Urea

Urea

SCHEMBL7500665

NC(N)=O.O=S(=O)(O)c1ccccc1

nearest known ligand 0.80

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BTKCACNA1CCACNA1DCACNA1FCACNA1SCACNA2D1CACNA2D2DRD2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQHRH1HTR2AP2RY12

The experimentally established mechanism targets of Urea. 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
TSHR P16473 4/20 0.80
SMN1; SMN2 Q16637 1/20 0.80
CYP2D6 P10635 2/20 0.54
POLB P06746 2/20 0.54
ALDH1A1 P00352 4/20 0.52
NT5E P21589 1/20 0.52
TDP1 Q9NUW8 4/20 0.50
HSD17B10 Q99714 3/20 0.50
CA1 P00915 2/20 0.50
CA2 P00918 2/20 0.50
CYP2C19 P33261 2/20 0.50
CA12 O43570 1/20 0.50
CA3 P07451 1/20 0.50
CA4 P22748 1/20 0.50
CA6 P23280 1/20 0.50
CA5A P35218 1/20 0.50
CA7 P43166 1/20 0.50
PLA2G7 Q13093 1/20 0.50
CA9 Q16790 1/20 0.50
CA13 Q8N1Q1 1/20 0.50

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
Urea SCHEMBL27768310 0.98 TSHR (0.76) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
Carbamic Acid SCHEMBL28801958 0.95 TSHR (0.80) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
Acetamide SCHEMBL7845790 0.91 TSHR (0.73) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
Bicarbonate SCHEMBL15282245 0.90 TSHR (0.89) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
Hydroxyamine SCHEMBL9651752 0.90 TSHR (0.89) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
Hydrazine SCHEMBL11223582 0.90 TSHR (0.89) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
Bicarbonate SCHEMBL28272077 0.90 TSHR (0.89) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
Hydrazine SCHEMBL5026988 0.90 TSHR (0.89) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
SCHEMBL597672 0.89 TSHR (1.00) TSHRSMN1; SMN2CYP2D6POLBALDH1A1
SCHEMBL2509 0.89 TSHR (1.00) TSHRSMN1; SMN2CYP2D6POLBALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106573913-A Acid addition salts of Trk inhibiting compounds 小野药品工业株式会社 2017-04-19 CN claimed
CN-101448796-B Salts and crystal modifications thereof NOVARTIS AG 2012-09-26 CN claimed
CN-101448796-A Salts and crystal modifications thereof NOVARTIS AG (CH) 2009-06-03 CN claimed
CN-1058705-C Substituted benzene sulfone urea, benzenesulfonyl thiourea its preparation, its application as medicine or diagnostic medicine and drugs containing it HOECHST AG (DE) 2000-11-22 CN claimed
CN-106573913-B Inhibit the acid-addition salts of the compound of Trk 小野药品工业株式会社 2019-11-19 CN disclosed
CN-106573913-A Acid addition salts of Trk inhibiting compounds 小野药品工业株式会社 2017-04-19 CN disclosed
CN-102015680-B New substituted indolin-2-one derivatives and use thereof as p38 mitogen-activated kinase inhibitors ALMIRALL SA 2013-11-20 CN disclosed
CN-101679413-B New 3-([1,2,4]triazolo[4,3-a]pyridin-7-yl)benzamide derivatives ALMIRALL LAB 2013-07-03 CN disclosed
CN-101448796-B Salts and crystal modifications thereof NOVARTIS AG 2012-09-26 CN disclosed
CN-102026972-A New substituted spiro[cycloalkyl-1,3'-indol]-2'(1'H)-one derivatives and their use as p38 mitogen-activated kinase inhibitors ALMIRALL SA 2011-04-20 CN disclosed
CN-102015680-A New substituted indolin-2-one derivatives and their use as p38 mitogen-activated kinase inhibitors ALMIRALL SA 2011-04-13 CN disclosed
CN-101679413-A New 3-([1,2,4]triazolo[4,3-a]pyridin-7-yl)benzamide derivatives ALMIRALL LAB 2010-03-24 CN disclosed
CN-101448796-A Salts and crystal modifications thereof NOVARTIS AG (CH) 2009-06-03 CN disclosed
CN-101268064-A Pyrazine derivatives useful as adenosine receptor antagonists ALMIRALL LAB (ES) 2008-09-17 CN disclosed
EP-1158980-A4 N-UREIDOALKYL-PIPERIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY DU PONT PHARM CO (US) 2002-04-03 EP disclosed
EP-1158980-A1 N-UREIDOALKYL-PIPERIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY Du Pont Pharmaceuticals Company (US) 2001-12-05 EP disclosed
WO-2000035453-A1 N-UREIDOALKYL-PIPERIDINES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY DU PONT PHARMACEUTICALS COMPANY (US) 2000-06-22 WO disclosed