SCHEMBL9906166

SCHEMBL9906166

CC(O)(c1ccccc1)C1CCCCC1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KEAP1 Q14145 1/20 0.56
NFE2L2 Q16236 1/20 0.56
CHRM2 P08172 6/20 0.51
CHRM1 P11229 6/20 0.51
CYP2D6 P10635 5/20 0.51
KCNH2 Q12809 4/20 0.51
CHRM3 P20309 6/20 0.49
CHRM4 P08173 3/20 0.49
CHRM5 P08912 3/20 0.49
HRH1 P35367 2/20 0.49
GRIN2D O15399 1/20 0.49
GRIN3B O60391 1/20 0.49
GRIN1 Q05586 1/20 0.49
GRIN2A Q12879 1/20 0.49
GRIN2B Q13224 1/20 0.49
GRIN2C Q14957 1/20 0.49
GRIN3A Q8TCU5 1/20 0.49
CYP3A4 P08684 1/20 0.49
TSHR P16473 1/20 0.49
NFKB1 P19838 1/20 0.49

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
SCHEMBL13429177 1.00 KEAP1 (0.56) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL18415154 1.00 KEAP1 (0.56) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL13131231 1.00 KEAP1 (0.56) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL17771882 0.98 KEAP1 (0.58) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL10306736 0.89 CYP2D6 (0.48) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL18911003 0.84 NPC1 (0.42) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL19130799 0.84 NPC1 (0.42) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL21141108 0.82 KEAP1 (0.51) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL20732594 0.82 KEAP1 (0.51) KEAP1NFE2L2CHRM2CHRM1CYP2D6
SCHEMBL18905366 0.82 KEAP1 (0.40) KEAP1NFE2L2CHRM2CHRM1CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113552235-A Method for measuring content of 1-cyclohexyl-1-phenethyl alcohol impurity in trihexyphenidyl hydrochloride by gas chromatography 江苏天士力帝益药业有限公司 2021-10-26 CN claimed
US-20220127266-A1 MALIC ENZYME INHIBITORS SUN PHARMA ADVANCED RESEARCH COMPANY LTD (IN) 2022-04-28 US disclosed
US-11225480-B2 Malic enzyme inhibitors SUN PHARMA ADVANCED RESEARCH COMPANY LTD (IN) 2022-01-18 US disclosed
CN-113552235-A Method for measuring content of 1-cyclohexyl-1-phenethyl alcohol impurity in trihexyphenidyl hydrochloride by gas chromatography 江苏天士力帝益药业有限公司 2021-10-26 CN disclosed
EP-3895705-A2 METHODS AND COMPOSITIONS FOR TREATMENT OF PERIPHERAL NEUROPATHIES University of Manitoba (CA) 2021-10-20 EP disclosed
US-20210115038-A1 MALIC ENZYME INHIBITORS SUN PHARMA ADVANCED RESEARCH COMPANY LTD (IN) 2021-04-22 US disclosed
WO-2020244452-A1 HETEROCYCLIC DERIVATIVE HAVING β2 RECEPTOR AGITATION AND M RECEPTOR ANTAGONISTIC ACTIVITY AND MEDICAL USE THEREOF 中国医药研究开发中心有限公司 2020-12-10 WO disclosed
US-20190185461-A1 BENZOCYCLIC DERIVATIVE HAVING B2-RECEPTOR AGONIST ACTIVITY AND M3-RECEPTOR ANTAGONIST ACTIVITY AND MEDICAL USE THEREOF SICHUAN HAISCO PHARMACEUTICAL CO., LTD. (CN) 2019-06-20 US disclosed
WO-2017012489-A1 BENZO RING DERIVATIVE WITH Β2 RECEPTOR AGONIST AND M3 RECEPTOR ANTAGONIST ACTIVITIES AND USE THEREOF IN MEDICINE 四川海思科制药有限公司 2017-01-26 WO disclosed
EP-1576108-B1 NITRILASES, NUCLEIC ACIDS ENCODING THEM AND METHODS FOR MAKING AND USING THEM BASF ENZYMES LLC (US) 2015-07-08 EP disclosed
US-8624024-B2 Phosphoramide compound, method for producing the same, ligand, complex, catalyst and method for producing optically active alcohol NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (JP) 2014-01-07 US disclosed
US-20130267506-A1 THERAPEUTIC COMPOSITIONS FOR DIABETIC SYMMETRICAL POLYNEUROPATHY UNIVERSITY OF MANITOBA (CA) 2013-10-10 US disclosed
US-20120214988-A1 PHOSPHORAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL SEKISUI MEDICAL CO., LTD. (JP) 2012-08-23 US disclosed
US-20120214988-A1 PHOSPHORAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL SEKISUI MEDICAL CO., LTD. (JP) 2012-08-23 US disclosed
US-8198445-B2 Phosphoramide compound, method for producing the same, ligand, complex, catalyst and method for producing optically active alcohol NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (JP) 2012-06-12 US disclosed
US-8198445-B2 Phosphoramide compound, method for producing the same, ligand, complex, catalyst and method for producing optically active alcohol NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (JP) 2012-06-12 US disclosed
US-20100113786-A1 PHOSPHORAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (JP) 2010-05-06 US disclosed
US-20100113786-A1 PHOSPHORAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL NATIONAL UNIVERSITY CORPORATION NAGOYA UNIVERSITY (JP) 2010-05-06 US disclosed
EP-2128167-A1 PHOSPHOROAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST, AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL National University Corporation Nagoya University (JP) 2009-12-02 EP disclosed
US-7608445-B1 Nitrilases, nucleic acids encoding them and methods for making and using them VERENIUM CORPORATION (US) 2009-10-27 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20210115038-A1 MALIC ENZYME INHIBITORS ME1, ME2, ME3 KEAP1 79/4885NFE2L2 494/4885CHRM2 4729/4885
US-20190185461-A1 BENZOCYCLIC DERIVATIVE HAVING B2-RECEPTOR AGONIST ACTIVITY AND M3-RECEPTOR ANTAGONIST ACTIVITY AND MEDICAL USE THEREOF HCAR2, CHRM3, BDKRB2 KEAP1 3592/4885NFE2L2 2057/4885CHRM2 4/4885
US-20130267506-A1 THERAPEUTIC COMPOSITIONS FOR DIABETIC SYMMETRICAL POLYNEUROPATHY CHRNA5, CHRM2, GAP43 KEAP1 3131/4885NFE2L2 4545/4885CHRM2 2/4885
US-11225480-B2 Malic enzyme inhibitors ME1, RNASE1, ME2 KEAP1 147/4885NFE2L2 1349/4885CHRM2 4098/4885
US-20220127266-A1 MALIC ENZYME INHIBITORS ME1, ME2, ME3 KEAP1 79/4885NFE2L2 494/4885CHRM2 4729/4885
US-20100113786-A1 PHOSPHORAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL ADH1C, ADH1A, DERA KEAP1 2748/4885NFE2L2 1705/4885CHRM2 2966/4885
US-20120214988-A1 PHOSPHORAMIDE COMPOUND, METHOD FOR PRODUCING THE SAME, LIGAND, COMPLEX, CATALYST AND METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOL ADH1C, ADH1A, DERA KEAP1 2748/4885NFE2L2 1705/4885CHRM2 2966/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.