SCHEMBL57855

SCHEMBL57855

Oc1ccc(N2CCC(Oc3ccc(OC(F)(F)F)cc3)CC2)cc1

nearest known ligand 0.53

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
KCNH2 Q12809 1/20 0.53
EPHX2 P34913 4/20 0.52
FAAH O00519 2/20 0.52
AADAC P22760 1/20 0.52
CHRM4 P08173 3/20 0.49
FFAR4 Q5NUL3 2/20 0.45
PTGS1 P23219 1/20 0.44
SLC6A2 P23975 1/20 0.44
SLC6A4 P31645 1/20 0.44
MMP2 P08253 1/20 0.44
MMP13 P45452 1/20 0.44
FPR2 P25090 2/20 0.43
PROKR1 Q8TCW9 2/20 0.43
FFAR1 O14842 3/20 0.43
ACACB O00763 1/20 0.43
PDE3B Q13370 1/20 0.43
PDE3A Q14432 1/20 0.43
KCNA5 P22460 1/20 0.43

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
SCHEMBL13281330 1.00 KCNH2 (0.53) KCNH2EPHX2FAAHAADACCHRM4
SCHEMBL3036120 0.99 KCNH2 (0.52) KCNH2EPHX2FAAHAADACCHRM4
SCHEMBL15441879 0.96 KCNH2 (0.50) KCNH2EPHX2FAAHAADACCHRM4
SCHEMBL13278969 0.91 KCNH2 (0.53) KCNH2EPHX2FAAHAADACCHRM4
SCHEMBL14405200 0.89 KCNH2 (0.46) KCNH2EPHX2FAAHAADACCHRM4
SCHEMBL2095407 0.89 KCNH2 (0.46) KCNH2EPHX2FAAHAADACCHRM4
Oxazole SCHEMBL5711296 0.87 KCNH2 (0.48) KCNH2EPHX2FAAHAADACCHRM4
SCHEMBL2056202 0.86 KCNH2 (0.58) KCNH2EPHX2FAAHCHRM4FFAR4
SCHEMBL13279685 0.86 DEGS1 (0.48) EPHX2MMP2MMP13FPR2PROKR1
SCHEMBL5541736 0.86 DEGS1 (0.48) EPHX2MMP2MMP13FPR2PROKR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107406386-B Process for producing 1- (4-hydroxyphenyl) -4- (4-trifluoromethoxyphenoxy) piperidine or salt thereof 大塚制药株式会社 2021-06-01 CN claimed
EP-3275862-B1 METHOD FOR PRODUCING 1-(4-HYDROXYPHENYL)-4-(4-TRIFLUOROMETHOXYPHENOXY)PIPERIDINE OR SALT THEREOF OTSUKA PHARMA CO LTD (JP) 2020-08-12 EP claimed
US-10252995-B2 Method for producing 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine or salt thereof OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2019-04-09 US claimed
US-20180065931-A1 METHOD FOR PRODUCING 1-(4-HYDROXYPHENYL)-4-(4-TRIFLUOROMETHOXYPHENOXY)PIPERIDINE OR SALT THEREOF OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2018-03-08 US claimed
EP-3275862-A1 METHOD FOR PRODUCING 1-(4-HYDROXYPHENYL)-4-(4-TRIFLUOROMETHOXYPHENOXY)PIPERIDINE OR SALT THEREOF Otsuka Pharmaceutical Co., Ltd. (JP) 2018-01-31 EP claimed
EP-1727782-B1 METHOD OF PRODUCING AMINOPHENOL COMPOUNDS OTSUKA PHARMA CO LTD (JP) 2012-08-22 EP claimed
US-7750156-B2 Method of producing aminophenol compounds OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2010-07-06 US claimed
US-20070219374-A1 Method of Producing Aminophenol Compounds OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2007-09-20 US claimed
EP-1727782-A1 METHOD OF PRODUCING AMINOPHENOL COMPOUNDS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-12-06 EP claimed
WO-2005092832-A1 METHOD OF PRODUCING AMINOPHENOL COMPOUNDS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-10-06 WO claimed
CN-113874341-B Process for preparing derivatives of 1, 1-dialkylethane-1, 2-diols useful as intermediates 科学与工业研究委员会 2024-05-31 CN disclosed
CN-110857294-B Crystal form of diramanib intermediate and preparation method thereof 华北制药集团新药研究开发有限责任公司 2022-11-18 CN disclosed
CN-113874341-A Process for preparing derivatives of 1, 1-dialkylethane-1, 2-diols as useful intermediates 科学与工业研究委员会 2021-12-31 CN disclosed
CN-107406386-B Process for producing 1- (4-hydroxyphenyl) -4- (4-trifluoromethoxyphenoxy) piperidine or salt thereof 大塚制药株式会社 2021-06-01 CN disclosed
CN-107406386-B Process for producing 1- (4-hydroxyphenyl) -4- (4-trifluoromethoxyphenoxy) piperidine or salt thereof 大塚制药株式会社 2021-06-01 CN disclosed
US-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-05-04 US disclosed
US-20060079697-A1 1-substituted-4-nitroimidazole compound and process for producing the same OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-04-13 US disclosed
WO-2005092832-A1 METHOD OF PRODUCING AMINOPHENOL COMPOUNDS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-10-06 WO disclosed
EP-1555267-A1 2,3-DIHYDRO-6-NITROIMIDAZO 2,1-b OXAZOLES OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-07-20 EP disclosed
EP-1553088-A1 1-SUBSTITUTED 4-NITROIMIDAZOLE COMPOUND AND PROCESS FOR PRODUCING THE SAME Otsuka Pharmaceutical Company, Limited (JP) 2005-07-13 EP 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 (5 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-20180065931-A1 METHOD FOR PRODUCING 1-(4-HYDROXYPHENYL)-4-(4-TRIFLUOROMETHOXYPHENOXY)PIPERIDINE OR SALT THEREOF DHPS, PAH, HPD KCNH2 174/4885EPHX2 1064/4885FAAH 2709/4885
US-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles NR2C2, NR4A3, NR4A2 KCNH2 3503/4885EPHX2 3662/4885FAAH 4363/4885
US-20060079697-A1 1-substituted-4-nitroimidazole compound and process for producing the same CBR1, CBR3, DCXR KCNH2 1539/4885EPHX2 3822/4885FAAH 3979/4885
US-20070219374-A1 Method of Producing Aminophenol Compounds PAH, CYP1A1, CYP1B1 KCNH2 3236/4885EPHX2 995/4885FAAH 2103/4885
US-10252995-B2 Method for producing 1-(4-hydroxyphenyl)-4-(4-trifluoromethoxyphenoxy)piperidine or salt thereof DHPS, PAH, HPD KCNH2 174/4885EPHX2 1064/4885FAAH 2709/4885

“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.