SCHEMBL7026151

SCHEMBL7026151

CNC1CCc2[nH]c3ccc(NC=O)cc3c2C1.CS(=O)(=O)O

nearest known ligand 0.59

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
HTR1B known ✓ P28222 4/20 0.59
HTR1A known ✓ P08908 2/20 0.59
HTR1D known ✓ P28221 2/20 0.59
DRD2 known ✓ P14416 1/20 0.52
DRD4 known ✓ P21917 1/20 0.52
HTR1E P28566 1/20 0.52
HTR7 P34969 1/20 0.52
OPRM1 P35372 1/20 0.52
TMEM97 Q5BJF2 1/20 0.52
HTR1F P30939 1/20 0.43
KMT2A Q03164 2/20 0.42
MEN1 O00255 1/20 0.42
BAZ2B Q9UIF8 1/20 0.40
HTR6 P50406 1/20 0.39

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
SCHEMBL980209 0.94 HTR1B (0.61) HTR1BHTR1AHTR1DDRD2DRD4
SCHEMBL7031093 0.94 HTR1B (0.61) HTR1BHTR1AHTR1DDRD2DRD4
SCHEMBL2301469 0.94 HTR1B (0.61) HTR1BHTR1AHTR1DDRD2DRD4
Bromide SCHEMBL7027435 0.93 HTR1B (0.60) HTR1BHTR1AHTR1DDRD2DRD4
Hydrochloric Acid SCHEMBL3466984 0.93 HTR1B (0.60) HTR1BHTR1AHTR1DDRD2DRD4
Oxalic Acid SCHEMBL7540895 0.92 HTR1B (0.62) HTR1BHTR1AHTR1DDRD2DRD4
Succinic Acid SCHEMBL7700352 0.89 HTR1B (0.68) HTR1BHTR1AHTR1DDRD2DRD4
Succinic Acid SCHEMBL7024837 0.89 HTR1B (0.68) HTR1BHTR1AHTR1DDRD2DRD4
Succinic Acid SCHEMBL16318529 0.88 HTR1B (0.69) HTR1BHTR1AHTR1DDRD2DRD4
Succinic Acid SCHEMBL7025602 0.88 HTR1B (0.69) HTR1BHTR1AHTR1DDRD2DRD4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0674621-B1 ENANTIOMERS OF CARBAZOLE DERIVATIVES AS 5-HT1-LIKE AGONISTS VERNALIS LTD (GB) 2003-02-26 EP claimed
US-5616603-A TREATING MIGRAINES SMITHKLINE BEECHAM PLC (GB) 1997-04-01 US claimed
EP-0674621-A1 ENANTIOMERS OF CARBAZOLE DERIVATIVES AS 5-HT1-LIKE AGONISTS SMITHKLINE BEECHAM PLC (GB) 1995-10-04 EP claimed
WO-1994014772-A1 ENANTIOMERS OF CARBAZOLE DERIVATIVES AS 5-HT1-LIKE AGONISTS SMITHKLINE BEECHAM PLC (GB) 1994-07-07 WO claimed
EP-0674621-B1 ENANTIOMERS OF CARBAZOLE DERIVATIVES AS 5-HT1-LIKE AGONISTS VERNALIS LTD (GB) 2003-02-26 EP disclosed
US-5962501-A HEADACHES SMITHKLINE BEECHAM, P.L.C. (GB) 1999-10-05 US disclosed
US-5917054-A ALKYLATING ENANTIOMER OF 3-AMINO-6-CARBOXAMIDO-1,2,3,4-TETRAHYDROCARBAZOLE OR A SALT SMITHKLINE BEECHAM P.L.C. (GB) 1999-06-29 US disclosed
US-5650426-A Enantiomers of carbazole derivatives as 5-HT.sub. 1-like agonists SMITHKLINE BEECHAM PLC (GB) 1997-07-22 US disclosed
US-5618947-A SEPARATING THE RACEMIC MIXTURE BY CHROMATOGRAPHY SMITHKLINE BEECHAM, P.L.C. (GB) 1997-04-08 US disclosed
US-5618948-A TREATMENT OF 6-CARBOXAMIDO-3-METHYLAMINO-1,2,3,4-TETRAHYDROCARBAZOLE WITH 2-PYRROLIDONE-5-CARBOXYLIC ACID, CRYSTALLIZATION SMITHKLINE BEECHAM P.L.C. (GB) 1997-04-08 US disclosed
US-5616603-A TREATING MIGRAINES SMITHKLINE BEECHAM PLC (GB) 1997-04-01 US disclosed