SCHEMBL6400531

SCHEMBL6400531

COc1ccc2c(c1)CCOC2(C)C(F)(F)F

nearest known ligand 0.43

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
PDK2 Q15119 2/20 0.43
KDM1A O60341 1/20 0.41
TACR1 P25103 2/20 0.41
CCR2 P41597 2/20 0.39
ESR1 P03372 1/20 0.39
ESR2 Q92731 1/20 0.39
DRD2 P14416 2/20 0.38
DRD3 P35462 2/20 0.38
DRD1 P21728 1/20 0.38
DRD5 P21918 1/20 0.38
ALDH1A1 P00352 1/20 0.38
ABHD6 Q9BV23 1/20 0.38
PARP1 P09874 1/20 0.38
BACE1 P56817 1/20 0.36
BCL2 P10415 1/20 0.36

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
SCHEMBL6406622 1.00 PDK2 (0.43) PDK2KDM1ATACR1CCR2ESR1
SCHEMBL6400509 1.00 PDK2 (0.43) PDK2KDM1ATACR1CCR2ESR1
SCHEMBL6403193 0.85 PDK2 (0.41) PDK2KDM1ATACR1ESR1ESR2
SCHEMBL6403380 0.85 PDK2 (0.41) PDK2KDM1ATACR1ESR1ESR2
SCHEMBL6401340 0.85 PDK2 (0.41) PDK2KDM1ATACR1ESR1ESR2
SCHEMBL6401391 0.84 CA2 (0.42) TACR1CCR2ESR1ALDH1A1
SCHEMBL6401257 0.84 CA2 (0.42) TACR1CCR2ESR1ALDH1A1
SCHEMBL6402105 0.79 ESR2 (0.41) PDK2TACR1ESR1ESR2DRD2
SCHEMBL6401424 0.79 ESR2 (0.41) PDK2TACR1ESR1ESR2DRD2
SCHEMBL6401576 0.79 ESR2 (0.41) PDK2TACR1ESR1ESR2DRD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050171354-A1 Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance P antagonists PFIZER INC. (US) 2005-08-04 US claimed
US-20030208079-A1 Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance P antagonists PFIZER INC. 2003-11-06 US claimed
EP-1032571-B1 PIPERIDINYLAMINOMETHYL TRIFLUOROMETHYL CYCLIC ETHER COMPOUNDS AS SUBSTANCE P ANTAGONISTS PFIZER (US) 2002-06-12 EP claimed
EP-1032571-A1 PIPERIDINYLAMINOMETHYL TRIFLUOROMETHYL CYCLIC ETHER COMPOUNDS AS SUBSTANCE P ANTAGONISTS PFIZER INC. (US) 2000-09-06 EP claimed
WO-1999025714-A1 PIPERIDINYLAMINOMETHYL TRIFLUOROMETHYL CYCLIC ETHER COMPOUNDS AS SUBSTANCE P ANTAGONISTS PFIZER PHARMACEUTICALS INC. (JP) 1999-05-27 WO claimed
US-20050171354-A1 Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance P antagonists PFIZER INC. (US) 2005-08-04 US disclosed
EP-1095939-B1 Process for the preparation of piperidinylaminomethyl trifluoromethyl cyclic ether compounds PFIZER PROD INC (US) 2004-01-07 EP disclosed
US-20030236268-A1 Process for the preparation of piperidinylaminomethyl trifluoromethyl cyclic ether compounds CARON STEPHANIE (US) 2003-12-25 US disclosed
US-20030208079-A1 Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance P antagonists PFIZER INC. 2003-11-06 US disclosed
EP-1178984-B1 1-TRIFLUOROMETHYL-4-HYDROXY-7-PIPERIDINYL-AMINOMETHYLCHROMAN DERIVATIVES PFIZER PROD INC (US) 2003-03-19 EP disclosed
US-6486325-B1 Process for the preparation of piperidinylaminomethyl trifluoromethyl cyclic ether compounds PFIZER INC 2002-11-26 US disclosed
EP-1032571-B1 PIPERIDINYLAMINOMETHYL TRIFLUOROMETHYL CYCLIC ETHER COMPOUNDS AS SUBSTANCE P ANTAGONISTS PFIZER (US) 2002-06-12 EP disclosed
EP-1178984-A2 1-TRIFLUOROMETHYL-4-HYDROXY-7-PIPERIDINYL-AMINOMETHYLCHROMAN DERIVATIVES Pfizer Products Inc. (US) 2002-02-13 EP disclosed
US-6239147-B1 TO TREAT CNS, GASTROINTESTINAL AND OTHER DISORDERS. SUBSTANCE P ANTAGONISTS HAVING IMPROVED ACTIVITY AND FEWER SIDE EFFECTS, TREATMENT OF EMESIS INDUCED BY ANTINEOPLASTIC AGENTS, ISOCHROMAN RING PFIZER INC 2001-05-29 US disclosed
EP-1095939-A2 Process for the preparation of piperidinylaminomethyl trifluoromethyl cyclic ether compounds Pfizer Products Inc. (US) 2001-05-02 EP disclosed
WO-2000071538-A2 1-TRIFLUOROMETHYL-4-HYDROXY-7-PIPERIDINYL-AMINOMETHYLCHROMAN DERIVATIVES PFIZER PRODUCTS INC. (US) 2000-11-30 WO disclosed
EP-1032571-A1 PIPERIDINYLAMINOMETHYL TRIFLUOROMETHYL CYCLIC ETHER COMPOUNDS AS SUBSTANCE P ANTAGONISTS PFIZER INC. (US) 2000-09-06 EP disclosed
WO-1999025714-A1 PIPERIDINYLAMINOMETHYL TRIFLUOROMETHYL CYCLIC ETHER COMPOUNDS AS SUBSTANCE P ANTAGONISTS PFIZER PHARMACEUTICALS INC. (JP) 1999-05-27 WO 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 (3 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-20050171354-A1 Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance P antagonists HRH2, TACR1, HRH4 PDK2 3515/4885KDM1A 2818/4885TACR1 2/4885
US-20030208079-A1 Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance P antagonists TACR1, HRH2, GRPR PDK2 4168/4885KDM1A 2139/4885TACR1 1/4885
US-20030236268-A1 Process for the preparation of piperidinylaminomethyl trifluoromethyl cyclic ether compounds H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CYP1B1, PAICS PDK2 3245/4885KDM1A 1019/4885TACR1 2311/4885

“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.