Rimonabant

Rimonabant

SCHEMBL4000441

Cl.[2H]C([2H])([2H])c1c(C(=O)NN2C([2H])([2H])CCCC2([2H])[2H])nn(-c2ccc(Cl)cc2Cl)c1-c1ccc(Cl)cc1

nearest known ligand 0.73

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CNR1

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CNR1 known ✓ P21554 8/20 0.73
CNR2 P34972 4/20 0.73
ACHE P22303 1/20 0.73
CYP2C9 P11712 2/20 0.72
GPR55 Q9Y2T6 2/20 0.72
ABCC4 O15439 1/20 0.72
MLNR O43193 1/20 0.72
ABCB11 O95342 1/20 0.72
CHRM2 P08172 1/20 0.72
ADORA3 P0DMS8 1/20 0.72
ADRA2B P18089 1/20 0.72
ADRA2C P18825 1/20 0.72
DRD1 P21728 1/20 0.72
TBXA2R P21731 1/20 0.72
SLC6A2 P23975 1/20 0.72
HRH2 P25021 1/20 0.72
HTR2A P28223 1/20 0.72
AGTR1 P30556 1/20 0.72
CCKAR P32238 1/20 0.72
CCKBR P32239 1/20 0.72

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
Rimonabant SCHEMBL4008814 0.94 CNR1 (0.82) CNR1CNR2ACHECYP2C9GPR55
Rimonabant SCHEMBL4000793 0.93 CNR1 (0.68) CNR1CNR2ACHECYP2C9GPR55
Rimonabant SCHEMBL13411625 0.92 CNR1 (0.67) CNR1CNR2ACHECYP2C9GPR55
Rimonabant SCHEMBL13411626 0.91 CNR1 (0.87) CNR1CNR2ACHECYP2C9GPR55
Rimonabant SCHEMBL4001384 0.87 CNR1 (0.76) CNR1CNR2ACHECYP2C9GPR55
Hydrochloric Acid SCHEMBL3996916 0.86 CNR1 (0.65) CNR1CNR2ACHECYP2C9GPR55
Hydrochloric Acid SCHEMBL3998232 0.86 CNR1 (0.70) CNR1CNR2ACHECYP2C9GPR55
Rimonabant SCHEMBL14338883 0.86 CNR1 (0.75) CNR1CNR2ACHECYP2C9GPR55
Hydrochloric Acid SCHEMBL4005602 0.85 CNR1 (0.71) CNR1CNR2ACHECYP2C9GPR55
Rimonabant SCHEMBL29835931 0.85 CNR1 (1.00) CNR1CNR2ACHECYP2C9GPR55

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090258902-A1 BIPHENYL-PYRAZOLECARBOXAMIDE COMPOUNDS CONCERT PHARMACEUTICALS INC. (US) 2009-10-15 US disclosed
US-7514068-B2 Biphenyl-pyrazolecarboxamide compounds CONCERT PHARMACEUTICALS INC. (US) 2009-04-07 US disclosed
US-20070276001-A1 Biphenyl-pyrazolecarboxamide compounds CONCERT PHARMACEUTICALS INC. (US) 2007-11-29 US disclosed
WO-2007033366-A2 BIPHENYL-PYRAZOLECARBOXAMIDE COMPOUNDS CONCERT PHARMACEUTICALS INC. (US) 2007-03-22 WO disclosed
US-20070066657-A1 obesity, smoking cessation, and normalization of blood lipid composition; reduced rates of hepatic oxidative metabolism, ability to penetrate the blood-brain barrier; 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-(trideuteromethyl)-1H-pyrazole-3-carboxylic acid; cannabinoid receptor antagonist CONCERT PHARMACEUTICALS INC. (US) 2007-03-22 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 (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-20090258902-A1 BIPHENYL-PYRAZOLECARBOXAMIDE COMPOUNDS CNR2, CNR1, GPR119 CNR1 2/4885CNR2 1/4885ACHE 1435/4885
US-20070276001-A1 Biphenyl-pyrazolecarboxamide compounds CNR2, CNR1, GPR119 CNR1 2/4885CNR2 1/4885ACHE 1435/4885
US-20070066657-A1 obesity, smoking cessation, and normalization of blood lipid composition; reduced rates of hepatic oxidative metabolism, ability to penetrate the blood-brain barrier; 5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-(trideuteromethyl)-1H-pyrazole-3-carboxylic acid; cannabinoid receptor antagonist CNR2, CNR1, GPR119 CNR1 2/4885CNR2 1/4885ACHE 933/4885

“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.