronic parts and adhesive tape TOMOEGAWA CO LTD 2014-12-03 CN disclosed
CN-103360973-A Masking sheet for manufacture of semiconductor device and method for manufacturing semiconductor device TOMOEGAWA PAPER CO LTD 2013-10-23 CN disclosed
CN-102812099-A Liquid adhesive for electronic parts and adhesive tape TOMOEGAWA CO LTD 2012-12-05 CN disclosed
US-8178273-B2 High density, durability; charging characteristics; dissolving coating in solution of supercritical and subcritical fluids; depositing on substrate by controlling pressure and/or temperature to reduce solubility RICOH COMPANY, LTD. (JP) 2012-05-15 US disclosed
US-8043785-B2 Coating material in carbon dioxide in liquid state, and forming coating layer on core material surface by reducing the solubility of the liquid RICOH COMPANY, LTD. (JP) 2011-10-25 US disclosed
US-20080138734-A1 CARRIER, METHOD FOR PRODUCING THE SAME, DEVELOPER, AND IMAGE FORMING METHOD RICOH COMPANY, LTD. (JP) 2008-06-12 US disclosed
US-20080063972-A1 CARRIER AND MANUFACTURING METHOD THEREOF, DEVELOPER, PROCESS CARTRIDGE, IMAGE FORMING APPARATUS, AND IMAGE FORMING METHOD RICOH COMPANY, LTD. (JP) 2008-03-13 US disclosed
WO-2008013987-A2 N-ALKYL SUBSTITUTED PIPERAZINYLMETHYLQUINAZOLINONES AND AZEPANYLMETHYLQUINAZOLINONES PROLEXYS PHARMACEUTICALS, INC. (US) 2008-01-31 WO disclosed
US-6057336-A ANTIINFLAMMATORY AGENTS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2000-05-02 US disclosed
CN-1020391-C FUNGICIDES PREPARING PROCESS ICI PLC (GB) 1993-05-05 CN disclosed
CN-1030749-A The method for preparing Fungicidal compounds ICI PLC (GB) 1989-02-01 CN disclosed
EP-0101602-B1 DERIVATIVES OF 7-OXO-4-OXA-DIAZABICYCLO-(3.2.0)-HEPT-2-EN NOT SUBSTITUTED IN POSITION 6, PROCESSES FOR THEIR PREPARATION AND THEIR USE AS INTERMEDIATES IN THE SYNTHESIS OF BETA-LACTAM ANTIBIOTICS BAYER AG (DE) 1988-06-01 EP disclosed
US-4616084-A Process for the preparation of 7-acylamino-3-hydroxy-cephem-4-carboxylic acids and 7-acylamino-3-hydroxy-1-dethia-1-oxacephem-4-carboxylic acids BAYER AKTIENGESELLSCHAFT (DE) 1986-10-07 US disclosed
US-4564473-A BETA-LACTAM ANTIBIOTIC INTERMEDIATES BAYER AKTIENGESELLSCHAFT (DE) 1986-01-14 US disclosed
EP-0133670-A2 Process for the preparation of 7-acylamino-3-hydroxy-cephem-4-carboxylic acids and 7-acylamino-3-hydroxy-1-dethia-1-oxacephem-4-carboxylic acids BAYER AG (DE) 1985-03-06 EP disclosed