Medetomidine

Medetomidine

SCHEMBL787913

Cc1cccc(C(C)c2c[nH]cn2)c1C.Cc1cccc([C@H](C)c2c[nH]cn2)c1C

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2C

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

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ADRA2A known ✓ P08913 4/20 0.50
ADRA2B known ✓ P18089 4/20 0.50
ADRA2C known ✓ P18825 4/20 0.50
ADRA1A P35348 3/20 0.50
ADRA1B P35368 3/20 0.50
ADRA1D P25100 2/20 0.50
KCNH2 Q12809 1/20 0.50
TP53 P04637 1/20 0.50
CYP1A2 P05177 1/20 0.50
CYP3A4 P08684 1/20 0.50
CYP2D6 P10635 1/20 0.50
CYP2C9 P11712 1/20 0.50
TSHR P16473 1/20 0.50
CYP2C19 P33261 1/20 0.50
SLC6A2 P23975 1/20 0.49
HTR7 P34969 1/20 0.49
TRPA1 O75762 1/20 0.31
ATM Q13315 1/20 0.31

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
Medetomidine SCHEMBL18497244 1.00 ADRA2A (0.50) ADRA2AADRA2BADRA2CADRA1AADRA1B
Dexmedetomidine SCHEMBL29431568 1.00 ADRA2A (0.50) ADRA2AADRA2BADRA2CADRA1AADRA1B
Dexmedetomidine SCHEMBL12092460 1.00 ADRA2A (0.50) ADRA2AADRA2BADRA2CADRA1AADRA1B
Medetomidine SCHEMBL26432 1.00 ADRA2A (0.50) ADRA2AADRA2BADRA2CADRA1AADRA1B
Dexmedetomidine SCHEMBL119382 1.00 ADRA2A (0.50) ADRA2AADRA2BADRA2CADRA1AADRA1B
Dexmedetomidine SCHEMBL14861666 1.00 ADRA2A (0.50) ADRA2AADRA2BADRA2CADRA1AADRA1B
Dexmedetomidine SCHEMBL14080529 0.98 ADRA2A (0.51) ADRA2AADRA2BADRA2CADRA1AADRA1B
Medetomidine SCHEMBL22616139 0.98 ADRA2A (0.49) ADRA2AADRA2BADRA2CADRA1AADRA1B
Dexmedetomidine SCHEMBL22476079 0.98 ADRA2A (0.49) ADRA2AADRA2BADRA2CADRA1AADRA1B
Medetomidine SCHEMBL204843 0.98 ADRA2A (0.51) ADRA2AADRA2BADRA2CADRA1AADRA1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2782569-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING 4-[1-(2,3-DIMETHYLPHENYL)ETHYL]-3H-IMIDAZOLE DERIVATIVES FOR TREATING RETINAL DISEASES ALLERGAN, INC. (US) 2014-10-01 EP disclosed
EP-2640382-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING (3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL)METHANOL Allergan, Inc. (US) 2013-09-25 EP disclosed
EP-2616068-A1 ESTER PRO-DRUGS OF [3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL]METHANOL FOR LOWERING INTRAOCULAR PRESSURE Allergan, Inc. (US) 2013-07-24 EP disclosed
EP-2616066-A1 ESTER PRO-DRUGS OF [3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL]METHANOL FOR TREATING RETINAL DISEASES Allergan, Inc. (US) 2013-07-24 EP disclosed
EP-2616067-A1 ESTER PRO-DRUGS OF [3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL]METHANOL FOR TREATING SKIN DISEASES AND CONDITIONS Allergan, Inc. (US) 2013-07-24 EP disclosed
EP-2616069-A1 ESTER PRO-DRUGS OF [3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL]METHANOL Allergan, Inc. (US) 2013-07-24 EP disclosed
WO-2013078151-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING 4-[1-(2,3-DIMETHYLPHENYL)ETHYL]-3H-IMIDAZOLE DERIVATIVES FOR TREATING RETINAL DISEASES ALLERGAN, INC. (US) 2013-05-30 WO disclosed
WO-2012067941-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING (3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL)METHANOL ALLERGAN, INC. (US) 2012-05-24 WO disclosed
WO-2012037453-A1 ESTER PRO-DRUGS OF [3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL] METHANOL FOR TREATING RETINAL DISEASES ALLERGAN, INC. (US) 2012-03-22 WO disclosed
WO-2012037499-A1 ESTER PRO-DRUGS OF [3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL] METHANOL ALLERGAN, INC. (US) 2012-03-22 WO disclosed
WO-2012037490-A1 ESTER PRO-DRUGS OF [3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL] METHANOL FOR LOWERING INTRAOCULAR PRESSURE ALLERGAN, INC. (US) 2012-03-22 WO disclosed
WO-2012037484-A1 ESTER PRO-DRUGS OF [3-(1-(1H-IMIDAZOL-4-YL)ETHYL)-2-METHYLPHENYL] METHANOL FOR TREATING SKIN DISEASES AND CONDITIONS ALLERGAN, INC. (US) 2012-03-22 WO disclosed
EP-2370136-A1 INHALATION DELIVERY METHODS AND DEVICES MAP Pharmaceuticals Inc (US) 2011-10-05 EP disclosed
US-20100196286-A1 INHALATION DELIVERY METHODS AND DEVICES MAP PHARMACEUTICALS, INC. 2010-08-05 US disclosed
WO-2010065547-A1 INHALATION DELIVERY METHODS AND DEVICES MAP PHARMACEUTICALS, INC. (US) 2010-06-10 WO disclosed
US-20070197622-A1 Methods for treating CNS disorders with 4-imidazole derivatives F. HOFFMANN-LA ROCHE AG, A SWISS COMPANY (CH) 2007-08-23 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 (1 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-20070197622-A1 Methods for treating CNS disorders with 4-imidazole derivatives CRY1, GPR119, MTNR1A ADRA2A 116/4885ADRA2B 107/4885ADRA2C 56/4885

“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.