SCHEMBL977933

SCHEMBL977933

O=C(Cl)C1CCN(C(=O)C(F)(F)F)CC1

nearest known ligand 0.53

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 5/20 0.46
EPHX2 P34913 4/20 0.44
KDM1A O60341 1/20 0.42
RIPK1 Q13546 1/20 0.42
PDK2 Q15119 2/20 0.36
MGLL Q99685 2/20 0.35
CYP2C19 P33261 1/20 0.34
HRH3 Q9Y5N1 1/20 0.34
GAA P10253 1/20 0.34
TDP1 Q9NUW8 1/20 0.34
LMNA P02545 1/20 0.33

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
SCHEMBL3285103 0.82 LMNA (0.50) EPHX1EPHX2KDM1ARIPK1GAA
SCHEMBL28278914 0.80 GAA (0.51) EPHX1EPHX2RIPK1GAATDP1
SCHEMBL12436970 0.80 EPHX1 (0.43) EPHX1EPHX2KDM1ARIPK1PDK2
Hydrochloric Acid SCHEMBL977934 0.80 LMNA (0.49) EPHX1EPHX2KDM1ARIPK1GAA
SCHEMBL7608711 0.77 EPHX1 (0.41) EPHX1EPHX2KDM1ARIPK1PDK2
SCHEMBL5758149 0.77 EPHX1 (0.46) EPHX1EPHX2KDM1ARIPK1
SCHEMBL3835392 0.76 EPHX1 (0.43) EPHX1EPHX2KDM1ARIPK1CYP2C19
SCHEMBL19195033 0.76 EPHX2 (0.43) EPHX2
SCHEMBL8486161 0.75 EPHX1 (0.45) EPHX1EPHX2KDM1ARIPK1CYP2C19
SCHEMBL4131266 0.75 EPHX1 (0.45) EPHX1EPHX2KDM1ARIPK1CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250257035-A1 1,4-Substituted Piperidine Derivatives CEPHALON LLC 2025-08-14 US disclosed
US-12098130-B2 1,4-substituted piperidine derivatives 89BIO LTD (IL) 2024-09-24 US disclosed
US-20230391723-A1 1,4-Substituted Piperidine Derivatives CEPHALON LLC 2023-12-07 US disclosed
US-11702388-B2 1,4-substituted piperidine derivatives 89BIO LTD (IL) 2023-07-18 US disclosed
US-11192868-B2 Modulators of indoleamine 2,3-dioxygenase and methods of using the same INCYTE CORPORATION (US) 2021-12-07 US disclosed
US-20210230116-A1 1,4-Substituted Piperidine Derivatives CEPHALON LLC 2021-07-29 US disclosed
CN-107847765-B 1, 4-substituted piperidine derivatives 89生物有限公司 2021-05-04 CN disclosed
US-10851057-B2 1,4-substituted piperidine derivatives 89BIO LTD (IL) 2020-12-01 US disclosed
EP-3310441-B1 1, 4-SUBSTITUTED PIPERIDINE DERIVATIVES 89BIO LTD (IL) 2020-07-29 EP disclosed
US-20190210985-A1 MODULATORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF USING THE SAME INCYTE CORPORATION 2019-07-11 US disclosed
US-20040192685-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists CAMERON KIMBERLY O (US) 2004-09-30 US disclosed
US-20030220494-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists CAMERON KIMBERLY O (US) 2003-11-27 US disclosed
US-6608203-B2 Devoid of unwanted side effects PFIZER INC. 2003-08-19 US disclosed
US-6602885-B2 Piperidine derivatives useful as CCR5 antagonists SCHERING CORPORATION 2003-08-05 US disclosed
US-20030004185-A1 Piperidine derivatives useful as CCR5 antagonists MERCK SHARP & DOHME CORP. 2003-01-02 US disclosed
US-6387930-B1 ANTIARTHRITIC AGENTS; ANTIALLERGENS; SKIN DISORDERS; INFLAMMATORY BOWEL DISORDERS SCHERING CORPORATION 2002-05-14 US disclosed
EP-1175402-A1 PIPERIDINE DERIVATIVES USEFUL AS CCR5 ANTAGONISTS SCHERING CORPORATION (US) 2002-01-30 EP disclosed
US-20010039285-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists CAMERON KIMBERLY O (US) 2001-11-08 US disclosed
EP-1113007-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists PFIZER INC. (US) 2001-07-04 EP disclosed
WO-2000066559-A1 PIPERIDINE DERIVATIVES USEFUL AS CCR5 ANTAGONISTS SCHERING CORPORATION (US) 2000-11-09 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 (12 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-20250257035-A1 1,4-Substituted Piperidine Derivatives FASN, CES1, CPT1A EPHX1 709/4885EPHX2 1352/4885KDM1A 489/4885
US-20010039285-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists GPER1, ESR1, ESR2 EPHX1 173/4885EPHX2 780/4885KDM1A 1196/4885
US-11192868-B2 Modulators of indoleamine 2,3-dioxygenase and methods of using the same IDO1, IDO2, INMT EPHX1 1059/4885EPHX2 611/4885KDM1A 271/4885
US-20230391723-A1 1,4-Substituted Piperidine Derivatives FASN, CES1, CPT1A EPHX1 709/4885EPHX2 1352/4885KDM1A 489/4885
US-20210230116-A1 1,4-Substituted Piperidine Derivatives FASN, CES1, CPT1A EPHX1 709/4885EPHX2 1352/4885KDM1A 489/4885
US-20030220494-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists GPER1, ESR1, ESR2 EPHX1 173/4885EPHX2 780/4885KDM1A 1196/4885
US-20040192685-A1 Tetrahydroisoquinoline compounds as estrogen agonists/antagonists GPER1, ESR1, ESR2 EPHX1 173/4885EPHX2 780/4885KDM1A 1196/4885
US-20190210985-A1 MODULATORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF USING THE SAME IDO1, IDO2, INMT EPHX1 1059/4885EPHX2 611/4885KDM1A 271/4885
US-11702388-B2 1,4-substituted piperidine derivatives FASN, CES1, CPT1A EPHX1 709/4885EPHX2 1352/4885KDM1A 489/4885
US-12098130-B2 1,4-substituted piperidine derivatives FASN, CES1, CPT1A EPHX1 709/4885EPHX2 1352/4885KDM1A 489/4885
US-10851057-B2 1,4-substituted piperidine derivatives FASN, CES1, CPT1A EPHX1 709/4885EPHX2 1352/4885KDM1A 489/4885
US-20030004185-A1 Piperidine derivatives useful as CCR5 antagonists CCR5, CCR1, CCR2 EPHX1 2674/4885EPHX2 1754/4885KDM1A 2934/4885

“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.