SCHEMBL8622049

SCHEMBL8622049

CCCCC1(CCCC)CCCCC1=O

nearest known ligand 0.35

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
SIRT2 Q8IXJ6 1/20 0.35
GRIN2D O15399 1/20 0.35
GRIN3B O60391 1/20 0.35
GRIN1 Q05586 1/20 0.35
GRIN2A Q12879 1/20 0.35
GRIN2B Q13224 1/20 0.35
GRIN2C Q14957 1/20 0.35
GRIN3A Q8TCU5 1/20 0.35
LMNA P02545 1/20 0.34
TSHR P16473 1/20 0.34
CETP P11597 4/20 0.34
ESR2 Q92731 1/20 0.34
HSD17B10 Q99714 1/20 0.33
CYP19A1 P11511 3/20 0.33
PTPN1 P18031 1/20 0.32
ACP1 P24666 1/20 0.32
CDC25B P30305 1/20 0.32
CNR2 P34972 4/20 0.31

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
SCHEMBL8622131 0.94 SIRT2 (0.41) SIRT2GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL8622062 0.94 SIRT2 (0.39) SIRT2ESR2HSD17B10CYP19A1
SCHEMBL8624874 0.92 SIRT2 (0.43) SIRT2CETPCYP19A1PTPN1ACP1
SCHEMBL5697005 0.91 SIRT2 (0.39) SIRT2GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL10581919 0.90 SIRT2 (0.37) SIRT2ESR2HSD17B10CYP19A1
SCHEMBL8622095 0.88 SIRT2 (0.45) SIRT2CYP19A1PTPN1ACP1CDC25B
SCHEMBL5257298 0.88 GRIN1 (0.37) SIRT2GRIN2DGRIN3BGRIN1GRIN2A
SCHEMBL8621156 0.86 SIRT2 (0.47) SIRT2CYP19A1PTPN1ACP1CDC25B
SCHEMBL8620532 0.85 ESR2 (0.36) SIRT2ESR2HSD17B10CYP19A1
SCHEMBL28848014 0.84 SIRT2 (0.35) SIRT2LMNACETP

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114431864-A Bioelectrode composition, bioelectrode, and method for producing bioelectrode 信越化学工业株式会社 2022-05-06 CN disclosed
CN-102575113-B Colorant multimer, colored curable composition, color filter and method for producing same, and solid-state image sensor, image display device, liquid crystal display device and organic EL display having the color filter FUJIFILM CORP 2015-06-17 CN disclosed
US-5852221-A Optically active β-aminoalkoxyborane complex NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1998-12-22 US disclosed
US-5808098-A REDUCING AGENT FROM AMINOALCOHOL NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1998-09-15 US disclosed
EP-0680484-B1 OPTICALLY ACTIVE BETA-AMINOALKOXYBORANE COMPLEXES NISSAN CHEMICAL IND LTD (JP) 1998-08-19 EP disclosed
US-5786485-A REACTING OPTICALLY ACTIVE BETA-AMINOALCOHOL WITH BORANE REAGENT TO PRODUCE OPTICALLY ACTIVE BETA-AMINOALKOXYBORANE COMPLEX NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 1998-07-28 US disclosed
US-5767277-A REDUCING AGENT FOR A CARBONYL COMPOUND TO PRODUCE A 1,3-SYN-DIOL COMPOUND NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1998-06-16 US disclosed
US-5739347-A REDUCING AGENTS FOR DECARBONYLATION NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1998-04-14 US disclosed
US-5663348-A REDUCTION OF DIKETONE WITH AMINOALKOXYBORANE COMPLEX TO FORM DIALCOHOL ESTER COMPOUND NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1997-09-02 US disclosed
EP-0680484-A1 OPTICALLY ACTIVE $g(b)-AMINOALKOXYBORANE COMPLEX NISSAN CHEMICAL INDUSTRIES, LIMITED (JP) 1995-11-08 EP disclosed
WO-1994017079-A1 OPTICALLY ACTIVE β-AMINOALKOXYBORANE COMPLEX NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1994-08-04 WO disclosed