Phenobarbital

Phenobarbital

SCHEMBL1171829

CCC1(c2ccccc2)C(=O)NC(=O)NC1=O.CCC1(c2ccccc2)C(=O)NCNC1=O

nearest known ligand 0.87

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9A

The experimentally established mechanism targets of Phenobarbital. 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
▸ SCN1A known ✓ P35498 1/20 0.40
▸ SCN4A known ✓ P35499 1/20 0.40
▸ SCN5A known ✓ Q14524 1/20 0.40
▸ SCN2A known ✓ Q99250 1/20 0.40
▸ SCN3A known ✓ Q9NY46 1/20 0.40
▸ KMT2A Q03164 2/20 0.87
▸ MEN1 O00255 1/20 0.87
▸ CYP1A2 P05177 1/20 0.87
▸ POLB P06746 1/20 0.87
▸ TSHR P16473 1/20 0.87
▸ APEX1 P27695 1/20 0.87
▸ TDP1 Q9NUW8 1/20 0.87
▸ MMP2 P08253 6/20 0.67
▸ MMP9 P14780 6/20 0.67
▸ MMP3 P08254 3/20 0.67
▸ LMNA P02545 4/20 0.53
▸ MMP13 P45452 2/20 0.49
▸ CYP2C19 P33261 1/20 0.48
▸ MMP8 P22894 1/20 0.44
▸ CACNA1F O60840 1/20 0.40

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
Primidone SCHEMBL34221 0.93 KMT2A (1.00) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL19991483 0.90 MMP2 (0.75) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL2592325 0.90 MMP2 (0.80) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL16583 0.90 MMP2 (0.80) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL18825042 0.90 MMP2 (0.80) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL28099657 0.90 MMP2 (0.80) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL2120028 0.88 MMP2 (0.77) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL1322895 0.88 MMP2 (0.77) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL22032658 0.88 MMP2 (0.77) KMT2AMEN1CYP1A2POLBTSHR
Phenobarbital SCHEMBL6807467 0.88 MMP2 (0.77) KMT2AMEN1CYP1A2POLBTSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2699572-A1 HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS Origenis GmbH (DE) 2014-02-26 — — EP disclosed
EP-2699579-A1 PYRAZOLO [4, 3-D]PYRIMIDINES USEFUL AS KINASE INHIBITORS Origenis GmbH (DE) 2014-02-26 — — EP disclosed
US-8478419-B2 Modulation and analysis of cerebral perfusion in epilepsy and other neurological disorders NEUROPACE, INC. (US) 2013-07-02 — — US disclosed
WO-2012143144-A1 PYRAZOLO [4, 3-D] PYRIMIDINES USEFUL AS KINASE INHIBITORS ORIGENIS GMBH (DE) 2012-10-26 — — WO disclosed
WO-2012143143-A1 HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS ORIGENIS GMBH (DE) 2012-10-26 — — WO disclosed
US-7892182-B2 Modulation and analysis of cerebral perfusion in epilepsy and other neurological disorders NEUROPACE, INC. (US) 2011-02-22 — — US disclosed
US-20090069863-A1 MODULATION AND ANALYSIS OF CEREBRAL PERFUSION IN EPILEPSY AND OTHER NEUROLOGICAL DISORDERS NEUROPACE, INC. (US) 2009-03-12 — — US disclosed
US-20080046026-A1 MODULATION AND ANALYSIS OF CEREBRAL PERFUSION IN EPILEPSY AND OTHER NEUROLOGICAL DISORDERS NEUROPACE, INC. (US) 2008-02-21 — — US disclosed
EP-1553952-A1 USE OF DIHYDROIMIDAZOLONES FOR THE TREATMENT OF EPILEPSY IN DOGS BOEHRINGER INGELHEIM VETMEDICA GMBH (DE) 2005-07-20 — — EP disclosed
WO-2004032938-A1 USE OF DIHYDROIMIDAZOLONES FOR THE TREATMENT OF EPILEPSY IN DOGS BOEHRINGER INGELHEIM VETMEDICA GMBH (DE) 2004-04-22 — — WO disclosed
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