SCHEMBL3676598

SCHEMBL3676598

CCCCCC(=O)ON1C(=O)c2ccccc2C1=O

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ASAH1 Q13510 1/20 0.48
ALDH1A1 P00352 4/20 0.47
POLM Q9NP87 1/20 0.46
POLK Q9UBT6 1/20 0.46
POLL Q9UGP5 1/20 0.46
POLH Q9Y253 1/20 0.46
MEN1 O00255 3/20 0.44
KMT2A Q03164 3/20 0.44
HSD17B10 Q99714 1/20 0.44
TDP1 Q9NUW8 1/20 0.43
NR1H2 P55055 1/20 0.42
NR1H3 Q13133 1/20 0.42
HPSE Q9Y251 1/20 0.42
CYP1A2 P05177 1/20 0.42
CYP2C9 P11712 1/20 0.42
CES2 O00748 1/20 0.41
CES1 P23141 1/20 0.41
MAPT P10636 1/20 0.41
GAA P10253 1/20 0.41
ALDH2 P05091 1/20 0.41

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL1537374 0.98 ASAH1 (0.50) ASAH1ALDH1A1POLMPOLKPOLL
SCHEMBL3678643 0.98 ASAH1 (0.50) ASAH1ALDH1A1POLMPOLKPOLL
SCHEMBL3678799 0.98 ASAH1 (0.50) ASAH1ALDH1A1POLMPOLKPOLL
SCHEMBL2040524 0.98 ASAH1 (0.50) ASAH1ALDH1A1POLMPOLKPOLL
SCHEMBL3678825 0.98 ASAH1 (0.50) ASAH1ALDH1A1POLMPOLKPOLL
SCHEMBL3679722 0.98 ASAH1 (0.50) ASAH1ALDH1A1POLMPOLKPOLL
SCHEMBL1537373 0.95 ALDH1A1 (0.48) ASAH1ALDH1A1POLMPOLKPOLL
SCHEMBL28693655 0.92 ALDH1A1 (0.47) ALDH1A1MEN1KMT2AHSD17B10TDP1
SCHEMBL30731584 0.90 ALDH1A1 (0.47) ALDH1A1MEN1KMT2AHSD17B10TDP1
SCHEMBL3678891 0.89 ALDH1A1 (0.50) ASAH1ALDH1A1MEN1KMT2ACYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102442703-A Preparation method of amino functionalized water-soluble manganese ferrate magnetic nanometer particles UNIV SHANGHAI 2012-05-09 CN claimed
CN-117083272-A 4-alkoxy-6-oxo-pyridazine derivatives that modulate NLRP3 詹森药业有限公司 2023-11-17 CN disclosed
CN-112746289-B Synthesis method of alkyl borate compound 合肥工业大学 2021-11-09 CN disclosed
CN-112746289-A Synthesis method of alkyl borate compound 合肥工业大学 2021-05-04 CN disclosed
CN-107074714-B Improvements in or relating to organic compounds 奇华顿股份有限公司 2020-11-06 CN disclosed
CN-102491400-B Amino-functional water-soluble gadolinium oxide nanometer sheet and preparation method and application thereof UNIV SHANGHAI 2013-12-25 CN disclosed
EP-1692253-B1 BIOCIDIC DETERGENT ECOLAB INC (US) 2013-07-24 EP disclosed
WO-2012076345-A1 COSMETIC COMPOSITION COMPRISING AN IMIDOPEROXYCARBOXYLIC ACID, AN IMIDOCARBOXYLIC ACID AND COPOLYMER OF 2-ACRYLAMIDO-2-METHYLPROPANESULPHONIC ACID L'OREAL (FR) 2012-06-14 WO disclosed
CN-102491400-A Amino-functional water-soluble gadolinium oxide nanometer sheet and preparation method and application thereof UNIV SHANGHAI 2012-06-13 CN disclosed
CN-101697303-B Preparation method of water-soluble ferroferric oxide magnetic nanoparticle with functional amidogen SHANGHAI NORMAL UNIVERSITY (CN) 2011-11-30 CN disclosed
EP-1338336-A1 CATALYSTS COMPRISING N-SUBSTITUTED CYCLIC IMIDES AND PROCESSES FOR PREPARING ORGANIC COMPOUNDS WITH THE CATALYSTS Daicel Chemical Industries, Ltd. (JP) 2003-08-27 EP disclosed
US-20030013603-A1 Catalyst comprising n-substituted cylic imides and processes for preparing organic compounds with the catalyst DAICEL CHEMICAL INDUSTRIES, LTD. (JP) 2003-01-16 US disclosed
CN-2284100-Y Microwave reaction unit INST OF MILITARY MEDICINE REAR (CN) 1998-06-17 CN disclosed
EP-0560155-B1 Process for separating phthalimidoperoxycaproic acid (PAP) from solution(s) in organic solvents AUSIMONT SPA (IT) 1996-05-08 EP disclosed
US-5487818-A EVAPORATING ORGANIC SOLVENT BY BUBBLING AN INERT GAS INTO SUSPENSION AUSIMONT S.P.A. (IT) 1996-01-30 US disclosed
EP-0556769-B1 Process for purifying phthalimidoperoxycaproic acid (PAP) which removes chlorinated solvent impurities from it AUSIMONT SPA (IT) 1995-09-13 EP disclosed
US-5310934-A Dissolving in a polar, nonvolatile solvent and crystallization AUSIMONT S.P.A. (IT) 1994-05-10 US disclosed
EP-0560155-A1 Process for separating phthalimidoperoxycaproic acid (PAP) from solution(s) in organic solvents AUSIMONT S.p.A. (IT) 1993-09-15 EP disclosed
EP-0556769-A1 Process for purifying phthalimidoperoxycaproic acid (PAP) which removes chlorinated solvent impurities from it AUSIMONT S.p.A. (IT) 1993-08-25 EP disclosed
EP-0435379-A2 Suspension, coating, agglomeration and uses of imidoperoxycarboxylic acids Akzo Nobel N.V. (NL) 1991-07-03 EP disclosed