SCHEMBL4078621

SCHEMBL4078621

COc1cccc(C(=O)C2CCN(CCc3ccc(F)cc3)CC2)c1OC

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 8/20 1.00
GRM2 Q14416 3/20 1.00
HTR7 P34969 6/20 0.82
HTR2C P28335 6/20 0.82
HTR2B P41595 5/20 0.82
HTR1A P08908 4/20 0.82
HTR1D P28221 3/20 0.82
DRD1 P21728 3/20 0.82
HRH1 P35367 3/20 0.82
ADRA2C P18825 2/20 0.82
DRD4 P21917 2/20 0.82
HRH2 P25021 2/20 0.82
HTR1B P28222 2/20 0.82
SLC6A4 P31645 2/20 0.82
HTR5A P47898 2/20 0.82
DRD2 P14416 2/20 0.82
ADRA1B P35368 2/20 0.82
ADRA2A P08913 1/20 0.82
DRD5 P21918 1/20 0.82
ADRA1A P35348 1/20 0.82

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
Hydrochloric Acid SCHEMBL4072830 0.99 HTR2A (0.98) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL13701274 0.92 HTR2A (0.84) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL22118461 0.91 HTR2A (0.83) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL5968621 0.91 HTR2A (1.00) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL5968525 0.89 HTR2A (0.79) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL13701275 0.83 HTR2A (0.71) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL22118484 0.82 HTR2A (0.69) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL6603889 0.81 HTR2A (0.68) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL14495114 0.78 HTR2A (0.64) HTR2AGRM2HTR7HTR2CHTR2B
SCHEMBL22118444 0.78 HTR2A (0.63) HTR2AGRM2HTR7HTR2CHTR2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250066302-A1 DEUTERATED FORMS AND DERIVATIVES OF VOLINANSERIN TERRAN BIOSCIENCES INC. 2025-02-27 US disclosed
US-20220106272-A1 Deuterated Forms And Derivatives Of Volinanserin TERRAN BIOSCIENCES, INC. 2022-04-07 US disclosed
US-20220106272-A1 Deuterated Forms And Derivatives Of Volinanserin TERRAN BIOSCIENCES, INC. 2022-04-07 US disclosed
EP-3897507-A1 DEUTERATED FORMS AND DERIVATIVES OF VOLINANSERIN Concert Pharmaceuticals Inc. (US) 2021-10-27 EP disclosed
WO-2020132461-A1 DEUTERATED FORMS AND DERIVATIVES OF VOLINANSERIN CONCERT PHARMACEUTICALS, INC. (US) 2020-06-25 WO disclosed
WO-2020132461-A1 DEUTERATED FORMS AND DERIVATIVES OF VOLINANSERIN CONCERT PHARMACEUTICALS, INC. (US) 2020-06-25 WO disclosed
US-20090227798-A1 NOVEL PROCESSES FOR THE PREPARATION OF (R)-ALPHA-(2,3-DIMETHOXYPHENYL)-1-[2-(4-FLUOROPHENYL)ETHYL]-4-PIPERIDINEMETHANOL SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2009-09-10 US disclosed
US-20090227798-A1 NOVEL PROCESSES FOR THE PREPARATION OF (R)-ALPHA-(2,3-DIMETHOXYPHENYL)-1-[2-(4-FLUOROPHENYL)ETHYL]-4-PIPERIDINEMETHANOL SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2009-09-10 US disclosed
EP-1362589-B1 Use of R(+)-alpha-(2,3-dimethoxyphenyl)-1-(2-(4-fluorophenyl)ethyl)-4- piperidinemethanol for the treatment of sleep disorders AVENTIS PHARMA INC (US) 2009-07-15 EP disclosed
EP-1937265-A2 COMINATION OF A HYPNOTIC AGENT AND R(+)-ALPHA-(2,3-DIMETHOXY-PHENYL)-1-[2-(4-FLUOROPHENL)ETHYL]-4-PIPERIDINEMETHANOL AND THERAPEUTIC APPLICATION THEREOF Aventis Pharmaceuticals Inc. (US) 2008-07-02 EP disclosed
EP-0796619-A1 Use of (+)-alpha-(2,3-dimethoxyphenyl)-1-(2-(4-fluorophenyl)ethyl)-4-piperidinemethanol in treating depressive disorders and bipolar disorders MERRELL PHARMACEUTICALS INC. (US) 1997-09-24 EP disclosed
US-5618824-A ADMINISTERING N-ARALKYL PIPERIDINEMETHANOL DERIVATIVES MERRELL PHARMACEUTICALS INC. (US) 1997-04-08 US disclosed
EP-0749309-A1 TREATMENT OF OBSESSIVE-COMPULSIVE DISORDERS WITH 5-HT 2? ANTAGONISTS MERRELL PHARMACEUTICALS INC. (US) 1996-12-27 EP disclosed
US-5561144-A TREATMENT OF SCHIZOPHRENIA MERRELL PHARMACEUTICALS INC. (US) 1996-10-01 US disclosed
WO-1995024194-A1 TREATMENT OF OBSESSIVE-COMPULSIVE DISORDERS WITH 5-HT2 ANTAGONISTS MERRELL PHARMACEUTICALS INC. (US) 1995-09-14 WO disclosed
EP-0531410-B1 (+)-ALPHA-(2,3-DIMETHOXYPHENYL)-1-[2-(FLUOROPHENYL)ETHYL]-4-PIPERIDINEMETHANOL MERRELL DOW PHARMA (US) 1994-11-30 EP disclosed
EP-0531410-A4 (+)--G(A)-(2,3-DIMETHOXYPHENYL)-1- 2-(4-FLUOROPHENYL)ETHYL)-4-PIPERIDINEMETHANOL 1993-05-26 EP disclosed
EP-0531410-A1 (+)-ALPHA-(2,3-DIMETHOXYPHENYL)-1-[2-(FLUOROPHENYL)ETHYL]-4-PIPERIDINEMETHANOL. MERRELL DOW PHARMA (US) 1993-03-17 EP disclosed
US-5134149-A Serotonin antagonist MERRELL DOW PHARMACEUTICALS INC. (US) 1992-07-28 US disclosed
WO-1991018602-A1 (+)-α-(2,3-DIMETHOXYPHENYL)-1-[2-(4-FLUOROPHENYL)ETHYL]-4-PIPERIDINEMETHANOL MERRELL DOW PHARMACEUTICALS INC. (US) 1991-12-12 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-20250066302-A1 DEUTERATED FORMS AND DERIVATIVES OF VOLINANSERIN DRD2, HTR3A, COMT HTR2A 16/4885GRM2 848/4885HTR7 21/4885
US-20090227798-A1 NOVEL PROCESSES FOR THE PREPARATION OF (R)-ALPHA-(2,3-DIMETHOXYPHENYL)-1-[2-(4-FLUOROPHENYL)ETHYL]-4-PIPERIDINEMETHANOL CYP2E1, CYP1A1, ADRM1 HTR2A 1477/4885GRM2 781/4885HTR7 889/4885
US-20220106272-A1 Deuterated Forms And Derivatives Of Volinanserin DRD2, HTR3A, COMT HTR2A 16/4885GRM2 848/4885HTR7 21/4885

“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.