Fipamezole

Fipamezole

SCHEMBL3901401

CCC1(c2c[nH]cn2)Cc2ccc(F)cc2C1.Cl

nearest known ligand 0.56

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2C

The experimentally established mechanism targets of Fipamezole. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
ADRA2A known ✓ P08913 2/20 0.56
ADRA2B known ✓ P18089 2/20 0.56
ADRA2C known ✓ P18825 2/20 0.56
ADRA1B P35368 2/20 0.56
HTR1D P28221 1/20 0.31
HTR1B P28222 1/20 0.31
CXCR5 P32302 1/20 0.30

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
Fipamezole SCHEMBL935549 0.99 ADRA2A (0.57) ADRA2AADRA2BADRA2CADRA1BHTR1D
Fipamezole SCHEMBL1271449 0.99 ADRA2A (0.57) ADRA2AADRA2BADRA2CADRA1BHTR1D
Fipamezole SCHEMBL9354688 0.90 ADRA2A (0.52) ADRA2AADRA2BADRA2CADRA1B
SCHEMBL4626063 0.85 ADRA2A (0.40) ADRA2AADRA2BADRA2CADRA1B
Atipamezole SCHEMBL3526769 0.83 ADRA2A (0.50) ADRA2AADRA2BADRA2CADRA1B
Atipamezole SCHEMBL31147780 0.83 ADRA2A (0.50) ADRA2AADRA2BADRA2CADRA1B
SCHEMBL7642900 0.83 ADRA2A (0.40) ADRA2AADRA2BADRA2CADRA1B
SCHEMBL8610304 0.83 ADRA2A (0.40) ADRA2AADRA2BADRA2CADRA1B
SCHEMBL8612885 0.83 ADRA2A (0.40) ADRA2AADRA2BADRA2CADRA1BHTR1D
Atipamezole SCHEMBL881064 0.82 ADRA2A (0.51) ADRA2AADRA2BADRA2CADRA1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2502917-A1 Solid state crystalline forms of 4-(2-ethyl-5-fluoro-2,3-dihydro-1H-inden-2-yl)-1H-imidazole Santhera Pharmaceuticals (Schweiz) AG (CH) 2012-09-26 EP claimed
WO-2012123129-A1 SOLID STATE CRYSTALLINE FORMS OF 4-(2-ETHYL-5-FLUORO-2,3-DIHYDRO-1H-INDEN-2-YL)-1H-IMIDAZOLE SANTHERA PHARMACEUTICALS (SCHWEIZ) AG (CH) 2012-09-20 WO claimed
EP-1560581-B1 OROMUCOSAL FORMULATION AND PROCESS FOR PREPARING THE SAME JUVANTIA PHARMA LTD OY (FI) 2007-01-10 EP claimed
US-20060052429-A1 Oromucosal formulation and process for preparing the same SANTHERA PHARMACEUTICALS (SWITZERLAND) LTD. (CH) 2006-03-09 US claimed
EP-1560581-A1 OROMUCOSAL FORMULATION AND PROCESS FOR PREPARING THE SAME Oy Juvantia Pharma Ltd (FI) 2005-08-10 EP claimed
WO-2004041271-A1 OROMUCOSAL FORMULATION AND PROCESS FOR PREPARING THE SAME OY JUVANTIA PHARMA LTD (FI) 2004-05-21 WO claimed
US-8653122-B2 Oromucosal formulation and process for preparing the same SANTHERA PHARMACEUTICALS (SWITZERLAND) LTD. (CH) 2014-02-18 US disclosed
EP-2502917-A1 Solid state crystalline forms of 4-(2-ethyl-5-fluoro-2,3-dihydro-1H-inden-2-yl)-1H-imidazole Santhera Pharmaceuticals (Schweiz) AG (CH) 2012-09-26 EP disclosed
EP-1581504-B1 PROCESS FOR PREPARING SUBSTITUTED IMIDAZOLE DERIVATIVES AND INTERMEDIATES USED IN THE PROCESS JUVANTIA PHARMA LTD OY (FI) 2009-03-18 EP disclosed
CN-100339368-C Process for the preparation of substituted imidazole derivatives and intermediates used in the process JUVANTIA PHARMA LTD OY (FI) 2007-09-26 CN disclosed
US-7223871-B2 Process for preparing substituted imidazole derivatives and intermediates used in the process OY JUVANTIA PHARMA LTD. (FI) 2007-05-29 US disclosed
EP-1560581-B1 OROMUCOSAL FORMULATION AND PROCESS FOR PREPARING THE SAME JUVANTIA PHARMA LTD OY (FI) 2007-01-10 EP disclosed
US-20060052429-A1 Oromucosal formulation and process for preparing the same SANTHERA PHARMACEUTICALS (SWITZERLAND) LTD. (CH) 2006-03-09 US disclosed
US-20060025465-A1 Process for preparing substituted imidazole derivates and intermediates used in the process OY JUVANTIA PHARMA LTD (FI) 2006-02-02 US disclosed
CN-1723202-A Process for preparing substituted imidazole derivates and intermediates used in the process JUVANTIA PHARMA LTD OY (FI) 2006-01-18 CN disclosed
EP-1581504-A1 PROCESS FOR PREPARING SUBSTITUTED IMIDAZOLE DERIVATIVES AND INTERMEDIATES USED IN THE PROCESS Oy Juvantia Pharma Ltd (FI) 2005-10-05 EP disclosed
EP-1560581-A1 OROMUCOSAL FORMULATION AND PROCESS FOR PREPARING THE SAME Oy Juvantia Pharma Ltd (FI) 2005-08-10 EP disclosed
WO-2004063168-A1 PROCESS FOR PREPARING SUBSTITUTED IMIDAZOLE DERIVATIVES AND INTERMEDIATES USED IN THE PROCESS OY JUVANTIA PHARMA LTD (FI) 2004-07-29 WO disclosed
WO-2004041271-A1 OROMUCOSAL FORMULATION AND PROCESS FOR PREPARING THE SAME OY JUVANTIA PHARMA LTD (FI) 2004-05-21 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 (2 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-20060025465-A1 Process for preparing substituted imidazole derivates and intermediates used in the process HRH2, HRH4, HRH3 ADRA2A 688/4885ADRA2B 782/4885ADRA2C 1118/4885
US-20060052429-A1 Oromucosal formulation and process for preparing the same HRH2, HRH1, CYP8B1 ADRA2A 1645/4885ADRA2B 1249/4885ADRA2C 1187/4885

“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.