SCHEMBL6700730

SCHEMBL6700730

Fc1ccc(C(CCCI)c2ccc(F)cc2)cc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP19A1 P11511 9/20 0.49
SCN5A Q14524 1/20 0.45
CACNA1B Q00975 2/20 0.41
SLC6A3 Q01959 2/20 0.41
HTR2A P28223 2/20 0.40
HRH1 P35367 2/20 0.40
MAPK1 P28482 2/20 0.39
FAAH O00519 1/20 0.39
CYP3A4 P08684 1/20 0.39
CYP2D6 P10635 1/20 0.39
TSHR P16473 1/20 0.39
ALOX12 P18054 1/20 0.39
MTOR P42345 1/20 0.39
RAB9A P51151 1/20 0.39
CACNA1F O60840 1/20 0.39
HTR1A P08908 1/20 0.39
ADORA3 P0DMS8 1/20 0.39
DRD4 P21917 1/20 0.39
DRD5 P21918 1/20 0.39
HRH2 P25021 1/20 0.39

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
SCHEMBL14299747 0.96 CYP19A1 (0.46) CYP19A1SCN5ACACNA1BSLC6A3HTR2A
SCHEMBL904927 0.80 CYP19A1 (0.47) CYP19A1SCN5ACACNA1BSLC6A3MAPK1
SCHEMBL8678280 0.80 CYP19A1 (0.47) CYP19A1SCN5ACACNA1BSLC6A3HTR2A
SCHEMBL2862310 0.80 HRH1 (0.65) CYP19A1SCN5ACACNA1BSLC6A3HTR2A
SCHEMBL6264296 0.80 CYP19A1 (0.47) CYP19A1SCN5ACACNA1BSLC6A3HTR2A
SCHEMBL5864161 0.80 CYP19A1 (0.47) CYP19A1SCN5ACACNA1BSLC6A3HTR2A
SCHEMBL318816 0.80 CYP19A1 (0.47) CYP19A1SCN5ACACNA1BSLC6A3HTR2A
Hydrochloric Acid SCHEMBL7389223 0.78 HRH1 (0.63) CYP19A1SCN5ACACNA1BSLC6A3HTR2A
SCHEMBL22028771 0.78 HRH1 (0.57) CYP19A1SCN5ACACNA1BSLC6A3HTR2A
SCHEMBL7331536 0.78 CYP19A1 (0.46) CYP19A1SCN5ACACNA1BSLC6A3TBXA2R

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2018011375-A1 MECLOZINE DERIVATIVES AND DICLAZURIL DERIVATIVES FOR USE IN THE PREVENTION AND/OR THE TREATMENT OF DISORDERS ASSOCIATED TO THE INFLAMMATION INDUCED BY P. ACNES UNIVERSITE PARIS DESCARTES (FR) 2018-01-18 WO disclosed
US-8354434-B2 Cyclourea compounds as calcium channel blockers PURDUE PHARMA L.P. (US) 2013-01-15 US disclosed
US-8354434-B2 Cyclourea compounds as calcium channel blockers PURDUE PHARMA L.P. (US) 2013-01-15 US disclosed
US-20120322830-A1 Cyclourea Compounds as Calcium Channel Blockers PURDUE PHARMA L.P. (US) 2012-12-20 US disclosed
US-20120322830-A1 Cyclourea Compounds as Calcium Channel Blockers PURDUE PHARMA L.P. (US) 2012-12-20 US disclosed
US-20120309778-A1 Fused and Spirocycle Compounds and the Use Thereof PURDUE PHARMA L.P. (US) 2012-12-06 US disclosed
US-20090176838-A1 Cyclourea Compounds as Calcium Channel Blockers PURDUE PHARMA L.P. (US) 2009-07-09 US disclosed
US-20090176838-A1 Cyclourea Compounds as Calcium Channel Blockers PURDUE PHARMA L.P. (US) 2009-07-09 US disclosed
WO-2007085357-A1 CYCLOUREA COMPOUNDS AS CALCIUM CHANNEL BLOCKERS EURO-CELTIQUE S.A. (LU) 2007-08-02 WO disclosed
US-20040006081-A1 Pharmaceutically active piperidine derivatives, in particular as modulators of chemokine receptor activity ASTRAZENECA AB (SE) 2004-01-08 US disclosed
EP-1289957-A1 PHARMACEUTICALLY ACTIVE PIPERIDINE DERIVATIVES, IN PARTICULAR AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY AstraZeneca AB (SE) 2003-03-12 EP disclosed
US-6403589-B1 NUCLEOSIDE TRANSPORT INHIBITOR JANSSEN PHARMACEUTICA N.V. (BE) 2002-06-11 US disclosed
WO-2001087839-A1 PHARMACEUTICALLY ACTIVE PIPERIDINE DERIVATIVES, IN PARTICULAR AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY ASTRAZENECA AB (SE) 2001-11-22 WO disclosed
EP-0999840-A1 USE OF DRAFLAZINE-ANALOGUES FOR TREATING PAIN JANSSEN PHARMACEUTICA N.V. (BE) 2000-05-17 EP disclosed
WO-1998057643-A1 USE OF DRAFLAZINE-ANALOGUES FOR TREATING PAIN JANSSEN PHARMACEUTICA N.V. (BE) 1998-12-23 WO disclosed
US-4766125-A N-aryl-piperazinealkanamides useful for protecting hearts from myocardial injury caused by ischaemia, anoxia or hypoxia JANSSEN PHARMACEUTICA N.V. (BE) 1988-08-23 US disclosed
EP-0068544-B1 NOVEL N-ARYL-PIPERAZINEALKANAMIDES JANSSEN PHARMACEUTICA N.V. (BE) 1987-06-03 EP disclosed
US-4410536-A 7,8,9,10-Tetrahydrothieno[3,2-e]pyrido[4,3-b]indole compounds and their anti-depressant use TROPONWERKE GMBH & CO. K.G. (DE) 1983-10-18 US disclosed
EP-0068544-A2 Novel N-aryl-piperazinealkanamides JANSSEN PHARMACEUTICA N.V. (BE) 1983-01-05 EP disclosed
US-3989707-A NEUROLEPTIC AGENTS JANSSEN PHARMACEUTICA N.V. (BE) 1976-11-02 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 (4 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-20120322830-A1 Cyclourea Compounds as Calcium Channel Blockers CACNA1E, CACNA1B, CACNA1D CYP19A1 4534/4885SCN5A 135/4885CACNA1B 2/4885
US-20090176838-A1 Cyclourea Compounds as Calcium Channel Blockers CACNA1E, CACNA1B, CACNA1D CYP19A1 4534/4885SCN5A 135/4885CACNA1B 2/4885
US-20040006081-A1 Pharmaceutically active piperidine derivatives, in particular as modulators of chemokine receptor activity CCR5, CCR2, CCR1 CYP19A1 2675/4885SCN5A 1579/4885CACNA1B 2141/4885
US-20120309778-A1 Fused and Spirocycle Compounds and the Use Thereof CACNA1A, CACNA1E, CACNA1C CYP19A1 909/4885SCN5A 33/4885CACNA1B 4/4885

“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.